V4890

Vindesine sulfate salt hydrate

≥95% (HPLC)

• Synonym(s): 3-(Aminocarbonyl)-O4-deacetyl-3-de(methoxycarbonyl)vincaleukoblastine sulfate salt hydrate, Desacetylvinblastine amide sulfate salt hydrate
• Empirical Formula (Hill Notation): C₄₃H₅₅N₅O₇ · H₂SO₄ · xH₂O
• CAS Number: 59917-39-4
• Molecular Weight: 852.00 (anhydrous basis)
• UNSPSC Code: 12352200
• PubChem Substance ID: 329829055
• NACRES: NA.77

Properties

• assay: ≥95% (HPLC)
• form: powder
• color: off-white to light yellow
• solubility: deionized water: ≥50 mg/mL
• originator: Eli Lilly
• storage temp.: −20°C
• SMILES string: O.OS(O)(=O)=O.CC[C@]1(O)C[C@H]2CN(CCc3c([nH]c4ccccc34)[C@@](C2)(C(=O)OC)c5cc6c(cc5OC)N(C)[C@H]7[C@](O)([C@H](O)[C@]8(CC)C=CC[N@H]9CC[C@]67[C@H]89)C(N)=O)C1
• InChI: 1S/C43H55N5O7.H2O4S.H2O/c1-6-39(52)21-25-22-42(38(51)55-5,33-27(13-17-47(23-25)24-39)26-11-8-9-12-30(26)45-33)29-19-28-31(20-32(29)54-4)46(3)35-41(28)15-18-48-16-10-14-40(7-2,34(41)48)36(49)43(35,53)37(44)50;1-5(2,3)4;/h8-12,14,19-20,25,34-36,45,49,52-53H,6-7,13,15-18,21-24H2,1-5H3,(H2,44,50);(H2,1,2,3,4);1H2/t25-,34+,35-,36-,39+,40-,41-,42+,43+;;/m1../s1
• InChI key: TUDLKTILIBRXNU-RIHOAIHNSA-N

Description

Biochem/physiol Actions

Microtubule inhibitor. Vindesine binds to and stabilizes tubulin, thereby preventing tubulin polymerization, preventing mitosis, and arresting cells in metaphase.

Features and Benefits

This compound was developed by Eli Lilly. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

Safety Information

• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable