| Weight | 641.758 g/mol |
|---|---|
| Formula | C35H47NO10 |
| Hydrogen Acceptors | 11 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 7 |
TAXINE (12607-93-1)
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LabBot
- Identification of six taxine alkaloids from Taxus baccata needles. (Journal of Natural Products, 1996)
- Semisynthesis of Some 7-Deoxypaclitaxel Analogs from Taxine B. (Journal of Organic Chemistry, 1996)
- Quantitative determination of taxine B in body fluids by LCMSMS (International Journal of Legal Medicine, 2006)
- Rvision structurale de la taxine B, alcalode majoritaire des feuilles de l'If d'Europe, Taxus baccata (Journal of Natural Products, 1991)
- Fatal Taxine Poisoning from Yew Leaf Ingestion (Journal of Forensic Sciences, 1991)
- Stable oil-in-water emulsions incorporating a taxine (taxol) and method of making same (1994)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=C2C(C(=O)C3(CC(=CC(C(C2(C)C)CC1OC(=O)C)OC(=O)C)C(CC3O)OC(=O)C(C(C4=CC=CC=C4)N(C)C)O)C)O
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InChIKeyKOTXAHKUCAQPQA-UHFFFAOYSA-N
- Pubchem - TAXINE
- Wikipedia - taxine
Taxine is a toxic alkaloid compound present in the Yew tree, Taxus baccata. It is composed of more than seven alkaloids, the main constituents being taxine A and taxine B; the other components are their derivatives, such as 2-deacetyltaxine A, isotaxine B and 1-deoxytaxine B. This substance is characterized by high melting and boiling point.
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CHEMBL93142
(O-acylation)
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