Basic information about inhibitors

IPAD-DB ID	S01253
Name	2-Phenylethyl cinnamate
Category	Synthetic compounds
2D Structure
3D Structure
Molecular Formula	C 1 7 H 1 6 O 2
Molecular Weight	252.31 g/mol
IUPAC Name	2-phenylethyl(E)-3-phenylprop-2-enoate
InChI	InChI=1S/C17H16O2/c18-17(12-11-15-7-3-1-4-8-15)19-14-13-16-9-5-2-6-10-16/h1-12H, 13-14H2/b12-11+
InChIKey	MJQVZIANGRDJBT-VAWYXSNFSA-N
Canonical SMILES	C1=CC=C(C=C1)CCOC(=O)C=CC2=CC=CC=C2
PubChem CID	5369459
DrugBank Accession Number	-
CAS Registry Number	103-53-7

Biological activity data

Ki	-
EC50	1040 μM(Aβ1-42)
IC50
Inhibition	<10%(10μM XOD inhibition), <10%(100μM XOD inhibition)
Toxicity
ROS(reactive oxygen species)	<10%(100μM DPPH radical scavenging activity), <10%(500μM DPPH radical scavenging activity)
Metal Chelating
BBB(blood-brain barrier)
Target Protein	Aβ1-42
Effects
Research Models	Molecular docking
Ref. Link

Physicochemical properties

Molecular Weight(Computed by SwissADME)	252.31
Hac(Computed by SwissADME)	19
Volume(Computed by ADMETlab 2.0)	281.964
Density(Computed by ADMETlab 2.0)	0.894
nRing(Computed by ADMETlab 2.0)	2
MaxRing(Computed by ADMETlab 2.0)	6
nHet(Computed by ADMETlab 2.0)	2
fChar(Computed by ADMETlab 2.0)	0
nRig(Computed by ADMETlab 2.0)	14
Flexibility(Computed by ADMETlab 2.0)	0.429
Stero Centers(Computed by ADMETlab 2.0)	0
LogS(Computed by ADMETlab 2.0)	-4.612
LogD(Computed by ADMETlab 2.0)	4.068

ADMET properties

logP(Computed by ADMETlab 2.0)	4.263
TPSA(Computed by SwissADME)	26.3
Hbond Acceptor(Computed by SwissADME)	2
Hbond Donor(Computed by SwissADME)	0
Rotatable Bonds(Computed by SwissADME)	6

Pharmacokinetics

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)	Yes
CYP3A4 Inhibitor(Computed by SwissADME)	No
log Kp(Skin Permeation)(Computed by SwissADME)	-4.59

Druglikeness

Lipinski(Computed by SwissADME)	0
Ghose(Computed by SwissADME)	0
Veber(Computed by SwissADME)	0
Egan(Computed by SwissADME)	0
Muegge(Computed by SwissADME)	0
Bioavailability Score(Computed by SwissADME)	0.55