Basic information about inhibitors

IPAD-DB ID	S01221
Name	Azure C
Category	Synthetic compounds
2D Structure
3D Structure
Molecular Formula	C 1 3 H 1 2 C l N 3 S
Molecular Weight	277.77 g/mol
IUPAC Name	7-methyliminophenothiazin-10-ium-3-amine;chloride
InChI	InChI=1S/C13H11N3S.ClH/c1-15-9-3-5-11-13(7-9)17-12-6-8(14)2-4-10(12)16-11;/h2-7H, 14H2, 1H3;1H
InChIKey	DDGMDTGNGDOUPX-UHFFFAOYSA-N
Canonical SMILES	CN=C1C=CC2=[NH+]C3=C(C=C(C=C3)N)SC2=C1.[Cl-]
PubChem CID	135421845
DrugBank Accession Number	-
CAS Registry Number	531-57-7

Biological activity data

Ki	-
EC50
IC50	0.09 ± 0.02 μM(Aβ42 oligomers )
Inhibition	0.9 ± 1.3%(Aβ42 fibril)
Toxicity
ROS(reactive oxygen species)
Metal Chelating
BBB(blood-brain barrier)
Target Protein	Aβ42 oligomers and fibrils
Effects
Research Models	In vitro
Ref. Link

Physicochemical properties

Molecular Weight(Computed by SwissADME)	277.77
Hac(Computed by SwissADME)	18
Volume(Computed by ADMETlab 2.0)	240.779
Density(Computed by ADMETlab 2.0)	1.001
nRing(Computed by ADMETlab 2.0)	3
MaxRing(Computed by ADMETlab 2.0)	14
nHet(Computed by ADMETlab 2.0)	4
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)	-3.118
LogD(Computed by ADMETlab 2.0)	2.08

ADMET properties

logP(Computed by ADMETlab 2.0)	2.803
TPSA(Computed by SwissADME)	80.76
Hbond Acceptor(Computed by SwissADME)	1
Hbond Donor(Computed by SwissADME)	2
Rotatable Bonds(Computed by SwissADME)	0

Pharmacokinetics

GI Absorption(Computed by SwissADME)	High
BBB(blood-brain barrier) Permeant(Computed by SwissADME)	No
P-gp Substrate(Computed by SwissADME)	No
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)	-6.35

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