Quinagolide
Compound with spectra: 11 MS (LC)
| SpectraBase Compound ID | 2BKOsi6Yw67 |
|---|---|
| InChI | InChI=1S/C20H33N3O3S/c1-4-10-22-14-17(21-27(25,26)23(5-2)6-3)11-16-12-18-15(13-19(16)22)8-7-9-20(18)24/h7-9,16-17,19,21,24H,4-6,10-14H2,1-3H3 |
| InChIKey | GDFGTRDCCWFXTG-UHFFFAOYSA-N |
| Mol Weight | 395.6 g/mol |
| Molecular Formula | C20H33N3O3S |
| Exact Mass | 395.224263 g/mol |
| Copyright | Copyright © 2018-2025 Wiley-VCH GmbH. All Rights Reserved. |
|---|---|
| Source of Spectrum | Maurer/Meyer/Helfer/Weber c/o Saarland University Homburg/Saar |
| Technique | HCD |
| Copyright | Copyright © 2018-2025 Wiley-VCH GmbH. All Rights Reserved. |
|---|---|
| Source of Spectrum | Maurer/Wissenbach/Weber, Saarland University |
| Technique | ITMS |
| Copyright | Copyright © 2012-2025 Herbert Oberacher. All Rights Reserved. |
|---|---|
| Source of Spectrum | Herbert Oberacher, Institute of Legal Medicine, Innsbruck/Austria |
| Technique | Q-TOF |
| Copyright | Copyright © 2012-2025 Herbert Oberacher. All Rights Reserved. |
|---|---|
| Source of Spectrum | Herbert Oberacher, Institute of Legal Medicine, Innsbruck/Austria |
| Technique | Q-TOF |
| Copyright | Copyright © 2012-2025 Herbert Oberacher. All Rights Reserved. |
|---|---|
| Source of Spectrum | Herbert Oberacher, Institute of Legal Medicine, Innsbruck/Austria |
| Technique | Q-TOF |
| Copyright | Copyright © 2012-2025 Herbert Oberacher. All Rights Reserved. |
|---|---|
| Source of Spectrum | Herbert Oberacher, Institute of Legal Medicine, Innsbruck/Austria |
| Technique | Q-TOF |
| Copyright | Copyright © 2012-2025 Herbert Oberacher. All Rights Reserved. |
|---|---|
| Source of Spectrum | Herbert Oberacher, Institute of Legal Medicine, Innsbruck/Austria |
| Technique | Q-TOF |
| Copyright | Copyright © 2012-2025 Herbert Oberacher. All Rights Reserved. |
|---|---|
| Source of Spectrum | Herbert Oberacher, Institute of Legal Medicine, Innsbruck/Austria |
| Technique | Q-TOF |
| Copyright | Copyright © 2012-2025 Herbert Oberacher. All Rights Reserved. |
|---|---|
| Source of Spectrum | Herbert Oberacher, Institute of Legal Medicine, Innsbruck/Austria |
| Technique | Q-TOF |
| Copyright | Copyright © 2012-2025 Herbert Oberacher. All Rights Reserved. |
|---|---|
| Source of Spectrum | Herbert Oberacher, Institute of Legal Medicine, Innsbruck/Austria |
| Technique | Q-TOF |
| Copyright | Copyright © 2012-2025 Herbert Oberacher. All Rights Reserved. |
|---|---|
| Source of Spectrum | Herbert Oberacher, Institute of Legal Medicine, Innsbruck/Austria |
| Technique | Q-TOF |
- Quinagolide MS2
- 3-(diethylsulfamoylamino)-6-hydroxy-1-propyl-3,4,4a,5,10,10a-hexahydro-2H-benzo[g]quinoline
trans-(+-)-Trifluoromethanesulfonic acid 4-Propyl-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolin-7-yl ester
cis-(+-)-Trifluoromethanesulfonic acid 4-Propyl-1,2,3,4,4a,5,6,10b-octahydrobenzo[f]quinolin-7-yl ester
IBWZVMAODGPSTI-JQFCIGGWSA-N
PFP-acyl derivative of DopAg
3-Benzazocine-3(2H)-carboxylic acid, 1,4,5,6-tetrahydro-8,9,10-trimethoxy-2-oxo-, phenylmethyl ester
1,4-Dibenzyl-6,7-dimethoxy-2-methyl-1,2,3,4-tetrahydro-isoquinoline
1-(12-hydroxy-1,2,3,4,6,11-hexahydrotetracen-2-yl)ethanone
Tramadol-M (HO-) 2 AC
10-O-DEMETHYLPROTOEMETINE
1-phenyl-1,3,9,9a-tetrahydroindeno[2,1-b]pyridin-2-one
This compound is available in the following databases:
Wiley Registry of Tandem Mass Spectral Data: MS for ID
Author: Herbert Oberacher, Institute of Legal Medicine, Innsbruck/Austria
The Wiley Registry® of Tandem Mass Spectral Data: MS for ID contains 10,000 positive and negative mode spectra of over 1200 compounds of interest for forensics, toxicology, and pathology. Learn more.
Maurer, Meyer, Helfer, Weber: LC-HR-MS & MS Library of Drugs, Poisons, and Their Metabolites
Author: Hans H. Maurer, Markus Meyer, Andreas G. Helfer, Armin A. Weber
Developed by toxicologist Hans H. Maurer and his team, the Maurer/Meyer/Helfer/Weber LC-HR-MS/MS Library of Drugs, Poisons, and Their Metabolites consists of spectra for parent drugs or poisons, and their metabolites or artifacts, in various compound classification groups. This metabolite-based library helps minimize the risk of false negative LC-MS results. Learn more.