Detailed Information for S00130

Basic information about inhibitors

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 -

Biological activity data

Ki -
EC50
IC50
Inhibition
Toxicity
ROS(reactive oxygen species)
Metal Chelating
BBB(blood-brain barrier)
Target Protein Aβ1-42
Effects Provided a significant degree of neuroprotection against Aβ exposure over the full concentration range of Aβ1-42, inhibit Aβ1-42  fibrils formation
Research Models Docking studies, in PC12 cells, in vitro
Ref. Link

Physicochemical properties

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

ADMET properties

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

Pharmacokinetics

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

Druglikeness

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