Similar articles for PMID: 12005180

Year	Number of Results
1997	6
1998	2
1999	4
2000	6
2001	10
2002	10
2003	11
2004	14
2005	3
2019	1
2024	0

1

The endocrine disruptor nonylphenol preferentially blocks cyclooxygenase-1.

Fujimoto Y, Sakuma S, Inoue T, Uno E, Fujita T. Fujimoto Y, et al. Life Sci. 2002 Mar 29;70(19):2209-14. doi: 10.1016/s0024-3205(01)01538-7. Life Sci. 2002. PMID: 12005180

2

Effects of endocrine disruptors on arachidonic acid metabolism in rabbit platelets.

Fujimoto Y, Sakuma S, Nishiwaki Y, Ikeda M, Fujita T. Fujimoto Y, et al. Toxicol Appl Pharmacol. 2003 Jun 1;189(2):96-9. doi: 10.1016/s0041-008x(03)00095-4. Toxicol Appl Pharmacol. 2003. PMID: 12781627

3

Mechanism of cyclooxygenase-2 inhibition by indanone derivatives.

Klein T, Nüsing RM. Klein T, et al. Adv Exp Med Biol. 1997;407:503-7. doi: 10.1007/978-1-4899-1813-0_75. Adv Exp Med Biol. 1997. PMID: 9321998 No abstract available.

4

Effects of endocrine disruptors on the formation of prostaglandin and arachidonoyl-CoA formed from arachidonic acid in rabbit kidney medulla microsomes.

Fujimoto Y, Usa K, Sakuma S. Fujimoto Y, et al. Prostaglandins Leukot Essent Fatty Acids. 2005 Dec;73(6):447-52. doi: 10.1016/j.plefa.2005.08.002. Epub 2005 Sep 21. Prostaglandins Leukot Essent Fatty Acids. 2005. PMID: 16181777

5

Synthesis, structure-activity relationships, and in vivo evaluations of substituted di-tert-butylphenols as a novel class of potent, selective, and orally active cyclooxygenase-2 inhibitors. 2. 1,3,4- and 1,2,4-thiadiazole series.

Song Y, Connor DT, Sercel AD, Sorenson RJ, Doubleday R, Unangst PC, Roth BD, Beylin VG, Gilbertsen RB, Chan K, Schrier DJ, Guglietta A, Bornemeier DA, Dyer RD. Song Y, et al. J Med Chem. 1999 Apr 8;42(7):1161-9. doi: 10.1021/jm980570y. J Med Chem. 1999. PMID: 10197960

6

Slow-binding inhibition of human prostaglandin endoperoxide synthase-2 with darbufelone, an isoform-selective antiinflammatory di-tert-butyl phenol.

Johnson AR, Marletta MA, Dyer RD. Johnson AR, et al. Biochemistry. 2001 Jun 26;40(25):7736-45. doi: 10.1021/bi002343f. Biochemistry. 2001. PMID: 11412128

7

Biochemical and pharmacological profile of a tetrasubstituted furanone as a highly selective COX-2 inhibitor.

Riendeau D, Percival MD, Boyce S, Brideau C, Charleson S, Cromlish W, Ethier D, Evans J, Falgueyret JP, Ford-Hutchinson AW, Gordon R, Greig G, Gresser M, Guay J, Kargman S, Léger S, Mancini JA, O'Neill G, Ouellet M, Rodger IW, Thérien M, Wang Z, Webb JK, Wong E, Chan CC, et al. Riendeau D, et al. Br J Pharmacol. 1997 May;121(1):105-17. doi: 10.1038/sj.bjp.0701076. Br J Pharmacol. 1997. PMID: 9146894 Free PMC article.

8

Synthesis, structure-activity relationships, and in vivo evaluations of substituted di-tert-butylphenols as a novel class of potent, selective, and orally active cyclooxygenase-2 inhibitors. 1. Thiazolone and oxazolone series.

Song Y, Connor DT, Doubleday R, Sorenson RJ, Sercel AD, Unangst PC, Roth BD, Gilbertsen RB, Chan K, Schrier DJ, Guglietta A, Bornemeier DA, Dyer RD. Song Y, et al. J Med Chem. 1999 Apr 8;42(7):1151-60. doi: 10.1021/jm9805081. J Med Chem. 1999. PMID: 10197959

9

Nonylphenol induces the death of neural stem cells due to activation of the caspase cascade and regulation of the cell cycle.

Kudo C, Wada K, Masuda T, Yonemura T, Shibuya A, Fujimoto Y, Nakajima A, Niwa H, Kamisaki Y. Kudo C, et al. J Neurochem. 2004 Mar;88(6):1416-23. doi: 10.1046/j.1471-4159.2003.02270.x. J Neurochem. 2004. PMID: 15009642 Free article.

10

3-(2-Methoxytetrahydrofuran-2-yl)pyrazoles: a novel class of potent, selective cyclooxygenase-2 (COX-2) inhibitors.

Ranatunge RR, Earl RA, Garvey DS, Janero DR, Letts LG, Martino AM, Murty MG, Richardson SK, Schwalb DJ, Young DV, Zemtseva IS. Ranatunge RR, et al. Bioorg Med Chem Lett. 2004 Dec 20;14(24):6049-52. doi: 10.1016/j.bmcl.2004.09.073. Bioorg Med Chem Lett. 2004. PMID: 15546727

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