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Journal Abstract Search
142 related items for PubMed ID: 4666087
1. [Research on substances with antineoplastic activity. XLVI. Synthesis of derivatives of 11H-benzo(e)-pyrrolo(1,2-a)-indole and 7H-benzo-(d,e)-pyrrolo-(1,2-a)-quinoline]. Vomero S, Chimenti F, Porretta GC, Giuliano R, Artico M. Farmaco Sci; 1972 Sep; 27(9):786-94. PubMed ID: 4666087 [No Abstract] [Full Text] [Related]
2. Research on compounds with antiblastic activity. 43. Synthesis of 9H-pyrrolo-(1,2-a)-indole derivatives. Artico M, Giuliano R, Porretta GC, Scalzo M. Farmaco Sci; 1972 Jan; 27(1):60-7. PubMed ID: 4666525 [No Abstract] [Full Text] [Related]
13. Synthesis and evaluation of stable bidentate transition metal complexes of 1-(chloromethyl)-5-hydroxy-3-(5,6,7-trimethoxyindol-2-ylcarbonyl)-2,3-dihydro-1H-pyrrolo[3,2-f]quinoline (seco-6-azaCBI-TMI) as hypoxia selective cytotoxins. Milbank JB, Stevenson RJ, Ware DC, Chang JY, Tercel M, Ahn GO, Wilson WR, Denny WA. J Med Chem; 2009 Nov 12; 52(21):6822-34. PubMed ID: 19821576 [Abstract] [Full Text] [Related]
15. Heterocyclic quinones. XVI. Pharmacomodulation in the series of 11H-indolo[3,2-c]quinolinediones: synthesis, cytotoxicity and antitumor activity of 3-substituted 11H-pyrido[3',4':4,5]pyrrolo[3,2-c]quinoline-1,4-diones. Helissey P, Giorgi-Renault S, Renault J, Cros S. Chem Pharm Bull (Tokyo); 1989 Sep 12; 37(9):2413-6. PubMed ID: 2557983 [Abstract] [Full Text] [Related]
19. Design and synthesis of 7H-pyrrolo[2,3-d]pyrimidines as focal adhesion kinase inhibitors. Part 1. Choi HS, Wang Z, Richmond W, He X, Yang K, Jiang T, Sim T, Karanewsky D, Gu XJ, Zhou V, Liu Y, Ohmori O, Caldwell J, Gray N, He Y. Bioorg Med Chem Lett; 2006 Apr 15; 16(8):2173-6. PubMed ID: 16458503 [Abstract] [Full Text] [Related]