Detailed Information for D00056

Basic information about inhibitors

IPAD-DB ID D00056
Name Risperidone
Category Drugs
2D Structure
3D Structure
Molecular Formula C 2 3 H 2 7 F N 4 O 2
Molecular Weight 410.5 g/mol
IUPAC Name 3-[2-[4-(6-fluoro-1,2-benzoxazol-3-yl)piperidin-1-yl]ethyl]-2-methyl-6,7,8,9-tetrahydropyrido[1,2-a]pyrimidin-4-one
InChI InChI=1S/C23H27FN4O2/c1-15-18(23(29)28-10-3-2-4-21(28)25-15)9-13-27-11-7-16(8-12-27)22-19-6-5-17(24)14-20(19)30-26-22/h5-6,14,16H,2-4,7-13H2,1H3
InChIKey RAPZEAPATHNIPO-UHFFFAOYSA-N
Canonical SMILES CC1=C(C(=O)N2CCCCC2=N1)CCN3CCC(CC3)C4=NOC5=C4C=CC(=C5)F
PubChem CID 5073
DrugBank Accession Number DB00734
CAS Registry Number 106266-06-2

Biological activity data

Ki
EC50
IC50
Inhibition
Toxicity
ROS(reactive oxygen species) -
Metal Chelating -
BBB(blood-brain barrier) -
Target Protein Aβ42
Effects
Research Models Molecular docking
Ref. Link

Physicochemical properties

Molecular Weight(Computed by SwissADME) 410.48
Hac(Computed by SwissADME) 30
Volume(Computed by ADMETlab 2.0) 412.762
Density(Computed by ADMETlab 2.0) 0.994
nRing(Computed by ADMETlab 2.0) 5
MaxRing(Computed by ADMETlab 2.0) 5
nHet(Computed by ADMETlab 2.0) 7
fChar(Computed by ADMETlab 2.0) 0
nRig(Computed by ADMETlab 2.0) 28
Flexibility(Computed by ADMETlab 2.0) 0.143
Stero Centers(Computed by ADMETlab 2.0) 0
LogS(Computed by ADMETlab 2.0) -2.384
LogD(Computed by ADMETlab 2.0) 2.82

ADMET properties

logP(Computed by ADMETlab 2.0) 2.924
TPSA(Computed by SwissADME) 64.16
Hbond Acceptor(Computed by SwissADME) 6
Hbond Donor(Computed by SwissADME) 0
Rotatable Bonds(Computed by SwissADME) 4

Pharmacokinetics

GI Absorption(Computed by SwissADME) High
BBB(blood-brain barrier) Permeant(Computed by SwissADME) Yes
P-gp Substrate(Computed by SwissADME) Yes
CYP1A2 Inhibitor(Computed by SwissADME) Yes
CYP2C19 Inhibitor(Computed by SwissADME) Yes
CYP2C9 Inhibitor(Computed by SwissADME) Yes
CYP2D6 Inhibitor(Computed by SwissADME) Yes
CYP3A4 Inhibitor(Computed by SwissADME) Yes
log Kp(Skin Permeation)(Computed by SwissADME) -6.87

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