Basic information about inhibitors

IPAD-DB ID	C01299
Name	Galangin
Category	Natural compounds
2D Structure
3D Structure
Molecular Formula	C 1 5 H 1 0 O 5
Molecular Weight	270.24 g/mol
IUPAC Name	3, 5, 7-trihydroxy-2-phenylchromen-4-one
InChI	InChI=1S/C15H10O5/c16-9-6-10(17)12-11(7-9)20-15(14(19)13(12)18)8-4-2-1-3-5-8/h1-7, 16-17, 19H
InChIKey	VCCRNZQBSJXYJD-UHFFFAOYSA-N
Canonical SMILES	C1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O
PubChem CID	5281616
DrugBank Accession Number	-
CAS Registry Number	548-83-4

Biological activity data

Ki	-
EC50	-
IC50	-
Inhibition	23.4%（BACE1）
Toxicity	-
ROS(reactive oxygen species)	-
Metal Chelating	-
BBB(blood-brain barrier)	-
Target Protein	β-site amyloid precursor protein cleaving enzyme 1 (BACE1)
Effects	Inhibit BACE1, reduce oxidative stress through scavenging activity
Research Models	QSAR model, in vitro
Main Source	Alpinia officinarum Hance
Ref. Link

Physicochemical properties

Molecular Weight(Computed by SwissADME)	270.24
Hac(Computed by SwissADME)	20
Volume(Computed by ADMETlab 2.0)	265.186
Density(Computed by ADMETlab 2.0)	1.018
nRing(Computed by ADMETlab 2.0)	3
MaxRing(Computed by ADMETlab 2.0)	10
nHet(Computed by ADMETlab 2.0)	5
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)	-3.491
LogD(Computed by ADMETlab 2.0)	2.497

ADMET properties

logP(Computed by ADMETlab 2.0)	3.26
TPSA(Computed by SwissADME)	90.9
Hbond Acceptor(Computed by SwissADME)	5
Hbond Donor(Computed by SwissADME)	3
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)	Yes
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)	-6.35

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