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Changwon Yang
Solubility: DMSO : 100 mg/mL (200
Molecular Weight: 2833
ML-792 inhibits SAE/SUMO1 and SAE/SUMO2 in ATP–inorganic pyrophosphate (PPi) exchange assays with IC50 of 3 nM and 11 nM
8)12-5-3-11-4-6-13-15(2
(±)-J 113397 imebutine maleate Changwon Yang() 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