Cytidine-5'-triphosphate disodium salt dihydrate - Moligand™,≥95% , CAS No.81012-87-5

CAS: 81012-87-5 Cat. No.: C137697 Molecular Weight: 563.15 EC Number: 815-308-8 PubChem CID: 51051624

GRADE & PURITY Moligand™, ≥95%

Synonyms

C76590 | CTP Disodium Dihydrate | CTP disodium salt dihydrate | Cytidine-5'-triphosphate disodium salt dihydrate | Cytidine 5'-triphosphate disodium salt

Storage

Protected from light,Store at -20°C

Shipped In

Ice chest + Ice pads

Overview

Cytidine 5′-triphosphate disodium salt is used as a nucleoside triphosphate for RNA synthesis reactions.

Specifications

Synonyms

C76590 | CTP Disodium Dihydrate | CTP disodium salt dihydrate | Cytidine-5'-triphosphate disodium salt dihydrate | Cytidine 5'-triphosphate disodium salt

Specifications & Purity

Moligand™, ≥95%

Biochemical and Physiological Mechanisms

CTP is incorporated into RNA via phosphodiester bond formation catalyzed by various RNA polymerases.

Storage

Protected from light, 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

≥95%

Names and Identifiers

• Pubchem Sid: 488201480
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488201480
• Canonical Smiles: C1=CN(C(=O)N=C1N)C2C(C(C(O2)COP(=O)(O)OP(=O)([O-])OP(=O)(O)[O-])O)O.O.O.[Na+].[Na+]
• IUPAC Name: disodium;[[[(2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-oxidophosphoryl] hydrogen phosphate;dihydrate
• InChIKey: KNSYTSUGTLJHPS-ODQFIEKDSA-L
• INCHI: 1S/C9H16N3O14P3.2Na.2H2O/c10-5-1-2-12(9(15)11-5)8-7(14)6(13)4(24-8)3-23-28(19,20)26-29(21,22)25-27(16,17)18;;;;/h1-2,4,6-8,13-14H,3H2,(H,19,20)(H,21,22)(H2,10,11,15)(H2,16,17,18);;;2*1H2/q;2*+1;;/p-2/t4-,6-,7-,8-;;;;/m1..../s1
• Isomeric SMILES: C1=CN(C(=O)N=C1N)[C@H]2[C@@H]([C@@H]([C@H](O2)COP(=O)(O)OP(=O)([O-])OP(=O)(O)[O-])O)O.O.O.[Na+].[Na+]
• PubChem CID: 51051624
• Molecular Weight: 563.15

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Nucleosides, nucleotides, and analogues
    • Class Pyrimidine nucleotides
      • Subclass Pyrimidine ribonucleotides

• Kingdom: Organic compounds
• Superclass: Nucleosides, nucleotides, and analogues
• Class: Pyrimidine nucleotides
• Subclass: Pyrimidine ribonucleotides
• Intermediate Tree Nodes: Not available
• Direct Parent: Pyrimidine ribonucleoside triphosphates
• Alternative Parents: Pentose phosphates Glycosylamines Monosaccharide phosphates Aminopyrimidines and derivatives Pyrimidones Alkyl phosphates Hydropyrimidines Imidolactams Tetrahydrofurans Heteroaromatic compounds 1,2-diols Secondary alcohols Oxacyclic compounds Azacyclic compounds Organic zwitterions Organopnictogen compounds Hydrocarbon derivatives Primary amines Organic oxides Organic sodium salts
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Pyrimidine ribonucleoside triphosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - Monosaccharide phosphate - Pentose monosaccharide - Aminopyrimidine - Pyrimidone - Hydropyrimidine - Monosaccharide - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Imidolactam - Tetrahydrofuran - Heteroaromatic compound - Secondary alcohol - 1,2-diol - Organic alkali metal salt - Organoheterocyclic compound - Azacycle - Oxacycle - Organic sodium salt - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Amine - Alcohol - Organic oxide - Organic nitrogen compound - Primary amine - Organic oxygen compound - Organic zwitterion - Organic salt - Organopnictogen compound - Aromatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as pyrimidine ribonucleoside triphosphates. These are pyrimidine ribobucleotides with triphosphate group linked to the ribose moiety.
• 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

• Sensitivity: Light sensitive
• Molecular Weight: 563.150 g/mol
• Hydrogen Bond Donor Count: 7
• Hydrogen Bond Acceptor Count: 16
• Rotatable Bond Count: 8
• Exact Mass: 562.97 Da
• Monoisotopic Mass: 562.97 Da
• Topological Polar Surface Area: 276.000 Ų
• Heavy Atom Count: 33
• Formal Charge: 0
• Complexity: 844.000
• 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: 5

XLogP3