Detailed Information for C00005

Basic information about inhibitors

IPAD-DB ID C00005
Name Hydroxytyrosol (HT)
Category Natural compounds
2D Structure
3D Structure
Molecular Formula C 8 H 1 0 O 3
Molecular Weight 154.16 g/mol
IUPAC Name 4-(2-hydroxyethyl)benzene-1, 2-diol
InChI InChI=1S/C8H10O3/c9-4-3-6-1-2-7(10)8(11)5-6/h1-2, 5, 9-11H, 3-4H2
InChIKey JUUBCHWRXWPFFH-UHFFFAOYSA-N
Canonical SMILES OCCC1=CC(O)=C(O)C=C1
PubChem CID -
DrugBank Accession Number -
CAS Registry Number -

Biological activity data

Ki -
EC50 -
IC50 2.85 μM(hIAPP)
Inhibition At a fixed concentration of 10 μM, HT was found to inhibit aggregation of 15 μM hIAPP by 52.16 ± 6.5% .
Toxicity -
ROS(reactive oxygen species) -
Metal Chelating -
BBB(blood-brain barrier) -
Target Protein HIAPP
Effects (1) Cell viability recovery was about 3% ±0.1% in the presence of HT-hIAPP,
Research Models In Vitro
Main Source Olive oil
Ref. Link

Physicochemical properties

Molecular Weight(Computed by SwissADME) 154.16
Hac(Computed by SwissADME) 11
Volume(Computed by ADMETlab 2.0) 156.829
Density(Computed by ADMETlab 2.0) 0.982
nRing(Computed by ADMETlab 2.0) 1
MaxRing(Computed by ADMETlab 2.0) 6
nHet(Computed by ADMETlab 2.0) 3
fChar(Computed by ADMETlab 2.0) 0
nRig(Computed by ADMETlab 2.0) 6
Flexibility(Computed by ADMETlab 2.0) 0.333
Stero Centers(Computed by ADMETlab 2.0) 0
LogS(Computed by ADMETlab 2.0) 0.151
LogD(Computed by ADMETlab 2.0) 0.458

ADMET properties

logP(Computed by ADMETlab 2.0) 0.63
TPSA(Computed by SwissADME) 60.69
Hbond Acceptor(Computed by SwissADME) 3
Hbond Donor(Computed by SwissADME) 3
Rotatable Bonds(Computed by SwissADME) 2

Pharmacokinetics

GI Absorption(Computed by SwissADME) High
BBB(blood-brain barrier) Permeant(Computed by SwissADME) No
P-gp Substrate(Computed by SwissADME) No
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) -7.75

Druglikeness

Lipinski(Computed by SwissADME) 0
Ghose(Computed by SwissADME) 1
Veber(Computed by SwissADME) 0
Egan(Computed by SwissADME) 0
Muegge(Computed by SwissADME) 1
Bioavailability Score(Computed by SwissADME) 0.55