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V8388

Vincristin -sulfat

meets USP testing specifications

Synonym(e):

Vincristin -sulfat (Salz), 22-Oxo-vincaleukoblastin -sulfat (Salz), Leurocristin -sulfat (Salz), VCR

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Über diesen Artikel

Empirische Formel (Hill-System):
C46H56N4O10 · H2SO4
CAS-Nummer:
Molekulargewicht:
923.04
UNSPSC Code:
12352210
NACRES:
NA.21
PubChem Substance ID:
EC Number:
218-190-0
Beilstein/REAXYS Number:
3924631
MDL number:
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Quality Level

agency

USP/NF, meets USP testing specifications

solubility

ethanol: slightly soluble, methanol: soluble, water: freely soluble

antibiotic activity spectrum

neoplastics

application(s)

pharmaceutical (small molecule)

mode of action

protein synthesis | interferes

storage temp.

−20°C

SMILES string

OS(O)(=O)=O.CC[C@]1(O)CC2CN(CCc3c([nH]c4ccccc34)[C@@](C2)(C(=O)OC)c5cc6c(cc5OC)N(C=O)C7[C@](O)([C@H](OC(C)=O)[C@]8(CC)C=CCN9CC[C@]67C89)C(=O)OC)C1

InChI

1S/C46H56N4O10.H2O4S/c1-7-42(55)22-28-23-45(40(53)58-5,36-30(14-18-48(24-28)25-42)29-12-9-10-13-33(29)47-36)32-20-31-34(21-35(32)57-4)50(26-51)38-44(31)16-19-49-17-11-15-43(8-2,37(44)49)39(60-27(3)52)46(38,56)41(54)59-6;1-5(2,3)4/h9-13,15,20-21,26,28,37-39,47,55-56H,7-8,14,16-19,22-25H2,1-6H3;(H2,1,2,3,4)/t28-,37-,38+,39+,42-,43+,44+,45-,46-;/m0./s1

InChI key

AQTQHPDCURKLKT-PNYVAJAMSA-N

General description

Vincristine sulfate is an alkaloid present in Cantharanthus roseus.[1]

Application

Vincristine sulfate has been used:
  • as a positive control in potato disc anti-tumor bioassay
  • as a standard cytotoxic agent
  • to treat cells for manipulation of the microtubule network

Widely used in cancer research. In studies on multi-drug resistance. Used to inhibit cell cycle progression at M-phase. Used to inhibit monoamine oxidase (MAO).

Biochem/physiol Actions

Vincristine sulfate possesses antitumor action targeting cell cycle. It prevents the action of tubulin by inhibiting microtubule polymerization. It also causes cell death and blocks metaphase in mitosis by preventing chromosome segregation. Vincristine sulfate inhibits angiogenesis mediated by factors such as vasculature endothelial growth factor. It decreases vascularization in tumors and normal tissues.[1]

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Dieser Artikel
1714007V0400000V8879
antibiotic activity spectrum

neoplastics

antibiotic activity spectrum

-

antibiotic activity spectrum

-

antibiotic activity spectrum

neoplastics

mode of action

protein synthesis | interferes

mode of action

-

mode of action

-

mode of action

protein synthesis | interferes

Quality Level

200

Quality Level

-

Quality Level

-

Quality Level

200

application(s)

pharmaceutical (small molecule)

application(s)

pharmaceutical (small molecule)

application(s)

pharmaceutical (small molecule)

application(s)

-

solubility

ethanol: slightly soluble, water: freely soluble, methanol: soluble

solubility

-

solubility

-

solubility

-

agency

USP/NF, meets USP testing specifications

agency

-

agency

-

agency

-


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pictograms

Skull and crossbonesHealth hazard

signalword

Danger

Hazard Classifications

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

Lagerklasse

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



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Molecularly characterized solvent extracts and saponins from Polygonum hydropiper L. show high anti-angiogenic, anti-tumor, brine shrimp, and fibroblast NIH/3T3 cell line cytotoxicity
Ayaz M, et al.
Frontiers in Pharmacology, 7, 74-74 (2016)
Haq Nawaz et al.
The Analyst, 138(20), 6177-6184 (2013-08-24)
Understanding the interaction of anticancer drugs with model cell lines is important to elucidate the mode of action of these drugs as well as to develop cost effective and rapid screening methods. Raman spectroscopy has been demonstrated to be a
The polyomavirus BK agnoprotein co-localizes with lipid droplets
Unterstab G, et al.
Virology, 399(2), 322-331 (2010)



Global Trade Item Number

SKUGTIN
V8388-25MG04061833276525
V8388-1MG04061837481475
V8388-5MG04061837481482

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