Pseudo-yohimbine
Compound with spectra: 5 NMR, and 1 FTIR
| SpectraBase Compound ID | CpxveqQM3uC |
|---|---|
| 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-AECJZGCLSA-N |
| Mol Weight | 354.45 g/mol |
| Molecular Formula | C21H26N2O3 |
| Exact Mass | 354.194343 g/mol |
| Enantiomer InChIKey | BLGXFZZNTVWLAY-LRTZBTEVSA-N |
| Copyright | Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Iowa State College, Ames, Iowa |
| Technique | KBr WAFER |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- 3-EPI-BETA-YOHIMBINE
- psi-YOHIMBINE
- PSI-YOHIMBINE M
Yohimbine - isomer
3-EPI-ALPHA-YOHIMBINE
(+-)-3-epialloyohimbine
Yohimbine II
(+-)-3-epi-17-epi-alloyohimbine
Corynanthine
Yohimbine
Allo-yohimbine
(+)-BETA-YOHIMBINE
.alpha.-Yohimbine
BLGXFZZNTVWLAY-UHFFFAOYSA-N
Benz[g]indolo[2,3-a]quinolizine, yohimban-16-carboxylic acid deriv.
17-epi-alloyohimbine
Corynanthine
Yohimbine
Yohimban-16-carboxylicacid,17-hydroxy-,methyl ester
3-EPI-BETA-YOHIMBINE;(3-BETA,16-ALPHA,17-BETA)-YOHIMBAN-16-CARBOXYLIC-ACID-17-HYDROXY-METHYLESTER
| Title | Journal or Book | Year |
|---|---|---|
| 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 |
| Alkaloid distribution in Malaysian Uncaria | Phytochemistry | 1992 |
| Dimeric indole alkaloids from Uncaria callophylla | Phytochemistry | 1991 |
| 3-epi-β-yohimbine from roots of Rauwolfia linearifolia | Phytochemistry | 1991 |
| 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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