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Results: 1-25 | 26-27
Results: 1-25/27
HIV-1 PROTEASE INHIBITORS BASED ON ACYCLIC CARBOHYDRATES
Authors: ZUCCARELLO G BOUZIDE A KVARNSTROM I NIKLASSON G SVENSSON SCT BRISANDER M DANIELSSON H NILLROTH U KARLEN A HALLBERG A CLASSON B SAMUELSSON B
Citation: G. Zuccarello et al., HIV-1 PROTEASE INHIBITORS BASED ON ACYCLIC CARBOHYDRATES, Journal of organic chemistry, 63(15), 1998, pp. 4898-4906
DESIGN AND SYNTHESIS OF NEW POTENT C-2-SYMMETRICAL HIV-1 PROTEASE INHIBITORS - USE OF L-MANNARIC ACID AS A PEPTIDOMIMETIC SCAFFOLD
Authors: ALTERMAN M BJORSNE M MUHLMAN A CLASSON B KVARNSTROM I DANIELSON H MARKGREN PO NILLROTH U UNGE T HALLBERG A SAMUELSSON B
Citation: M. Alterman et al., DESIGN AND SYNTHESIS OF NEW POTENT C-2-SYMMETRICAL HIV-1 PROTEASE INHIBITORS - USE OF L-MANNARIC ACID AS A PEPTIDOMIMETIC SCAFFOLD, Journal of medicinal chemistry, 41(20), 1998, pp. 3782-3792
SYNTHESIS OF NOVEL FLUORO CARBOCYCLIC PURINE NUCLEOSIDE ANALOGS
Authors: WACHTMEISTER J CLASSON B KVARNSTROM I SAMUELSSON B
Citation: J. Wachtmeister et al., SYNTHESIS OF NOVEL FLUORO CARBOCYCLIC PURINE NUCLEOSIDE ANALOGS, Nucleosides & nucleotides, 16(5-6), 1997, pp. 809-814
A CONVENIENT SYNTHESIS OF )-(T-BUTYLOXYCARBONYLAMINO)-2'-PHENYLETHYL]OXIRANE - A USEFUL BUILDING-BLOCK IN THE SYNTHESIS OF HIV PROTEASE INHIBITORS
Authors: BRANALT J KVARNSTROM I CLASSON B SAMUELSSON B NILLROTH U DANIELSON UH KARLEN A HALLBERG A
Citation: J. Branalt et al., A CONVENIENT SYNTHESIS OF )-(T-BUTYLOXYCARBONYLAMINO)-2'-PHENYLETHYL]OXIRANE - A USEFUL BUILDING-BLOCK IN THE SYNTHESIS OF HIV PROTEASE INHIBITORS, Tetrahedron letters, 38(19), 1997, pp. 3483-3486
SYNTHESIS OF CARBOCYCLIC 2',3'-DIDEOXY-2'-FLUORO-3'-C-HYDROXYMETHYL NUCLEOSIDE ANALOGS AS POTENTIAL INHIBITORS OF HIV AND HSV
Authors: WACHTMEISTER J CLASSON B SAMUELSSON B KVARNSTROM I
Citation: J. Wachtmeister et al., SYNTHESIS OF CARBOCYCLIC 2',3'-DIDEOXY-2'-FLUORO-3'-C-HYDROXYMETHYL NUCLEOSIDE ANALOGS AS POTENTIAL INHIBITORS OF HIV AND HSV, Tetrahedron, 53(5), 1997, pp. 1861-1872
SYNTHESIS OF ENANTIOMERICALLY PURE CIS AND TRANS 2-AMINOCYCLOPENTANECARBOXYLIC ACIDS - USE OF PROLINE REPLACEMENTS IN POTENTIAL HIV-PROTEASE INHIBITORS
Authors: NOTEBERG D BRANALT J KVARNSTROM I CLASSON B SAMUELSSON B NILLROTH U DANIELSON H KARLEN A HALLBERG A
Citation: D. Noteberg et al., SYNTHESIS OF ENANTIOMERICALLY PURE CIS AND TRANS 2-AMINOCYCLOPENTANECARBOXYLIC ACIDS - USE OF PROLINE REPLACEMENTS IN POTENTIAL HIV-PROTEASE INHIBITORS, Tetrahedron, 53(23), 1997, pp. 7975-7984
CYCLIC HIV-1 PROTEASE INHIBITORS DERIVED FROM MANNITOL - SYNTHESIS, INHIBITORY POTENCIES, AND COMPUTATIONAL PREDICTIONS OF BINDING AFFINITIES
Authors: HULTEN J BONHAM NM NILLROTH U HANSSON T ZUCCARELLO G BOUZIDE A AQVIST J CLASSON B DANIELSON UH KARLEN A KVARNSTROM I SAMUELSSON B HALLBERG A
Citation: J. Hulten et al., CYCLIC HIV-1 PROTEASE INHIBITORS DERIVED FROM MANNITOL - SYNTHESIS, INHIBITORY POTENCIES, AND COMPUTATIONAL PREDICTIONS OF BINDING AFFINITIES, Journal of medicinal chemistry, 40(6), 1997, pp. 885-897
SYNTHESIS OF C-2 SYMMETRICAL POTENTIAL INHIBITORS OF HIV-1 PROTEASE FROM D-MANNITOL
Authors: NIKLASSON G KVARNSTROM I CLASSON B SAMUELSSON B NILLROTH U DANIELSON H KARLEN A HALLBERG A
Citation: G. Niklasson et al., SYNTHESIS OF C-2 SYMMETRICAL POTENTIAL INHIBITORS OF HIV-1 PROTEASE FROM D-MANNITOL, Journal of carbohydrate chemistry, 15(5), 1996, pp. 555-569
SYNTHESIS OF ENANTIOMERICALLY PURE BIS(HYDROXYMETHYL)-BRANCHED CYCLOHEXENYL AND CYCLOHEXYL PURINES AS POTENTIAL INHIBITORS OF HIV
Authors: ROSENQUIST A KVARNSTROM I CLASSON B SAMUELSSON B
Citation: A. Rosenquist et al., SYNTHESIS OF ENANTIOMERICALLY PURE BIS(HYDROXYMETHYL)-BRANCHED CYCLOHEXENYL AND CYCLOHEXYL PURINES AS POTENTIAL INHIBITORS OF HIV, Journal of organic chemistry, 61(18), 1996, pp. 6282-6288
SYNTHESIS OF 5-BIS(HYDROXYMETHYL)-1,3-DIOXOLAN-2-YL]NUCLEOSIDES AS POTENTIAL INHIBITORS OF HIV
Authors: BRANALT J KVARNSTROM I CLASSON B SAMUELSSON B
Citation: J. Branalt et al., SYNTHESIS OF 5-BIS(HYDROXYMETHYL)-1,3-DIOXOLAN-2-YL]NUCLEOSIDES AS POTENTIAL INHIBITORS OF HIV, Journal of organic chemistry, 61(11), 1996, pp. 3599-3603
SYNTHESIS OF BIS(HYDROXYMETHYL)-1,3-OXATHIOLAN-2-YL]NUCLEOSIDES AS POTENTIAL INHIBITORS OF HIV VIA STEREOSPECIFIC BASE-INDUCED REARRANGEMENT OF A 2,3-EPOXY THIOACETATE
Authors: BRANALT J KVARNSTROM I CLASSON B SAMUELSSON B
Citation: J. Branalt et al., SYNTHESIS OF BIS(HYDROXYMETHYL)-1,3-OXATHIOLAN-2-YL]NUCLEOSIDES AS POTENTIAL INHIBITORS OF HIV VIA STEREOSPECIFIC BASE-INDUCED REARRANGEMENT OF A 2,3-EPOXY THIOACETATE, Journal of organic chemistry, 61(11), 1996, pp. 3604-3610
SYNTHESIS OF -BIS(HYDROXYMETHYL)-1,3-DITHIOLAN-2-YL]NUCLEOSIDES AS POTENTIAL INHIBITORS OF HIV
Authors: BRANALT J KVARNSTROM I CLASSON B SAMUELSSON B
Citation: J. Branalt et al., SYNTHESIS OF -BIS(HYDROXYMETHYL)-1,3-DITHIOLAN-2-YL]NUCLEOSIDES AS POTENTIAL INHIBITORS OF HIV, Journal of organic chemistry, 61(11), 1996, pp. 3611-3615
SYNTHESIS OF 2',3'-DIDEOXY-3',4'-DIHYDROXYMETHYL SUBSTITUTED PYRIMIDINE NUCLEOSIDE ANALOGS
Authors: BJORSNE M CLASSON B KERS I SAMUELSSON B KVARNSTROM I
Citation: M. Bjorsne et al., SYNTHESIS OF 2',3'-DIDEOXY-3',4'-DIHYDROXYMETHYL SUBSTITUTED PYRIMIDINE NUCLEOSIDE ANALOGS, Bioorganic & medicinal chemistry letters, 5(1), 1995, pp. 43-46
SYNTHESIS OF METHYL-2',3',4'-TRIDEOXY-BETA-THREO-PENTOPYRANOSYL NUCLEOSIDES AS POTENTIAL INHIBITORS OF HIV
Authors: LUNDQUIST A KVARNSTROM I SVENSSON SCT CLASSON B SAMUELSSON B
Citation: A. Lundquist et al., SYNTHESIS OF METHYL-2',3',4'-TRIDEOXY-BETA-THREO-PENTOPYRANOSYL NUCLEOSIDES AS POTENTIAL INHIBITORS OF HIV, Nucleosides & nucleotides, 14(7), 1995, pp. 1493-1502
SYNTHESIS AND ANTIVIRAL PROPERTIES OF 2',3'-DIDEOXY-3',4'DIHYDROXYMETHYL SUBSTITUTED PYRIMIDINE NUCLEOSIDE ANALOGS
Authors: BJORSNE M CLASSON B KERS I SAMUELSSON B
Citation: M. Bjorsne et al., SYNTHESIS AND ANTIVIRAL PROPERTIES OF 2',3'-DIDEOXY-3',4'DIHYDROXYMETHYL SUBSTITUTED PYRIMIDINE NUCLEOSIDE ANALOGS, Nucleosides & nucleotides, 14(3-5), 1995, pp. 283-286
SYNTHESIS OF NOVEL OLEFINIC CARBOCYCLIC PURINE NUCLEOSIDE ANALOGS
Authors: WACHTMEISTER J CLASSON B SAMUELSSON B
Citation: J. Wachtmeister et al., SYNTHESIS OF NOVEL OLEFINIC CARBOCYCLIC PURINE NUCLEOSIDE ANALOGS, Nucleosides & nucleotides, 14(3-5), 1995, pp. 405-408
SYNTHESIS OF 2',3'-DIDEOXYCYCLO-2'-PENTENYL-3'-C-HYDROXYMETHYL CARBOCYCLIC NUCLEOSIDE ANALOGS AS POTENTIAL ANTIVIRAL AGENTS
Authors: WACHTMEISTER J CLASSON B SAMUELSSON B KVARNSTROM I
Citation: J. Wachtmeister et al., SYNTHESIS OF 2',3'-DIDEOXYCYCLO-2'-PENTENYL-3'-C-HYDROXYMETHYL CARBOCYCLIC NUCLEOSIDE ANALOGS AS POTENTIAL ANTIVIRAL AGENTS, Tetrahedron, 51(7), 1995, pp. 2029-2038
SYNTHESIS OF CARBOCYCLIC 2',3'-DIDEOXY-2'-C-HYDROXYMETHYL NUCLEOSIDESAS POTENTIAL INHIBITORS OF HIV
Authors: ROSENQUIST A KVARNSTROM I SVENSSON SCT CLASSON B SAMUELSSON B
Citation: A. Rosenquist et al., SYNTHESIS OF CARBOCYCLIC 2',3'-DIDEOXY-2'-C-HYDROXYMETHYL NUCLEOSIDESAS POTENTIAL INHIBITORS OF HIV, Journal of organic chemistry, 59(7), 1994, pp. 1779-1782
SYNTHESIS OF 3'-DIDEOXY-3'-C-(HYDROXYMETHYL)-4'-THIONUCLEOSIDES AS POTENTIAL INHIBITORS OF HIV
Authors: BRANALT J KVARNSTROM I NIKLASSON G SVENSSON SCT CLASSON B SAMUELSSON B
Citation: J. Branalt et al., SYNTHESIS OF 3'-DIDEOXY-3'-C-(HYDROXYMETHYL)-4'-THIONUCLEOSIDES AS POTENTIAL INHIBITORS OF HIV, Journal of organic chemistry, 59(7), 1994, pp. 1783-1788
A NEW SYNTHESIS OF 4-THIOFURANOSIDES VIA REGIOSELECTIVE OPENING OF ANEPISULFIDE WITH ALLYLMAGNESIUM BROMIDE
Authors: BRANALT J KVARNSTROM I SVENSSON SCT CLASSON B SAMUELSSON B
Citation: J. Branalt et al., A NEW SYNTHESIS OF 4-THIOFURANOSIDES VIA REGIOSELECTIVE OPENING OF ANEPISULFIDE WITH ALLYLMAGNESIUM BROMIDE, Journal of organic chemistry, 59(16), 1994, pp. 4430-4432
MOLECULAR CHARACTERIZATION OF THE ANTIGEN RECOGNIZED BY THE LYMPHOSTROMAL MARKER MTS-32
Authors: MALIN M FRASER S BOYD R CLASSON B
Citation: M. Malin et al., MOLECULAR CHARACTERIZATION OF THE ANTIGEN RECOGNIZED BY THE LYMPHOSTROMAL MARKER MTS-32, Journal of leukocyte biology, 1993, pp. 55-55
EXPRESSION OF A SOLUBLE FORM OF THE FAS ANTIGEN
Authors: CLASSON B COVERDALE L TARLINTON D
Citation: B. Classon et al., EXPRESSION OF A SOLUBLE FORM OF THE FAS ANTIGEN, Journal of leukocyte biology, 1993, pp. 63-63
SYNTHESIS OF 2',3'-DIDEHYDRO-2',3'-DIDEOXY-3'-C-METHYL SUBSTITUTED NUCLEOSIDES
Authors: IOANNIDIS P CLASSON B SAMUELSSON B KVARNSTROM I
Citation: P. Ioannidis et al., SYNTHESIS OF 2',3'-DIDEHYDRO-2',3'-DIDEOXY-3'-C-METHYL SUBSTITUTED NUCLEOSIDES, Nucleosides & nucleotides, 12(8), 1993, pp. 865-877
SYNTHESIS OF 2',3'-DIDEHYDRO-2',3'-DIDEOXY-2'-C- METHYLSUBSTITUTED NUCLEOSIDES USING A NOVEL SN2' TYPE REACTION
Authors: IONNIDIS P CLASSON B SAMUELSSON B KVARNSTROM I
Citation: P. Ionnidis et al., SYNTHESIS OF 2',3'-DIDEHYDRO-2',3'-DIDEOXY-2'-C- METHYLSUBSTITUTED NUCLEOSIDES USING A NOVEL SN2' TYPE REACTION, Nucleosides & nucleotides, 12(5), 1993, pp. 449-462
SYNTHESIS OF MIMICS TO THYMIDINE TRIPHOSPHATE AND 3'-DEOXY-3'-FLUOROTHYMIDINE TRIPHOSPHATE
Authors: BJORSNE M CLASSON B KVARNSTROM I SAMUELSSON B
Citation: M. Bjorsne et al., SYNTHESIS OF MIMICS TO THYMIDINE TRIPHOSPHATE AND 3'-DEOXY-3'-FLUOROTHYMIDINE TRIPHOSPHATE, Nucleosides & nucleotides, 12(5), 1993, pp. 529-536
Risultati: 1-25 | 26-27