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Effect of biodegradable chelating agents on heavy metals phytoextraction with Mirabilis jalapa and on its associated bacteriaCAO, Alessia; CARUCCI, Alessandra; LAI, Tiziana et al.European journal of soil biology. 2007, Vol 43, Num 4, pp 200-206, issn 1164-5563, 7 p.Conference Paper

Synthesis and biological evaluation of azole derivatives, analogues of bifonazole, with a phenylisoxazolyl or phenylpyrimidinyl moietyMENOZZI, Giulia; MOSTI, Luisa; FOSSA, Paola et al.Il Farmaco (Pavia). 2001, Vol 56, Num 9, pp 633-640, issn 0014-827XArticle

A new class of antifungal agents. Synthesis and antimycotic activity of disubstituted N-azolylaminesCASTELLANO, Sabrina; STEFANCICH, Giorgio; MUSIU, Chiara et al.Archiv der Pharmazie (Weinheim). 2000, Vol 333, Num 9, pp 299-304, issn 0365-6233Article

Anti-HIV evaluation of benzo[d]isothiazole hydrazonesVICINI, Paola; INCERTI, Matteo; LA COLLA, Paolo et al.European journal of medicinal chemistry. 2009, Vol 44, Num 4, pp 1801-1807, issn 0223-5234, 7 p.Article

Structure-activity relationship studies on new dabos: effect of substitutions at pyrimidine C-5 and C-6 positions on anti-HIV-1 activitySBARDELLA, Gianluca; MAI, Antonello; ARTICO, Marino et al.Antiviral chemistry & chemotherapy. 2001, Vol 12, Num 1, pp 37-50, issn 0956-3202Article

Antitumor agents. 3. Design, synthesis, and biological evaluation of new pyridoisoquinolindione and dihydrothienoquinolindione derivatives with potent cytotoxic activityBOLOGNESE, Adele; CORREALE, Gaetano; MANFRA, Michele et al.Journal of medicinal chemistry (Print). 2004, Vol 47, Num 4, pp 849-858, issn 0022-2623, 10 p.Article

The use of a new in vitro reaction substrate reproducing both U3 and U5 regions of the HIV-1 3'-ends increases the correlation between the in vitro and in vivo effects of the HIV-1 integrase inhibitorsTRAMONTANO, Enzo; ONIDI, Loredana; ESPOSITO, Francesca et al.Biochemical pharmacology. 2004, Vol 67, Num 9, pp 1751-1761, issn 0006-2952, 11 p.Article

Surface-active compounds and their role in the access to hydrocarbons in Gordonia strainsFRANZETTI, Andrea; BESTETTI, Giuseppina; CAREDDA, Paolo et al.FEMS microbiology ecology. 2008, Vol 63, Num 2, pp 238-248, issn 0168-6496, 11 p.Article

Synthesis and antiproliferative activity of benzo[d]isothiazole hydrazonesVICINI, Paola; INCERTI, Matteo; DOYTCHINOVA, Irini A et al.European journal of medicinal chemistry. 2006, Vol 41, Num 5, pp 624-632, issn 0223-5234, 9 p.Article

Synthesis and antiviral activity of new dimeric inhibitors against HIV-1DANEL, Krzysztof; LARSEN, Louise M; PEDERSEN, Erik B et al.Bioorganic & medicinal chemistry. 2008, Vol 16, Num 1, pp 511-517, issn 0968-0896, 7 p.Article

6-[1-(4-Fluorophenyl)methyl-1H-pyrrol-2-yl]-2,4-dioxo-5-hexenoic acid ethyl ester a novel diketo acid derivative which selectively inhibits the HIV-1 viral replication in cell culture and the ribonuclease H activity in vitroTRAMONTANO, Enzo; ESPOSITO, Francesca; BADAS, Roberta et al.Antiviral research. 2005, Vol 65, Num 2, pp 117-124, issn 0166-3542, 8 p.Article

Activity and molecular modeling of a new small molecule active against NNRTI-resistant HIV-1 mutantsCARTA, Antonio; PRICL, Sabrina; PIRAS, Sandra et al.European journal of medicinal chemistry. 2009, Vol 44, Num 12, pp 5117-5122, issn 0223-5234, 6 p.Article

Antimicrobial activity of 10-(diphenylmethylene)-4-azatricyclo [5.2.1.02,6]dec-8-ene-3,5-dione derivativesSTEFANSKA, Joanna; BIELENICA, Anna; STRUGA, Marta et al.Annals of microbiology. 2010, Vol 60, Num 1, pp 151-155, issn 1590-4261, 5 p.Article

Thiocarbamates as non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 2. Parallel synthesis, molecular modelling and structure-activity relationship studies on analogues of O-(2-phenylethyl)-N-phenylthiocarbamateCESARINI, Sara; SPALLAROSSA, Andrea; RANISE, Angelo et al.Bioorganic & medicinal chemistry. 2008, Vol 16, Num 7, pp 4173-4185, issn 0968-0896, 13 p.Article

Design, synthesis, SAR, and molecular modeling studies of acylthiocarbamates: A novel series of potent non-nucleoside HIV-1 reverse transcriptase inhibitors structurally related to phenethylthiazolylthiourea derivativesRANISE, Angelo; SPALLAROSSA, Andrea; SCHENONE, Silvia et al.Journal of medicinal chemistry (Print). 2003, Vol 46, Num 5, pp 768-781, issn 0022-2623, 14 p.Article

Synthesis and studies of 3'-C-trifluoromethyl nucleoside analogues bearing adenine or cytosine as the basesJEANNOT, Frédéric; GOSSELIN, Gilles; STANDRING, David et al.Bioorganic & medicinal chemistry. 2002, Vol 10, Num 10, pp 3153-3161, issn 0968-0896Article

Design, synthesis and QSAR studies on N-aryl heteroarylisopropanolamines, a new class of non-peptidic HIV-1 protease inhibitorsDI SANTO, Roberto; COSTI, Roberta; ARTICO, Marino et al.Bioorganic & medicinal chemistry. 2002, Vol 10, Num 8, pp 2511-2526, issn 0968-0896Article

Synthesis and anti-HIV-1 activity of new delavirdine analogues carrying arylpyrrole moietiesPINNA, Gérard Aimè; LORIGA, Giovanni; MURINEDDU, Gabriele et al.Chemical and pharmaceutical bulletin. 2001, Vol 49, Num 11, pp 1406-1411, issn 0009-2363Article

N-Acylated and N,N'-diacylated imidazolidine-2-thione derivatives and N,N'-diacylated tetrahydropyrimidine-2(1H)-thione analogues : Synthesis and antiproliferative activityCESARINI, Sara; SPALLAROSSA, Andrea; RANISE, Angelo et al.European journal of medicinal chemistry. 2009, Vol 44, Num 3, pp 1106-1118, issn 0223-5234, 13 p.Article

Thiocarbamates as non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 1. Parallel synthesis, molecular modelling and structure-activity relationship studies on 0-[2-(hetero)arylethyl]-N-phenylthiocarbamatesCESARINI, Sara; SPALLAROSSA, Andrea; RANISE, Angelo et al.Bioorganic & medicinal chemistry. 2008, Vol 16, Num 7, pp 4160-4172, issn 0968-0896, 13 p.Article

Synthesis and biological evaluation of benzo[d]isothiazole, benzothiazole and thiazole Schiff basesVICINI, Paola; GERONIKAKI, Athina; INCERTI, Matteo et al.Bioorganic & medicinal chemistry. 2003, Vol 11, Num 22, pp 4785-4789, issn 0968-0896, 5 p.Article

3,4-Dihydro-2-alkoxy-6-benzyl-oxopyrimidines [DABOs]: Development of a potent class of non-nucleoside reverse transcriptase inhibitorsMARONGIU, M. Elena; PANI, Alessandra; MUSIU, Chiara et al.Recent research developments in medicinal chemistry (Vol. 1 (2001) ). Recent developments in antiviral research. 2001, pp 65-92, isbn 81-7895-012-X, 28 p.Book Chapter

Novel modifications in the series of O-(2-phthalimidoethyl)-N-substituted thiocarbamates and their ring-opened congeners as non-nucleoside HIV-1 reverse transcriptase inhibitorsSPALLAROSSA, Andrea; CESARINI, Sara; RANISE, Angelo et al.European journal of medicinal chemistry. 2009, Vol 44, Num 4, pp 1650-1663, issn 0223-5234, 14 p.Article

Design, synthesis, and preliminary in vitro and in silico antiviral activity of [4,7]phenantrolines and 1-oxo-1,4-dihydro-[4,7]phenantrolines against single-stranded positive-sense RNA genome virusesCARTA, Antonio; LORIGA, Mario; PAGLIETTI, Giuseppe et al.Bioorganic & medicinal chemistry. 2007, Vol 15, Num 5, pp 1914-1927, issn 0968-0896, 14 p.Article

Computer-aided design, synthesis, and anti-HIV-1 activity in vitro of 2-alkylamino-6-[1-(2,6-difluorophenyl)alkyl]-3,4-dihydro-5-alkylpyrimidin-4(3H)- ones as novel potent non-nucleoside reverse transcriptase inhibitors, also active against the Y181C variantRAGNO, Rino; MAI, Antonello; SBARDELLA, Gianluca et al.Journal of medicinal chemistry (Print). 2004, Vol 47, Num 4, pp 928-934, issn 0022-2623, 7 p.Article

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