Basic information about inhibitors

IPAD-DB ID	C00663
Name	Luteolin
Category	Natural compounds
2D Structure
3D Structure
Molecular Formula	C 1 5 H 1 0 O 6
Molecular Weight	286.24 g/mol
IUPAC Name	2-(3, 4-dihydroxyphenyl)-5, 7-dihydroxychromen-4-one
InChI	InChI=1S/C15H10O6/c16-8-4-11(19)15-12(20)6-13(21-14(15)5-8)7-1-2-9(17)10(18)3-7/h1-6, 16-19H
InChIKey	IQPNAANSBPBGFQ-UHFFFAOYSA-N
Canonical SMILES	C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O
PubChem CID	5280445
DrugBank Accession Number	-
CAS Registry Number	491-70-3

Biological activity data

Ki	-
EC50	-
IC50	-
Inhibition	25% Aβ（1-40）, 49%Aβ（1-42）
Toxicity	-
ROS(reactive oxygen species)	-
Metal Chelating	-
BBB(blood-brain barrier)	-
Target Protein	Aβ1-40
Effects	(1) Reduce amyloidogenesis determined by APP mutations related with familial AD and traumatic brain injury,
Research Models	Tg2576 mice
Main Source	-
Ref. Link

Physicochemical properties

Molecular Weight(Computed by SwissADME)	286.24
Hac(Computed by SwissADME)	21
Volume(Computed by ADMETlab 2.0)	273.977
Density(Computed by ADMETlab 2.0)	1.044
nRing(Computed by ADMETlab 2.0)	3
MaxRing(Computed by ADMETlab 2.0)	10
nHet(Computed by ADMETlab 2.0)	6
fChar(Computed by ADMETlab 2.0)	0
nRig(Computed by ADMETlab 2.0)	18
Flexibility(Computed by ADMETlab 2.0)	0.056
Stero Centers(Computed by ADMETlab 2.0)	0
LogS(Computed by ADMETlab 2.0)	-3.629
LogD(Computed by ADMETlab 2.0)	2.361

ADMET properties

logP(Computed by ADMETlab 2.0)	2.28
TPSA(Computed by SwissADME)	111.13 Ų
Hbond Acceptor(Computed by SwissADME)	6
Hbond Donor(Computed by SwissADME)	4
Rotatable Bonds(Computed by SwissADME)	1

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)	Yes
CYP3A4 Inhibitor(Computed by SwissADME)	Yes
log Kp(Skin Permeation)(Computed by SwissADME)	-6.25 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