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Results: 1-19 |
Results: 19
SYNTHESIS AND CHARACTERIZATION OF A HIGHLY POTENT AND SELECTIVE ISOTOPICALLY LABELED RETINOIC ACID RECEPTOR-LIGAND, ALRT1550
Authors: BENNANI YL MARRON KS MAIS DE FLATTEN K NADZAN AM BOEHM MF
Citation: Yl. Bennani et al., SYNTHESIS AND CHARACTERIZATION OF A HIGHLY POTENT AND SELECTIVE ISOTOPICALLY LABELED RETINOIC ACID RECEPTOR-LIGAND, ALRT1550, Journal of organic chemistry, 63(3), 1998, pp. 543-550
SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF POTENT CONFORMATIONALLY RESTRICTED RETINOID-X-RECEPTOR LIGANDS
Authors: FARMER LJ ZHI L JEONG S KALLEL EA CROSTON G FLATTEN KS HEYMAN RA NADZAN AM
Citation: Lj. Farmer et al., SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF POTENT CONFORMATIONALLY RESTRICTED RETINOID-X-RECEPTOR LIGANDS, Bioorganic & medicinal chemistry letters, 7(21), 1997, pp. 2747-2752
SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF POTENT RETINOID-X-RECEPTOR LIGANDS
Authors: FARMER LJ JEONG S KALLEL EA KOCH SSC CROSTON GE FLATTEN KS HEYMAN RA NADZAN AM
Citation: Lj. Farmer et al., SYNTHESIS AND STRUCTURE-ACTIVITY-RELATIONSHIPS OF POTENT RETINOID-X-RECEPTOR LIGANDS, Bioorganic & medicinal chemistry letters, 7(18), 1997, pp. 2393-2398
SENSITIZATION OF DIABETIC AND OBESE MICE TO INSULIN BY RETINOID-X-RECEPTOR AGONISTS
Authors: MUKHERJEE R DAVIES PJA CROMBIE DL BISCHOFF ED CESARIO RM JOW L HAMANN LG BOEHM MF MONDON CE NADZAN AM PATERNITI JR HEYMAN RA
Citation: R. Mukherjee et al., SENSITIZATION OF DIABETIC AND OBESE MICE TO INSULIN BY RETINOID-X-RECEPTOR AGONISTS, Nature, 386(6623), 1997, pp. 407-410
A NOVEL RETINOIC ACID RECEPTOR-SELECTIVE RETINOID, ALRT1550, HAS POTENT ANTITUMOR-ACTIVITY AGAINST HUMAN ORAL SQUAMOUS CARCINOMA XENOGRAFTSIN NUDE-MICE
Authors: SHALINSKY DR BISCHOFF ED LAMPH WW ZHANG L BOEHM MF DAVIES PJA NADZAN AM HEYMAN RA
Citation: Dr. Shalinsky et al., A NOVEL RETINOIC ACID RECEPTOR-SELECTIVE RETINOID, ALRT1550, HAS POTENT ANTITUMOR-ACTIVITY AGAINST HUMAN ORAL SQUAMOUS CARCINOMA XENOGRAFTSIN NUDE-MICE, Cancer research, 57(1), 1997, pp. 162-168
SYNTHESIS OF GEOMETRICALLY DEFINED EXOCYCLIC OLEFINS
Authors: BENNANI YL HWANG CK KOCH SSC MARRON KS DARDASHTI LJ BADEA BA NADZAN AM
Citation: Yl. Bennani et al., SYNTHESIS OF GEOMETRICALLY DEFINED EXOCYCLIC OLEFINS, Tetrahedron letters, 37(45), 1996, pp. 8109-8112
ACTIVATION OF SPECIFIC RXR HETERODIMERS BY AN ANTAGONIST OF RXR HOMODIMERS
Authors: LALA DS MUKHERJEE R SCHULMAN IG KOCH SSC DARDASHTI LJ NADZAN AM CROSTON GE EVANS RM HEYMAN RA
Citation: Ds. Lala et al., ACTIVATION OF SPECIFIC RXR HETERODIMERS BY AN ANTAGONIST OF RXR HOMODIMERS, Nature, 383(6599), 1996, pp. 450-453
IDENTIFICATION OF THE FIRST RETINOID-X RECEPTOR HOMODIMER ANTAGONIST
Authors: KOCH SSC DARDASHTI LJ HEBERT JJ WHITE SK CROSTON GE FLATTEN KS HEYMAN RA NADZAN AM
Citation: Ssc. Koch et al., IDENTIFICATION OF THE FIRST RETINOID-X RECEPTOR HOMODIMER ANTAGONIST, Journal of medicinal chemistry, 39(17), 1996, pp. 3229-3234
DISCOVERY OF NOVEL RETINOIC ACID RECEPTOR AGONISTS HAVING POTENT ANTIPROLIFERATIVE ACTIVITY IN CERVICAL-CANCER CELLS
Authors: ZHANG L NADZAN AM HEYMAN RA LOVE DL MAIS DE CROSTON G LAMPH WW BOEHM MF
Citation: L. Zhang et al., DISCOVERY OF NOVEL RETINOIC ACID RECEPTOR AGONISTS HAVING POTENT ANTIPROLIFERATIVE ACTIVITY IN CERVICAL-CANCER CELLS, Journal of medicinal chemistry, 39(14), 1996, pp. 2659-2663
AMINO ACID-DERIVED PIPREIDIDES AS NOVEL CCKB LIGANDS WITH ANXIOLYTIC-LIKE PROPERTIES
Authors: HOLLADAY MW BENNETT MJ BAI H RALSTON JW KERWIN JF STASHKO M MILLER TR ONEILL AB NADZAN AM BRIONI J LIN CW
Citation: Mw. Holladay et al., AMINO ACID-DERIVED PIPREIDIDES AS NOVEL CCKB LIGANDS WITH ANXIOLYTIC-LIKE PROPERTIES, Bioorganic & medicinal chemistry letters, 5(24), 1995, pp. 3057-3062
DESIGN OF NOVEL RXR - SELECTIVE RETINOIDS
Authors: NADZAN AM BOEHM MF ZHANG L BADEA BA ZHI L WHITE SK MAIS DE BERGER E SUTO CM MCCLURG MR DAVIES PJA HEYMAN RA
Citation: Am. Nadzan et al., DESIGN OF NOVEL RXR - SELECTIVE RETINOIDS, European journal of medicinal chemistry, 30, 1995, pp. 519-533
INTRACELLULAR RECEPTORS AND SIGNAL TRANSDUCERS AND ACTIVATORS OF TRANSCRIPTION SUPERFAMILIES - NOVEL TARGETS FOR SMALL-MOLECULE DRUG DISCOVERY
Authors: ROSEN J DAY A JONES TK JONES ETT NADZAN AM STEIN RB
Citation: J. Rosen et al., INTRACELLULAR RECEPTORS AND SIGNAL TRANSDUCERS AND ACTIVATORS OF TRANSCRIPTION SUPERFAMILIES - NOVEL TARGETS FOR SMALL-MOLECULE DRUG DISCOVERY, Journal of medicinal chemistry, 38(25), 1995, pp. 4855-4874
DESIGN AND SYNTHESIS OF POTENT RETINOID-X RECEPTOR-SELECTIVE LIGANDS THAT INDUCE APOPTOSIS IN LEUKEMIA-CELLS
Authors: BOEHM MF ZHANG L ZHI L MCCLURG MR BERGER E WAGONER M MAIS DE SUTO CM DAVIES PJA HEYMAN RA NADZAN AM
Citation: Mf. Boehm et al., DESIGN AND SYNTHESIS OF POTENT RETINOID-X RECEPTOR-SELECTIVE LIGANDS THAT INDUCE APOPTOSIS IN LEUKEMIA-CELLS, Journal of medicinal chemistry, 38(16), 1995, pp. 3146-3155
TETRAPEPTIDE CCK-A AGONISTS - EFFECT OF BACKBONE N-METHYLATIONS ON IN-VITRO AND IN-VIVO CCK ACTIVITY
Authors: HOLLADAY MW KOPECKA H MILLER TR BEDNARZ L NIKKEL AL BIANCHI BR WITTE DG SHIOSAKI K LIN CW ASIN KE NADZAN AM
Citation: Mw. Holladay et al., TETRAPEPTIDE CCK-A AGONISTS - EFFECT OF BACKBONE N-METHYLATIONS ON IN-VITRO AND IN-VIVO CCK ACTIVITY, Journal of medicinal chemistry, 37(5), 1994, pp. 630-635
TETRAPEPTIDE CCK AGONISTS - STRUCTURE-ACTIVITY STUDIES ON MODIFICATIONS AT THE N-TERMINUS
Authors: ELLIOTT RL KOPECKA H BENNETT MJ SHUE YK CRAIG R LIN CW BIANCHI BR MILLER TR WITTE DG STASHKO MA ASIN KE NIKKEL A BEDNARZ L NADZAN AM
Citation: Rl. Elliott et al., TETRAPEPTIDE CCK AGONISTS - STRUCTURE-ACTIVITY STUDIES ON MODIFICATIONS AT THE N-TERMINUS, Journal of medicinal chemistry, 37(2), 1994, pp. 309-313
NOVEL ASP(32)-REPLACEMENT TETRAPEPTIDE ANALOGS AS POTENT AND SELECTIVE CCK-A AGONISTS
Authors: ELLIOTT RL KOPECKA H TUFANO MD SHUE YK GAURI AJ LIN CW BIANCHI BR MILLER TR WITTE DG STASHKO MA ASIN KE NIKKEL AL BEDNARZ L NADZAN AM
Citation: Rl. Elliott et al., NOVEL ASP(32)-REPLACEMENT TETRAPEPTIDE ANALOGS AS POTENT AND SELECTIVE CCK-A AGONISTS, Journal of medicinal chemistry, 37(11), 1994, pp. 1562-1568
CCK-A-SELECTIVE TETRAPEPTIDES CONTAINING LYS(N-E)-AMIDE RESIDUES - FAVORABLE IN-VIVO AND IN-VITRO EFFECTS OF N-METHYLATION AT THE ASPARTYL RESIDUE
Authors: BENNETT MJ NIKKEL AL BIANCHI BR MILLER TR BEDNARZ L WITTE DG STASHKO M WANG SS GORE PA ASIN KE LIN CW NADZAN AM HOLLADAY MW
Citation: Mj. Bennett et al., CCK-A-SELECTIVE TETRAPEPTIDES CONTAINING LYS(N-E)-AMIDE RESIDUES - FAVORABLE IN-VIVO AND IN-VITRO EFFECTS OF N-METHYLATION AT THE ASPARTYL RESIDUE, Journal of medicinal chemistry, 37(11), 1994, pp. 1569-1571
TOWARD DEVELOPING PEPTIDOMIMETICS - SUCCESSFUL REPLACEMENT OF BACKBONE AMIDE BONDS IN TETRAPEPTIDE-BASED CCK-A RECEPTOR AGONISTS
Authors: SHIOSAKI K LIN CW LEANNA MR MORTON HE MILLER TR WITTE D STASHKO M NADZAN AM
Citation: K. Shiosaki et al., TOWARD DEVELOPING PEPTIDOMIMETICS - SUCCESSFUL REPLACEMENT OF BACKBONE AMIDE BONDS IN TETRAPEPTIDE-BASED CCK-A RECEPTOR AGONISTS, Bioorganic & medicinal chemistry letters, 3(5), 1993, pp. 855-860
CONFORMATIONALLY CONSTRAINED AMINO-ACIDS .2. ON THE SYNTHESIS OF 4-SUBSTITUTED 8-MEMBERED CYCLIC TRYPTOPHAN DERIVATIVES
Authors: CHUNG JYL WASICAK JT NADZAN AM
Citation: Jyl. Chung et al., CONFORMATIONALLY CONSTRAINED AMINO-ACIDS .2. ON THE SYNTHESIS OF 4-SUBSTITUTED 8-MEMBERED CYCLIC TRYPTOPHAN DERIVATIVES, Synthetic communications, 22(7), 1992, pp. 1039-1048
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