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UNC-0642

  Cat. No.:  DC7750   Featured
Chemical Structure
1481677-78-4
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More than 5000 active chemicals with high quality for research!
Field of application
UNC0642 is a novel highly potent, selective and cell permeable inhibitor of the homologous protein lysine methyltransferases, G9a and GLP, with IC50 < 2.5 nM.
Chemicals PropertiesBiological activity COA & MSDSRelated productsDatasheet
Cas No.: 1481677-78-4
Chemical Name: UNC-0642，UNC0642，UNC 0642
Synonyms: UNC-0642，UNC0642，UNC 0642
SMILES: N1=C2C(C=C(OC)C(OCCCN3CCCC3)=C2)=C(NC2CCN(C(C)C)CC2)N=C1N1CCC(F)(F)CC1
Formula: C29H44F2N6O2
M.Wt: 546.7
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: UNC0642 is a potent and selective G9a/GLP inhibitor, with an IC50 of less than 2.5 nM.
In Vivo: A single intraperitoneal (IP) injection (5 mg/kg) of UNC0642results in a plasma Cmax (maximum concentration) of 947 ng/mL and an AUC (area under the curve) of 1265 hr*ng/mL[1].
In Vitro: UNC0642 displays high in vitro and cellular potency, low cell toxicity, and excellent selectivity. UNC0642 is competitive with the peptide substrate and non-competitive with the cofactor SAM. The Ki of UNC0642 is determined to be 3.7±1 nM. UNC0642 displays high in vitro potency for GLP (IC50< 2.5 nM), similar to G9a. UNC0642 is more than 300-fold selective for G9a and GLP over a broad range of kinases, GPCRs, transporters, and ion channels. UNC0642 exhibits high potency at reducing the H3K9me2 mark, low cell toxicity, and good separation of functional potency and cell toxicity in a number of cell lines. It reduces clonogenicity in PANC-1 cells, a pancreatic carcinoma cell line[1].
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
2018-0101
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