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GSK1324726A (I-BET726)

GSK1324726A (I-BET726) Suppliers list
Company Name: Hubei Jusheng Technology Co.,Ltd.
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Products Intro: Product Name:GSK1324726A (I-BET726)
CAS:1300031-52-0
Purity:0.99 Package:5KG;1KG
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Products Intro: Product Name:GSK1324726A
CAS:1300031-52-0
Purity:86799% Package:10kg 25kg 200 kilograms per barrel Remarks:good
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Products Intro: Product Name:GSK1324726A (I-BET726)
CAS:1300031-52-0
Purity:99.9% Package:25kgs/Drum;200kgs/Drum Remarks:FDA GMP CEP Approved Manufacturer
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Products Intro: Product Name:GSK1324726A (I-BET-726)
CAS:1300031-52-0
Purity:98% Package:1mg Remarks:V0422
GSK1324726A (I-BET726) Basic information
Product Name:GSK1324726A (I-BET726)
Synonyms:4-((2S,4R)-1-acetyl-4-(4-chlorophenylamino)-2-methyl-1,2,3,4-tetrahydroquinolin-6-yl)benzoic acid;4-[(2S,4R)-1-Acetyl-4-[(4-chlorophenyl)amino]-2-methyl-1,2,3,4-tetrahydro-6-quinolinyl]benzoic acid;GSK1324726A (I-BET726);4-(cis-1-Acetyl-4-((4-chlorophenyl)amino)-2-methyl-1,2,3,4-tetrahydroquinolin-6-yl)benzoic acid;I-BET726; I-BET 726;CS-1736;4-[(2S,4R)-1-Acetyl-4-[(4-chlorophenyl)amino]-1,2,3,4-tetrahydro-2-methyl-6-quinolinyl]benzoic acid;I-BET726
CAS:1300031-52-0
MF:C25H23ClN2O3
MW:434.91
EINECS:
Product Categories:Inhibitors
Mol File:1300031-52-0.mol
GSK1324726A (I-BET726) Structure
GSK1324726A (I-BET726) Chemical Properties
Boiling point 707.3±60.0 °C(Predicted)
density 1.304±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility insoluble in H2O; ≥1.87 mg/mL in EtOH with gentle warming and ultrasonic; ≥17.7 mg/mL in DMSO
form Powder
pka4.20±0.10(Predicted)
InChIKeyFAWSUKOIROHXAP-NPMXOYFQSA-N
SMILESC(O)(=O)C1=CC=C(C2C=CC3=C(C=2)[C@H](NC2=CC=C(Cl)C=C2)C[C@H](C)N3C(C)=O)C=C1
Safety Information
MSDS Information
GSK1324726A (I-BET726) Usage And Synthesis
DescriptionI-BET726 is an inhibitor of BET family proteins that binds BRD2, BRD3, and BRD4 with high affinity (IC50s = 41, 31, and 22 nM, respectively) and competes with tetra-acetylated histone 4 peptides for binding to the bromodomains of these proteins. It exhibits >1,000-fold selectivity for these proteins over other bromodomain-containing homologs. I-BET726 inhibits cell growth and induces cytotoxicity in neuroblastoma cell lines by modulating the expression of genes involved in apoptosis and Myc signaling. I-BET726 can be administered orally to animals, and it reduces tumor growth in mouse xenograft models of human neuroblastoma.
targetBRD2
references[1] wyce a, ganji g, smitheman kn, chung cw, korenchuk s, bai y, barbash o, le b, craggs pd, mccabe mt, kennedy-wilson km, sanchez lv, gosmini rl, parr n, mchugh cf, dhanak d, prinjha rk, auger kr, tummino pj. bet inhibition silences expression of mycn and bcl2 and induces cytotoxicity in neuroblastoma tumor models. plos one. 2013 aug 23;8(8):e72967.
GSK1324726A (I-BET726) Preparation Products And Raw materials
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