General Information of the Compound
Compound ID
CP0016295
Compound Name
4-[4-(4-fluorophenyl)-2-(4-methanesulfinylphenyl)-1H-imidazol-5-yl]pyridine
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Synonyms
152121-47-6
4-(4-(4-fluorophenyl)-2-(4-(methylsulfinyl)phenyl)-1H-imidazol-5-yl)pyridine
4-(4-Fluorophenyl)-2-(4-methylsulfinylphenyl)-5-(4-pyridyl)-1H-imidazole
4-(4-Fluorophenyl)-2-(4-methylsulfinylphenyl)-5-(4-pyridyl)1H-imidazole
4-(4-Fluorophenyl)-2-[4-(methylsulfinyl)phenyl]-5-(4-pyridyl)-1H-imidazole
4-[4-(4-fluorophenyl)-2-(4-methylsulfinylphenyl)-1H-imidazol-5-yl]pyridine
CHEBI:90705
CHEMBL10
PB 203580
RWJ 64809
SB 203580
SB-203580
SB203580
UNII-WS78QR6DSV
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Structure
Formula
C21H16FN3OS
Molecular Weight
377.444
Canonical SMILES
CS(=O)c1ccc(cc1)-c1nc(c([nH]1)-c1ccc(F)cc1)-c1ccncc1
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InChI
InChI=1S/C21H16FN3OS/c1-27(26)18-8-4-16(5-9-18)21-24-19(14-2-6-17(22)7-3-14)20(25-21)15-10-12-23-13-11-15/h2-13H,1H3,(H,24,25)
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InChIKey
CDMGBJANTYXAIV-UHFFFAOYSA-N
Physicochemical Property
logP
4.6822
Rotatable Bonds
4
Heavy Atom Count
27
Polar Areas
58.64
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
3
Complexity
27

"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: 176155
SID: 49684193
ChEMBL ID
CHEMBL10
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: PT01002, Cytochrome P450 1A2
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000023 BTI-Tn-5B1-4 Trichoplusia ni (Cabbage looper)  1
1
IC50 = 2000 nM
   TI
   LI
   LO
   TS
Protein ID: PT01049, Cytochrome P450 2C19
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000023 BTI-Tn-5B1-4 Trichoplusia ni (Cabbage looper)  1
1
IC50 = 800 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 Potency = 39.8 nM
Protein ID: PT00905, Cytochrome P450 2C9
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000023 BTI-Tn-5B1-4 Trichoplusia ni (Cabbage looper)  1
1
IC50 = 1000 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 Potency = 1995.3 nM
Protein ID: PT00817, Cytochrome P450 2D6
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000023 BTI-Tn-5B1-4 Trichoplusia ni (Cabbage looper)  1
1
IC50 = 2000 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 Potency = 39810.7 nM
Protein ID: PT00861, Mitogen-activated protein kinase 14
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000013 Sf9 Spodoptera frugiperda (Fall armyworm)  1
1
IC50 = 35 nM
   TI
   LI
   LO
   TS
CL000012 Sf21 Spodoptera frugiperda (Fall armyworm)  1
1
Kd = 21.7 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 IC50 = 10 nM
2 IC50 = 19 nM
3 IC50 = 20 nM
4 IC50 = 25 nM
5 IC50 = 30 nM
6 IC50 = 35 nM
7 IC50 = 37 nM
8 IC50 = 38 nM
9 IC50 = 39 nM
10 IC50 = 40 nM
11 IC50 = 41 nM
12 IC50 = 44 nM
13 IC50 = 45 nM
14 IC50 = 48 nM
15 IC50 = 50 nM
16 IC50 = 55 nM
17 IC50 = 62 nM
18 IC50 = 65 nM
19 IC50 = 68 nM
20 IC50 = 70 nM
21 IC50 = 72 nM
22 IC50 = 100 nM
23 IC50 = 159 nM
24 IC50 = 273 nM
25 IC50 = 290 nM
26 IC50 = 462 nM
27 IC50 = 500 nM
28 IC50 = 723 nM
29 IC50 = 2000 nM
30 IC50 = 6000 nM
31 IC50 = 7000 nM
32 Kd = 4.1 nM
33 Kd = 12 nM
34 Kd = 17 nM
35 Ki = 18 nM
36 Ki = 57 nM
Protein ID: PT01743, Polyunsaturated fatty acid 5-lipoxygenase
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000194 RBL-1 Rattus norvegicus (Rat)  1
1
IC50 = 58000 nM
   TI
   LI
   LO
   TS
Clinical Information about the Compound
Drug 1 ( SB 203580 )
Drug Name SB 203580
Target(s)
Prostaglandin G/H synthase 2 (COX-2)
Inhibitor
Interleukin 1 receptor type 1 (IL1R1)
Antagonist
Stress-activated protein kinase 2a (p38 alpha)
Inhibitor