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Volumn 78, Issue 1, 2009, Pages 62-69

Differential interactions of the catalytic subunits of adenylyl cyclase with forskolin analogs

Author keywords

Adenylyl cyclase; Diterpenes; Fluorescence spectroscopy; Forskolin; MANT GTP

Indexed keywords

1 DEOXYFORSKOLIN; 1,9 DIDEOXYFORSKOLIN; 6 ACETYL 7 DEACETYLFORSKOLIN; 7 DEACETYL 1 DEOXYFORSKOLIN; 7 DEACETYL 1,9 DIDEOXYFORSKOLIN; 7 DEACETYL 7 (N METHYLPIPERAZINO GAMMA BUTYRYLOXY)FORSKOLIN; 7 DEACETYLFORSKOLIN; 9 DEOXYFORSKOLIN; ADENYLATE CYCLASE; DITERPENE; FORSKOLIN; FORSKOLIN DERIVATIVE; UNCLASSIFIED DRUG;

EID: 67349241188     PISSN: 00062952     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bcp.2009.03.023     Document Type: Article
Times cited : (19)

References (23)
  • 2
    • 0031820874 scopus 로고    scopus 로고
    • Catalytic mechanism and regulation of mammalian adenylyl cyclases
    • Tang W.J., and Hurley J.H. Catalytic mechanism and regulation of mammalian adenylyl cyclases. Mol Pharmacol 54 (1998) 231-240
    • (1998) Mol Pharmacol , vol.54 , pp. 231-240
    • Tang, W.J.1    Hurley, J.H.2
  • 3
    • 0035040818 scopus 로고    scopus 로고
    • Regulation and role of adenylyl cyclase isoforms
    • Hanoune J., and Defer N. Regulation and role of adenylyl cyclase isoforms. Annu Rev Pharmacol Toxicol 41 (2001) 145-174
    • (2001) Annu Rev Pharmacol Toxicol , vol.41 , pp. 145-174
    • Hanoune, J.1    Defer, N.2
  • 5
    • 0024443061 scopus 로고
    • Forskolin: a specific stimulator of adenylyl cyclase or a diterpene with multiple sites of action?
    • Laurenza A., Sutkowski E.M., and Seamon K.B. Forskolin: a specific stimulator of adenylyl cyclase or a diterpene with multiple sites of action?. Trends Pharmacol Sci 10 (1989) 442-447
    • (1989) Trends Pharmacol Sci , vol.10 , pp. 442-447
    • Laurenza, A.1    Sutkowski, E.M.2    Seamon, K.B.3
  • 6
    • 0029900539 scopus 로고    scopus 로고
    • Forskolin carbamates: binding and activation studies with type I adenylyl cyclase
    • Robbins J.D., Boring D.L., Tang W.J., Shank R., and Seamon K.B. Forskolin carbamates: binding and activation studies with type I adenylyl cyclase. J Med Chem 39 (1996) 2745-2752
    • (1996) J Med Chem , vol.39 , pp. 2745-2752
    • Robbins, J.D.1    Boring, D.L.2    Tang, W.J.3    Shank, R.4    Seamon, K.B.5
  • 7
    • 0038717215 scopus 로고    scopus 로고
    • Isoform-specific regulation of adenylyl cyclase: a potential target in future pharmacotherapy
    • Iwatsubo K., Tsunematsu T., and Ishikawa Y. Isoform-specific regulation of adenylyl cyclase: a potential target in future pharmacotherapy. Expert Opin Ther Targets 7 (2003) 441-451
    • (2003) Expert Opin Ther Targets , vol.7 , pp. 441-451
    • Iwatsubo, K.1    Tsunematsu, T.2    Ishikawa, Y.3
  • 8
    • 0035930583 scopus 로고    scopus 로고
    • Type-specific regulation of adenylyl cyclase. Selective pharmacological stimulation and inhibition of adenylyl cyclase isoforms
    • Onda T., Hashimoto Y., Nagai M., Kuramochi H., Saito S., Yamazaki H., et al. Type-specific regulation of adenylyl cyclase. Selective pharmacological stimulation and inhibition of adenylyl cyclase isoforms. J Biol Chem 276 (2001) 47785-47793
    • (2001) J Biol Chem , vol.276 , pp. 47785-47793
    • Onda, T.1    Hashimoto, Y.2    Nagai, M.3    Kuramochi, H.4    Saito, S.5    Yamazaki, H.6
  • 10
    • 0030832040 scopus 로고    scopus 로고
    • Interactions of forskolin and ATP with the cytosolic domains of mammalian adenylyl cyclase
    • Dessauer C.W., Scully T.T., and Gilman A.G. Interactions of forskolin and ATP with the cytosolic domains of mammalian adenylyl cyclase. J Biol Chem 272 (1997) 22272-22277
    • (1997) J Biol Chem , vol.272 , pp. 22272-22277
    • Dessauer, C.W.1    Scully, T.T.2    Gilman, A.G.3
  • 13
    • 14844299755 scopus 로고    scopus 로고
    • Structural basis for the inhibition of mammalian membrane adenylyl cyclase by 2′(3′)-O-(N-methylanthraniloyl)-guanosine 5′-triphosphate
    • Mou T.C., Gille A., Fancy D.A., Seifert R., and Sprang S.R. Structural basis for the inhibition of mammalian membrane adenylyl cyclase by 2′(3′)-O-(N-methylanthraniloyl)-guanosine 5′-triphosphate. J Biol Chem 280 (2005) 7253-7261
    • (2005) J Biol Chem , vol.280 , pp. 7253-7261
    • Mou, T.C.1    Gille, A.2    Fancy, D.A.3    Seifert, R.4    Sprang, S.R.5
  • 14
    • 33747624168 scopus 로고    scopus 로고
    • Broad specificity of mammalian adenylyl cyclase for interaction with 2′, 3′-substituted purine- and pyrimidine nucleotide inhibitors
    • Mou T.C., Gille A., Suryanarayana S., Richter M., Seifert R., and Sprang S.R. Broad specificity of mammalian adenylyl cyclase for interaction with 2′, 3′-substituted purine- and pyrimidine nucleotide inhibitors. Mol Pharmacol 70 (2006) 878-886
    • (2006) Mol Pharmacol , vol.70 , pp. 878-886
    • Mou, T.C.1    Gille, A.2    Suryanarayana, S.3    Richter, M.4    Seifert, R.5    Sprang, S.R.6
  • 16
    • 0030901637 scopus 로고    scopus 로고
    • Structure of the adenylyl cyclase catalytic core
    • Zhang G., Liu Y., Ruoho A.E., and Hurley J.H. Structure of the adenylyl cyclase catalytic core. Nature 386 (1997) 247-253
    • (1997) Nature , vol.386 , pp. 247-253
    • Zhang, G.1    Liu, Y.2    Ruoho, A.E.3    Hurley, J.H.4
  • 17
    • 0020682114 scopus 로고
    • Structure-activity relationships for activation of adenylate cyclase by the diterpene forskolin and its derivatives
    • Seamon K.B., Daly J.W., Metzger H., de Souza N.J., and Reden J. Structure-activity relationships for activation of adenylate cyclase by the diterpene forskolin and its derivatives. J Med Chem 26 (1983) 436-439
    • (1983) J Med Chem , vol.26 , pp. 436-439
    • Seamon, K.B.1    Daly, J.W.2    Metzger, H.3    de Souza, N.J.4    Reden, J.5
  • 19
    • 0036033424 scopus 로고    scopus 로고
    • Constitutive activity of G-protein-coupled receptors: cause of disease and common property of wild-type receptors
    • Seifert R., and Wenzel-Seifert K. Constitutive activity of G-protein-coupled receptors: cause of disease and common property of wild-type receptors. Naunyn-Schmiedeberg's Arch Pharmacol 366 (2002) 381-416
    • (2002) Naunyn-Schmiedeberg's Arch Pharmacol , vol.366 , pp. 381-416
    • Seifert, R.1    Wenzel-Seifert, K.2
  • 20
    • 0345490945 scopus 로고    scopus 로고
    • International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification. International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification. XXXVIII. Update on terms and symbols in quantitative pharmacology
    • Neubig R.R., Spedding M., Kenakin T., and Christopoulos A. International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification. International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification. XXXVIII. Update on terms and symbols in quantitative pharmacology. Pharmacol Rev 55 (2003) 597-606
    • (2003) Pharmacol Rev , vol.55 , pp. 597-606
    • Neubig, R.R.1    Spedding, M.2    Kenakin, T.3    Christopoulos, A.4
  • 21
    • 33751183557 scopus 로고    scopus 로고
    • Determining the potency and molecular mechanism of action of insurmountable antagonists
    • Kenakin T., Jenkinson S., and Watson C. Determining the potency and molecular mechanism of action of insurmountable antagonists. J Pharmacol Exp Ther 319 (2006) 710-723
    • (2006) J Pharmacol Exp Ther , vol.319 , pp. 710-723
    • Kenakin, T.1    Jenkinson, S.2    Watson, C.3
  • 22
    • 2442506761 scopus 로고    scopus 로고
    • Differential inhibition of adenylyl cyclase isoforms and soluble guanylyl cyclase by purine and pyrimidine nucleotides
    • Gille A., Lushington G.H., Mou T.C., Doughty M.B., Johnson R.A., and Seifert R. Differential inhibition of adenylyl cyclase isoforms and soluble guanylyl cyclase by purine and pyrimidine nucleotides. J Biol Chem 279 (2004) 19955-19969
    • (2004) J Biol Chem , vol.279 , pp. 19955-19969
    • Gille, A.1    Lushington, G.H.2    Mou, T.C.3    Doughty, M.B.4    Johnson, R.A.5    Seifert, R.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.