D-(+)-Glucose - Moligand™, ≥99.5% , CAS No.50-99-7

CAS: 50-99-7 Cat. No.: G116302 Formula: C₆H₁₂O₆ Molecular Weight: 180.16 Beilstein Registry Number: 1724615 EC Number: 200-075-1

GRADE & PURITY Moligand™, ≥99.5%

Synonyms

ANHYDROUS DEXTROSE [II] | GLUCOSE [MI] | D-Glucose;Grape sugar;Glucopyranose | DTXCID701436386 | GLUCOSE [WHO-DD] | NSC-406891 | (C13)D-Glucose | CAS-50-99-7 | DTXSID4048729 | Glucose (C-14) | SW220288-1 | (2R,3S,4R,5R)-2,3,4,5,6-pentakis(oxidanyl)hexanal

Storage

Room temperature,Argon charged

Shipped In

Normal

Overview

D(+)Glucose, Anhydrous is a granular monosaccharide.
A primary source of energy for living organisms

Specifications

Synonyms

ANHYDROUS DEXTROSE [II] | GLUCOSE [MI] | D-Glucose;Grape sugar;Glucopyranose | DTXCID701436386 | GLUCOSE [WHO-DD] | NSC-406891 | (C13)D-Glucose | CAS-50-99-7 | DTXSID4048729 | Glucose (C-14) | SW220288-1 | (2R,3S,4R,5R)-2,3,4,5,6-pentakis(oxidanyl)hexanal

Specifications & Purity

Moligand™, ≥99.5%

Biochemical and Physiological Mechanisms

Energy source for aerobic respiration or anaerobic respiration. Glycolysis metabolic pathway substrate. Product of gluconeogenesis. Orally active.

Storage

Room temperature,Argon charged

Shipped In

Normal

Grade

Moligand™

Note

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Purity

≥99.5%

Names and Identifiers

Pubchem Sid

488187412

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488187412

Canonical Smiles

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

Isomeric SMILES

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

WGK Germany

1

RTECS

LZ6600000

Molecular Weight

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
    • Class Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates
        • Level5 Monosaccharides
          • Level6 Hexoses

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Class: 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
• Description: 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

Associated Targets(non-human)

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

Mechanisms of Action

Chemical and Physical Properties

• Solubility: Soluble in water (0.9 g/ml at 25 °C), alcohol (slightly), methanol ( at 20 °C), absolute alcohol (very sparingly), ether (very sparingly), acetone (very sparingly), hot glacial acetic acid, pyridine, aniline, ethanol (<1 mg/mL at 25 °C), and DMSO (36 m
• Sensitivity: Moisture sensitive.
• Specific Rotation[α]: 53 ° (C=10, H2O)
• Melt Point(°C): 146°C
• Molecular Weight: 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