DL-Methionine - 10mM in Water , CAS No.59-51-8

CAS: 59-51-8 Cat. No.: D424961 Formule: C₅H₁₁NO₂S Poids moléculaire: 149.21 Beilstein Registry Number: 636185 Numéro CE: 200-432-1

QUALITÉ & PURETÉ 10mM in Water

Synonyms

alpha-Amino-gamma-(methylthio)butyric acid|Racemethionine [USAN:USP:NF]|.alpha.-Amino-.gamma.-methylmercaptobutyric acid|Mertionin|(+/-)-Methionine|D,L-METHIONINE [FHFI]|DL-2-Amino-4-(methylthio)butanoic acid|Dyprin|Lobamine|RACEMETHIONINE (USP-RS)|dl-methionin|Met248|Methionine, DL-|Amurex|2-Amino-4-(methylmercapto)butyric acid|2-amino-4-methylsulfanylbutanoic acid|2-amino-4-methylsulfanyl-butanoic acid|DL-METHIONINE [WHO-DD]|Metion|(+-)-Methionine|H-DL-Met-OH|Hmet|Racemethionine (USAN:USP:NF)|(.+/-.)-Methionine|DL-2-Amino-4-(methylthio)butyric acid|2-amino-4-(methylthio) butyric acid|DL-2-Amino-4-methylthiobutanoic acid|Metione|Urimeth|METHIONINE,L-|alpha-Amino-gamma-methylmercaptobutyric acid|DL-Methionine (JAN)|Cynaron|DL-METHIONINE [EP MONOGRAPH]|Acimetion|DL-CH3SCH2CH2CH(NH2)COOH|2-Amino-4-methylthiobutanoic acid|Methionine DL-|Methionine dl-form|Petameth|Racemethionine [USAN]|DL-METHIONINE [JAN]|methionine|Methionine, amorphous|D,L-methionine|Racemethionine, USAN|DL-METHIONINE [WHO-IP]|DL-Methionine;|Methio-Form|DL-METHIONINE|METHIONINE DL-FORM [MI]|DL-METHIONINE [EP IMPURITY]|DL-Methioninum|Methilonin|R-Methionine|RACEMETHIONINE [USP-RS]|DL-Met|DL-Methionine-3,3,4,4-d4|DL-METHIONINE [FCC]|DL-2-Amino-4-(methylthio)-butyric acid|Racemethionine|2-amino-4-(methylsulfanyl)butanoic acid|2-amino-4-methylsulfanyl-butyric acid|2-Amino-4-(methylthio)butyric acid|2-amino-4-(methylthio)-butyric acid|alpha-Amino-gamma-methylmercaptobutyric acid (VAN)|DL-METHIONINE [MART.]|(+/-)-2-Amino-4-(methylmercapto)butyric acid|Padameth (TN)|DL-Methionine (Racemethionine)|Meonine|Pedameth|Neston|Padameth

Storage

Protected from light,Store at -80°C

Shipped In

Dry ice packs + Cold packs

Vue d’ensemble

DL-Methionine is an essential nonpolar α-amino acid with oxidative stress defense properties.
An essential nonpolar amino acid with oxidative stress defense properties

Spécifications

Synonymes

alpha-Amino-gamma-(methylthio)butyric acid | Racemethionine [USAN:USP:NF] | .alpha.-Amino-.gamma.-methylmercaptobutyric acid | Mertionin | (+/-)-Methionine | D,L-METHIONINE [FHFI] | DL-2-Amino-4-(methylthio)butanoic acid | Dyprin | Lobamine | RACEMETHIONINE (USP-RS) | dl-methionin | Met248 | Methionine, DL- | Amurex | 2-Amino-4-(methylmer Afficher plus

Spécifications et pureté

10mM in Water

Mécanismes biochimiques et physiologiques

Methionine can prevent diseases related to hair, skin and nails. It increases the production of lecithin in liver, thus reducing cholesterol level. It is naturally used as a heavy metal chelating agent to regulate ammonia concentration in urine. This can

Conditions de stockage de stockage

Protected from light,Store at -80°C

Expédié en

Dry ice packs + Cold packs

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Type d'action

INHIBITOR

Noms et identifiants

Pubchem Sid

528764175

Sourires canoniques

CSCCC(C(=O)O)N

IUPAC Name

2-amino-4-methylsulfanylbutanoic acid

InChIKey

FFEARJCKVFRZRR-UHFFFAOYSA-N

INCHI

1S/C5H11NO2S/c1-9-3-2-4(6)5(7)8/h4H,2-3,6H2,1H3,(H,7,8)

Isomères SMILES

CSCCC(C(=O)O)N

WGK Allemagne

1

RTECS

PD0456000

Poids moléculaire

149.21

Beilstein

636185

Reaxy-Rn

636185

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=636185&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Level5 Amino acids and derivatives
          • Level6 Alpha amino acids and derivatives
            • Level7 Methionine and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Amino acids, peptides, and analogues
• Intermediate Tree Nodes: Amino acids and derivatives - Alpha amino acids and derivatives
• Direct Parent: Methionine and derivatives
• Alternative Parents: Alpha amino acids Thia fatty acids Amino acids Sulfenyl compounds Monocarboxylic acids and derivatives Dialkylthioethers Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Methionine or derivatives - Alpha-amino acid - Thia fatty acid - Fatty acid - Fatty acyl - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Thioether - Sulfenyl compound - Dialkylthioether - Amine - Organic oxygen compound - Primary amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Primary aliphatic amine - Carbonyl group - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as methionine and derivatives. These are compounds containing methionine or a derivative thereof resulting from reaction of methionine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
• External Descriptors: sulfur-containing amino acid - alpha-amino acid

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Cibles associées (non humaines)

Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mécanismes d'action

Propriétés chimiques et physiques

• Sensibilité: Light sensitive.
• Point de fusion (°C): 281°C
• Poids moléculaire: 149.210 g/mol
• XLogP3: -1.900
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 149.051 Da
• Monoisotopic Mass: 149.051 Da
• Topological Polar Surface Area: 88.600 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 97.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1