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Elaeodendroside V

PubChem CID: 42636949

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Compound Synonyms ELAEODENDROSIDE V, CHEBI:65830, sarmentologenin-3beta-O-[beta-allosyl-(1->4)-beta-6-deoxyalloside], (3beta,5beta,11alpha)-3-{[4-O-(beta-D-allopyranosyl)-6-deoxy-beta-D-allopyranosyl]oxy}-5,11,14,19-tetrahydroxycard-20(22)-enolide, Sarmentologenin-3b-O-(b-allosyl-(1->4)-b-6-deoxyalloside), Sarmentologenin-3b-O-[b-allosyl-(1->4)-b-6-deoxyalloside], Sarmentologenin-3beta-O-(beta-allosyl-(1->4)-beta-6-deoxyalloside), Sarmentologenin-3I2-O-(I2-allosyl-(1->4)-I2-6-deoxyalloside), Sarmentologenin-3I2-O-[I2-allosyl-(1->4)-I2-6-deoxyalloside], (3beta,5beta,11alpha)-3-((4-O-(beta-D-allopyranosyl)-6-deoxy-beta-D-allopyranosyl)oxy)-5,11,14,19-tetrahydroxycard-20(22)-enolide, 3-((3S,5S,8R,9S,10R,11R,13R,14S,17R)-3-((2R,3R,4S,5S,6R)-3,4-dihydroxy-6-methyl-5-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxyoxan-2-yl)oxy-5,11,14-trihydroxy-10-(hydroxymethyl)-13-methyl-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta(a)phenanthren-17-yl)-2H-furan-5-one, 3-[(3S,5S,8R,9S,10R,11R,13R,14S,17R)-3-[(2R,3R,4S,5S,6R)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,11,14-trihydroxy-10-(hydroxymethyl)-13-methyl-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2H-furan-5-one, CHEMBL501316, Q27134323
Topological Polar Surface Area 266.0
Hydrogen Bond Donor Count 10.0
Heavy Atom Count 51.0
Isotope Atom Count 0.0
Molecular Complexity 1350.0
Database Name cmaup_ingredients;npass_chem_all;pubchem
Defined Atom Stereocenter Count 19.0
Iupac Name 3-[(3S,5S,8R,9S,10R,11R,13R,14S,17R)-3-[(2R,3R,4S,5S,6R)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,11,14-trihydroxy-10-(hydroxymethyl)-13-methyl-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2H-furan-5-one
Prediction Hob 0.0
Xlogp -2.3
Molecular Formula C35H54O16
Prediction Swissadme 0.0
Inchi Key YPZVRDVFGRFZHP-PCUDRXQQSA-N
Fcsp3 0.9142857142857144
Logs -2.429
Rotatable Bond Count 7.0
Logd -0.274
Compound Name Elaeodendroside V
Prediction Hob Swissadme 0.0
Exact Mass 730.341
Formal Charge 0.0
Monoisotopic Mass 730.341
Hydrogen Bond Acceptor Count 16.0
Molecular Weight 730.8
Covalent Unit Count 1.0
Total Atom Stereocenter Count 19.0
Total Bond Stereocenter Count 0.0
Esol -2.4473662000000043
Inchi InChI=1S/C35H54O16/c1-15-29(51-31-27(43)25(41)24(40)21(12-36)50-31)26(42)28(44)30(48-15)49-17-3-6-33(14-37)23-19(4-7-34(33,45)10-17)35(46)8-5-18(16-9-22(39)47-13-16)32(35,2)11-20(23)38/h9,15,17-21,23-31,36-38,40-46H,3-8,10-14H2,1-2H3/t15-,17+,18-,19-,20-,21-,23-,24-,25-,26+,27-,28-,29-,30+,31+,32-,33+,34+,35+/m1/s1
Smiles C[C@@H]1[C@H]([C@H]([C@H]([C@@H](O1)O[C@H]2CC[C@@]3([C@@H]4[C@@H](CC[C@@]3(C2)O)[C@]5(CC[C@@H]([C@]5(C[C@H]4O)C)C6=CC(=O)OC6)O)CO)O)O)O[C@H]7[C@@H]([C@@H]([C@@H]([C@H](O7)CO)O)O)O
Nring 7.0
Defined Bond Stereocenter Count 0.0