sulfuric acid hydrate methyl (13S,15S,17S)-13-[(1R,9R,10S,11R,12R,19R)-10-carbamoyl-12-ethyl-10,11-dihydroxy-5-methoxy-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2(7),3,5,13-tetraen-4-yl]-17-ethyl-17-hydroxy-1,11-diazatetracyclo[13.3.1.04,12.05,10]nonadeca-4(12),5,7,9-tetraene-13-carboxylate

• ChemBase ID: 154892
• Molecular Formular: C43H59N5O12S
• Molecular Mass: 870.01986
• Monoisotopic Mass: 869.38809335
• SMILES: CC[C@@]1(C[C@@H]2C[C@@](c3c(c4ccccc4[nH]3)CCN(C2)C1)(c1cc2c(cc1OC)N([C@@H]1[C@@]32CCN2[C@H]3[C@@](C=CC2)([C@H]([C@@]1(C(=O)N)O)O)CC)C)C(=O)OC)O.O.OS(=O)(=O)O
• Canonical SMILES: OS(=O)(=O)O.COc1cc2N(C)[C@@H]3[C@@]4(c2cc1[C@]1(C[C@@H]2CN(CCc5c1[nH]c1c5cccc1)C[C@](C2)(O)CC)C(=O)OC)CCN1[C@H]4[C@@]([C@H]([C@]3(O)C(=O)N)O)(CC)C=CC1.O
• InChI: 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
• InChIKey: TUDLKTILIBRXNU-RIHOAIHNSA-N

NAMES AND DATABASE IDS

Names

• IUPAC name: sulfuric acid hydrate methyl (13S,15S,17S)-13-[(1R,9R,10S,11R,12R,19R)-10-carbamoyl-12-ethyl-10,11-dihydroxy-5-methoxy-8-methyl-8,16-diazapentacyclo[10.6.1.0^1,^9.0^2,^7.0^1^6,^1^9]nonadeca-2(7),3,5,13-tetraen-4-yl]-17-ethyl-17-hydroxy-1,11-diazatetracyclo[13.3.1.0^4,^1^2.0^5,^1^0]nonadeca-4(12),5,7,9-tetraene-13-carboxylate
• IUPAC Traditional name: sulfuric acid vindesine hydrate
• Synonyms: 3-(Aminocarbonyl)-O4-deacetyl-3-de(methoxycarbonyl)vincaleukoblastine sulfate salt hydrate; Desacetylvinblastine amide sulfate salt hydrate; Vindesine sulfate salt hydrate

Database IDs

• CAS Number: 59917-39-4(anhydrous)
• PubChem SID: 162249030
• PubChem CID: 71312023

CALCULATED PROPERTIES

• Acid pKa: 11.342998
• H Acceptors: 9
• H Donor: 5
• LogD (pH = 5.5): -2.6965613
• LogD (pH = 7.4): 0.8213256
• Log P: 2.7891831
• Molar Refractivity: 210.3222 cm^3
• Polarizability: 82.5302 Å^3
• Polar Surface Area: 164.82 Å^2
• Rotatable Bonds: 7
• Lipinski's Rule of Five: false

PROPERTIES

Physical Property

• Solubility: deionized water: ≥50 mg/mL
• Apperance: off-white to light yellow powder

Safety Information

• German water hazard class: 3
• Storage Temperature: -20°C

Product Information

• Purity: ≥95% (HPLC)
• Empirical Formula (Hill Notation): C43H55N5O7 · H2SO4 · xH2O

DETAILS

Sigma Aldrich - V4890

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