IPAD-DB ID | C00850 |
Name | 3, 4-Dihydroxycinnamic acid |
Category | Natural compounds |
2D Structure |
|
3D Structure | |
Molecular Formula | C 9 H 8 O 4 |
Molecular Weight | 180.16g/mol |
IUPAC Name | (E)-3-(3, 4-dihydroxyphenyl)prop-2-enoic acid |
InChI | InChI=1S/C9H8O4/c10-7-3-1-6(5-8(7)11)2-4-9(12)13/h1-5, 10-11H, (H, 12, 13)/b4-2+ |
InChIKey | QAIPRVGONGVQAS-DUXPYHPUSA-N |
Canonical SMILES | C1=CC(=C(C=C1C=CC(=O)O)O)O |
PubChem CID | 689043 |
DrugBank Accession Number | - |
CAS Registry Number | 501-16-6, 331-39-5 |
Molecular Weight(Computed by SwissADME) | 180.16 |
Hac(Computed by SwissADME) | 13 |
Volume(Computed by ADMETlab 2.0) | 177.642 |
Density(Computed by ADMETlab 2.0) | 1.013 |
nRing(Computed by ADMETlab 2.0) | 1 |
MaxRing(Computed by ADMETlab 2.0) | 6 |
nHet(Computed by ADMETlab 2.0) | 4 |
fChar(Computed by ADMETlab 2.0) | 0 |
nRig(Computed by ADMETlab 2.0) | 8 |
Flexibility(Computed by ADMETlab 2.0) | 0.25 |
Stero Centers(Computed by ADMETlab 2.0) | 0 |
LogS(Computed by ADMETlab 2.0) | -1.118 |
LogD(Computed by ADMETlab 2.0) | 1.02 |
logP(Computed by ADMETlab 2.0) | 1.43 |
TPSA(Computed by SwissADME) | 77.76 |
Hbond Acceptor(Computed by SwissADME) | 4 |
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) | -6.58 |
Lipinski(Computed by SwissADME) | 0 |
Ghose(Computed by SwissADME) | 0 |
Veber(Computed by SwissADME) | 0 |
Egan(Computed by SwissADME) | 0 |
Muegge(Computed by SwissADME) | 1 |
Bioavailability Score(Computed by SwissADME) | 0.56 |