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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 - Gs-441524 - Vitamin D Analogs - Antibiotics

Catalog No	CAS NO	Product name
CR2309	955977-50-1	PI-3065 PI3065 is a p110δ isoform of phosphoinositide-3-OH kinase (PI(3)K) inhibitor. Inhibitors against the p110δ isoform of phosphoino..
CR2308	1202757-89-8	AVL-292 Spebrutinib Spebrutinib, also known as AVL-292 or CC-292, is an orally bioavailable, selective inhibitor of BrutonÂ’s agammaglobulinemia..
CR2307	1206161-97-8	Filgotinib (GLPG0634) Filgotinib, also known as GLPG0634, is a potent and selective JAK1 inhibitor under investigation for the treatment of rheumatoid a..
CR2306	1226895-15-3	FLLL32 FLLL32, a novel curcumin analogue, is a potent STAT3 inhibitor. FLLL32 specifically reduced STAT3 phosphorylation at Tyr705 (pSTAT..
CR2305	52214-84-3	Ciprofibrate Ciprofibrate is a peroxisome proliferator-activated receptor agonist. Target: PPAR Ciprofibrate is a hypolipidemic compound that c..
CR2304	1415238-77-5	5S rRNA modificator 5S rRNA modificator is a rRNA modification agent. 5S rRNA modificator worked as an electrophile for 2'-hydroxyl acylation on s..
CR2303	173352-39-1	CM346 Afobazole hydrochloride Fabomotizole hydrochloride is an anxiolytic drug; produces anxiolytic and neuroprotective effects without any sedative or muscle r..
CR2302	67469-81-2	GBR 12935 dihydrochloride GBR-12935 is a potent and selective dopamine reuptake inhibitor. It was originally developed in its 3H radiolabelled form for the ..
CR2301	1515856-92-4	XEN445 XEN445 is potent and selective endothelial lipase inhibitor, that showed good ADME and PK properties, and demonstrated in vivo eff..
CR2300	1395084-25-9	MS436 MS436 is a BRD4 inhibitor. MS436, through a set of water-mediated interactions, exhibits low nanomolar affinity (estimated Ki of 3..

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