522-94-1 Usage
Description
Allo-yohimbine is a chemical compound derived from yohimbine, an alkaloid found in the bark of the yohimbe tree. It is structurally similar to yohimbine and exhibits similar physiological effects, such as acting as an alpha-2 adrenergic receptor antagonist. Allo-yohimbine is being studied for its potential therapeutic applications, including the treatment of erectile dysfunction, metabolism and weight loss, as well as its potential as an antidepressant and anxiolytic agent.
Used in Pharmaceutical Industry:
Allo-yohimbine is used as a therapeutic agent for the treatment of erectile dysfunction due to its effects on alpha-2 adrenergic receptors, which may help improve erectile function.
Used in Metabolism and Weight Loss Applications:
Allo-yohimbine is used as a metabolic enhancer and weight loss aid, as it may help increase fat metabolism and promote weight loss.
Used in Antidepressant and Anxiolytic Applications:
Allo-yohimbine is used as a potential antidepressant and anxiolytic agent, as it is being investigated for its effects on mood and anxiety.
Research on allo-yohimbine is ongoing, and its full range of pharmacological effects and potential therapeutic applications are still being explored.
Check Digit Verification of cas no
The CAS Registry Mumber 522-94-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,2 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 522-94:
(5*5)+(4*2)+(3*2)+(2*9)+(1*4)=61
61 % 10 = 1
So 522-94-1 is a valid CAS Registry Number.
InChI:InChI=1/C21H26N2O3/c1-26-21(25)19-15-10-17-20-14(13-4-2-3-5-16(13)22-20)8-9-23(17)11-12(15)6-7-18(19)24/h2-5,12,15,17-19,22,24H,6-11H2,1H3/t12-,15+,17+,18+,19-/m1/s1
522-94-1Relevant articles and documents
Total Syntheses of Yohimbe Alkaloids, with Stereoselection for the Normal, Allo, and 3-Epiallo Series, Based on Annelations of 4-Methoxy-1,2-dihydropyridones
Kuehne, Martin E.,Muth, Randy S.
, p. 2701 - 2712 (2007/10/02)
N--2,3-dihydro-4-pyridone (31) was generated in two steps (77percent yield) from tryptamine and N-methyl-4-piperidone methiodide.Its cyclization (90percent yield) and oxidation (91percent yield) provided the tetracyclic analogue 32.O-Methylation and Robinson-type annelation of these vinylogous lactams (the latter in form of its Na-carbamate) furnished the dienones 38 (64percent) and 43 (90percent).Further elaboration by cyclization and/or reduction reactions selectively provided the 15,16-didehydroyohimbinones 7 and 44.Their reductions then led to yohimbinone (52, 20percent overall yield from tryptamine), alloyohimbinone (11, 19percent overall yield), and 3-epi-alloyohimbinone (10, 23percent overall yield), which led to yohimbine (3), β-yohimbine (9), 3-epi-alloyohimbine (53), and 3-epi-17-epi-alloyohimbine (54).
Total synthesis of yohimbine.
van Tamelen,Shamma,Burgstahler,Wolinsky,Tamm,Aldrich
, p. 7315 - 7333 (2007/10/04)
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