Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C14H16N2 |
| Molecular Weight | 212.2902 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC(N)=C(NCC2=CC=CC=C2)C=C1
InChI
InChIKey=BXKFJRIHXLNJPC-UHFFFAOYSA-N
InChI=1S/C14H16N2/c1-11-7-8-14(13(15)9-11)16-10-12-5-3-2-4-6-12/h2-9,16H,10,15H2,1H3
| Molecular Formula | C14H16N2 |
| Molecular Weight | 212.2902 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Suppressive effect of novel aromatic diamine compound on nuclear factor-kappaB-dependent expression of inducible nitric oxide synthase in macrophages. | 2005-10-03 |
|
| Anti-inflammatory benzene diamine compound inhibited toll-like receptor 4-mediated inducible nitric oxide synthase expression and nuclear factor-kappa B activation. | 2005-05 |
|
| Anti-inflammatory effects of N1-benzyl-4-methylbenzene-1,2-diamine (JSH-21) analogs on nitric oxide production and nuclear factor-kappa B transcriptional activity in lipopolysaccharide-stimulated macrophages RAW 264.7. | 2004-10 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:40:50 GMT 2025
by
admin
on
Mon Mar 31 23:40:50 GMT 2025
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| Record UNII |
1JB5C96T8S
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| Record Status |
Validated (UNII)
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| Record Version |
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1JB5C96T8S
Created by
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10727275
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39235-93-3
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admin on Mon Mar 31 23:40:50 GMT 2025 , Edited by admin on Mon Mar 31 23:40:50 GMT 2025
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DTXSID501254833
Created by
admin on Mon Mar 31 23:40:50 GMT 2025 , Edited by admin on Mon Mar 31 23:40:50 GMT 2025
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