2-Deoxy-L-ribose - ≥98% , CAS No.18546-37-7

CAS: 18546-37-7 Cat. No.: D118253 Formula: C₅H₁₀O₄ Peso molecolare: 134.13 Numero EC: 606-054-7

GRADE & PURITY ≥98%

Synonyms

GS-3353 | AKOS006282569 | DTXSID50939972 | SCHEMBL574324 | (3R,4S)-3,4,5-tris(oxidanyl)pentanal | L-erythro-Pentose, 2-deoxy- | (3R,4S)-3,4,5-trihydroxypentanal | L-erythro-Pentose,2-deoxy- | Q6456094 | A812964 | 2-Deoxy-L-ribose, >=97.0% (TLC) | MFCD0988

Storage

Store at 2-8°C

Shipped In

Wet ice

Panoramica

2-Deoxy-L-ribose is a stereoisomer of 2-Deoxy-d-ribose that inhibits 2-Deoxy-d-ribose anti-apoptotic effects. 2-Deoxy-L-ribose suppresses metastasis of tumor cells overexpressing thymidine phosphorylase.

Specifications

Sinonimi

GS-3353 | AKOS006282569 | DTXSID50939972 | SCHEMBL574324 | (3R,4S)-3,4,5-tris(oxidanyl)pentanal | L-erythro-Pentose, 2-deoxy- | (3R,4S)-3,4,5-trihydroxypentanal | L-erythro-Pentose,2-deoxy- | Q6456094 | A812964 | 2-Deoxy-L-ribose, >=97.0% (TLC) | MFCD0988

Specifiche e purezza

≥98%

Meccanismi biochimici e fisiologici

Inhibitor of enzymes and valuable building block for synthesis

Condizioni di conservazione di stoccaggio

Store at 2-8°C

Spedito in

Wet ice

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

Purezza

≥98%

Nomi e identificatori

• Pubchem Sid: 504764458
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504764458
• Sorrisi canonici: C(C=O)C(C(CO)O)O
• IUPAC Name: (3R,4S)-3,4,5-trihydroxypentanal
• InChIKey: ASJSAQIRZKANQN-UHNVWZDZSA-N
• INCHI: 1S/C5H10O4/c6-2-1-4(8)5(9)3-7/h2,4-5,7-9H,1,3H2/t4-,5+/m1/s1
• Isomeri SMILES: C(C=O)[C@H]([C@H](CO)O)O
• Peso molecolare: 134.13
• 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
    • Classe Organooxygen compounds
      • Subclass Carbonyl compounds
        • Level5 Aldehydes
          • Level6 Beta-hydroxy aldehydes

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: 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
• Descrizione: 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

Proprietà chimiche e fisiche

• Peso molecolare: 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