DL-Cysteine - Moligand™,≥97% , CAS No.3374-22-9

CAS: 3374-22-9 Cat. No.: C110437 Formule: C₃H₇NO₂S Poids moléculaire: 121.16 Beilstein Registry Number: 1721406 Numéro CE: 222-160-2

GRADE & PURITY Moligand™, ≥97%

Synonyms

SR-01000944791 | Tox21_111766_1 | [35s]cysteine | A821916 | CCRIS 8598 | FD21272 | NCGC00248803-03 | SY009625 | d,l-cysteine | CAS-3374-22-9 | Zystein | CAS_5862 | L-Cysteine-13C3 | NSC 63864 | CHEBI:15356 | Hcys | UNII-5CM45Q5YAF | AB02703 | L-CYSTEINE (

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Vue d’ensemble

Product Description

Cysteine is a non-essential amino acid that can be synthesized by the human body under normal physiological conditions if a sufficient quantity of methionine is available. Cysteine is commonly used as a precursor in the food and pharmaceutical industries. Cysteine is used as a processing aid for baking, as an additive in cigarettes, as well as in the preparation of meat flavours.

Product Application
NMDA agonist that is an agonist at quisqualate receptors at high concentration.

Specifications

Synonymes

SR-01000944791 | Tox21_111766_1 | [35s]cysteine | A821916 | CCRIS 8598 | FD21272 | NCGC00248803-03 | SY009625 | d,l-cysteine | CAS-3374-22-9 | Zystein | CAS_5862 | L-Cysteine-13C3 | NSC 63864 | CHEBI:15356 | Hcys | UNII-5CM45Q5YAF | AB02703 | L-CYSTEINE (

Spécifications et pureté

Moligand™, ≥97%

Mécanismes biochimiques et physiologiques

NMDA agonist that is an agonist at quisqualate receptors at high concentration.

Conditions de stockage de stockage

Store at 2-8°C,Argon charged

Expédié en

Wet ice

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

Grade

Moligand™

Pureté

≥97%

Noms et identifiants

• Pubchem Sid: 508810488
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/508810488
• Sourires canoniques: C(C(C(=O)O)N)S
• IUPAC Name: 2-amino-3-sulfanylpropanoic acid
• InChIKey: XUJNEKJLAYXESH-UHFFFAOYSA-N
• INCHI: 1S/C3H7NO2S/c4-2(1-7)3(5)6/h2,7H,1,4H2,(H,5,6)
• Isomères SMILES: C(C(C(=O)O)N)S
• WGK Allemagne: 3
• Poids moléculaire: 121.16
• Beilstein: 1721406
• Reaxy-Rn: 1721406
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1721406&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 Cysteine 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: Cysteine and derivatives
• Alternative Parents: Alpha amino acids Amino acids Monocarboxylic acids and derivatives Carboxylic acids Alkylthiols Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Cysteine or derivatives - Alpha-amino acid - Amino acid - Alkylthiol - Carboxylic acid - Monocarboxylic acid or derivatives - Organic nitrogen compound - Hydrocarbon derivative - Primary amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Primary aliphatic amine - Organopnictogen compound - Carbonyl group - Amine - Organic oxygen compound - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as cysteine and derivatives. These are compounds containing cysteine or a derivative thereof resulting from reaction of cysteine 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

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VDR Tclin Vitamin D receptor (26531 Activities)

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HepG2 (196354 Activities)

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EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)

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TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

Discover Target: TDP1

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LMNA Tbio Prelamin-A/C (36751 Activities)

Discover Target: LMNA

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Adam17 ADAM17 (14 Activities)

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Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)

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ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)

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Mécanismes d'action

Propriétés chimiques et physiques

• Solubilité: Soluble in water (partly), 1 N HCl (25 mg/ml), ethanol, and acetic acid. Insoluble in acetone.
• Sensibilité: light sensitive;Air sensitive;Moisture sensitive
• Point de fusion (°C): 225°C
• Poids moléculaire: 121.160 g/mol
• XLogP3: -2.500
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 121.02 Da
• Monoisotopic Mass: 121.02 Da
• Topological Polar Surface Area: 64.300 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 75.300
• 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