Details
Stereochemistry | ACHIRAL |
Molecular Formula | C16H12FN3S |
Molecular Weight | 297.35 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
FC1=CC=C(C=C1)C2=C(N3CCSC3=N2)C4=CC=NC=C4
InChI
InChIKey=YOELZIQOLWZLQC-UHFFFAOYSA-N
InChI=1S/C16H12FN3S/c17-13-3-1-11(2-4-13)14-15(12-5-7-18-8-6-12)20-9-10-21-16(20)19-14/h1-8H,9-10H2
Molecular Formula | C16H12FN3S |
Molecular Weight | 297.35 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: P09917 Gene ID: 240.0 Gene Symbol: ALOX5 Target Organism: Homo sapiens (Human) Sources: https://www.ncbi.nlm.nih.gov/pubmed/8831759 |
10.0 µM [IC50] | ||
Target ID: P23219|||Q5T7T7 Gene ID: 5742.0 Gene Symbol: PTGS1 Target Organism: Homo sapiens (Human) Sources: https://www.ncbi.nlm.nih.gov/pubmed/8831759 |
5.4 µM [IC50] | ||
Target ID: CHEMBL2094115 Sources: https://www.ncbi.nlm.nih.gov/pubmed/9525949 |
PubMed
Title | Date | PubMed |
---|---|---|
1-substituted 4-aryl-5-pyridinylimidazoles: a new class of cytokine suppressive drugs with low 5-lipoxygenase and cyclooxygenase inhibitory potency. | 1996 Sep 27 |
|
p38 mitogen-activated protein kinase-dependent and -independent intracellular signal transduction pathways leading to apoptosis in human neutrophils. | 1998 Apr 3 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:34:31 GMT 2023
by
admin
on
Sat Dec 16 09:34:31 GMT 2023
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Record UNII |
9R6QDF1UO7
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Record Status |
Validated (UNII)
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Record Version |
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72873-74-6
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Related Record | Type | Details | ||
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TARGET -> INHIBITOR |