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NP-313

CAS No.: 5397-78-4

NP-313 (NSC-4264) is a potent antithrombotic agent that inhibits platelet aggregation and activation by inhibiting throm
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Description NP-313 (NSC-4264) is a potent antithrombotic agent that inhibits platelet aggregation and activation by inhibiting thromboxane A 2 synthesis and selectively inhibiting SOCC-mediated Ca2+ efflux.
In vitro NP-313 (0-80 μM) can inhibit platelet aggregation in a dose-dependent manner. Among them, NP-313 can inhibit thrombin- and A23187-induced platelet aggregation to a maximum extent of about 80% and 60%, respectively.[1] NP-313 (0-8 μM) concentration-dependently inhibits P-selectin expression and collagen- or thrombin-induced thromboxane B 2 (TXB2) production in human platelets. Meanwhile, NP-313 inhibits COX-1 and TXA 2 synthase with IC50 values of 1.5 and 3.9 µM, respectively.[1]
In vivo NP-313 (4-16 µg/g; i.v.) significantly prolongs time-to-occlusion (TTO), prolongs bleeding time, and inhibits platelet aggregation induced by collagen (10 µg/mL) in male ICR mice.[1]
Target activity COX-1:1.5 µM, TXA2:3.9 µM
Synonyms NP 313, NSC 4264, NSC-4264, NSC4264
molecular weight 249.65
Molecular formula C12H8ClNO3
CAS 5397-78-4
Storage Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility DMSO: 60 mg/mL (240.34 mM)
References 1. Gornostaev L M, et al. On the Reaction of 2-Benzylamino-1, 4-naphthoquinones with Nitrosylsulfuric Acid. Russian Journal of Organic Chemistry. 2019;55: 608-614. 2. Kuo HL, et al. NP-313, 2-acetylamino-3-chloro-1,4-naphthoquinone, a novel antithrombotic agent with dual inhibition of thromboxane A(2) synthesis and calcium entry. Br J Pharmacol. 2011 Apr;162(8):1871-83.