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

Catalog No	CAS NO	Product name
CR3934	960201-86-9	Zanubrutinib Impurity 7 Synonyms: 1-Piperidinecarboxylic acid, 4-[3-(dimethylamino)-1-oxo-2-propen-1-yl]-, 1,1-dim;4-[3-(DiMethylaMino)-1-oxo-2-propen-1-y..
CR3933	1094-61-7	β-Nicotinamide mononucleotide Nicotinamide Mononucleotide, also known as ("NMN" and "β-NMN") is a nucleotide derived from ribose and nicoti..
CR3932	2222112-77-6	ARV-110 ARV-110 is a first-in-class PROTAC that effectively targets the wild type Androgen Receptor (AR) and certain genomic alterations o..
CR3931	2296729-00-3	Sotorasib (AMG510) Sotorasib (AMG-510) is a first-in-class, orally bioavailable, and selective KRAS G12C covalent inhibitor. Sotorasib irreversibly i..
CR3930	1899922-76-9	3-(2-Chloropyrimidin-4-yl)-1-cyclopropyl-1H-indole Synonyms: 3-(2-Chloropyrimidin-4-yl)-1-cyclopropyl-1H-indole;1H-Indole, 3-(2-chloro-4-pyrimidinyl)-1-cyclopropyl-Chemical & P..
CR3929	236743-98-9	Trabectedin intermediate Chemical Name: (6aS,7R,13S,14R,16R)-5-(allyloxy)-16-(hydroxymethyl)-9-methoxy-8-(methoxymethoxy)-4,10,17-trimethyl-6,6a,7,13,14,16..
CR3928	2291328-15-7	Trabectedin intermediate M19 Chemical Properties: Density: 1.30±0.1 g/cm3(Predicted)pka: 3.70±0.60(Predicted) Related Products: Trabected..
CR3927	265134-87-0	Trabectedin intermediate Chemical Name: (6aS,7R,13S,14R,16R)-16-(((tert-butyldimethylsilyl)oxy)methyl)-5-hydroxy-9-methoxy-8-(methoxymethoxy)-4,10,17-trime..
CR3926	182201-77-0	S-((9H-fluoren-9-yl)methyl)-N-((allyloxy)carbonyl)-L-cysteine Chemical Name: S-(9H-Fluoren-9-ylmethyl)-N-[(2-propen-1-yloxy)carbonyl]-L-cysteineSynonyms: L-Cysteine, S-(9H-fluoren-9-ylmethyl)-..
CR3925	2267329-76-8	EGFR-IN-7 TQB3804, also known as EGFR-IN-7, is a selective and potent EGFR kinase inhibitor. TQB3804 displayed potent enzymatic activities f..

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