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   CAS NO.    Products Name
    Etrasimod  more...
   Etrasimod (APD334) is a potent, selective and orally available antagonist of the sphingosine-1-phosphate-1 (S1P1) receptor with an IC50 value of 1.88 nM in CHO cells....
    Etrasimod  more...
   Etrasimod (APD334) is a potent, selective and orally available antagonist of the sphingosine-1-phosphate-1 (S1P1) receptor with an IC50 value of 1.88 nM in CHO cells....
    Etrasimod  more...
   Etrasimod (APD334) is a potent, selective and orally available antagonist of the sphingosine-1-phosphate-1 (S1P1) receptor with an IC50 value of 1.88 nM in CHO cells....
   947620-48-6 RVT-501  more...
   RVT-501 (E6005) potently and selectively inhibits human PDE4 activity with an IC50 of 2.8 nM and suppresses the production of various cytokines from human lymphocytes and monocytes wit...
   1799633-27-4 S63845  more...
   S63845 is a potent and selective myeloid cell leukemia 1 (MCL1) inhibitor; binds human MCL1 with a Kd of 0.19 nM....
   1434635-54-7 ND 630  more...
   ND-630 is an acetyl-CoA carboxylase (ACC) inhibitor; inhibits human ACC1 and ACC2 with IC50 values of 2.1 and 6.1 nM, respectively....
   1708971-55-4 FGF401  more...
   FGF401 is an inhibitor of human fibroblast growth factor receptor 4 (FGFR4), with potential antineoplastic activity. Upon administration, FGF401 binds to and inhibits the activity of FG...
   1429749-41-6 Thiomyristoyl  more...
   Thiomyristoyl is a potent and specific SIRT2 inhibitor with an IC50 of 28 nM....
   256477-09-5 UK-371804  more...
   UK-371804 is a urokinase-type plasminogen activator (uPA) inhibitor with a Ki of 10 nM....
   1185851-52-8 Tafluprost ethyl amide  more...
   Tafluprost ethyl amide is derived from 17-phenyl trinor Prostaglandin F2α(17-phenyl trinor PGF2α). A number of 17-phenyl trinor PGF2α derivatives have been approved for the treatment of...

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