Citidin-trifosfat

Citidin-trifosfat
	[(2R,3S,4R,5R)-5-(4-amino-2-oxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl(hydroxy-phosphonooxyphosphoryl)hydrogen phosphate
Drugi nazivi	CTP; Cytidine-5'-triphosphate; Cytidine 5'-(tetrahydrogen triphosphate)
Identifikacija
CAS registarski broj	65-47-4
PubChem	6176
ChemSpider	5941
MeSH	Cytidine+triphosphate
IUPHAR ligand	1741
Jmol-3D slike	Slika 1
SMILES
	O=P(O)(O)OP(=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
InChI
	InChI=1S/C9H13N3O5.3H3O4P/c10-5-1-2-12(9(16)11-5)8-7(15)6(14)4(3-13)17-8;31-5(2,3)4/h1-2,4,6-8,13-15H,3H2,(H2,10,11,16);3(H3,1,2,3,4)/t4-,6-,7-,8-;;;/m1.../s1 ; Kod: PCDQPRRSZKQHHS-XVFCMESISA-N InChI=1/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; Kod: PCDQPRRSZKQHHS-XVFCMESIBL
Svojstva
Molekulska formula	C9H16N3O14P3
Molarna masa	483.156
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

Citidin trifosfat je pirimidinski nukleotid.^[4] CTP je supstrat u RNK sintezi.

CTP je visokoenergijski molekul poput ATP, međutim njegova uloga u organizmu je specifičnija od ATP. CTP se koristi kao izvor energije, i kao koenzim u metaboličkim reakcijama, kao što je sinteza glicerofosfolipida^[5]^[6] i glikozilacija proteina.

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Literatura[uredi | uredi kod]

↑ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit
↑ Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.
↑ Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit
↑ Donald Voet, Judith G. Voet (2005). Biochemistry (3 izd.). Wiley. str. 93-95,1221. ISBN 978-0-471-19350-0.
↑ Horrocks, Lloyd A.; Farooqui, Akhlaq A. (2007). Glycerophospholipids in the brain phospholipases A2 in neurological disorders. Berlin: Springer. ISBN 0-387-36602-4.
↑ „Wiley Online Library: Book Article”.

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Portal Hemija

MeSH Citidine+triphosphate

[1] Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit

[2] Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.

[3] Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit

[4] Donald Voet, Judith G. Voet (2005). Biochemistry (3 izd.). Wiley. str. 93-95,1221. ISBN 978-0-471-19350-0.

[isbn0-387-36602-4-5] Horrocks, Lloyd A.; Farooqui, Akhlaq A. (2007). Glycerophospholipids in the brain phospholipases A2 in neurological disorders. Berlin: Springer. ISBN 0-387-36602-4.

[urlWiley_Online_Library:_Book_Article-6] „Wiley Online Library: Book Article”.

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Citidin-trifosfat

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