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RECOMMENDED PRODUCTS

Catalog NoChemical NameCAS NumberPurityChemical Structure
18381JPH203 HCl ( Nanvuranlat )1597402-27-1≧95.0%
JPH203, also known as KYT-0353, is a potent and selective LAT1 selective ( L-type ami
18435Ritlecitinib ( PF-06651600 )1792180-81-4≧98.0%
Ritlecitinib ( PF-06651600 ) is a potent and selective JAK3 inhibitor. PF-06651600, a
184321Ensartinib ( X396 )1370651-20-9>98%
Ensartinib is an orally available small molecule inhibitor of the receptor tyrosine k
512194Lazertinib1903008-80-998% Min.
Description:Lazertinib is a an orally available third-generation, selective inhibi
185235Trilaciclib (G1T28)1374743-00-6>98%
TRILACICLIB (G1T28), A HIGHLY POTENT, TRANSIENT CDK 4/6 INHIBITOR WITHIC50s OF 1 nM A
18722Fezolinetant1629229-37-3>98%
Fezolinetant, also known as ESN-364, is Neurokinin-3 (NK-3) receptor antagonist which
187122Gefapixant1015787-98-098%
Gefapixant, also known as AF-219 or MK-7264, is a P2X3 receptor antagonist. Gefapixan
188281Arimoclomol maleate289893-26-198%
Arimoclomol, also known as BRX-220, is potentially useful for the treatment of Nieman
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