
D64131
CAS No. 74588-78-6
D64131( D-64131 | D 64131 | D64131 )
Catalog No. M15845 CAS No. 74588-78-6
D-64131 is a tubulin polymerization inhibitor with an IC50 value of 0.53 μM.
Purity : >98% (HPLC)






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Biological Information
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Product NameD64131
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NoteResearch use only, not for human use.
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Brief DescriptionD-64131 is a tubulin polymerization inhibitor with an IC50 value of 0.53 μM.
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DescriptionD-64131 is a tubulin polymerization inhibitor with an IC50 value of 0.53 μM. The polymerization of bovine brain tubulin as well as binding of [3H] colchicine to biotinylated αβ-tubulin was dose-dependently inhibited by D-64131. Many Y cells display abnormal microtubule structures, such as fragmented mitotic spindles or multiple spindle poles after treatment with D-64131. Nuclear blebbing and abnormal nuclear structures typical for apoptotic cells are detectable in many cells treated with D-64131. In nude mice, D-64131 proved to be well tolerated and highly active against the human amelanoic melanoma MEXF 989 tumor xenograft. D-64131 treatment resulted in significant tumor growth inhibition during treatment.
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In VitroD-64131 is antimitotic by binding to β-tubulin, thereby destabilizing microtubules and arresting mitotic cells in the M-phase.D-64131 inhibits the proliferation of tumor cells from 12 of 14 different organs and tissues with mean IC50s of 62 nM.D-64131 is cytotoxic toward MDR/MRP tumor cell lines.D-64131 suppresses U373 proliferation and cell cycle with IC50s of 74 nM and 62.7nM, respectively. Cell Cycle Analysis Cell Line:HeLa/KB cervical carcinoma cells Concentration:1 nM-1 μM Incubation Time:48 hours Result:Induced dose-dependently arrested in G2-M before induction of apoptotic cell death.
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In VivoD-64131 (200-400 mg/kg; p.o.; daily; days 1-5, 8-9, and 15-18) significantly inhibits tumor growth in the human amelanoic melanoma MEXF 989 tumor xenograft mice model.D-64131 has oral bioavailability and is well tolerated at efficacious doses. Animal Model:Outbred nude mice (6-8 weeks),human amelanoic melanoma MEXF 989 tumor xenograft model Dosage:200 mg/kg, 400 mg/kg Administration:Oral administration, daily, on days 1-5, 8-9, and 15-18 after xenograft Result:Resulted in significant tumor growth inhibition during treatment.
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SynonymsD-64131 | D 64131 | D64131
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PathwayCytoskeleton/Cell Adhesion Molecules
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TargetMicrotubule/Tubulin
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RecptorTubulin polymerization
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Research AreaCancer
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Indication——
Chemical Information
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CAS Number74588-78-6
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Formula Weight251.28
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Molecular FormulaC16H13NO2
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Purity>98% (HPLC)
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SolubilitySoluble in DMSO
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SMILESO=C(C(N1)=CC2=C1C=CC(OC)=C2)C3=CC=CC=C3
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Chemical Name(5-Methoxy-1H-indol-2-yl)phenylmeth?anone
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.Beckers T, et al. Y Res. 2002 Jun 1;62(11):3113-9.
molnova catalog



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