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RECOMMENDED PRODUCTS

Catalog NoChemical NameCAS NumberPurityChemical Structure
20103003ML3801627138-52-6≧98.0%
ML380 is a highly potent and the first CNS penetrant M5 positive allosteric modulator
2071535Danicopan1903768-17-1≧98.0%
Danicopan, aslo known as ACH-4471 and ACH-0144471, is a highly potent, orally active
20259Elinzanetant ( NT-814 )929046-33-3≧98.0%
Elinzanetant, previously known as NT-814 (45), is a dual NK1,3R antagonist and theref
19381Abrocitinib1622902-68-4>98%
Abrocitinib, Bulk in stock, contact us by email for the quotation. Kg scale intermedi
20294Paltusotine ( CRN-00808 )2172870-89-0≧98.0%
Paltusotine is a new class of oral, selective, nonpeptide, somatostatin receptor type
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
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
52023DCC-2036(Rebastinib)1020172-07-998%
Rebastinib(DCC-2036;DCC2036) is an inhibitor of tyrosine kinases TIE2 and ABL1.Rebast
52019GSK 26561571337532-29-298% 
GSK2656157 is an ATP-competitive and highly selective inhibitor ofPERKwithIC50of 0.9
51608SSR128129E848318-25-298% 
SSR128129E is an orally-active and allostericFGFR1inhibitor withIC50of 1.9 M, while n