Basic information about inhibitors

IPAD-DB ID	C01039
Name	Moracin O
Category	Natural compounds
2D Structure
3D Structure
Molecular Formula	C 1 9 H 1 8 O 5
Molecular Weight	326.3g/mol
IUPAC Name	5-[6-(2-hydroxypropan-2-yl)-5, 6-dihydrofuro[3, 2-f][1]benzofuran-2-yl]benzene-1, 3-diol
InChI	InChI=1S/C19H18O5/c1-19(2, 22)18-7-11-3-10-6-15(23-16(10)9-17(11)24-18)12-4-13(20)8-14(21)5-12/h3-6, 8-9, 18, 20-22H, 7H2, 1-2H3
InChIKey	HMTMYIWMPJSCAZ-UHFFFAOYSA-N
Canonical SMILES	CC(C)(C1CC2=C(O1)C=C3C(=C2)C=C(O3)C4=CC(=CC(=C4)O)O)O
PubChem CID	14539883
DrugBank Accession Number	-
CAS Registry Number	123702-97-6

Biological activity data

Ki	-
EC50	-
IC50	-
Inhibition	-
Toxicity	-
ROS(reactive oxygen species)	-
Metal Chelating	-
BBB(blood-brain barrier)	-
Target Protein	Monoamine Oxidase B (MAOB)
Effects	-
Research Models	In vitro, Molecular docking, molecular dynamics (MD) simulations
Main Source	From Morus macroura leaf
Ref. Link

Physicochemical properties

Molecular Weight(Computed by SwissADME)	326.34
Hac(Computed by SwissADME)	24
Volume(Computed by ADMETlab 2.0)	328.45
Density(Computed by ADMETlab 2.0)	0.993
nRing(Computed by ADMETlab 2.0)	4
MaxRing(Computed by ADMETlab 2.0)	12
nHet(Computed by ADMETlab 2.0)	5
fChar(Computed by ADMETlab 2.0)	0
nRig(Computed by ADMETlab 2.0)	20
Flexibility(Computed by ADMETlab 2.0)	0.1
Stero Centers(Computed by ADMETlab 2.0)	1
LogS(Computed by ADMETlab 2.0)	-3.591
LogD(Computed by ADMETlab 2.0)	2.965

ADMET properties

logP(Computed by ADMETlab 2.0)	3.59
TPSA(Computed by SwissADME)	83.06 Ų
Hbond Acceptor(Computed by SwissADME)	5
Hbond Donor(Computed by SwissADME)	3
Rotatable Bonds(Computed by SwissADME)	2

Pharmacokinetics

GI Absorption(Computed by SwissADME)	High
BBB(blood-brain barrier) Permeant(Computed by SwissADME)	No
P-gp Substrate(Computed by SwissADME)	Yes
CYP1A2 Inhibitor(Computed by SwissADME)	Yes
CYP2C19 Inhibitor(Computed by SwissADME)	Yes
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)	-5.96 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