YM-60828 (hydrochloride)


CAS No. : 179755-65-8

179755-65-8
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Cat. No. : HY-10279
M.Wt: 610.55
Formula: C27H33Cl2N5O5S
Purity: >98 %
Solubility:
Introduction of 179755-65-8 :

YM-60828 hydrochloride is an orally active, selective and competitive factor Xa inhibitor with a Ki of 1.3 nM and an IC50 of 2.3 nM. YM-60828 hydrochloride inhibits thrombus formation and platelet aggregation. YM-60828 hydrochloride can be used for the research of venous thrombosis, arterial thrombosis, and thromboembolic disorders[1][2][3][4][5]. In Vitro:YM-60828 hydrochloride potently prolongs prothrombin time in pooled mouse plasma, with a CT2 value of 0.70 μM[2].
YM-60828 (3 min) hydrochloride dose-dependently prolongs human plasma factor Xa clotting time, prothrombin time, and activated partial thromboplastin time, with CT2 values of 0.10 μM, 0.21 μM, and 0.24 μM respectively, and does not affect thrombin time at concentrations up to 100 μM[5].
YM-60828 hydrochloride dose-dependently prolongs prothrombin time and activated partial thromboplastin time in plasma from multiple species, with the highest potency in squirrel monkey plasma (CT2 0.16 μM for PT, 0.18 μM for APTT) and lowest potency in guinea pig plasma (CT2 2.79 μM for PT, 1.36 μM for APTT)[5].
YM-60828 (0.1-100 nM) hydrochloride dose-dependently inhibits thrombin generation in the prothrombinase complex on washed human platelet surfaces, with an IC50 of 7.7 nM[5].
YM-60828 hydrochloride dose-dependently inhibits agonist-induced aggregation of human platelets, with IC50 values ranging from 3.3 μM (TRAP-induced in PRP) to 23.4 μM (Thrombin-induced in washed platelets)[5]. In Vivo:YM-60828 (i.v.; single dose) hydrochloride dose-dependently inhibits venous thrombus formation in guinea pigs, with an ID50 of 0.012 mg/kg and significant activity at 0.03 mg/kg[1].
YM-60828 (i.v.; single dose) hydrochloride dose-dependently inhibits thrombus formation in a guinea pig arterio-venous shunt model, with an ID50 of 0.0094 mg/kg and significant activity at 0.01 mg/kg[1].
YM-60828 (i.v.; single dose) hydrochloride dose-dependently inhibits carotid artery thrombus formation in guinea pigs, with an ID50 of 0.14 mg/kg and significant activity at 0.3 mg/kg[1].
YM-60828 (100 mg/kg; p.o.; single dose) hydrochloride exhibits anticoagulant activity in ICR mice[2].
YM-60828 (0.1-1 mg/kg bolus + 0.3-3 mg/kg/h infusion; i.v.; 60 min) hydrochloride dose-dependently improves carotid artery patency after moPA-induced thrombolysis in rats with electrically-induced arterial thrombosis[3].
YM-60828 (10-100 mg/kg; p.o.; single dose; 60 min pre-stimulation) hydrochloride improves carotid artery patency in a rat arterial thrombosis model[4].
YM-60828 (0.3 (i.v.) and 3 mg/kg (p.o.); single dose) hydrochloride exhibits anticoagulant activity in squirrel monkeys[5].

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