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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
CR3517	1369489-71-3	E-7046 E7046 is a potent and selective antagonist of the type 4 prostaglandin E2 (PGE2) receptor EP4. EP4 Antagonism by E7046 diminishes ..
CR3516	1311423-89-8	YF-2 YF-2 is a highly selective, blood-brain-barrier permeable histone acetyltransferase activator. YF-2 acetylates H3 in the hippocamp..
CR3515	1257423-87-2	BTdCPU BTdCPU is an activator of HRI. The eIF2-alpha kinase HRI is a novel therapeutic target in multiple myeloma. Combination therapy wi..
CR3514	314761-14-3	BTSA1 BTSA1 is a potent, high affinity and orally active BAX activator with an IC50 of 250 nM and an EC50 of 144 nM. BTSA1 binds with hi..
CR3513	1269662-73-8	SHR-1258 Pyrotinib Pyrotinibm, also known as SHR-1258, is an orally bioavailable, dual kinase inhibitor of the epidermal growth factor receptor (EGFR..
CR3511	375823-41-9	anti-IL-6R Tocilizumab Tocilizumab (Anti-Human IL6R, Humanized Antibody) is an anti-human interleukin-6 receptor (IL-6R) neutralizing antibody, prevents ..
CR3510	1891087-61-8	BAY-1816032 BAY-1816032 is a potent and oral available BUB1 (budding uninhibited by benzimidazoles 1) kinase inhibitor with an IC50 of 7 nM. B..
CR3508	152831-36-2	NE-10790 3-PEHPC NE10790 is a risedronate analog, which belongs to the group of phosphonocarboxylates in which one of the phosphonate groups is sub..
CR3507	162490-88-2	sordidin Synonyms: 2,8-Dioxabicyclo[3.2.1]octane, 1-ethyl-3,5,7-trimethyl-, (1S,3R,5R,7S)-;sexual pheromone of Cosmopolites sordidus Germar
CR3506	7252-84-8	3-Amino-6-methoxypyridazine Chemical Name: 3-Amino-6-methoxypyridazine Synonyms: 6-methoxypyridazin-3-amine

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