Detailed Information for C00538

Basic information about inhibitors

IPAD-DB ID C00538
Name Viniferol E
Category Natural compounds
2D Structure
3D Structure
Molecular Formula C 5 6 H 4 4 O 1 3
Molecular Weight 924.9g/mol
IUPAC Name 5-[(2S, 3S)-5-[(2R, 3S, 4S, 5S)-4-[(2S, 3S)-3-(3, 5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2, 3-dihydro-1-benzofuran-5-yl]-2, 5-bis(4-hydroxyphenyl)oxolan-3-yl]-6-hydroxy-2-(4-hydroxyphenyl)-2, 3-dihydro-1-benzofuran-3-yl]benzene-1, 3-diol
InChI InChI=1S/C56H44O13/c57-33-9-1-27(2-10-33)53-49(31-17-37(61)21-38(62)18-31)43-23-41(45(65)25-47(43)67-53)51-52(56(30-7-15-36(60)16-8-30)69-55(51)29-5-13-35(59)14-6-29)42-24-44-48(26-46(42)66)68-54(28-3-11-34(58)12-4-28)50(44)32-19-39(63)22-40(64)20-32/h1-26, 49-66H/t49-, 50-, 51+, 52+, 53+, 54+, 55-, 56+/m0/s1
InChIKey SLSQRFIWGCSNDI-ZBYKJNIJSA-N
Canonical SMILES C1=CC(=CC=C1C2C(C(C(O2)C3=CC=C(C=C3)O)C4=CC5=C(C=C4O)OC(C5C6=CC(=CC(=C6)O)O)C7=CC=C(C=C7)O)C8=CC9=C(C=C8O)OC(C9C1=CC(=CC(=C1)O)O)C1=CC=C(C=C1)O)O
PubChem CID 46890016
DrugBank Accession Number -
CAS Registry Number -

Biological activity data

Ki -
EC50 -
IC50 -
Inhibition 17 ± 10%(Aβ fibril)
Toxicity -
ROS(reactive oxygen species) -
Metal Chelating -
BBB(blood-brain barrier) -
Target Protein
Effects -
Research Models -
Main Source -
Ref. Link

Physicochemical properties

Molecular Weight(Computed by SwissADME) 924.94
Hac(Computed by SwissADME) 69
Volume(Computed by ADMETlab 2.0) 934.009
Density(Computed by ADMETlab 2.0) 0.99
nRing(Computed by ADMETlab 2.0) 11
MaxRing(Computed by ADMETlab 2.0) 9
nHet(Computed by ADMETlab 2.0) 13
fChar(Computed by ADMETlab 2.0) 0
nRig(Computed by ADMETlab 2.0) 61
Flexibility(Computed by ADMETlab 2.0) 0.131
Stero Centers(Computed by ADMETlab 2.0) 8
LogS(Computed by ADMETlab 2.0) -2.838
LogD(Computed by ADMETlab 2.0) 3.913

ADMET properties

logP(Computed by ADMETlab 2.0) 10.65
TPSA(Computed by SwissADME) 229.99 Ų
Hbond Acceptor(Computed by SwissADME) 13
Hbond Donor(Computed by SwissADME) 10
Rotatable Bonds(Computed by SwissADME) 8

Pharmacokinetics

GI Absorption(Computed by SwissADME) Low
BBB(blood-brain barrier) Permeant(Computed by SwissADME) No
P-gp Substrate(Computed by SwissADME) Yes
CYP1A2 Inhibitor(Computed by SwissADME) No
CYP2C19 Inhibitor(Computed by SwissADME) No
CYP2C9 Inhibitor(Computed by SwissADME) No
CYP2D6 Inhibitor(Computed by SwissADME) No
CYP3A4 Inhibitor(Computed by SwissADME) No
log Kp(Skin Permeation)(Computed by SwissADME) -5.67 cm/s

Druglikeness

Lipinski(Computed by SwissADME) No, 3 violations: MW>500, NorO>10, NHorOH>5
Ghose(Computed by SwissADME) No, 4 violations: MW>480, WLOGP>5.6, MR>130, #atoms>70
Veber(Computed by SwissADME) No, 1 violation: TPSA>140
Egan(Computed by SwissADME) No, 2 violations: WLOGP>5.88, TPSA>131.6
Muegge(Computed by SwissADME) No, 6 violations: MW>600, XLOGP3>5, TPSA>150, #rings>7, H-acc>10, H-don>5
Bioavailability Score(Computed by SwissADME) 0.17