IPAD-DB ID | S00638 |
Name | N1-((7-Methoxybenzo[d][1, 3]dioxol-5-yl)methyl)-N5-(1, 2, 4-tetrahydroacridin-9-yl)pentane-1, 5-diamine |
Category | Synthetic compounds |
2D Structure |
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3D Structure | |
Molecular Formula | - |
Molecular Weight | - |
IUPAC Name | - |
InChI | - |
InChIKey | - |
Canonical SMILES | - |
PubChem CID | - |
DrugBank Accession Number | - |
CAS Registry Number | - |
Molecular Weight(Computed by SwissADME) | |
Hac(Computed by SwissADME) | |
Volume(Computed by ADMETlab 2.0) | |
Density(Computed by ADMETlab 2.0) | |
nRing(Computed by ADMETlab 2.0) | |
MaxRing(Computed by ADMETlab 2.0) | |
nHet(Computed by ADMETlab 2.0) | |
fChar(Computed by ADMETlab 2.0) | |
nRig(Computed by ADMETlab 2.0) | |
Flexibility(Computed by ADMETlab 2.0) | |
Stero Centers(Computed by ADMETlab 2.0) | |
LogS(Computed by ADMETlab 2.0) | |
LogD(Computed by ADMETlab 2.0) |
logP(Computed by ADMETlab 2.0) | |
TPSA(Computed by SwissADME) | |
Hbond Acceptor(Computed by SwissADME) | |
Hbond Donor(Computed by SwissADME) | |
Rotatable Bonds(Computed by SwissADME) |
GI Absorption(Computed by SwissADME) | |
BBB(blood-brain barrier) Permeant(Computed by SwissADME) | |
P-gp Substrate(Computed by SwissADME) | |
CYP1A2 Inhibitor(Computed by SwissADME) | |
CYP2C19 Inhibitor(Computed by SwissADME) | |
CYP2C9 Inhibitor(Computed by SwissADME) | |
CYP2D6 Inhibitor(Computed by SwissADME) | |
CYP3A4 Inhibitor(Computed by SwissADME) | |
log Kp(Skin Permeation)(Computed by SwissADME) |
Lipinski(Computed by SwissADME) | |
Ghose(Computed by SwissADME) | |
Veber(Computed by SwissADME) | |
Egan(Computed by SwissADME) | |
Muegge(Computed by SwissADME) | |
Bioavailability Score(Computed by SwissADME) |