Ribitol

Ribitol
	D-ribitol
Drugi nazivi	Adonit, Adonitol, Adonitrol, Pentitol, 1,2,3,4,5-Pentanepentol, 1,2,3,4,5-Pentanol, (2R,3s,4S)-Pentan-1,2,3,4,5-pentol, Pentan-1,2,3,4,5-pentol
Identifikacija
CAS registarski broj	488-81-3
PubChem	827
ChemSpider	10254628
KEGG	C00474
ChEBI	15963
Jmol-3D slike	Slika 1
SMILES
	O[C@H](CO)[C@@H](O)[C@@H](O)CO
InChI
	InChI=1S/C5H12O5/c6-1-3(8)5(10)4(9)2-7/h3-10H,1-2H2/t3-,4+,5- ; Kod: HEBKCHPVOIAQTA-ZXFHETKHSA-N InChI=1/C5H12O5/c6-1-3(8)5(10)4(9)2-7/h3-10H,1-2H2/t3-,4+,5-
Svojstva
Molekulska formula	C5H12O5
Molarna masa	152.15 g mol−1
Tačka topljenja	102 °C, 375 K, 216 °F
Opasnost
R-oznake	—
S-oznake	S22 S24/25
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

Ribitol (adonitol) je kristalni pentozni alkohol (C₅H₁₂O₅) formiran redukcijom riboze. On se prirodno javlja u biljci Adonis vernalis, kao i u ćelijskim zidovima Gram pozitivne bakterije (posebno kao ribitol fosfat u teihoinskim kiselinama).^[5] On takođe sačinjava deo strukture riboflavina.^[6]

Literatura

↑ 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
↑ 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.
↑ Bracha R, Chang M, Fiedler F, Glaser L (1978). „Biosynthesis of teichoic acids”. Methods Enzymol 50: 387-40. PMID 661594.
↑ David L. Nelson, Michael M. Cox (2005). Principles of Biochemistry (4th izd.). New York: W. H. Freeman. ISBN 0-7167-4339-6.

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