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Ilomastat

    95%

Ilomastat

源葉(MedMol)
S80347
142880-36-2
C20H28N4O4
388.461
伊洛馬司他;伊諾馬司他;ILOMASTAT (GM6001, GALARDIN);(r)-n4-hydroxy-n1-[(s)-2-(1h-indol-3-yl)-1-methylcarbamoly-ethyl]-2-isobutyl-succinamide;galardin tm;(R)-N4-Hydroxy-N1-[(S)-2-(1H-indol-3-yl)-1-methylcarbamoyl
品牌 貨號(hào) 產(chǎn)品規(guī)格 價(jià)格(RMB) 庫(kù)存(上海) 北京 武漢 南京 購(gòu)買數(shù)量
源葉(MedMol) S80347-2mg 95% ¥180.00元 7 - - -
源葉(MedMol) S80347-5mg 95% ¥240.00元 5 - - -
源葉(MedMol) S80347-10mg 95% ¥380.00元 7 - - -
源葉(MedMol) S80347-25mg 95% ¥720.00元 5 - - -
源葉(MedMol) S80347-50mg 95% ¥1200.00元 4 - - -
源葉(MedMol) S80347-100mg 95% ¥1900.00元 預(yù)計(jì)交期:2-3天 - - -
產(chǎn)品介紹 參考文獻(xiàn) 質(zhì)檢證書(COA) 摩爾濃度計(jì)算器 相關(guān)產(chǎn)品

產(chǎn)品介紹

Ilomastat (GM6001) is a potent and broad spectrum matrix metalloprotease (MMP) inhibitor, inhibits MMPs (IC50s, 1.5 nM for MMP-1; 1.1 nM for MMP-2; 1.9 nM for MMP-3; 0.5 nM for MMP-9), with a Ki of 0.4 nM for human skin fibroblast collagenase (MMP-1).
產(chǎn)品描述: Ilomastat (GM6001) is a potent and broad spectrum matrix metalloprotease (MMP) inhibitor, inhibits MMPs (IC50s, 1.5 nM for MMP-1; 1.1 nM for MMP-2; 1.9 nM for MMP-3; 0.5 nM for MMP-9), with a Ki of 0.4 nM for human skin fibroblast collagenase (MMP-1).
靶點(diǎn): Fibroblast collagenase:0.4 nM (Ki, Human skin);MMP-1:1.5 nM (IC50);MMP-2:1.1 nM (IC50);MMP-3:1.9 nM (IC50);MMP-9:0.5 nM (IC50);Thermolysin:20 nM (Ki);Eastase:20 nM (Ki);MMP
體內(nèi)研究: Ilomastat (GM6001) (400 μg/mL) inhibits corneal ulceration after severe alkali injury in animals. Ilomastat (GM6001) significantly suppresses intimal hyperplasia and intimalcollagen content. Ilomastat increases lumen area in stented arteries, shows no activity on proliferation rates in rabbit model after stenting
參考文獻(xiàn): 1. Grobelny D, et al. Inhibition of human skin fibroblast collagenase, thermolysin, and Pseudomonas aeruginosa elastase by peptide hydroxamic acids. Biochemistry. 1992 Aug 11;31(31):7152-4. 2. Schultz GS, et al. Treatment of alkali-injured rabbit corneas with a synthetic inhibitor of matrix metalloproteinases. Invest Ophthalmol Vis Sci. 1992 Nov;33(12):3325-31. 3. Li C, et al. Arterial repair after stenting and the effects of GM6001, a matrix metalloproteinase inhibitor. J Am Coll Cardiol. 2002 Jun 5;39(11):1852-8. 4. Leppert D, et al. T cell gelatinases mediate basement membrane transmigration in vitro. J Immunol. 1995 May 1;154(9):4379-89. 5. Yamamoto M, et al. Inhibition of membrane-type 1 matrix metalloproteinase by hydroxamate inhibitors: an examination of the subsite pocket. J Med Chem. 1998 Apr 9;41(8):1209-17.
溶解性: DMSO  :  ≥  47  mg/mL  (120.99  mM)
保存條件: 2-8℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 2.574 ml 12.871 ml 25.743 ml
5 mM 0.515 ml 2.574 ml 5.149 ml
10 mM 0.257 ml 1.287 ml 2.574 ml
50 mM 0.051 ml 0.257 ml 0.515 ml
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