glutathione
5-L-glutamyl-L-cysteinylglycine
 
Notes:
a tripeptide with many roles in cells. it conjugates to drugs to make them more soluble for excretion, is a cofactor for some enzymes, is involved in protein disulfide bond rearrangement and reduces peroxides. Glutathione (GSH) - reduced glutathione - is a tripeptide with a gamma peptide linkage between the amine group of cysteine (which is attached by normal peptide linkage to a glycine) and the carboxyl group of the glutamate side-chain. It is an antioxidant, preventing damage to important cellular components caused by reactive oxygen species such as free radicals and peroxides. [Wikipedia]
  • BOC Sciences
    • BOC Sciences
      Best of Chemicals Supplier
      Quality supplier of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecule and chiral compounds.
      BOC Sciences provides a wide range of services to support the pharmaceutical industry through all stages of drug discovery including Custom Synthesis of those chemicals that are not in stock, Isotope Labeling Service, Chiral Synthesis and Resolution, Bioconjugation, PEGylation services, analytical services.
      BOC Sciences is a brand of BOCSCI Inc. We leverage our wide spectrum of business in the fields of development, manufacturing, marketing, and distribution to help you make best-informed decisions tailored to your evolving needs for premium chemicals. Our complete suite of CRO services spans the entire molecule development pipeline including contract research for target identification, building blocks, compound synthesis, biochemical and cellular analysis, preclinical animal tests, and clinical studies.
      Email: Marketing
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      US Email: Sales
      Voice: 1-631-485-4226
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      Product(s):
      70-18-8 Glutathione >98%
       
  • Charkit Chemical
    • Charkit Chemical Corporation
      The Specialty Chemical Specialists
      Explore this website to discover the products and services that Charkit provides for your industry and please contact us directly to find out how we can be of service to you.
      about: Since 1982, Charkit has been committed to expanding the markets we serve as our roster of products and services continues to grow with us. Our substantial portfolio of personal care ingredients now include a wide array of luxury and exotic components to compliment the key products we have always offered. We have expanded our offerings to the nutraceutical, industrial, and resin markets with a growing roster of versatile and unique ingredients. We continue to lead the way in our traditional markets such as Metal and Water Treatment, Imaging, Flavor & Fragrance, Aroma and Food. Our Pharmaceutical offerings continue to expand, still anchored by the Boronic Derivatives that meet the demands of Suzuki coupling reactions. Please contact us to learn how we can help you reach your goals.
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      Product(s):
      GLUTATHIONE, L-
      GLUTATHIONE REDUCED, L-
       
  • Glentham Life Sciences
  • Jiangyin Healthway
    • Jiangyin Healthway International Trade Co., Ltd
      Independent Ingredients Supplier
      We provide custom synthesis and contract manufacturing from milligrams to metric tonnes.
      Jiangyin Healthway International Trade Co., Ltd is a professional company, main engaged in manufacturing and exporting aroma chemicals ,food additives , cosmetic ingredient ,pharmaceutical intermediates & other fine chemicals; especially on aroma chemicals , as the major manufacturer of heterocyclic and sulphur aroma compounds , we are the leading independent ingredients supplier to the flavour and fragrance industries in China, can offer hundreds of different high quality aroma chemicals.
      Email: Info
      Email: Sales
      Voice: 86-510-86023169
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      Services
      Biochemical
      Natural Food Colour
      New functional food ingredients
      Product(s):
      HLCFD-126 Reduced Glutathione
       
  • Penta International
    • Penta International Corporation
      Chemistry innovation
      At Penta, our products and services help businesses do business better.
      For over 30 years, Penta Manufacturing Company has played a growing role in worldwide chemistry innovations and applications. As an industry leader, Penta continues to pioneer chemistry-based solutions for practically every area of commerce. Our products and expertise have helped fuel technical advances in dozens of commercial applications including flavoring, coloring, fragrances and chemical processes.
      US Email: Technical Services
      US Email: Sales
      US Voice: (973) 740-2300
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      Product(s):
      07-31000 GLUTATHIONE REDUCED
       
Synonyms   Articles   Notes   Search
CAS Number: 70-18-8Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 200-725-4
FDA UNII: GAN16C9B8O
Nikkaji Web: J10.686K
Beilstein Number: 1729812
MDL: MFCD00065939
XlogP3-AA: -4.50 (est)
Molecular Weight: 307.32669000
Formula: C10 H17 N3 O6 S
NMR Predictor: Predict (works with chrome or firefox)
Category: nutrient adjuncts, dietary supplements, nutrient agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Perfumer and Flavorist: Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
 FDA/DG SANTE Petitions, Reviews, Notices:
GRN 293 Glutathione View - notice PDF
GRN 244 Glutathione View - notice PDF
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Physical Properties:
Appearance: white powder (est)
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Melting Point: 195.00 °C. @ 760.00 mm Hg
Boiling Point: 754.00 to  755.00 °C. @ 760.00 mm Hg (est)
Flash Point: 770.00 °F. TCC ( 410.10 °C. ) (est)
logP (o/w): -1.645 (est)
Soluble in:
 water, 1.927e+005 mg/L @ 25 °C (est)
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: reducing agents
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Suppliers:
AIDP
L-Glutathione (Reduced) 98.0%
Alfa Biotechnology
For experimental / research use only.
Glutathione 98%
Bio Springer
Springer® 4000 yeast extracts
Flavor: characteristic
The Springer® 4000 yeast extracts provide Kokumi taste, or mouthfullness, thanks to the naturally occurring sulfur amino acids and peptides they contain. They provide intense poultry stock flavour and enhance meat and cheese flavours. These glutathione-rich extracts work well on their own or in synergy with one of our Springer® yeast extracts.
BOC Sciences
For experimental / research use only.
Glutathione >98%
Carbosynth
For experimental / research use only.
L-Glutathione, reduced
Charkit Chemical
GLUTATHIONE REDUCED, L-
Charkit Chemical
GLUTATHIONE, L-
George Uhe Company
Glutathione
Glentham Life Sciences
Glutathione reduced
Graham Chemical
L-Glutathione
Jiangyin Healthway
Reduced Glutathione
New functional food ingredients
Meafo
For experimental / research use only.
L-Glutathione Reduced 98%
Penta International
GLUTATHIONE REDUCED
Prinova
L-Glutathione
Santa Cruz Biotechnology
For experimental / research use only.
Glutathione, reduced ≥98%
Sigma-Aldrich
For experimental / research use only.
L-Glutathione reduced ≥98.0%
WILD Flavors
L-Glutathione
Flavor: taste
L-Glutathione is a small protein consisting of three amino acids: cysteine, glutamic acid and glycine. It neutralizes free radicals that can cause cellular damage. It also acts as a regulator for other antioxidants in the body, such as Vitamins C & E, and is found in every cell in the body. It plays an important role in cellular metabolism, immunity and overall health and wellness.
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Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
intravenous-rabbit LD50  > 2000 mg/kg
Biochemical Journal. Vol. 41, Pg. 325, 1947.

oral-mouse LD50  5000 mg/kg
"Modern Pharmaceuticals of Japan, IV," Tokyo, Japan Pharmaceutical, Medical and Dental Supply Exporters' Assoc., 1972Vol. -, Pg. 93, 1972.

intravenous-mouse LD50  2238 mg/kg
Japanese Journal of Antibiotics. Vol. 38, Pg. 137, 1985.

intraperitoneal-mouse LD50  4020 mg/kg
"Modern Pharmaceuticals of Japan, IV," Tokyo, Japan Pharmaceutical, Medical and Dental Supply Exporters' Assoc., 1972Vol. -, Pg. 93, 1972.

intramuscular-mouse LD50  4000 mg/kg
"Modern Pharmaceuticals of Japan, III," Tokyo, Japan Pharmaceutical, Medical and Dental Suppl Exporters' Assoc., 1968Vol. -, Pg. 97, 1968.

Dermal Toxicity:
subcutaneous-mouse LD50 5000 mg/kg
"Modern Pharmaceuticals of Japan, IV," Tokyo, Japan Pharmaceutical, Medical and Dental Supply Exporters' Assoc., 1972Vol. -, Pg. 93, 1972.

Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: nutrient adjuncts, dietary supplements, nutrient agents
Recommendation for glutathione usage levels up to:
 not for fragrance use.
 
Recommendation for glutathione flavor usage levels up to:
 not for flavor use.
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Safety References:
European Food Safety Authority (EFSA) reference(s):
EFSA scientific advice to EC on accumulating formaldehyde in GM soybeans
View page or View pdf
EPI System: View
ClinicalTrials.gov: search
Daily Med: search
Chemical Carcinogenesis Research Information System: Search
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA GENetic TOXicology: Search
EPA Substance Registry Services (TSCA): 70-18-8
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 124886
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 2
 (2S)-2-amino-5-[[(2R)-1-(carboxymethylamino)-1-oxo-3-sulfanylpropan-2-yl]amino]-5-oxopentanoic acid
Chemidplus: 0000070188
RTECS: MC0556000 for cas# 70-18-8
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References:
 (2S)-2-amino-5-[[(2R)-1-(carboxymethylamino)-1-oxo-3-sulfanylpropan-2-yl]amino]-5-oxopentanoic acid
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 70-18-8
Pubchem (cid): 124886
Pubchem (sid): 134971822
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Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
CHEBI: View
CHEMBL: View
KEGG (GenomeNet): C00051
HMDB (The Human Metabolome Database): HMDB00125
FooDB: FDB001498
YMDB (Yeast Metabolome Database): YMDB00690
Export Tariff Code: 2930.90.5050
FDA Listing of Food Additive Status: View
MedlinePlusSupp: View
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
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Potential Blenders and core components note
 
None Found
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 biological additives 
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 bean black bean root
Search Trop  Picture
 bean fava bean
Search Trop  Picture
 bean mung bean sprout
Search Trop  Picture
 black gram seed
Search Trop  Picture
 corn fruit
Search Trop  Picture
 corn root
Search Trop  Picture
 corn seed
Search Trop  Picture
 garlic bulb
Search Trop  Picture
 lotus indian lotus seed
Search Trop  Picture
 onion bulb
Search Trop  Picture
 peanut seed
Search Trop  Picture
 potato plant
Search Trop  Picture
 purslane herb
Search Trop  Picture
 spinach plant
Search Trop  Picture
Synonyms   Articles   Notes   Search   Top
Synonyms:
(S)-2-amino-5-((R)-1-(carboxymethylamino)-3-mercapto-1-oxopropan-2-ylamino)-5-oxopentanoic acid
(2S)-2-amino-5-({(2R)-1-[(carboxymethyl)amino]-1-oxo-3-sulfanyl-2-propanyl}amino)-5-oxopentanoic acid
(2S)-2-amino-5-[[(2R)-1-(carboxymethylamino)-1-oxo-3-sulfanylpropan-2-yl]amino]-5-oxopentanoic acid
 deltathione
N-(N-L-g-glutamyl-L-cysteinyl)glycine
N-(N-L-gamma-glutamyl-L-cysteinyl)glycine
5-L-glutamyl-L-cysteinylglycine
L-glutamyl-L-cysteinylglycine
 glutathiol
L-glutathione
L-glutathione reduced
 glutathione reduced form
 glutathione, reduced form
L-glutatione
Synonyms   Articles   Notes   Search   Top
Articles:
PubMed: Evolved Saccharomyces cerevisiae wine strains with enhanced glutathione production obtained by an evolution-based strategy.
PubMed: Secretion expression of SOD1 and its overlapping function with GSH in brewing yeast strain for better flavor and anti-aging ability.
PubMed: Protective effects of N-acetylcysteine against monosodium glutamate-induced astrocytic cell death.
PubMed: Direct accurate analysis of cysteinylated and glutathionylated precursors of 4-mercapto-4-methyl-2-pentanone and 3-mercaptohexan-1-ol in must by ultrahigh performance liquid chromatography coupled to mass spectrometry.
PubMed: Leaf proteome profiling of transgenic mint infected with Alternaria alternata.
PubMed: Restoration of brain antioxidant status by hydroalcoholic extract of Mimusops elengi flowers in rats treated with monosodium glutamate.
PubMed: New insights into sulfur metabolism in yeasts as revealed by studies of Yarrowia lipolytica.
PubMed: Response surface methodology for meat-like odorants from Maillard reaction with glutathione I: the optimization analysis and the general pathway exploration.
PubMed: Integrated expression of the α-amylase, dextranase and glutathione gene in an industrial brewer's yeast strain.
PubMed: Construction of self-cloning, indigenous wine strains of Saccharomyces cerevisiae with enhanced glycerol and glutathione production.
PubMed: Sensory characteristics and consumer acceptability of beef stock containing the glutathione-xylose Maillard reaction product and/or monosodium glutamate.
PubMed: 4-(2-Hydroxypropan-2-yl)-1-methylcyclohexane-1,2-diol prevents xenobiotic induced cytotoxicity.
PubMed: Response surface methodology for meat-like odorants from the Maillard reaction with glutathione II: the tendencies analysis of meat-like donors.
PubMed: Effect of monosodium glutamate on lipid peroxidation and certain antioxidant enzymes in cardiac tissue of alcoholic adult male mice.
PubMed: Toxic effects of some synthetic food colorants and/or flavor additives on male rats.
PubMed: Development of Saccharomyces cerevisiae producing higher levels of sulfur dioxide and glutathione to improve beer flavor stability.
PubMed: Metabolomic approach for determination of key volatile compounds related to beef flavor in glutathione-Maillard reaction products.
PubMed: Sensory characteristics and consumer acceptability of beef stock containing glutathione Maillard reaction products prepared at various conditions.
PubMed: Impacts of glutathione Maillard reaction products on sensory characteristics and consumer acceptability of beef soup.
PubMed: Identification of impact odorants contributing to fresh mushroom off-flavor in wines: incidence of their reactivity with nitrogen compounds on the decrease of the olfactory defect.
PubMed: Construction of amylolytic industrial brewing yeast strain with high glutathione content for manufacturing beer with improved anti-staling capability and flavor.
PubMed: Environmental stress enhances biosynthesis of flavor precursors, S-3-(hexan-1-ol)-glutathione and S-3-(hexan-1-ol)-L-cysteine, in grapevine through glutathione S-transferase activation.
PubMed: The cinnamon-derived dietary factor cinnamic aldehyde activates the Nrf2-dependent antioxidant response in human epithelial colon cells.
PubMed: Sensory characteristics and consumer acceptability of beef soup with added glutathione and/or MSG.
PubMed: Glutamate. Its applications in food and contribution to health.
PubMed: A review of fatty acid profiles and antioxidant content in grass-fed and grain-fed beef.
PubMed: Free amino acid production during tomato fruit ripening: a focus on L-glutamate.
PubMed: [Effects of knockout ECM25/YJL201W gene in brewing yeast on beer flavor stability].
PubMed: Over-expression of GSH1 gene and disruption of PEP4 gene in self-cloning industrial brewer's yeast.
PubMed: Cytotoxicity and gene expression profiles in cell cultures exposed to whole smoke from three types of cigarettes.
PubMed: Monosodium glutamate-induced oxidative damage and genotoxicity in the rat: modulatory role of vitamin C, vitamin E and quercetin.
PubMed: The Saccharomyces cerevisiae EHT1 and EEB1 genes encode novel enzymes with medium-chain fatty acid ethyl ester synthesis and hydrolysis capacity.
PubMed: A comparative study of the antioxidant/prooxidant activities of eugenol and isoeugenol with various concentrations and oxidation conditions.
PubMed: Chemometric modeling to relate antioxidants, neutral lipid fatty acids, and flavor components in chicken breasts.
PubMed: Isothiocyanates in cancer prevention.
PubMed: NTP toxicology and carcinogensis Studies of 2,4-hexadienal (89% trans,trans isomer, CAS No. 142-83-6; 11% cis,trans isomer) (Gavage Studies).
PubMed: II. Glutamine and glutamate.
PubMed: Constituents of the essential oil of the Cinnamomum cassia stem bark and the biological properties.
PubMed: Mechanisms of inhibition of chemical toxicity and carcinogenesis by diallyl sulfide (DAS) and related compounds from garlic.
PubMed: Decrease of hepatic catalase level by treatment with diallyl sulfide and garlic homogenates in rats and mice.
PubMed: Flavor characteristics of glutathione in raw and cooked foodstuffs.
PubMed: Metabolism of the chemoprotective agent diallyl sulfide to glutathione conjugates in rats.
PubMed: Pathways of metabolism of [1'-14C]-trans-anethole in the rat and mouse.
PubMed: Protective effects of garlic and related organosulfur compounds on acetaminophen-induced hepatotoxicity in mice.
PubMed: Differential induction of glutathione transferase isoenzymes of mice stomach by diallyl sulfide, a naturally occurring anticarcinogen.
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