IPAD-DB ID | C00467 |
Name | 3-Ethoxy-4-isopropyloxycinnamic acid |
Category | Natural compounds |
2D Structure |
|
3D Structure | |
Molecular Formula | C 1 4 H 1 8 O 4 |
Molecular Weight | 250.29 g/mol |
IUPAC Name | (E)-3-(3-ethoxy-4-isopropoxyphenyl)acrylic acid |
InChI | InChI=1S/C14H18O4/c1-4-17-13-9-11(6-8-14(15)16)5-7-12(13)18-10(2)3/h5-10H, 4H2, 1-3H3, (H, 15, 16)/b8-6+ |
InChIKey | FFPWDFCCBUVIIX-SOFGYWHQSA-N |
Canonical SMILES | O=C(O)/C=C/C1=CC(OCC)=C(C=C1)OC(C)C |
PubChem CID | 19617860 |
DrugBank Accession Number | - |
CAS Registry Number | - |
Molecular Weight(Computed by SwissADME) | 250.29 |
Hac(Computed by SwissADME) | 18 |
Volume(Computed by ADMETlab 2.0) | 264.122 |
Density(Computed by ADMETlab 2.0) | 0.947 |
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) | 0.75 |
Stero Centers(Computed by ADMETlab 2.0) | 0 |
LogS(Computed by ADMETlab 2.0) | -3.857 |
LogD(Computed by ADMETlab 2.0) | 3.061 |
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) | 6 |
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) | Yes |
CYP2C19 Inhibitor(Computed by SwissADME) | Yes |
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) | -5.33 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 |