
Tubulin inhibitor 11
CAS No. 2366260-33-3
Tubulin inhibitor 11( —— )
Catalog No. M36093 CAS No. 2366260-33-3
Tubulin Inhibitor 11 is a potent, orally active agent that inhibits tubulin by targeting the Colchicine binding site. It impedes tubulin polymerization, leading to mitotic blockade and apoptosis.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
2MG | 76 | Get Quote |
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5MG | 116 | Get Quote |
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10MG | 187 | Get Quote |
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25MG | 419 | Get Quote |
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50MG | 618 | Get Quote |
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100MG | 860 | Get Quote |
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500MG | 1728 | Get Quote |
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1G | Get Quote | Get Quote |
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Biological Information
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Product NameTubulin inhibitor 11
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NoteResearch use only, not for human use.
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Brief DescriptionTubulin Inhibitor 11 is a potent, orally active agent that inhibits tubulin by targeting the Colchicine binding site. It impedes tubulin polymerization, leading to mitotic blockade and apoptosis.
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DescriptionTubulin inhibitor 11 is a potent and orally active tubulin inhibitor. Tubulin inhibitor 11 targets the Colchicine binding site on tubulin, inhibits tubulin polymerization, promotes mitotic blockade and apoptosis.
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In VitroTubulin inhibitor 11 (Compound 48; 0.03-0.1 μM; 12 hours) causes cell cycle arrest at G2/M phase. Tubulin inhibitor 11 reduces cdc2 phosphorylation and increases cyclin B1 and phosphorylation of histone H3 at Ser10 in cells.Tubulin inhibitor 11 (Compound 48; 0.03-0.3 μM; 48 hours) causes cancer cell apoptosis.Tubulin inhibitor 11 (Compound 48) demonstrates favorable antiproliferative activities in DU145 cells with an IC50 of 8 nM.Tubulin inhibitor 11 (Compound 48; 0.03-0.3 μM) significantly reduces the expression levels of acetyl-α-tubulin and α-tubulin in a dose-dependent manner.Cell Cycle Analysis Cell Line:DU145 cells Concentration:0.01 μM, 0.03 μM, and 0.1 μM Incubation Time:12 hours Result:Caused cell cycle arrest at G2/M phase.Apoptosis Analysis Cell Line:DU145 cells Concentration:0.03 μM, 0.1 μM, and 0.3 μM Incubation Time:48 hours Result: Induced cancer cell apoptosis.Western Blot Analysis Cell Line:DU145 cells Concentration:0.01 μM, 0.03 μM, and 0.1 μM Incubation Time:12 hours Result:Reduced cdc2 phosphorylation and increased cyclin B1 and phosphorylation of histone H3 at Ser10 in cells.
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In VivoTubulin inhibitor 11 (Compound 48; 5-10 mg/kg; p.o; once daily) shows robust in vivo antitumor efficacies.Animal Model:Male athymic BALB/c nude mice (18-20 g) injected with DU145, NCI-H1299 or A549R cells Dosage:5 mg/kg, 10 mg/kg Administration:p.o; once dailyResult:Effectively suppressed tumor growth.
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorMicrotubule Associated | Apoptosis
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Research Area——
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Indication——
Chemical Information
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CAS Number2366260-33-3
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Formula Weight409.5
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Molecular FormulaC22H23N3O3S
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (244.20 mM; Ultrasonic )
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SMILESN(S(=O)(=O)C1=CC=C(C)C=C1)C2=CC(C(NCC=3C=CC(C)=NC3)=O)=CC=C2C
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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. Songwen Lin, et al. Optimization of Benzamide Derivatives as Potent and Orally Active Tubulin Inhibitors Targeting the Colchicine Binding Site. J Med Chem. 2022 Dec 22;65(24):16372-16391. ?
molnova catalog



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