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PUBMED FOR HANDHELDS

Journal Abstract Search

121 related items for PubMed ID: 6069771

  • 1. Ring-D-bridged steroid analogs. V. 14-alpha,17-alpha-etheno-15,16-di(trifluoromethyl)pregna-4,15-diene-3,20-dione and 14-alpha,17-alpha-ethano-15-beta,16-beta-di(trifluoromethyl)pregn-4-ene-3,20-dione.
    Solo AJ, Singh B.
    J Med Chem; 1967 Nov; 10(6):1048-51. PubMed ID: 6069771
    [No Abstract] [Full Text] [Related]

  • 2. Investigations on sterols. 39. Synthesis and progestational activities of some 16-methylene-17 -acetoxy-9 ,10 -pregna-4,6-diene-3,20-dione derivatives.
    Hartog J, Wittelaar JI, Morsink L, de Wachter AM.
    J Med Chem; 1972 Dec; 15(12):1292-7. PubMed ID: 4635977
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  • 4. Ring D bridged steroid analogs. 11. The high Clauberg activity of 19-nor-14, 17-ethano-4-pregnene-3,20-dione.
    Solo AJ, Kapoor JN.
    J Med Chem; 1973 Mar; 16(3):270-3. PubMed ID: 4733110
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  • 6. Ring-d-bridged steroid analogs. II. 14-alpha, 17-alpha-etheno-16-alpha-carbomethoxypregn-4-ene-3, 20-dione.
    Solo AJ, Singh B.
    J Med Chem; 1966 Mar; 9(2):179-81. PubMed ID: 5916499
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  • 7. Synthesis and biological activity of some 6,7-dihalo-delta5-pregnenes and some 6,6-dihalo-5,7-cyclo-5beta-pregnane derivatives.
    Rosen P, Boris A, Karasiewicz R.
    J Med Chem; 1974 Feb; 17(2):182-4. PubMed ID: 4809254
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  • 13. Synthesis of 6-chloro-16-methylene-17-alpha-- hydroxy-21-fluoro-4,6-pregnadiene-3,20-dione 17-acetate, a potent progestational agent.
    Popper TL, Carlon FE, Shapiro EL, Neri R.
    J Med Chem; 1971 Jan; 14(1):33-5. PubMed ID: 5539741
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  • 14. Sustained release hormonal preparations. 3. Biological effectivness of 6-methyl-17-alpha-acetoxypregna-4,6-diene-3,20-dione.
    Chang CC, Kincl FA.
    Steroids; 1968 Dec; 12(6):689-96. PubMed ID: 5726404
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  • 16. Antiandrogenic and antiuterotropic activities of three synthetic progestagens.
    McKinney GR, Braselton JP.
    Steroids; 1970 Mar; 15(3):405-11. PubMed ID: 5461225
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  • 17. Ring-D-bridged steroid analogs. X. Synthesis and nuclear magnetic resonance spectral properties of 3 -acetoxy-14 ,17 -ethano-5,15-pregnadien-20-one, 3 -acetoxy-14 ,17 -ethano-5-pregnen-20-one, and 3 -acetoxy-16,16'-cyclo-14 ,17 -ethano-5-pregnen-20-one.
    Solo AJ, Eng S, Singh B.
    J Org Chem; 1972 Nov 03; 37(22):3542-3. PubMed ID: 5077646
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  • 20. Preparation of 7-chloro steroids.
    Guthrie RW, Boris A, Mennona FA, Mullin JG, Kierstead RW.
    J Med Chem; 1973 Jan 03; 16(1):65-8. PubMed ID: 4682203
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