Crene Biotechnology,API,pharmaceutical intermediates,small molecules,prostaglandins,chemicals

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- Prostaglandins - Custom Synthesis - PARP Inhibitors - PI3K Inhibitors - FAK Inhibitors - AKT Inhibitors - C-Kit Inhibitors - VEGFR Inhibitors - c-Met Inhibitors - CDK Inhibitors - CYP17 Inhibitors - DNA/RNA Inhibitors - mTOR Inhibitors - SRC Inhibitors - Others - Veterinary APIs

Catalog No	CAS NO	Product name
CR3227	72882-78-1	PF-9366 PF-9366 is a Mat2A inhibitor, with an IC50 of 420 nM and a Kd of 170 nM. PF-9366 displays no substantial off-target activity i..
CR3226	1423715-37-0	Seclidemstat Seclidemstat (Compound 2577) reduces tumor volume at 40, 80 mg/kg by i.p. and also shows such effect at 80 mg/kg via p.o. dosing.
CR3225	594839-88-0	Tafamidis Tafamidis, Tafamidis, also known as Fx-1006 or PF-06291826, is a drug for the amelioration of transthyretin-related hereditary amy..
CR3224	1532593-30-8	ML355 ML355 is a potent and selective inhibitors of 12-Lipoxygenase(12-LOX) with IC50 of 0.34 μM, excellent selectivity over related li..
CR3223	1218942-37-0	Setanaxib GKT137831 Setanaxib (GKT137831), also known as GTK831, is a novel and potent Nox4 inhibitor. GKT137831 reduced the increased leukocyte adher..
CR3222	1604810-83-4	THZ1 THZ1 is a selective CDK7 inhibitor that preferentially diminishes transcription in cancer cells. THZ1 has the unprecedented abilit..
CR3221	877636-42-5	ML221 ML221 is a potent apelin receptor (APJ) functional antagonist in cell-based assays that is >37-fold selective over the closely ..
CR3220	1052147-86-0	LP-211 LP-211 (10 mg/kg, i.p.) rapidly reaches the systemic circulation in the mouse, with mean Cmax of 0.76 ± 0.32 μg/mL at 30 m..
CR3219	1456858-58-4	HG-9-91-01 HG-9-91-01 inhibits a number of protein tyrosine kinases that possess a threonine residue at the gatekeeper site, such as Src fami..
CR3218	1338545-07-5	OTS964 HCl OTS964 is a potent and selective TOPK inhibitor with potential anticancer activity. OTS964 inhibits TOPK kinase activity with high..

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