(±)-J 113397 imebutine maleate Smiles: OC1=CC=C(CCNCCN(C2CCCCC2)C(=O)CCNCCC2=CC(Cl)=C(Cl)C=C2)C2OCC(=O)NC=21

Smiles: OC1=CC=C(CCNCCN(C2CCCCC2)C(=O)CCNCCC2=CC(Cl)=C(Cl)C=C2)C2OCC(=O)NC=21

Smiles: C[C@]12CC[C@H]3[C@@H](CCC4C=C(O)C(=CC=43)OC)[C@@H]1CCC2=O

ML-792 inhibits SAE/SUMO1 and SAE/SUMO2 in ATP–inorganic pyrophosphate (PPi) exchange assays with IC50 of 3 nM and 11 nM

Identification of ellagic acid as potent inhibitor of protein kinase CK2: a successful example of a virtual screening application

8a-trimethyl-1

(±)-J 113397 imebutine maleate Smiles: OC1=CC=C(CCNCCN(C2CCCCC2)C(=O)CCNCCC2=CC(Cl)=C(Cl)C=C2)C2OCC(=O)NC=21() J 113397 is a potent and selective non peptidyl antagonist of ORL1 receptor, with a Ki value of 1. 8 nM for cloned human ORL1 . The ORL1 receptor is a G protein coupled. It is structurally related to the opioid receptors. The heptadecapeptide nociceptin orphanin FQ is the endogenous ligand . In CHO ORL1 cells, nociceptinr orphanin FQ dose dependently suppressed the accumulation of cyclic AMP stimulated by forskolin with an EC value of 0. 22 0. 011