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Melongoside G

PubChem CID: 131752997

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Compound Synonyms Melongoside G, CHEBI:192877, DTXSID201107691, 2-[3-hydroxy-2-(hydroxymethyl)-6-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl)oxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl]oxy-6-methyloxane-3,4,5-triol, 94805-86-4, I(2)-D-Glucopyranoside, (3I(2),5I+/-,25R)-spirostan-3-yl O-6-deoxy-I+/--L-mannopyranosyl-(1a3)-O-[I(2)-D-glucopyranosyl-(1a2)]-
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 256.0
Hydrogen Bond Donor Count 9.0
Pfizer 3 75 Rule True
Scaffold Graph Level C1CCC(CC2CCCC(CC3CCC4C(CCC5C4CCC4C6CC7(CCCCC7)CC6CC45)C3)C2CC2CCCCC2)CC1
Np Classifier Class Spirostane steroids
Deep Smiles OCCOCOCCCCCC6)CCCC6CCCC6CCC5CC)CO5)CCCCO6))C))))))))))C)))))))))C))))))CCC6O))OCOCC)CCC6O))O))O)))))))OCOCCO))CCC6O))O))O
Heavy Atom Count 62.0
Classyfire Class Steroids and steroid derivatives
Description Constituent of aubergine (Solanum melongena). Melongoside G is found in fruits and eggplant.
Scaffold Graph Node Level C1CCC(OC2CCOC(OC3CCC4C(CCC5C4CCC4C6CC7(CCCCO7)OC6CC45)C3)C2OC2CCCCO2)OC1
Classyfire Subclass Steroidal glycosides
Isotope Atom Count 0.0
Molecular Complexity 1560.0
Database Name fooddb_chem_all;hmdb_chem_all;imppat_phytochem;pubchem
Defined Atom Stereocenter Count 0.0
Iupac Name 2-[3-hydroxy-2-(hydroxymethyl)-6-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl)oxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl]oxy-6-methyloxane-3,4,5-triol
Class Steroids and steroid derivatives
Veber Rule False
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 2.2
Superclass Lipids and lipid-like molecules
Subclass Steroidal glycosides
Gsk 4 400 Rule False
Molecular Formula C45H74O17
Scaffold Graph Node Bond Level C1CCC(OC2CCOC(OC3CCC4C(CCC5C4CCC4C6CC7(CCCCO7)OC6CC45)C3)C2OC2CCCCO2)OC1
Inchi Key GVSGITAPQDRRJB-UHFFFAOYSA-N
Silicos It Class Soluble
Rotatable Bond Count 8.0
Synonyms Melongoside G, melongoside g
Substituent Name Steroidal saponin, Polycyclic triterpenoid, Triterpenoid, Spirostane skeleton, Oligosaccharide, O-glycosyl compound, Glycosyl compound, Oxane, Saccharide, Oxolane, Secondary alcohol, Polyol, 1,2-diol, Oxacycle, Organoheterocyclic compound, Ether, Acetal, Hydrocarbon derivative, Primary alcohol, Organooxygen compound, Alcohol, Aliphatic heteropolycyclic compound
Esol Class Poorly soluble
Functional Groups CO, COC(C)(C)OC, COC(C)OC
Compound Name Melongoside G
Kingdom Organic compounds
Exact Mass 886.493
Formal Charge 0.0
Monoisotopic Mass 886.493
Hydrogen Bond Acceptor Count 17.0
Molecular Weight 887.1
Gi Absorption False
Covalent Unit Count 1.0
Total Atom Stereocenter Count 27.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 False
Inchi InChI=1S/C45H74O17/c1-19-8-13-45(55-18-19)20(2)30-27(62-45)15-26-24-7-6-22-14-23(9-11-43(22,4)25(24)10-12-44(26,30)5)57-42-39(61-41-37(54)35(52)32(49)28(16-46)58-41)38(33(50)29(17-47)59-42)60-40-36(53)34(51)31(48)21(3)56-40/h19-42,46-54H,6-18H2,1-5H3
Smiles CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)C)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)OC1
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule False
Taxonomy Direct Parent Steroidal saponins
Np Classifier Superclass Steroids

  • 1. Outgoing r'ship FOUND_IN to/from Solanum Melongena (Plant) Rel Props:Reference:ISBN:9788185042138