Basic information about inhibitors

IPAD-DB ID	C00748
Name	Piperettine
Category	Natural compounds
2D Structure
3D Structure
Molecular Formula	C 1 9 H 2 1 N O 3
Molecular Weight	311.4 g/mol
IUPAC Name	(2E, 4E, 6E)-7-(1, 3-benzodioxol-5-yl)-1-piperidin-1-ylhepta-2, 4, 6-trien-1-one
InChI	InChI=1S/C19H21NO3/c21-19(20-12-6-3-7-13-20)9-5-2-1-4-8-16-10-11-17-18(14-16)23-15-22-17/h1-2, 4-5, 8-11, 14H, 3, 6-7, 12-13, 15H2/b2-1+, 8-4+, 9-5+
InChIKey	DLKOUKNODPCIHZ-UMYWTXKFSA-N
Canonical SMILES	C1CCN(CC1)C(=O)C=CC=CC=CC2=CC3=C(C=C2)OCO3
PubChem CID	10244953
DrugBank Accession Number	-
CAS Registry Number	583-34-6

Biological activity data

Ki	-
EC50	-
IC50	-
Inhibition	200 μg/mL:24.14%(BChE), 51.41%(Aβ1–42)
Toxicity	-
ROS(reactive oxygen species)	-
Metal Chelating	-
BBB(blood-brain barrier)	-
Target Protein	Aβ1-42
Effects	-
Research Models	Molecular docking, in vitro
Main Source	From Piper nigrum fruits
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Physicochemical properties

Molecular Weight(Computed by SwissADME)	311.37
Hac(Computed by SwissADME)	23
Volume(Computed by ADMETlab 2.0)	330.423
Density(Computed by ADMETlab 2.0)	0.942
nRing(Computed by ADMETlab 2.0)	3
MaxRing(Computed by ADMETlab 2.0)	9
nHet(Computed by ADMETlab 2.0)	4
fChar(Computed by ADMETlab 2.0)	0
nRig(Computed by ADMETlab 2.0)	20
Flexibility(Computed by ADMETlab 2.0)	0.25
Stero Centers(Computed by ADMETlab 2.0)	0
LogS(Computed by ADMETlab 2.0)	-4.521
LogD(Computed by ADMETlab 2.0)	3.583

ADMET properties

logP(Computed by ADMETlab 2.0)	3.55
TPSA(Computed by SwissADME)	38.77 Ų
Hbond Acceptor(Computed by SwissADME)	3
Hbond Donor(Computed by SwissADME)	0
Rotatable Bonds(Computed by SwissADME)	5

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)	Yes
CYP2D6 Inhibitor(Computed by SwissADME)	No
CYP3A4 Inhibitor(Computed by SwissADME)	Yes
log Kp(Skin Permeation)(Computed by SwissADME)	-5.28 cm/s

Druglikeness

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)	0.55