| Weight | 383.4 g/mol |
|---|---|
| Formula | C21H21NO6 |
| Hydrogen Acceptors | 7 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
HYDRASTINE (118-08-1)
hydrastine, (R-(R*,R*))-isomer · hydrastine, (R-(R*,S*))-isomer · isocoryne
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- Effect of strychnine, hydrastine, and apamine on synaptic transmission in smooth muscle cells (Neirofiziologiia, 1979)
- Antitubercular Natural Products: Berberine from the Roots of Commercial Hydrastis canadensis Powder. Isolation of Inactive 8-Oxotetrahydrothalifendine, Canadine, -Hydrastine, and Two New Quinic Acid Esters, Hycandinic Acid Esters-1 and -2 (Journal of Natural Products, 1998)
- THE BIOSYNTHESIS OF HYDRASTINE AND BERBERINE (Canadian Journal of Chemistry, 1963)
- Highperformance liquid chromatography determination of hydrastine and berberine in dietary supplements containing goldenseal (Journal of Pharmaceutical Sciences, 2001)
- (+)Hydrastine, a potent competitive antagonist at mammalian GABAA receptors (British Journal of Pharmacology, 1990)
- A COMPARATIVE STUDY OF HYDRASTINE, BICUCULLINE AND ADLUMINE (Journal of Pharmacology and Experimental Therapeutics, 1934)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - hydrastine, (R-(R*,R*))-isomer
- hydrastine, (R-(R*,S*))-isomer
- isocoryne
- beta-hydrastine
- hydrastine hydrochloride, (S-(R*,S*))-isomer
-
SMILESCN1CCC2=CC3=C(C=C2C1C4C5=C(C(=C(C=C5)OC)OC)C(=O)O4)OCO3
-
InChIKeyJZUTXVTYJDCMDU-UHFFFAOYSA-N
- Pubchem - HYDRASTINE
- Wikipedia - Hydrastine
Hydrastine is an alkaloid which was discovered in 1851 by Alfred P. Durand. Hydrolysis of hydrastine yields hydrastinine, which was patented by Bayer as a haemostatic drug during the 1910s.
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