This website is for informational and educational purposes only. Please do not self-medicate; contact a medical professional for advice before administration. This website is for informational and educational purposes only. Please do not self-medicate; contact a medical professional for advice before administration.

methyl (1R,4aS,6S,7R,7aS)-6-[(2S,3R,4S)-4-(2,2-dimethoxyethyl)-3-ethenyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carbonyl]oxy-1-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate

PubChem CID: 122228280

Connections displayed (default: 10).
Loading graph...

Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 209.0
Hydrogen Bond Donor Count 5.0
Pfizer 3 75 Rule True
Scaffold Graph Level CC(CC1CC2CCCCC2C1)C1CCC(CC2CCCCC2)CC1
Np Classifier Class Iridoids monoterpenoids, Secoiridoid monoterpenoids
Deep Smiles COCC[C@H][C@@H]C=C))[C@@H]OC=C6C=O)O[C@H]C[C@H][C@@H][C@H]5C))[C@H]O)OC=C6C=O)OC))))))))))))))))O[C@@H]O[C@H]CO))[C@H][C@@H][C@H]6O))O))O))))))))))OC
Heavy Atom Count 44.0
Classyfire Class Prenol lipids
Scaffold Graph Node Level OC(OC1CC2CCOCC2C1)C1CCC(OC2CCCCO2)OC1
Classyfire Subclass Terpene glycosides
Isotope Atom Count 0.0
Molecular Complexity 1090.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 13.0
Iupac Name methyl (1R,4aS,6S,7R,7aS)-6-[(2S,3R,4S)-4-(2,2-dimethoxyethyl)-3-ethenyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carbonyl]oxy-1-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate
Veber Rule False
Classyfire Superclass Lipids and lipid-like molecules
Xlogp -0.2
Gsk 4 400 Rule False
Molecular Formula C29H42O15
Scaffold Graph Node Bond Level O=C(OC1CC2C=COCC2C1)C1=COC(OC2CCCCO2)CC1
Inchi Key OLQSEMGEQKAMCH-UXPRVSINSA-N
Silicos It Class Soluble
Rotatable Bond Count 13.0
Synonyms sylvestroside iii dimethyl acetal
Esol Class Soluble
Functional Groups C=CC, CO, COC(=O)C1=CO[C@@H](O)CC1, COC(=O)C1=CO[C@@H](O[C@@H](C)OC)CC1, COC(C)OC
Compound Name methyl (1R,4aS,6S,7R,7aS)-6-[(2S,3R,4S)-4-(2,2-dimethoxyethyl)-3-ethenyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carbonyl]oxy-1-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate
Exact Mass 630.252
Formal Charge 0.0
Monoisotopic Mass 630.252
Hydrogen Bond Acceptor Count 15.0
Molecular Weight 630.6
Gi Absorption False
Covalent Unit Count 1.0
Total Atom Stereocenter Count 13.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 False
Inchi InChI=1S/C29H42O15/c1-6-13-14(8-20(37-3)38-4)16(11-41-28(13)44-29-24(33)23(32)22(31)19(9-30)43-29)26(35)42-18-7-15-17(25(34)39-5)10-40-27(36)21(15)12(18)2/h6,10-15,18-24,27-33,36H,1,7-9H2,2-5H3/t12-,13+,14-,15+,18-,19+,21+,22+,23-,24+,27+,28-,29-/m0/s1
Smiles C[C@H]1[C@H](C[C@H]2[C@@H]1[C@@H](OC=C2C(=O)OC)O)OC(=O)C3=CO[C@H]([C@@H]([C@@H]3CC(OC)OC)C=C)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)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 Scaevola Taccada (Plant) Rel Props:Reference:ISBN:9788185042145