Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
25149 | Safusidenib | 1898206-17-1 | ≧98.0% | ![]() |
Safusidenib, also known as DS-1001, is an oral isocitrate dehydrogenase [NADP] cytopl | ||||
41788 | CB-6644 | 2316817-88-4 | 96.33% | ![]() |
CB-6644 acts as a noncompetitive ATPase inhibitor. Additionally, it can inhibit RUVBL | ||||
25148 | Atebimetinib | 2669009-92-9 | ≧98.0% | ![]() |
Atebimetinib (IMM-1-104) is an oral, small-molecule allosteric inhibitor of the MEK1 | ||||
25075 | LLL12 | 1260247-42-4 | ≧97.0% | ![]() |
LLL12 is a potent STAT3 inhibitor. | ||||
25176 | AG-270 | 2201056-66-6 | ≧98.0% | ![]() |
MAT2A Inhibitor AG-270 is an orally available small molecule inhibitor of methionine | ||||
25177 | Dencatistat | 2377000-84-3 | ≧98.0% | ![]() |
Dencatistat is an orally bioavailable, small molecule inhibitor of cytidine triphosph | ||||
24107 | LXH-3-71 | 2251753-65-6 | ≧97.0% | ![]() |
LXH-3-71 isnovel "molecular glue"that induces the interaction between PHGDH | ||||
20509 | GLPG3667 | 2308520-97-8 | ≧98.0% | ![]() |
GLPG3667 is an oral potent and selective small-molecule TYK2 inhibitor in development | ||||
121431 | KW-2478 | 819812-04-9 | 98% | ![]() |
KW-2478 is an agent that targets the human heat-shock protein 90 (Hsp90) with potenti | ||||
18576 | VU0467154 | 1451993-15-9 | ≧98.0% | ![]() |
VU0467154 is a positive allosteric modulator of theM4 muscarinic acetylcholine recept | ||||
171452 | BGB-15025 | 2766481-17-6 | ≧98.0% | ![]() |
BGB-15025 is a potent and selective HPK1 inhibitor that is efficacious as a single ag | ||||
17021601 | LY3039478 ( Crenigacestat ) | 1421438-81-4 | ≧98.0% | ![]() |
LY3039478 ( Crenigacestat ), a selective NOTCH1 inhibitor, reduces intrahepatic chola |
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