SYNTHESIS OF 2,3,5,6-TETRAHYDROIMIDAZO (1,2-C) QUINAZOLINE DERIVATIVES AS POTENTIAL NARCOTIC ANTAGONISTSANTONINI I; CRISTALLI G; FRANCHETTI P et al.1980; J. HETEROCYCL. CHEM.; USA; DA. 1980; VOL. 17; NO 1; PP. 155-157; BIBL. 6 REF.Article

SYNTHESIS OF N¹-ARYL- AND N¹-BENZYL SUBSTITUTED IMIDAZOLE-4- AND IMIDAZOLE-5-CARBALDEHYDESANTONINI I; CRISTALLI G; FRANCHETTI P et al.1983; SYNTHESIS (STUTTG.); ISSN 0039-7881; DEU; DA. 1983; NO 1; PP. 47-49; BIBL. 3 REF.Article

INDOLIZINE DERIVATIVES WITH BIOLOGICAL ACTIVITY. IV: 3-(2-AMINOETHYL)-2-METHYLINDOLIZINE, 3-(2-AMINOETHYL)-2-METHYL-5,6,7,8-TETRAHYDROINDOLIZINE, AND THEIR N-ALKYL DERIVATIVESANTONINI I; CLAUDI F; GULINI U et al.1979; J. PHARM. SCI.; USA; DA. 1979; VOL. 68; NO 3; PP. 321-324; BIBL. 8 REF.Article

STRUCTURE-ACTIVITY RELATIONSHIPS IN REACTIVATORS OF ORGANOPHOSPHORUS-INHIBITED ACETYLCHOLINESTERASE. XI. BISQUARTERNARY COMPOUNDS OF BETA -(4-PYRIDYL) ACRALDOXIME.ANTONINI I; CRISTALLI G; FRANCHETTI P et al.1977; FARMACO, ED. SCI.; ITAL.; DA. 1977; VOL. 32; NO 12; PP. 905-908; ABS. ITAL.; BIBL. 4 REF.Article

The synthesis of a new polycyclic heterocyclic ring system : pyrimido[5,6,1-d,e]acridineANTONINI, I; MARTELLI, S.Journal of heterocyclic chemistry. 1992, Vol 29, Num 2, pp 471-473, issn 0022-152XArticle

ACID-CATALYSED, NUCLEOPHILE-CATALYSED AND THERMAL DECOMPOSITION OF 2-AMINO-3-(2',2' DIMETHYLAZIRIDINO)-1,4-NAPHTHOQUINONEANTONINI I; CLAUDI F; CRISTALLI G et al.1980; J. HETEROCYCL. CHEM.; USA; DA. 1980; VOL. 17; NO 1; PP. 181-185; BIBL. 18 REF.Article

ELUCIDATION OF THE STRUCTURE OF THE ANTINEOPLASTIC AGENTS, 2-FORMYLPYRIDINE AND 1-FORMYLISOQUINOLINE THIOSEMICARBAZONES.ANTONINI I; CLAUDI F; FRANCHETTI P et al.1977; J. MEDICIN. CHEM.; U.S.A.; DA. 1977; VOL. 20; NO 3; PP. 447-449; BIBL. 18 REF.Article

HETEROCYCLIC QUINONES WITH POTENTIAL ANTITUMOR ACTIVITY A CONVENIENT SYNTHESIS OF 5,6-DIMETHYL-4,7-BENZIMIDAZOLEDIONESANTONINI I; CRISTALLI G; FRANCHETTI P et al.1982; HETEROCYCLES; ISSN 0385-5414; JPN; DA. 1982; VOL. 19; NO 12; PP. 2313-2317; BIBL. 15 REF.Article

THERMAL DECOMPOSITION OF 2-AMINO-3-AZIRIDINO-1,4-NAPHTHOQUINONES (1,2)ANTONINI I; CLAUDI F; CRISTALLI G et al.1981; J. HETEROCYCL. CHEM.; ISSN 0022-152X; USA; DA. 1981; VOL. 18; NO 2; PP. 399-404; BIBL. 18 REF.Article

SYNTHESIS OF 4-AMINO-1-BETA -D-RIBOFURANOSYL-1H-PYRROLO (2,3-B) PYRIDINE (1-DEAZATUBERCIDIN) AS A POTENTIAL ANTITUMOR AGENTANTONINI I; CLAUDI F; CRISTALLI G et al.1982; J. MED. CHEM.; ISSN 0022-2623; USA; DA. 1982; VOL. 25; NO 10; PP. 1258-1261; BIBL. 15 REF.Article

PLATELET AGGREGATION INHIBITORS. II. N-HETEROCYCLIC ALDOXIME METHIODIDES.ANTONINI I; FRANCHETTI P; GRIFANTINI M et al.1976; FARMACO, ED. SCI.; ITAL.; DA. 1976; VOL. 31; NO 11; PP. 809-816; ABS. ITAL.; BIBL. 23 REF.Article

INDOLIZINE DERIVATIVES WITH BIOLOGICAL ACTIVITY. III. 3-(3-(AMINOPROPYL)-2-METHYLINDOLIZINE, 3-(3-AMINOPROPYL)-2-METHYL-5,6,7,8-TETRAHYDROINDOLIZINE, AND THEIR N-ALKYL DERIVATIVES.ANTONINI I; CARDELLINI M; CLAUDI F et al.1977; J. PHARM. SCI.; U.S.A.; DA. 1977; VOL. 66; NO 12; PP. 1692-1696; BIBL. 23 REF.Article

Characterization and dissolution studies of PEG 4000/fenofibrate solid dispersionsPALMIERI, G. F; ANTONINI, I; MARTELLI, S et al.STP pharma sciences. 1996, Vol 6, Num 3, pp 188-194, issn 1157-1489Article

Synthesis and ¹H NMR charaterization of substituted 1-amino-9-imino-4-nitro-9,10-dihydroacridines as potential antitumor agentsCHOLODY, W. M; KONOPA, J; ANTONINI, I et al.Journal of heterocyclic chemistry. 1991, Vol 28, Num 2, pp 209-214, issn 0022-152X, 6 p.Article

Heterocyclic quinones with potential antitumor activity. II: Synthesis and antitumor activity of some benzimidazole-4,7-dione derivativesANTONINI, I; CLAUDI, F; CRISTALLI, G et al.Journal of medicinal chemistry (Print). 1988, Vol 31, Num 1, pp 260-264, issn 0022-2623Article

Adenosine deaminase inhibitors. Synthesis of deaza analogues of erythro-9-(2-hydroxy-3-nonyl)adenineANTONINI, I; CRISTALLI, G; FRANCHETTI, P et al.Journal of medicinal chemistry (Print). 1984, Vol 27, Num 3, pp 274-278, issn 0022-2623Article

2,3-dimethyl-1,4-naphthoquinone derivatives as bioreductive alkylating agents with cross-linking potentialLIN, T.-S; ANTONINI, I; COSBY, L. A et al.Journal of medicinal chemistry (Print). 1984, Vol 27, Num 6, pp 813-815, issn 0022-2623Article

Deaza analogues of adenosine as inhibitors of blood platelet aggregationANTONINI, I; CRISTALLI, G; FRANCHETTI, P et al.Journal of pharmaceutical sciences. 1984, Vol 73, Num 3, pp 366-369, issn 0022-3549Article

2,3-Dihydro-1H, 7H-pyrimido[5,6,1-de]acridine-1,3,7-trione derivatives, a class of cytotoxic agents active on multidrug-resistant cell lines : Synthesis, biological evaluation, and structure-activity relationshipsANTONINI, I; POLUCCI, P; KELLAND, L. R et al.Journal of medicinal chemistry (Print). 1999, Vol 42, Num 14, pp 2535-2541, issn 0022-2623Article

Synthesis of 7-oxo-7H-benzo[e]perimidine-4-carboxamides as potential antitumor drugsANTONINI, I; POLUCCI, P; COLA, D et al.Il Farmaco (Pavia). 1992, Vol 47, Num 11, pp 1385-1393, issn 0014-827XArticle

Synthesis of 9,10-anthraquinone monoalkylaminoalkylhydrazones as potential antitumor drugsANTONINI, I; POLUCCI, P; COLA, D et al.Il Farmaco (Pavia). 1993, Vol 48, Num 12, pp 1641-1648, issn 0014-827XArticle

N₁-aryl- and N₁-benzyl-4-formylimidazole thiosemicarbazones with potential antineoplastic activityANTONINI, I; CLAUDI, F; CRISTALLI, G et al.European journal of medicinal chemistry. 1984, Vol 19, Num 3, pp 285-287, issn 0223-5234Article

Pyrimido[4,5,6-kl]acridines, a new class of potential anticancer agents. Synthesis and biological evaluationANTONINI, I; POLUCCI, P; COLA, D et al.Anti-cancer drug design. 1996, Vol 11, Num 4, pp 339-349, issn 0266-9536Article

(o- and p-nitrobenzyloxycarbonyl)-5-fluorouracil derivatives as potential conjugated bioreductive alkylating agentsTAI-SHUN LIN; LIN WANG; ANTONINI, I et al.Journal of medicinal chemistry (Print). 1986, Vol 29, Num 1, pp 84-89, issn 0022-2623Article