Basic information about inhibitors

IPAD-DB ID	S00008
Name	3-Amino-N-[4-(6-methyl-benzothiazol-2-yl)-phenyl]-benzamide
Category	Synthetic compounds
2D Structure
3D Structure
Molecular Formula	C 2 1 H 1 7 N 3 O S
Molecular Weight	359.4 g/mol
IUPAC Name	3-amino-N-[4-(6-methyl-1, 3-benzothiazol-2-yl)phenyl]benzamide
InChI	InChI=1S/C21H17N3OS/c1-13-5-10-18-19(11-13)26-21(24-18)14-6-8-17(9-7-14)23-20(25)15-3-2-4-16(22)12-15/h2-12H, 22H2, 1H3, (H, 23, 25)
InChIKey	SVSXKCQZEGVZIW-UHFFFAOYSA-N
Canonical SMILES	CC1=CC2=C(C=C1)N=C(S2)C3=CC=C(C=C3)NC(=O)C4=CC(=CC=C4)N
PubChem CID	10361109
DrugBank Accession Number	-
CAS Registry Number	-

Biological activity data

Ki	-
EC50
IC50	8.2±0.5 μM(HD exon 1)
Inhibition
Toxicity
ROS(reactive oxygen species)
Metal Chelating
BBB(blood-brain barrier)
Target Protein	HD exon 1
Effects	Inhibit huntingtin fibrillogenesis in a dose-dependent
Research Models	In 293 Tet-Off cells, in vitro
Ref. Link

Physicochemical properties

Molecular Weight(Computed by SwissADME)	359.44
Hac(Computed by SwissADME)	26
Volume(Computed by ADMETlab 2.0)	368.835
Density(Computed by ADMETlab 2.0)	0.974
nRing(Computed by ADMETlab 2.0)	4
MaxRing(Computed by ADMETlab 2.0)	9
nHet(Computed by ADMETlab 2.0)	5
fChar(Computed by ADMETlab 2.0)	0
nRig(Computed by ADMETlab 2.0)	23
Flexibility(Computed by ADMETlab 2.0)	0.174
Stero Centers(Computed by ADMETlab 2.0)	0
LogS(Computed by ADMETlab 2.0)	-5.698
LogD(Computed by ADMETlab 2.0)	3.65

ADMET properties

logP(Computed by ADMETlab 2.0)	4.649
TPSA(Computed by SwissADME)	96.25
Hbond Acceptor(Computed by SwissADME)	2
Hbond Donor(Computed by SwissADME)	2
Rotatable Bonds(Computed by SwissADME)	4

Pharmacokinetics

GI Absorption(Computed by SwissADME)	High
BBB(blood-brain barrier) Permeant(Computed by SwissADME)	No
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)	-5.26

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