Capsianside F
PubChem CID: 131751078
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| Compound Synonyms | Capsianoside F, Capsianside F |
|---|---|
| Ghose Rule | False |
| Classyfire Kingdom | Organic compounds |
| Topological Polar Surface Area | 580.0 |
| Hydrogen Bond Donor Count | 21.0 |
| 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)))))/C)))))O)))))))CCC6O))O))O)))))))O)))))))/C)))))C)))))C)))))C=C))C)))CCC6O))O))OCOCCO))CCC6O))O))O |
| Heavy Atom Count | 119.0 |
| 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 | 3300.0 |
| 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-2,6,10,14-tetramethylhexadeca-2,6,10,15-tetraenoate |
| Class | Fatty Acyls |
| Veber Rule | False |
| Classyfire Superclass | Lipids and lipid-like molecules |
| Xlogp | 0.4 |
| Superclass | Lipids and lipid-like molecules |
| Subclass | Fatty acyl glycosides |
| Gsk 4 400 Rule | False |
| Molecular Formula | C82H134O37 |
| Scaffold Graph Node Bond Level | O=C(C=CCCC=CCCC=CCCCOC1OCCCC1OC1CCCCO1)OC1CCOC(OCC2CCCC(OC3CCOC(OCC=CCCC=CCCC=CCCCOC4OCCCC4OC4CCCCO4)C3)O2)C1 |
| Inchi Key | XIQPUQZGYSYODK-JZKHGTLTSA-N |
| Rotatable Bond Count | 43.0 |
| Synonyms | Capsianside F, 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}-2,6,10,14-tetramethylhexadeca-2,6,10,15-tetraenoic acid, capsianoside f |
| 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 | Capsianside F |
| Kingdom | Organic compounds |
| Exact Mass | 1710.86 |
| Formal Charge | 0.0 |
| Monoisotopic Mass | 1710.86 |
| Hydrogen Bond Acceptor Count | 37.0 |
| Molecular Weight | 1711.9 |
| Covalent Unit Count | 1.0 |
| Total Atom Stereocenter Count | 37.0 |
| Total Bond Stereocenter Count | 6.0 |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Lipinski Rule Of 5 | False |
| Inchi | InChI=1S/C82H134O37/c1-13-81(11,118-79-71(62(97)56(91)49(35-85)111-79)116-76-64(99)59(94)54(89)47(33-83)109-76)31-19-28-41(5)23-15-21-39(3)25-17-27-43(7)37-105-74-68(103)70(53(88)46(10)107-74)115-78-66(101)61(96)58(93)51(113-78)38-106-75-67(102)69(52(87)45(9)108-75)114-73(104)44(8)30-18-26-40(4)22-16-24-42(6)29-20-32-82(12,14-2)119-80-72(63(98)57(92)50(36-86)112-80)117-77-65(100)60(95)55(90)48(34-84)110-77/h13-14,21-22,27-30,45-72,74-80,83-103H,1-2,15-20,23-26,31-38H2,3-12H3/b39-21+,40-22+,41-28+,42-29+,43-27-,44-30+ |
| 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/CC/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)/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_INto/from Capsicum Annuum (Plant) Rel Props:Reference:ISBN:9788172362089