Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
18381 | JPH203 HCl ( Nanvuranlat ) | 1597402-27-1 | ≧95.0% | ![]() |
JPH203, also known as KYT-0353, is a potent and selective LAT1 selective ( L-type ami | ||||
18435 | Ritlecitinib ( PF-06651600 ) | 1792180-81-4 | ≧98.0% | ![]() |
Ritlecitinib ( PF-06651600 ) is a potent and selective JAK3 inhibitor. PF-06651600, a | ||||
184321 | Ensartinib ( X396 ) | 1370651-20-9 | >98% | ![]() |
Ensartinib is an orally available small molecule inhibitor of the receptor tyrosine k | ||||
512194 | Lazertinib | 1903008-80-9 | 98% Min. | ![]() |
Description:Lazertinib is a an orally available third-generation, selective inhibi | ||||
185235 | Trilaciclib (G1T28) | 1374743-00-6 | >98% | ![]() |
TRILACICLIB (G1T28), A HIGHLY POTENT, TRANSIENT CDK 4/6 INHIBITOR WITHIC50s OF 1 nM A | ||||
18722 | Fezolinetant | 1629229-37-3 | >98% | ![]() |
Fezolinetant, also known as ESN-364, is Neurokinin-3 (NK-3) receptor antagonist which | ||||
187122 | Gefapixant | 1015787-98-0 | 98% | ![]() |
Gefapixant, also known as AF-219 or MK-7264, is a P2X3 receptor antagonist. Gefapixan | ||||
188281 | Arimoclomol maleate | 289893-26-1 | 98% | ![]() |
Arimoclomol, also known as BRX-220, is potentially useful for the treatment of Nieman | ||||
1810163 | BMS-986165 | 1609392-27-9 | >99% | ![]() |
BMS-986165 potently binds to the Tyk2 pseudokinase domain (Ki = 0.02 nM). BMS-986165 | ||||
1810164 | Pemigatinib (INCB054828) | 1513857-77-6 | 98% | ![]() |
Pemigatinib (INCB054828) is an orally active, selectiveFGFRinhibitor withIC50s of 0.4 | ||||
1811121 | DCC-2618 ( Ripretinib ) | 1442472-39-0 | >98% | ![]() |
Ripretinib, also known as DCC-2618, is a potent, orally active and selective KIT/PDGF | ||||
1811162 | PF-05231023 | 1037589-69-7 | >98% | ![]() |
PF-05231023 is a long-acting FGF21 mimetic. PF-05231023 decreases body weight and imp |
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