TG6-129

TG6-129 (订货以CAS编码或英文名称为准)

TG6-129 is an antagonist of the EP2 receptor, suppressing PGE2-induced elevation of cAMP in cells expressing EP2 with an IC50 value of 1.6 μM. It is without effect on EP4, DP1, IP, and β2-adrenergic receptors.
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编号:MED20677
分子式:C20H18FN5O3S3
CAS号:1164464-14-5
分子量:491.58
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中文名称: TG6-129
英文名称: TG6-129
英文别名: MLS000548650;SMR000171256;(E)-N-[[4-[(5-ethyl-1,3,4-thiadiazol-2-yl)sulfamoyl]phenyl]carbamothioyl]-3-(4-fluorophenyl)prop-2-enamide;(E)-N-((4-(N-(5-ethyl-1,3,4-thiadiazol-2-yl)sulfamoyl)phenyl)carbamothioyl)-3-(4-fluorophenyl)acrylamide;N-(5-Ethyl-[1,3,4]thiadiazol-2-yl)-4-{3-[3-(4-fluoro-phenyl)-acryloyl]-thioureido}-benzenesulfonamide;GTPL9283;C20H18FN5O3S3;BDBM53793;cid_1987175;HMS2521G21;BDBM50492529;STK842336;CID 1987175;NCGC0035
CAS号: 1164464-14-5
分子式: C20H18FN5O3S3
分子量: 491.58
外观: A crystalline solid
储存条件 -20°C

TG6-129 is an antagonist of the EP2 receptor, suppressing PGE2-induced elevation of cAMP in cells expressing EP2 with an IC50 value of 1.6 μM. It is without effect on EP4, DP1, IP, and β2-adrenergic receptors. TG6-129 reduces the expression of COX-2, IL-1β, IL-12, IL-23, IL-6, and TNF-α induced by the EP2-selective agonist butaprost in P388D1 macrophages.

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