Galanolakton
IUPAC ime
(3E)-3-[2-[(1R,2S)-5,5,8a-trimetilspiro[3,4,4a,6,7,8-heksahidro- 1H-naftalen-2,2'-oksiran]-1-il]etiliden]oksolan-2-on
Identifikacija
CAS registarski broj
115753-79-2 Y =
PubChem [ 1] [ 2] 11141699
ChemSpider [ 3] 9316811 Y
MeSH
galanolactone
Jmol -3D slike
Slika 1
O=C/1OCCC\1=C\C[C@@H]4[C@@]2([C@H](C(CCC2)(C)C)CC[C@]43OC3)C
InChI=1S/C20H30O3/c1-18(2)9-4-10-19(3)15(18)7-11-20(13-23-20)16(19)6-5-14-8-12-22-17(14)21/h5,15-16H,4,6-13H2,1-3H3/b14-5 /t15-,16 ,19-,20 /m0/s1 N N
InChI=1/C20H30O3/c1-18(2)9-4-10-19(3)15(18)7-11-20(13-23-20)16(19)6-5-14-8-12-22-17(14)21/h5,15-16H,4,6-13H2,1-3H3/b14-5 /t15-,16 ,19-,20 /m0/s1
Svojstva
Molekulska formula
C20 H30 O3
Molarna masa
318,45 g/mol
Rastvorljivost u aceton
Rastvoran je
Y (šta je ovo?)
(verifikuj)
Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
Infobox references
Galanolakton je diterpenoidni lakton koji je originalno izolovan iz đumbira . Poznato je da je prisutan u acetonskim ekstraktima đumbira. On je antagonist 5-HT3 receptora .[ 4]
↑ 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 ↑ Huang, Q.; Iwamoto, Y.; Aoki; Tanaka; Tajima; Yamahara; Takaishi; Yoshida i dr.. (1991). „Anti-5-hydroxytryptamine3 effect of galanolactone, diterpenoid isolated from ginger”. Chemical & pharmaceutical bulletin 39 (2): 397–399. DOI :10.1248/cpb.39.397 . PMID 2054863 .
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