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Merck

V1377

Sigma-Aldrich

Vinblastine sulfate salt

≥97% (HPLC), powder, plant alkaloid

Sinónimos:

VLB, Vincaleukoblastine sulfate salt

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1 MG
$41.000
5 MG
$91.400
10 MG
$165.000
25 MG
$331.000
50 MG
$561.000

$41.000


Fecha estimada de envío29 de abril de 2025


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1 MG
$41.000
5 MG
$91.400
10 MG
$165.000
25 MG
$331.000
50 MG
$561.000

About This Item

Fórmula empírica (notación de Hill):
C46H58N4O9 · H2SO4
Número de CAS:
Peso molecular:
909.05
Beilstein:
3659812
Número CE:
Número MDL:
Código UNSPSC:
12352200
ID de la sustancia en PubChem:
NACRES:
NA.77

$41.000


Fecha estimada de envío29 de abril de 2025


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Nombre del producto

Vinblastine sulfate salt, ≥97% (HPLC)

Nivel de calidad

Ensayo

≥97% (HPLC)

Formulario

(powder or amorphous or crystalline powder)

color

white to light yellow

mp

267 °C (dec.) (lit.)

Absorción

14 at 270 nm in 0.1 M phosphate buffer at 1 mM
16.2 at 259 nm in ethanol at 1 mM
53.7 at 214 nm in ethanol at 1 mM

espectro de actividad antibiótica

neoplastics

Modo de acción

DNA synthesis | interferes

emisor

Eli Lilly

temp. de almacenamiento

2-8°C

cadena SMILES

OS(O)(=O)=O.[H][C@@]12CN(CCc3c([nH]c4ccccc34)[C@@](C1)(C(=O)OC)c5cc6c(cc5OC)N(C)[C@@]7([H])[C@](O)([C@H](OC(C)=O)[C@]8(CC)C=CCN9CC[C@]67[C@]89[H])C(=O)OC)C[C@](O)(CC)C2

InChI

1S/C46H58N4O9.H2O4S/c1-8-42(54)23-28-24-45(40(52)57-6,36-30(15-19-49(25-28)26-42)29-13-10-11-14-33(29)47-36)32-21-31-34(22-35(32)56-5)48(4)38-44(31)17-20-50-18-12-16-43(9-2,37(44)50)39(59-27(3)51)46(38,55)41(53)58-7;1-5(2,3)4/h10-14,16,21-22,28,37-39,47,54-55H,8-9,15,17-20,23-26H2,1-7H3;(H2,1,2,3,4)/t28-,37-,38+,39+,42-,43+,44+,45-,46-;/m0./s1

Clave InChI

KDQAABAKXDWYSZ-PNYVAJAMSA-N

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Categorías relacionadas

Aplicación

Vinblastine sulfate salt has been used:
  • as a microtubule depolymerizing drug for the synchronization of human cell lines in G2/M phase[1]
  • as a multidrug resistance screening substrate in human colon cancer cell line (HCT116) cell line[2]
  • as an antimicrotubule agent in sub perineural glia of Drosophila brain[3]

Acciones bioquímicas o fisiológicas

Plant alkaloid that inhibits microtubule assembly by binding tubulin and inducing self-association in spiral aggregates in a reaction that appears to be regulated by the C-terminus of β-tubulin and is enhanced by GDP and GTP. Depolymerizes microtubules. Arrests the cell cycle in G2/M-phase by blocking mitotic spindle formation. Triggers Raf-1 activation, phosphorylation of bcl-2-family proteins, induction of p53 expression, and apoptosis in several tumor cell lines. Substrate of Pgp and CYP3A4.

Características y beneficios

This compound is a featured product for ADME Tox research. Click here to discover more featured ADME Tox products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.
This compound was developed by Eli Lilly. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

Pictogramas

Health hazardExclamation mark

Palabra de señalización

Warning

Frases de peligro

Clasificaciones de peligro

Acute Tox. 4 Oral - Muta. 2 - Repr. 2

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3


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Use of drugs to study role of microtubule assembly dynamics in living cells.
M A Jordan et al.
Methods in enzymology, 298, 252-276 (1998-09-30)
DrugTargetSeqR: a genomics-and CRISPR-Cas9-based method to analyze drug targets
Kasap C, et al.
Nature chemical biology, 10(8), 626-626 (2014)
Phosphorylation of mixed lineage leukemia 5 by CDC2 affects its cellular distribution and is required for mitotic entry
Liu J, et al.
The Journal of Biological Chemistry, 285(27), 20904-20914 (2010)
Noelle S Williams et al.
Proceedings of the National Academy of Sciences of the United States of America, 104(7), 2074-2079 (2007-02-09)
Blocking cell division through the inhibition of mitosis is one of the most successful clinical strategies for the treatment of cancer. Taxanes and vinca alkaloids are in widespread use and have demonstrated substantive therapeutic efficacy. Both classes of compounds bind
M V Blagosklonny et al.
Cancer research, 57(1), 130-135 (1997-01-01)
Recent studies have shown that paclitaxel leads to activation of Raf-1 kinase and have suggested that this activation is essential for bcl-2 phosphorylation and apoptosis. In the present study, we demonstrate that, in addition to paclitaxel, other agents that interact

Artículos

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Questions

  1. What is the composition of vinblastine sulfate salt. I mean what is the ratio of vinblastine: salt in this powder

    1 answer
    1. The minimum purity of this Vinblastine Sulfate product is 96%. The exact purity is lot specific and reported on the product Certificate of Analysis. Maximum limits allowable are also set for several residual solvents and related substances. Total impurities may not exceed 3%. The H2SO4 makes up 10.7% of the purified compound based on the molecular formula: C46H58N4O9 · H2SO4. Please see the link below to access a sample or lot specific Certificate:
      https://www.sigmaaldrich.com/product/sigma/v1377#product-documentation

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