| Weight | 808.973 g/mol |
|---|---|
| Formula | C46H56N4O9 |
| Hydrogen Acceptors | 12 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 7 |
LEUROSINE (54081-68-4)
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- Antitumor Principles Derived from Vinca rosea Linn I. Vincaleukoblastine and Leurosine (Cancer Research, 1960)
- VINCA ALKALOIDS. III.1CHARACTERIZATION OF LEUROSINE AND VINCALEUKOBLASTINE, NEW ALKALOIDS FROM VINCA ROSEA LINN. (Journal of the American Chemical Society, 1959)
- VINCA ALKALOIDS.1IV. STRUCTURAL FEATURES OF LEUROSINE AND VINCALEUKOBLASTINE, REPRESENTATIVES OF A NEW TYPE OF INDOLE-INDOLINE ALKALOIDS (Journal of the American Chemical Society, 1959)
- Total synthesis of indole and dihydroindole alkaloids. XII. Selective functionalization of various bisindoles. Efficient syntheses of leurosine and related bisindole alkaloid derivatives (Canadian Journal of Chemistry, 1978)
- Catharanthus alkaloids, XXXVIII. Confirming structural evidence and antineoplastic activity of the bisindole alkaloids leurosine-N'b-oxide (pleurosine), roseadine and vindolicine from Catharanthus roseus. (Journal of Natural Products, 1983)
- Selective deoxygenation of leurosine: concise access to anhydrovinblastine. (Journal of Organic Chemistry, 2002)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCC12CN3CCC4=C(C(CC(C3)C1O2)(C5=C(C=C6C(=C5)C78CCN9C7C(C=CC9)(C(C(C8N6C)(C(=O)OC)O)OC(=O)C)CC)OC)C(=O)OC)NC1=CC=CC=C41
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InChIKeyLPGWZGMPDKDHEP-UHFFFAOYSA-N
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