L-2-Phosphoglyceric acid disodium salt hydrate - Moligand™, ≥80% , CAS No.23295-92-3

CAS: 23295-92-3 Cat. No.: S1223229 Molecular Weight: 230.02 (anhydrous basis)

GRADE & PURITY Moligand™, ≥80%

Synonyms

L-Glycerate 2-phosphate disodium salt | Disodium L-2-phosphoglycerate

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Overview

L-2-Phosphoglyceric acid disodium salt hydrate is a glyceric acid which serves as the substrate in the ninth step of glycolysis. It is catalyzed by enolase into phosphoenolpyruvate (PEP), the penultimate step in the conversion of glucose to pyruvate.

Specifications

Synonyms

L-Glycerate 2-phosphate disodium salt | Disodium L-2-phosphoglycerate

Specifications & Purity

Moligand™, ≥80%

Biochemical and Physiological Mechanisms

Opposite enantiomer to the standard configuration found in glycolysis/gluconeogenesis.

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

This product requires cold chain shipping. Ground and other economy services are not available.

Grade

Moligand™

Purity

≥80%

Names and Identifiers

• Canonical Smiles: C([C@@H](C(=O)O)OP(=O)(O)O)O
• IUPAC Name: (2S)-3-hydroxy-2-phosphonooxypropanoic acid
• InChIKey: GXIURPTVHJPJLF-REOHCLBHSA-N
• INCHI: 1S/C3H7O7P/c4-1-2(3(5)6)10-11(7,8)9/h2,4H,1H2,(H,5,6)(H2,7,8,9)/t2-/m0/s1
• Molecular Weight: 230.02 (anhydrous basis)

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Class Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Class: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Not available
• Direct Parent: Sugar acids and derivatives
• Alternative Parents: Monoalkyl phosphates Beta hydroxy acids and derivatives Monosaccharides Monocarboxylic acids and derivatives Carboxylic acids Primary alcohols Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Beta-hydroxy acid - Glyceric_acid - Monoalkyl phosphate - Hydroxy acid - Monosaccharide - Organic phosphoric acid derivative - Phosphoric acid ester - Alkyl phosphate - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Alcohol - Organic oxide - Carbonyl group - Primary alcohol - Hydrocarbon derivative - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as sugar acids and derivatives. These are compounds containing a saccharide unit which bears a carboxylic acid group.
• External Descriptors: Not available

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

Chemical and Physical Properties

• Molecular Weight: 186.060 g/mol
• XLogP3: -2.600
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 4
• Exact Mass: 185.993 Da
• Monoisotopic Mass: 185.993 Da
• Topological Polar Surface Area: 124.000 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 182.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• 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