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Home > Encyclopedia > Cytidine 5′-(tetrahydrogen triphosphate), sodium salt (1:2)

Cytidine 5′-(tetrahydrogen triphosphate), sodium salt (1:2)

pharmaceutical raw materials
Cytidine 5′-(tetrahydrogen triphosphate), sodium salt (1:2) structure

Cytidine 5′-(tetrahydrogen triphosphate), sodium salt (1:2) 

structure
  • CAS No:

    36051-68-0

  • Formula:

    C9H16N3O14P3.2Na

  • Chemical Name:

    Cytidine 5′-(tetrahydrogen triphosphate), sodium salt (1:2)

  • Synonyms:

    Cytidine 5′-(tetrahydrogen triphosphate),sodium salt (1:2);Cytidine 5′-(tetrahydrogen triphosphate),disodium salt;Cytidine-5′-triphosphate disodium salt;NSC 20261;Cytidine triphosphate disodium salt;Disodium cytidine triphosphate

  • Categories:

    Biochemical Engineering  >  Nucleoside Drugs

Description

White powder

Cytidine 5′-(tetrahydrogen triphosphate), sodium salt (1:2) Basic Attributes

527.12

526.948425

252-849-3

20261

29349990

Characteristics

305.51000

-0.75440

White Powder

2.5g/cm3

849.2°C at 760 mmHg

113 °C

soluble in water. Insoluble in ethanol, chloroform and ether.H2O: 50 mg/mL, clear, colorless

−20°C

Safety Information

NONH for all modes of transport

3

24/25

Cytidine 5′-(tetrahydrogen triphosphate), sodium salt (1:2) Use and Manufacturing

Cytidine 5'-triphosphate (CTP) is a pyrimidine nucleoside triphosphate that is involved in a variety of biochemical reactions. It is used in the synthesis of RNA by RNA polymerases. In the formation of phosphatidylcholine (PC), CTP reacts with phosphocholine, via CTP:phosphocholine cytidylyltransferases, to produce CDP-choline and diphosphate. This is the rate-limiting step in PC synthesis and, as a pivotal step in cell proliferation, can be important in cancer. CTP also interacts with N-acylneuraminate, in a reaction mediated by N-acylneuraminate cytidylyltransferase, to generate an intermediate that is required for sialylation, namely CMP-N-acylneuraminic acid.[Cayman Chemical]

Computed Properties

Molecular Weight:483.16
XLogP3:-5.6
Hydrogen Bond Donor Count:7
Hydrogen Bond Acceptor Count:14
Rotatable Bond Count:8
Exact Mass:482.98451319
Monoisotopic Mass:482.98451319
Topological Polar Surface Area:268
Heavy Atom Count:29
Complexity:855
Undefined Atom Stereocenter Count:4
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Drug Function and Efficacy

Coenzyme drugs are nucleotide derivatives that participate in the synthesis and metabolism of phospholipids and nucleic acids in the body. They are intermediate products and energy sources for brain phospholipid synthesis and nucleic acid metabolism.

This ingredient has been used in drugs with the following functions (note: it does not mean that the ingredient itself has the following health functions)

Related Drugs

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