Basic information about inhibitors

IPAD-DB ID	C00215
Name	Amentoflavone
Category	Natural compounds
2D Structure
3D Structure
Molecular Formula	C 3 0 H 1 8 O 1 0
Molecular Weight	538.5g/mol
IUPAC Name	8-[5-(5, 7-dihydroxy-4-oxochromen-2-yl)-2-hydroxyphenyl]-5, 7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one
InChI	InChI=1S/C30H18O10/c31-15-4-1-13(2-5-15)24-12-23(38)29-21(36)10-20(35)27(30(29)40-24)17-7-14(3-6-18(17)33)25-11-22(37)28-19(34)8-16(32)9-26(28)39-25/h1-12, 31-36H
InChIKey	YUSWMAULDXZHPY-UHFFFAOYSA-N
Canonical SMILES	C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O
PubChem CID	5281600
DrugBank Accession Number	-
CAS Registry Number	1617-53-4

Biological activity data

Ki	-
EC50	-
IC50	3.37 ± 0.40 μM(Aβ42 polymerization), 6.91 ± 0.43 μM(Aβ42 extension), 20.8 ± 1.4 μM(Aβ42 destabilization)
Inhibition	-
Toxicity	-
ROS(reactive oxygen species)	-
Metal Chelating	-
BBB(blood-brain barrier)	-
Target Protein	Aβ1-42
Effects	(1) Biflavonoids exert their cytoprotective effect in Aβ-induced toxicity by accumulating nontoxic oligomers, (2)effectively inhibit Aβ toxicity and fibrillogenesis,
Research Models	SH-SY5Y
Main Source	-
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Physicochemical properties

Molecular Weight(Computed by SwissADME)	538.46
Hac(Computed by SwissADME)	40
Volume(Computed by ADMETlab 2.0)	521.816
Density(Computed by ADMETlab 2.0)	1.031
nRing(Computed by ADMETlab 2.0)	6
MaxRing(Computed by ADMETlab 2.0)	10
nHet(Computed by ADMETlab 2.0)	10
fChar(Computed by ADMETlab 2.0)	0
nRig(Computed by ADMETlab 2.0)	36
Flexibility(Computed by ADMETlab 2.0)	0.083
Stero Centers(Computed by ADMETlab 2.0)	0
LogS(Computed by ADMETlab 2.0)	-4.576
LogD(Computed by ADMETlab 2.0)	2.383

ADMET properties

logP(Computed by ADMETlab 2.0)	6.003
TPSA(Computed by SwissADME)	181.8
Hbond Acceptor(Computed by SwissADME)	10
Hbond Donor(Computed by SwissADME)	6
Rotatable Bonds(Computed by SwissADME)	3

Pharmacokinetics

GI Absorption(Computed by SwissADME)	Low
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)	-6.01

Druglikeness

Lipinski(Computed by SwissADME)	2
Ghose(Computed by SwissADME)	2
Veber(Computed by SwissADME)	1
Egan(Computed by SwissADME)	1
Muegge(Computed by SwissADME)	3
Bioavailability Score(Computed by SwissADME)	0.17