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A MILD AND EFFECTIVE TWO-STEP CONVERSION OF DISUBSTITUTED CYANAMIDES TO SECONDARY AMINESDONETTI A; BELLORA E.1972; J. ORG. CHEM.; U.S.A.; DA. 1972; VOL. 37; NO 21; PP. 3352-3353; BIBL. 13 REF.Serial Issue

SYNTHESIS OF THE DIACETATE OF 4-CHLORO-2-HYDROXYMETHYL-2-BUTEN-1-OL: A USEFUL SYNTHON IN THE CHEMISTRY OF THE ISOPRENE UNITCEREDA E; BELLORA E; DONETTI A et al.1980; TETRAHEDRON LETT.; ISSN 0040-4039; GBR; DA. 1980; VOL. 21; NO 51; PP. 4977-4980; BIBL. 17 REF.Article

PHASE-TRANSFER CATALYZED OXIDATIVE DECYANATION OF ALPHA -SECONDARY NITRILES: A CONVENIENT SYNTHESIS OF AROMATIC KETONESDONETTI A; BONIARDI O; EZHAYA A et al.1980; SYNTHESIS (STUTTG.); ISSN 0039-7881; DEU; DA. 1980; NO 12; PP. 1009-1011; BIBL. 20 REF.Article

N-TRISUBSTITUTED METHYLIMIDAZOLES AS ANTIFUNGAL AGENTSCASADIO S; DONETTI A; COPPI G et al.1973; J. PHARM. SCI.; U.S.A.; DA. 1973; VOL. 62; NO 5; PP. 773-778; BIBL. 13REF.Serial Issue

ANALGETIC-ANTIINFLAMMATORY ACTIVITY OF PRENYL DERIVATIVES OF BASIC NAPHTHYLALKYLNITRILES AND NAPHTHYLALKYLAMIDES CHEMICALLY RELATED TO NAPHTHYPRAMIDEPALA G; DONETTI A; LUMACHI B et al.1973; J. MEDICIN. CHEM.; U.S.A.; DA. 1973; VOL. 16; NO 6; PP. 720-723; BIBL. 16REF.Serial Issue

THE ACETATE OF (Z)-4-CHLORO-2-METHYL-2-BUTEN-1-OL. STEREOSELECTIVE WITTIG SYNTHESIS OF A NEW HEMITERPENOID SYNTHONCEREDA E; ATTOLINI M; BELLORA E et al.1982; TETRAHEDRON LETT.; ISSN 0040-4039; GBR; DA. 1982; VOL. 23; NO 21; PP. 2219-2222; BIBL. 12 REF.Article

SPECIES DIFFERENCES IN THE METABOLISM OF FEPRAZONE, AN ANTIINFLAMMATORY DRUGGAETANI M; YAMAGUCHI H; VIDI A et al.1979; PHARMACOL. RES. COMMUNIC.; GBR; DA. 1979; VOL. 11; NO 8; PP. 719-730; BIBL. 9 REF.Article

TERPENE COMPOUNDS AS DRUGS. XV. BASIC ETHOXYETHYLETHERS OF GUAIACOL AND EUGENOL AS ANTITUSSIVESMANTEGANI A; DONETTI A; BONARDI G et al.1972; CHIM. THERAPEUT.; FR.; DA. 1972; VOL. 7; NO 6; PP. 483-485; ABS. FR. ALLEM.; BIBL. 5REF.Serial Issue

THE METABOLISM OF (¹⁴C) PRENAZONE IN THE RAT.TOFT P; DRING LG; HIROM PC et al.1975; XENOBIOTICA; G.B.; DA. 1975; VOL. 5; NO 12; PP. 729-739; BIBL. 13 REF.Article

SYNTHESIS AND ANALGETIC ACTIVITY OF N-SUBSTITUTED 6,7-BENZOMORPHANSBELLORA E; CEREDA E; EZHAYA A et al.1980; FARMACO, ED. SCI.; ITA; DA. 1980; VOL. 35; NO 6; PP. 490-497; ABS. ITA; BIBL. 18 REF.Article

Hexocyclium derivatives with a high selectivity for smooth muscle muscarinic receptorsMICHELETTI, R; SCHIAVONE, A; CEREDA, E et al.British journal of pharmacology. 1990, Vol 100, Num 1, pp 150-152, issn 0007-1188Article

The effect of DAU 6215, a novel 5HT-2 antagonist, in animal models of anxietyBORSINI, F; BRAMBILLA, A; CESANA, R et al.Pharmacological research. 1993, Vol 27, Num 2, pp 151-164, issn 1043-6618Article

N-(Fluoroethyl)(imidazolylphenyl)formamidines. The issue of the active species of mifentidineDONETTI, A; CEREDA, E; EZHAYA, A et al.Journal of medicinal chemistry (Print). 1989, Vol 32, Num 5, pp 957-961, issn 0022-2623, 5 p.Article

4-DAMP analogues reveal heterogeneity of M₁ muscarinic receptorsMICHELETTI, R; GIUDICI, L; TURCONI, M et al.British journal of pharmacology. 1990, Vol 100, Num 3, pp 395-397, issn 0007-1188, 3 p.Article

A new, convenient synthesis of N²-aryl-N¹-alkylformamidines and N²-aryl-N¹,N¹-dialkylformamidinesCEREDA, E; BELLORA, E; DONETTI, A et al.Synthesis (Stuttgart). 1986, Num 4, pp 288-291, issn 0039-7881Article

TERPENE COMPOUNDS AS DRUGS. XIII. O-TERPENYLAMINOMETHYLPHENOLS AND THEIR N-METHYL DERIVATIVESDONETTI A; CASADIO S; MOLINO C et al.1972; J. MEDICIN. CHEM.; U.S.A.; DA. 1972; VOL. 15; NO 10; PP. 1089-1091; BIBL. 11REF.Serial Issue

Guanylpirenzepine distinguishes between neuronal m₁ and m₄ muscarinic receptor subtypesMONFERINI, E; CEREDA, E; LADINSKY, H et al.Journal of receptor research. 1990, Vol 10, Num 1-2, pp 81-96, issn 0197-5110, 16 p.Article

Cimetidine, Ranitidine and Mifentidine in Specific gastric and duodenal ulcer modelsDEL SOLDATO, P; GHIORZI, A; CEREDA, E et al.Pharmacology. 1985, Vol 30, Num 1, pp 45-51, issn 0031-7012Article

Ionization, tautomerism and molecular conformation in aqueous solution of the histamine H₂-receptor antagonist mifentidineBAZZANO, C; VANONI, P. C; MONDONI, M et al.European journal of medicinal chemistry. 1986, Vol 21, Num 1, pp 27-33, issn 0223-5234Article

Are the imidazoles of cimetidine and mifentidine bioisostere?BIETTI, G; CEREDA, E; GIACHETTI, A et al.European journal of medicinal chemistry. 1988, Vol 23, Num 3, pp 267-273, issn 0223-5234Article

Synthesis and biological evaluation of new muscarinic receptor antagonists bearing cyclic amidines as cationic headsNICOLA, M; SCHIAVI, G. B; MICHELETTI, R et al.Farmaco (Il) : (1989). 1991, Vol 46, Num 4, pp 539-553, 15 p.Article

Affinity profile of the novel muscarinic antagonist, guanylpirenzepineMICHELETTI, R; SCHIAVONE, A; ANGELICI, O et al.Life sciences (1973). 1990, Vol 47, Num 15, pp PL55-PL58, issn 0024-3205Article

Conformational studies of two histamine H₂-receptor antagonistic phenylformamidines: mifentidine and its guanidinothiazole analogue DA 4643DONETTI, A; TRUMMLITZ, G; BIETTI, G et al.Arzneimittel-Forschung. 1985, Vol 35, Num 1A, pp 306-315, issn 0004-4172Article

Anti-secretory and anti-ulcer activities of some new 2-(2-pyridylmethyl-sulfinyl)-benzimidazolesCEREDA, E; TURCONI, M; EZHAYA, A et al.European journal of medicinal chemistry. 1987, Vol 22, Num 6, pp 527-537, issn 0223-5234Article