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Asparagoside E

PubChem CID: 131751196

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Compound Synonyms Asparagoside E, CHEBI:197033, 2-[4-[16-[3,5-dihydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-hydroxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosan-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 307.0
Hydrogen Bond Donor Count 12.0
Pfizer 3 75 Rule True
Scaffold Graph Level C1CCC(CCCCCC2CC3CC4C(CCC5C6CCC(CC7CCCC(CC8CCCCC8)C7)CC6CCC54)C3C2)CC1
Np Classifier Class Furostane steroids
Deep Smiles OCCOCOCCCCCC6)CCCC6CCCC6CCC5CC)CO5)O)CCCCOCOCCO))CCC6O))O))O)))))))C))))))))))C)))))))))C))))))CCC6O))OCOCCO))CCC6O))O))O)))))))O
Heavy Atom Count 64.0
Classyfire Class Steroids and steroid derivatives
Description Constituent of Asparagus officinalis (asparagus). Asparagoside E is found in asparagus and green vegetables.
Scaffold Graph Node Level C(CCC1CC2C(CC3C2CCC2C4CCC(OC5CC(OC6CCCCO6)CCO5)CC4CCC23)O1)COC1CCCCO1
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-[4-[16-[3,5-dihydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-hydroxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosan-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol
Class Steroids and steroid derivatives
Veber Rule False
Classyfire Superclass Lipids and lipid-like molecules
Xlogp 0.7
Superclass Lipids and lipid-like molecules
Subclass Steroidal glycosides
Gsk 4 400 Rule False
Molecular Formula C45H76O19
Scaffold Graph Node Bond Level C(CCC1CC2C(CC3C2CCC2C4CCC(OC5CC(OC6CCCCO6)CCO5)CC4CCC23)O1)COC1CCCCO1
Inchi Key STAKUOVRJNVEFG-UHFFFAOYSA-N
Silicos It Class Soluble
Rotatable Bond Count 13.0
State Solid
Synonyms Asparagoside E, asparagoside e
Esol Class Moderately soluble
Functional Groups CO, COC(C)(C)O, COC(C)OC
Compound Name Asparagoside E
Kingdom Organic compounds
Exact Mass 920.498
Formal Charge 0.0
Monoisotopic Mass 920.498
Hydrogen Bond Acceptor Count 19.0
Molecular Weight 921.1
Gi Absorption False
Covalent Unit Count 1.0
Total Atom Stereocenter Count 27.0
Total Bond Stereocenter Count 0.0
Molecular Framework Aliphatic heteropolycyclic compounds
Lipinski Rule Of 5 False
Inchi InChI=1S/C45H76O19/c1-19(18-58-40-36(54)34(52)31(49)27(15-46)60-40)7-12-45(57)20(2)30-26(64-45)14-25-23-6-5-21-13-22(8-10-43(21,3)24(23)9-11-44(25,30)4)59-42-38(56)39(33(51)29(17-48)62-42)63-41-37(55)35(53)32(50)28(16-47)61-41/h19-42,46-57H,5-18H2,1-4H3
Smiles CC1C2C(CC3C2(CCC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)OC1(CCC(C)COC8C(C(C(C(O8)CO)O)O)O)O
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule False
Taxonomy Direct Parent Steroidal saponins
Np Classifier Superclass Steroids