2'-O-ANTHRANILOYL AND 2'-O-(N-METHYLANTHRANILOYL) DERIVATIVES OF CAMP AND CGMP AS ACTIVE-SITE PROBES OF CYCLIC-NUCLEOTIDE PHOSPHODIESTERASES

被引：0
|
作者：
KARUPPIAH, N [1 ]
TALPAS, CJ [1 ]
MUTUS, B [1 ]
机构：
[1] UNIV WINDSOR,DEPT CHEM & BIOCHEM,WINDSOR N9B 3P4,ONTARIO,CANADA
来源：
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY | 1988年 / 195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：121 / BIOL
相关论文
共 33 条
  • [1] 2'-O-ANTHRANILOYL AND 2'-O-(N-METHYLANTHRANILOYL) DERIVATIVES OF CAMP AND CGMP AS ACTIVE-SITE PROBES OF CYCLIC-NUCLEOTIDE PHOSPHODIESTERASES
    KARUPPIAH, N
    TALPAS, CJ
    MUTUS, B
    BIOCHEMISTRY, 1988, 27 (08) : 3101 - 3102
  • [2] INTRAMOLECULAR INTERACTIONS IN 2'-O-ANTHRANILOYL AND 2'-O-(N-METHYLANTHRANILOYL) DERIVATIVES OF CAMP AND CGMP
    LEUNG, T
    AROCA, R
    KEAY, BA
    MUTUS, B
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1988, 195 : 122 - BIOL
  • [3] INTRAMOLECULAR INTERACTIONS IN 2'-O-ANTHRANILOYL AND 2'-O-(N-METHYLANTHRANILOYL) DERIVATIVES OF CAMP AND CGMP
    LEUNG, T
    AROCA, R
    KEAY, BA
    MUTUS, B
    BIOCHEMISTRY, 1988, 27 (08) : 3102 - 3102
  • [4] A COMPARATIVE KINETIC-STUDY OF BOVINE CALMODULIN-DEPENDENT CYCLIC-NUCLEOTIDE PHOSPHODIESTERASE ISOZYMES UTILIZING CAMP, CGMP AND THEIR 2'-O-ANTHRANILOYL-DERIVATIVE,2'-O-(N-METHYLANTHRANILOYL)-DERIVATIVE AS SUBSTRATES
    GREWAL, J
    KARUPPIAH, N
    MUTUS, B
    BIOCHEMISTRY INTERNATIONAL, 1989, 19 (06): : 1287 - 1295
  • [5] Probing the nucleotide binding sites of axonemal dynein with the fluorescent nucleotide analogue 2′(3′)-O-(-N-methylanthraniloyl)-adenosine 5′-triphosphate
    Mocz, G
    Helms, MK
    Jameson, DM
    Gibbons, IR
    BIOCHEMISTRY, 1998, 37 (27) : 9862 - 9869
  • [6] Functional adenylyl cyclase inhibition in murine cardiomyocytes by 2′(3′)-O-(N-methylanthraniloyl)-guanosine 5′-[γ-thio]triphosphate
    Rottlaender, Dennis
    Matthes, Jan
    Vatner, Stephen F.
    Seifert, Roland
    Herzig, Stefan
    JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2007, 321 (02): : 608 - 615
  • [7] Structural basis for the inhibition of mammalian membrane adenylyl cyclase by 2′(3′)-O-(N-methylanthraniloyl)-guanosine 5′-triphosphate
    Mou, TC
    Gille, A
    Fancy, DA
    Seifert, R
    Sprang, SR
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (08) : 7253 - 7261
  • [8] 2′(3′)-O-(N-methylanthraniloyl)-substituted GTP analogs:: A novel class of potent competitive adenylyl cyclase inhibitors
    Gille, A
    Seifert, R
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (15) : 12672 - 12679
  • [9] Interaction of 2'(3')-O-(N-methylanthraniloyl) adenosine 5'-triphosphate (Mant-ATP) with axonemal dynein measured by fluorescence anisotropy.
    Mocz, G
    Helms, M
    Jameson, DM
    Gibbons, IR
    MOLECULAR BIOLOGY OF THE CELL, 1996, 7 : 3309 - 3309
  • [10] Structural Basis for the High-Affinity Inhibition of Mammalian Membranous Adenylyl Cyclase by 2′,3′-O-(N-Methylanthraniloyl)-Inosine 5′-Triphosphate
    Huebner, Melanie
    Dixit, Anshuman
    Mou, Tung-Chung
    Lushington, Gerald H.
    Pinto, Cibele
    Gille, Andreas
    Geduhn, Jens
    Koenig, Burkhard
    Sprang, Stephen R.
    Seifert, Roland
    MOLECULAR PHARMACOLOGY, 2011, 80 (01) : 87 - 96
1234