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Ramnoza
	(2R,3R,4R,5R,6S)-6-methyloxane-2,3,4,5-tetrol
Drugi nazivi	izodulcit; alfa-L-Ramnoza; L-ramnoza; L-manometiloza; alfa-L-Ra; alfa-L-Ramnosid; alfa-L-Manometiloza; 6-dezoksi-L-manoza
Identifikacija
CAS registarski broj	10485-94-6
PubChem	19233
ChemSpider	18150
UNII	QN34XC755A
DrugBank	DB01869
KEGG	C00507
ChEBI	16055
Jmol-3D slike	Slika 1
SMILES
	O=C[C@H](O)[C@H](O)[C@@H](O)[C@@H](O)C
InChI
	InChI=1S/C6H12O5/c1-3(8)5(10)6(11)4(9)2-7/h2-6,8-11H,1H3/t3-,4-,5-,6-/m0/s1 ; Kod: PNNNRSAQSRJVSB-BXKVDMCESA-N InChI=1/C6H12O5/c1-3(8)5(10)6(11)4(9)2-7/h2-6,8-11H,1H3/t3-,4-,5-,6-/m0/s1; Kod: PNNNRSAQSRJVSB-BXKVDMCEBH
Svojstva
Molekulska formula	C6H12O5
Molarna masa	164.16 g/mol
Tačka topljenja	91-93 °C (monohidrat)
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

Ramnoza (Rham) je dezoksi šećer koji se javlja u prirodi. Ona se može klasifikovati kao bilo metil-pentoza ili 6-deoksi-heksoza. Ramnoza se javlja u prirodi u svojoj L-formi kao L-ramnoza (6-dezoksi-L-manoza). To je neuobičajeno, pošto su većina prirodnih šećera u D-formi. Izuzeci su metil pentoze L-fukoza i L-ramnoza i pentoza L-arabinoza.

Ramnoza može biti izolovana iz pasjakovine i biljki iz genusa Uncaria.^[6]

Literatura

↑ The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals (11th izd.). Merck Publishing. 1989. str. 8171. ISBN 0-911910-28-X.
↑ 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.
↑ „Chemical from tropical flower latest weapon against wrinkles”. The Daily Telegraph. 6. 02. 2011.. Arhivirano iz originala na datum 2011-02-08. Pristupljeno 7. 01. 2011.

Vanjske veze

Upotreba L-ramnoze u studijama ireverziblne apsorpcije bakteriofaga PL-1

[1] The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals (11th izd.). Merck Publishing. 1989. str. 8171. ISBN 0-911910-28-X.

[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. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit

[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] 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

[5] 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.

[6] „Chemical from tropical flower latest weapon against wrinkles”. The Daily Telegraph. 6. 02. 2011.. Arhivirano iz originala na datum 2011-02-08. Pristupljeno 7. 01. 2011.

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