wherein R1=H, Me; R2=H; R3=CH2COOMe, CH(Me)COOMe, CH(Et)COOMe, CH(CH2CH2SMe)COOMe, CH2COOH, CH(Me)COOH, CH(Et)COOH, CH(CH2CH2SMe)COOH, CH2CH2CH2CH2CH(NH2)COOH, CH2CH2CH2CH(NH2)COOH; R2, R3=CH2CH2CH2CH(COOMe); R2, R3=CH2CH2CH2CH(COOH). The above compounds are administered parenterally in a dose of 0.5-90 mg/kg, particularly in a dose of 1-3 mg/kg 10-120 minutes before administering nonsteroidal anti-inflammatory agents (e.g. aspirin or indomethacin), particularly 30 minutes before administering the nonsteroidal anti-inflammatory agents (e.g. aspirin or indomethacin) that enables reducing an area of erosions and ulcers of the gastric mucosa by 2-4 times as compared to a reference group receiving the nonsteroidal anti-inflammatory agents and receiving no declared compounds. The above phenylthioacetamides are applicable for preventing and treating the gastric ulcer caused by administering the therapeutic agents containing the nonsteroidal anti-inflammatory preparations of salycylates and acetic acid derivatives. The areas of the ulcer formation caused by the action of the nonsteroidal anti-inflammatory agents of salycylates (e.g. aspirin-containing) and acetic acid derivatives (e.g. indomethacin-containing) decrease after administering the phenylthioacetamide derivatives in the mammalian gastric mucosa.;EFFECT: higher clinical effectiveness.;6 cl, 12 ex, 9 dwg"/> METHOD FOR PREVENTING AND TREATING GASTRIC ULCER LESION CAUSED BY ADMINISTERING NONSTEROIDAL ANTIINFLAMMATORY AGENTS
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METHOD FOR PREVENTING AND TREATING GASTRIC ULCER LESION CAUSED BY ADMINISTERING NONSTEROIDAL ANTIINFLAMMATORY AGENTS

机译:预防非甾体类抗炎剂引起的胃溃疡病的防治方法

摘要

FIELD: medicine.;SUBSTANCE: preventive agent is presented by one of phenylthioacetamide derivatives of the general formula: wherein R1=H, Me; R2=H; R3=CH2COOMe, CH(Me)COOMe, CH(Et)COOMe, CH(CH2CH2SMe)COOMe, CH2COOH, CH(Me)COOH, CH(Et)COOH, CH(CH2CH2SMe)COOH, CH2CH2CH2CH2CH(NH2)COOH, CH2CH2CH2CH(NH2)COOH; R2, R3=CH2CH2CH2CH(COOMe); R2, R3=CH2CH2CH2CH(COOH). The above compounds are administered parenterally in a dose of 0.5-90 mg/kg, particularly in a dose of 1-3 mg/kg 10-120 minutes before administering nonsteroidal anti-inflammatory agents (e.g. aspirin or indomethacin), particularly 30 minutes before administering the nonsteroidal anti-inflammatory agents (e.g. aspirin or indomethacin) that enables reducing an area of erosions and ulcers of the gastric mucosa by 2-4 times as compared to a reference group receiving the nonsteroidal anti-inflammatory agents and receiving no declared compounds. The above phenylthioacetamides are applicable for preventing and treating the gastric ulcer caused by administering the therapeutic agents containing the nonsteroidal anti-inflammatory preparations of salycylates and acetic acid derivatives. The areas of the ulcer formation caused by the action of the nonsteroidal anti-inflammatory agents of salycylates (e.g. aspirin-containing) and acetic acid derivatives (e.g. indomethacin-containing) decrease after administering the phenylthioacetamide derivatives in the mammalian gastric mucosa.;EFFECT: higher clinical effectiveness.;6 cl, 12 ex, 9 dwg
机译:领域:药物;物质:预防剂由以下通式的苯硫基乙酰胺衍生物之一提供:其中R 1 = H,Me; R 2 = H; R 3 = CH 2 COOMe,CH(Me)COOMe,CH(Et)COOMe,CH(CH 2 CH 2 < / Sub> SMe)COOMe,CH 2 COOH,CH(Me)COOH,CH(Et)COOH,CH(CH 2 CH 2 SMe)COOH,CH 2 CH 2 CH 2 CH 2 CH(NH 2 )COOH,CH 2 CH 2 CH 2 CH(NH 2 )COOH; R 2 ,R 3 = CH 2 CH 2 CH 2 CH(COOMe ); R 2 ,R 3 = CH 2 CH 2 CH 2 CH(COOH )。在非甾体抗炎药(例如阿司匹林或消炎痛)给药前10-120分钟,以0.5-90 mg / kg的剂量,特别是以1-3 mg / kg的剂量,肠胃外给药上述化合物,特别是在给药前30分钟给予非甾体类抗炎药(例如阿司匹林或消炎痛),与接受非甾体类抗炎药且不接受已申报化合物的对照组相比,可使胃粘膜的糜烂和溃疡面积减少2-4倍。上述苯基硫代乙酰胺可用于预防和治疗因服用含有水杨酸盐和乙酸衍生物的非甾体抗炎剂的治疗剂而引起的胃溃疡。在哺乳动物胃粘膜中施用苯硫基乙酰胺衍生物后,由水杨酸盐(例如含阿司匹林)和乙酸衍生物(例如含吲哚美辛)的非甾体类抗炎药作用引起的溃疡形成面积减少。更高的临床疗效。; 6 cl,12 ex,9 dwg

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