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Results: 1-17 |
Results: 17
SOLID-PHASE SYNTHESIS OF UREA LIBRARIES USING A DIVERSIFIABLE THIOPHENOXY CARBONYL LINKER
Authors: DRESSMAN BA SINGH U KALDOR SW
Citation: Ba. Dressman et al., SOLID-PHASE SYNTHESIS OF UREA LIBRARIES USING A DIVERSIFIABLE THIOPHENOXY CARBONYL LINKER, Tetrahedron letters, 39(22), 1998, pp. 3631-3634
COMBINATORIAL CHEMISTRY USING POLYMER-SUPPORTED REAGENTS
Authors: KALDOR SW SIEGEL MG
Citation: Sw. Kaldor et Mg. Siegel, COMBINATORIAL CHEMISTRY USING POLYMER-SUPPORTED REAGENTS, CURRENT OPINION IN CHEMICAL BIOLOGY, 1(1), 1997, pp. 101-106
5-HT1F RECEPTOR AGONISTS INHIBIT NEUROGENIC DURAL INFLAMMATION IN GUINEA-PIGS
Authors: JOHNSON KW SCHAUS JM DURKIN MM AUDIA JE KALDOR SW FLAUGH ME ADHAM N ZGOMBICK JM COHEN ML BRANCHEK TA PHEBUS LA
Citation: Kw. Johnson et al., 5-HT1F RECEPTOR AGONISTS INHIBIT NEUROGENIC DURAL INFLAMMATION IN GUINEA-PIGS, NeuroReport, 8(9-10), 1997, pp. 2237-2240
SYNTHESIS OF 2',3'-DIDEOXY-3'-HYDROXYMETHYLCYTIDINE - A NOVEL HYDROFORMYLATION ROUTE
Authors: KALDOR SW FRITZ JE WARD JA
Citation: Sw. Kaldor et al., SYNTHESIS OF 2',3'-DIDEOXY-3'-HYDROXYMETHYLCYTIDINE - A NOVEL HYDROFORMYLATION ROUTE, Tetrahedron letters, 38(9), 1997, pp. 1509-1510
RAPID PURIFICATION OF SMALL-MOLECULE LIBRARIES BY ION-EXCHANGE CHROMATOGRAPHY
Authors: SIEGEL MG HAHN PJ DRESSMAN BA FRITZ JE GRUNWELL JR KALDOR SW
Citation: Mg. Siegel et al., RAPID PURIFICATION OF SMALL-MOLECULE LIBRARIES BY ION-EXCHANGE CHROMATOGRAPHY, Tetrahedron letters, 38(19), 1997, pp. 3357-3360
SYNTHESIS OF 2',3'-DIDEOXY-3'-HYDROXYMETHYLCYTIDINE - A UNIQUE ANTIVIRAL NUCLEOSIDE
Authors: FAUL MM HUFF BE DUNLAP SE FRANK SA FRITZ JE KALDOR SW LETOURNEAU ME STASZAK MA WARD JA WERNER JA WINNEROSKI LL
Citation: Mm. Faul et al., SYNTHESIS OF 2',3'-DIDEOXY-3'-HYDROXYMETHYLCYTIDINE - A UNIQUE ANTIVIRAL NUCLEOSIDE, Tetrahedron, 53(24), 1997, pp. 8085-8104
VIRACEPT (NELFINAVIR MESYLATE, AG1343) - A POTENT, ORALLY BIOAVAILABLE INHIBITOR OF HIV-1 PROTEASE
Authors: KALDOR SW KALISH VJ DAVIES JF SHETTY BV FRITZ JE APPELT K BURGESS JA CAMPANALE KM CHIRGADZE NY CLAWSON DK DRESSMAN BA HATCH SD KHALIL DA KOSA MB LUBBEHUSEN PP MUESING MA PATICK AK REICH SH SU KS TATLOCK JH
Citation: Sw. Kaldor et al., VIRACEPT (NELFINAVIR MESYLATE, AG1343) - A POTENT, ORALLY BIOAVAILABLE INHIBITOR OF HIV-1 PROTEASE, Journal of medicinal chemistry, 40(24), 1997, pp. 3979-3985
DISCOVERY OF ANTIRHINOVIRAL LEADS BY SCREENING A COMBINATORIAL LIBRARY OF UREAS PREPARED USING COVALENT SCAVENGERS
Authors: KALDOR SW FRITZ JE TANG J MCKINNEY ER
Citation: Sw. Kaldor et al., DISCOVERY OF ANTIRHINOVIRAL LEADS BY SCREENING A COMBINATORIAL LIBRARY OF UREAS PREPARED USING COVALENT SCAVENGERS, Bioorganic & medicinal chemistry letters, 6(24), 1996, pp. 3041-3044
SIMPLE IN-VITRO TRANSLATION ASSAY TO ANALYZE INHIBITORS OF RHINOVIRUSPROTEASES
Authors: HEINZ BA TANG J LABUS JM CHADWELL FW KALDOR SW HAMMOND M
Citation: Ba. Heinz et al., SIMPLE IN-VITRO TRANSLATION ASSAY TO ANALYZE INHIBITORS OF RHINOVIRUSPROTEASES, Antimicrobial agents and chemotherapy, 40(1), 1996, pp. 267-270
SOLID-PHASE SYNTHESIS OF HYDANTOINS USING A CARBAMATE LINKER AND A NOVEL CYCLIZATION CLEAVAGE STEP
Authors: DRESSMAN BA SPANGLE LA KALDOR SW
Citation: Ba. Dressman et al., SOLID-PHASE SYNTHESIS OF HYDANTOINS USING A CARBAMATE LINKER AND A NOVEL CYCLIZATION CLEAVAGE STEP, Tetrahedron letters, 37(7), 1996, pp. 937-940
USE OF SOLID SUPPORTED NUCLEOPHILES AND ELECTROPHILES FOR THE PURIFICATION OF NONPEPTIDE SMALL-MOLECULE LIBRARIES
Authors: KALDOR SW SIEGEL MG FRITZ JE DRESSMAN BA HAHN PJ
Citation: Sw. Kaldor et al., USE OF SOLID SUPPORTED NUCLEOPHILES AND ELECTROPHILES FOR THE PURIFICATION OF NONPEPTIDE SMALL-MOLECULE LIBRARIES, Tetrahedron letters, 37(40), 1996, pp. 7193-7196
A SYSTEMATIC STUDY OF P-1-P-3 SPANNING SIDE-CHAINS FOR THE INHIBITIONOF HIV-1 PROTEASE
Authors: KALDOR SW APPELT K FRITZ JE HAMMOND M CROWELL TA BAXTER AJ HATCH SD WISKERCHEN M MUESING MA
Citation: Sw. Kaldor et al., A SYSTEMATIC STUDY OF P-1-P-3 SPANNING SIDE-CHAINS FOR THE INHIBITIONOF HIV-1 PROTEASE, Bioorganic & medicinal chemistry letters, 5(7), 1995, pp. 715-720
ISOPHTHALIC ACID-DERIVATIVES - AMINO-ACID SURROGATES FOR THE INHIBITION OF HIV-1 PROTEASE
Authors: KALDOR SW DRESSMAN BA HAMMOND M APPELT K BURGESS JA LUBBEHUSEN PP MUESING MA HATCH SD WISKERCHEN MA BAXTER AJ
Citation: Sw. Kaldor et al., ISOPHTHALIC ACID-DERIVATIVES - AMINO-ACID SURROGATES FOR THE INHIBITION OF HIV-1 PROTEASE, Bioorganic & medicinal chemistry letters, 5(7), 1995, pp. 721-726
STRUCTURE-BASED DRUG DESIGN OF NONPEPTIDIC P-2 SUBSTITUENTS FOR HIV-1PROTEASE INHIBITORS
Authors: KALISH VJ TATLOCK JH DAVIES JF KALDOR SW DRESSMAN BA REICH S PINO M NYUGEN D APPELT K MUSICK L WU BW
Citation: Vj. Kalish et al., STRUCTURE-BASED DRUG DESIGN OF NONPEPTIDIC P-2 SUBSTITUENTS FOR HIV-1PROTEASE INHIBITORS, Bioorganic & medicinal chemistry letters, 5(7), 1995, pp. 727-732
GLUTAMINE-DERIVED ALDEHYDES FOR THE INHIBITION OF HUMAN RHINOVIRUS 3CPROTEASE
Authors: KALDOR SW HAMMOND M DRESSMAN BA LABUS JM CHADWELL FW KLINE AD HEINZ BA
Citation: Sw. Kaldor et al., GLUTAMINE-DERIVED ALDEHYDES FOR THE INHIBITION OF HUMAN RHINOVIRUS 3CPROTEASE, Bioorganic & medicinal chemistry letters, 5(17), 1995, pp. 2021-2026
A CONVENIENT, LARGE-SCALE SYNTHESIS OF N-CBZ-(S-PHENYL)-L-CYSTEINE
Authors: MARZONI G KALDOR SW TRIPPE AJ SHAMBLIN BM FRITZ JE
Citation: G. Marzoni et al., A CONVENIENT, LARGE-SCALE SYNTHESIS OF N-CBZ-(S-PHENYL)-L-CYSTEINE, Synthetic communications, 25(16), 1995, pp. 2475-2482
NEW DIPEPTIDE ISOSTERES USEFUL FOR THE INHIBITION OF HIV-1 PROTEASE
Authors: KALDOR SW HAMMOND M DRESSMAN BA FRITZ JE CROWELL TA HERMANN RA
Citation: Sw. Kaldor et al., NEW DIPEPTIDE ISOSTERES USEFUL FOR THE INHIBITION OF HIV-1 PROTEASE, Bioorganic & medicinal chemistry letters, 4(11), 1994, pp. 1385-1390
Risultati: 1-17 |