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 | - |
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 |
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 |
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 |
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 |