Detailed Information for C01375

Basic information about inhibitors

IPAD-DB ID C01375
Name 6-Methoxymellein
Category Natural compounds
2D Structure
3D Structure
Molecular Formula C 1 1 H 1 2 O 4
Molecular Weight 208.21 g/mol
IUPAC Name (3R)-8-hydroxy-6-methoxy-3-methyl-3, 4-dihydroisochromen-1-one
InChI InChI=1S/C11H12O4/c1-6-3-7-4-8(14-2)5-9(12)10(7)11(13)15-6/h4-6, 12H, 3H2, 1-2H3/t6-/m1/s1
InChIKey AIFNAMVERSBWPS-ZCFIWIBFSA-N
Canonical SMILES CC1CC2=C(C(=CC(=C2)OC)O)C(=O)O1
PubChem CID 83412
DrugBank Accession Number -
CAS Registry Number 13410-15-6

Biological activity data

Ki -
EC50 -
IC50 11.4±0.8 μM(eeAChE), 98±3 μM(Aβ1-40 aggregation)
Inhibition -
Toxicity -
ROS(reactive oxygen species) -
Metal Chelating -
BBB(blood-brain barrier) -
Target Protein Aβ1-40
Effects Inhibit Aβ1–40 aggregation in the low micromolar range
Research Models In Vitro
Main Source Carrots
Ref. Link

Physicochemical properties

Molecular Weight(Computed by SwissADME) 208.21
Hac(Computed by SwissADME) 15
Volume(Computed by ADMETlab 2.0) 206.314
Density(Computed by ADMETlab 2.0) 1.009
nRing(Computed by ADMETlab 2.0) 2
MaxRing(Computed by ADMETlab 2.0) 10
nHet(Computed by ADMETlab 2.0) 4
fChar(Computed by ADMETlab 2.0) 0
nRig(Computed by ADMETlab 2.0) 12
Flexibility(Computed by ADMETlab 2.0) 0.083
Stero Centers(Computed by ADMETlab 2.0) 1
LogS(Computed by ADMETlab 2.0) -2.714
LogD(Computed by ADMETlab 2.0) 2.213

ADMET properties

logP(Computed by ADMETlab 2.0) 2.95
TPSA(Computed by SwissADME) 55.76
Hbond Acceptor(Computed by SwissADME) 4
Hbond Donor(Computed by SwissADME) 1
Rotatable Bonds(Computed by SwissADME)

Pharmacokinetics

GI Absorption(Computed by SwissADME) High
BBB(blood-brain barrier) Permeant(Computed by SwissADME) Yes
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) No
CYP3A4 Inhibitor(Computed by SwissADME) No
log Kp(Skin Permeation)(Computed by SwissADME) -5.86

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