2-Deoxy-D-Ribose - Moligand™, 10mM in DMSO , CAS No.533-67-5

CAS: 533-67-5 Cat. No.: D424566 分子式: C₅H₁₀O₄ 分子量: 134.13 Beilstein Registry Number: 1721978 EC番号: 208-573-0

GRADE & PURITY Moligand™, 10mM in DMSO

Synonyms

2-Deoxy-D-ribose, 97% | CHEBI:28816 | NSC-772796 | ASJSAQIRZKANQN-CRCLSJGQSA-N | BBL012499 | 2-Deoxy-D-ribose | 2-Deoxy-D-ribose, >=99.0% (TLC) | AM20100306 | 4-01-00-04181 (Beilstein Handbook Reference) | aldehydo-2-deoxy-D-ribose | D-erythro-Pentose, 2-

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Specifications

同義語

2-Deoxy-D-ribose, 97% | CHEBI:28816 | NSC-772796 | ASJSAQIRZKANQN-CRCLSJGQSA-N | BBL012499 | 2-Deoxy-D-ribose | 2-Deoxy-D-ribose, >=99.0% (TLC) | AM20100306 | 4-01-00-04181 (Beilstein Handbook Reference) | aldehydo-2-deoxy-D-ribose | D-erythro-Pentose, 2-

仕様と純度

Moligand™, 10mM in DMSO

生化学的・生理学的メカニズム

Reducing sugar used to study processes of oxidative stress and glycation in vivo and in vitro . Induces apoptosis by inhibiting the synthesis and increasing the efflux of glutathione. Endothelial-cell chemoattractant and angiogenesis-inducing factor

保管条件

Store at -80°C

入荷

Dry ice packs + Cold packs

この製品は冷冷この冷このこの製品の運送が必要です。地上およびその他の経済サービスは利用できません。

等級

Moligand™

名前と識別子

• パブケム・シド: 508808533
• カノニカル・スマイル: C(C=O)C(C(CO)O)O
• IUPAC Name: (3S,4R)-3,4,5-trihydroxypentanal
• InChIKey: ASJSAQIRZKANQN-CRCLSJGQSA-N
• INCHI: 1S/C5H10O4/c6-2-1-4(8)5(9)3-7/h2,4-5,7-9H,1,3H2/t4-,5+/m0/s1
• 異性体SMILES: C(C=O)[C@@H]([C@@H](CO)O)O
• WGKドイツ: 3
• RTECS: SB7230000
• 分子量: 134.13
• Beilstein: 1721978
• Reaxy-Rn: 1904591
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1904591&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • 分類 Organooxygen compounds
      • Subclass Carbonyl compounds
        • Level5 Aldehydes
          • Level6 Beta-hydroxy aldehydes

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• 分類: Organooxygen compounds
• Subclass: Carbonyl compounds
• Intermediate Tree Nodes: Aldehydes
• Direct Parent: Beta-hydroxy aldehydes
• Alternative Parents: Alpha-hydrogen aldehydes Secondary alcohols Polyols Short-chain aldehydes Primary alcohols Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Beta-hydroxy aldehyde - Alpha-hydrogen aldehyde - Secondary alcohol - Polyol - Organic oxide - Hydrocarbon derivative - Short-chain aldehyde - Primary alcohol - Alcohol - Aliphatic acyclic compound
• 説明: This compound belongs to the class of organic compounds known as beta-hydroxy aldehydes. These are organic compounds containing an aldehyde substituted with a hydroxy group on the second carbon atom.
• External Descriptors: deoxypentose

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

化学的性質と物理的性質

• 感度: Hygroscopic
• 比旋光度［α］: -56 ° (C=1, H2O)
• 融点（°C）: 91°C
• 分子量: 134.130 g/mol
• XLogP3: -2.300
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 134.058 Da
• Monoisotopic Mass: 134.058 Da
• Topological Polar Surface Area: 77.800 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 83.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 2
• 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

参考文献

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