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Results: 1-9 |
Results: 9
Three-dimensional structure of a complex of galanthamine (Nivalin (R)) with acetylcholinesterase from Torpedo californica: Implications for the design of new anti-Alzheimer drugs
Authors: Bartolucci, C Perola, E Pilger, C Fels, G Lamba, D
Citation: C. Bartolucci et al., Three-dimensional structure of a complex of galanthamine (Nivalin (R)) with acetylcholinesterase from Torpedo californica: Implications for the design of new anti-Alzheimer drugs, PROTEINS, 42(2), 2001, pp. 182-191
EUDOC: A computer program for identification of drug interaction sites in macromolecules and drug leads from chemical databases
Authors: Pang, YP Perola, E Xu, K Prendergast, FG
Citation: Yp. Pang et al., EUDOC: A computer program for identification of drug interaction sites in macromolecules and drug leads from chemical databases, J COMPUT CH, 22(15), 2001, pp. 1750-1771
Discovery of a new inhibitor lead of adenovirus proteinase: steps toward selective, irreversible inhibitors of cysteine proteinases
Authors: Pang, YP Xu, K Kollmeyer, TM Perola, E McGrath, WJ Green, DT Mangel, WF
Citation: Yp. Pang et al., Discovery of a new inhibitor lead of adenovirus proteinase: steps toward selective, irreversible inhibitors of cysteine proteinases, FEBS LETTER, 502(3), 2001, pp. 93-97
Dimerization of an inactive fragment of huperzine A produces a drug with twice the potency of the natural product
Authors: Carlier, PR Du, DM Han, YF Liu, J Perola, E Williams, ID Pang, YP
Citation: Pr. Carlier et al., Dimerization of an inactive fragment of huperzine A produces a drug with twice the potency of the natural product, ANGEW CHEM, 39(10), 2000, pp. 1775
Successful virtual screening of a chemical database for farnesyltransferase inhibitor leads
Authors: Perola, E Xu, K Kollmeyer, TM Kaufmann, SH Prendergast, FG Pang, YP
Citation: E. Perola et al., Successful virtual screening of a chemical database for farnesyltransferase inhibitor leads, J MED CHEM, 43(3), 2000, pp. 401-408
Models of ternary complexes for nonpeptidic farnesyltransferase inhibitors: Insights into structure-based screen and design of potential anticancer therapeutics
Authors: Xu, K Perola, E Prendergast, FG Pang, YP
Citation: K. Xu et al., Models of ternary complexes for nonpeptidic farnesyltransferase inhibitors: Insights into structure-based screen and design of potential anticancer therapeutics, J MOL MODEL, 5(10), 1999, pp. 203-217
Fractions of chemically oversulphated galactosaminoglycan sulphates inhibit three enveloped viruses: human immunodeficiency virus type 1, herpes simplex virus type 1 and human cytomegalovirus
Authors: Di Caro, A Perola, E Bartolini, B Marzano, M Liverani, L Mascellani, G Benedetto, A Cellai, L
Citation: A. Di Caro et al., Fractions of chemically oversulphated galactosaminoglycan sulphates inhibit three enveloped viruses: human immunodeficiency virus type 1, herpes simplex virus type 1 and human cytomegalovirus, ANTIVIR CHE, 10(1), 1999, pp. 33-38
NMR structure of the chimeric hybrid duplex r(gcaguggc)center dot r(gcca)d(CTGC) comprising the tRNA-DNA junction formed during initiation of HIV-1 reverse transcription
Authors: Szyperski, T Gotte, M Billeter, M Perola, E Cellai, L Heumann, H Wuthrich, K
Citation: T. Szyperski et al., NMR structure of the chimeric hybrid duplex r(gcaguggc)center dot r(gcca)d(CTGC) comprising the tRNA-DNA junction formed during initiation of HIV-1 reverse transcription, J BIOM NMR, 13(4), 1999, pp. 343-355
"Back door" opening implied by the crystal structure of a carbamoylated acetylcholinesterase
Authors: Bartolucci, C Perola, E Cellai, L Brufani, M Lamba, D
Citation: C. Bartolucci et al., "Back door" opening implied by the crystal structure of a carbamoylated acetylcholinesterase, BIOCHEM, 38(18), 1999, pp. 5714-5719
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