D-(+)-Glucosa - AR, used for D-(+)-glucose has been used for: As a supplement to Duchenne phosphate-buffered saline (DPBS) for standardized serum bactericidal assays (SBA) using human complement; As a component of Tyrode's solution (HEPES)-buffered for tr

CAS: 50-99-7 Cat. No.: G116300 Fórmula: C₆H₁₂O₆ Peso molecular: 180.16 Beilstein Registry Number: 1724615 Número EC: 200-075-1

GRADE & PURITY AR

Synonyms

DEXTROSA ANHIDROSA [II] | GLUCOSA [MI] | D-Glucosa;Azúcar de uva;Glucopiranosa | DTXCID701436386 | GLUCOSA [WHO-DD] | NSC-406891 | (C13)D-Glucosa | CAS-50-99-7 | DTXSID4048729 | Glucosa (C-14) | SW220288-1 | (2R,3S,4R,5R)-2,3,4,5,6-pentakis(oxidanil)hexan

Storage

Argón cargado

Shipped In

Normal

Descripción general

La D(+)Glucosa, Anhidra es un monosacárido granular.
Una fuente primaria de energía para los organismos vivos

Specifications

Sinónimos

DEXTROSA ANHIDROSA [II] | GLUCOSA [MI] | D-Glucosa;Azúcar de uva;Glucopiranosa | DTXCID701436386 | GLUCOSA [WHO-DD] | NSC-406891 | (C13)D-Glucosa | CAS-50-99-7 | DTXSID4048729 | Glucosa (C-14) | SW220288-1 | (2R,3S,4R,5R)-2,3,4,5,6-pentakis(oxidanil)hexan

Especificaciones y pureza

AR

Mecanismos bioquímicos y fisiológicos

La glucosa es una fuente de energía universal para todas las células humanas y un precursor importante para la producción y transformación de diversos hidratos de carbono posteriores. La ingesta de glucosa es un indicador clave del metabolismo energético

Aplicación

D-(+)-glucose has been used for: As a supplement to Duchenne phosphate-buffered saline (DPBS) for standardized serum bactericidal assays (SBA) using human complement; As a component of Tyrode's solution (HEPES)-buffered for treating excised diaphragmatic

Condiciones de almacenamiento de almacenamiento

Argón cargado

Enviado en

Normal

Grado

AR

Nombres e identificadores

Pubchem Sid

508810412

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508810412

Sonrisas canónicas

OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@@H]1O

IUPAC Name

(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal

InChIKey

GZCGUPFRVQAUEE-SLPGGIOYSA-N

INCHI

1S/C6H12O6/c7-1-3(9)5(11)6(12)4(10)2-8/h1,3-6,8-12H,2H2/t3-,4+,5+,6+/m0/s1

Isómeros SMILES

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

WGK Alemania

1

RTECS

LZ6600000

Peso molecular

180.16

Beilstein

1724615

Reaxy-Rn

1281608

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1281608&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Clase Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates
        • Level5 Monosaccharides
          • Level6 Hexoses

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Clase: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Monosaccharides
• Direct Parent: Hexoses
• Alternative Parents: Medium-chain aldehydes Beta-hydroxy aldehydes Alpha-hydroxyaldehydes Secondary alcohols Polyols Primary alcohols Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Hexose monosaccharide - Medium-chain aldehyde - Beta-hydroxy aldehyde - Alpha-hydroxyaldehyde - Secondary alcohol - Polyol - Organic oxide - Hydrocarbon derivative - Primary alcohol - Carbonyl group - Aldehyde - Alcohol - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as hexoses. These are monosaccharides in which the sugar unit is a is a six-carbon containing moeity.
• External Descriptors: aldehydo-glucose - D-glucose

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

Objetivos asociados (no humanos)

Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

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

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

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

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Soluble in water, insoluble in alcohol, ether
• Sensibilidad: Moisture sensitive.
• Rotación específica [α]: 53 ° (C=10, H2O)
• Punto de fusión (°C): 146°C
• Peso molecular: 180.160 g/mol
• XLogP3: -2.900
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 5
• Exact Mass: 180.063 Da
• Monoisotopic Mass: 180.063 Da
• Topological Polar Surface Area: 118.000 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 138.000
• 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