E. Bisagni

发表

A new series of pyridinone derivatives as potent non-nucleoside human immunodeficiency virus type 1 specific reverse transcriptase inhibitors.

C. Nguyen, M. Andreola, V. Dollé, 1995, Journal of medicinal chemistry.

Synthesis and antiviral activity of 4-benzyl pyridinone derivatives as potent and selective non-nucleoside human immunodeficiency virus type 1 reverse transcriptase inhibitors.

C. Nguyen, M. Andreola, V. Dollé, 2000, Journal of medicinal chemistry.

Synthesis and 13C, 15N NMR study of a new functionalized pyrido[2,3‐b]indole derivative

J. Buisson, C. Monneret, E. Bisagni, 1996 .

In Vitro Evaluation of a Novel 2,6,9‐Trisubstituted Purine Acting As a Cyclin‐Dependent Kinase Inhibitor

L. Meijer, S. Leclerc, V. Favaudon, 1999, Annals of the New York Academy of Sciences.

Synthesis of C2 alkynylated purines, a new family of potent inhibitors of cyclin-dependent kinases.

L Meijer, L. Meijer, S. Leclerc, 1998, Bioorganic & medicinal chemistry letters.

Sequence-specific artificial photo-induced endonucleases based on triple helix-forming oligonucleotides

C. Giovannangeli, T. Doan, C. Hélène, 1990, Nature.

Rational design of a triple helix-specific intercalating ligand.

C. Nguyen, C. Hélène, E. Bisagni, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Binding geometries of triple helix selective benzopyrido [4,3-b]indole ligands complexed with double- and triple-helical polynucleotides

B. Nordén, C. Nguyen, Jian-sheng Sun, 1997 .

Triple helix-specific ligands.

M. Rougée, J. Mergny, C. Nguyen, 1992, Science.

Stabilization of triple helical DNA by a benzopyridoquinoxaline intercalator.

M. Waring, C. Bailly, C. Nguyen, 1996, Biochemistry.

Photosensitized cross-linking and cleavage of pBR322 and M13 DNA: comparison of 4,4',6-trimethylangelicin and 3-carbethoxypsoralen.

D. Averbeck, J. Kagan, F. Dall'acqua, 1994, Journal of photochemistry and photobiology. B, Biology.

Photochemotherapy (PUVA) of psoriasis using 3‐carbethoxypsoralen, a non‐carcinogenic compound in mice

D. Averbeck, E. Moustacchi, L. Dubertret, 1979, The British journal of dermatology.

Five-coordinate iron(II) porphyrins derived from meso-α,β,γ,δ tetraphenylporphin: synthesis, characterization, and coordinating properties

M. Rougée, M. Momenteau, E. Bisagni, 1979 .

A new route to 2,5-diamino-4,6-dichloropyrimidine, a key precursor of 9-substituted guanines

E. Bisagni, M. Legraverend, H. Boumchita, 1990 .

Synthesis of new (+-)-3,5-dihydroxypentyl nucleoside analogues from 1-amino-5-(benzyloxy)pentan-3-ol and their antiviral evaluation.

M. Lemaitre, E. Bisagni, M. Legraverend, 1990, Journal of medicinal chemistry.

Synthesis of C2 Alkynylated Purines, a New Family of Potent Inhibitors of Cyclin‐Dependent Kinases.

L. Meijer, S. Leclerc, E. Bisagni, 1998 .

In vitro cytotoxicity of S16020-2, a new olivacine derivative

E. Bisagni, A. Pierré, S. Léonce, 2004, Investigational New Drugs.

Sequence-selective binding of an ellipticine derivative to DNA.

M. Waring, C. Bailly, J. Hénichart, 1990, Nucleic acids research.

Genistein analogues: effects on epidermal growth factor receptor tyrosine kinase and on stress-activated pathways.

A. Jacquemin-Sablon, A. Croisy, E. Bisagni, 1997, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

5-Methoxypsoralen, the melanogenic additive in sun-tan preparations, is tumorigenic in mice exposed to 365 nm u.v. radiation.

E. Bisagni, F. Zajdela, 1981, Carcinogenesis.

Alternate strand recognition of double-helical DNA by (T,G)-containing oligonucleotides in the presence of a triple helix-specific ligand.

T. de Bizemont, E. Bisagni, T. Garestier, 1996, Nucleic acids research.

Self-association and DNA-binding properties of two triple helix-specific ligands: comparison of a benzo[e]pyridoindole and a benzo[g]pyridoindole

D. S. Pilch, C. Nguyen, Jian-sheng Sun, 1993 .

Two-photon ionisation of the antitumor drug pazelliptine (BD40) by 355 nm laser photolysis.

M. Fontaine‐Aupart, E. Bisagni, C. Rivalle, 1993, Journal of photochemistry and photobiology. B, Biology.

Premiere synthese de methyl-4-5h- pyrido ¦3',4':4,5¦pyrrolo ¦3,2-c¦pyridines, analogues tricycliques des aza-9 ellipticines

E. Bisagni, N. C. Hung, 1986 .

Imidazo[1,5-g][1,4]diazepines, TIBO analogues lacking the phenyl ring: synthesis and evaluation as anti-HIV agents.

C. Monneret, D. Grierson, A. Aubertin, 1996 .

Synthesis and Antiviral Evaluation of Two New Carbocyclic Pyrrolo [2,3-d] Pyrimidine Nucleosides

M. Lemaitre, E. Bisagni, M. Legraverend, 1990 .

Localized chemical reactivity in double-stranded DNA associated with the intercalative binding of benzo[e]pyridoindole and benzo[g]pyridoindole triple-helix-stabilizing ligands.

M. Waring, C. Bailly, C. Marchand, 1995, European journal of biochemistry.

Stimulation by γ-carboline derivatives (simplified analogues of antitumor ellipticines) of site specific DNA cleavage by calf DNA topoisomerase II

C. Nguyen, C. Paoletti, P. Fossé, 1990 .

SPECTROSCOPIC PROPERTIES OF PSORALEN DERIVATIVES SUBSTITUTED BY CARBETHOXY GROUPS AT THE 3,4 AND/OR 4,5' REACTION SITE

D. Averbeck, P. Vigny, F. Gaboriau, 1979 .

Recognition and photo-induced cleavage and cross-linking of nucleic acids by oligonucleotides covalently linked to ellipticine.

E. Bisagni, N. Thuong, U. Asseline, 1991, Antisense research and development.

Synthesis and evaluation of "AZT-HEPT", "AZT-pyridinone", and "ddC-HEPT" conjugates as inhibitors of HIV reverse transcriptase.

C. Nguyen, C. Monneret, D. Grierson, 2000, Journal of medicinal chemistry.

Synthesis and antitumor activity of 1-[[(dialkylamino)alkyl]amino]-4-methyl-5H-pyrido[4,3-b]benzo[e]- and -benzo[g])indoles. A new class of antineoplastic agents.

C. Nguyen, E. Bisagni, F. Lavelle, 1990, Journal of medicinal chemistry.

On the methylation of 3-cyano-6-hydroxypyridine-2(1H)-ones

E. Bisagni, M. Legraverend, Y. Janin, 1999 .

Diphenyl quinolines and isoquinolines: synthesis and primary biological evaluation.

G. Leclercq, P. Ducrot, D. Carrez, 2000, Bioorganic & medicinal chemistry.

A new route to [g]-fused 5-methyl-1-functionalized isoquinolines

E. Bisagni, M. Rautureau, 1987 .

NEW HETEROCYCLIC REARRANGEMENT: TRANSFORMATION OF 1-SUBSTITUTED 4-(ALKYLAMINO)-1H-PYRROLO(3,2-C)PYRIDINES INTO 1-SUBSTITUTED 4-(ALKYLAMINO)-1H-PYRROLO(2,3-B)PYRIDINES (5-AZA TO 7-AZAINDOLES)

E. Bisagni, M. Legraverend, J. Lhoste, 1982 .

Intoplicine (RP 60475) and its derivatives, a new class of antitumor agents inhibiting both topoisomerase I and II activities.

C. Nguyen, A. Larsen, J. Riou, 1993, Cancer research.

Synthesis of 4‐methylfuro[3′,2′:5,6]benzofuro[3,2‐c]pyridine

E. Bisagni, J. Morón, 1986 .

Spectroscopic study of the interaction of pazelliptine with nucleic acids.

M. Fontaine‐Aupart, E. Bisagni, É. Renault, 1997, Journal of photochemistry and photobiology. B, Biology.

Synthesis and evaluation of new 6-amino-substituted benzo[c]phenanthridine derivatives.

J. Riou, A. Croisy, E. Bisagni, 1993, Journal of medicinal chemistry.

New cyclobutyl analogs of adenosine and guanosine. Part 1. Synthesis of the 9‐[3,3‐bis(hydroxymethyl)cyclobutyl]purine nucleoside analogs

E. Bisagni, M. Legraverend, C. Huel, 1990 .

An efficient synthesis of 9-[(1-hydroxymethyl)-cyclubut-1-ene-3-yl] adenine and 1-(adenin-9-yl)-3-methylidene-but-1-ene-4-ol via regiospecific addition of phenyl selenenyl bromide to the alkene precursor.

E. Bisagni, M. Legraverend, T. Gharbaoui, 1992 .

New cyclobutyl analogs of nucleosides. Part 2. Synthesis and antiviral evaluation of 2-amino-7-[3,3-bis (hydroxymethyl)cyclobut-1-yl]-3H,7H-pyrrolo-[2,3-d]pyrimidin-4-one and of cyclobutyl analogs of the pyrimidine nucleosides

Marc Lemaitre, M. Lemaitre, E. Bisagni, 1991 .

New Cyclobutyl Analogs of Adenosine and Guanosine. Part 1. Synthesis of the 9‐(3,3‐Bis(hydroxymethyl)cyclobutyl)purine Nucleoside Analogs.

E. Bisagni, M. Legraverend, C. Huel, 1991 .

Synthesis of 1-functionalized-6-hydroxy-4-methyl and 6,11-dihydroxy-4-methylnaphtho[2,3-g]isoquinoline-5,12-quinones

A. Croisy, E. Bisagni, C. Huel, 1991 .

Reaction of ortho-lithiated protected anilines with o-hydroxycarbonyl compounds: formation of quino- and pyranoquino-acridines

E. Bisagni, C. Rivalle, C. Huel, 1995 .

Synthesis of C-nucleosides. 13. s-Triazol (4,3-a)- and -(1,5-a)pyridine derivatives.

T. Huynh-Dinh, E. Bisagni, J. Igolen, 1976, The Journal of organic chemistry.

Synthesis of s-triazolo[4,3-b]pyridazine C-nucleosides†

E. Bisagni, M. Legraverend, J. Lhoste, 1981 .

Synthesis of various pyrido- and indolo [g] fused 1H-quinolin-4-one derivatives

E. Bisagni, C. Huel, J. Morón, 1993 .

Synthesis of C-nucleosides. 17. s-Triazolo[4,3-a]pyrazines

E. Bisagni, J. Igolen, C. Gouyette, 1979 .

Synthesis of Pyrano[2,3-h]quinolines as Tricyclic Acronycine Analogues

E. Bisagni, C. Rivalle, C. Jolivet, 1996 .

A formal new access to the benzo[c]phenanthridine alkaloids, synthesis of nitidine and o-methyl fagaronine analogues.

E. Bisagni, Y. Janin, 1993 .

A new series of ellipticine derivatives (1-(alkylamino)-9-methoxyellipticine). Synthesis, DNA binding, and biological properties.

L. Larue, C. Paoletti, E. Bisagni, 1988, Journal of medicinal chemistry.

A new route to 7-deazaguanine derivatives

E. Bisagni, M. Legraverend, 1985 .

Photocyclization of 1-(1-chloroisoquinolin-6-yl)-1H-v-triazolo[4,5-c]pyridines to 10-chloro-5H-pyrido[3',4':4,5]pyrrolo[2,3-g]isoquinolines (azaellipticines)

E. Bisagni, C. Rivalle, C. Ducrocq, 1980 .

SYNTHESIS OF 10‐SUBSTITUTED 5H‐PYRIDO(3′,4′:4,5)PYRROLO(2,3‐G)ISOQUINOLINES

E. Bisagni, C. Rivalle, C. Ducrocq, 1979 .

Synthesis of new carbocyclic oxetanocin analogues

A. Aubertin, E. Bisagni, M. Legraverend, 1995 .

An Efficient Synthesis of 9-((1-Hydroxymethyl)cyclobut-1-ene-3-yl) adenine and 1-(Adenin-9-yl)-3-methylidenebut-1-ene-4-ol via Regiospecific Addition of Phenylselenenyl Bromide to the Alkene Precursor.

E. Bisagni, M. Legraverend, T. Gharbaoui, 1993 .

Synthesis of Carbocyclic Oxetanocin Analogues as Potential Anti-HIV Agents. Part 3

E. Bisagni, M. Legraverend, J. Guilhem, 1991 .

Synthesis of new carbocyclic analogues of oxetanocin A and oxetanocin G

E. Bisagni, M. Legraverend, P. Pecquet, 1992 .

Synthesis of 9-O-substituted derivatives of 9-hydroxy-5, 6-dimethyl-6H-pyrido[4,3-b]carbazole-1-carboxylic acid (2-(dimethylamino)ethyl)amide and their 10- and 11-methyl analogues with improved antitumor activity.

E. Bisagni, L. Kraus-Berthier, S. Léonce, 1999, Journal of medicinal chemistry.

13H-benzo[6-7]indolo[3,2-c]quinolines(B[6,7]IQ): optimization of their DNA triplex-specific stabilizationproperties

C. Nguyen, Jian-sheng Sun, D. Grierson, 2000 .

SYNTHESIS OF 9-(HEXANE-1,6-DIOL-3-YL)PURINES, A NOVEL SERIES OF ACYCLIC NUCLEOSIDE ANALOGS AND ANTIVIRAL EVALUATION

E. Bisagni, M. Legraverend, H. Boumchita, 1990 .

Reaction of noracronycine and 1-hydroxy-3-methoxy-10-methylacridone with alkyl- and aryl-lithiums: formation of quinone methides

E. Bisagni, C. Rivalle, C. Jolivet, 1995 .

Synthesis, DNA binding, and cleaving properties of an ellipticine-salen.copper conjugate.

C. Bailly, P. Colson, C. Houssier, 1997, Bioconjugate chemistry.

Reaction of a biscationic distamycin-ellipticine hybrid ligand with DNA. Mode and sequence specificity of binding.

C. Bailly, P. Colson, C. Houssier, 1994, Biochemistry.

Ligand-induced formation of triple helices with antiparallel third strands containing G and T.

C. Nguyen, E. Bisagni, C. Escudé, 1996, Biochemistry.

Characterization of a triple helix-specific ligand. BePI (3-methoxy-7H-8-methyl-11- [(3'-amino)propylamino]-benzo[e]pyrido[4,3-b]indole) intercalates into both double-helical and triple-helical DNA.

M. Waring, M. Rougée, D. S. Pilch, 1993, Journal of molecular biology.

Biological effects and repair of damage photoinduced by a derivative of psoralen substituted at the 3,4 reaction site: photoreactivity of this compound and lethal effect in yeast.

D. Averbeck, E. Moustacchi, E. Bisagni, 1978, Biochimica et biophysica acta.

Lethal and mutagenic effects photoinduced in haploid yeast (Saccharomyces cerevisiae) by two new monofunctional pyridopsoralens compared to 3-carbethoxypsoralen and 8-methoxypsoralen.

D. Averbeck, E. Bisagni, S. Averbeck, 1985, Mutation research.

Triple‐Helix Directed Cleavage of Double‐Stranded DNA by Benzoquinoquinoxaline‐1,10‐phenanthroline Conjugates

C. Nguyen, R. Zain, Jian-sheng Sun, 2004, Chembiochem : a European journal of chemical biology.

Optimization of Triple‐Helix‐Directed DNA Cleavage by Benzoquinoquinoxaline–Ethylenediaminetetraacetic Acid Conjugates

C. Nguyen, R. Zain, Jian-sheng Sun, 2003, Chembiochem : a European journal of chemical biology.

Design of a triple-helix-specific cleaving reagent.

C. Nguyen, R. Zain, C. Marchand, 1999, Chemistry & biology.

A new family of sequence-specific DNA-cleaving agents directed by triple-helical structures: benzopyridoindole-EDTA conjugates.

C. Nguyen, C. Marchand, E. Bisagni, 2000, Chemistry.

Synthesis of 13H-Benzo[6,7]- and 13H-Benzo[4,5]indolo[3,2-c]quinolines: A New Series of Potent Specific Ligands for Triplex DNA.

C. Marchand, E. Bisagni, T. Garestier, 1998 .

Synthesis of 13H-Benzo[6,7]- and 13H-Benzo[4,5]indolo[3,2-c]- quinolines: A New Series of Potent Specific Ligands for Triplex DNA

C. Nguyen, C. Marchand, E. Bisagni, 1998 .

Triple-helix specific ligands stabilize H-DNA conformation.

J. Mergny, T. de Bizemont, M. Takasugi, 1995, Journal of molecular biology.

SELECTIVE STABILIZATION OF DNA TRIPLE HELICES BY BENZOPYRIDOINDOLE DERIVATIVES

J. Mergny, C. Nguyen, E. Bisagni, 1995 .

Synthesis and biological evaluation of amino-substituted benzo[f]pyrido[4,3-b] and pyrido[3,4-b]quinoxalines: a new class of antineoplastic agents.

P. Vrignaud, C. Nguyen, J. Riou, 1995, Anti-cancer drug design.

A New Access to 1-Naphthylamines by an Equivalent Semmler-Wolff Reaction

E. Bisagni, Y. Janin, 1993 .

PHOTOREACTION OF MONOFUNCTIONAL 3‐CARBETHOXYPSORALEN WITH DNA: IDENTIFICATION AND CONFORMATIONAL STUDY OF THE PREDOMINANT cis‐syn FURAN SIDE MONOADDUCT TO THYMINE

J. Cadet, P. Vigny, F. Gaboriau, 1987, Photochemistry and photobiology.

Role of the superoxide anion in the oxidative activation of the new antitumor drug BD40: a radiolysis study.

A. Croisy, E. Bisagni, C. Rivalle, 1989, International journal of radiation biology.

PHOTO‐CIDNP AS A TOOL FOR THE STUDY OF THE REACTIVITY OF PHOTOSENSITIZING DRUGS: THE FUROCOUMARINS

G. Vermeersch, E. Bisagni, J. Marko, 1988 .

SOME PROPERTIES OF THE TRIPLET EXCITED STATE OF THE PHOTOSENSITIZING FUROCOUMARIN: 3‐CARBETHOXYPSORALEN

D. Averbeck, E. Land, E. Bisagni, 1982 .

PSEUDONUCLEOSIDE DERIVATIVES OF PYRROLO(2,3‐D)PYRIMIDINES. SYNTHESIS AND BIOLOGICAL ACTIVITY

E. Bisagni, M. Legraverend, J. Lhoste, 1984 .

Synthese de formyl-3 carbethoxy-4 et carbethoxy-4 formyl-5 pyrazoles N1-substitues

E. Bisagni, J. Bourzat, J. Marquet, 1973 .

CORRELATION BETWEEN THE TRIPLET PHOTOPHYSICAL PROPERTIES AND THE PHOTOBIOLOGICAL ACTION IN YEAST OF TWO MONOFUNCTIONAL PYRIDOPSORALENS

D. Averbeck, E. Land, R. Bensasson, 1987 .

Sensitizers for the room temperature phosphorescence of biacetyl in fats

J. Blais, A. Cepeda, P. Prognon, 1991 .

Epoxidation of 2-azabicyclo[2.2.1]hept-5-en-3-one

E. Bisagni, M. Legraverend, C. Huel, 2009 .

4-benzyl- and 4-benzoyl-3-dimethylaminopyridin-2(1H)-ones, a new family of potent anti-HIV agents: optimization and in vitro evaluation against clinically important HIV mutant strains.

R. Pauwels, C. Nguyen, C. Monneret, 2004, Journal of Medicinal Chemistry.

(+/-)-2-Amino-3,4-dihydro-7-[2,3-dihydroxy-4-(hydroxymethyl)-1- cyclopentyl]-7H-pyrrolo[2,3-d]pyrimidin-4-ones: new carbocyclic analogues of 7-deazaguanosine with antiviral activity.

E. Bisagni, M. Legraverend, A. Zerial, 1985, Journal of Medicinal Chemistry.

Synthesis and Biological Evaluation of 3-Deazacytidine and 3-Deazauridine Derivatives

C. Nguyen, E. Bisagni, M. Legraverend, 1986 .

Ligand-induced formation of hoogsteen-paired parallel DNA.

C. Nguyen, E. Taillandier, J. Liquier, 1996, Chemistry and Biology.

Synthesis and antiviral activity of 4-benzyl pyridinone derivatives as potent and selective non-nucleoside human immunodeficiency virus type 1 reverse transcriptase inhibitors.

C. Nguyen, M. Andreola, V. Dollé, 2000, Journal of medicinal chemistry.

Triple helices formed at oligopyrimidine*oligopurine sequences with base pair inversions: effect of a triplex-specific ligand on stability and selectivity.

D. M. Brown, C. Nguyen, D. Loakes, 1998, Nucleic acids research.

Synthesis of C-nucleosides. Part 14. 5(3)-Glycosyl-1,2,4-triazole-3(5)-carboxamides as analogues of ribavirin.

T. Huynh-Dinh, E. Bisagni, J. Igolen, 1977, Journal of the Chemical Society. Perkin transactions 1.

Conformational studies of some carbocyclic nucleoside analogues

E. Bisagni, M. Legraverend, J. Lhoste, 1984 .

Synthesis and in vitro evaluation of novel 2,6,9-trisubstituted purines acting as cyclin-dependent kinase inhibitors.

L. Meijer, S. Leclerc, V. Favaudon, 1999, Bioorganic & medicinal chemistry.

Synthesis of Ring-enlarged Cyclobut-A and Cyclobut-G Analogues as HIV Inhibitors. Part 4

E. Bisagni, M. Legraverend, H. Boumchita, 1991 .

Synthesis of psoralens and analogues.

E. Bisagni, 1992, Journal of photochemistry and photobiology. B, Biology.

SPECTROSCOPIC PROPERTIES AND PHOTOREACTIVITY WITH DNA OF NEW MONOFUNCTIONAL PYRIDOPSORALENS

J. Blais, P. Vigny, E. Bisagni, 1984, Photochemistry and photobiology.

Synthesis of 5H-furo[3′,2′ : 6,7][1]benzopyrano[3,4-c]pyridin-5-ones and 8H-pyrano[3′,2′ : 5,6]benzofuro[3,2-c]pyridin-8-ones (pyridopsoralens)

C. Nguyen, E. Bisagni, J. Morón, 1983 .

Spectroscopic study of the dar interaction and of the photoreaction between a new monofunctional psoralen: 3-carbethoxy psoralen, and DNA.

D. Averbeck, P. Vigny, F. Gaboriau, 1982, Biochimie.

PHOTOBIOLOGICAL ACTIVITY IN YEAST OF DERIVATIVES OF PSORALEN SUBSTITUTED AT THE 3,4 AND/OR THE 4',5' REACTION SITE

D. Averbeck, P. Vigny, F. Gaboriau, 1979, Photochemistry and photobiology.

Further SAR in the new antitumor 1-amino-substituted gamma-carbolines and 5H-benzo[e]pyrido[4,3-b]indoles series.

C. Nguyen, J. Riou, E. Bisagni, 1992, Anti-cancer drug design.

AZAINDOLES. III. SYNTHESIS OF 4-AMINO-5-AZAINDOLE AND THE CORRESPONDNG N-5 RIBONUCLEOSIDE (ISO-1-DEAZATUBERCIDINE)

J. Defaye, J. Mispelter, E. Bisagni, 1976 .

Synthesis and Anti-HIV Evaluation of 7-Deaza Analogues of Carbovir

A. Aubertin, E. Bisagni, M. Legraverend, 1994 .

(±)‐2‐Amino‐3,4‐dihydro‐7‐[2,3‐dihydroxy‐4‐(hydroxymethyl)‐1‐cyclopentyl]‐7H‐ pyrrolo[2,3‐d]pyrimidin‐4‐ones: New Carbocyclic Analogues of 7‐Deazaguanosine with Antiviral Activity.

E. Bisagni, M. Legraverend, A. Zerial, 1986 .

Antiviral activities of 54.247-RP, a carbocyclic analog of 7-deazaguanosine, in cell cultures and animals

M. Zerial, E. Bisagni, M. Legraverend, 1986 .

In vivo antitumor activity of S 16020-2, a new olivacine derivative

E. Bisagni, L. Kraus-Berthier, M. Visalli, 1996, Cancer Chemotherapy and Pharmacology.

Antitumoral activity of dipyrido [4,3-b] [3,4-f] indoles on L 1210 leukemia.

J. Chermann, J. Gruest, L. Montagnier, 1980, Bulletin du cancer.

Likelihood of the new antitumoral drug 10-[gamma-diethylaminopropylamino]-6-methyl-5H-pyrido[3',4':4,5]pyrrolo [2,3-g]isoquinoline (BD-40), a pyridopyrroloisoquinoline derivative, to induce DNA strand breaks in vivo and its nonmutagenicity in yeast.

E. Moustacchi, V. Favaudon, E. Bisagni, 1983, Cancer research.

Photochemotherapy using pyridopsoralens.

D. Averbeck, J. Blais, D. Papadopoulo, 1985, Biochimie.

Antitumor activity of intoplicine (RP 60475, NSC 645008), a new benzo-pyrido-indole: evaluation against solid tumors and leukemias in mice

P. Vrignaud, C. Nguyen, M. Bissery, 1993, Investigational New Drugs.

Interrelationship between affinity for DNA, cytotoxicity and induction of DNA-breaks in cultured L1210 cells for two series of tricyclic intercalators. Simplified analogues of ellipticine derivatives.

P. Gros, C. Nguyen, E. Bisagni, 1989, Biochemical pharmacology.

Synthesis of 11-amino-substituted-5,6-dimethyl-5H-pyrido[3',4':4,5]pyrrolo-[2,3-g]isoquinolines as new ellipticine analogues

E. Bisagni, C. Rivalle, J. Belehradek, 1991 .

Structure-activity relationships in a series of newly synthesized 1-amino-substituted ellipticine derivatives.

J. Chermann, F. Wendling, E. Bisagni, 1980, Journal of Medicinal Chemistry.

Synthesis of 11-Amino-Substituted-5,6-dimethyl-5H-pyrido(3′,4′:4,5) pyrrolo(2,3-g)isoquinolines as New Ellipticine Analogues.

E. Bisagni, C. Rivalle, J. Belehradek, 1992 .

1-Amino-substituted 4-methyl-5H-pyrido[3',4':4,5]pyrrolo[3,2-c]pyridines: a new class of antineoplastic agents.

C. Nguyen, E. Bisagni, P. de Cointet, 1987, Journal of medicinal chemistry.

Antitumor amino-substituted pyrido[3',4':4,5]pyrrolo[2,3-g]isoquinolines and pyrido[4,3-b]carbazole derivatives: synthesis and evaluation of compounds resulting from new side chain and heterocycle modifications.

J. Chermann, F. Wendling, E. Bisagni, 1983, Journal of medicinal chemistry.

Intercalative binding to DNA of new antitumoral agents: dipyrido [4,3-b] [3,4-f] indoles.

E. Bisagni, C. Rivalle, F. Pochon, 1980, Bulletin du cancer.

Binding of a distamycin-ellipticine hybrid molecule to DNA and chromatin: spectroscopic, biochemical, and molecular modeling investigations.

M. Waring, P. Colson, C. Houssier, 1992, Biochemistry.

A convenient synthesis of 2-amino-6-methoxy-1-methyl (and 1,4-dimethyl)carbazole derivatives and their 6-aza analogues

E. Bisagni, J. Morón, C. Landras, 1992 .

Synthesis of 11-amino-substituted-9-methoxy-5-methyl-6H-pyrido[4,3-b]-carbazoles

C. Paoletti, E. Bisagni, C. Rivalle, 1991 .

Aminoalkylamino derivatives of dihydroxy-benzo [g] isoquinoline dione and of trihydroxy-naphtho [2,3-g] isoquinoline dione: synthesis and anti-tumor evaluation

D. Carrez, E. Bisagni, M. Croisy-Delcey, 1988 .

Synthese et etude de 5H-pyrido[4,3-b]-benzo[f]indoloquinones-6,11 apparentees aux ellipticines et aux anthracyclines

J. Chermann, E. Bisagni, C. Rivalle, 1985 .

STRUCTURE-ACTIVITY RELATIONSHIPS IN A SERIES OF NEWLY SYNTHESIZED 1-AMINO-SUBSTITUTED ELLIPTICINE DERIVATIVES

J. Chermann, F. Wendling, E. Bisagni, 1981 .

Synthesis and antitumor properties of new 4-methyl-substituted- pyrido[4,3-b]indoles (gamma-carbolines).

C. Nguyen, E. Bisagni, F. Lavelle, 1992, Anti-cancer drug design.

Synthesis and evaluation of 9-hydroxy-5-methyl-(and 5,6-dimethyl)-6H-pyrido[4,3-b]carbazole-1-N- [(dialkylamino)alkyl]carboxamides, a new promising series of antitumor olivacine derivatives.

J. Prost, E. Bisagni, L. Kraus-Berthier, 1994, Journal of medicinal chemistry.

Synthesis and biological properties of new benz[h]isoquinoline derivatives.

J. Riou, D. Carrez, E. Bisagni, 1994, Chemical & pharmaceutical bulletin.

1-Amino-substituted 4-methyl-5H-pyrido[4,3-b]indoles (gamma-carbolines) as tricyclic analogues of ellipticines: a new class of antineoplastic agents.

P. Gros, C. Nguyen, E. Bisagni, 1988, Journal of medicinal chemistry.

A convenient way to dibenzo[c,h]-1,5-naphthyridines (11-aza-benzo[c] phenanthridines)

E. Bisagni, C. Huel, Sylvie Thirot, 1996 .

A Convenient Way to Dibenzo(c,h)-1,5-naphthyridines (11-Aza-benzo(c) phenanthridines).

E. Bisagni, C. Huel, Sylvie Thirot, 1996 .

NOVEL OLIVACINE AND ELLIPTICINE DERIVATIVES : S-16020-2 AND RELATED COMPOUNDS AS POTENTIAL ANTITUMOR AGENTS

E. Bisagni, G. Atassi, M. Devissaguet, 1997 .

Direct determination of biacetyl in fats by sensitized room temperature phosphorescence

P. Prognon, G. Mahuzier, E. Bisagni, 1989 .

Preparation and characterization of a new meso-substituted tetrapyrrole macrocyclc: Meso-tetra[2-(3-carboxyethyl)furyl]porphine, [TF CO 2 EtP]

M. Momenteau, E. Bisagni, B. Loock, 1979 .

Synthesis of 11H-furo[3',2':7,8]benzopyrano[3,4-c]pyridin-11-one and 6,8-dimethyl-10H-pyrano[2',3':4,5]benzofuro[3,2-c]pyridin-10-one (pyridoangelicins)

E. Bisagni, C. Huel, J. Morón, 1992 .

Aza analogues of lucanthone: synthesis and antitumor and bactericidal properties.

E. Bisagni, M. Croisy-Delcey, 1983, Journal of medicinal chemistry.

Both-faces hindered porphyrins. Part 1. Synthesis and characterization of basket-handle porphyrins and their iron complexes

J. Mispelter, M. Momenteau, E. Bisagni, 1983 .

126. Oxygen heterocycles. Part VII. Spasmolytic ketones in the benzofuran series, and related compounds

E. Bisagni, N. P. Buu‐Hoï, R. Royer, 1957 .