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Cytidine-5'-triphosphate

CAT: 0804-HY-125818-01Size: 100 mgDry Ice: NoHazardous: No
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CAT#:0804-HY-125818-01Size:100 mg
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Description
Cytidine 5′-triphosphate (Cytidine triphosphate; 5'-CTP) is a nucleoside triphosphate and serves as a building block for nucleotides and nucleic acids, lipid biosynthesis. Cytidine triphosphate synthase can catalyze the formation of cytidine 5′-triphosphate from uridine 5′-triphosphate (UTP) . Cytidine 5′-triphosphate is an essential biomolecule in the de novo pyrimidine biosynthetic pathway in T. gondii[1].
CAS Number
65-47-4
Product Name Alternative
Cytidine triphosphate; 5'-CTP
UNSPSC
12352005
Hazard Statement
H315, H319
Target
DNA/RNA Synthesis; Endogenous Metabolite; Nucleoside Antimetabolite/Analog
Type
Oligonucleotides
Related Pathways
Cell Cycle/DNA Damage; Metabolic Enzyme/Protease
Applications
COVID-19-anti-virus
Field of Research
Metabolic Disease
Assay Protocol
https://www.medchemexpress.com/cytidine-5-triphosphate.html
Purity
98.0
Solubility
H2O : ≥ 200 mg/mL
Smiles
O[C@H]1[C@@H](O)[C@H](N2C(N=C(N)C=C2)=O)O[C@@H]1COP(OP(OP(O)(O)=O)(O)=O)(O)=O
Molecular Formula
C9H16N3O14P3
Molecular Weight
483.16
Precautions
H315, H319
References & Citations
[1]Heidy Y Narvaez-Ortiz, et al. A CTP Synthase Undergoing Stage-Specific Spatial Expression Is Essential for the Survival of the Intracellular Parasite Toxoplasma gondii. Front Cell Infect Microbiol. 2018 Mar 22;8:83.|[2]Hatch GM, et al., Regulation of cardiolipin biosynthesis in H9c2 cardiac myoblasts by cytidine 5'-triphosphate. J Biol Chem. 1996 Oct 18;271 (42) :25810-6.|[3]Matsumoto S, et al., An equilibrium binding study of the interaction of aspartate transcarbamylase with cytidine 5'-triphosphate and adenosine 5'-triphosphate. Biochemistry. 1973 Mar 27;12 (7) :1388-94.
Shipping Conditions
Blue Ice
Storage Conditions
-20°C (Powder, sealed storage, away from moisture)
Scientific Category
Oligonucleotides
Clinical Information
No Development Reported
Isoform
Human Endogenous Metabolite

Chemical Information

5'-Ctp

CTP is a cytidine 5'-phosphate and a pyrimidine ribonucleoside 5'-triphosphate. It has a role as a mouse metabolite and an Escherichia coli metabolite. It is a conjugate acid of a CTP(4-) and a CTP(3-).

CAS Number65-47-4
PubChem CID6176
IUPAC Name[[(2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate
Molecular FormulaC9H16N3O14P3
Molecular Weight483.16
XLogP-5.6
Topological Polar Surface Area268
Hydrogen Bond Donor Count7
Hydrogen Bond Acceptor Count14
Rotatable Bond Count8
Heavy Atom Count29
Formal Charge0
Complexity855
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
InChI
InChI=1S/C9H16N3O14P3/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)/t4-,6-,7-,8-/m1/s1
InChIKey
PCDQPRRSZKQHHS-XVFCMESISA-N
Chemical Structure
2D Structure
2D structure of 5'-Ctp
CAS: 65-47-4
CID: 6176
Formula: C9H16N3O14P3
MW: 483.16
Interactive 3D Structure
Loading 3D structure...
View on PubChemRaw 3D data
Computed Properties
PropertyValue
Molecular Weight483.16
XLogP3-5.6
Hydrogen Bond Donor Count7
Hydrogen Bond Acceptor Count14
Rotatable Bond Count8
Exact Mass482.98451319
Monoisotopic Mass482.98451319
Topological Polar Surface Area268 Ų
Heavy Atom Count29
Formal Charge0
Complexity855
Isotope Atom Count0
Defined Atom Stereocenter Count4
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count1
Compound Is CanonicalizedYes

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