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

+ AII PRODUCTS

- 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
CR3495	1172854-54-4	NS-3-008 hydrochloride NS-3-008 hydrochloride is an orally active transcriptional inhibitor of G0/G1 switch 2 (G0s2) with an IC50 of 2.25 μM. NS-3-008 h..
CR3494	1550053-02-5	BRD3308 BRD3308 is a highly selective HDAC3 inhibitor with an IC50 of 54 nM. BRD3308 is 23-fold selectivity for HDAC3 over HDAC1 (IC50 of ..
CR3493	1186649-91-1	ML-109 ML-109 is a potent and full thyroid stimulating hormone receptor (TSHR) agonist, with an EC50 of 40 nM.Chemical Name: N-(4-(5-(3-B..
CR3492	702662-50-8	STING agonist-1 G10 STING agonist-1 (G10) is human-specific STING agonist that elicits antiviral activity against emerging Alphaviruses. G10 potently ..
CR3491	1354707-41-7	Mitochonic Acid 5 Mitochonic acid 5 binds mitochondria and ameliorates renal tubular and cardiac myocyte damage. Mitochonic acid 5 modulates mitocho..
CR3490	1799328-86-1	ASTX660 ASTX660 is an orally bioavailable, non-peptidomimetic antagonist of both X chromosome-linked inhibitor of apoptosis protein (XIAP)..
CR3489	GMB-475	GMB-475 GMB-475 is a degrader of BCR-ABL1 tyrosine kinase based on PROTAC, overcoming BCR-ABL1-dependent drug resistance. GMB-475 targets ..
CR3488	1597403-47-8	ISRIB trans-isomer ISRIB (trans-isomer) is a potent inhibitor of PERK with an IC50 of 5 nM.IC50 & Target: IC50: 5 nM (PERK)[1]In Vitro: Trans-ISR..
CR3487	1286739-19-2	FRAX597 FRAX597 is a potent and selective inhibitor of the p21-activated kinases. FRAX597 inhibits tumorigenesis of neurofibromatosis type..
CR3486	1438391-30-0	CC-401 Hydrochloride CC-401 hydrochloride is a potent inhibitor of all three forms of JNK with Ki of 25 to 50 nM.

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