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Results: 1-8 |
Results: 8
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
HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 PROTEINASE RESISTANCE TO SYMMETRICAL CYCLIC UREA INHIBITOR ANALOGS
Authors: NILLROTH U VRANG L MARKGREN PO HULTEN J HALLBERG A DANIELSON UH
Citation: U. Nillroth et al., HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 PROTEINASE RESISTANCE TO SYMMETRICAL CYCLIC UREA INHIBITOR ANALOGS, Antimicrobial agents and chemotherapy, 41(11), 1997, pp. 2383-2388
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 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
THE USE OF 5'-PHOSPHATE DERIVATIVES OF NUCLEOSIDE ANALOGS AS INHIBITORS OF HIV-1 REPLICATION
Authors: NILLROTH U VRANG L AHLSEN G BESIDSKY Y CHATTOPADHYAYA J UGI I DANIELSON UH
Citation: U. Nillroth et al., THE USE OF 5'-PHOSPHATE DERIVATIVES OF NUCLEOSIDE ANALOGS AS INHIBITORS OF HIV-1 REPLICATION, Antiviral chemistry & chemotherapy, 6(1), 1995, pp. 50-64
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