Sel sulfate de Vincristine, (HPLC) ,95 - 10,5% ( HPLC), poudre

Code: v8879-1mg D2-231

Non disponible en dehors du Royaume-Uni et de l'Irlande

Analysis Note

Freely soluble in water, Soluble in methanol, slightly soluble in ethanol

Application

Vincristine is an antitumor alkaloid isolated...


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Votre prix
$200.10 1MG

Non disponible en dehors du Royaume-Uni et de l'Irlande

Analysis Note

Freely soluble in water, Soluble in methanol, slightly soluble in ethanol

Application

Vincristine is an antitumor alkaloid isolated from Vinca Rosea. It is used to treat acute leukaemia, malignant lymphoma, Hodgkin′s disease, acute erythraemia, acute panmyelosis, breast cancer, Kaposi’;s sarcoma and testicular cancer. Vincristine is widely used in cancer research. It is used to study multi-drug resistance. It is used to inhibit cell cycle progression at M-phase and to inhibit monoamine oxidase (MAO) .

Biochem/physiol Actions

Vincristine is a plant alkaloid that inhibits microtubule assembly by binding tubulin and inducing coiled spiral aggregate formation. It arrests cell cycle in G2/M-phase by blocking mitotic spindle formation. Vincristine triggers Raf-1 activation, phosphorylation of bcl-2-family proteins, induction of p53 expression, and apoptosis in several tumor cell lines. It inhibits VEGF production in leukemia cell lines. It is a substrate for Pgp and CYP3A4. MRP1 transports vincristine in an ATP- and GSH-dependent manner. Vincristine has some immunosuppressant effect. Vincristine may also interfere with amino acid, cyclic AMP, and glutathione metabolism, calmodulin-dependent Ca2+-transport, cellular respiration, and nucleic acid and lipid biosynthesis.

Other Notes

Keep container tightly closed in a dry and well-ventilated place. Keep in a dry place.

Packaging

1, 5, 25 mg in glass bottle

antibiotic activity spectrumneoplastics
assay95.0-105.0% (HPLC)
biological sourceStreptomyces roseosporus
colorwhite to slightly yellow
formpowder or crystals
InChI keyAQTQHPDCURKLKT-PNYVAJAMSA-N
InChI1S/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
mode of actionprotein synthesis | interferes
Quality Level200
SMILES stringOS(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
storage condition(Keep container tightly closed in a dry and well-ventilated place. Keep in a dry place.)
storage temp.−20°C
Code
Description
Unité de vente
Prix annoncé
Qté
V8879-25MG
Unité:25MG
Prix annoncé: $2,349.00
Source:Prix annoncé
V8879-5MG
Unité:5MG
Prix annoncé: $698.90
Source:Prix annoncé
Cas Number2068-78-2
Hazard Class6.1
Un Number2811
Pack GroupII
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