S-(2-aminoethyl) Isothiourea (dihydrobromide) 684PADS tetrasodium 3E)-5-hydroxy-3-methylpenta-1

3E)-5-hydroxy-3-methylpenta-1

selective and cell permeable Jumonji histone demethylase inhibitor

Dose-response studies reveal that 30 nM Go-6976 is sufficient to cause abrogation of S-phase arrest in 6 h and abrogation of G2 arrest followed by lethal mitosis in 24 h

NC(=N)C1C=CC(=CC=1)N/N=N/C1C=CC(=CC=1)C(N)=N

InChi: InChI=1S/C10H14ClN3

S-(2-aminoethyl) Isothiourea (dihydrobromide) 684PADS tetrasodium 3E)-5-hydroxy-3-methylpenta-1S (2 aminoethyl) Isothiourea (dihydrobromide) is a potent and non selective inhibitor of NOS with Ki values of 1. 8, 2. 1, and 0. 59 M for human nNOS, eNOS, and iNOS, respectively . In the brain, nitric oxide (NO), which is synthesized from L arginine (Arg) by NO synthase (NOS), acts as both an intra and an intercellular second messenger. Nitric oxide synthase (iNOS, eNOS, and nNOS) catalyzed the production of NO in the two step oxidation of L