Basic information about inhibitors

IPAD-DB ID	C00040
Name	Liensinine
Category	Natural compounds
2D Structure
3D Structure
Molecular Formula	C 3 7 H 4 2 N 2 O 6
Molecular Weight	610.7 g/mol
IUPAC Name	4-[[(1R)-6, 7-dimethoxy-2-methyl-3, 4-dihydro-1H-isoquinolin-1-yl]methyl]-2-[[(1R)-1-[(4-hydroxyphenyl)methyl]-6-methoxy-2-methyl-3, 4-dihydro-1H-isoquinolin-7-yl]oxy]phenol
InChI	InChI=1S/C37H42N2O6/c1-38-14-13-26-20-35(43-4)37(22-29(26)30(38)16-23-6-9-27(40)10-7-23)45-33-18-24(8-11-32(33)41)17-31-28-21-36(44-5)34(42-3)19-25(28)12-15-39(31)2/h6-11, 18-22, 30-31, 40-41H, 12-17H2, 1-5H3/t30-, 31-/m1/s1
InChIKey	XCUCMLUTCAKSOZ-FIRIVFDPSA-N
Canonical SMILES	CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)OC4=C(C=CC(=C4)CC5C6=CC(=C(C=C6CCN5C)OC)OC)O)OC
PubChem CID	160644
DrugBank Accession Number	-
CAS Registry Number	2586-96-1

Biological activity data

Ki	-
EC50	-
IC50	0.34 ± 0.02 μM(AChE), 9.96 ± 0.47 μM(BChE), 6.37 ± 0.13 μM(BACE1),
Inhibition	-
Toxicity	-
ROS(reactive oxygen species)	-
Metal Chelating	-
BBB(blood-brain barrier)	-
Target Protein	Butyrylcholinesterase (BChE)
Effects	-
Research Models	In Vitro
Main Source	From Nelumbo nucifera embryos fractions
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Physicochemical properties

Molecular Weight(Computed by SwissADME)	610.74
Hac(Computed by SwissADME)	45
Volume(Computed by ADMETlab 2.0)	640.267
Density(Computed by ADMETlab 2.0)	0.953
nRing(Computed by ADMETlab 2.0)	6
MaxRing(Computed by ADMETlab 2.0)	10
nHet(Computed by ADMETlab 2.0)	8
fChar(Computed by ADMETlab 2.0)	0
nRig(Computed by ADMETlab 2.0)	34
Flexibility(Computed by ADMETlab 2.0)	0.265
Stero Centers(Computed by ADMETlab 2.0)	2
LogS(Computed by ADMETlab 2.0)	-2.956
LogD(Computed by ADMETlab 2.0)	4.026

ADMET properties

logP(Computed by ADMETlab 2.0)
TPSA(Computed by SwissADME)	83.86
Hbond Acceptor(Computed by SwissADME)	8
Hbond Donor(Computed by SwissADME)	2
Rotatable Bonds(Computed by SwissADME)	9

Pharmacokinetics

GI Absorption(Computed by SwissADME)	High
BBB(blood-brain barrier) Permeant(Computed by SwissADME)	No
P-gp Substrate(Computed by SwissADME)	No
CYP1A2 Inhibitor(Computed by SwissADME)	No
CYP2C19 Inhibitor(Computed by SwissADME)	No
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)	-5.5

Druglikeness

Lipinski(Computed by SwissADME)	1
Ghose(Computed by SwissADME)	3
Veber(Computed by SwissADME)	0
Egan(Computed by SwissADME)	0
Muegge(Computed by SwissADME)	2
Bioavailability Score(Computed by SwissADME)	0.55