Have you ever wondered what it means when you go to the store and look at al.

Showing 1–12 of 19 results

CAS NO. PRODUCT NAME OVERVIEW
    1163-36-6 Clemizole HCL (1163-36-6)

    Clemizole hydrochloride is an H1 histamine receptor antagonist, is found to substantially inhibit HCV replication. The IC50 of Clemizole for ...

    1621862-70-1 CPI-1205 (1621862-70-1)

    CPI-1205 is an orally available selective inhibitor of the histone lysine methyltransferase EZH2, with potential antineoplastic activity.

    ...
    1616391-65-1 EPZ015666 (1616391-65-1)

    EPZ015666 is a potent, selective PRMT5 inhibitor (Ki of 5 nM); displays >20,000-fold selectivity over other PMTs. EPZ015666 acts by blocki...

    1380288-87-8 EPZ5676 (1380288-87-8)

    Pinometostat, also known as EPZ-5676. Pinometostat has been used in trials studying the treatment of Leukemia, Acute Leukemias, Acute Myeloid...

    1403254-99-8 EPZ6438 (1403254-99-8)

    Tazemetostat (EPZ-6438) is a potent, selective and orally available EZH2 inhibitor. Tazemetostat has been used in trials studying the treatme...

    1373423-53-0 GSK J4 (1373423-53-0)

    GSK-J4 has been used to study the effect of KDM2B (Jumonji (JmjC) domain histone 3 lysine 36 (H3K36) di-demethylase) inhibition on the surviv...

    1431368-48-7 GSK-LSD1 2HCl (1431368-48-7)

    GSK-LSD1 has been used as a lysine specific demethylase 1 (LSD1) inhibitor in mice to study sepsis-induced mortality. It has also been used a...

    1346704-33-3 GSK343 (1346704-33-3)

    GSK343 is a potent and selective EZH2 inhibitor with IC50 of 4 nM, showing 60 fold selectivity against EZH1, and >1000 fold selectivity ag...

    1640282-31-0 I-CBP112 (1640282-31-0)

    I-CBP112 is a specific and potent acetyl-lysine competitive protein-protein interactioninhibitor, that targets the CBP/p300 bromodomains.

    ...
    199596-05-9 JIB-04 (199596-05-9)

    JIB-04 is a pan-selective Jumonji histone demethylase inihibitor with IC50s of 230, 340, 855, 445, 435, 1100, and 290 nM for JARID1A, JMJD2E,...

    1357302-64-7 OG-L002 (1357302-64-7)

    OG-L002 is a potent LSD1 inhibitor that has been found to inhibit herpes simplex virus (HSV) immediate early gene expression and viral yield ...

    1431326-61-2 ORY-1001 (1431326-61-2)

    ORY-1001 is a potent and selective inhibitor of LSD1 (IC₅₀ < 20 nM). It targets acute myeloid leukemia (AML) stem cells and significantly ...

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