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Vindesine sulfate

pharmaceutical raw materials
Vindesine sulfate structure

Vindesine sulfate 

structure
  • CAS No:

    59917-39-4

  • Formula:

    C43H55N5O7.H2O4S

  • Chemical Name:

    Vindesine sulfate

  • 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

  • Categories:

    Active Pharmaceutical Ingredients  >  Antineoplastic Agents

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).

Vindesine sulfate Basic Attributes

852

851.377502

261-984-7

DTXSID0049074

2942000000

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.

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

Related Drugs

Registered Holders

  • Guangzhou Baiyunshan Hanfang Modern Pharmaceutical Co., Ltd.

    China China
    Active
  • Minsheng Group Shaoxing Pharmaceutical Co., Ltd.

    China China
    Active
  • Yangtze River Pharmaceutical Group Jiangsu HaiCi Biological Pharmaceutical Co., Ltd.

    China China
    Active

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