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Products

Catalog NoChemical NameCAS NumberPurityChemical Structure
52007SRT17201001645-58-498% 
SRT1720 is a selectiveSIRT1activator withEC50of 0.16 M, but is >230-fold less pote
20294Paltusotine ( CRN-00808 )2172870-89-0≧98.0%
Paltusotine is a new class of oral, selective, nonpeptide, somatostatin receptor type
19381Abrocitinib1622902-68-4>98%
Abrocitinib, Bulk in stock, contact us by email for the quotation. Kg scale intermedi
24003NVL-655 ( ALK-IN-27 )2739866-40-9≧98.0%
NVL-655 is a novel, brain-penetrant, ALK-selective inhibitor that was designed to add
61726Ensifentrine ( RPL554 )1884461-72-6≧98.0%
Ensifentrine (RPL554) is an investigational, first-in-class, inhaled dual inhibitor o
20513ZINC40099027 (ZN27)1211825-25-0≧98.0%
ZINC40099027 (ZN27) is a specific focal adhesion kinase (FAK) activator that promotes
20510CC-92480 ( Mezigdomide )2259648-80-9≧98.0%
CC-92480 Is a Novel Cereblon E3 Ligase Modulator with Enhanced Tumoricidal and Immuno
51703Luminespib ( NVP-AUY922 ; VER-52296 )747412-49-398%
NVP-AUY922 is an experimental drug candidate for the treatment of cancer. It was disc
51902AT131481056901-62-2≧98%
AT13148, a first-in-class multi-AGC kinase inhibitor, against gastric cancer cells. A
51702AZD12081204144-28-498%
AZD1208 is a potent, highly selective, and orally available Pim kinase inhibitor that
51603AZD64821173900-33-8≧98.0%
AZD6482 is aPI3Kinhibitor withIC50of 10 nM, 8-, 87- and 109-fold more selective to PI
51905CPI-613(Devimistat )95809-78-2≧98.0%
CPI-613( Devimistat ) is an E1 pyruvate dehydrogenase (PDH) modulator that prevents c