Pioglitazone hydrochloride

ENMD-1068 hydrochloride is a selective protease-activated receptor 2 ( PAR2 ) antagonist. ENMD-1068 hydrochloride reduces hepatic stellate cell activation and collagen expression by inhibiting TGF-β1/Smad signaling. ENMD-1068 hydrochloride also

ENMD-1068 hydrochloride is a selective protease-activated receptor 2 ( PAR2 ) antagonist. ENMD-1068 hydrochloride reduces hepatic stellate cell activation and collagen expression by inhibiting TGF-β1/Smad signaling. ENMD-1068 hydrochloride also

ERα degrader-2 is a selective estrogen receptor degrader ( SERD ) with potent binding affinity with ERα ( IC 50 =17.1 nM), good degradation efficacy ( EC 50 =0.3 nM). ERα degrader-2 exhibits favorable pharmacokinetic properties and excellent

ERα degrader-2 is a selective estrogen receptor degrader ( SERD ) with potent binding affinity with ERα ( IC 50 =17.1 nM), good degradation efficacy ( EC 50 =0.3 nM). ERα degrader-2 exhibits favorable pharmacokinetic properties and excellent

ERα degrader-2 is a selective estrogen receptor degrader ( SERD ) with potent binding affinity with ERα ( IC 50 =17.1 nM), good degradation efficacy ( EC 50 =0.3 nM). ERα degrader-2 exhibits favorable pharmacokinetic properties and excellent

InformationEstriol (NSC-12169) is an antagonist of the G-protein coupledestrogen receptorin estrogen receptor-negative breast cancer cells.In vitroMTT assays using G-1 shows that, in SkBr3 cells, the proliferative effect induced by 100 nM G-1 is

Application Etifoxine hydrochloride has been used as a &#947:-aminobutyric acid (GABA)-receptor agonist to study its effects on insulin expression in &#945: cell line (&#945:TC1) Biochem/physiol Actions Etifoxine is an anxiolytic

Potent PI 3-kinase inhibitor: also inhibits DNA-PK and mTOR.

Potent PI 3-kinase inhibitor: also inhibits DNA-PK and mTOR.

Potent PI 3-kinase inhibitor: also inhibits DNA-PK and mTOR.

Potent PI 3-kinase inhibitor: also inhibits DNA-PK and mTOR.

Potent PI 3-kinase inhibitor: also inhibits DNA-PK and mTOR.