General Information of the Compound
Compound ID
CP0015550
Compound Name
2-(4-(benzo[d][1,3]dioxol-5-yl)-2-tert-butyl-1H-imidazol-5-yl)-6-methylpyridine
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Synonyms
2-(4-(benzo[d][1,3]dioxol-5-yl)-2-tert-butyl-1H-imidazol-5-yl)-6-methylpyridine
2-[4-(1,3-Benzodioxol-5-yl)-2-(tert-butyl)-1H-imidazol-5-yl]-6-methylpyridine
2-[4-(2H-1,3-benzodioxol-5-yl)-2-tert-butyl-1H-imidazol-5-yl]-6-methylpyridine
2-[5-(1,3-Benzodioxol-5-yl)-2-(1,1-dimethylethyl)-1H-imidazol-4-yl]-6-methylpyridine
694433-59-5
AOB1766
AOB5688
CHEBI:100922
CHEMBL226838
CTK8E3615
DTXSID50431926
EX-A217
GTPL6049
KS-00000XPS
MLS006010969
MolPort-021-804-897
SB 505124
SB-505124
SB505124
SCHEMBL373422
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Structure
Formula
C20H21N3O2
Molecular Weight
335.407
Canonical SMILES
Cc1cccc(n1)-c1nc([nH]c1-c1ccc2OCOc2c1)C(C)(C)C
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InChI
InChI=1S/C20H21N3O2/c1-12-6-5-7-14(21-12)18-17(22-19(23-18)20(2,3)4)13-8-9-15-16(10-13)25-11-24-15/h5-10H,11H2,1-4H3,(H,22,23)
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InChIKey
WGZOTBUYUFBEPZ-UHFFFAOYSA-N
Physicochemical Property
logP
4.47332
Rotatable Bonds
2
Heavy Atom Count
25
Polar Areas
60.03
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
4
Complexity
25

"RO5" indicates the cutoff set by lipinski's rule of five:

(1) Molecular weight less than 500 Dalton;

(2) xlogp less than 5;

(3) No more than 5 hbonddonor (Hydrogen Bond Donor Count);

(4) No more than 10 hbondacc (Hydrogen Bond Acceptor Count);

(5) No more than 10 rotbonds (Rotatable Bond Count).

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PubChem ID
CID: 9858940
SID: 14822144
ChEMBL ID
CHEMBL226838
Map of Molecular Bioactivity Related to the Compound
Map of Molecular Bioactivity Related to the Compound

Compound
Cell Line
Protein

Bioactivity Value:

<= 0.1 μM
> 0.1 μM and <= 10 μM
> 10 μM
Imprecise Activity
Table of Molecular Bioactivities Related to the Compound
Protein ID: PT01221, TGF-beta receptor type-1
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000013 Sf9 Spodoptera frugiperda (Fall armyworm)  4
1
IC50 = 34.9 nM
   TI
   LI
   LO
   TS
2
IC50 = 54 nM
   TI
   LI
   LO
   TS
3
IC50 = 54.4 nM
   TI
   LI
   LO
   TS
4
IC50 = 169 nM
   TI
   LI
   LO
   TS
CL000150 HaCaT Homo sapiens (Human)  1
1
IC50 = 43.8 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 IC50 = 47 nM
Protein ID: PT04556, TGF-beta receptor type-1
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000245 4T1 Mus musculus (Mouse)  1
1
IC50 = 76.6 nM
   TI
   LI
   LO
   TS
Clinical Information about the Compound
Drug 1 ( SB-505124 )
Drug Name SB-505124
Target(s)
TGF-beta receptor type I (TGFBR1)
Inhibitor