IPAD-DB ID | D01417 |
Name | Tacrine |
Category | Drugs |
2D Structure |
|
3D Structure | |
Molecular Formula | C 1 3 H 1 4 N 2 |
Molecular Weight | 198.26 g/mol |
IUPAC Name | 1,2,3,4-tetrahydroacridin-9-amine |
InChI | InChI=1S/C13H14N2/c14-13-9-5-1-3-7-11(9)15-12-8-4-2-6-10(12)13/h1,3,5,7H,2,4,6,8H2,(H2,14,15) |
InChIKey | YLJREFDVOIBQDA-UHFFFAOYSA-N |
Canonical SMILES | C1CCC2=NC3=CC=CC=C3C(=C2C1)N |
PubChem CID | 1935 |
DrugBank Accession Number | DB00382 |
CAS Registry Number | 321-64-2 |
Molecular Weight(Computed by SwissADME) | 198.26 |
Hac(Computed by SwissADME) | 15 |
Volume(Computed by ADMETlab 2.0) | 216.546 |
Density(Computed by ADMETlab 2.0) | 0.915 |
nRing(Computed by ADMETlab 2.0) | 3 |
MaxRing(Computed by ADMETlab 2.0) | 14 |
nHet(Computed by ADMETlab 2.0) | 2 |
fChar(Computed by ADMETlab 2.0) | 0 |
nRig(Computed by ADMETlab 2.0) | 17 |
Flexibility(Computed by ADMETlab 2.0) | 0 |
Stero Centers(Computed by ADMETlab 2.0) | 0 |
LogS(Computed by ADMETlab 2.0) | -2.967 |
LogD(Computed by ADMETlab 2.0) | 2.534 |
logP(Computed by ADMETlab 2.0) | 2.813 |
TPSA(Computed by SwissADME) | 38.91 |
Hbond Acceptor(Computed by SwissADME) | 1 |
Hbond Donor(Computed by SwissADME) | 1 |
Rotatable Bonds(Computed by SwissADME) | 0 |
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) | No |
CYP2C9 Inhibitor(Computed by SwissADME) | No |
CYP2D6 Inhibitor(Computed by SwissADME) | No |
CYP3A4 Inhibitor(Computed by SwissADME) | Yes |
log Kp(Skin Permeation)(Computed by SwissADME) | -5.59 |
Lipinski(Computed by SwissADME) | 0 |
Ghose(Computed by SwissADME) | 0 |
Veber(Computed by SwissADME) | 0 |
Egan(Computed by SwissADME) | 0 |
Muegge(Computed by SwissADME) | 1 |
Bioavailability Score(Computed by SwissADME) | 0.55 |