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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
1810164Pemigatinib (INCB054828)1513857-77-698%
Pemigatinib (INCB054828) is an orally active, selectiveFGFRinhibitor withIC50s of 0.4
1811121DCC-2618 ( Ripretinib )1442472-39-0>98%
Ripretinib, also known as DCC-2618, is a potent, orally active and selective KIT/PDGF
1811162PF-052310231037589-69-7>98%
PF-05231023 is a long-acting FGF21 mimetic. PF-05231023 decreases body weight and imp
5141902Avatrombopag maleate677007-74-896%
Avatrombopag maleate is an orally bioavailable, small molecule thrombopoietin recepto
1811211Anlotinib HCl ( AL-3818 )1360460-82-7≧98.0%
Anlotinib is a novel oral tyrosine kinase inhibitor (TKI) targeting c-kit, platelet-d
191146AR-9281913548-29-5>98%
AR-9281 is a soluble epoxide hydrolase (s-EH) inhibitor potentially for the treatment
19356AZ876898800-26-5>98%
AZ876, also known as AZ-876, is a liver X receptor agonist. AZ876 protects against pa
S510901Cenicriviroc Mesylate497223-28-698% Min.
Cenicriviroc (CVC) is an oral, once-daily, potent immunomodulator that blocks two che
6111901UNC25411612782-86-198% Min.
UNC2541 is a potent and MerTK-specific inhibitor and exhibits sub-micro molar inhibit
6111904Lemborexant (E-2006)1369764-02-298% Min.
Lemborexant(CAS 1369764-02-2)is a novel investigational small molecule that inhib
112191Aprocitentan1103522-45-798% Min.
Aprocitentan is an orally active, dual endothelin (ET) receptor antagonist developed