PubMed (MeSH Keyword) for id: 7048

Year	Number of Results
1985	1
1991	2
1994	1
1995	1
1996	2
1999	1
2002	1
2004	3
2005	1
2006	2
2008	1
2009	1
2010	1
2011	3
2014	1
2015	1
2016	1
2017	1
2020	1
2024	0

1

Carcinogenicity of some aromatic amines and related compounds.

IARC Monographs Vol 127 group. IARC Monographs Vol 127 group. Lancet Oncol. 2020 Aug;21(8):1017-1018. doi: 10.1016/S1470-2045(20)30375-2. Epub 2020 Jun 25. Lancet Oncol. 2020. PMID: 32593317 No abstract available.

2

2-Nitroanisole-induced oxidative DNA damage in Salmonella typhimurium and in rat urinary bladder cells.

Wada K, Katoh Y, Ohnuma-Koyama A, Takahashi N, Yamada M, Matsumoto K. Wada K, et al. Mutat Res Genet Toxicol Environ Mutagen. 2017 Apr;816-817:18-23. doi: 10.1016/j.mrgentox.2017.03.002. Epub 2017 Mar 27. Mutat Res Genet Toxicol Environ Mutagen. 2017. PMID: 28464992

3

Immunohistochemical Expression of Cyclin D1, Cytokeratin 20, and Uroplakin III in Proliferative Urinary Bladder Lesions Induced by o-Nitroanisole in Fischer 344/N Rats.

Willson CJ, Flake GP, Sills RC, Kissling GE, Cesta MF. Willson CJ, et al. Vet Pathol. 2016 May;53(3):682-90. doi: 10.1177/0300985815603432. Epub 2015 Aug 28. Vet Pathol. 2016. PMID: 26319780

4

Theoretical and experimental calculations, Mulliken charges and thermodynamic properties of 4-chloro-2-nitroanisole.

Arunagiri C, Arivazhagan M, Subashini A, Maruthaiveeran N. Arunagiri C, et al. Spectrochim Acta A Mol Biomol Spectrosc. 2014 Oct 15;131:647-56. doi: 10.1016/j.saa.2014.03.116. Epub 2014 Apr 16. Spectrochim Acta A Mol Biomol Spectrosc. 2014. PMID: 24915766

5

FT-IR and FT-Raman spectroscopic investigation, computed vibrational frequency analysis and IR intensity and Raman activity peak resemblance analysis on 2-nitroanisole using HF and DFT (B3LYP and B3PW91) calculations.

Prabhu T, Periandy S, Ramalingam S. Prabhu T, et al. Spectrochim Acta A Mol Biomol Spectrosc. 2011 Dec;83(1):8-16. doi: 10.1016/j.saa.2011.04.004. Epub 2011 Apr 29. Spectrochim Acta A Mol Biomol Spectrosc. 2011. PMID: 21963192

6

Human cytochrome-P450 enzymes metabolize N-(2-methoxyphenyl)hydroxylamine, a metabolite of the carcinogens o-anisidine and o-nitroanisole, thereby dictating its genotoxicity.

Naiman K, Martínková M, Schmeiser HH, Frei E, Stiborová M. Naiman K, et al. Mutat Res. 2011 Dec 24;726(2):160-8. doi: 10.1016/j.mrgentox.2011.09.010. Epub 2011 Sep 18. Mutat Res. 2011. PMID: 21946300

7

o-Nitroanisole.

National Toxicology Program. National Toxicology Program. Rep Carcinog. 2011;12:285-6. Rep Carcinog. 2011. PMID: 21860492 Free article. No abstract available.

8

Identification of rat cytochromes P450 metabolizing N-(2-methoxyphenyl)hydroxylamine, a human metabolite of the environmental pollutants and carcinogens o-anisidine and o-nitroanisole.

Naiman K, Frei E, Stiborova M. Naiman K, et al. Neuro Endocrinol Lett. 2010;31 Suppl 2:36-45. Neuro Endocrinol Lett. 2010. PMID: 21187827

9

o-Nitroanisole.

[No authors listed] [No authors listed] Rep Carcinog. 2004;11:III185-6. Rep Carcinog. 2004. PMID: 21089917 No abstract available.

10

Rat cytochromes P450 oxidize 2-nitrophenol, a human metabolite of carcinogenic 2-nitroanisole.

Svobodova M, Martinkova M, Dracinska H, Frei E, Stiborova M. Svobodova M, et al. Neuro Endocrinol Lett. 2009;30 Suppl 1:46-51. Neuro Endocrinol Lett. 2009. PMID: 20027144

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