Pioglitazone hydrochloride

A cell-permeable quinone reductase inhibitor with anti-coagulant properties. Binds competitively with NADH or NADPH to inhibit NAD(P)H:quinone oxidoreductase (NQO1).

Diisopropanolamine was used to study its effects upon choline uptake and phospholipid synthesis in Chinese hamster ovary (CHO) cells.

Diisopropanolamine was used to study its effects upon choline uptake and phospholipid synthesis in Chinese hamster ovary (CHO) cells.

Diisopropanolamine was used to study its effects upon choline uptake and phospholipid synthesis in Chinese hamster ovary (CHO) cells.

Cell Line Origin Mouse mammary, drug-resistant Cell Line Description The cisplatin-resistant variant of the mouse mammary tumour cell line EMT6/P (Sigma Catalogue number. 96042344) was derived by continuous in vitro exposure to increasing

A selective ERR&beta/&gamma receptor agonist (EC₅₀ = 130 nM) used to potentiate ERR&gamma-induced growth inhibition in LNCaP and DU145 prostate cancer cell lines.

Ebopiprant (OBE022) is an oral and selective prostaglandin F 2α ( PGF 2α ) receptor antagonist, with K i s of 1 nM, 26 nM for human and rat FP receptors, respectively.In VitroEbopiprant (OBE022) and OBE002 are assayed for FP binding affinity by

Ebopiprant (OBE022) is an oral and selective prostaglandin F 2α ( PGF 2α ) receptor antagonist, with K i s of 1 nM, 26 nM for human and rat FP receptors, respectively.In VitroEbopiprant (OBE022) and OBE002 are assayed for FP binding affinity by

InformationElimusertib (BAY-1895344) hydrochloride is a potent, highly selective and orally availableATRinhibitor with an IC50 of 7 nM.TargetsATR (Cell-free assay) 7 nMIn vitroBAY 1895344 is shown to be a very potent and highly selective ATR

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

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