BDBM225241 3-Nitro-N-(2-phenylbenzo[d]oxazol-6-yl)benzenesulfonamide (2)::MT-pep

SMILES CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](Cc1ccc(OP(O)(O)=O)cc1)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)N)[C@@H](C)CC)C(=O)N[C@@H](Cc1ccc(O)cc1)C(O)=O

InChI Key InChIKey=PDAKWZXYKUNQKV-RMOSGFMZSA-N

Data  1 IC50  2 ITC

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 225241   

TargetHistone-lysine N-methyltransferase EHMT2(Homo sapiens (Human))
Shenyang Pharmaceutical University

LigandBDBM225241(3-Nitro-N-(2-phenylbenzo[d]oxazol-6-yl)benzenesulf...)Copy SMILESCopy InChI

Affinity DataIC50: >4.00E+4nMpH: 8.5 T: 2°CAssay Description:Biochemical activity of G9a was measured as described [Kubicek et al., Mol. Cell, 25:473-481]. Assays were performed in white, opaque 384-well plates...More data for this Ligand-Target Pair

Target InfoPDBReactome pathway
UniProtKB/SwissProt
GoogleScholar

Ligand InfoKEGGPC cidPC sid

In DepthDetails ArticlePubMed
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