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ML-345

目录号 : GC44225

An inhibitor of the insulin-degrading enzyme

ML-345 Chemical Structure

Cas No.:1632125-79-1

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1mg
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5mg
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10mg
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产品描述

Insulin-degrading enzyme (IDE) is a thiol-sensitive zinc-metallopeptidase that acts as the major insulin-degrading protease in vivo, mediating the termination of insulin signaling. [1] In addition to regulating insulin action in diabetes pathogenesis, IDE plays a role in Varicella-Zoster virus infection and degradation of amyloid-β, a peptide implicated in Alzheimer's disease. ML-345 is a small molecule inhibitor that selectively targets cysteine819 in IDE with an EC50 value of 188 nM. [2] It demonstrates 10-fold selectivity for IDE over a panel of enzymes with reactive cysteine residues.[2] 

Reference:
[1]. Maianti, J.P., McFedries, A., Foda, Z.H., et al. Anti-diabetic activity of insulin-degrading enzyme inhibitors mediated by multiple hormones. Nature 511(7507), 94-98 (2014).
[2]. Bannister, T.D., Wang, H., Abdul-Hay, S.O., et al. ML345, a small-molecule inhibitor of the insulin-degrading enzyme (IDE). 1 R03 DA024888-01 (MLSCN cycle 6), 1-41 (2014).

Chemical Properties

Cas No. 1632125-79-1 SDF
化学名 5-fluoro-2-[2-(4-morpholinyl)-5-(4-morpholinylsulfonyl)phenyl]-1,2-benzisothiazol-3(2H)-one
Canonical SMILES O=C(C(C=C(F)C=C1)=C1S2)N2C3=CC(S(N4CCOCC4)(=O)=O)=CC=C3N5CCOCC5
分子式 C21H22FN3O5S2 分子量 479.5
溶解度 DMF: 5 mg/ml,DMF:PBS(pH 7.2)(1:1): 0.5 mg/ml,DMSO: 1 mg/ml 储存条件 Store at -20°C
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1 mg 5 mg 10 mg
1 mM 2.0855 mL 10.4275 mL 20.8551 mL
5 mM 0.4171 mL 2.0855 mL 4.171 mL
10 mM 0.2086 mL 1.0428 mL 2.0855 mL
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Research Update

Effects of water deficit stress on growth, water relations and osmolyte accumulation in Medicago truncatula and M. laciniata populations

C R Biol 2010 Mar;333(3):205-13.PMID:20338538DOI:10.1016/j.crvi.2009.12.010

The effects of water stress were investigated in two Tunisian Medicago truncatula populations collected from arid (Mt-173) and sub-humid (Mt-664) climates and two Tunisian M. laciniata populations originating from arid (Ml-173) and semi-arid (ML-345) regions. After a pre-treatment phase (24 days after sowing, DAS) of watering at 100% of field capacity (FC), the plants were either irrigated at 100% FC or at only 33% FC. After 12 days of treatment (36 DAS), one lot of dehydrated plants was rewatered at 100% FC. A final harvest was carried out after 24 days of treatment (48 DAS). Measured parameters were total dry weight (TDW), root shoot ratio (RSR), leaf relative water content (RWC), osmotic potential (OP), photosynthetic parameters (CO(2) net assimilation A, stomatal conductance g(s) and transpiration E), malondialdehyde (MDA) concentration and leaf contents in inorganic (Na(+) and K(+)) and organic solutes (proline and soluble sugars). Under water deficit conditions, compared to M. laciniata, M. truncatula populations showed a higher reduction in TDW, A, g(s) and RWC associated with a higher increase in MDA concentration. Thus, the relative tolerance of M. laciniata populations to water shortage would be related to their lower intrinsic growth rate and stomatal control of gas exchange. TDW, A, g(s), E and RWC were more decreased by water deficit in ML-345 than in Ml-173. Drought tolerance of Ml-173 was found to be associated with a more pronounced decrease of OP and a lower reduction in RWC due to the accumulation of solutes such as proline, soluble sugars and K(+). In addition, Ml-173 showed the highest water use efficiency values (WUE) and the lowest MDA concentrations under water deficit stress.