Salicin

Salicin^[1]
Nazivi
	IUPAC naziv (2R,3S,4S,5R,6S)-2-(Hidroksimetil)-6-[2-(hidroksimetil)fenoksi]oksan-3, 4,5-triol
	Drugi nazivi D-(−)-Salicin; Salikozid; 2-(Hidroksimetil)fenil; -β-D-glukopiranozid
Identifikacija
CAS broj	138-52-3 ;
ECHA InfoCard	100.004.847
KEGG	C01451 ;
PubChem C ID	439503;
RTECS	LZ5901700
UNII	4649620TBZ ;
Svojstva
Hemijska formula	C13H18O7
Molarna masa	286,28 g·mol−1
Tačka topljenja	197-200 °C
	Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje materijala (na 25 °C [77 °F], 100 kPa).
	verifikuj (šta je ?)
	Reference infokutije

Salicin je alkoholni β-glukozid. On je antiinflamatorni agens koji se može izdvojiti iz kore vrbe.^[5]

Salicin ima blisko srodnu hemijsku strukturu sa aspirinom. Kad se konzumira, acetalni etarski most se razlaže. Dva dela molekula, glukoza i benzoil alkohol, zatim podležu zasebnom metabolizmu. Oksidacijom alkohola od aromatičnog dela se formira salicilna kiselina.

Salicin ima gorak ukus poput hinina.^{[тражи се извор]}

Reference

^ Susan Budavari, ур. (2001). The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals (13th изд.). Merck Publishing. ISBN 0911910131.
^ 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.
^ Uchytil RJ (1991). „Salix drummondiana”. Fire Effects Information System,. Online. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Приступљено 19. 7. 2006.

Literatura

Spoljašnje veze

[Merck13th-1] Susan Budavari, ур. (2001). The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals (13th изд.). Merck Publishing. ISBN 0911910131.

[2] 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.

[3] 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

[4] 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.

[5] Uchytil RJ (1991). „Salix drummondiana”. Fire Effects Information System,. Online. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory (Producer). Приступљено 19. 7. 2006.

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