(-)-Vindoline
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(-)-Vindoline
structure -
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CAS No:
2182-14-1
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Formula:
C25H32N2O6
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Chemical Name:
(-)-Vindoline
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Synonyms:
Aspidospermidine-3-carboxylic acid,4-(acetyloxy)-6,7-didehydro-3-hydroxy-16-methoxy-1-methyl-,methyl ester,(2β,3β,4β,5α,12R,19α)-;Vindoline,(-)-;Aspidospermidine-3-carboxylic acid,4-(acetyloxy)-6,7-didehydro-3-hydroxy-16-methoxy-1-methyl-,methyl ester,(2β,3β,4β,5α,12β,19α)-;1H-Indolizino[8,1-cd]carbazole,aspidospermidine-3-carboxylic acid deriv.;Vindolin;(-)-Vindoline;Vindoline;NSC 91994;7616-06-0
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CAS No:
Description
Vindoline, a vinca alkaloid extracted from the leaves of Catharanthus roseus, weakly inhibits tubulin self-assembly[1].
Characteristics
88.54000
2.20
White or offwhite powder
1.3±0.1 g/cm3
164-165 °C
569.8±50.0 °C at 760 mmHg
298.4±30.1 °C
1.626
-20°C Freezer
0mmHg at 25°C
D20 -18° (chloroform); D27 +42° (chloroform)
Safety Information
NONH for all modes of transport
68
36/37-24/25
CJ0120000
Xn
P281
H341
|Warning|H341 (97.5%): Suspected of causing genetic defects [Warning Germ cell mutagenicity]|P201, P202, P281, P308+P313, P405, and P501|Aggregated GHS information provided by 40 companies from 2 notifications to the ECHA C&L Inventory.
(-)-Vindoline Use and Manufacturing
A novel antitumor agent Vendolin has antibacterial, anti-inflammatory and anti-cancer effects; a monomeric vinblastine, which exhibits anti-mitotic activity by inhibiting the assembly of microtubules.
Computed Properties
Molecular Weight:456.5
XLogP3:1.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:6
Exact Mass:456.22603674
Monoisotopic Mass:456.22603674
Topological Polar Surface Area:88.5
Heavy Atom Count:33
Complexity:864
Defined Atom Stereocenter Count:5
Undefined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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