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产品详情
产品名称 英文名称:BIX-01294 同义词 BIX-01294、935693-62-2、N-(1-benzylpiperidin-4-yl)-6,7-dimethoxy-2-(4-methyl-1,4-diazepan-1-yl)quinazolin-4-amine、BIX01294、BIX 01294 trihydrochloride hydrate、CHEMBL569864、2-(Hexahydro-4-methyl-1H-1,4-diazepin-1-yl)-6,7-dimethoxy-N-[1-(phenylmethyl)-4-piperi 产品性质 CAS编号:935693-62-2 分子式:C28H38N6O2 分子量:490.64 PubChem编号:25150857 英文别名:BIX-01294|935693-62-2|N-(1-benzylpiperidin-4-yl)-6,7-dimethoxy-2-(4-methyl-1,4-diazepan-1-yl)quinazolin-4-amine|BIX01294|BIX 01294 trihydrochloride hydrate|CHEMBL569864|2-(Hexahydro-4-methyl-1H-1,4-diazepin-1-yl)-6,7-dimethoxy-N-[1-(phenylmethyl)-4-piperi 规格或纯度:≥98% 英文名称:BIX-01294 生化机理:BIX-01294, a diazepin-quinazolinamine derivative, is a selective inhibitor of G9a histone methyl transferase (G9a HMTase) that impairs G9a HMTase and generation of H3K9me2 in vitro. In its inhibition of the histone lysine methyltransferases, BIX-01294 does not compete with cofactor S-adenosyl-methionine. G9a HMTase regulates gene expression including one of the pluripotency genes Oct4. It is reported that BIX-01294 enhances reprogramming efficiency of neural progenitor cells to the same levels as when four transcription factors (Oct4, Klf4, Sox2 and c-Myc) were introduced to somatic cells for generation of induced pluripotent stem cells. BIX-01294 and valproic acid, a histone deacetylase (HDAC) inhibitor, may replace the requirement for ectopic OCT4 (POU5F1) and cMyc respectively in pluripotent stem cell induction (iPS) recipes.Potent, selective G9a and G9a-like protein histone lysine methyltransferase inhibitor (IC 50 values are 1.7 and 0.7 μM at G9a and G9a-like protein, respectively). No activity at other HMT up to 37 μM. Antimalarial agent. Active in vitro . 储存温度:-20°C储存 运输条件:超低温冰袋运输 备注:如果有可能,您尽量在使用的当天配置溶液,并在当天使用完它。但是,如果您需要预先配制储备溶液,我们建议您将溶液等份保存在-20°C的密封小瓶中。通常,它们最多可以使用一个月。在使用前和打开样品瓶之前,我们建议您让您的产品在室温下平衡至少1小时。需要更多关于溶解度,用法和处理的建议吗?请访问我们的常见问题(FAQ)页面以获取更多详细信息。 产品介绍:BIX01294是G9a组蛋白甲基转移酶(HMTase)抑制剂,IC50为2.7 μM。A selective large conductance calcium activated potassium channel activatorBIX01294 is an inhibitor of G9a histone methyltransferase with IC50 of 2.7 μMA selective large conductance calcium activated potassium channel activator IUPAC Name:N-(1-benzylpiperidin-4-yl)-6,7-dimethoxy-2-(4-methyl-1,4-diazepan-1-yl)quinazolin-4-amine INCHI:InChI=1S/C28H38N6O2/c1-32-12-7-13-34(17-16-32)28-30-24-19-26(36-3)25(35-2)18-23(24)27(31-28)29-22-10-14-33(15-11-22)20-21-8-5-4-6-9-21/h4-6,8-9,18-19,22H,7,10-17,20H2,1-3H3,(H,29,30,31) InChi Key:OSXFATOLZGZLSK-UHFFFAOYSA-N Canonical SMILES:CN1CCCN(CC1)C2=NC3=CC(=C(C=C3C(=N2)NC4CCN(CC4)CC5=CC=CC=C5)OC)OC Isomeric SMILES:CN1CCCN(CC1)C2=NC3=CC(=C(C=C3C(=N2)NC4CCN(CC4)CC5=CC=CC=C5)OC)OC PubChem CID:25150857 CAS Registry No.:935693-62-2 ChEMBL Ligand:CHEMBL569864 RCSB PDB Ligand:Q4A 溶解性:≥5.1 mg/mL in EtOH with ultrasonic; ≥51.2 mg/mL in H2O 密度:1.6 折光率:1.54 熔点:178.44°C 产品包装
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