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Catalog NoChemical NameCAS NumberPurityChemical Structure
1810163BMS-9861651609392-27-9>99%
BMS-986165 potently binds to the Tyk2 pseudokinase domain (Ki = 0.02 nM). BMS-986165
90731GDC-0810 ( Brilanestrant , ARN-810 )1365888-06-7≧98.0%
GDC-0810 (Brilanestrant, ARN-810, RG6046) is a selective estrogen receptor degrader (
51702AZD12081204144-28-498%
AZD1208 is a potent, highly selective, and orally available Pim kinase inhibitor that
19356AZ876898800-26-5>98%
AZ876, also known as AZ-876, is a liver X receptor agonist. AZ876 protects against pa
6111904Lemborexant (E-2006)1369764-02-298% Min.
Lemborexant(CAS 1369764-02-2)is a novel investigational small molecule that inhib
52007SRT17201001645-58-498% 
SRT1720 is a selectiveSIRT1activator withEC50of 0.16 M, but is >230-fold less pote
112101AV-412451492-95-899.38%
AV-412 is an EGFR/HER2 inhibitor that binds to and inhibits the epidermal growth fact
188281Arimoclomol maleate289893-26-198%
Arimoclomol, also known as BRX-220, is potentially useful for the treatment of Nieman
6111901UNC25411612782-86-198% Min.
UNC2541 is a potent and MerTK-specific inhibitor and exhibits sub-micro molar inhibit
122919Tenapanor1234423-95-098% 
Tenapanoris an inhibitor of the sodium-proton exchanger NHE3. Thisantiporter protein
52003Zosuquidar trihydrochloride167465-36-399% 
zosuquidar trihydrochloride is adifluorocyclopropyl quinoline. Zosuquidar trihydrochl
6111110Nastorazepide209219-38-598% 
Nastorazepide (Z-360) is a selective, orally available, 1,5-benzodiazepine-derivative