FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Chemical: PD169316
Open Close
General Information
Name
PD169316
FlyBase ID
FBch0003160
ChEBI Name
PD169316
ChEBI ID
CHEBI:93358
PubChem Name
PD-169316
PubChem ID
CID:4712
Chemical Structure
Chemical structure of PD169316
PD169316
InChIKey

BGIYKDUASORTBB-UHFFFAOYSA-N

Definition (ChEBI)

A member of the class of imidazoles that is 1H-imidazole in which the hydrogens at positions 2, 4, and 5 are replaced by 4-nitrophenyl, 4-fluorophenyl, and pyridin-4-yl groups, respectively. It is a potent inhibitor of p38 MAP kinase (IC50 = 89 nM). ChEBI: 4-[4-(4-fluorophenyl)-2-(4-nitrophenyl)-1H-imidazol-5-yl]pyridine is a member of imidazoles.

Roles Classification (ChEBI)
Comment
Synonyms and Secondary IDs (14)
Synonyms
152121-53-4
(PubChem, 2019-)
2-(4-Nitrophenyl)-4-(4-fluorophenyl)-5-(4-pyridinyl)-1H-imidazole
(PubChem, 2019-)
2-(4-nitrophenyl)-4-(4-fluorophenyl)-5-(4-pyridinyl)-1H-imidazole
(ChEBI, 2019-)
4-(4-(4-fluorophenyl)-2-(4-nitrophenyl)-1H-imidazol-5-yl)pyridine
(PubChem, 2019-)
4-(4-fluorophenyl)-2-(4-nitrophenyl)-5-(4-pyridyl)-1H-imidazole
(ChEBI, 2019-)
4-[4-(4-fluorophenyl)-2-(4-nitrophenyl)-1H-imidazol-5-yl]pyridine
(ChEBI, 2019-, PubChem, 2019-)
4-[5-(4-fluorophenyl)-2-(4-nitrophenyl)-1H-imidazol-4-yl]-pyridine
(ChEBI, 2019-)
GX3Y2V80CV
(PubChem, 2019-)
J1.342.800J
(ChEBI, 2019-, PubChem, 2019-)
PD 169316
(ChEBI, 2019-, PubChem, 2019-)
PD-169316
(ChEBI, 2019-, PubChem, 2019-)
PD168316
(PubChem, 2019-)
PD169316
(Gregor et al., 2025, ChEBI, 2019-, PubChem, 2019-)
PubChem:4712
(PubChem, 2019-)
Secondary FlyBase IDs
    References (3)