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Results: 1-12 |
Results: 12
DESIGN AND SELECTION OF DMP-850 AND DMP-851 - THE NEXT-GENERATION OF CYCLIC UREA HIV PROTEASE INHIBITORS (VOL 5, PG 597, 1998)
Authors: RODGERS JD LAM PYS JOHNSON BL WANG HS LI RH RU Y KO SS SEITZ SP TRAINOR GL ANDERSON PS KLABE RM BACHELER LT CORDOVA B GARBER S REID C WRIGHT MR CHANG CH ERICKSONVIITANEN S
Citation: Jd. Rodgers et al., DESIGN AND SELECTION OF DMP-850 AND DMP-851 - THE NEXT-GENERATION OF CYCLIC UREA HIV PROTEASE INHIBITORS (VOL 5, PG 597, 1998), Chemistry & biology, 5(11), 1998, pp. 312-312
DESIGN AND SELECTION OF DMP-850 AND DMP-851 - THE NEXT-GENERATION OF CYCLIC UREA HIV PROTEASE INHIBITORS
Authors: RODGERS JD LAM PYS JOHNSON BL WANG HS KO SS SEITZ SP TRAINOR GL ANDERSON PS KLABE RM BACHELER LT CORDOVA B GARBER S REID C WRIGHT MR CHANG CH ERICKSONVIITANEN S
Citation: Jd. Rodgers et al., DESIGN AND SELECTION OF DMP-850 AND DMP-851 - THE NEXT-GENERATION OF CYCLIC UREA HIV PROTEASE INHIBITORS, Chemistry & biology, 5(10), 1998, pp. 597-608
MEK INHIBITORS - THE CHEMISTRY AND BIOLOGICAL-ACTIVITY OF U0126, ITS ANALOGS, AND CYCLIZATION PRODUCTS
Authors: DUNCIA JV SANTELLA JB HIGLEY CA PITTS WJ WITYAK J FRIETZE WE RANKIN FW SUN JH EARL RA TABAKA AC TELEHA CA BLOM KF FAVATA MF MANOS EJ DAULERIO AJ STRADLEY DA HORIUCHI K COPELAND RA SCHERLE PA TRZASKOS JM MAGOLDA RL TRAINOR GL WEXLER RR HOBBS FW OLSON RE
Citation: Jv. Duncia et al., MEK INHIBITORS - THE CHEMISTRY AND BIOLOGICAL-ACTIVITY OF U0126, ITS ANALOGS, AND CYCLIZATION PRODUCTS, Bioorganic & medicinal chemistry letters, 8(20), 1998, pp. 2839-2844
NONSYMMETRIC P2 P2' CYCLIC UREA HIV PROTEASE INHIBITORS - STRUCTURE-ACTIVITY RELATIONSHIP, BIOAVAILABILITY, AND RESISTANCE PROFILE OF MONOINDAZOLE-SUBSTITUTED P2 ANALOGS/
Authors: DELUCCA GV KIM UT LIANG J CORDOVA B KLABE RM GARBER S BACHELER LT LAM GN WRIGHT MR LOGUE KA ERICKSONVIITANEN S KO SS TRAINOR GL
Citation: Gv. Delucca et al., NONSYMMETRIC P2 P2' CYCLIC UREA HIV PROTEASE INHIBITORS - STRUCTURE-ACTIVITY RELATIONSHIP, BIOAVAILABILITY, AND RESISTANCE PROFILE OF MONOINDAZOLE-SUBSTITUTED P2 ANALOGS/, Journal of medicinal chemistry, 41(13), 1998, pp. 2411-2423
THE SYNTHESIS AND ANTITUMOR EVALUATION OF UNSYMMETRICAL BIS-IMIDES
Authors: CHERNEY RJ SWARTZ SG PATTEN AD AKAMIKE E SUN JH KALTENBACH RF SEITZ SP BEHRENS CH GETAHUN Z TRAINOR GL VAVALA M KIRSHENBAUM MR PAPP LM STAFFORD MP CZERNIAK PM DIAMOND RJ MCRIPLEY RJ PAGE RJ GROSS JL
Citation: Rj. Cherney et al., THE SYNTHESIS AND ANTITUMOR EVALUATION OF UNSYMMETRICAL BIS-IMIDES, Bioorganic & medicinal chemistry letters, 7(2), 1997, pp. 163-168
MOLECULAR RECOGNITION OF CYCLIC HIV PROTEASE INHIBITORS - NONSYMMETRIC CYCLIC UREAS WITH EXCELLENT ORAL BIOAVAILABILITY AND LOW DRUG-RESISTANCE PROFILES
Authors: LAM PYS RODGERS JD LI R RU Y JADHAV PK CHANG CH CLARK CG SEITZ SP KO SS BACHELER LT KLABE RM LAM GN WRIGHT MR ERICKSONVIITANEN S TRAINOR GL ANDERSON PS
Citation: Pys. Lam et al., MOLECULAR RECOGNITION OF CYCLIC HIV PROTEASE INHIBITORS - NONSYMMETRIC CYCLIC UREAS WITH EXCELLENT ORAL BIOAVAILABILITY AND LOW DRUG-RESISTANCE PROFILES, The FASEB journal, 11(9), 1997, pp. 48-48
ANTISENSE THERAPEUTICS - PROGRESS AND PROSPECTS - PREFACE
Authors: TRAINOR GL
Citation: Gl. Trainor, ANTISENSE THERAPEUTICS - PROGRESS AND PROSPECTS - PREFACE, Perspectives in drug discovery and design, 4, 1996, pp. 5-6
POTENT ANTISENSE OLIGONUCLEOTIDES TO THE HUMAN MULTIDRUG RESISTANCE-1MESSENGER-RNA ARE RATIONALLY SELECTED BY MAPPING RNA-ACCESSIBLE SITESWITH OLIGONUCLEOTIDE LIBRARIES
Authors: HO SP BRITTON DHO STONE BA BEHRENS DL LEFFET LM HOBBS FW MILLER JA TRAINOR GL
Citation: Sp. Ho et al., POTENT ANTISENSE OLIGONUCLEOTIDES TO THE HUMAN MULTIDRUG RESISTANCE-1MESSENGER-RNA ARE RATIONALLY SELECTED BY MAPPING RNA-ACCESSIBLE SITESWITH OLIGONUCLEOTIDE LIBRARIES, Nucleic acids research, 24(10), 1996, pp. 1901-1907
BIODISTRIBUTION AND METABOLISM OF H-3 INTERNAL LABELED OLIGONUCLEOTIDES - COMPARISON OF A PHOSPHOTHIOATE TO BOTH 3'5' BLOCKED AND UNBLOCKEDPHOSPHODIESTERS
Authors: SANDS H GOREYFERET L HO SP BAO Y COCUZZA AJ CHIDESTER D TRAINOR GL HOBBS FW
Citation: H. Sands et al., BIODISTRIBUTION AND METABOLISM OF H-3 INTERNAL LABELED OLIGONUCLEOTIDES - COMPARISON OF A PHOSPHOTHIOATE TO BOTH 3'5' BLOCKED AND UNBLOCKEDPHOSPHODIESTERS, Journal of cellular biochemistry, 1995, pp. 167-167
MODIFIED OLIGONUCLEOTIDES - INTRODUCTION
Authors: TRAINOR GL
Citation: Gl. Trainor, MODIFIED OLIGONUCLEOTIDES - INTRODUCTION, Bioorganic & medicinal chemistry letters, 4(8), 1994, pp. 963-963
GENETIC BIT ANALYSIS - A SOLID-PHASE METHOD FOR TYPING SINGLE NUCLEOTIDE POLYMORPHISMS
Authors: NIKIFOROV TT RENDLE RB GOELET P ROGERS YH KOTEWICZ ML ANDERSON S TRAINOR GL KNAPP MR
Citation: Tt. Nikiforov et al., GENETIC BIT ANALYSIS - A SOLID-PHASE METHOD FOR TYPING SINGLE NUCLEOTIDE POLYMORPHISMS, Nucleic acids research, 22(20), 1994, pp. 4167-4175
BIODISTRIBUTION AND METABOLISM OF INTERNALLY H-3 LABELED OLIGONUCLEOTIDES .1. COMPARISON OF A PHOSPHODIESTER AND A PHOSPHOROTHIOATE
Authors: SANDS H GOREYFERET LJ COCUZZA AJ HOBBS FW CHIDESTER D TRAINOR GL
Citation: H. Sands et al., BIODISTRIBUTION AND METABOLISM OF INTERNALLY H-3 LABELED OLIGONUCLEOTIDES .1. COMPARISON OF A PHOSPHODIESTER AND A PHOSPHOROTHIOATE, Molecular pharmacology, 45(5), 1994, pp. 932-943
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