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Results: 1-25 | 26-35
Results: 1-25/35
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
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
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
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, 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
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
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
SYNTHESIS, ANTIVIRAL AND ANTIPROLIFERATIVE ACTIVITY OF A NEW CLASS OF5-(ALKYL OR ARYLTHIO)-6-VINYL URACILS
Authors: BARALDI PG CACCIARI B ROMAGNOLI R SPALLUTO G GARUTI L ROBERTI M PANI A PERRA G SCINTU F PINNA N MUSIU C LACOLLA P
Citation: Pg. Baraldi et al., SYNTHESIS, ANTIVIRAL AND ANTIPROLIFERATIVE ACTIVITY OF A NEW CLASS OF5-(ALKYL OR ARYLTHIO)-6-VINYL URACILS, Anti-cancer drug design, 11(8), 1996, pp. 597-609
4-ISOPROPYL-2-OXAZOEIN-5-ONE ANION AS MASKED UMPOLED SYNTHON FOR BOTHFORMYL AND HYDROXYCARBONYL ANIONS - GENERATION, REACTIVITY AND SYNTHETIC APPLICATIONS
Authors: BARCO A BENETTI S DERISI C POLLINI GP SPALLUTO G ZANIRATO V
Citation: A. Barco et al., 4-ISOPROPYL-2-OXAZOEIN-5-ONE ANION AS MASKED UMPOLED SYNTHON FOR BOTHFORMYL AND HYDROXYCARBONYL ANIONS - GENERATION, REACTIVITY AND SYNTHETIC APPLICATIONS, Tetrahedron, 52(13), 1996, pp. 4719-4734
PYRAZOLO[4,3-E]-1,2,4-TRIAZOLO[1,5-C]PYRIMIDINE DERIVATIVES - POTENT AND SELECTIVE A(2A) ADENOSINE ANTAGONISTS
Authors: BARALDI PG CACCIARI B SPALLUTO G VILLATORO MJPDIY ZOCCHI C DIONISOTTI S ONGINI E
Citation: Pg. Baraldi et al., PYRAZOLO[4,3-E]-1,2,4-TRIAZOLO[1,5-C]PYRIMIDINE DERIVATIVES - POTENT AND SELECTIVE A(2A) ADENOSINE ANTAGONISTS, Journal of medicinal chemistry, 39(5), 1996, pp. 1164-1171
NOVEL UBSTITUTED-PHENYLCARBAMOYL)ADENOSINE-5'-URONAMIDES AS POTENT AGONISTS FOR A(3) ADENOSINE RECEPTORS
Authors: BARALDI PG CACCIARI B SPALLUTO G JI XD OLAH ME STILES G DIONISOTTI S ZOCCHI C ONGINI E JACOBSON KA
Citation: Pg. Baraldi et al., NOVEL UBSTITUTED-PHENYLCARBAMOYL)ADENOSINE-5'-URONAMIDES AS POTENT AGONISTS FOR A(3) ADENOSINE RECEPTORS, Journal of medicinal chemistry, 39(3), 1996, pp. 802-806
2,3-TRIAZOLO[5,4-E]1,2,4-TRIAZOLO[1,5-C]PYRIMIDINE DERIVATIVES - A NEW CLASS OF A(2A) ADENOSINE RECEPTOR ANTAGONISTS
Authors: BARALDI PG CACCIARI B SPALLUTO G DELASINFANTS MJP ZOCCHI C FERRARA S DIONISOTTI S
Citation: Pg. Baraldi et al., 2,3-TRIAZOLO[5,4-E]1,2,4-TRIAZOLO[1,5-C]PYRIMIDINE DERIVATIVES - A NEW CLASS OF A(2A) ADENOSINE RECEPTOR ANTAGONISTS, Il Farmaco, 51(4), 1996, pp. 297-300
1H-PYRAZOLO[4,3-D]PYRIMIDINE-7(6H)-ONE AND 5H-PYRAZOLO[4,3-D] 1,2,3-TRIAZIN-4(3H)-ONE DERIVATIVES - SYNTHESIS AND IN-VITRO BIOLOGICAL-ACTIVITY AT ADENOSINE A(1) AND A(2A) RECEPTORS
Authors: BARALDI PG CACCIARI B DALPIAZ A DIONISOTTI S ZOCCHI C DELASINFANTAS MJP SPALLUTO G VARANI K
Citation: Pg. Baraldi et al., 1H-PYRAZOLO[4,3-D]PYRIMIDINE-7(6H)-ONE AND 5H-PYRAZOLO[4,3-D] 1,2,3-TRIAZIN-4(3H)-ONE DERIVATIVES - SYNTHESIS AND IN-VITRO BIOLOGICAL-ACTIVITY AT ADENOSINE A(1) AND A(2A) RECEPTORS, Arzneimittel-Forschung, 46(4), 1996, pp. 365-368
UNUSUAL RING-OPENING REACTION OF 6,7-DIHYDROTHIENO[3,2-D]PYRIMIDINE-2,4-DIONE DERIVATIVES LEADING TO 5-(ALKYLTHIO)-6-VINYLURACILS
Authors: BARALDI PG CACCIARI B MANFREDINI S POLLINI GP SIMONI D SPALLUTO G ZANIRATO V
Citation: Pg. Baraldi et al., UNUSUAL RING-OPENING REACTION OF 6,7-DIHYDROTHIENO[3,2-D]PYRIMIDINE-2,4-DIONE DERIVATIVES LEADING TO 5-(ALKYLTHIO)-6-VINYLURACILS, Journal of organic chemistry, 60(5), 1995, pp. 1461-1463
MASTERING BETA-KETO-ESTERS
Authors: BENETTI S ROMAGNOLI R DERISI C SPALLUTO G ZANIRATO V
Citation: S. Benetti et al., MASTERING BETA-KETO-ESTERS, Chemical reviews, 95(4), 1995, pp. 1065-1114
Risultati: 1-25 | 26-35