Tubulin polymerization-IN-28 structure
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Common Name | Tubulin polymerization-IN-28 | ||
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CAS Number | 2481404-89-9 | Molecular Weight | 662.77 | |
Density | N/A | Boiling Point | N/A | |
Molecular Formula | C37H46N2O9 | Melting Point | N/A | |
MSDS | N/A | Flash Point | N/A |
Use of Tubulin polymerization-IN-28Tubulin polymerization-IN-28 (compound-4) is a microtubule protein polymerization inhibitor with highly selective anticancer activity. Tubulin polymerization-IN-28 can be activated by NQO1 and effectively release combretastatin A-4 to kill tumor cells. Tubulin polymerization-IN-28 can induce cell apoptosis and be used in anti-cancer research[1]. |
Name | Tubulin polymerization-IN-28 |
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Description | Tubulin polymerization-IN-28 (compound-4) is a microtubule protein polymerization inhibitor with highly selective anticancer activity. Tubulin polymerization-IN-28 can be activated by NQO1 and effectively release combretastatin A-4 to kill tumor cells. Tubulin polymerization-IN-28 can induce cell apoptosis and be used in anti-cancer research[1]. |
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Related Catalog | |
In Vitro | Tubulin polymerization-IN-28 (compound-4) (9-381 nM,48 hours)has a significant inhibitory effect on tumor cells[1]. Tubulin polymerization-IN-28 (compound-4) (10 nM,48 hours) inhibits microtubule assembly with anti-tumor activity[1]. Tubulin polymerization-IN-28 (compound-4) (10 nM,48 hours) causes G2/M phase arrest in cells[1]. Tubulin polymerization-IN-28 (compound-4) (10 nM,24 hours) leads to significant cell apoptosis[1]. Cell Proliferation Assaysup>[1] Cell Line: NQO1-Overexpressing A549, HepG2; Hypoxia-exposed A549 (A549/Hyp), HepG2 (HepG2/Hyp) cells; Taxol-resistant A549 cells (A549/T) Concentration: 9-381 nM Incubation Time: 48 hours Result: Inhibited A549, HepG2, A549/Hyp, HepG2/Hyp, A549/T with IC50values of 10 nM, 26 nM, 72 nM, 85 nM, 56 nM, 74 nM and 88 nM respectively. Immunofluorescencesup>[1] Cell Line: HepG2 Concentration: 10 nM Incubation Time: 48 hours Result: Showed that Tubulin polymerization-IN-28 converted to CA-4, thereby inhibiting microtubule assembly, in the presence of NQO1. Cell Cycle Analysis[1] Cell Line: HepG2 Concentration: 0 nM,10 nM Incubation Time: 48 hours Result: Resulted in an increase in the percentage of G2/M phase cells from 12.71% to 33.49%. Apoptosis Analysis[1] Cell Line: HepG2 Concentration: 0 nM,10 nM Incubation Time: 24 hours Result: Showed the apoptosis rate of cells increasing from 6.54% to 23.93%. |
In Vivo | Tubulin polymerization-IN-28 (compound-4) (intraperitoneal injection, every day, 17days) exhibits good anti-cancer activity in HepG2 xenograft-bearing BALB/c mice model in vivo[1]. Animal Model: HepG2 xenograft-bearing BALB/c mice[1] Dosage: 20 mg/kg, 40 mg/kg Administration: Intraperitoneal injection; every day; 17days Result: Resulted in 47.49% reduction in tumor growth at a concentration of 20 mg/kg. Resulted in 54.87% reduction in tumor growth at a concentration of 40 mg/kg. |
References |
Molecular Formula | C37H46N2O9 |
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Molecular Weight | 662.77 |