L-Methionine(H-Met-OH) - Moligand™, 10mM in Water , CAS No.63-68-3

CAS: 63-68-3 Cat. No.: L425234 Summenformel: C₅H₁₁NO₂S Molekulargewicht: 149.21 Beilstein Registry Number: 1722294 EG-Nummer: 200-562-9

GRADE & PURITY Moligand™, 10mM in Water

Synonyms

L-methionine|63-68-3|methionine|h-Met-oh|(S)-2-Amino-4-(methylthio)butanoic acid|Cymethion|L-(-)-Methionine|S-Methionine|Liquimeth|Neo-methidin|L-Methioninum|Methilanin|(L)-Methionine|Acimethin|(S)-methionine|metionina|Methionine (VAN)|Methioninum|Metioni

Storage

Protected from light,Store at -80°C

Shipped In

Dry ice packs + Cold packs

Übersicht

L-Methionine is an essential amino acid for human development, hepatoprotectant, acetominophen poisoning antidote, and urinary acidifier.
An essential amino acid

Specifications

Synonyme

L-methionine | 63-68-3 | methionine | h-Met-oh | (S)-2-Amino-4-(methylthio)butanoic acid | Cymethion | L-(-)-Methionine | S-Methionine | Liquimeth | Neo-methidin | L-Methioninum | Methilanin | (L)-Methionine | Acimethin | (S)-methionine | metionina | Methionine (VAN) | Methioninum | Metioni

Spezifikationen & Reinheit

Moligand™, 10mM in Water

Biochemische und physiologische Mechanismen

Methionine is an essential amino acid which acts a precursor for transmethylation and transsulphuration. In proteins, L-methionine is the biologically active form.The adenosylation of methionine results in the formation of S-adenosyl-L-methionine (SAM), w

Storage

Protected from light,Store at -80°C

Verschickt in

Dry ice packs + Cold packs

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Note

Moligand™

Namen und Kennungen

Pubchem Sid

528765194

Kanonisches Lächeln

CSCC[C@H](N)C(O)=O

IUPAC Name

(2S)-2-amino-4-methylsulfanylbutanoic acid

InChIKey

FFEARJCKVFRZRR-BYPYZUCNSA-N

INCHI

1S/C5H11NO2S/c1-9-3-2-4(6)5(7)8/h4H,2-3,6H2,1H3,(H,7,8)/t4-/m0/s1

Isomere SMILES

CSCC[C@@H](C(=O)O)N

WGK Deutschland

1

RTECS

PD0457000

Molekulargewicht

149.21

Beilstein

1722294

Reaxy-Rn

1722294

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1722294&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Klasse Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Ebene5 Amino acids and derivatives
          • Ebene6 Alpha amino acids and derivatives
            • Ebene7 Methionine and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Klasse: 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: L-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 - L-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
• Beschreibung: 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: Common amino acids

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

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F2 Tclin Thrombin (11687 Activities)

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ESR1 Tclin Estrogen receptor alpha (17718 Activities)

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PGR Tclin Progesterone receptor (8562 Activities)

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CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)

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HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)

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ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)

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AR Tclin Androgen Receptor (11781 Activities)

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CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)

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GABRA1 Tclin GABA receptor alpha-1 subunit (399 Activities)

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MAOA Tclin Monoamine oxidase A (11911 Activities)

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DRD1 Tclin Dopamine D1 receptor (9720 Activities)

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ACHE Tclin Acetylcholinesterase (18204 Activities)

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PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)

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SLC6A2 Tclin Norepinephrine transporter (10102 Activities)

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ADORA1 Tclin Adenosine A1 receptor (17603 Activities)

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SLC6A4 Tclin Serotonin transporter (12625 Activities)

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ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)

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OPRM1 Tclin Mu opioid receptor (19785 Activities)

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DRD3 Tclin Dopamine D3 receptor (14368 Activities)

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SLC6A3 Tclin Dopamine transporter (10535 Activities)

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PDE3A Tclin Phosphodiesterase 3A (3309 Activities)

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HTR2B Tclin Serotonin 2b (5-HT2b) receptor (10323 Activities)

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TBXA2R Tclin Thromboxane A2 receptor (5717 Activities)

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PDE4A Tclin Phosphodiesterase 4A (1943 Activities)

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HRH3 Tclin Histamine H3 receptor (10389 Activities)

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FASN Tchem Fatty acid synthase (3390 Activities)

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Homo sapiens (32628 Activities)

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SLC7A5 Tchem L-type amino acid transporter 1 (388 Activities)

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Mat1a S-adenosylmethionine synthetase alpha and beta forms (31 Activities)

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Mat2a S-adenosylmethionine synthetase gamma form (83 Activities)

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Hdac6 Histone deacetylase 6 (222 Activities)

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Pkm Pyruvate kinase isozymes M1/M2 (66 Activities)

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Ggt1 Gamma-glutamyltranspeptidase 1 (36 Activities)

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Pyricularia grisea (1253 Activities)

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Oryza sativa (2923 Activities)

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luxS S-ribosylhomocysteine lyase (12 Activities)

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rep Replicase polyprotein 1ab (378 Activities)

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Slc16a10 Monocarboxylate transporter 10 (73 Activities)

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Mat1a S-adenosylmethionine synthetase (MAT 1 and MAT 2) (155 Activities)

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Slc1a5 Amino acid transporter (271 Activities)

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Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Empfindlichkeit: Light sensitive.
• Spezifische Drehung [α]: 24° (C=8,HCl (1+1))
• Schmelzpunkt (°C): 280-282°C
• Molekulargewicht: 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: 1
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1