Search Results - "FERLIN, M. G"

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  1. 1

    Discovery of a new anilino-3H-pyrrolo[3,2-f]quinoline derivative as potential anti-cancer agent by VIA, L. Dalla, GIA, O, GASPAROTTO, V, FERLIN, M. G

    Published in European journal of medicinal chemistry (01-02-2008)
    “…The newly synthesized 1-[4-(3H-pyrrolo[3,2-f]quinolin-9-ylamino)-phenyl]-ethanone hydrochloride showed high antiproliferative activity by mixed mechanisms of…”
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  2. 2

    Novel Pyrrolo[3,2- f]quinolines: Synthesis and Antiproliferative Activity by Ferlin, M.G, Gatto, B, Chiarelotto, G, Palumbo, M

    Published in Bioorganic & medicinal chemistry (01-07-2001)
    “…Novel pyrrolo[3,2, f]quinoline derivatives have been synthesized and tested as antiproliferative agents. They are characterized by an angular aromatic…”
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  3. 3

    Pyrrolo-quinoline derivatives as potential antineoplastic drugs by FERLIN, M. G, GATTO, B, CHIARELOTTO, G, PALUMBO, M

    Published in Bioorganic & medicinal chemistry (01-06-2000)
    “…Some novel pyrrolo-quinoline derivatives have been synthesized as potential antineoplastic agents. They contain an angular aromatic tricyclic or tetracyclic…”
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  4. 4

    Synthesis and antiproliferative activity of some new DNA-targeted alkylating pyrroloquinolines by Ferlin, M.G., Dalla Via, L., Gia, O.M.

    Published in Bioorganic & medicinal chemistry (15-02-2004)
    “…Two novel DNA-direct alkylating agents, consisting of aniline mustard linked to an angular 3H-pyrrolo[3,2- f]quinoline nucleus, were synthetized and assayed…”
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  5. 5

    Synthesis and antiproliferative activity of some variously substituted acridine and azacridine derivatives by FERLIN, M. G, MARZANO, C, CHIARELOTTO, G, BACCICHETTI, F, BORDIN, F

    Published in European journal of medicinal chemistry (01-09-2000)
    “…A group of 9-substituted acridine and azacridine derivatives (m-AMSA analogues) were synthesised following classical procedures as potential antitumour agents…”
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  6. 6
  7. 7

    Synthesis and biological properties of a new series of N-pyrido substituted tetrahydrocarbazoles by Ferlin, M.G., Chiarelotto, G., Marzano, C., Severin, E., Baccichetti, F., Carlassare, F., Simonato, M., Bordin, F.

    Published in Farmaco (Società chimica italiana : 1989) (30-06-1998)
    “…A series of methyl and ethyl quaternary pyridiniumtetrahydrocarbazoles was synthesized and studied in comparison with ellipticine, chosen as a reference. In…”
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  8. 8

    Antiproliferative activity of some unsubstituted angular analogoues of ellipticine by Ferlin, M G, Chiarelotto, G, Marzano, C, Mobilio, S, Carlassare, F, Baccichetti, F

    Published in Farmaco (Società chimica italiana : 1989) (01-02-1995)
    “…With the aim of obtaining further knowledge on the antiproliferative activity of pyrroloquinolines and isoquinolines, we prepared four unsubstituted angular…”
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  9. 9

    New mono- and bis-intercalating compounds between DNA base pairs by Chiarelotto, G, Ferlin, M G, Vedaldi, D, Dall'Acqua, F, Rodighiero, G

    Published in Farmaco (Società chimica italiana : 1989) (01-06-1993)
    “…With the aim to obtain new bis-intercalating agents in DNA a series of compounds was prepared linking two identical tricyclic moieties (two…”
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  10. 10

    A mass spectrometric investigation on some 4,7-dioxo-4,5,6,7-tetrahydroindole derivatives by Bertazzo, A., Ferlin, M. G., Chiarelotto, G., Catinella, S., Traldi, P.

    Published in Journal of heterocyclic chemistry (01-12-1993)
    “…The mass spectrometric behaviour of a series of 2‐aryl substituted 4,7‐dioxo‐4,5,6,7‐tetrahydroindoles has been studied in different ionization conditions…”
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  11. 11

    2-substituted 1H-pyrrolo [3,2-h] quinoline derivatives: synthesis and aspects of their biological activity by Ferlin, M G, Chiarelotto, G, Baccichetti, F, Carlassare, F, Toniolo, L, Bordin, F

    Published in Farmaco (Società chimica italiana : 1989) (01-12-1992)
    “…Certain 2-substituted 1H-pyrrolo [3,2-h] quinolines have been prepared and their biological activity in mammalian cells and in some microorganisms have been…”
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  12. 12

    Preparation and antiproliferative activity of 1H-pyrrolo [2,3-f]quinolinium and isoquinolinium iodides by Ferlin, M G, Chiarelotto, G, Gia, O, Baccichetti, F, Carlassare, F

    Published in Farmaco (Società chimica italiana : 1989) (01-06-1991)
    “…2-Carbomethoxy-N-methyl-1H-pyrrolo[2,3-f]quinolinium and isoquinolinium iodides were prepared. Their in vitro ability to form complexes with DNA is enhanced in…”
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  13. 13

    1H-pyrrolo[2,3-f]quinoline and isoquinoline derivatives: synthesis and antiproliferative activity by Ferlin, M G, Chiarelotto, G, Basadonna, O, Gia, O, Mobilio, S, Baccichetti, F, Carlassare, F

    Published in Farmaco (Società chimica italiana : 1989) (01-12-1989)
    “…Fischer indol synthesis is reported for the preparation of some 2-substituted 1H-pyrrolo[2,3-f]quinoline and isoquinoline derivatives having a structural…”
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  14. 14

    Synthesis of 4,8-dimethoxy-3H-benz[f]indol-3-one. Anomalous behaviour to cyclization of 1,4,5-trimethoxy-3-amino-γ-chloroalkylnaphthalene intermediates by Malesani, Giorgio, Ferlin, Maria Grazia

    Published in Journal of heterocyclic chemistry (01-03-1987)
    “…A new linear benz[f]indole derivative 15 bearing two methoxyls in the fused naphthalene moiety was prepared as a potential chemotherapeutic agent. The…”
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  15. 15

    Synthesis and in Vitro and in Vivo Antitumor Activity of 2-Phenylpyrroloquinolin-4-ones by Ferlin, Maria Grazia, Chiarelotto, Gianfranco, Gasparotto, Venusia, Dalla Via, Lisa, Pezzi, Vincenzo, Barzon, Luisa, Palù, Giorgio, Castagliuolo, Ignazio

    Published in Journal of medicinal chemistry (05-05-2005)
    “…In our search for potential new anticancer drugs, we designed and synthesized a series of tricyclic compounds containing the antimitotic 2-phenylazaflavone…”
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  16. 16

    Synthesis of 4,9-dimethoxy-1H-benz[f]indole by Malesani, Giorgio, Ferlin, Maria Grazia

    Published in Journal of heterocyclic chemistry (01-07-1985)
    “…A three‐step synthesis of 4,9‐dimethoxy‐1H‐benz[f]indole (4) starting from 1,4‐dimethoxy‐2‐aminonaphthalene (1) is described. Compound 1 was condensed with…”
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  17. 17

    Electrocatalytic reduction of arylethyl chlorides at silver cathodes in the presence of carbon dioxide: Synthesis of 2-arylpropanoic acids by Isse, Abdirisak Ahmed, Ferlin, Maria Grazia, Gennaro, Armando

    “…The electrochemical reduction of some arylethyl chlorides ArCH(CH 3)Cl (Ar = 4-isobutylphenyl, 3-phenoxyphenyl, 6-methoxy-2-naphthyl), which are used as…”
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  18. 18

    Novel anellated pyrazoloquinolin-3-ones: synthesis and in vitro BZR activity by Ferlin, Maria Grazia, Chiarelotto, Gianfranco, Dall’Acqua, Stefano, Maciocco, Elisabetta, Mascia, Maria Paola, Pisu, Maria Giuseppina, Biggio, Giovanni

    Published in Bioorganic & medicinal chemistry (16-05-2005)
    “…New pyrazolopyrroloquinolinones were synthesized and showed high affinity for central BZRs acting as antagonists. None turned out to be active in inhibiting…”
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  19. 19

    Bis-pyridoquinolines as new bifunctional intercalators for DNA by Malesani, G, Chiarelotto, G, Ferlin, M G, Bordin, F, Baccichetti, F, Carlassare, F, Vedaldi, D, Dall'Acqua, F

    Published in Il Farmaco; edizione scientifica (01-11-1984)
    “…With the aim of obtaining new bifunctional intercalators for DNA, a new series of bis-pyridoquinolines were synthesized by joining two tricyclic planar…”
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  20. 20

    Mannich bases of 3H-pyrrolo[3,2-f]quinoline having vasorelaxing activity by FERLIN, Maria Grazia, CHIARELOTTO, Gianfranco, ANTONUCCI, Francesca, CAPARROTTA, Laura, FROLDI, Guglielmina

    Published in European journal of medicinal chemistry (01-05-2002)
    “…Mannich bases obtained by aminoalkylation of 3H-pyrrolo[3,2-f]quinoline were designed and prepared as potential vasorelaxing agents. Compounds Ia-Va were…”
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