Meseclazone (W2395)
(Synonyms: 美西拉宗; W2395; NSC297623) 目录号 : GC31970Meseclazone (W2395) (W2395;NSC276923) 表现出对第二相 ADP 聚集的抑制效力。
Cas No.:29053-27-8
Sample solution is provided at 25 µL, 10mM.
Quality Control & SDS
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- Purity: >98.00%
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Meseclazone (W2395;NSC297623) exhibits inhibitory potency of secondary phase ADP aggregation. Meseclazone possesses anti-inflammatory, analgesic and antipyretic activity.
Meseclazone inhibits collagen-induced aggregation 1 and 4 hr after oral administration[1]. Intravenous administration of Meseclazone and other nonsteroidal anti-inflammatory drugs caused a dose-dependent inhibition of bronchoconstriction resulting in the following order of descending potency: isoproterenol congruent to indomethacin greater than fenoprofen greater than tolmetin greater than aspirin greater than naproxen congruent to ibuprofen greater than phenylbutazone greater than diflunisal greater than Meseclazone greater than 5-CSA[2].
[1]. Diamantis W, et al. Meseclazone, 5-chlorosalicylic acid and acetylsalicylic acid. Comparison of their effects on in vitro and ex vivo platelet aggregation. Thromb Haemost. 1978 Aug 31;40(1):24-36. [2]. Diamantis W, et al. Antagonism by meseclazone and other nonsteroidal anti-inflammatory drugs of bradykinin-induced bronchospasm. Pharmacology. 1982;24(4):243-7.
制备储备液 | |||
1 mg | 5 mg | 10 mg | |
1 mM | 4.1726 mL | 20.8629 mL | 41.7258 mL |
5 mM | 0.8345 mL | 4.1726 mL | 8.3452 mL |
10 mM | 0.4173 mL | 2.0863 mL | 4.1726 mL |
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