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BMS-986120

Chemical Structure : BMS-986120

CAS No.: 1478712-37-6

BMS-986120 (BMS 986120;BMS986120)

Catalog No.: PC-60548Not For Human Use, Lab Use Only.

BMS-986120 (BMS986120) is a potent, selective, orally bioavailable, and reversible PAR4 antagonist with Kd of 0.098 nM for human PAR4.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

    Biological Activity

    BMS-986120 (BMS986120) is a potent, selective, orally bioavailable, and reversible PAR4 antagonist with Kd of 0.098 nM for human PAR4.
    BMS-986120 selectivity inhibits PAR4 AP-induced cellular calcium mobilization in HEK cells with IC5o of 0.56 nM, with no activity on PAR1 and PAR2.
    BMS-986120 inhibits human PRP aggregation in response to γ-thrombin in vitro with IC50 of 7.3 nM.
    BMS-986120 demonstrates potent and highly efficacious antithrombotic activity with low bleeding in vivo.

    Physicochemical Properties

    M.Wt 513.587
    Formula C23H23N5O5S2
    Appearance Solid
    CAS No.
    Storage
    Solide Powder
    -20 °C 12 Months; 4°C 6 Months
    In Solvent
    -80 °C 6 Months; -20°C 6 Months
    Shipping
    Solubility

    10 mM in DMSO

    Chemical Name/SMILES

    4-(4-(((6-methoxy-2-(2-methoxyimidazo[2,1-b][1,3,4]thiadiazol-6-yl)benzofuran-4-yl)oxy)methyl)-5-methylthiazol-2-yl)morpholine

    References

    1. Wong PC, et al. Sci Transl Med. 2017 Jan 4;9(371). pii: eaaf5294.

    2. Moschonas IC, et al. Platelets. 2017 Dec;28(8):812-821.

    3. Wilson SJ, et al. Arterioscler Thromb Vasc Biol. 2017 Dec 21. pii: ATVBAHA.117.310104.

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