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HA-155
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。
HA-155图片
CAS NO:1229652-22-5
包装与价格:
包装价格(元)
5mg电议
10mg电议
25mg电议

产品介绍

化学性质

Physical AppearanceA crystalline solid
StorageStore at -20°C
M.Wt463.3
Cas No.1229652-22-5
FormulaC24H19BFNO5S
SynonymsAutotaxin Inhibitor IV
Solubility≤30mg/ml in DMSO;50mg/ml in dimethyl formamide
Chemical NameB-[4-[[4-[[3-[(4-fluorophenyl)methyl]-2,4-dioxo-5-thiazolidinylidene]methyl]phenoxy]methyl]phenyl]-boronic acid
Canonical SMILESFC1=CC=C(CN2C(/C(SC2=O)=C/C3=CC=C(OCC4=CC=C(B(O)O)C=C4)C=C3)=O)C=C1
运输条件蓝冰运输或根据您的需求运输。
一般建议为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同厂家不同批次产品溶解度各有差异,仅做参考。若实验所需浓度过大至产品溶解极限,请添加助溶剂助溶或自行调整浓度。溶液形式一般不宜长期储存,请尽快用完。

资料参考

IC50 = 5.7 nM

HA155 is an autotaxin inhibitor.

Autotaxin (ATX), a secreted phosphodiesterase, hydrolyzes the abundant phospholipid lysophosphatidylcholine (LPC) to produce lysophosphatidic acid (LPA). The ATX-LPA signaling axis has been reported to be involved in fibrosis, inflammation, and tumor progression, rendering ATX an attractive drug target.

In vitro: HA155 was identified as a boronic acid-based inhibitor of ATX based on the crystal structure of ATX in complex with HA155. Furthermore, the syntheses and activities of HA155 could be explained by structural data. In order to further understand the difference in activity, molecular docking experiments were performed. The molecular docking indicated a remarkable binding pose for one of the isomers, which differed from the original binding pose of HA155 for ATX. Moreover, the thrombin-mediated increase in platelet-derived LPA was completely attenuated in a dose-dependent manner by HA155. HA-155 could inhibit autotaxin by selectively binding to its catalytic threonine. HA155 showed to dose-dependently block thrombin-induced LPA secretion in platelets [1,2].

In vivo: Up to now, there is no animal in vivo data reported.

Clinical trial: So far, no clinical study has been conducted.

References:
[1] Albers, H. M.H.G.,Hendrickx, L.J.D.,van Tol, R.J.P., et al. Structure-based design of novel boronic acid-based inhibitors of autotaxin. Journal of Medicinal Chemistry 54(13), 4619-4626 (2011).
[2] Fulkerson, Z. ,Wu, T.,Sunkara, M., et al. Binding of autotaxin to integrins localizes lysophosphatidic acid production to platelets and mammalian cells. The Journal of Biological Chemisty 286(40), 34654-34663 (2011).