Fig. 1 · Structure

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Vinblastine sulfate

Cat. No. A13661 CAS 143-67-9

microtubule dynamics inhibitor

Vinblastine sulfate inhibits microtubule formation and suppresses nAChR activity with IC50 of 8.9 μM in a cell-free assay, used to treat certain kinds of cancer.

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Biological Activity

Cellular Effect

Cell Line Activity Value Description Reference
A-375 IC50 7.2 μM Cytotoxicity against human A375 cells after 48 hrs by SRB assay [PMID: 19467877]
A549 IC50 2.36 μM Antiproliferative activity against human A549 cells after 48 hrs by MTS assay [PMID: 22546674]
A549 IC50 67.3 μM Cytotoxicity against human A549 cells after 48 hrs by SRB assay [PMID: 19467877]
ACHN IC50 22.7 μM Cytotoxicity against human ACHN cells after 48 hrs by SRB assay [PMID: 19467877]
BXPC-3 IC50 1.13 μM Antiproliferative activity against human BxPC3 cells after 48 hrs by MTS assay [PMID: 22546674]
C32 IC50 3 μM Cytotoxicity against human C32 cells after 48 hrs by SRB assay [PMID: 19467877]
Caco-2 IC50 69 μM Cytotoxicity against human Caco-2 cells after 48 hrs by SRB assay [PMID: 19467877]
COR-L23 IC50 45.5 μM Cytotoxicity against human COR-L23 cells after 48 hrs by SRB assay [PMID: 19467877]
DU-145 IC50 4.25 μM Antiproliferative activity against human DU145 cells after 48 hrs by MTS assay [PMID: 22546674]
HepG2 IC50 0.019 μM Cytotoxicity against human HepG2 cells assessed as growth inhibition after 72 hrs by MTT assay [PMID: 23708010]
HepG2 IC50 0.056 μM Cytotoxicity against adriamycin-resistant human HepG2 cells assessed as growth inhibition after 72 hrs by MTT assay [PMID: 23708010]
HepG2 IC50 0.16 μM Antiproliferative activity against human HepG2 cells after 48 hrs by MTS assay [PMID: 22546674]
HT-29 IC50 0.55 μM Cytotoxicity against human HT-29 cells after 48 hrs by MTS assay [PMID: 21920762]
HT-29 IC50 11.18 μM Antiproliferative activity against human HT-29 cells after 48 hrs by MTS assay [PMID: 22546674]
K562 IC50 0.001 μM Antiproliferative activity against human K562 cells after 48 hrs by hemocytometer [PMID: 21705223]
K562 IC50 0.001 μM Antiproliferative activity against human K562 cells after 48 hrs by hemocytometric analysis [PMID: 21563750]
K562 IC50 0.001 μM Cell growth inhibition of human K562 cells after 48 hrs [PMID: 20546980]
K562 IC50 0.001 μM Antiproliferative activity against human K562 cells after 48 hrs [PMID: 20537765]
K562 IC50 0.001 μM Antiproliferative activity against human K562 cells after 48 hrs [PMID: 19220018]
K562 IC50 0.001 μM Antiproliferative activity against human K562 cells after 48 hrs [PMID: 17973361]
K562 IC50 0.016 μM Cytotoxicity against human K562 cells assessed as growth inhibition after 72 hrs by MTT assay

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Specifications

Manufacturer Adooq Bioscience
Actions Inhibitor
CAS Number 143-67-9
Applications microtubule dynamics inhibitor
Formula C46H58N4O9.H2SO4
Molecular Weight 909.05
Synonyms Vincaleukoblastine sulfate salt
SMILES
CCC1(CC2CC(C3=C(CCN(C2)C1)C4=CC=CC=C4N3)(C5=C(C=C6C(=C5)C78CCN9C7C(C=CC9)(C(C(C8N6C)(C(=O)OC)O)OC(=O)C)CC)OC)C(=O)OC)O.OS(=O)(=O)O

Storage & Solubility

In Vitro Solubility

Reported Solubility

SolventReported Solubility
DMSO 93 mg/mL (102.3 mM)
Water Insoluble
Ethanol Insoluble

Preparing Stock Solutions

Stock preparation is unavailable for this product molecular weight.

Calculated stock concentrations do not establish solvent solubility. Refer to the reported solubility data for experimental guidance.

Storage

Store powder at -20°C, keep desiccated.
In powder form, the chemical is stable for 36 months.
In solution, store at -20°C and use within 1 month to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.

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