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SYNTHESIS OF 1-AMINO-3-HYDROXY-ADAMANTANEDONETTI A; BELLORA E.1974; SYNTHET. COMMUNIC.; U.S.A.; DA. 1974; VOL. 3; NO 2; PP. 165-166; BIBL. 4 REF.Article

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

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 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

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

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

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

Gastroprokinetic properties of the benzimidazolone derivative BIMU 1, an agonist at 5-hydroxytryptamine4 and antagonist at 5-hydroxytryptamine3 receptorsRIZZI, C. A; SAGRADA, A; SCHIAVONE, A et al.Naunyn-Schmiedeberg's archives of pharmacology. 1994, Vol 349, Num 4, pp 338-345, issn 0028-1298Article

Substituent effect on the stereochemistry of H2-receptor antagonists of the phenylformamidine series. A conformation-dependent mode of interaction with the H2 receptorDONETTI, A; BASTIAANS, H. M. M; KRAMER, K et al.Journal of medicinal chemistry (Print). 1991, Vol 34, Num 6, pp 1772-1776, issn 0022-2623, 5 p.Article

Pharmacological properties of a novel class of 5-HT3 receptor antagonistsTURCONI, M; DONETTI, A; SCHIAVONE, A et al.European journal of pharmacology. 1991, Vol 203, Num 2, pp 203-211, issn 0014-2999Article

New pyrrolidin-, piperidin- and azepin-2-oxocarboxylic acid esters are preferential M1, M3 muscarinic antagonists. Synthesis and bronchospasmolytic activityCEREDA, E; EZHAYA, A; BELLORA, E et al.European journal of medicinal chemistry. 1994, Vol 29, Num 6, pp 411-421, issn 0223-5234Article

Synthesis and biological evaluation of new antimuscarinic compounds with amidine basic centers. A useful bioisosteric replacement of classical cationic headsCEREDA, E; ZEHAYA, A; GIL QUINTERO, M et al.Journal of medicinal chemistry (Print). 1990, Vol 33, Num 8, pp 2108-2113, issn 0022-2623, 6 p.Article

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