Basic information about inhibitors

IPAD-DB ID	C00250
Name	Nodakenetin
Category	Natural compounds
2D Structure
3D Structure
Molecular Formula	C 1 4 H 1 4 O 4
Molecular Weight	246.26g/mol
IUPAC Name	(2R)-2-(2-hydroxypropan-2-yl)-2, 3-dihydrofuro[3, 2-g]chromen-7-one
InChI	InChI=1S/C14H14O4/c1-14(2, 16)12-6-9-5-8-3-4-13(15)18-10(8)7-11(9)17-12/h3-5, 7, 12, 16H, 6H2, 1-2H3/t12-/m1/s1
InChIKey	FWYSBEAFFPBAQU-GFCCVEGCSA-N
Canonical SMILES	CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)OC4C(C(C(C(O4)CO)O)O)O
PubChem CID	26305
DrugBank Accession Number	-
CAS Registry Number	495-32-9

Biological activity data

Ki	-
EC50	-
IC50	407.98 ± 2.90 µM(PTP1B), 720.29 ± 1.89 µM(α-Glucosidase), 266.39 ± 1.02 µM(RLAR), 46.19 ± 0.29 µM(AChE), 46.07 ± 0.56 µM(BChE), 153.46 ± 0.91 µM(BACE1)
Inhibition	-
Toxicity	-
ROS(reactive oxygen species)	-
Metal Chelating	-
BBB(blood-brain barrier)	-
Target Protein	Butyrylcholinesterase (BChE)
Effects	-
Research Models	Sprague–Dawley rats, In vitro
Main Source	From Angelica decursiva
Ref. Link

Physicochemical properties

Molecular Weight(Computed by SwissADME)	408.4
Hac(Computed by SwissADME)	29
Volume(Computed by ADMETlab 2.0)	386.18
Density(Computed by ADMETlab 2.0)	1.057
nRing(Computed by ADMETlab 2.0)	4
MaxRing(Computed by ADMETlab 2.0)	13
nHet(Computed by ADMETlab 2.0)	9
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)	6
LogS(Computed by ADMETlab 2.0)	-2.736
LogD(Computed by ADMETlab 2.0)	0.99

ADMET properties

logP(Computed by ADMETlab 2.0)	-0.31
TPSA(Computed by SwissADME)	138.82 Ų
Hbond Acceptor(Computed by SwissADME)	9
Hbond Donor(Computed by SwissADME)	4
Rotatable Bonds(Computed by SwissADME)	4

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)	-8.56 cm/s

Druglikeness

Lipinski(Computed by SwissADME)	Yes, 0 violation
Ghose(Computed by SwissADME)	Yes
Veber(Computed by SwissADME)	Yes
Egan(Computed by SwissADME)	No, 1 violation: TPSA>131.6
Muegge(Computed by SwissADME)	Yes
Bioavailability Score(Computed by SwissADME)	0.55