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Fargesin

PubChem CID: 10926754

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Compound Synonyms Fargesin, 31008-19-2, (+/-)-Fargesin, Demethoxyaschantin, 5-[(3S,3aR,6R,6aR)-6-(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-1,3-benzodioxole, rel-5-((1S,3aR,4R,6aR)-4-(3,4-Dimethoxyphenyl)tetrahydro-1H,3H-furo[3,4-c]furan-1-yl)benzo[d][1,3]dioxole, ( inverted exclamation markA)-Fargesin, (A+/-)-Fargesin, CHEMBL2442732, SCHEMBL15273910, DTXSID901317922, MFCD07781423, s9285, AKOS025311589, CCG-268297, FF41812, AS-55997, DA-53117, F1188, 1H,3H-FURO(3,4-C)FURAN, 1.ALPHA.-(3,4-DIMETHOXYPHENYL)-3A.BETA.,4,6,6A.BETA.-TETRAHYDRO-4.BETA.-((3,4-METHYLENEDIOXY)PHENYL)-, rel-5-[(1R,3aS,4S,6aS)-4-(3,4-Dimethoxyphenyl)tetrahydro-1H,3H-furo[3,4-c]furan-1-yl]-1,3-benzodioxole
Ghose Rule True
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 55.4
Hydrogen Bond Donor Count 0.0
Pfizer 3 75 Rule False
Scaffold Graph Level C1CCC(C2CCC3C(C4CCC5CCCC5C4)CCC23)CC1
Np Classifier Class Furofuranoid lignans
Deep Smiles COcccccc6OC)))))[C@@H]OC[C@H][C@@H]5CO[C@@H]5cccccc6)OCO5
Heavy Atom Count 27.0
Classyfire Class Furanoid lignans
Scaffold Graph Node Level C1CCC(C2OCC3C2COC3C2CCC3OCOC3C2)CC1
Isotope Atom Count 0.0
Molecular Complexity 515.0
Database Name cmaup_ingredients;imppat_phytochem;npass_chem_all;pubchem
Defined Atom Stereocenter Count 4.0
Iupac Name 5-[(3S,3aR,6R,6aR)-6-(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-1,3-benzodioxole
Prediction Hob 1.0
Veber Rule True
Classyfire Superclass Lignans, neolignans and related compounds
Xlogp 2.8
Gsk 4 400 Rule True
Molecular Formula C21H22O6
Scaffold Graph Node Bond Level c1ccc(C2OCC3C(c4ccc5c(c4)OCO5)OCC23)cc1
Prediction Swissadme 1.0
Inchi Key AWOGQCSIVCQXBT-LATRNWQMSA-N
Silicos It Class Moderately soluble
Fcsp3 0.4285714285714285
Logs -5.245
Rotatable Bond Count 4.0
Logd 3.252
Synonyms (+)-methylpluviatilol(fargesin), fargesin, methyl pluviatilol(fargesin)
Esol Class Soluble
Functional Groups COC, c1cOCO1, cOC
Compound Name Fargesin
Prediction Hob Swissadme 1.0
Exact Mass 370.142
Formal Charge 0.0
Monoisotopic Mass 370.142
Hydrogen Bond Acceptor Count 6.0
Molecular Weight 370.4
Gi Absorption True
Covalent Unit Count 1.0
Total Atom Stereocenter Count 4.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 True
Esol -3.9716750888888903
Inchi InChI=1S/C21H22O6/c1-22-16-5-3-12(7-18(16)23-2)20-14-9-25-21(15(14)10-24-20)13-4-6-17-19(8-13)27-11-26-17/h3-8,14-15,20-21H,9-11H2,1-2H3/t14-,15-,20-,21+/m0/s1
Smiles COC1=C(C=C(C=C1)[C@H]2[C@H]3CO[C@@H]([C@H]3CO2)C4=CC5=C(C=C4)OCO5)OC
Nring 5.0
Np Classifier Biosynthetic Pathway Shikimates and Phenylpropanoids
Defined Bond Stereocenter Count 0.0
Egan Rule True
Np Classifier Superclass Lignans

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