IPAD-DB ID | C00463 |
Name | 3-Methoxy-4-ethoxycinnamic acid |
Category | Natural compounds |
2D Structure |
|
3D Structure | |
Molecular Formula | C 1 3 H 1 6 O 4 |
Molecular Weight | 236.26 g/mol |
IUPAC Name | methyl (E)-3-(4-ethoxy-3-methoxyphenyl)prop-2-enoate |
InChI | InChI=1S/C13H16O4/c1-4-17-11-7-5-10(9-12(11)15-2)6-8-13(14)16-3/h5-9H, 4H2, 1-3H3/b8-6+ |
InChIKey | SFYMFSUPKNCUPC-SOFGYWHQSA-N |
Canonical SMILES | CCOC1=C(C=C(C=C1)C=CC(=O)OC)OC |
PubChem CID | 15686803 |
DrugBank Accession Number | - |
CAS Registry Number | - |
Molecular Weight(Computed by SwissADME) | 222.24 |
Hac(Computed by SwissADME) | 16 |
Volume(Computed by ADMETlab 2.0) | 229.53 |
Density(Computed by ADMETlab 2.0) | 0.968 |
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) | 0.625 |
Stero Centers(Computed by ADMETlab 2.0) | 0 |
LogS(Computed by ADMETlab 2.0) | -3.317 |
LogD(Computed by ADMETlab 2.0) | 1.905 |
logP(Computed by ADMETlab 2.0) | |
TPSA(Computed by SwissADME) | 55.76 Ų |
Hbond Acceptor(Computed by SwissADME) | 4 |
Hbond Donor(Computed by SwissADME) | 1 |
Rotatable Bonds(Computed by SwissADME) | 5 |
GI Absorption(Computed by SwissADME) | High |
BBB(blood-brain barrier) Permeant(Computed by SwissADME) | Yes |
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) | -5.73 cm/s |
Lipinski(Computed by SwissADME) | Yes; 0 violation |
Ghose(Computed by SwissADME) | Yes |
Veber(Computed by SwissADME) | Yes |
Egan(Computed by SwissADME) | Yes |
Muegge(Computed by SwissADME) | Yes |
Bioavailability Score(Computed by SwissADME) | 0.85 |