跳转至内容
Merck
  • Non-carboxylic analogues of arylpropionic acids: synthesis, anti-inflammatory activity and ulcerogenic potential.

Non-carboxylic analogues of arylpropionic acids: synthesis, anti-inflammatory activity and ulcerogenic potential.

European journal of medicinal chemistry (2006-10-21)
Kamel A Metwally, Shada H Yaseen, El-Sayed M Lashine, Hassan M El-Fayomi, Mohamed E El-Sadek
摘要

Two series of 1,2,4-triazoles and 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazoles derived from three selected arylpropionic acids namely, ibuprofen, flurbiprofen and naproxen, were synthesized and evaluated for anti-inflammatory activity and ulcerogenic potential. All the tested compounds exhibited anti-inflammatory activity comparable to that of hydrocortisone. Compared to ibuprofen, however, all the tested compounds displayed more potent anti-inflammatory activity. Compounds tested for ulcerogenicity showed no or minimal ulcerogenic effect compared to indomethacin.

材料
货号
品牌
产品描述

Sigma-Aldrich
氢化可的松, BioReagent, suitable for cell culture
Sigma-Aldrich
氢化可的松, γ-irradiated, powder, BioXtra, suitable for cell culture
Sigma-Aldrich
氢化可的松 溶液, 50 μM, sterile-filtered, BioXtra, suitable for cell culture
Sigma-Aldrich
布洛芬, ≥98% (GC)
Sigma-Aldrich
氢化可的松, ≥98% (HPLC)
Sigma-Aldrich
吲哚美辛, 98.5-100.5% (in accordance with EP)
Sigma-Aldrich
氢化可的松-水溶性, BioReagent, suitable for cell culture
Supelco
布洛芬
Sigma-Aldrich
吲哚美辛, meets USP testing specifications
Sigma-Aldrich
氢化可的松, meets USP testing specifications
Sigma-Aldrich
布洛芬, meets USP testing specifications