2,4-Dihidroksibenzojeva kiselina

2,4-Dihidroksibenzojeva kiselina
Nazivi
	IUPAC naziv 2,4-dihydroxybenzoic acid
	Drugi nazivi beta-Rezorcilna kiselina; beta-Rezorcinolinska kiselina; p-Hidroksisalicilna kiselina; 2,4-DHBA
Identifikacija
CAS broj	89-86-1 =;
3D model (Jmol)	interaktivna slika;
ChemSpider	1446 ;
DrugBank	DB02839 ;
ECHA InfoCard	100.001.770
PubChem C ID	1491;
	SMILES C1=CC(=C(C=C1O)O)C(=O)O; ; ; ; ; ;
Svojstva
Hemijska formula	C7H6O4
Molarna masa	154,12 g/mol
	Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje materijala (na 25 °C [77 °F], 100 kPa).
	verifikuj (šta je ?)
	Reference infokutije

2,4-Dihidroksibenzoinska kiselina (β-rezorcilna kiselina) je dihidroksibenzojeva kiselina‎.

Rezorcilna kiselina je jedna od tri izomerne kristalne kiseline koje su karboksilni derivati rezorcinola i dihidroksi derivati benzojeve kiseline.^[3]

Ona je degradacioni proizvod cijanidin glikozida iz trešanja.^[4] On je takođe metabolit koji je nađen u ljudskoj plazmi nakon konzumacije soka od brusnica.^[5]

Reference

^ 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.
^ Resorcyclic acid on merriam-webster on-line dictionary
^ Seeram, Navindra P.; Bourquin, Leslie D.; Nair, Muraleedharan G. (2001). „Degradation Products of Cyanidin Glycosides from Tart Cherries and Their Bioactivities”. Journal of Agricultural and Food Chemistry. 49 (10): 4924—4929. PMID 11600045. doi:10.1021/jf0107508.
^ Zhang, Kai; Zuo, Yuegang (2004). „GC-MS Determination of Flavonoids and Phenolic and Benzoic Acids in Human Plasma after Consumption of Cranberry Juice”. Journal of Agricultural and Food Chemistry. 52 (2): 222—227. PMID 14733499. doi:10.1021/jf035073r.

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

[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] Resorcyclic acid on merriam-webster on-line dictionary

[4] Seeram, Navindra P.; Bourquin, Leslie D.; Nair, Muraleedharan G. (2001). „Degradation Products of Cyanidin Glycosides from Tart Cherries and Their Bioactivities”. Journal of Agricultural and Food Chemistry. 49 (10): 4924—4929. PMID 11600045. doi:10.1021/jf0107508.

[5] Zhang, Kai; Zuo, Yuegang (2004). „GC-MS Determination of Flavonoids and Phenolic and Benzoic Acids in Human Plasma after Consumption of Cranberry Juice”. Journal of Agricultural and Food Chemistry. 52 (2): 222—227. PMID 14733499. doi:10.1021/jf035073r.

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