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SKU | Size | Availability | Price | Qty |
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C422308-1ml | 1ml | Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience! | $253.90 |
Histone Acetyltransferase Inhibitors
Specifications & Purity | 10mM in DMSO |
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Biochemical and Physiological Mechanisms | CPI-637 is a selective and cell-active benzodiazepinone CBP/EP300 bromodomain inhibitor with IC50 values of 0.03 μM and 0.051μM for CBP and EP300 respectively in TR-FRET assay. It is highly selective against other bromodomains, displaying substantial bioc |
Storage Temp | Store at -80°C |
Shipped In | Ice chest + Ice pads |
Product Description | Information CPI-637 CPI-637 is a selective and cell-active benzodiazepinone CBP/EP300 bromodomain inhibitor with IC50 values of 0.03 μM and 0.051μM for CBP and EP300 respectively in TR-FRET assay. It is highly selective against other bromodomains, displaying substantial biochemical activity only against BRD9. Targets CBP (Cell-free assay); EP300 (Cell-free assay) 0.03 μM; 0.051 μM In vitro CPI-637 inhibits MYC expression in AMO-1 cells (EC50=0.60 μM). Cell Research(from reference) Cell lines:AMO-1 cells Concentrations:0-5 μM Incubation Time:6 h |
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IUPAC Name | (4R)-4-methyl-6-[1-methyl-3-(1-methylpyrazol-4-yl)indazol-5-yl]-1,3,4,5-tetrahydro-1,5-benzodiazepin-2-one |
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INCHI | InChI=1S/C22H22N6O/c1-13-9-20(29)25-18-6-4-5-16(22(18)24-13)14-7-8-19-17(10-14)21(26-28(19)3)15-11-23-27(2)12-15/h4-8,10-13,24H,9H2,1-3H3,(H,25,29)/t13-/m1/s1 |
InChi Key | BFTKDWYIRJGJCA-CYBMUJFWSA-N |
Canonical SMILES | CC1CC(=O)NC2=CC=CC(=C2N1)C3=CC4=C(C=C3)N(N=C4C5=CN(N=C5)C)C |
Isomeric SMILES | C[C@@H]1CC(=O)NC2=CC=CC(=C2N1)C3=CC4=C(C=C3)N(N=C4C5=CN(N=C5)C)C |
PubChem CID | 121271792 |
Molecular Weight | 386.45 |
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RIDADR | NONHforallmodesoftransport |
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