Betaine - Moligand™, 10mM in DMSO , CAS No.107-43-7

CAS: 107-43-7 Cat. No.: B420528 Formula: C₅H₁₁NO₂ Peso molecolare: 117.15 Beilstein Registry Number: 3537113 Numero EC: 203-490-6

GRADE & PURITY Moligand™, 10mM in DMSO

Synonyms

betaine|107-43-7|glycine betaine|oxyneurine|Trimethylglycine|lycine|Abromine|Trimethylglycocoll|Glycocoll betaine|Glycylbetaine|Rubrine C|Jortaine|BETAINE, ANHYDROUS|acidin-pepsin|alpha-Earleine|trimethylammonioacetate|2-(trimethylazaniumyl)acetate|N,N,N-

Storage

Protected from light,Store at -80°C

Shipped In

Dry ice packs + Cold packs

Panoramica

Betaine is a quaternary ammonium zwitterion, extensively present in animals, plants and microorganisms. It also forms a good dietary source as it is found in wheat, spinach, shellfish and sugar beets. Betaine is a methyl derivative of the amino acid glycine. It is known by different names such as trimethylglycine, glycine betaine, lycine and oxyneurine.

Specifications

Sinonimi

betaine | 107-43-7 | glycine betaine | oxyneurine | Trimethylglycine | lycine | Abromine | Trimethylglycocoll | Glycocoll betaine | Glycylbetaine | Rubrine C | Jortaine | BETAINE, ANHYDROUS | acidin-pepsin | alpha-Earleine | trimethylammonioacetate | 2-(trimethylazaniumyl)acetate | N,N,N-

Specifiche e purezza

Moligand™, 10mM in DMSO

Meccanismi biochimici e fisiologici

Apart from betaine taking part in transmethylation, it acts as an organic osmolyte in protecting cells under stress. This is being significantly observed in plants and microorganisms. Betaine is also known to increase the levels of S-adenosylmethionine an

Condizioni di conservazione di stoccaggio

Protected from light,Store at -80°C

Spedito in

Dry ice packs + Cold packs

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Grado

Moligand™

Nomi e identificatori

Pubchem Sid

528773394

Sorrisi canonici

C[N+](C)(C)CC(=O)[O-]

IUPAC Name

2-(trimethylazaniumyl)acetate

InChIKey

KWIUHFFTVRNATP-UHFFFAOYSA-N

INCHI

1S/C5H11NO2/c1-6(2,3)4-5(7)8/h4H2,1-3H3

Isomeri SMILES

C[N+](C)(C)CC(=O)[O-]

WGK Germania

3

RTECS

DS5900000

Peso molecolare

117.15

Beilstein

3537113

Reaxy-Rn

3537113

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3537113&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 Alpha amino acids

• 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: Alpha amino acids
• Alternative Parents: Tetraalkylammonium salts Carboxylic acid salts Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organic salts Organic oxides Hydrocarbon derivatives Carbonyl compounds Amines
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Alpha-amino acid - Quaternary ammonium salt - Tetraalkylammonium salt - Carboxylic acid salt - Monocarboxylic acid or derivatives - Carboxylic acid - Organopnictogen compound - Hydrocarbon derivative - Organic salt - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Carbonyl group - Amine - Organic nitrogen compound - Organic oxide - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as alpha amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon).
• External Descriptors: a methylated methyl acceptor

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

Obiettivi associati (non umani)

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Sensibilità: Light sensitive.
• Punto di fusione (°C): 293°C
• Peso molecolare: 117.150 g/mol
• XLogP3: 0.500
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 117.079 Da
• Monoisotopic Mass: 117.079 Da
• Topological Polar Surface Area: 40.100 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 87.600
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• 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