Yohimbine
Compound with spectra: 7 NMR, 3 FTIR, 1 Raman, and 5 MS (GC)
| 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 |
| Copyright | Copyright © 2012-2024 John Wiley & Sons, Inc. Portions provided by AAFS, Toxicology Section. All Rights Reserved. |
|---|---|
| Source of Spectrum | Mass Spectrometry Committee of the Toxicology Section of the American Academy of Forensic Sciences |
| Copyright | Copyright © 2012-2024 John Wiley & Sons, Inc. Portions provided by AAFS, Toxicology Section. All Rights Reserved. |
|---|---|
| Source of Spectrum | Mass Spectrometry Committee of the Toxicology Section of the American Academy of Forensic Sciences |
| Copyright | Copyright © 2012-2024 John Wiley & Sons, Inc. Portions provided by AAFS, Toxicology Section. All Rights Reserved. |
|---|---|
| Source of Spectrum | Mass Spectrometry Committee of the Toxicology Section of the American Academy of Forensic Sciences |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | J-56-2712-3 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | SWG-33-2030-0 |
| Copyright | Copyright © 2012-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Spectrum Chemical Manufacturing Corp. |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | Free base of Y1024 |
| Copyright | Copyright © 2018-2024 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2018-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Aldrich |
| Catalog Number | 230480 |
| 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 | CD3OD |
| 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 | CD3OD |
| Copyright | Copyright © 2021-2024 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2021 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Sigma-Aldrich Co. LLC. |
| Source of Spectrum | Sigma-Aldrich Co. LLC. |
| Catalog Number | 230480 |
| Solvent | CDCl3 |
| Copyright | Copyright © 2021-2024 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2021 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Sigma-Aldrich Co. LLC. |
| Source of Spectrum | Sigma-Aldrich Co. LLC. |
| Catalog Number | 230480 |
| Solvent | CDCl3 |
| Copyright | Copyright © 2018-2024 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2018-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Aldrich |
| Source of Spectrum | Sigma-Aldrich Co. LLC. |
| Catalog Number | 230480 |
| Technique | Mull |
| Copyright | Copyright © 2017-2024 Sigma-Aldrich Co. LLC. - Database Compilation Copyright © 2017-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Catalog Number | 230480 |
- Corynanthin
Pseudo-yohimbine
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
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 |
|---|---|---|
| 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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