Sancilio L F, Nolan J C, Wagner L E, Gathright C E, Droppleman D D, Alphin R S, Walsh D A, Welstead W J
Department of Pharmacology, A.H. Robins Co., Inc., Richmond, VA 23261-6609.
Agents Actions. 1990 Aug;31(1-2):117-26. doi: 10.1007/BF02003231.
AHR-10037 is an anti-inflammatory compound possessing analgesic and antipyretic properties and a high therapeutic index. AHR-10037 was comparable to indomethacin in suppressing acute (Evans blue-carrageenan pleural effusion) and chronic (adjuvant-induced arthritis) inflammation. There was a delayed onset of antipyresis (yeast-induced hyperthermia in rats), analgesia (acetylcholine-induced abdominal constriction in mice) and inhibition of caster oil-induced diarrhea in rats. Antipyresis occurred 3 hours after administration of AHR-10037, 4 mg/kg, PO. vs 1 hour after administration of acetylsalicylic acid, 100 mg/kg, PO; maximum analgesic activity (ED50 = 4.1 mg/kg) occurred at 4 hours. AHR-10037 was inferior to indomethacin in suppressing castor oil-induced diarrhea in rats. The therapeutic index of AHR-10037 (relating acute anti-inflammatory potency to gastric toxicity potency relative to indomethacin) ranged from 56-91. The pharmacological profile suggests that AHR-10037 is a prodrug converted in vivo to a cyclooxygenase inhibitor.
AHR - 10037是一种具有抗炎、镇痛和解热特性且治疗指数高的化合物。在抑制急性(伊文思蓝 - 角叉菜胶性胸腔积液)和慢性(佐剂性关节炎)炎症方面,AHR - 10037与吲哚美辛相当。在大鼠酵母诱导的发热、小鼠乙酰胆碱诱导的腹部收缩以及大鼠蓖麻油诱导的腹泻抑制方面,AHR - 10037的起效延迟。给予4mg/kg的AHR - 10037口服后3小时出现解热作用,而给予100mg/kg的乙酰水杨酸口服后1小时出现解热作用;最大镇痛活性(ED50 = 4.1mg/kg)在4小时出现。在抑制大鼠蓖麻油诱导的腹泻方面,AHR - 10037不如吲哚美辛。AHR - 10037的治疗指数(相对于吲哚美辛,将急性抗炎效力与胃毒性效力相关联)范围为56 - 91。药理学特征表明AHR - 10037是一种在体内转化为环氧化酶抑制剂的前药。