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ScientificNameLabel
Beta-sitosterol-3-O-beta-D-glucoside
PHCD compound ID : 506
Chemical Names :
Beta-sitosterol-3-O-beta-D-glucoside , Beta-sitosterol-3-O-beta-D-glucopyranoside , Beta-Sitosterol beta-D-glucopyranoside
Molecular Formula : C35H60O6
Molecular Weight : 576.43899
More Details :
Names & Synonyms: (2S,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(1R,4R)-4-ethyl-1,5-dimethyl-hexyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol , (2S,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol , (2S,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methyl-heptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol , (2S,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(1R,4R)-4-ethyl-1,5-dimethyl-hexyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-methylol-tetrahydropyran-3,4,5-triol
Smiles: CC[C@@H](C(C)C)CC[C@H]([C@H]1CC[C@@H]2[C@]1(C)CC[C@H]1[C@H]2CC=C2[C@]1(C)CC[C@@H](C2)O[C@H]1O[C@H](CO)[C@H]([C@@H]([C@H]1O)O)O)C
InChi : InChI=1S/C35H60O6/c1-7-22(20(2)3)9-8-21(4)26-12-13-27-25-11-10-23-18-24(14-16-34(23,5)28(25)15-17-35(26,27)6)40-33-32(39)31(38)30(37)29(19-36)41-33/h10,20-22,24-33,36-39H,7-9,11-19H2,1-6H3/t21-,22-,24+,25+,26-,27+,28+,29-,30-,31+,32-,33+,34+,35-/m1/s1
InChi Key : InChIKey=NPJICTMALKLTFW-KUENWNPSSA-N
PubChem ID : 12309073
Rotatable bond count : 9 Rule of five : 1
Hydrogen bond acceptor count : 6 Ionization potential : 9.316037
Hydrogen bond donor count : 4 Electric dipole moment : 3.587
XLogP : 10.487 VDW volume : 602.238529
Molecular weight : 576.43899 HOMO-LUMO gap : 10.479000
Herb list :
Refrences & Litretures:
  
31.      Journal:'Global Journal of Pharmacology'      Year:'2013'      Volume:'7'      Page:'377'      DOI:'10.5829/idosi.gjp.2013.7.4.1114'      Title:'Steryl Glycosides, Lipoidal Matter and Volatile Constituents of Urtica pilulifera'
278.      Journal:'Cancer Chemother Pharmacol'      Year:'2007'      Volume:'59'      Page:'589'      DOI:'10.1007/s00280-006-0300-z'      Title:'In vitro anti-cancer activity and structure–activity relationships of natural products isolated from fruits of Panax ginseng'
295.      Journal:'Chemistry of Natural Compounds'      Year:'2011'      Volume:'47'      Page:'140'      DOI:''      Title:'CHEMICAL CONSTITUENTS OF Alhagi pseudalhagi'
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