Vindesine sulfate
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Vindesine sulfate
structure -
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CAS No:
59917-39-4
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Formula:
C43H55N5O7.H2O4S
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Chemical Name:
Vindesine sulfate
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Synonyms:
Vincaleukoblastine,3-(aminocarbonyl)-O4-deacetyl-3-de(methoxycarbonyl)-,sulfate (1:1);Vincaleukoblastine,3-(aminocarbonyl)-O4-deacetyl-3-de(methoxycarbonyl)-,sulfate (1:1) (salt);1H-Indolizino[8,1-cd]carbazole,vincaleukoblastine deriv.;2H-3,7-Methanoazacycloundecino[5,4-b]indole,vincaleukoblastine deriv.;Vindesine sulfate;Desacetylvinblastine amide sulfate;DAVA;Lilly 99094;NSC 245467;Eldesine;Eldisine;LY 099094;Fildesin;Xi Ai Ke Vial
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CAS No:
Description
Amorphous Solid
Vindesine sulfate is an alkaloid sulfate salt. It has a role as an antineoplastic agent. It derives from a vindesine.|Vinblastine derivative with antineoplastic activity against CANCER. Major side effects are myelosuppression and neurotoxicity. Vindesine is used extensively in chemotherapy protocols (ANTINEOPLASTIC COMBINED CHEMOTHERAPY PROTOCOLS).
Characteristics
247.80000
3.80150
off-white to light yellow
1.41 g/cm3
>250 °C
deionized water: ≥50mg/mL
2-8°C
LD50 in mice, rats (mg/kg): 6.3 ± 0.6, 2.0 ± 0.2 i.v. (Todd); in mice: 8.8 ± 2.5 i.p. (Owellen, Biochem. Pharmacol.)
Safety Information
II
6.1(a)
1544
3
40
26-36
YY8090000
Xn
|Danger|H300 (100%): Fatal if swallowed [Danger Acute toxicity, oral]|P201, P202, P264, P270, P280, P281, P301+P310, P305+P351+P338, P308+P313, P310, P321, P330, P405, and P501|The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.
Drug Information
Agents obtained from higher plants that have demonstrable cytostatic or antineoplastic activity. (See all compounds classified as Antineoplastic Agents, Phytogenic.)|Agents that interact with TUBULIN to inhibit or promote polymerization of MICROTUBULES. (See all compounds classified as Tubulin Modulators.)
Compound 112531
Vindesine sulfate Use and Manufacturing
Synthetic derivative of the dimeric Catharanthus alkaloid vinblastine. Antineoplastic
Computed Properties
Molecular Weight:852.0
Hydrogen Bond Donor Count:7
Hydrogen Bond Acceptor Count:14
Rotatable Bond Count:7
Exact Mass:851.37752882
Monoisotopic Mass:851.37752882
Topological Polar Surface Area:248
Heavy Atom Count:60
Complexity:1650
Defined Atom Stereocenter Count:9
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes
Drug Function and Efficacy
It is a cell cycle-specific antitumor drug that inhibits the polymerization of intracellular tubulin, prevents the formation of spindles in the mitosis of proliferating cells, and stops cell division at the metaphase of mitosis. This product has a broad antitumor spectrum for transplanted animal tumors and has no complete cross-resistance with vinblastine and vincristine.
Registered Holders
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Guangzhou Baiyunshan Hanfang Modern Pharmaceutical Co., Ltd.
Active
China
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Minsheng Group Shaoxing Pharmaceutical Co., Ltd.
Active
China
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Yangtze River Pharmaceutical Group Jiangsu HaiCi Biological Pharmaceutical Co., Ltd.
Active
China
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