Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
S-203041 | [4-(2,2,2-trifluoroethoxy)phenyl]boronic acid | 886536-37-4 | 95% | ![]() |
g scale to Kg scale may be provided. | ||||
23178 | AC-90179 HCl | 359878-19-6 | 98% Min. | ![]() |
AC-90179 is a high selective 5-hydroxytryptamine2A receptor inverse agonist. It is an | ||||
2051510 | LML-134 | 1542135-76-1 | 98% | ![]() |
LML134 is an orally active and high selective Histamine 3 receptor (H3R) inverse agon | ||||
2051515 | Asapiprant | 932372-01-5 | 98% Min. | ![]() |
Asapiprant is a potent and selective DP1 receptor antagonist, with a Ki of 0.44 nM. A | ||||
615201 | CLEFMA | 1246964-32-8 | 98% Min. | ![]() |
CLEFMA has anti-proliferative activity in H441 cells. CLEFMA may induce autophagic ce | ||||
2062004 | ((1R,2S)-2-(3-fluorophenyl)-2-(hydroxymethyl)cyclopropyl)methyl acetate | 1369768-29-5 | ≧95.0% | ![]() |
262324 | 2-(3-Fluoro-4-isopropoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | 1350426-06-0 | 98% Min. | ![]() |
20732 | Lanraplenib | 1800046-95-0 | 98% | ![]() |
Lanraplenib (GS-9876) is a highly selective and orally active SYK inhibitor in develo | ||||
52004 | Belnacasan | 273404-37-8 | 98% | ![]() |
Belnacasan is a prodrug ofVRT-043198, a caspase-1 inhibitor that was developed by Ver | ||||
2071401 | Pimodivir ( VX-787 ) | 1629869-44-8 | 98% Min. | ![]() |
Pimodivir, also known as VX-787, JNJ-872, is a novel inhibitor of influenza virus rep | ||||
2073107 | Trilaciclib hydrochloride (G1T28 hydrochloride) | 1977495-97-8 | 98% Min. | ![]() |
TRILACICLIB (G1T28), A HIGHLY POTENT, TRANSIENT CDK 4/6 INHIBITOR WITHIC50s OF 1 nM A | ||||
2073108 | PF-06802861 ( ARRY 371797 ; ARRY-797 ) | 1034189-82-6 | ≧98.0% | ![]() |
ARRY 797 (also known as ARRY 371797 or PF 06802861) is an orally active, selective p3 |
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