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Results: 1-8 |
Results: 8
RAPID IDENTIFICATION OF SUBTYPE-SELECTIVE AGONISTS OF THE SOMATOSTATIN RECEPTOR THROUGH COMBINATORIAL CHEMISTRY
Authors: ROHRER SP BIRZIN ET MOSLEY RT BERK SC HUTCHINS SM SHEN DM XIONG YS HAYES EC PARMAR RM FOOR F MITRA SW DEGRADO SJ SHU M KLOPP JM CAI SJ BLAKE A CHAN WWS PASTERNAK A YANG LH PATCHETT AA SMITH RG CHAPMAN KT SCHAEFFER JM
Citation: Sp. Rohrer et al., RAPID IDENTIFICATION OF SUBTYPE-SELECTIVE AGONISTS OF THE SOMATOSTATIN RECEPTOR THROUGH COMBINATORIAL CHEMISTRY, Science, 282(5389), 1998, pp. 737-740
SYNTHESIS AND BIOLOGICAL-ACTIVITIES OF POTENT PEPTIDOMIMETICS SELECTIVE FOR SOMATOSTATIN RECEPTOR SUBTYPE-2
Authors: YANG LH BERK SC ROHRER SP MOSLEY RT GUO LQ UNDERWOOD DJ ARISON BH BIRZIN ET HAYES EC MITRA SW PARMAR RM CHENG K WU TJ BUTLER BS FOOR F PASTERNAK A PAN YP SILVA M FREIDINGER RM SMITH RG CHAPMAN K SCHAEFFER JM PATCHETT AA
Citation: Lh. Yang et al., SYNTHESIS AND BIOLOGICAL-ACTIVITIES OF POTENT PEPTIDOMIMETICS SELECTIVE FOR SOMATOSTATIN RECEPTOR SUBTYPE-2, Proceedings of the National Academy of Sciences of the United Statesof America, 95(18), 1998, pp. 10836-10841
NOVEL TRANSANNULAR REARRANGEMENTS OF AZALIDE IMINOETHERS
Authors: WILKENING RR RATCLIFFE RW DOSS GA MOSLEY RT BALL RG
Citation: Rr. Wilkening et al., NOVEL TRANSANNULAR REARRANGEMENTS OF AZALIDE IMINOETHERS, Tetrahedron, 53(50), 1997, pp. 16923-16944
CHEMICAL SIMILARITY USING PHYSIOCHEMICAL PROPERTY DESCRIPTORS
Authors: KEARSLEY SK SALLAMACK S FLUDER EM ANDOSE JD MOSLEY RT SHERIDAN RP
Citation: Sk. Kearsley et al., CHEMICAL SIMILARITY USING PHYSIOCHEMICAL PROPERTY DESCRIPTORS, Journal of chemical information and computer sciences, 36(1), 1996, pp. 118-127
O-5-ALPHA-ANDROST-1-ENE-17-BETA-N-ARYLCARBOXAMIDES AS DUAL INHIBITORSOF HUMAN TYPE-1 AND TYPE-2 STEROID 5-ALPHA-REDUCTASES - DRAMATIC EFFECT OF N-ARYL SUBSTITUENTS ON TYPE-1 AND TYPE-2 5-ALPHA-REDUCTASE INHIBITORY POTENCY (VOL 38, PG 3190, 1995)
Authors: BAKSHI RK RASMUSSON GH PATEL GF MOSLEY RT CHANG B ELLSWORTH K HARRIS GS TOLMAN RL
Citation: Rk. Bakshi et al., O-5-ALPHA-ANDROST-1-ENE-17-BETA-N-ARYLCARBOXAMIDES AS DUAL INHIBITORSOF HUMAN TYPE-1 AND TYPE-2 STEROID 5-ALPHA-REDUCTASES - DRAMATIC EFFECT OF N-ARYL SUBSTITUENTS ON TYPE-1 AND TYPE-2 5-ALPHA-REDUCTASE INHIBITORY POTENCY (VOL 38, PG 3190, 1995), Journal of medicinal chemistry, 39(5), 1996, pp. 1192-1192
-5-ALPHA-ANDROST-1-ENE-17-BETA-N-ARYL-CARBOXAMIDES AS DUAL INHIBITORSOF HUMAN TYPE-1 AND TYPE-2 STEROID 5-ALPHA-REDUCTASES - DRAMATIC EFFECT OF N-ARYL SUBSTITUENTS ON TYPE-1 AND TYPE-2 5-ALPHA-REDUCTASE INHIBITORY POTENCY
Authors: BAKSHI RK RASMUSSON GH PATEL GF MOSLEY RT CHANG B ELLSWORTH K HARRIS GS TOLMAN RL
Citation: Rk. Bakshi et al., -5-ALPHA-ANDROST-1-ENE-17-BETA-N-ARYL-CARBOXAMIDES AS DUAL INHIBITORSOF HUMAN TYPE-1 AND TYPE-2 STEROID 5-ALPHA-REDUCTASES - DRAMATIC EFFECT OF N-ARYL SUBSTITUENTS ON TYPE-1 AND TYPE-2 5-ALPHA-REDUCTASE INHIBITORY POTENCY, Journal of medicinal chemistry, 38(17), 1995, pp. 3189-3192
SYNTHESIS, BIOLOGICAL-ACTIVITY AND ELECTROSTATIC PROPERTIES OF [(3-AMINO-1,2,4-THIADIAZOL-5-YL)METHYL]-1H-INDOLE, A NOVEL 5-HT1D RECEPTOR AGONIST
Authors: CASTRO JL MATASSA VG BROUGHTON HB MOSLEY RT STREET LJ BAKER R
Citation: Jl. Castro et al., SYNTHESIS, BIOLOGICAL-ACTIVITY AND ELECTROSTATIC PROPERTIES OF [(3-AMINO-1,2,4-THIADIAZOL-5-YL)METHYL]-1H-INDOLE, A NOVEL 5-HT1D RECEPTOR AGONIST, Bioorganic & medicinal chemistry letters, 3(6), 1993, pp. 993-997
ISOLATION AND STRUCTURE OF CHAETOMELLIC ACIDS A AND B FROM CHAETOMELLA-ACUTISETA - FARNESYL PYROPHOSPHATE MIMIC INHIBITORS OF RAS FARNESYL-PROTEIN TRANSFERASE
Authors: SINGH SB ZINK DL LIESCH JM GOETZ MA JENKINS RG NALLINOMSTEAD M SILVERMAN KC BILLS GF MOSLEY RT GIBBS JB ALBERSSCHONBERG G LINGHAM RB
Citation: Sb. Singh et al., ISOLATION AND STRUCTURE OF CHAETOMELLIC ACIDS A AND B FROM CHAETOMELLA-ACUTISETA - FARNESYL PYROPHOSPHATE MIMIC INHIBITORS OF RAS FARNESYL-PROTEIN TRANSFERASE, Tetrahedron, 49(27), 1993, pp. 5917-5926
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