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PAT-048
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
PAT-048图片
CAS NO:1359983-15-5
包装与价格:
包装价格(元)
100mg电议
250mg电议
500mg电议

产品介绍
PAT-048 是一种有效、选择性、可口服的自分泌运动因子 autotaxin 抑制剂,抑制 IL-6 mRNA 的表达,但在肺部纤维化模型中,对 autotaxin 蛋白水平和溶血磷脂酸 (LPA) 的产生无明显作用。在小鼠血浆中对 autotaxin 的 IC50 和 IC90 值分别为 20 nM 和 200 nM。在体内实验中,PAT-048 可降低皮肤纤维化。
Cas No.1359983-15-5
Canonical SMILESCCCN1N=CC(N2C3=C(C(SC4=CC=CC(C(O)=O)=C4F)=C2C)C=CC(Cl)=C3F)=C1
分子式C22H18ClF2N3O2S
分子量461.91
溶解度Soluble in DMSO
储存条件Store at -20°C
General tipsFor obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.
Shipping ConditionEvaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request
产品描述

PAT-048 is a potent, selective and orally active autotaxin inhibitor, inhibits IL-6 mRNA expression, but shows no effect on autotaxin protein and pulmonary lysophosphatidic acid (LPA) production in lung fibrosis model. PAT-048 shows an IC50 and IC90 of 20 nM and 200 nM for autotaxin in mouse plasma. PAT-048 reduces dermal fibrosis in vivo[1][2]. IC50: 20 nM (Autotaxin, in mouse plasma)[1] IC90: 200 nM (Autotaxin, in mouse plasma)[1]

[1]. Castelino FV, et al. An Autotaxin/Lysophosphatidic Acid/Interleukin-6 Amplification Loop Drives Scleroderma Fibrosis. Arthritis Rheumatol. 2016 Dec;68(12):2964-2974. [2]. Black KE, et al. Autotaxin activity increases locally following lung injury, but is not required for pulmonary lysophosphatidic acid production or fibrosis. FASEB J. 2016 Jun;30(6):2435-50.