IPAD-DB ID | S00130 |
Name | 1, 3-dibenzyl-2-[3-(benzyloxy)phenyl]imidazolidine |
Category | Synthetic compounds |
2D Structure |
|
3D Structure | |
Molecular Formula | C 3 0 H 3 0 N 2 O |
Molecular Weight | 434.6 g/mol |
IUPAC Name | 1, 3-dibenzyl-2-(3-phenylmethoxyphenyl)imidazolidine |
InChI | |
InChIKey | LZTISNFRXHXPBF-UHFFFAOYSA-N |
Canonical SMILES | C1CN(C(N1CC2=CC=CC=C2)C3=CC(=CC=C3)OCC4=CC=CC=C4)CC5=CC=CC=C5 |
PubChem CID | 563624 |
DrugBank Accession Number | - |
CAS Registry Number | - |
Molecular Weight(Computed by SwissADME) | 434.57 |
Hac(Computed by SwissADME) | 33 |
Volume(Computed by ADMETlab 2.0) | 483.8 |
Density(Computed by ADMETlab 2.0) | 0.898 |
nRing(Computed by ADMETlab 2.0) | 5 |
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) | 29 |
Flexibility(Computed by ADMETlab 2.0) | 0.276 |
Stero Centers(Computed by ADMETlab 2.0) | 0 |
LogS(Computed by ADMETlab 2.0) | -4.034 |
LogD(Computed by ADMETlab 2.0) | 4.694 |
logP(Computed by ADMETlab 2.0) | 5.25 |
TPSA(Computed by SwissADME) | 15.71 |
Hbond Acceptor(Computed by SwissADME) | 3 |
Hbond Donor(Computed by SwissADME) | 0 |
Rotatable Bonds(Computed by SwissADME) | 8 |
GI Absorption(Computed by SwissADME) | High |
BBB(blood-brain barrier) Permeant(Computed by SwissADME) | Yes |
P-gp Substrate(Computed by SwissADME) | Yes |
CYP1A2 Inhibitor(Computed by SwissADME) | Yes |
CYP2C19 Inhibitor(Computed by SwissADME) | Yes |
CYP2C9 Inhibitor(Computed by SwissADME) | No |
CYP2D6 Inhibitor(Computed by SwissADME) | Yes |
CYP3A4 Inhibitor(Computed by SwissADME) | Yes |
log Kp(Skin Permeation)(Computed by SwissADME) | -4.58 |
Lipinski(Computed by SwissADME) | 1 |
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 |