| Weight | 369.417 g/mol |
|---|---|
| Formula | C21H23NO5 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
Allocryptopine (24240-04-8, 485-91-6)
allo-cryptopine
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- Sigma-Aldrich - Allocryptopine128.75 USD
- Fisher Scientific - Search for Allocryptopine
- TCI - Search for Allocryptopine
- Protopine and allocryptopine increase mRNA levels of cytochromes P450 1A in human hepatocytes and HepG2 cells independently of AhR (Toxicology Letters, 2011)
- Rapid determination of protopine, allocryptopine, sanguinarine and chelerythrine in fruits of Macleaya cordata by Microwave-assisted solvent extraction and HPLC-ESI/MS (Phytochemical Analysis, 2006)
- THE CHEMICAL AND BIOLOGICAL PROPERTIES OF PROTOPINE AND ALLOCRYPTOPINE (Heterocycles, 2010)
- Effects of Allocryptopine, an Alkaloid Isolated from Glaucium arabicum on Rat Isolated Ileum and Urinary Bladder (General Pharmacology-the Vascular System, 1997)
- Optimization of microwave-assisted extraction of protopine and allocryptopine from stems of Macleaya cordata (Willd) R. Br. using response surface methodology. (Journal of Separation Science, 2010)
- The Hydroxylation of Anhydromethyltetrahydroberberine-A. 13-Hydroxydihydro-allocryptopine (Journal of the American Chemical Society, 1956)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - allo-cryptopine
-
SMILESCN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C(=C(C=C4)OC)OC)OCO3
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InChIKeyHYBRYAPKQCZIAE-UHFFFAOYSA-N
- Pubchem - Allocryptopine
- Wikipedia - allocryptopine
Allocryptopine is a bioactive alkaloid from Glaucium arabicum.
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Allocryptopine
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