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Meseclazone (W2395) Sale

(Synonyms: 美西拉宗; W2395; NSC297623) 目录号 : GC31970

Meseclazone (W2395) (W2395;NSC276923) 表现出对第二相 ADP 聚集的抑制效力。

Meseclazone (W2395) Chemical Structure

Cas No.:29053-27-8

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1mg
¥2,678.00
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5mg
¥5,355.00
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10mg
¥9,104.00
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20mg
¥16,065.00
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Sample solution is provided at 25 µL, 10mM.

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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.

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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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