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Capsianoside D

PubChem CID: 131751077

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Compound Synonyms Capsianoside D, Capsianside D
Ghose Rule False
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 601.0
Hydrogen Bond Donor Count 22.0
Pfizer 3 75 Rule True
Scaffold Graph Level CC(CCCCCCCCCCCCCCC1CCCCC1CC1CCCCC1)CC1CCCC(CCC2CCCC(CC3CCCC(CCCCCCCCCCCCCCCCC4CCCCC4CC4CCCCC4)C3)C2)C1
Np Classifier Class Labdane diterpenoids, Phytane diterpenoids
Deep Smiles OCCOCOCCC/C=C/CC/C=C/CC/C=CCOCOCC)CCC6O))OCOCCOCOCC)CCC6O))OC=O)/C=C/CC/C=C/CC/C=C/CCCOCOCCO))CCC6OCOCCO))CCC6O))O))O)))))))O))O))))))C=C))C)))))/C)))))/C)))O)))/C)))))O)))))))CCC6O))O))O)))))))O)))))))/C)))))C)))))C)))))C=C))C)))CCC6O))O))OCOCCO))CCC6O))O))O
Heavy Atom Count 120.0
Classyfire Class Fatty acyls
Scaffold Graph Node Level OC(CCCCCCCCCCCCCOC1OCCCC1OC1CCCCO1)OC1CCOC(OCC2CCCC(OC3CCOC(OCCCCCCCCCCCCCCOC4OCCCC4OC4CCCCO4)C3)O2)C1
Classyfire Subclass Fatty acyl glycosides
Isotope Atom Count 0.0
Molecular Complexity 3340.0
Database Name hmdb_chem_all;imppat_phytochem;pubchem
Defined Atom Stereocenter Count 0.0
Iupac Name [2-[[6-[2-[(2Z,6E,10E)-14-[4,5-dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,6,10,14-tetramethylhexadeca-2,6,10,15-tetraenoxy]-3,5-dihydroxy-6-methyloxan-4-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3,5-dihydroxy-6-methyloxan-4-yl] (2E,6E,10E)-14-[4,5-dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-2,6,10,14-tetramethylhexadeca-2,6,10,15-tetraenoate
Class Fatty Acyls
Veber Rule False
Classyfire Superclass Lipids and lipid-like molecules
Xlogp -0.7
Superclass Lipids and lipid-like molecules
Subclass Fatty acyl glycosides
Gsk 4 400 Rule False
Molecular Formula C82H134O38
Scaffold Graph Node Bond Level O=C(C=CCCC=CCCC=CCCCOC1OCCCC1OC1CCCCO1)OC1CCOC(OCC2CCCC(OC3CCOC(OCC=CCCC=CCCC=CCCCOC4OCCCC4OC4CCCCO4)C3)O2)C1
Inchi Key BHQXDVVPOFDEHV-RPQRBYGFSA-N
Rotatable Bond Count 43.0
Synonyms Capsianside D, N-(3-Methylbut-3-enyl)-7H-purin-6-amine, 2-({6-[(2-{[(2Z,6E,10E)-14-{[4,5-dihydroxy-6-(hydroxymethyl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-2,6,10,14-tetramethylhexadeca-2,6,10,15-tetraen-1-yl]oxy}-3,5-dihydroxy-6-methyloxan-4-yl)oxy]-3,4,5-trihydroxyoxan-2-yl}methoxy)-3,5-dihydroxy-6-methyloxan-4-yl (2E,6E,10E)-14-{[4,5-dihydroxy-6-(hydroxymethyl)-3-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxan-2-yl]oxy}-4-hydroxy-2,6,10,14-tetramethylhexadeca-2,6,10,15-tetraenoic acid, capsianoside d
Functional Groups C/C=C(/C)C, C/C=C(C)C, C/C=C(C)C(=O)OC, C=CC, CO, COC(C)OC
Compound Name Capsianoside D
Kingdom Organic compounds
Exact Mass 1726.86
Formal Charge 0.0
Monoisotopic Mass 1726.86
Hydrogen Bond Acceptor Count 38.0
Molecular Weight 1727.9
Covalent Unit Count 1.0
Total Atom Stereocenter Count 38.0
Total Bond Stereocenter Count 6.0
Molecular Framework Aliphatic heteromonocyclic compounds
Lipinski Rule Of 5 False
Inchi InChI=1S/C82H134O38/c1-13-81(11,119-79-71(62(98)56(92)49(34-85)112-79)117-76-64(100)59(95)54(90)47(32-83)110-76)28-18-26-39(4)21-15-20-38(3)23-17-25-42(7)36-106-74-68(104)70(53(89)45(10)108-74)116-78-66(102)61(97)58(94)51(114-78)37-107-75-67(103)69(52(88)44(9)109-75)115-73(105)43(8)31-46(87)30-41(6)24-16-22-40(5)27-19-29-82(12,14-2)120-80-72(63(99)57(93)50(35-86)113-80)118-77-65(101)60(96)55(91)48(33-84)111-77/h13-14,20,24-27,31,44-72,74-80,83-104H,1-2,15-19,21-23,28-30,32-37H2,3-12H3/b38-20+,39-26+,40-27+,41-24+,42-25-,43-31+
Smiles CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3C(C(OC(C3O)OC/C(=C\CC/C(=C/CC/C(=C/CCC(C)(C=C)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)/C)/C)/C)C)O)O)O)O)O)OC(=O)/C(=C/C(C/C(=C/CC/C(=C/CCC(C)(C=C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)/C)/C)O)/C)O
Np Classifier Biosynthetic Pathway Terpenoids
Defined Bond Stereocenter Count 6.0
Egan Rule False
Taxonomy Direct Parent Sophorolipids
Np Classifier Superclass Diterpenoids

  • 1. Outgoing r'ship FOUND_IN to/from Capsicum Annuum (Plant) Rel Props:Reference:ISBN:9788172362089