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Macrophyllicinin

PubChem CID: 44151714

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Compound Synonyms Macrophyllicinin, 153288-84-7, (3beta,6beta,16alpha)-28-(Acetyloxy)-6,16-dihydroxyolean-12-en-3-yl O-6-deoxy-alpha-L-mannopyranosyl-(1-2)-O-beta-D-glucopyranosyl-(1-2)-O-beta-D-galactopyranosyl-(1-2)-beta-D-Glucopyranosiduronic acid, 3beta-O-(alpha-L-Rhamnopyranosyl-(1-2)-beta-D-glucopyranosyl-(1-2)-beta-D-galactopyranosyl-(1-2)-beta-D-glucuronopyranosyl)-6beta,16alpha-dihydroxyolean-12-en-28-acetate, beta-D-Glucopyranosiduronic acid, (3beta,6beta,16alpha)-28-(acetyloxy)-6,16-dihydroxyolean-12-en-3-yl O-6-deoxy-alpha-L-mannopyranosyl-(1-2)-O-beta-D-glucopyranosyl-(1-2)-O-beta-D-galactopyranosyl-(1-2)-, 3 beta-O-(alpha-L-rhamnopyranosyl-(-->2)-beta-D-glucopyranosyl-(-->2)-beta-D-galactopyranosyl-(-->2)-beta-D-glucuronopyranosyl)-6 beta,16 alpha-dihydroxy-olean-12-en-28-acetate
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 400.0
Hydrogen Bond Donor Count 14.0
Pfizer 3 75 Rule True
Scaffold Graph Level CC(CC1CCC2C(CCC3C2CCC2C4CCCCC4CCC23)C1)C1CC(CC2CCCCC2)C(CC2CCCCC2)C(CC2CCCCC2)C1
Np Classifier Class Oleanane triterpenoids
Deep Smiles OC[C@H]O[C@H]O[C@H]O[C@H]C=O)OCCC[C@]CC6C)C))[C@@H]O)C[C@@]C6CC=C[C@@]6C)C[C@@H][C@@][C@@H]6CCC)C)CC6)))))COC=O)C)))))O))))))))C)))))C)))))))[C@H][C@@H][C@H]6O[C@H]O[C@H]CO))[C@H][C@@H][C@H]6O))O))O)))))))O[C@@H]O[C@@H]C)[C@@H][C@H][C@H]6O))O))O)))))))O))))))[C@@H][C@H][C@H]6O))O))O
Heavy Atom Count 81.0
Classyfire Class Prenol lipids
Scaffold Graph Node Level OC(OC1CCC2C(CCC3C2CCC2C4CCCCC4CCC23)C1)C1CC(OC2CCCCO2)C(OC2CCCCO2)C(OC2CCCCO2)O1
Classyfire Subclass Triterpenoids
Isotope Atom Count 0.0
Molecular Complexity 2290.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 27.0
Iupac Name [(5S,6aR,6bS,8S,8aS,12aR,14bR)-8a-(acetyloxymethyl)-5,8-dihydroxy-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] (2S,3S,4S,5R,6R)-3-hydroxy-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxane-2-carboxylate
Veber Rule False
Classyfire Superclass Lipids and lipid-like molecules
Xlogp -0.2
Gsk 4 400 Rule False
Molecular Formula C56H90O25
Scaffold Graph Node Bond Level O=C(OC1CCC2C(CCC3C4CCC5CCCCC5C4=CCC23)C1)C1CC(OC2CCCCO2)C(OC2CCCCO2)C(OC2CCCCO2)O1
Inchi Key UTSJMDCMTNWPES-XKWSIZEHSA-N
Rotatable Bond Count 14.0
Synonyms macrophyllicinin
Functional Groups CC=C(C)C, CO, COC(C)=O, CO[C@@H](C)OC, CO[C@@H](C)O[C@H](C)OC, CO[C@H](C)OC
Compound Name Macrophyllicinin
Exact Mass 1162.58
Formal Charge 0.0
Monoisotopic Mass 1162.58
Hydrogen Bond Acceptor Count 25.0
Molecular Weight 1163.3
Covalent Unit Count 1.0
Total Atom Stereocenter Count 30.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 False
Inchi InChI=1S/C56H90O25/c1-22-32(62)35(65)38(68)47(74-22)78-42-41(71)43(79-50(81-49-40(70)37(67)34(64)28(20-58)76-49)44(42)80-48-39(69)36(66)33(63)27(19-57)75-48)46(72)77-31-12-13-53(7)29-11-10-24-25-16-51(3,4)14-15-56(25,21-73-23(2)59)30(61)18-54(24,8)55(29,9)17-26(60)45(53)52(31,5)6/h10,22,25-45,47-50,57-58,60-71H,11-21H2,1-9H3/t22-,25+,26-,27+,28+,29?,30-,31?,32-,33+,34-,35+,36-,37-,38+,39+,40+,41-,42-,43-,44+,45?,47-,48+,49+,50+,53+,54+,55+,56+/m0/s1
Smiles C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@H]2[C@@H]([C@H](O[C@@H]([C@@H]2O[C@@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)O[C@@H]4[C@@H]([C@H]([C@H]([C@H](O4)CO)O)O)O)C(=O)OC5CC[C@@]6(C7CC=C8[C@H]9CC(CC[C@@]9([C@H](C[C@]8([C@@]7(C[C@@H](C6C5(C)C)O)C)C)O)COC(=O)C)(C)C)C)O)O)O)O
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 0.0
Egan Rule False
Np Classifier Superclass Triterpenoids

  • 1. Outgoing r'ship FOUND_IN to/from Primula Macrophylla (Plant) Rel Props:Reference:https://www.ncbi.nlm.nih.gov/pubmed/8254351