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目录号 : GC61924

JFD01307SC ([(1,1-dioxidotetrahydrothien-3-yl)amino]acetic acid) shows activity against M.tuberculosis with minimum inhibitory concentrations (MICs) in the range of 8 to 16 ?g/ml. JFD01307SC may targets enzymes involved in glutamine biosynthesis.

JFD01307SC Chemical Structure

Cas No.:51070-56-5

规格 价格 库存 购买数量
10 mg
¥450.00
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25 mg
¥810.00
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50 mg
¥1,350.00
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100 mg
¥2,250.00
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Sample solution is provided at 25 µL, 10mM.

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产品描述

JFD01307SC ([(1,1-dioxidotetrahydrothien-3-yl)amino]acetic acid) shows activity against M.tuberculosis with minimum inhibitory concentrations (MICs) in the range of 8 to 16 ?g/ml. JFD01307SC may targets enzymes involved in glutamine biosynthesis.

[1] Gyanu Lamichhane, et al. 2011 Feb 1;2(1):e00301-10.

Chemical Properties

Cas No. 51070-56-5 SDF
Canonical SMILES O=C(O)CNC(CC1)CS1(=O)=O
分子式 C6H11NO4S 分子量 193.22
溶解度 DMSO : 2 mg/mL (10.35 mM; ultrasonic and warming and heat to 80°C) 储存条件 Store at -20°C
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储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
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1 mg 5 mg 10 mg
1 mM 5.1754 mL 25.8772 mL 51.7545 mL
5 mM 1.0351 mL 5.1754 mL 10.3509 mL
10 mM 0.5175 mL 2.5877 mL 5.1754 mL
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Research Update

Essential metabolites of Mycobacterium tuberculosis and their mimics

mBio 2011 Feb 1;2(1):e00301-10.PMID:21285434DOI:PMC3031304

An organism requires a range of biomolecules for its growth. By definition, these are essential molecules which constitute the basic metabolic requirements of an organism. A small organic molecule with chemical similarity to that of an essential metabolite may bind to the enzyme that catalyzes its production and inhibit it, likely resulting in the stasis or death of the organism. Here, we report a high-throughput approach for identifying essential metabolites of an organism using genetic and biochemical approaches and then implement computational approaches to identify metabolite mimics. We generated and genotyped 5,126 Mycobacterium tuberculosis mutants and performed a statistical analysis to determine putative essential genes. The essential molecules of M. tuberculosis were classified as products of enzymes that are encoded by genes in this list. Although incomplete, as many enzymes of M. tuberculosis have yet to be identified and characterized, this is the first report of a large number of essential molecules of the organism. We identified essential metabolites of three distinct metabolic pathways in M. tuberculosis and selected molecules with chemical similarity using cheminformatics strategies that illustrate a variety of different pharmacophores. Our approach is aimed at systematic identification of essential molecules and their mimics as a blueprint for development of effective chemical probes of M. tuberculosis metabolism, with the ultimate goal of seeking drugs that can kill this pathogen. As an illustration of this approach, we report that compounds JFD01307SC and l-methionine-S-sulfoximine, which share chemical similarity with an essential molecule of M. tuberculosis, inhibited the growth of this organism at micromolar concentrations.