Basic information about inhibitors

IPAD-DB ID	S00832
Name	5, 7-Dichloro-8-hydroxyquinolin-2-yl)methyl-1H-indole-2-carboxylate
Category	Synthetic compounds
2D Structure
3D Structure
Molecular Formula	C 1 9 H 1 2 C l 2 N 2 O 3
Molecular Weight	387.2 g/mol
IUPAC Name	(5, 7-dichloro-8-hydroxyquinolin-2-yl)methyl 1H-indole-2-carboxylate
InChI	InChI=1S/C19H12Cl2N2O3/c20-13-8-14(21)18(24)17-12(13)6-5-11(22-17)9-26-19(25)16-7-10-3-1-2-4-15(10)23-16/h1-8, 23-24H, 9H2
InChIKey	DTMGDZDJTHMJDY-UHFFFAOYSA-N
Canonical SMILES	C1=CC=C2C(=C1)C=C(N2)C(=O)OCC3=NC4=C(C=C3)C(=CC(=C4O)Cl)Cl
PubChem CID	162395046
DrugBank Accession Number	-
CAS Registry Number	-

Biological activity data

Ki	-
EC50	9.28 μM(Aβ1-42)
IC50
Inhibition
Toxicity
ROS(reactive oxygen species)
Metal Chelating
BBB(blood-brain barrier)
Target Protein	Aβ1-42
Effects
Research Models	SY5Y-APPSw cells, Molecular docking, In vitro
Ref. Link

Physicochemical properties

Molecular Weight(Computed by SwissADME)	387.22
Hac(Computed by SwissADME)	26
Volume(Computed by ADMETlab 2.0)	355.376
Density(Computed by ADMETlab 2.0)	1.086
nRing(Computed by ADMETlab 2.0)	4
MaxRing(Computed by ADMETlab 2.0)	10
nHet(Computed by ADMETlab 2.0)	7
fChar(Computed by ADMETlab 2.0)	0
nRig(Computed by ADMETlab 2.0)	22
Flexibility(Computed by ADMETlab 2.0)	0.182
Stero Centers(Computed by ADMETlab 2.0)	0
LogS(Computed by ADMETlab 2.0)	-4.123
LogD(Computed by ADMETlab 2.0)	3.412

ADMET properties

logP(Computed by ADMETlab 2.0)	4.838
TPSA(Computed by SwissADME)	75.21
Hbond Acceptor(Computed by SwissADME)	4
Hbond Donor(Computed by SwissADME)	2
Rotatable Bonds(Computed by SwissADME)	4

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)	Yes
CYP2C19 Inhibitor(Computed by SwissADME)	Yes
CYP2C9 Inhibitor(Computed by SwissADME)	Yes
CYP2D6 Inhibitor(Computed by SwissADME)	Yes
CYP3A4 Inhibitor(Computed by SwissADME)	Yes
log Kp(Skin Permeation)(Computed by SwissADME)	-5.16

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