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1983 1
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Page 1
Anticooperativity and Competition in Some Cocrystals Featuring Iodine-Nitrogen Halogen Bonds.
Côté M, Ovens JS, Bryce DL. Côté M, et al. Chem Asian J. 2023 Mar 14;18(6):e202201221. doi: 10.1002/asia.202201221. Epub 2023 Feb 17. Chem Asian J. 2023. PMID: 36688875
We describe the preparation of four cocrystals of 1,3,5-trifluoro-2,4,6-triiodobenzene with N-heterocyclic compounds, namely acridine, 3-aminopyridine, 4-methylaminopyridine, and 1,2-di(4-pyridyl)ethane. The cocrystals, which are characterized by single-crystal and …
We describe the preparation of four cocrystals of 1,3,5-trifluoro-2,4,6-triiodobenzene with N-heterocyclic compounds, namely acridine, 3-ami …
Preparation, Characterization, and Insecticidal Activity of Avermectin-Grafted-Carboxymethyl Chitosan.
Li Y, Qin Y, Liu S, Xing R, Yu H, Li K, Li P. Li Y, et al. Biomed Res Int. 2016;2016:9805675. doi: 10.1155/2016/9805675. Epub 2016 Apr 24. Biomed Res Int. 2016. PMID: 27213156 Free PMC article.
Avermectin-grafted-N,O-carboxymethyl chitosan (NOCC) derivative was obtained by esterification reaction using dicyclohexylcarbodiimide (DCC) as dehydrating agent and 4-methylaminopyridine as catalyst. The structures of the conjugate were confirmed by FT-IR, (1)H NMR …
Avermectin-grafted-N,O-carboxymethyl chitosan (NOCC) derivative was obtained by esterification reaction using dicyclohexylcarbodiimide (DCC) …
Alkylaminopyridine-modified aluminum aminoterephthalate metal-organic frameworks as components of reactive self-detoxifying materials.
Bromberg L, Klichko Y, Chang EP, Speakman S, Straut CM, Wilusz E, Hatton TA. Bromberg L, et al. ACS Appl Mater Interfaces. 2012 Sep 26;4(9):4595-602. doi: 10.1021/am3009696. Epub 2012 Aug 21. ACS Appl Mater Interfaces. 2012. PMID: 22871803
Following MOF attachment and curing, the MOF primary amino groups were functionalized with highly nucleophilic 4-methylaminopyridine (4-MAP) by disuccinimidyl suberate-activated conjugation. ...
Following MOF attachment and curing, the MOF primary amino groups were functionalized with highly nucleophilic 4-methylaminopyridi …
2-aminopyridines as highly selective inducible nitric oxide synthase inhibitors. Differential binding modes dependent on nitrogen substitution.
Connolly S, Aberg A, Arvai A, Beaton HG, Cheshire DR, Cook AR, Cooper S, Cox D, Hamley P, Mallinder P, Millichip I, Nicholls DJ, Rosenfeld RJ, St-Gallay SA, Tainer J, Tinker AC, Wallace AV. Connolly S, et al. J Med Chem. 2004 Jun 3;47(12):3320-3. doi: 10.1021/jm031035n. J Med Chem. 2004. PMID: 15163211
4-Methylaminopyridine (4-MAP) (5) is a potent but nonselective nitric oxide synthase (NOS) inhibitor. ...
4-Methylaminopyridine (4-MAP) (5) is a potent but nonselective nitric oxide synthase (NOS) inhibitor. ...
Restraining the motion of a ligand for modulating the structural phase transition in two isomorphic polar coordination polymers.
Wang BY, Xu WJ, Xue W, Lin RB, Du ZY, Zhou DD, Zhang WX, Chen XM. Wang BY, et al. Dalton Trans. 2014 Jun 28;43(24):9008-11. doi: 10.1039/c4dt00675e. Dalton Trans. 2014. PMID: 24805838
Restraining such motion in an isomorphic compound [Cu(NCS)2(4-MeAPy)2]n (4-MeAPy = 4-methylaminopyridine) results in distinct phase transition behaviour. ...
Restraining such motion in an isomorphic compound [Cu(NCS)2(4-MeAPy)2]n (4-MeAPy = 4-methylaminopyridine) results in distinct …
Metabolism of carcinogenic and non-carcinogenic N-nitroso-N-methylaminopyridines. II. Investigations in vivo.
Heydt-Zapf G, Haubner R, Preussmann R, Eisenbrand G. Heydt-Zapf G, et al. Carcinogenesis. 1983;4(6):729-31. doi: 10.1093/carcin/4.6.729. Carcinogenesis. 1983. PMID: 6688042
Formation of the latter is thought to result from demethylation of the denitrosation product 4-methylaminopyridine. In contrast to metabolism of carcinogenic 2-NMPY, no 4-hydroxypyridine, indicative for activation of 4-NMPY to a diazonium intermediate, was detectabl …
Formation of the latter is thought to result from demethylation of the denitrosation product 4-methylaminopyridine. In contras …
Novel bioactive metabolites of dipyrone (metamizol).
Rogosch T, Sinning C, Podlewski A, Watzer B, Schlosburg J, Lichtman AH, Cascio MG, Bisogno T, Di Marzo V, Nüsing R, Imming P. Rogosch T, et al. Bioorg Med Chem. 2012 Jan 1;20(1):101-7. doi: 10.1016/j.bmc.2011.11.028. Epub 2011 Nov 25. Bioorg Med Chem. 2012. PMID: 22172309 Free PMC article.
[Antagonistic effect of 4-aminopyridine derivatives on dTc induced block].
Amaki Y, Koyama T, Wada T, Kobayashi K, Futaki R. Amaki Y, et al. Masui. 1989 May;38(5):661-5. Masui. 1989. PMID: 2778952 Japanese.
In order to obtain 4-AMP derivatives with less side effect and the same antagonizing effect on dTc block as that of 4-AMP, three types of derivatives were synthesized. They were 4-methylaminopyridine (4-MAMP), 4-dimethylaminopyridine (4-DAMP), and 4-trimethylaminopy …
In order to obtain 4-AMP derivatives with less side effect and the same antagonizing effect on dTc block as that of 4-AMP, three types of de …