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Secologanate

PubChem CID: 439612

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Compound Synonyms Secologanate, 22864-93-3, (2S,3R,4S)-3-ethenyl-4-(2-oxoethyl)-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylic acid, C01957, (2S,3R,4S)-4-(2-oxoethyl)-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-3-vinyl-3,4-dihydro-2H-pyran-5-carboxylic acid, AC1L97OQ, Secologansaeure, (2S,3R,4S)-3-ethenyl-4-(2-oxoethyl)-2-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxy-3,4-dihydro-2H-pyran-5-carboxylic acid, (2S,3R,4S)-4-(2-oxoethyl)-2-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl)oxy-3-vinyl-3,4-dihydro-2H-pyran-5-carboxylic acid, CHEBI:9075, SCHEMBL2135809, AKOS040746336, DA-57772, HY-121380, CS-0081832, Q27108262
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 163.0
Hydrogen Bond Donor Count 5.0
Pfizer 3 75 Rule True
Scaffold Graph Level C1CCC(CC2CCCCC2)CC1
Np Classifier Class Secoiridoid monoterpenoids
Deep Smiles O=CC[C@H][C@@H]C=C))[C@@H]OC=C6C=O)O)))))O[C@@H]O[C@H]CO))[C@H][C@@H][C@H]6O))O))O
Heavy Atom Count 26.0
Classyfire Class Prenol lipids
Scaffold Graph Node Level C1CCC(OC2CCCCO2)OC1
Classyfire Subclass Terpene glycosides
Isotope Atom Count 0.0
Molecular Complexity 561.0
Database Name cmaup_ingredients;imppat_phytochem;npass_chem_all;pubchem
Defined Atom Stereocenter Count 8.0
Iupac Name (2S,3R,4S)-3-ethenyl-4-(2-oxoethyl)-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylic acid
Prediction Hob 0.0
Veber Rule False
Classyfire Superclass Lipids and lipid-like molecules
Xlogp -1.9
Gsk 4 400 Rule True
Molecular Formula C16H22O10
Scaffold Graph Node Bond Level C1=COC(OC2CCCCO2)CC1
Prediction Swissadme 0.0
Inchi Key PUEUIRDVQIKCCG-ZASXJUAOSA-N
Silicos It Class Soluble
Fcsp3 0.625
Rotatable Bond Count 7.0
Synonyms secologanic acid
Esol Class Very soluble
Functional Groups C=CC, CC=O, CO, CO[C@H](C)O[C@H]1CCC(C(=O)O)=CO1
Compound Name Secologanate
Prediction Hob Swissadme 0.0
Exact Mass 374.121
Formal Charge 0.0
Monoisotopic Mass 374.121
Hydrogen Bond Acceptor Count 10.0
Molecular Weight 374.34
Gi Absorption False
Covalent Unit Count 1.0
Total Atom Stereocenter Count 8.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 True
Esol -0.47042040000000046
Inchi InChI=1S/C16H22O10/c1-2-7-8(3-4-17)9(14(22)23)6-24-15(7)26-16-13(21)12(20)11(19)10(5-18)25-16/h2,4,6-8,10-13,15-16,18-21H,1,3,5H2,(H,22,23)/t7-,8+,10-,11-,12+,13-,15+,16+/m1/s1
Smiles C=C[C@@H]1[C@@H](C(=CO[C@H]1O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)C(=O)O)CC=O
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule False
Np Classifier Superclass Monoterpenoids

  • 1. Outgoing r'ship FOUND_IN to/from Catharanthus Roseus (Plant) Rel Props:Reference:ISBN:9788172360481
  • 2. Outgoing r'ship FOUND_IN to/from Lonicera Japonica (Plant) Rel Props:Source_db:cmaup_ingredients;npass_chem_all