SpectraBase Compound ID | 5nrjDA6vgV1 |
---|---|
InChI | InChI=1S/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+/m0/s1 |
InChIKey | BLGXFZZNTVWLAY-SCYLSFHTSA-N |
Mol Weight | 354.45 g/mol |
Molecular Formula | C21H26N2O3 |
Exact Mass | 354.194343 g/mol |
Enantiomer InChIKey | BLGXFZZNTVWLAY-RWULDMNWSA-N |
Title | Journal or Book | Year |
---|---|---|
Chemical Composition of Aspidosperma ulei Markgr. and Antiplasmodial Activity of Selected Indole Alkaloids | Molecules | 2013 |
Hydroxylation of Yohimbine in Superacidic Media: One-Step Access to Human Metabolites 10 and 11-Hydroxyyohimbine | Journal of Natural Products | 2001 |
A Reinvestigation of the Oxidative Rearrangement of Yohimbane‐Type Alkaloids. Part A. Formation of pseudoindoxyl ( = 1,2‐dihydro‐3H‐indol‐3‐one) derivatives | Helvetica Chimica Acta | 1994 |
17α-O-Methylyohimbine and vallesiachotamine from roots ofAmsonia elliptica | Phytochemistry | 1990 |
General methods of synthesis of indole alkaloids. 14. Short routes of construction of yohimboid and ajmalicinoid alkaloid systems and their carbon-13 nuclear magnetic resonance spectral analysis | Journal of the American Chemical Society | 1976 |
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