Cytidine diphosphate

Names
IUPAC name Cytidine 5′-(trihydrogen diphosphate)
Systematic IUPAC name [(2R,3S,4R,5R)-5-(4-Amino-2-oxopyrimidin-1(2H)-yl)-3,4-dihydroxyoxolan-2-yl]methyl trihydrogen diphosphate
Identifiers
CAS Number	63-38-7 Y 54394-9-0 (disodium salt) Y 34393-59-4 (trisodium salt) Y
3D model (JSmol)	Interactive image
ChEBI	CHEBI:17239 Y
ChEMBL	ChEMBL425252 Y
ChemSpider	5902 Y
DrugBank	DB04555
ECHA InfoCard	100.000.507
EC Number	200-557-1
KEGG	C00112
PubChemCID	290
UNII	1ZH821MXU5 Y F8B9F7OXES (disodium salt) Y 0TZ883O8PW (trisodium salt) Y
CompTox Dashboard(EPA)	DTXSID501014481
InChI InChI=1S/C9H15N3O11P2/c10-5-1-2-12(9(15)11-5)8-7(14)6(13)4(22-8)3-21-25(19,20)23-24(16,17)18/h1-2,4,6-8,13-14H,3H2,(H,19,20)(H2,10,11,15)(H2,16,17,18)/t4-,6-,7-,8-/m1/s1 Y Key: ZWIADYZPOWUWEW-XVFCMESISA-N Y InChI=1/C9H15N3O11P2/c10-5-1-2-12(9(15)11-5)8-7(14)6(13)4(22-8)3-21-25(19,20)23-24(16,17)18/h1-2,4,6-8,13-14H,3H2,(H,19,20)(H2,10,11,15)(H2,16,17,18)/t4-,6-,7-,8-/m1/s1 Key: ZWIADYZPOWUWEW-XVFCMESIBF
SMILES O=P(O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N/1C(=O)/N=C(/N)\C=C\1)[C@H](O)[C@@H]2O
Properties
Chemical formula	C9H15N3O11P2
Molar mass	403.176422
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references

Cytidine diphosphate, abbreviatedCDP, is anucleoside diphosphate. It is anester ofpyrophosphoric acid with thenucleosidecytidine. CDP consists of thepyrophosphategroup, thepentosesugarribose, and thenucleobasecytosine.

InBacillus subtilis andStaphylococcus aureus, CDP-activatedglycerol andribitol are necessary to build wallteichoic acid.^[1]

InRhodothermus marinus, CDP-activatedinositol is necessary to form thephospholipid dialkylether glycerophosphoinositide, which contains inositolphosphate andether-linkedalkyl chains.^[2]

CDP is commonly formed in the reactiondolichol +cytidine triphosphate (CTP) ⟶dolichol-phosphate + CDP, which is prevalent in manybiochemical pathways.^[3]

• Nucleoside
• Nucleotide
• DNA
• RNA
• Oligonucleotide

• Nucleotides
• Pyrimidones
• Pyrophosphate esters

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