n-(3-(aminomethyl)benzyl)acetamidine has been researched along with Acute Liver Injury, Drug-Induced in 1 studies
N-(3-(aminomethyl)benzyl)acetamidine: structure in first source
N-[3-(aminomethyl)benzyl]acetamidine : An aralkylamine that is Nbenzylacetamidine substituted at position 3 on the benzene ring by an aminomethyl group. An inhibitor of nitric oxide synthase.
| Excerpt | Relevance | Reference |
|---|---|---|
| " Nitric oxide can combine with superoxide to form peroxynitrite, a molecule that may participate in the toxic mechanisms of hepatotoxins, such as acetaminophen and bacterial endotoxin." | 1.31 | iNOS-null mice are not resistant to cadmium chloride-induced hepatotoxicity. ( Harstad, EB; Klaassen, CD, 2002) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Harstad, EB | 1 |
| Klaassen, CD | 1 |
1 other study available for n-(3-(aminomethyl)benzyl)acetamidine and Acute Liver Injury, Drug-Induced
| Article | Year |
|---|---|
iNOS-null mice are not resistant to cadmium chloride-induced hepatotoxicity.
Topics: Alanine Transaminase; Amidines; Animals; Benzylamines; Cadmium Chloride; Chemical and Drug Induced L | 2002 |