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#31 Hebbeh

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Posted 20 April 2013 - 03:34 AM

Is anyone still interested in this? I'll probably be leaving the forum after I can get this synthesized. Just way too much searching for some holy grail ideal compound. I'd be satisfied with this and tDCS. for all my nootropic purposes. AMPA'rs are a two edged sword with glutamate, C16 can have serious immunosuppresive side effects, like having your whole brain infected with the herpes virus, gabaa alpha 5 inverse agonists are a pain to synthesize; but have a great half life since they're based on a benzo structure, alpha 7 nicotinic PAM's are also elusive and have tough chemical structures. The list goes on.


I'm game...count me in.

#32 lourdaud

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Posted 20 April 2013 - 08:42 AM

Is anyone still interested in this? I'll probably be leaving the forum after I can get this synthesized. Just way too much searching for some holy grail ideal compound. I'd be satisfied with this and tDCS. for all my nootropic purposes. AMPA'rs are a two edged sword with glutamate, C16 can have serious immunosuppresive side effects, like having your whole brain infected with the herpes virus, gabaa alpha 5 inverse agonists are a pain to synthesize; but have a great half life since they're based on a benzo structure, alpha 7 nicotinic PAM's are also elusive and have tough chemical structures. The list goes on.


+1
This is probably the substance I'm most interested in. Really curious to see how it'd work for ADHD.
So please count me in, if there'll be any form of group purchase!

Edited by lourdaud, 20 April 2013 - 08:43 AM.


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#33 Reformed-Redan

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Posted 21 April 2013 - 03:49 PM

How's this looking? As a selegiline user I'd like to move on to Dr. Knoll's next more enhanced pro-life compound, anyone else?

My father would also benefit from this also, AFAIK.
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#34 Reformed-Redan

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Posted 21 April 2013 - 05:18 PM

Here is an awesome interview with Dr. Joseph Knoll M.D

Shattering the Barriers of Maximum Life Span: An Interview with Dr. Joseph Knoll
By David Jay Brown
Joseph Knoll, M.D., is a Hungarian neurochemist and pharmacologist. He is probably best known for developing the drug deprenyl (also known as Selegiline), the first selective MAO-B inhibitor, and he has researched the properties of deprenyl for over half a century.

[Quick Note: MAO is Monoa-mine Oxidase, an enzyme in the brain that breaks down neurotransmitters. By inhibiting the production of MAO, you increase the longevity of neurotransmitters in the synapses between neurons, and, consequently, the effects of those neurotransmitters. MAO-B is specific to break down the excitatory neurotransmitter dopamine. So by inhibiting MAO-B, you enhance the effects of dopamine in the brain.]

Dr. Knoll is also the author of the recently published book The Brain and Its Self: A Neurochemical Concept of Innate and Acquired Drives (Springer, 2005), which summarizes his life's research and his fascinating speculations about the relationship between brain activity and culture. In this book, Dr. Knoll describes how his experience as a Nazi concentration camp survivor helped to inspire and motivate much of his scientific research. Although his parents were sent to the gas chamber when he was a teenager, Dr. Knoll survived because he spoke fluent German and was chosen to serve as the personal servant to the Chief of the SS guards. In 1945, after the war, Dr. Knoll returned to his native city of Budapest. He earned his M.D. from the University of Budapest in 1951, and later became a professor and the head of the Department of Pharmacology at the Semmelweiss University of Medicine in Budapest.

In the early 1950s, Dr. Knoll helped to pioneer research into the physiological basis of innate and acquired drives in animals. Trying to make sense of his experience in the Nazi concentration camp, Dr. Knoll became interested in how animals acquire new drives. The research that resulted from Dr. Knoll's interest in this subject centered around studying the brain changes in rats that had been trained to have an acquired drive for an unnatural object—a glass cylinder.

This acquired drive—which urged the animals to search for, and jump to, the rim of a thirty centimeter-high glass-cylinder, and then crawl inside—would often override the animals' instinctive drives for food and sex.

Dr. Knoll first synthesized deprenyl in his Budapest laboratory in 1961.

He showed that deprenyl improves the availability of dopamine, and slows its age-related decline by acting as a selective MAO-B inhibitor. Even more importantly, according to Dr. Knoll, it has an enhancer effect, and it helps maintain healthy brain cells, particularly in the dopamine-producing area of the brain known as the substantia nigra—the area of the brain that degenerates with Parkinson's Disease. For this reason deprenyl has been used as an effective treatment for Parkinson's Disease. It has also been shown to be an effective treatment for Alzheimer's Disease and other brain disorders that result in cognitive decline.

Deprenyl has been shown to have many uses as a cognitive enhancer. It is a moderate-level stimulant and antidepressant that has been shown to improve memory, protect the brain against cell damage, alleviate depression, extend the life span of laboratory animals, and heighten sexual desire in both men and women. This impressive substance is available by prescription in the U.S., and although it is primarily prescribed to help people with Parkinson's disease, memory disorder problems, and sometimes depression, a lot of healthy people also use deprenyl to improve their mental performance. In fact, Dr. Knoll himself takes deprenyl every day, and recommends that every sexually mature person should be doing the same.

I've personally been using deprenyl as an antidepressant and cognitive enhancer for over ten years, and I can attest to its powerful brain-boosting effects. It improves my mental performance so dramtically that I've used it before every public talk that I've given since 1995.

Along with other cognitive enhancers, such as hydergine and piracetam, I think that deprenyl has incredible potential for enhancing memory, accelerating intelligence, and improving concentration. There is a good deal of scientific evidence to support these claims. For an excellent summary of the scientific studies in this area see John Morgenthaler and Ward Dean's book Smart Drugs and Nutrients II.

Many people report that deprenyl and other "smart drugs" have sexually-enhancing "side-effects," although deprenyl appears to have the leading reputation in this area. According to Dr. Dean—the coauthor of Smart Drugs and Nutrients—"anything that improves brain function is probably going to improve sexual functioning." This is probably because sexuality and health go hand-in-hand, and sexual vitality is a pretty good indicator of overall health.

Dr. Knoll and colleagues first reported indications for deprenyl's potential as a sexuality enhancer in 1983, with reports that old male rats had increased their "mounting frequency" and "intromission" when they were treated with deprenyl. This contrasted dramatically with the untreated control animals. Many anecdotal reports, from both men and women, have confirmed that these aphrodisiac-like effects apply to humans as well. Because deprenyl inhibits MAO—the dopamine-destroying enzyme—levels of the excitatory neurotransmitter dopamine rise in the brain, which generally causes people to feel more pleasure and become more physiologically aroused.

Interestingly, unlike most other MAO inhibitor drugs (such as the antidepressant Nardil), there are usually no dietary restrictions necessary when one takes deprenyl. When taken at moderate levels (under 10 mg), deprenyl only inhibits the action of a specific type of MAO—MAO B—which doesn't interfere with the body's ability to metabolize the dietary amine tyramine, like a broad-spectrum MAO inhibitor does. This is why most other MAO-inhibiting drugs carry the serious danger of triggering a hypertensive reaction if one eats tyramine-rich foods, like cheese or wine. Deprenyl has been described by researchers as working with great precision in this regard, and the physicians that I spoke with agreed that it was unusually safe.

In fact, deprenyl is better than safe. This truly remarkable drug has also been shown to increase the maximum lifespan of laboratory animals by close to forty percent. This is the equivalent of a human being living to be around one hundred fifty years of age. Giving deprenyl to animals is the only experimental treatment—besides caloric restriction—that has been shown to increase maximum life span.

[Quick Note: Extending maximum life span—as opposed to extending average life span—means extending the maximum number of years that the longest-lived members of a particular species has been known to attain.]

To fully appreciate how significant deprenyl's life extension potential is, one has to understand the difference between maximum life span and average life span. Many factors can affect the average lifespan (or the "normal life expectancy") that an animal lives—genetics, diet, exercise, nutritional supplements, mental attitude, etc. However, even under the very best of conditions, there is an upper limit at which the longest-lived animals of a particular species can survive, and that is the animal's maximum life span.

The average life span of a human being is approximately seventy to eighty years. However, the maximum life span of a human being is around one hundred twenty years. The laboratory animals in the deprenyl studies showed a forty percent increase in maximum life span, the human equivalent of living one hundred fifty years. Since deprenyl's primary effects work the same in all mammalian brains, it stands to reason that deprenyl's life extension effects are likely to carry over to humans, just as the mental benefits do. Many people have certainly verified that the increase in sex drive occurs in both humans and laboratory animals.

Following are some excerpts from the interview that I conducted with Dr. Knoll. Born in 1925, Dr. Knoll was eighty at the time of this interview. We spoke about how his experience with the holocaust influenced his decision to become a research scientist, how people can utilize deprenyl for its cognitive enhancing and anti-aging benefits, and what type of anti-aging treatments might be available in the future.

Q: How did your experience with the holocaust when you were young influence your decision to become a research scientist, and what inspired your interest in neurochemistry?
Dr. Knoll: It is a horrifying fact that in Germany millions of single-minded little-men, who had previously lived an honest, simple life and never belonged to extremist groups, dramatically changed within a few years after 1933 and, imbued with the Nazi ideology, became unbelievably cool-headed murders of innocent civilians during the Second World War. This phenomenon has been documented from many angles in dozens of novels, films, and so on. However, we are still waiting for an adequate elucidation of the brain mechanism responsible for this dramatic and rapid change in the behavior of millions.
As a survivor of Auschwitz, and one of the 1,300 survivors of the "Dachau Death Train," I had the opportunity to directly experience a few typical representatives of this type of manipulated human beings, and had more than enough time and direct experience to reflect upon the essential changes in the physiological manipulability of the human brain. It was therefore not just by mere chance that, when in the early 1950s I finally had the opportunity to approach this problem experimentally, I decided to develop a rat model to follow the changes in the brain in the course of the acquisition of a drive from the start of training until its manifestation.

Q: What are some of the disorders that deprenyl has proven itself to be an effective treatment for?
Dr. Knoll: Successful clinical studies with deprenyl were executed in depression and in the two age-related neurodegenerative diseases: Parkinson's Disease and Alzheimer's Disease. The first clinical study performed in depressed patients by Dr. Varga with deprenyl was published in 1965. The clinical use of deprenyl in Parkinson's Disease started in 1977. The first two papers demonstrating the effectiveness of deprenyl in Alzheimer's Disease appeared in 1987. Deprenyl was originally developed with the intention to be used as a new spectrum antidepressant. Its effectiveness was first demonstrated with the racemic form of the compound by Dr. Varga and his coworkers in 1965 and 1967, and with the enantiomer in 1971. The first study that corroborated the antidepressant effect of deprenyl was published by Dr. Mann and Dr. Gershon in 1980.

The realization of the peculiar effect of deprenyl—first in Parkinson's Disease and later in Alzheimer's Disease—distracted attention from its antidepressant property which remains unutilized. Even an especially interesting aspect of this problem fell into oblivion. In a depression study performed by Dr. Birkmayer and his coworkers in 1984 on a 102 outpatients and 53 inpatients, deprenyl was given together with phenylalanine. The latter is the precursor of phenylethylamine (PEA) that, in contrast to PEA, crosses the blood-brain barrier and, as it is metabolized in the brain, increases the concentration of this natural enhancer substance. Nearly seventy percent of the patients achieved full remission from depression. The outstanding clinical efficiency was equaled only with that of electroconvulsive treatment, but without the latter's side effect of memory-loss.

Q: How might healthy people utilize deprenyl for its cognitive enhancing and antiaging benefits?
Dr. Knoll: They should take one milligram of deprenyl daily from sexual maturity until death.

Q: Some studies have shown that deprenyl can significantly increase the maximum life span of laboratory animals, yet some of the longevity researchers that I've spoken with told me that these findings have been difficult to replicate. Why do you think this is, and what are your thoughts about this?
Dr. Knoll: Our finding that deprenyl prolongs life was corroborated in mice, in rats, in hamsters, and in dogs. Nevertheless, variation in the extent of the prolongation of life between the longevity studies performed in different laboratories was unusually high. The reason for this variation is now clear. A bell-shaped concentration effect curve is characteristic to the enhancer effect of the synthetic mesencephalic enhancer substances. Thus, there is an optimum dose for the enhancer effect.
Concerning the optimum dose of deprenyl there are, not only species, but also strain differences. On the other hand, even the effect of an optimum dose depends on the selected experimental conditions. We worked, for example, with the long-lived, robust, Wistar-Logan strain, which seldom grows tumors. The age of rats at the start of treatment was two years in our first study and roughly eight months in our second study.

In both studies a substantial number of rats treated with deprenyl lived longer than the estimated technical life span of three and a half years.

Dr. Milgram and colleagues were the first who repeated our survival study with deprenyl. They clearly intended to hold tightly to the parameters we used in our first study, and started experiments with two year old rats and treated them with 0.25 milligrams per kilogram of deprenyl. They changed, however, an important parameter. They worked with the short-lived Fischer 344 strain of rats, thus, they started treatment too late and found only a sixteen percent marginally significant prolongation of life span. Nevertheless, they found a convincingly significant increase in the longer survival.

Dr. Kitani and colleagues, who conducted the second control survival study with deprenyl, also used Fischer 344 rats. They obviously considered that these rats are shorter living than the Wistar-Logan rats, and they started to work with one and a half year old rats. This was an advantageous change in the experimental conditions and found a satisfyingly significant, thirty-four percent prolongation of the average life span.

However, in the hope to increase the effectiveness of their treatment they doubled the dose of deprenyl. Although a higher dose is usually more effective than a lower one, the doubling of the dose was in this special case an unfavorable change. We know now that 0.01 milligrams per kilogram of deprenyl is sufficient to exert an enhancer effect. Thus the 0.5 milligrams per kilogram dose was obviously enormously high, and this explains why Kitani and colleagues found no sign of the significant extension in the longest survival which appeared in our studies and in the Milgram et al. study.

All in all, in future longevity studies with a synthetic mesencephalic enhancer substance, it is reasonable to treat the animals with a dose that in preliminary studies proved to exert a peak effect in enhancing the release of catecholamines and serotonin in the brain stem.

Q: What do you think are the primary causes of aging in general?
Dr. Knoll: Various species live together on earth in a harmonious proportion. This is obviously carefully regulated. One of the seemingly principal regulatory mechanisms that produces equilibrium among living organisms is brain aging. It ultimately leads to the elimination of those individuals who have already fulfilled their duty in nurturing the new generation.
Accordingly, the period from weaning until sexual maturity is reached is the most delightful phase of life, the glorious uphill journey. The individual progressively takes possession, on a mature level, of all abilities crucial for survival and maintenance of the species. It learns to avoid dangerous situations, masters the techniques to obtain its food, develops procreative powers for sexual reproduction and copulates.

This is, at the same time, the climax of developmental longevity. The fully sexually mature individual fulfills its duty. Thus, to maintain the precisely balanced out natural equilibrium among living organisms, the biologically "useless" individual has to be eliminated. According to the inborn program, the postdevelopmental stage of life (aging) begins. The essence of this stage is progressive decay of the efficiency of the catecholaminergic system during the postdevelopmental life span until at some point, in an emergency situation, the integration of the parts in a highly sophisticated entity can no longer be maintained and "natural death," signaled by the disappearance of the EEG signal, sets in.

Q: What do you think are currently the best ways to slow down, or reverse, the aging process and extend the human life span?
Dr. Knoll: Regarding the quality and duration of life, the most important aging process is the continuous, slow, age-related decline of the mesencephalic enhancer regulation during the postdevelopment phase of life. This can not be reversed, but its progress can be slowed by the prophylactic administration of a synthetic mesencephalic enhancer substance (for the time being with the daily administration of one milligram of deprenyl). The earlier this protective treatment starts, the better are the prospects to improve the quality of life in the latter decades, which necessarily goes together with an extension of life span.

Q: How long do you think it's possible for the human life span to be extended?
Dr. Knoll: The average life span in the most developed countries has already exceeded the eighty year level. This change has come about due to the prevention of premature deaths owing to the development of hygiene, immunology, and chemotherapy. The human technical life span (TLSh), close to one hundred twenty years, has remained, however, unchanged.
In my view, to extend the human life span beyond the TLSh needs the elaboration of an ultimate technique for the prophylactic, daily small-dose administration of a safe synthetic mesencephalic enhancer substance from sexual maturity until death. The attainable upper limit in the extension of the TLSh is obviously unpredictable at present.

Nevertheless, if brain research could, at some time in the future, achieve just a doubling of the TLSh, this will mean for humans the most significant accomplishment that science has ever achieved, since nothing can be more important for the individual than the quality and duration of his/her life.

Q: What are some of the new anti-aging treatments that you foresee coming along in the near future?
Dr. Knoll: In the developed countries the proportion of the aged is high, and the estimated number of individuals over sixty-five will increase to 1.1 billion by 2050. Accordingly, the demand on anti-aging therapy is rapidly increasing. This trend explains the already high-sounding proposals for anti-aging treatments.
My view is that since the brain alone ensures that the mammalian organism works as a purposeful, motivated, goal-directed entity, the age-related changes in the central nervous system are of particular importance. And since the enhancer-sensitive neurons in the brain stem work as the engine of the brain, the slow, continuous, postdevelopmental functional decline of the mesencephalic enhancer regulation is of primary importance in the maintenance of the well-balanced equilibrium among living organisms, because it helps to eliminate the individuals who already fulfilled their duty in nurturing the new generation.

For the time being the prestigious task—the maintenance of the mesencephalic enhancer regulation during the postdevelopmental phase of life on the enhanced level characteristic of developmental longevity—cannot be fully accomplished. However, it is already feasible to modestly slow the age-related decay of the catecholaminergic and trace-aminergic tone in the brain via the prophylactic administration of one milligram of deprenyl daily.

The development of BPAP—a synthetic mesencephalic enhancer substance that is at least a hundred times more potent than deprenyl—is by itself a hint that our present knowledge about the mesencephalic enhancer regulation is in a very early stage. The high potency of BPAP indicates already that much more potent natural enhancer substances than PEA and tryptamine might exist. Better understanding of mesencephalic enhancer regulation promises to develop more efficient techniques in the future to slow brain aging and prolong human life beyond the TLSh. According to my judgment, this is the only physiologically well-founded, feasible, antiaging therapy that I foresee coming along in the future that has a chance, in the long run, to remain the method to continuously improve the quality, and prolong the duration of human life.

We shall never forget that humans obviously cannot change natural laws, but by discovering their mechanisms of action they learn to make use of this knowledge. By conquering gravitation man stepped across his naturally given limit and ultimately landed on the moon. By conquering the age-related decline of the mesencephalic enhancer regulation man might in the future step across also this naturally given limit and extend human life span beyond the TLSh.

Q: What are you currently working on?
Dr. Knoll: My ambition is to develop a more efficient compound than deprenyl for slowing the age-related decay of the mesencephalic enhancer regulation, and to detect the envisioned unknown mesencephalic enhancer substances, expected to be several thousand times more active than PEA or tryptamine. Currently we are trying to clarify in more detail the pharmacological spectrum of BPAP—our newly developed, tryptamine-derived, synthetic mesencephalic enhancer substance.

David Jay Brown is the author of four volumes of interviews with leading-edge thinkers, Mavericks of the Mind, Voices from the Edge, Conversations on the Edge of the Apocalypse, and Mavericks of Medicine. (Mavericks of Medicine will be published by Smart Publications as a book in late 2006.) He is also the author of two science fiction novels, Brainchild and Virus. David holds a master’s degree in psychobiology from New York University, and was responsible for the California-based research in two of British biologist Rupert Sheldrake’s bestselling books on unexplained phenomena in science: Dogs That Know When Their Owners Are Coming Home and The Sense of Being Stared At. To find out more about David’s work visit his award-winning web site: www.mavericksofthemind.com.


Edited by yadayada, 21 April 2013 - 05:19 PM.

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#35 **DEACTIVATED**

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Posted 21 April 2013 - 05:44 PM

yadayada,

I've gone over everything so far, i'll read the "Shattering the Barriers of Maximum Life Span: An Interview with Dr. Joseph Knoll" later.

Consider having one more. Do you have the link to the LEF thread with the first hand experiences?
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#36 violetechos

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Posted 21 April 2013 - 06:58 PM

<------------WANTS!

Willing to shell out under 50 $ us for a years supply.

#37 meatsauce

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Posted 21 April 2013 - 11:04 PM

I am interested in a group buy
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#38 SUB-Rx

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Posted 21 April 2013 - 11:18 PM

I would contribute to a group buy as well.
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#39 Passion

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Posted 22 April 2013 - 01:52 AM

Have there been any studies that measure the effects of BPAP on the lifespan/cognition of rodents or is BPAP's predicted success fully based Deprenyll? I've never looked into Deprenyll but after reading that interview posted by yadayada, I'm really thinking about it! If BPAP is even more effective than Deprenyll, I'm definitely in for a group buy as well but I think I'd like to see at least some rodent studies.

If we did a group buy, could we be certain that the substance would last several years without degrading?

P.S.: I plan on buying Deprenyll right after this post. Thanks for that awesome interview yadayada.
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#40 Reformed-Redan

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Posted 22 April 2013 - 02:06 AM

Have there been any studies that measure the effects of BPAP on the lifespan/cognition of rodents or is BPAP's predicted success fully based Deprenyll? I've never looked into Deprenyll but after reading that interview posted by yadayada, I'm really thinking about it! If BPAP is even more effective than Deprenyll, I'm definitely in for a group buy as well but I think I'd like to see at least some rodent studies.

If we did a group buy, could we be certain that the substance would last several years without degrading?

P.S.: I plan on buying Deprenyll right after this post. Thanks for that awesome interview yadayada.

Dr. Knoll explains that the longevity effect of deprenyl is mediated by the enhancement of catelocholamine pathways. Obviously, I haven;t read everything about deprenyl; but, I'll still look around.

lol, some jerk is down-rating posts above.
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#41 daouda

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Posted 22 April 2013 - 11:38 PM

OK thanks to yadayada's post in another thread I got my attention attracted to this compound and it does look very good. Ive had great results from low dose selegiline and rasagiline (alternatively not simultaneously), so I would probably benefit from BPAP.
How is the group buy functioning ?

#42 Reformed-Redan

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Posted 23 April 2013 - 12:50 AM

I think there is a misconception of rasagiline if one wants to extend their lifespan. Rasagiline AFAIK does not posses the longevity promoting catecholamine enhancer effects of deprenyl or the newer and mroe potent catecholamine enhancer, BPAP.

lol, I'm uprating the downrated post that some jerk is downrating in this thread. lol
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#43 ricko321

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Posted 23 April 2013 - 04:56 AM

hi im interested in the group buy also can we do overnight shipping

#44 Reformed-Redan

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Posted 23 April 2013 - 05:20 AM

More info on (-)-BPAP from Paul Wakfer.

R-(-)-1-(benzofuran-2-yl)-2-propylaminopentane - (-)-BPAP

A chemical for brain health, nootropic potential, mood enhancement and potentially life extension, often compared with Deprenyl.


Below we present a summary of the major research results for (-)-BPAP, taken from published studies in the peer-reviewed literature. In summary:
(-)-BPAP is a powerful catecholaminergic/serotoninergic activity enhancer over 100 times as effective as deprenyl (which it was invented to replace), with a broader spectrum of neurotransmitter enhancement effects and without the negative amphetamine and MOA inhibition side effects. It has been shown to have anti-depression, neurotrophic and brain antioxidative benefits. Moreover, with a better safety profile than deprenyl, BPAP appears to have even more life extension potential than deprenyl although this last is yet untested in any mammal.

Safety, Pharmacology and Interactions

1. "(-)-Deprenyl, the only synthetic enhancer substance in clinical use is known to be a safe, well-tolerated drug. Since (-)-BPAP, ... a deprenyl-derived enhancer substance being free of the MAO-B inhibitory property ... which is ... at least 100-times more potent than (-)-deprenyl, has even a better safety margin than (-)-deprenyl, we may expect that 100-times higher doses of (-)-BPAP than the ones that exert an enhancer effect can be administered without risk of significant side-effects."R

2. "(-)-BPAP did not show any effects on spontaneous norepinephrine release. Thus, (-)-BPAP did not exert tyramine-like norepinephrine releasing action. ... Furthermore, we demonstrated that (-)-BPAP inhibited tyramine-induced norepinephrine release ... (-)-BPAP, as demonstrated here, has a similar action to (-)-deprenyl ["a blockade of (-)-deprenyl against the 'cheese effect' induced by tyramine"] concerning potential to participate in hypertensive crisis. As (-)-BPAP has an affinity to catecholamine transporters which are also carriers for tyramine, the inhibitory action of (-)-BPAP on tyramineinduced norepinephrine release may be due to its tyramine uptake inhibitory action. In the present study, (-)-BPAP was also demonstrated not to influence spontaneous dopamine release, and to reduce tyramine-induced dopamine release, as was the case for norepinephrine. Thus, (-)-BPAP inhibits the effect of tyramine."R

3. "in rats ... (-)-BPAP-14C ... was well absorbed after i.p., s.c. and oral treatment and Cmax has been reached at 30 to 60 min following drug administration. A second peak, detected at 4 hours, indicated enterohepatic circulation of the substance. The highest tissue levels ... were reached at 30 min following s.c. treatment. ... A similar distribution profile was observed in the brain regions with a peak level at 30 min. ... is preferentially eliminated through the urine, the secondary route of excretion was the stool. More than 90% of the substance was recovered in the excreta during 72 hours. The t1/2 beta was found to be 5.5 to 5.8 hours. (-)-BPAP was well absorbed and penetrated the brain. Its elimination was fast and enterohepatic circulation was observed in rats."R

4. "(-)Deprenyl (Selegiline), for the time being the only CAE [catecholaminergic activity enhancer] substance in clinical use free of the catecholamine releasing property, is metabolized to methamphetamine and amphetamine and is also a highly potent and selective MAO-B inhibitor. To get rid of these, from point of view of the CAE effect, disadvantageous properties of the compound, we synthetized [sic] in the early '90s deprenyl analogues not metabolized to amphetamines and free of the MAO inhibitory effect."

5. "Our selected reference compound, (-)-BPAP, ... a much more potent enhancer of the impulse propagation mediated release of catecholamines and serotonin in the brain than ... (-)-deprenyl ... and a compound structurally unrelated to PEA [phenylethylamine] and the amphetamines, seems to be an especially promising experimental tool for studying the nature and the physiological role of the CAE/SAE [catecholaminergic/serotoninergic activity enhancer] mechanism in the brain. ..."

6. "(-)-BPAP, obviously because of its close structural similarity to tryptamine, is a weak, selective inhibitor of MAO-A, but this effect is from pharmacological point of view not significant."R


Proven Benefits

1. In cultured rat and human cells, which "work under catecholaminergic influence", subjected to hypoxia, "(-)-BPAP and (-)-deprenyl, due to their enhancer effect, exerted a significant cytoprotective effect"R

2. "in rat mesencephalic slice cultures ... R-(-)-BPAP significantly increased the mRNA and protein levels of BDNF [brain-derived neurotrophic factor], without affecting the level of NT-3 mRNA. In addition, R-(-)-BPAP significantly increased the mRNA level of trkB [a cell receptor], but not that of p75(NTR) [another cell receptor]. These effects of R-(-)-BPAP may result in enhanced BDNF/trkB signaling, and could thus underlie the potential neurotrophic and antidepressant actions of this drug."

3. "Brain-derived neurotrophic factor (BDNF) is a member of the neurotrophin family that plays an important role in regulating survival, differentiation, and functional integrity of central neurons. BDNF interacts with a specific trkB receptor kinase and with a low-affinity receptor p75NTR. Deficiencies of neurotrophins and their receptors are regarded as an important aspect of the pathogenesis of neurodegenerative disorders. Dopaminergic neuronal death in Parkinson's disease has been associated with the depletion of neurotrophins, such as BDNF and nerve growth factor (NGF). Indeed, the levels of neurotrophins, especially BDNF, were markedly reduced in the substantia nigra of Parkinson's disease patients, in whom selective degeneration of dopaminergic neurons is evident. Therefore, pharmacological stimulation of endogenous neurotrophin synthesis is expected to become a useful therapeutic approach for Parkinson's disease. R-(-)-1-(Benzofuran-2-yl)-2-propylaminopentane [R-(-)-BPAP], a potent

4. "catecholaminergic and serotonergic activity enhancer", enhances the electric field stimulation-induced release of catecholamine and serotonin from isolated rat brain stem. Because of its "catecholaminergic and serotonergic activity enhancer" effects, R-(-)-BPAP ameliorates motor deficits in reserpine-treated rats and improves active avoidance behavior in rats under tetrabenazine-induced depression. Therefore, this drug is a promising candidate as a treatment for symptoms of depression as well as for Parkinson's disease. .... Recently, the induction of BDNF/trkB signal was implicated as an important mechanism of action of antidepressants. For example, the infusion of BDNF into the midbrain produces antidepressant-like effects in an animal model of depression. Interestingly, R-(-)-BPAP is reported to produce antidepressant-like activity in rats with tetrabenazine-induced depression. ... Our findings suggest that R-(-)-BPAP, in addition to action mediated by its "catecholaminergic and serotonergic activity enhancer" effect, may serve as a neuroprotective agent for the treatment of progressive neurodegenerative disorders."R

5. "(-)-Deprenyl, a prototype of the phenylethylamine-derived synthetic enhancer substances, stimulates the catecholaminergic neurons in the brain but is almost ineffective on the serotonergic neurons. R-(-)-1-(benzofuran-2-yl)-2-propylaminopentane, (-)-BPAP, the recently developed tryptamine-derived selective synthetic enhancer substance, is a hundred times more potent enhancer of the catecholaminergic neuronal activity than (-)-deprenyl, and is also a highly potent stimulant of the serotonergic neurons. Evaluation of the peculiar pharmacological profile, the high potency and unusual safeness and tolerability of (-)-BPAP cherish the hope that this compound by itself and in combination with uptake inhibitors may improve the effectiveness of drug therapy in major depression and diminish the number of therapy resistant cases. ... (-)-BPAP, the first tryptamine-derived selective and highly potent synthetic enhancer substance that opens a previously unknown possibility to keep the activity of the noradrenergic, dopaminergic, and serotonergic neurons in the brain on a higher activity level. ... Since (-)-deprenyl is a highly potent and selective inhibitor of MAO-B, a structure-activity relationship study was performed to develop a deprenyl-derived enhancer substance being free of the MAO-B inhibitory property, and (-)-PPAP is at present the reference substance with this pharmacological profile."R1,R2

6. "(-)-BPAP may block tyramine-induced adverse effects such as hypertensive crisis. The actions of (-)-BPAP on the spontaneous and tyramine-induced dopamine release resembled its effects on norepinephrine release. We conclude that (-)-BPAP is not only catecholaminergic and serotonergic activity enhancer, but also a norepinephrine and dopamine uptake inhibitor and a weak serotonin uptake inhibitor that does not possess a tyramine-like action on catecholamine release, and is an inhibitor of tyramine-induced release of norepinephrine. ... Based on the dopamine deficiency theory, activation of the dopaminergic system by (-)-BPAP may be useful for the improvement of motor deficits in patients with early Parkinson's disease. (-)-BPAP is also expected to improve the non-motor functional deficits such as depression that is observed in Parkinson's disease, is unresponsive to anti-Parkinsonian drugs"R

7. "in cultured mouse astrocytes ... The amounts of NGF [nerve growth factor], BDNF [brain-derived neurotrophic factor], and GDNF [glial cell line-derived neurotrophic factor] secreted from astrocytes into the culture medium increased by up to 120, two, and seven times higher than those of the control, respectively, by treatment with 0.35 mM (-)-BPAP for 24 h. ... Furthermore, the treatment with (-)-BPAP for 6 h increased the mRNA expression of NGF, BDNF, and GDNF. These results suggest that (-)-BPAP up-regulated neurotrophic factor synthesis in cultured astrocytes."R

8. "These findings suggested that a "catecholaminergic and serotoninergic activity enhancer" compound, (-)-BPAP, stimulates motor function in rats and improves motor deficits in animal models of Parkinson's disease due to its ability to induce dopamine release."R

9. "The chemical reactions between (-)-BPAP and .OH were studied ... (-)-BPAP was proved to be a good radical scavenger. It was found that every atom of the benzofuran ring, except carbon 3, was capable of easily trapping the radical, where the most active site was carbon 1 on the furan part. ... Since the single radical trapping products were still radicals, these could trap further radicals by way of cascade without any activation energy. Thus, the double radical trapping products were very stable ..."R

10. "These findings suggest that (-)-BPAP [has] unique survival activity on cortical neurons through sigma receptors."R


Potential Benefits

1. "This paper presents that a series of benzofuran derivatives prevented apoptosis induced by an endogenous neurotoxin ... it remains to be clarified whether BPAP derivatives activate transcription factors, such as NF-KB, to induce anti-apoptotic genes. In addition, the relation of the gene induction to catecholaminergic-serotonergic enhancing effects should be further examined to elucidate the mechanism behind neuroprotection by a series of BPAP derivatives."R

2. "This substance [(-)-BPAP], which is specific and hundreds of times more potent than selegiline, is now the best experimental tool to study the enhancer regulation in the mesencephalon and a promising candidate to significantly surpass the therapeutic efficiency of selegiline in depression, Parkinson’s disease, and Alzheimer’s disease."R

3. "Antiaging compounds: (-)deprenyl (selegeline) and (-)1-(benzofuran-2-yl)-2-propylaminopentane, [(-)-BPAP], a selective highly potent enhancer of the impulse propagation mediated release of catecholamine and serotonin in the brain."

4. "Hundreds of millions of people now die over the age of 80 years primarily due to twentieth century progress in hygiene, chemotherapy, and immunology. With a longer average lifespan, the need to improve quality of life during the latter decades is more compelling. "Aging--The Epidemic of the New Millenium," a recent international conference (Monte Carlo, June 17-18, 2000), showed with peculiar clarity that a safe and efficient drug strategy to slow the age-related decay of brain performance is still missing. This review summarizes the physiologic and pharmacologic arguments in favor of a peculiar lifelong prophylactic medication with reasonable chances to keep in check brain aging and decrease the precipitation of age-related neurological diseases."R


Additional Related Papers

1. "The recent discovery of the enhancer regulation in the mammalian brain brought a different perspective to the brain-organized realization of goal-oriented behavior, which is the quintessence of plastic behavioral descriptions such as drive or motivation. According to this new approach, ‘drive’ means that special endogenous enhancer substances enhance the impulse-propagation-mediated release of transmitters in a proper population of enhancersensitive neurons, and keep these neurons in the state of enhanced excitability until the goal is reached. However, to reach any goal needs the participation of the catecholaminergic machinery, the engine of the brain. We developed a method to detect the specific enhancer effect of synthetic enhancer substances [(-)-deprenyl, (-)-PPAP, (-)-BPAP] by measuring the release of transmitters from freshly isolated selected discrete brain areas (striatum, substantia nigra, tuberculum olfactorium, locus coeruleus, raphe) by the aid of HPLC with electrochemical detection. To test the validity of the working hypothesis that in any form of goal-seeking behavior the catecholaminergic and serotonergic neurons work on a higher activity level, we compared the amount of norepinephrine, dopamine, and serotonin released from selected discrete brain areas isolated from the brain of sated and food-deprived rats. Rats were deprived of food for 48 and 72 hours, respectively, and the state of excitability of their catecholaminergic and serotonergic neurons in comparison to that of sated rats was measured. We tested the orienting–searching reflex activity of the rats in a special open field, isolated thereafter selected discrete brain areas and measured the release of norepinephrine, dopamine, and serotonin from the proper tissue samples into the organ bath. The orienting–searching reflex activity of the rats increased proportionally to the time elapsed from the last feed and the amount of dopamine released from the striatum, substantia nigra and tuberculum olfactorium, that of norepinephrine released from the locus coeruleus and that of serotonin released from the raphe increased significantly in the hungry rats proportionally to the time of fasting. For example: the amount of dopamine released from the substantia nigra of sated rats (4.62 +- 0.20 nmoles/g wet weight) increased to 5.95 +- 0.37 (P < 0.05) and 10.67 +- 0.44 (P < 0.01) in rats deprived of food for 48 and 72 hours, respectively."R

2 . "In the cultured astrocytes incubated for 24 h with selegiline, the synthesis of NGF [nerve growth factor] and BDNF [brain-derived neurotrophic factor] was significantly enhanced in the concentration dependent manner, with minimum effective concentrations of 4 x 10-4 and 5 x 10-4 M, respectively. (–)-BPAP also enhanced the NGF,BDNF andGDNF synthesis, with minimum effective concentrations of 5 x 10-5, 1 x 10-5, and 1 x 10-6 M, respectively."R

3. "As (-)-BPAP is for the time being the most selective and most potent available stimulant of the enhancer-sensitive midbrain neurons, we prefer to use this compound in examining the mechanism of action of the enhancer substances. This study is an in vivo and ex vivo analysis of the characteristic dose/concentration dependency of the enhancer effect of (-)-BPAP on catecholaminergic and serotoninergic neurons."R




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From: http://morelife.org/...chems/BPAP.html

Edited by yadayada, 23 April 2013 - 05:23 AM.

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#45 autopilot

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Posted 23 April 2013 - 09:51 AM

Just a bit off topic- i cant seem to get an answer how to take my 1/4 pill of 1.25 mg selegiline-orally or sublingually. i have now started taking it orally with food after getting my mouth sore with sublingual intake in just four days.
i am happy to get in group buy. sounds promising.

#46 autopilot

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Posted 23 April 2013 - 09:58 AM

Is anyone still interested in this? I'll probably be leaving the forum after I can get this synthesized. Just way too much searching for some holy grail ideal compound. I'd be satisfied with this and tDCS. for all my nootropic purposes. AMPA'rs are a two edged sword with glutamate, C16 can have serious immunosuppresive side effects, like having your whole brain infected with the herpes virus, gabaa alpha 5 inverse agonists are a pain to synthesize; but have a great half life since they're based on a benzo structure, alpha 7 nicotinic PAM's are also elusive and have tough chemical structures. The list goes on.


are you alreaady into tDCS? any suggestions how to make a start?
thanks

#47 eddielang

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Posted 23 April 2013 - 11:20 AM

I am also interested in the group buy.

#48 datrat

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Posted 23 April 2013 - 05:09 PM

Count me in on the group buy.

#49 **DEACTIVATED**

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Posted 23 April 2013 - 08:14 PM

Damn.. I can't find hardly any anecdotal experiences with this chemical.. It looks like "Paul Wakfer", whoever this man is, gave it a shot but discontinued it's use after 15 months and no clear benefits. His response to the drug can be seen here: http://health.groups...fe/message/1990

Note that he also doesn't receive any noticeable effects from Deprenyl either, weird.

Stephen_b, a member of this forum also discontinued it's use. He did not go into full detail but stated that it had the same effects Deprenyl does, but that he could not tolerate it. Scroll down to post #12 in this thread for that: http://www.longecity...lement-regimen/

By chance I happen to stumbled upon a later post on a yahoo message board where "Stephen Boulet", probably Stephen_B, considered trying BPAP out again! But, there's still no data regarding it's effects even in this yahoo discussion. The post can be viewed here with it's replies: http://health.groups...fe/message/1977

Ultimately it looks like we're on our own but everything points to the chemical being on the safe side.. I'm still feeling adventurous.

In the interview above it states that BPAP acts as a dopamine reuptake inhibitor. Could it be safe to combine with Deprenyl then?
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#50 Reformed-Redan

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Posted 23 April 2013 - 08:19 PM

Damn.. I can't find hardly any anecdotal experiences with this chemical.. It looks like "Paul Wakfer", whoever this man is, gave it a shot but discontinued it's use after 15 months and no clear benefits. His response to the drug can be seen here: http://health.groups...fe/message/1990

Note that he also doesn't receive any noticeable effects from Deprenyl either, weird.

Stephen_b, a member of this forum also discontinued it's use. He did not go into full detail but stated that it had the same effects Deprenyl does, but that he could not tolerate it. Scroll down to post #12 in this thread for that: http://www.longecity...lement-regimen/

By chance I happen to stumbled upon a later post on a yahoo message board where "Stephen Boulet", probably Stephen_B, considered trying BPAP out again! But, there's still no data regarding it's effects even in this yahoo discussion. The post can be viewed here with it's replies: http://health.groups...fe/message/1977

Ultimately it looks like we're on our own but everything points to the chemical being on the safe side.. I'm still feeling adventurous.

In the interview above it states that BPAP acts as a dopamine reuptake inhibitor. Could it be safe to combine with Deprenyl then?

I sent him an e-mail a while back about BPAP. He restarted taking it as long as he has the vials afaik. Mind you, he takes some fifty other supplements so at that amoun of supplements I don't see how you can discern the effect of one compound from another. As for me, I'd just stick with this compound, maybe combine it with deprenyl as I suggested to Paul Wakfer and continue my simple supplements. Bacopa and ALCAR, zinc, aspirin, exercise, b vitamines. I don't have the time nor inclination (monetary ability) to do too many group buys.

Edited by yadayada, 23 April 2013 - 08:21 PM.

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#51 Reformed-Redan

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Posted 24 April 2013 - 03:33 AM

I'll be looking for a supplier soon. Anyone else is open to do so also and see prices and specifications.
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#52 Reformed-Redan

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Posted 24 April 2013 - 04:58 AM

So, we have 15 people interested in the group buy so far.
Metagene
peakplasma
Hebbeh, can always count on you for a group buy. :D
lourdaud
CrackaLackN, though has been on the fence.
lenses,
meatsauce
SUB-Rx
Passion, >?
daouda, pleasure to have you, :D
ricko321
indranghimiray
eddielang
datrat
and me

Nice

Anyone else who is willing and able to be in this group buy please let me know. Five more spots to claim.

This compound and IDRA-21 and I'm done here. Haha!
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#53 **DEACTIVATED**

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Posted 24 April 2013 - 05:22 AM

Hah, signing off the board completely then? You'll miss the next big thing ;). I am in btw.

#54 Reformed-Redan

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Posted 24 April 2013 - 05:39 AM

Hah, signing off the board completely then? You'll miss the next big thing ;). I am in btw.

Yeah, just don't have that much time. Might lurk around just watching for that next big thing. Hah. Awesome that you're in. :-D

#55 Reformed-Redan

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Posted 24 April 2013 - 05:26 PM

Did I mention that 1g of BPAP would last you your lifetime? lol

#56 Googoltarian

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Posted 24 April 2013 - 07:27 PM

Shattering the Barriers of Maximum Life Span: An Interview with Dr. Joseph Knoll

Did I mention that 1g of BPAP would last you your lifetime? lol


Acorrding to material you quoted this statment might not be true... ;)

#57 Reformed-Redan

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Posted 24 April 2013 - 07:29 PM

Well it depends when you die. But i agree 34 years is likely not a lifetime

Edited by yadayada, 24 April 2013 - 07:32 PM.

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#58 Reformed-Redan

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Posted 24 April 2013 - 09:23 PM

Q did it! has joined the fray. We'll most likely be doing a smaller group buy composed of 10 people including myself. Can I please get a hands up for a cost of possibly $200 per each person. I still have yet to contact suppliers and get a definitive quote. This group buy will take some time since the last couple of group buys may have exhausted available funds from longecity users.
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#59 SUB-Rx

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Posted 24 April 2013 - 09:26 PM

I'm still interested at that price.

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#60 eddielang

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Posted 24 April 2013 - 10:14 PM

Still in




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