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
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
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
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
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
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
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
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
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
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
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
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
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
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
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