Ganirelix acetate

This nuclear receptor assay system utilizes proprietary non-human mammalian cells engineered to provide constitutive, high-level expression of full-length, unmodified human androgen receptor (NR3C4), a ligand-dependent transcription factor commonly

Auglurant (VU0424238) is a novel and selective mGlu5 antagonist with an IC 50 value of 11 nM (rat) and an IC 50 value of 14 nM (human). Auglurant (VU0424238) has an acceptable CNS penetrationIn VitroAuglurant (VU0424238) with an IC 50 value of 14 nM

Auglurant (VU0424238) is a novel and selective mGlu5 antagonist with an IC 50 value of 11 nM (rat) and an IC 50 value of 14 nM (human). Auglurant (VU0424238) has an acceptable CNS penetrationIn VitroAuglurant (VU0424238) with an IC 50 value of 14 nM

Auglurant (VU0424238) is a novel and selective mGlu5 antagonist with an IC 50 value of 11 nM (rat) and an IC 50 value of 14 nM (human). Auglurant (VU0424238) has an acceptable CNS penetrationIn VitroAuglurant (VU0424238) with an IC 50 value of 14 nM

Cotadutide (MEDI0382) acetate is a potent dual agonist of Glukagon-like peptide-1 (GLP-1) and GCGR with EC 50 values of 6.9 pM and 10.2 pM, respectively. Cotadutide acetate exhibits ability to facilitate both weight loss and glycaemic control, and

InformationFasiglifam (TAK-875) Fasiglifam (TAK-875) is a selective GPR40 agonist with EC50 of 14 nM in human GPR40 expressing CHO cell line, 400-fold more potent than oleic acid.In vitroTAK-875 exhibits potent agonist activity and high binding

InformationGaleterone (TOK-001) is a selectiveCYP17inhibitor andandrogen receptor (AR)antagonist withIC50of 300 nM and 384 nM, respectively, and is a potent inhibitor of human prostate tumor growth. Phase 2.In vitroGaleterone is effective at

Biochem/physiol Actions Ganirelix is a decapeptide GnRH antagonist. Ganirelix acts by blocking the action of GnRH upon the pituitary, thus rapidly suppressing the production and action of LH and FSH.

Biochem/physiol Actions Ganirelix is a decapeptide GnRH antagonist. Ganirelix acts by blocking the action of GnRH upon the pituitary, thus rapidly suppressing the production and action of LH and FSH.

Ganodermanondiol is a melanogenesis inhibitor isolated from the Ganoderma lucidum .Ganodermanondiol exhibits potent cytoprotective effects on tert-butyl hydroperoxide-induced hepatotoxicity . Ganodermanondiol shows significant anti- HIV-1 protease

Ganodermanondiol is a melanogenesis inhibitor isolated from the Ganoderma lucidum .Ganodermanondiol exhibits potent cytoprotective effects on tert-butyl hydroperoxide-induced hepatotoxicity . Ganodermanondiol shows significant anti- HIV-1 protease

InformationHPOB is a potent, selectiveHDAC6inhibitor withIC50of 56 nM, &gt:30-fold selectivity over other HDACs.TargetsHDAC6 : HDAC3 : HDAC8 : HDAC1 : HDAC10 14965,56 nM: 1.7 μM: 2.8 μM: 2.9 μM: 3.0 μMIn vitroIn normal (HFS) and transformed (LNCaP,