Showing 1–12 of 53 results

CAS NO. PRODUCT NAME OVERVIEW
    164178-33-0 AM630 (164178-33-0)

    Iodopravadoline, also known as AM630, is an inverse agonist at the human cannabinoid CB1 receptor. Iodopravadoline has been found to attenuat...

    942398-84-7 Amiselimod (942398-84-7)

    Amiselimod hydrochloride is a novel sphingosine 1-phosphate receptor-1 (S1P1) modulator, designed to reduce the bradycardia effects associate...

    1206123-37-6 APD334 (1206123-37-6)

    APD334, also known as Etrasimod, is a potent, centrally available, functional antagonists of the S1P1 receptor for use as next generation the...

    1629268-00-3 ARS853 (1629268-00-3)

    ARS-853 (ARS853) is a selective, covalent KRAS(G12C) inhibitor that inhibits mutant KRAS-driven signaling by binding to the GDP-bound oncopro...

    406205-74-1 BAY59-3074 (406205-74-1)

    Bay 59-3074 is a novel, selective CB1/CB2 receptor partial agonist with Ki values of 48.3 and 45.5 nM at human CB1 and CB2 receptors respecti...

    133085-33-3 BIBS39 (133085-33-3)

    BIBS39 is a nonpeptide angiotensin II (AII) receptor antagonists that displaced [125I] AII from its specific binding sites with a K(i) value ...

    1703793-34-3 BLU285 (1703793-34-3)

    BLU-285 is a dual inhibitor of KIT receptor and platelet-derived growth factor receptor α (PDGFRα) tyrosine kinases with activating loop muta...

    1257213-50-5 BMS-986020 (1257213-50-5)

    BMS-986020, is a potent G protein-coupled lysophosphatidic acid receptor 1 (LPA1) antagonist. BMS-986020 , also known as AM152 and AP-3152 fr...

    1637739-82-2 BQU57 (1637739-82-2)

    BQU57, a derivative of RBC8, is a selective GTPase Ral inhibitor relative to the GTPases Ras and RhoA.

    1262414-04-9 Cenerimod (1262414-04-9)

    Cenerimod (ACT-334441) is a potent and orally available sphingosine 1-phosphate 1 receptor (S1P1) agonist extracted from patent WO 2016184939...

    1437321-24-8 CEP-40783 (1437321-24-8)

    CEP-40783, also known as RXDX-106,is an orally-available, potent and selective TAM(TYRO3, AXL, MER)/MET inhibitor displaying low nanomolar bi...

    124431-80-7 CGS21680 HCL (124431-80-7)

    CGS 21680 HCL is a potent, selective agonist of the adenosine A2A receptor (Ki = 11-46 nM).It is less effective at adenosine A1 and A3 recept...

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