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L-Cysteine hydrochloride Sale

(Synonyms: L-半胱氨酸盐酸盐) 目录号 : GC36431

A conditionally essential amino acid

L-Cysteine hydrochloride Chemical Structure

Cas No.:52-89-1

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1g
¥450.00
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产品描述

L-Cysteine is a conditionally essential amino acid.1,2 It is produced from L-methionine through the transsulfuration pathway.1 L-Cysteine can also be derived from dietary sources and protein turnover. It is a precursor in the biosynthesis of the intracellular antioxidant glutathione . L-Cysteine supplementation increases GSH levels as well as decreases oxidative stress and pro-inflammatory cytokine levels in various rat and porcine disease models, including type 2 diabetes, aging, and inflammatory bowel disease (IBD). It is also an excitotoxin, inducing neuronal damage by overactivation of NMDA receptors.2

1.Yin, J., Ren, W., Yang, G., et al.L-Cysteine metabolism and its nutritional implicationsMol. Nutr. Food Res.60(1)134-146(2016) 2.Janáky, R., Varga, V., Hermann, A., et al.Mechanisms of L-cysteine neurotoxicityNeurochem. Res.25(9-10)1397-1405(2000)

Chemical Properties

Cas No. 52-89-1 SDF
别名 L-半胱氨酸盐酸盐
Canonical SMILES N[C@@H](CS)C(O)=O.[H]Cl
分子式 C3H8ClNO2S 分子量 157.62
溶解度 Water: 100 mg/mL (634.44 mM) 储存条件 Store at RT
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1 mg 5 mg 10 mg
1 mM 6.3444 mL 31.7219 mL 63.4437 mL
5 mM 1.2689 mL 6.3444 mL 12.6887 mL
10 mM 0.6344 mL 3.1722 mL 6.3444 mL
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Research Update

An ESR study of radical kinetics in L-alpha-amino-n-butyric acid hydrochloride containing L-Cysteine hydrochloride

Radiat Res 1989 Dec;120(3):430-41.PMID:2556732doi

On annealing at temperatures near 100 degrees C, carbon-centered radicals migrate to sulfur-centered radicals in X-irradiated crystals of L-alpha-amino-n-butyric acid hydrochloride, CH3CH2CH(NH3-Cl)COOH, containing L-Cysteine hydrochloride, SHCH2CH(NH3Cl)COOH. Samples containing 0, 0.5, 1.0, and 1.5% L-Cysteine hydrochloride were studied. When no cysteine is present, the carbon-centered radical formed by X irradiation, CH3CH2CHOOH, decays according to a second-order diffusion-controlled rate equation. In samples containing cysteine, the same carbon-centered radicals are formed, but on annealing, they migrate to cysteine, where a perithiyl radical, RSS, is formed. The transfer of carbon-centered radicals to perthiyl radicals follows a pseudo first-order rate equation with an activation energy of 1.15 eV. A decrease in the initial concentration of the carbon-centered radicals or an increase in the initial concentration of cysteine results in an increase in the transfer efficiency. The rate of growth of the perthiyl radical depends on both the initial concentration of cysteine and the initial concentration of carbon-centered radicals. The pseudo first-order rate constant increases when either the initial carbon-centered radical concentration increases or the initial cysteine concentration increases. The mechanism by which radicals move from one lattice site to another in the crystalline material is most likely hydrogen abstraction from a neighboring molecule.