
Tubulin inhibitor 24
CAS No. 2415761-65-6
Tubulin inhibitor 24( —— )
Catalog No. M28918 CAS No. 2415761-65-6
Tubulin inhibitor 24 is a potent inhibitor that can inhibit tubulin polymerization.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 393 | Get Quote |
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10MG | 581 | Get Quote |
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25MG | 888 | Get Quote |
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50MG | 1242 | Get Quote |
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100MG | 1674 | Get Quote |
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500MG | 3348 | Get Quote |
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1G | Get Quote | Get Quote |
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Biological Information
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Product NameTubulin inhibitor 24
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NoteResearch use only, not for human use.
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Brief DescriptionTubulin inhibitor 24 is a potent inhibitor that can inhibit tubulin polymerization.
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DescriptionTubulin inhibitor 24 is a potent inhibitor that can inhibit tubulin polymerization.
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In VitroTubulin inhibitor 24 (compound 1b) () shows high antiproliferative activity with IC50s of 0.021, 0.047, 0.003, 0.048 μM for Hela, MCF-7, A549, HCT-116, B16-F10 cells, respectively.Tubulin inhibitor 24 inhibites tubulin polymerization with an IC50 value of 2.1 μM.Tubulin inhibitor 24 (5, 10 nM) induces cell cycle arrest at the G2/M phase in a concentration-dependent manner.Tubulin inhibitor 24 (10, 20, 40 nM; 24 h) inhibits MCF-7 cancer cells migration in a dose-dependent manner.Tubulin inhibitor 24 (40 nM; 6 h) destabilizes microtubule by inhibiting tubulin polymerization and disturbing microtubule networks in B16-F10 cells. Cell Proliferation Assay Cell Line:Hela, MCF-7, A549, HCT-116, B16-F10 cells Concentration:0.00098, 0.0039, 0.016, 0.0625, 0.25, 1.0, 4.0, 16, 64 μM Incubation Time:48 hResult:Showed high antiproliferative activity with IC50s of 0.021, 0.047, 0.003, 0.048 μM for Hela, MCF-7, A549, HCT-116, B16-F10 cells, respectively.Cell Cycle Analysis Cell Line:MCF-7 cells Concentration:5, 10 nM Incubation Time:48 h Result:Cells were arrested at the G2/M phase in a concentration-dependent manner.
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In VivoTubulin inhibitor 24 (10, 20 mg/kg; i.p.; per day for 16 days) shows antitumor activity with no obvious toxicity. Animal Model:4-6 weeks, male C57/BL mice (B16e-10 tumor model)Dosage:10, 20 mg/kg (formulated in 5% DMSO, 40% PEG-300 and 55% saline)Administration: I.p.; per day, 16 days Result:Showed antitumor activity with no obvious toxicity.
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Synonyms——
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PathwayCytoskeleton/Cell Adhesion Molecules
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TargetMicrotubule/Tubulin
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number2415761-65-6
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Formula Weight375.42
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Molecular FormulaC22H21N3O3
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Purity>98% (HPLC)
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Solubility——
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SMILESCOC1=CC(=CC(OC)=C1OC)C1=CC=NC2=CC(=NN12)C1=CC=C(C)C=C1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.KASAI, R, MATSUMOTO, et al. 3,4-SECO-LUPANE TYPE TRITERPENE GLYCOSYL ESTERS FROM A KOREAN MEDICINAL PLANT, ACANTHOPANAX-CHIISANENSIS (ARALIACEAE)[J]. Chem Pharm Bull Tokyo, 1986.
molnova catalog



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