Search Results - "CHIARELOTTO, G"

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  1. 1

    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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  2. 2

    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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  3. 3

    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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  4. 4

    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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  5. 5
  6. 6

    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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  7. 7

    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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  8. 8

    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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  9. 9

    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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  10. 10

    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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  11. 11

    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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  12. 12

    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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  13. 13

    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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  14. 14

    Synthesis and characterization of some N-mannich bases of [1,2,3]triazoloquinolines by Ferlin, Maria Grazia, Chiarelotto, Gianfranco, Castagliuolo, Ignazio

    Published in Journal of heterocyclic chemistry (01-07-2002)
    “…Some novel N‐Mannich bases of [1,2,3]‐triazolo[4,5‐f] and [4,5‐h]quinolines were synthesized following the classical experimental procedure for Mannich base…”
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  15. 15
  16. 16

    Synthesis of novel methoxy and hydroxy derivatives of 2-phenyl-1H-benz[g]indoles by Ferlin, Maria Grazia, Chiarelotto, Gianfranco, Malesani, Giorgio

    Published in Journal of heterocyclic chemistry (01-01-1989)
    “…The synthesis of novel methoxy‐derivatives of 2‐phenyl‐1H‐benz[g]indole 3 by condensation of α‐naphthyl‐amines 1 with N‐phenacyl‐pyridinium salts 2 is…”
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  17. 17

    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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  18. 18

    Antimicrobial properties of some 3-acyl-4,7-disubstituted indoles by Malesani, G, Chiarelotto, G, Dall'Acqua, F, Vedaldi, D

    Published in Il Farmaco; edizione scientifica (01-02-1975)
    “…In continuation of research on indole derivatives as potential chemotherapeutic agents, the antimicrobial properties of some 4,7-disubstituted 3-acylindoles…”
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  19. 19

    Carboxylation and acylation of 4,7-dimethoxyindoles and a study of the corresponding dealkylated derivatives by Malesani, Giorgio, Chiarelotto, Gianfranco, Ferlin, Maria Grazia, Masiero, Sergio

    Published in Journal of heterocyclic chemistry (01-05-1981)
    “…Treatment of 4,7‐dimethoxyindoles 1 and 9 with ethylmagnesium bromide and ethyl chloroformate in refluxing dry ether gives the corresponding…”
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  20. 20

    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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