D-Glucuronic acid - Moligand™, 10mM in DMSO , CAS No.6556-12-3

CAS: 6556-12-3 Cat. No.: D425310 Fórmula: C₆H₁₀O₇ Peso molecular: 194.14 Beilstein Registry Number: 1727083 Número CE: 229-486-4

GRADE & PURITY Moligand™, 10mM in DMSO

Synonyms

BP-12303 | AKOS006271885 | D-GLUCURONIC ACID [MI] | D-Glucuronic Acid; Glucuronic acid, D- (8CI); D-(+)-Glucuronic acid; Glucosiduronic acid; Glucuronic acid | MFCD00166981 | (d)-glucuronic acid | IAJILQKETJEXLJ-QTBDOELSSA-N | AT25131 | DTXSID60859531 | G

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Visão geral

The level of carbohydrates in a sample of alginate purified from P.aeruginosa was determined by using a phenol-sulfuric acid aβay where D- glucuronic acid was used as the standard

Specifications

Sinónimos

BP-12303 | AKOS006271885 | D-GLUCURONIC ACID [MI] | D-Glucuronic Acid; Glucuronic acid, D- (8CI); D-(+)-Glucuronic acid; Glucosiduronic acid; Glucuronic acid | MFCD00166981 | (d)-glucuronic acid | IAJILQKETJEXLJ-QTBDOELSSA-N | AT25131 | DTXSID60859531 | G

Especificações e pureza

Moligand™, 10mM in DMSO

Mecanismos bioquímicos e fisiológicos

In humans, glucuronic acid conjugation with steroidal compounds and drugs is an important step in phase II metabolic reactions. This influences the biotransformation process of the compound.Water soluble sugar acid formed by oxidation of the C-6 carbon of

Condições de armazenamento de armazenamento

Store at -80°C

Enviado em

Dry ice packs + Cold packs

Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.

Grau

Moligand™

Tipo de ação

AGONIST

Nomes e identificadores

Pubchem Sid

528764062

Sorrisos canónicos

C(=O)C(C(C(C(C(=O)O)O)O)O)O

IUPAC Name

(2S,3S,4S,5R)-2,3,4,5-tetrahydroxy-6-oxohexanoic acid

InChIKey

IAJILQKETJEXLJ-QTBDOELSSA-N

INCHI

1S/C6H10O7/c7-1-2(8)3(9)4(10)5(11)6(12)13/h1-5,8-11H,(H,12,13)/t2-,3+,4-,5-/m0/s1

SMILES isoméricas

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

WGK Alemanha

3

RTECS

LZ8836600

Peso molecular

194.14

Beilstein

1727083

Reaxy-Rn

2330562

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2330562&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates
        • Level5 Sugar acids and derivatives
          • Level6 Glucuronic acid derivatives

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Sugar acids and derivatives
• Direct Parent: Glucuronic acid derivatives
• Alternative Parents: Hexoses Medium-chain hydroxy acids and derivatives Medium-chain fatty acids Hydroxy fatty acids Beta hydroxy acids and derivatives Beta-hydroxy aldehydes Alpha hydroxy acids and derivatives Alpha-hydroxyaldehydes Secondary alcohols Polyols Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Glucuronic acid or derivatives - Hexose monosaccharide - Medium-chain hydroxy acid - Medium-chain fatty acid - Hydroxy fatty acid - Beta-hydroxy acid - Fatty acyl - Fatty acid - Monosaccharide - Hydroxy acid - Beta-hydroxy aldehyde - Alpha-hydroxy acid - Alpha-hydroxyaldehyde - Secondary alcohol - Polyol - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxide - Hydrocarbon derivative - Carbonyl group - Aldehyde - Alcohol - Aliphatic acyclic compound
• Descrição: This compound belongs to the class of organic compounds known as glucuronic acid derivatives. These are compounds containing a glucuronic acid moiety (or a derivative), which consists of a glucose moiety with the C6 carbon oxidized to a carboxylic acid.
• External Descriptors: D-glucuronic 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

Propriedades químicas e físicas

• Sensibilidade: Moisture sensitive.
• Rotação específica [α]: 36 ° (C=6, H2O)
• Ponto de fusão (°C): 165°C
• Peso molecular: 194.140 g/mol
• XLogP3: -2.600
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 5
• Exact Mass: 194.043 Da
• Monoisotopic Mass: 194.043 Da
• Topological Polar Surface Area: 135.000 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 191.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 4
• 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