SYNTHESIS AND BIOLOGICAL EVALUATION OF FORSKOLIN CARBAMATES AS POTENTIAL ADENYLYL-CYCLASE ISOFORM SELECTIVE LIGANDS

被引：0
|
作者：
ROBBINS, JD
BORING, DL
TANG, WJ
SHANK, R
SEAMON, KB
机构：
[1] UNIV TEXAS,HLTH SCI CTR,SW MED SCH,DALLAS,TX 75235
[2] US FDA,CTR BIOL EVALUAT & RES,DBB,LMP,BETHESDA,MD 20892
[3] DAVDP,ODE 2,CTR DRUG EVALUAT & RES,ROCKVILLE,MD 20890
来源：
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY | 1994年 / 207卷
关键词：
D O I：
暂无
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
引用
收藏
页码：248 / MEDI
相关论文
共 50 条
  • [41] SYNTHESIS OF IODO-ARYL-AZIDO ADENOSINE-ANALOGS AS AFFINITY LIGANDS FOR ADENYLYL CYCLASE
    JOHNSON, RA
    SHOSHANI, I
    QUI, H
    JOHNSON, F
    FASEB JOURNAL, 1993, 7 (07): : A1152 - A1152
  • [42] Synthesis and use of 3′-(azidoiodosalicyl) derivatives of 2′,5′-dideoxyadenosine as photoaffinity ligands for adenylyl cyclase
    Shoshani, I
    Taussig, R
    Iyengar, R
    Johnson, RA
    ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2000, 376 (01) : 221 - 228
  • [43] Projuvenoids: Synthesis and biological evaluation of sulfenylated, sulfinylated, and sulfonylated carbamates
    Ujvary, I
    Matolcsy, G
    Belai, I
    Szurdoki, F
    Bauer, K
    Varjas, L
    Kramer, KJ
    ARCHIVES OF INSECT BIOCHEMISTRY AND PHYSIOLOGY, 1996, 32 (3-4) : 659 - 669
  • [44] Synthesis and biological evaluation of potential isoform-selective benzimidazole-4-carboxamide inhibitors of poly(ADP-ribose)polymerases
    Pickles, James
    Cano, Celine
    Golding, Bernard
    Harnor, Suzannah
    Jackson, Steve
    Newell, Herbie
    Travers, Jon
    Griffin, Roger
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2015, 249
  • [45] Design, Synthesis, and Biological Evaluation of 4,4′-Difluorobenzhydrol Carbamates as Selective M1 Antagonists
    Kilian, Jonas
    Ozenil, Marius
    Millard, Marlon
    Fuertoes, Dorka
    Maisetschlaeger, Verena
    Holzer, Wolfgang
    Wadsak, Wolfgang
    Hacker, Marcus
    Langer, Thierry
    Pichler, Verena
    PHARMACEUTICALS, 2022, 15 (02)
  • [46] A3 adenosine receptors:: Synthesis and biological evaluation of new potent and selective ligands
    Volpini, R
    Lambertucci, C
    Taffi, S
    Vittori, S
    Klotz, KN
    Cristalli, G
    Chemistry of Nucleic Acid Components, 2005, 7 : 297 - 300
  • [47] Design, synthesis, and biological evaluation of α3 GABAergic subtype selective ligands for anxiety disorders
    Namjoshi, Ojas A.
    Johnson, Yun Teng
    Roth, Bryan L.
    Majumder, Samarpan
    Ramerstorfer, Joachim
    Sieghart, Werner
    Cook, James M.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2011, 241
  • [48] THE EFFECT OF GTP ON THE ALUMINUM FLUORIDE-ACTIVATED AND FORSKOLIN-ACTIVATED ADENYLYL-CYCLASE FROM HUMAN EMBRYONIC KIDNEY 293-CELLS (VOL 109, PG 359, 1994)
    SANCHEZYAGUC, J
    RODRIGUEZ, MC
    LLANILLO, M
    HERNANDEZHERNANDEZ, A
    COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 1995, 110 (04): : 823 - 823
  • [49] Focused Library Screening for Isoform Selective Adenylyl Cyclase 1 Inhibitors as Non-Opioid Alternatives for Chronic and Inflammatory Pain
    Hayes, Michael
    Wiernicki, Todd
    Martinez-Grau, Maria
    Burris, Kevin
    Watts, Val
    FASEB JOURNAL, 2020, 34
  • [50] Design, Synthesis, and Preliminary Biological Evaluation of New Isoform-Selective f-Current Blockers
    Melchiorre, Michele
    Del Lungo, Martina
    Guandalini, Luca
    Martini, Elisabetta
    Dei, Silvia
    Manetti, Dina
    Scapecchi, Serena
    Teodori, Elisabetta
    Sartiani, Laura
    Mugelli, Alessandro
    Cerbai, Elisabetta
    Romanelli, Maria Novella
    JOURNAL OF MEDICINAL CHEMISTRY, 2010, 53 (18) : 6773 - 6777
12345