Bolinakvinon

Bolinakvinon
	3[(1R,2R,4aS,8aS)-1,2,4a,5-Tetramethyl-1,2,3,4,4a,7,8,8a-oktahidronaftalen-2-il]metil2-hidroksi-5-metoksicikloheksa-2,5-dien-1,4-dion
Drugi nazivi	Bolinakvinon
Identifikacija
PubChem	10066979
ChemSpider	8242519
ChEMBL	CHEMBL477692
Jmol-3D slike	Slika 1
SMILES
	COC1=CC(=O)C(=C(C[C@@]2(C)CC[C@@]3(C)[C@@H](CCC=C3C)[C@H]2C)C1=O)O
InChI
	InChI=1S/C22H30O4/c1-13-7-6-8-16-14(2)21(3,9-10-22(13,16)4)12-15-19(24)17(23)11-18(26-5)20(15)25/h7,11,14,16,24H,6,8-10,12H2,1-5H3/t14-,16+,21-,22-/m1/s1 ; Kod: PYUXUMSQSVWNDS-NSAJDELNSA-N InChI=1/C22H30O4/c1-13-7-6-8-16-14(2)21(3,9-10-22(13,16)4)12-15-19(24)17(23)11-18(26-5)20(15)25/h7,11,14,16,24H,6,8-10,12H2,1-5H3/t14-,16+,21-,22-/m1/s1; Kod: PYUXUMSQSVWNDS-NSAJDELNBY
Svojstva
Molekulska formula	C22H30O4
Molarna masa	358.47 g mol−1
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

Bolinakvinon je hidroksihinonski morski metabolit. On je poznat po tome što je potentan antiinflamatorni agens.^[5]

Reference[uredi | uredi kod]

↑ 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
↑ Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594. edit
↑ Petronzi, C; et al (2010). „Structure-based design, synthesis and preliminary anti-inflammatory activity of bolinaquinone analogues”. European Journal of Medicinal Chemistry 46 (2): 488–96. PMID 21163556.

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