Basic information about inhibitors

IPAD-DB ID	C00062
Name	10-Hydroxy-infractopicrin
Category	Natural compounds
2D Structure
3D Structure
Molecular Formula	C 1 7 H 1 3 C l N 2 O 2
Molecular Weight	312.7 g/mol
IUPAC Name	5-hydroxy-1-aza-11-azoniapentacyclo[9.6.2.02, 7.08, 18.015, 19]nonadeca-2(7), 3, 5, 8(18), 9, 11(19), 15-heptaen-17-one;chloride
InChI	InChI=1S/C17H12N2O2.ClH/c20-11-3-4-14-13(9-11)12-5-7-18-6-1-2-10-8-15(21)19(14)17(12)16(10)18;/h3-5, 7-9H, 1-2, 6H2;1H
InChIKey	NTHWONPMICHNIA-UHFFFAOYSA-N
Canonical SMILES	C1CC2=CC(=O)N3C4=C(C=C(C=C4)O)C5=C3C2=[N+](C1)C=C5.[Cl-]
PubChem CID	46228997
DrugBank Accession Number	-
CAS Registry Number	-

Biological activity data

Ki	-
EC50	-
IC50	12.7±0.16 μM（AChE）
Inhibition	-
Toxicity	-
ROS(reactive oxygen species)	-
Metal Chelating	-
BBB(blood-brain barrier)	-
Target Protein	Aβ1-40
Effects	Inhibit self-aggregation of Aβ1-40 and AChE
Research Models	In HepG2 and SH-SY5Y cells, Molecular modeling, in vitro
Main Source	Cortinarius infractus
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Physicochemical properties

Molecular Weight(Computed by SwissADME)	312.75
Hac(Computed by SwissADME)	22
Volume(Computed by ADMETlab 2.0)	279.606
Density(Computed by ADMETlab 2.0)	0.991
nRing(Computed by ADMETlab 2.0)	5
MaxRing(Computed by ADMETlab 2.0)	17
nHet(Computed by ADMETlab 2.0)	4
fChar(Computed by ADMETlab 2.0)	1
nRig(Computed by ADMETlab 2.0)	24
Flexibility(Computed by ADMETlab 2.0)	0
Stero Centers(Computed by ADMETlab 2.0)	0
LogS(Computed by ADMETlab 2.0)	-4.847
LogD(Computed by ADMETlab 2.0)	2.692

ADMET properties

logP(Computed by ADMETlab 2.0)	2.762
TPSA(Computed by SwissADME)	45.59
Hbond Acceptor(Computed by SwissADME)	2
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)	No
P-gp Substrate(Computed by SwissADME)	Yes
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)	-6.17

Druglikeness

Lipinski(Computed by SwissADME)	0
Ghose(Computed by SwissADME)	1
Veber(Computed by SwissADME)	0
Egan(Computed by SwissADME)	0
Muegge(Computed by SwissADME)	0
Bioavailability Score(Computed by SwissADME)	0.55