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Results: 1-25 | 26-50
Results: 1-25/50
1-METHYL-3-NITRO-5-METHOXYCARBONYL PYRAZOLE
Authors: BARALDI PG CACCIARI B ROMAGNOLI R SPALLUTO G
Citation: Pg. Baraldi et al., 1-METHYL-3-NITRO-5-METHOXYCARBONYL PYRAZOLE, Molecules, 3(2), 1998, pp. 46
ETHYL-(R,S)-5-ACETYL-4,5-DIHYDRO-3-ISOXAZOLE ACETATE
Authors: BARALDI PG CACCIARI B ROMAGNOLI R SPALLUTO G
Citation: Pg. Baraldi et al., ETHYL-(R,S)-5-ACETYL-4,5-DIHYDRO-3-ISOXAZOLE ACETATE, Molecules, 3(2), 1998, pp. 47
HETEROCYCLIC-ANALOGS OF DNA MINOR-GROOVE ALKYLATING-AGENTS
Authors: BARALDI PG CACCIARI B GUIOTTO A ROMAGNOLI R ZAID AN SPALLUTO G
Citation: Pg. Baraldi et al., HETEROCYCLIC-ANALOGS OF DNA MINOR-GROOVE ALKYLATING-AGENTS, Current pharmaceutical design, 4(3), 1998, pp. 249-276
SYNTHESIS OF NOVEL C7-ARYL SUBSTITUTED PYRROLO[2,1-C][1,4]BENZODIAZEPINES (PBDS) VIA PRO-N-10-TROC PROTECTION AND SUZUKI COUPLING
Authors: GUIOTTO A HOWARD PW BARALDI PG THURSTON DE
Citation: A. Guiotto et al., SYNTHESIS OF NOVEL C7-ARYL SUBSTITUTED PYRROLO[2,1-C][1,4]BENZODIAZEPINES (PBDS) VIA PRO-N-10-TROC PROTECTION AND SUZUKI COUPLING, Bioorganic & medicinal chemistry letters, 8(21), 1998, pp. 3017-3018
DESIGN, SYNTHESIS AND BIOLOGICAL-ACTIVITY OF A PYRROLO[2,1-C][1,4]BENZODIAZEPINE (PBD)-DISTAMYCIN HYBRID
Authors: BARALDI PG CACCIARI B GUIOTTO A LEONI A ROMAGNOLI R SPALLUTO G MONGELLI N HOWARD PW THURSTON DE BIANCHI N GAMBARI R
Citation: Pg. Baraldi et al., DESIGN, SYNTHESIS AND BIOLOGICAL-ACTIVITY OF A PYRROLO[2,1-C][1,4]BENZODIAZEPINE (PBD)-DISTAMYCIN HYBRID, Bioorganic & medicinal chemistry letters, 8(21), 1998, pp. 3019-3024
ENZYMATIC-SYNTHESIS OF 2'-O-ACYL PRODRUGS OF BETA-D-ARABINOFURANOSYL)-5(E)-(2-BROMOVINYL)URACIL AND OF 2'-O-ACYL-ARAU, 2'-O-ACYL-ARAC AND 2'-O-ACYL-ARAA
Authors: MANFREDINI S BARALDI PG BAZZANINI R BORTOLOTTI F VERTUANI S ASHIDA N MACHIDA H
Citation: S. Manfredini et al., ENZYMATIC-SYNTHESIS OF 2'-O-ACYL PRODRUGS OF BETA-D-ARABINOFURANOSYL)-5(E)-(2-BROMOVINYL)URACIL AND OF 2'-O-ACYL-ARAU, 2'-O-ACYL-ARAC AND 2'-O-ACYL-ARAA, Antiviral chemistry & chemotherapy, 9(1), 1998, pp. 25-31
SYNTHESIS AND ANTI-HSV-1 ACTIVITY OF 6 SUBSTITUTED PYRAZOLO[3,4-D]PYRIDAZIN-7-ONE NUCLEOSIDES
Authors: BARALDI PG MANFREDINI S ROMAGNOLI R STEVANATO L ZAID AN MANSERVIGI R
Citation: Pg. Baraldi et al., SYNTHESIS AND ANTI-HSV-1 ACTIVITY OF 6 SUBSTITUTED PYRAZOLO[3,4-D]PYRIDAZIN-7-ONE NUCLEOSIDES, Nucleosides & nucleotides, 17(12), 1998, pp. 2165-2173
A MILD ONE-POT SYNTHESIS OF THIENO[3,4-C]PYRAZOLES AND THEIR CONVERSION INTO PYRAZOLE ANALOGS OF O-QUINODIMETHANE
Authors: BARALDI PG ELKASHEF H MANFREDINI S DELASINFANTAS MJP ROMAGNOLI R SPALLUTO G
Citation: Pg. Baraldi et al., A MILD ONE-POT SYNTHESIS OF THIENO[3,4-C]PYRAZOLES AND THEIR CONVERSION INTO PYRAZOLE ANALOGS OF O-QUINODIMETHANE, Synthesis, (9), 1998, pp. 1331-1334
BINDING-AFFINITY OF ADENOSINE RECEPTOR AGONISTS AND ANTAGONISTS AT HUMAN CLONED A(3) ADENOSINE RECEPTORS
Authors: VARANI K CACCIARI B BARALDI PG DIONISOTTI S ONGINI E BOREA PA
Citation: K. Varani et al., BINDING-AFFINITY OF ADENOSINE RECEPTOR AGONISTS AND ANTAGONISTS AT HUMAN CLONED A(3) ADENOSINE RECEPTORS, Life sciences (1973), 63(5), 1998, pp. 81-87
SYNTHESIS AND BIOLOGICAL-ACTIVITY OF A NEW SERIES OF N-6-ARYLCARBAMOYL, 2-(AR)ALKYNYL-N-6-ARYLCARBAMOYL, AND N-6-CARBOXAMIDO DERIVATIVES OFADENOSINE-5'-N-ETHYLURONAMIDE AS A(1) AND A(3) ADENOSINE RECEPTOR AGONISTS
Authors: BARALDI PG CACCIARI B DELASINFANTAS MJP ROMAGNOLI R SPALLUTO G VOLPINI R COSTANZI S VITTORI S CRISTALLI G MELMAN N PARK KS JI XD JACOBSON KA
Citation: Pg. Baraldi et al., SYNTHESIS AND BIOLOGICAL-ACTIVITY OF A NEW SERIES OF N-6-ARYLCARBAMOYL, 2-(AR)ALKYNYL-N-6-ARYLCARBAMOYL, AND N-6-CARBOXAMIDO DERIVATIVES OFADENOSINE-5'-N-ETHYLURONAMIDE AS A(1) AND A(3) ADENOSINE RECEPTOR AGONISTS, Journal of medicinal chemistry, 41(17), 1998, pp. 3174-3185
DESIGN, SYNTHESIS, AND BIOLOGICAL EVALUATION OF A 2ND-GENERATION OF PYRAZOLO[4,3-E]-1,2,4-TRIAZOLO[1,5-C]PYRIMIDINES AS POTENT AND SELECTIVE A(2A) ADENOSINE RECEPTOR ANTAGONISTS
Authors: BARALDI PG CACCIARI B SPALLUTO G BERGONZONI M DIONISOTTI S ONGINI E VARANI K BOREA PA
Citation: Pg. Baraldi et al., DESIGN, SYNTHESIS, AND BIOLOGICAL EVALUATION OF A 2ND-GENERATION OF PYRAZOLO[4,3-E]-1,2,4-TRIAZOLO[1,5-C]PYRIMIDINES AS POTENT AND SELECTIVE A(2A) ADENOSINE RECEPTOR ANTAGONISTS, Journal of medicinal chemistry, 41(12), 1998, pp. 2126-2133
A(2A)-ADENOSINE RECEPTOR RESERVE FOR CORONARY VASODILATION
Authors: SHRYOCK JC SNOWDY S BARALDI PG CACCIARI B SPALLUTO G MONOPOLI A ONGINI E BAKER SP BELARDINELLI L
Citation: Jc. Shryock et al., A(2A)-ADENOSINE RECEPTOR RESERVE FOR CORONARY VASODILATION, Circulation, 98(7), 1998, pp. 711-718
SYNTHESIS AND ANTIPROLIFERATIVE ACTIVITY OF 2'-O-ALLYL-1-BETA-D-ARABINOFURANOSYL-URACIL, 2'-O-ALLYL-1-BETA-D-ARABINOFURANOSYL-CYTOSINE AND 2'-O-ALLYL-1-BETA-D-ARABINOFURANOSYL-ADENINE
Authors: MANFREDINI S BARALDI PG BAZZANINI R SIMONI D BALZARINI J DECLERCQ E
Citation: S. Manfredini et al., SYNTHESIS AND ANTIPROLIFERATIVE ACTIVITY OF 2'-O-ALLYL-1-BETA-D-ARABINOFURANOSYL-URACIL, 2'-O-ALLYL-1-BETA-D-ARABINOFURANOSYL-CYTOSINE AND 2'-O-ALLYL-1-BETA-D-ARABINOFURANOSYL-ADENINE, Bioorganic & medicinal chemistry letters, 7(4), 1997, pp. 473-478
SYNTHESIS, CYTOTOXICITY, ANTITUMOR-ACTIVITY AND SEQUENCE SELECTIVE BINDING OF 2 PYRAZOLE ANALOGS STRUCTURALLY RELATED TO THE ANTITUMOR AGENTS U-71,184 AND ADOZELESIN
Authors: BARALDI PG CACCIARI B ROMAGNOLI R SPALLUTO G GAMBARI R BIANCHI N PASSADORE M AMBROSINO P MONGELLI N COZZI P GERONI C
Citation: Pg. Baraldi et al., SYNTHESIS, CYTOTOXICITY, ANTITUMOR-ACTIVITY AND SEQUENCE SELECTIVE BINDING OF 2 PYRAZOLE ANALOGS STRUCTURALLY RELATED TO THE ANTITUMOR AGENTS U-71,184 AND ADOZELESIN, Anti-cancer drug design, 12(7), 1997, pp. 555-576
SYNTHESIS, CHEMICAL SOLVOLYTIC STABILITY AND PRELIMINARY BIOLOGICAL EVALUATION OF (+ -)-N-BOC-CPZI - A PYRAZOLE ANALOG OF THE LEFT-HAND SEGMENT OF THE ANTITUMOR AGENT CC-1065/
Authors: BARALDI PG CACCIARI B DELASINFANTAS MJP ROMAGNOLI R SPALLUTO G COZZI P MONGELLI N
Citation: Pg. Baraldi et al., SYNTHESIS, CHEMICAL SOLVOLYTIC STABILITY AND PRELIMINARY BIOLOGICAL EVALUATION OF (+ -)-N-BOC-CPZI - A PYRAZOLE ANALOG OF THE LEFT-HAND SEGMENT OF THE ANTITUMOR AGENT CC-1065/, Anti-cancer drug design, 12(1), 1997, pp. 67-74
A NEW SYNTHETIC APPROACH TO INDAZOLE SYNTHESIS
Authors: BARALDI PG CACCIARI B SPALLUTO G ROMAGNOLI R BRACCIOLI G ZAID AN DELASINFANTAS MJP
Citation: Pg. Baraldi et al., A NEW SYNTHETIC APPROACH TO INDAZOLE SYNTHESIS, Synthesis, (10), 1997, pp. 1140
SYNTHESIS, CYTOTOXICITY AND ANTITUMOR-ACTIVITY OF SOME NEW SIMPLIFIEDPYRAZOLE ANALOGS OF THE ANTITUMOR AGENT CC-1065 - EFFECT OF AN HYDROPHOBIC GROUP, ON ANTITUMOR-ACTIVITY
Authors: BARALDI PG CACCIARI B GUIOTTO A ROMAGNOLI R SPALLUTO G ZAID AN
Citation: Pg. Baraldi et al., SYNTHESIS, CYTOTOXICITY AND ANTITUMOR-ACTIVITY OF SOME NEW SIMPLIFIEDPYRAZOLE ANALOGS OF THE ANTITUMOR AGENT CC-1065 - EFFECT OF AN HYDROPHOBIC GROUP, ON ANTITUMOR-ACTIVITY, Il Farmaco, 52(12), 1997, pp. 711-716
SYNTHESIS, SOLVOLYTIC STABILITY AND CYTOTOXICITY OF A MODIFIED DERIVATIVE OF CPZI, A PYRAZOLE ANALOG OF THE ALKYLATION SUBUNIT OF THE ANTITUMOR AGENT CC-1065 - EFFECT OF THE NITROGEN SUBSTITUTION ON THE FUNCTIONAL REACTIVITY
Authors: BARALDI PG CACCIARI B GUIOTTO A ROMAGNOLI R SPALLUTO G ZAID AN
Citation: Pg. Baraldi et al., SYNTHESIS, SOLVOLYTIC STABILITY AND CYTOTOXICITY OF A MODIFIED DERIVATIVE OF CPZI, A PYRAZOLE ANALOG OF THE ALKYLATION SUBUNIT OF THE ANTITUMOR AGENT CC-1065 - EFFECT OF THE NITROGEN SUBSTITUTION ON THE FUNCTIONAL REACTIVITY, Il Farmaco, 52(12), 1997, pp. 717-723
FSPTP - THE FIRST IRREVERSIBLE ANTAGONIST OF THE A2A-ADENOSINE RECEPTOR
Authors: SHRYOCK JC SNOWDY S BARALDI PG CACCIARI B SPALLUTO G BAKER SP BELARDINELLI L
Citation: Jc. Shryock et al., FSPTP - THE FIRST IRREVERSIBLE ANTAGONIST OF THE A2A-ADENOSINE RECEPTOR, Circulation, 96(8), 1997, pp. 287-287
PYRAZOLE-RELATED NUCLEOSIDES - DESIGN, SYNTHESIS AND ANTIPROLIFERATIVE ACTIVITY OF METHYL -IODO-1-BETA-D-RIBOFURANOSYLPYRAZOLE-3-CARBOXYLATE (IPCAR), AND DERIVATIVES, AGAINST HUMAN LEUKEMIAS, LYMPHOMAS AND SOLID TUMORS CELL-LINES IN-VITRO
Authors: MANFREDINI S BAZZANINI R BARALDI PG SIMONI D VERTUANI S PANI A PINNA E SCINTU F DEMONTIS A LACOLLA P
Citation: S. Manfredini et al., PYRAZOLE-RELATED NUCLEOSIDES - DESIGN, SYNTHESIS AND ANTIPROLIFERATIVE ACTIVITY OF METHYL -IODO-1-BETA-D-RIBOFURANOSYLPYRAZOLE-3-CARBOXYLATE (IPCAR), AND DERIVATIVES, AGAINST HUMAN LEUKEMIAS, LYMPHOMAS AND SOLID TUMORS CELL-LINES IN-VITRO, Medicinal chemistry research, 6(5), 1996, pp. 293-311
A PLE-BASED RESOLUTION OF COCAINE, PSEUDOCOCAINE, AND 6-METHOXYLATED AND 7-METHOXYLATED COCAINE ANALOGS
Authors: KOZIKOWSKI AP SIMONI D BARALDI PG LAMPRONTI I MANFREDINI S
Citation: Ap. Kozikowski et al., A PLE-BASED RESOLUTION OF COCAINE, PSEUDOCOCAINE, AND 6-METHOXYLATED AND 7-METHOXYLATED COCAINE ANALOGS, Bioorganic & medicinal chemistry letters, 6(4), 1996, pp. 441-444
SYNTHESIS AND ANTITUMOR-ACTIVITY OF NOVEL DISTAMYCIN DERIVATIVES
Authors: BARALDI PG BERIA I CACCIARI B COZZI P FRANZETTI C MONGELLI N ROMAGNOLI R SPALLUTO G
Citation: Pg. Baraldi et al., SYNTHESIS AND ANTITUMOR-ACTIVITY OF NOVEL DISTAMYCIN DERIVATIVES, Bioorganic & medicinal chemistry letters, 6(11), 1996, pp. 1241-1246
STRUCTURE-ACTIVITY RELATIONSHIP OF NOVEL TALLIMUSTINE DERIVATIVES - SYNTHESIS AND ANTITUMOR-ACTIVITY
Authors: BARALDI PG BERIA I CACCIARI B CAPOLONGO L COZZI P MONGELLI N ROMAGNOLI R SPALLUTO G
Citation: Pg. Baraldi et al., STRUCTURE-ACTIVITY RELATIONSHIP OF NOVEL TALLIMUSTINE DERIVATIVES - SYNTHESIS AND ANTITUMOR-ACTIVITY, Bioorganic & medicinal chemistry letters, 6(11), 1996, pp. 1247-1252
DESIGN, SYNTHESIS AND ANTIPROLIFERATIVE ACTIVITY OF METHYL IODO-1-BETA-D-RIBOFURANOSYL-PYRAZOLE-3-CARBOXYLATE AND RELATED-COMPOUNDS
Authors: MANFREDINI S BAZZANINI R BARALDI PG SIMONI D VERTUANI S PANI A PINNA E SCINTU F LICHINO D LACOLLA P
Citation: S. Manfredini et al., DESIGN, SYNTHESIS AND ANTIPROLIFERATIVE ACTIVITY OF METHYL IODO-1-BETA-D-RIBOFURANOSYL-PYRAZOLE-3-CARBOXYLATE AND RELATED-COMPOUNDS, Bioorganic & medicinal chemistry letters, 6(11), 1996, pp. 1279-1284
SYNTHESIS OF THE TRITIUM-LABELED SCH-58261, A NEW NONXANTHINE A(2A)-ADENOSINE RECEPTOR ANTAGONIST
Authors: BARALDI PG CACCIARI B DIONISOTTI S EGAN J SPALLUTO G ZOCCHI C
Citation: Pg. Baraldi et al., SYNTHESIS OF THE TRITIUM-LABELED SCH-58261, A NEW NONXANTHINE A(2A)-ADENOSINE RECEPTOR ANTAGONIST, Journal of labelled compounds & radiopharmaceuticals, 38(8), 1996, pp. 725-732
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