Pantetein

Pantetein
Nazivi
	IUPAC naziv 2,4-Dihidroksi-3,3-dimetil-N-[2-(2-sulfaniletilkarbamoil)etil]butanamid
Identifikacija
CAS broj	496-65-1 R;
3D model (Jmol)	interaktivna slika; interaktivna slika;
3DMet	B00185
Bajlštajn	1714196 R
ChEBI	CHEBI:16753 ;
ChemSpider	466 ; 388453 R ;
ECHA InfoCard	100.007.114
EC broj	207-824-1
KEGG	C00831 ;
MeSH	Pantetheine
PubChem C ID	479; 439322 R;
	SMILES CC(C)(CO)C(O)c(:[o]):[nH]CCc(:[o]):[nH]CCS; CC(C)(CO)C(O)C(=O)NCCC(=O)NCCS; ; ; ; ;
Svojstva
Hemijska formula	C11H22N2O4S
Molarna masa	278,37 g·mol−1
Srodna jedinjenja
Srodna jedinjenja	Bis-tris propan; Oktopin; Nopalin; Spermin;
	Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje materijala (na 25 °C [77 °F], 100 kPa).
	verifikuj (šta je ?)
	Reference infokutije

Pantetein je cisteaminski amidni analog pantoteinske kiseline (vitamina B₅). Dimer ovog jedinjenja, pantetin je široko poznat, i smatra se potentnijim oblikom vitamina B₅ od pantotenske kiseline. Pantetein je intermedijar u produkciji koenzima A u telu.^[4]

Reference

^ Joanne Wixon; Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast. 17 (1): 48—55. doi:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.
^ 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. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди
^ 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.
^ Suriender Kumar; G.T. Phillips; John W. Porter (februar 1972). „Comparative biochemistry of fatty acid synthesizing enzyme systems: A review”. International Journal of Biochemistry. 3: 15—32.

Spoljašnje veze

[1] Joanne Wixon; Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast. 17 (1): 48—55. doi:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.

[2] 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. PMID 20970519. doi:10.1016/j.drudis.2010.10.003. уреди

[3] 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.

[4] Suriender Kumar; G.T. Phillips; John W. Porter (februar 1972). „Comparative biochemistry of fatty acid synthesizing enzyme systems: A review”. International Journal of Biochemistry. 3: 15—32.

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