82 related articles for article (PubMed ID: 3136917)
1. Structure-activity relationships defining the cytotoxicity of catechol analogues against human malignant melanoma.
Kern DH; Shoemaker RH; Hildebrand-Zanki SU; Driscoll JS
Cancer Res; 1988 Sep; 48(18):5178-82. PubMed ID: 3136917
[TBL] [Abstract][Full Text] [Related]
2. Synthesis and antimelanoma activity of sterically congested tertiary amide analogues of N-acetyl-4-S-cysteaminylphenol.
Ferguson J; Rogers PM; Kelland LR; Robins DJ
Oncol Res; 2005; 15(2):87-94. PubMed ID: 16119006
[TBL] [Abstract][Full Text] [Related]
3. Synthesis and anti-melanoma activity of analogues of N-acetyl-4-S-cysteaminylphenol substituted with two methyl groups alpha to the nitrogen.
Lant NJ; McKeown P; Timoney MC; Kelland LR; Rogers PM; Robins DJ
Anticancer Drug Des; 2001 Feb; 16(1):49-55. PubMed ID: 11762644
[TBL] [Abstract][Full Text] [Related]
4. Comparison of in vitro cytotoxicity of N-acetyl and N-propionyl derivatives of phenolic thioether amines in melanoma and neuroblastoma cells and the relationship to tyrosinase and tyrosine hydroxylase enzyme activity.
Gili A; Thomas PD; Ota M; Jimbow K
Melanoma Res; 2000 Feb; 10(1):9-15. PubMed ID: 10711635
[TBL] [Abstract][Full Text] [Related]
5. The effect of functional groups on reduction and activation of quinone bioreductive agents by DT-diaphorase.
Fourie J; Oleschuk CJ; Guziec F; Guziec L; Fiterman DJ; Monterrosa C; Begleiter A
Cancer Chemother Pharmacol; 2002 Feb; 49(2):101-10. PubMed ID: 11862423
[TBL] [Abstract][Full Text] [Related]
6. Increase in melanin formation and promotion of cytotoxicity in cultured melanoma cells caused by phosphorylated isomers of L-dopa.
Pawelek JM; Murray M
Cancer Res; 1986 Feb; 46(2):493-7. PubMed ID: 3079662
[TBL] [Abstract][Full Text] [Related]
7. Analogues of N-hydroxy-N'-phenylthiourea and N-hydroxy-N'-phenylurea as inhibitors of tyrosinase and melanin formation.
Criton M; Le Mellay-Hamon V
Bioorg Med Chem Lett; 2008 Jun; 18(12):3607-10. PubMed ID: 18501598
[TBL] [Abstract][Full Text] [Related]
8. Data mining the NCI cancer cell line compound GI(50) values: identifying quinone subtypes effective against melanoma and leukemia cell classes.
Marx KA; O'Neil P; Hoffman P; Ujwal ML
J Chem Inf Comput Sci; 2003; 43(5):1652-67. PubMed ID: 14502500
[TBL] [Abstract][Full Text] [Related]
9. Analogues of N alpha-(4-amino-4-deoxypteroyl)-N delta-hemiphthaloyl-L-ornithine (PT523) modified in the side chain: synthesis and biological evaluation.
Rosowsky A; Vaidya CM; Bader H; Wright JE; Teicher BA
J Med Chem; 1997 Jan; 40(3):286-99. PubMed ID: 9022795
[TBL] [Abstract][Full Text] [Related]
10. Synthesis and antimelanoma activity of analogues of N-acetyl-4-S-cysteaminylphenol.
Lant NJ; McKeown P; Kelland LR; Rogers PM; Robins DJ
Anticancer Drug Des; 2000 Aug; 15(4):295-302. PubMed ID: 11200505
[TBL] [Abstract][Full Text] [Related]
11. Synthesis and potent antifolate activity and cytotoxicity of B-ring deaza analogues of the nonpolyglutamatable dihydrofolate reductase inhibitor Nalpha-(4-amino-4-deoxypteroyl)-Ndelta-hemiphthaloyl- L-ornithine (PT523).
Rosowsky A; Wright JE; Vaidya CM; Bader H; Forsch RA; Mota CE; Pardo J; Chen CS; Chen YN
J Med Chem; 1998 Dec; 41(26):5310-9. PubMed ID: 9857098
[TBL] [Abstract][Full Text] [Related]
12. Inhibition of human melanoma growth by prostaglandin A, D, and J analogues.
Bregman MD; Funk C; Fukushima M
Cancer Res; 1986 Jun; 46(6):2740-4. PubMed ID: 3698005
[TBL] [Abstract][Full Text] [Related]
13. Apoptosis induction by 4-nerolidylcatechol in melanoma cell lines.
Brohem CA; Sawada TC; Massaro RR; Almeida RL; Rivelli DP; Ropke CD; da Silva VV; de Lima TM; Curi R; Barros SB; Maria-Engler SS
Toxicol In Vitro; 2009 Feb; 23(1):111-9. PubMed ID: 19059332
[TBL] [Abstract][Full Text] [Related]
14. Tyrosinase-mediated cytotoxicity of 4-substituted phenols: quantitative structure-thiol-reactivity relationships of the derived o-quinones.
Cooksey CJ; Land EJ; Ramsden CA; Riley PA
Anticancer Drug Des; 1995 Mar; 10(2):119-29. PubMed ID: 7710634
[TBL] [Abstract][Full Text] [Related]
15. Chemical transformations of oxyresveratrol (trans-2,4,3',5'-tetrahydroxystilbene) into a potent tyrosinase inhibitor and a strong cytotoxic agent.
Likhitwitayawuid K; Sornsute A; Sritularak B; Ploypradith P
Bioorg Med Chem Lett; 2006 Nov; 16(21):5650-3. PubMed ID: 16919455
[TBL] [Abstract][Full Text] [Related]
16. Effects of latanoprost on tyrosinase activity and mitotic index of cultured melanoma lines.
Dutkiewicz R; Albert DM; Levin LA
Exp Eye Res; 2000 May; 70(5):563-9. PubMed ID: 10870514
[TBL] [Abstract][Full Text] [Related]
17. Evaluation of the in vivo antitumor activity and in vitro cytotoxic properties of auranofin, a coordinated gold compound, in murine tumor models.
Mirabelli CK; Johnson RK; Sung CM; Faucette L; Muirhead K; Crooke ST
Cancer Res; 1985 Jan; 45(1):32-9. PubMed ID: 3917372
[TBL] [Abstract][Full Text] [Related]
18. Synthesis and evaluation of N-acylamino acids derivatives of triazenes. Activation by tyrosinase in human melanoma cell lines.
Monteiro AS; Almeida J; Cabral G; Severino P; Videira PA; Sousa A; Nunes R; Pereira JD; Francisco AP; Perry MJ; Mendes E
Eur J Med Chem; 2013; 70():1-9. PubMed ID: 24125877
[TBL] [Abstract][Full Text] [Related]
19. Effects of novel spermine analogues on cell cycle progression and apoptosis in MALME-3M human melanoma cells.
Kramer DL; Fogel-Petrovic M; Diegelman P; Cooley JM; Bernacki RJ; McManis JS; Bergeron RJ; Porter CW
Cancer Res; 1997 Dec; 57(24):5521-7. PubMed ID: 9407962
[TBL] [Abstract][Full Text] [Related]
20. Tyrosine kinase inhibitors. 6. Structure-activity relationships among N- and 3-substituted 2,2'-diselenobis(1H-indoles) for inhibition of protein tyrosine kinases and comparative in vitro and in vivo studies against selected sulfur congeners.
Showalter HD; Sercel AD; Leja BM; Wolfangel CD; Ambroso LA; Elliott WL; Fry DW; Kraker AJ; Howard CT; Lu GH; Moore CW; Nelson JM; Roberts BJ; Vincent PW; Denny WA; Thompson AM
J Med Chem; 1997 Feb; 40(4):413-26. PubMed ID: 9046331
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
