Detailed Information for S00802

Basic information about inhibitors

IPAD-DB ID S00802
Name 3, 3‘-bis(β-hydroxyethyl)-9-ethyl-5, 5‘-dimethoxythiacarbocyanine iodide
Category Synthetic compounds
2D Structure
3D Structure
Molecular Formula -
Molecular Weight
IUPAC Name
InChI
InChIKey
Canonical SMILES
PubChem CID
DrugBank Accession Number -
CAS Registry Number -

Biological activity data

Ki -
EC50
IC50 300 nM(tau protein), 294 ± 23nM(total filament length), 272 ± 17 nM(total filament number)
Inhibition
Toxicity
ROS(reactive oxygen species)
Metal Chelating
BBB(blood-brain barrier)
Target Protein α-synuclein
Effects (1)In the presence of increasing concentrations of N744 up to 4.1 μM(i.e., ≈1:1 molar stoichiometry with respect to tau protomer), however, aggregation as reflected in either the total number or total length of all filaments was greatly inhibited, (2) N744 can inhibit fibrillization of tau isoforms containing three or four repeats, (3)N744 at substoichiometric concentrations did not inhibit Aβ and α-synuclein aggregation,
Research Models In vitro
Ref. Link

Physicochemical properties

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)

ADMET properties

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)

Pharmacokinetics

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)

Druglikeness

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)