tcsc1568 Ansamitocin P-3

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Product Description

Ansamitocin P-3 is a microtubule inhibitor. Ansamitocin P-3 is a macrocyclic antitumor antibiotic.

IC50 & Target: Microtubule[1]

In Vitro: Ansamitocin P3 potently inhibits the proliferation of MCF-7, HeLa, EMT-6/AR1 and MDA-MB-231 cells in culture with a half-maximal inhibitory concentration of 20±3, 50±0.5, 140±17, and 150±1.1 pM, respectively. Further, Ansamitocin P3 is found to bind to purified tubulin in vitro with a dissociation constant (Kd) of 1.3±0.7 µM. The binding of Ansamitocin P3 induces conformational changes in tubulin. Ansamitocin P3 inhibits the proliferation of MCF-7, HeLa, EMT-6/AR1 and MDA-MB-231 cells in culture in a concentration dependent manner. Flow cytometric analysis of PI-stained cells suggests that Ansamitocin P3 inhibits the cell cycle progression of MCF-7 cells in G2/M phase. For example, 26, 50 and 70% of the cells are found to be in G2/M phase in the absence and presence of 50 and 100 pM Ansamitocin P3, respectively[2].

Information

CAS No66584-72-3
FormulaC32H43ClN2O9
Clinical Informationclinicalinformation
PathwayCell Cycle/DNA Damage
Cytoskeleton
Antibody-drug Conjugate/ADC Related
TargetMicrotubule/Tubulin
Microtubule/Tubulin
ADC Cytotoxin

Specifications

Purity / Grade>98%
Solubility10 mM in DMSO
Smilessmiles

Misc Information

Alternative NamesAntibiotic C 15003P3;Maytansinol butyrate;C15003P3
Observed Molecular Weight635.14
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