메뉴 건너뛰기




Volumn 49, Issue 13, 2006, Pages 3753-3756

A thienopyridazinone-based melanin-concentrating hormone receptor 1 antagonist with potent in vivo anorectic properties

Author keywords

[No Author keywords available]

Indexed keywords

ANOREXIGENIC AGENT; BENZOPYRIDAZINONE DERIVATIVE; HORMONE RECEPTOR; MELANIN CONCENTRATING HORMONE RECEPTOR 1; MELANIN CONCENTRATING HORMONE RECEPTOR 1 ANTAGONIST; PYRIDAZINONE DERIVATIVE; RECEPTOR BLOCKING AGENT; THIENOPYRIDAZINONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 33745666463     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm051263c     Document Type: Article
Times cited : (43)

References (36)
  • 4
    • 0036797774 scopus 로고    scopus 로고
    • Acute and chronic administration of melanin-concentrating hormone enhances food intake and body weight in Wistar and Sprague-Dawley rats
    • Della-Zuana, O.; Presse, F.; Ortola, C.; Duhault, J.; Nahon, J. L.; Levens, N. Acute and chronic administration of melanin-concentrating hormone enhances food intake and body weight in Wistar and Sprague-Dawley rats. Int. J. Obes. 2002, 26, 289-1295.
    • (2002) Int. J. Obes. , vol.26 , pp. 289-1295
    • Della-Zuana, O.1    Presse, F.2    Ortola, C.3    Duhault, J.4    Nahon, J.L.5    Levens, N.6
  • 5
    • 0032542294 scopus 로고    scopus 로고
    • Mice lacking melanin-concentrating hormone are hypophagic and lean
    • Shimada, M.; Tritos, N. A.; Lowell, B. B.; Flier, J. S.; Maratos-Flier, E. Mice lacking melanin-concentrating hormone are hypophagic and lean. Nature 1998, 396, 670-674.
    • (1998) Nature , vol.396 , pp. 670-674
    • Shimada, M.1    Tritos, N.A.2    Lowell, B.B.3    Flier, J.S.4    Maratos-Flier, E.5
  • 16
    • 24944458852 scopus 로고    scopus 로고
    • Discovery and characterization of aminopiperidinecoumarin melanin concentrating hormone receptor 1 antagonists
    • (i) Kym, P. R.; Iyengar, R.; Souers, A. J.; Lynch, J. K.; Judd, A. S.; Gao, J.; et al. Discovery and characterization of aminopiperidinecoumarin melanin concentrating hormone receptor 1 antagonists. J. Med. Chem. 2005, 48, 5888-5891.
    • (2005) J. Med. Chem. , vol.48 , pp. 5888-5891
    • Kym, P.R.1    Iyengar, R.2    Souers, A.J.3    Lynch, J.K.4    Judd, A.S.5    Gao, J.6
  • 20
    • 33645693576 scopus 로고    scopus 로고
    • Screening for cardiovascular safety: A structure-activity approach for guiding lead selection of melanin concentrating hormone receptor 1 antagonists
    • (m) Kym, P. R.; Souers, A. J.; Campbell, T. J.; Lynch, J. K.; Judd, A. S.; Iyengar, R.; et al. Screening for cardiovascular safety: a structure-activity approach for guiding lead selection of melanin concentrating hormone receptor 1 antagonists. J. Med. Chem. 2006, 49, 2339-2352.
    • (2006) J. Med. Chem. , vol.49 , pp. 2339-2352
    • Kym, P.R.1    Souers, A.J.2    Campbell, T.J.3    Lynch, J.K.4    Judd, A.S.5    Iyengar, R.6
  • 22
    • 33745648411 scopus 로고    scopus 로고
    • (a) Amgen, 2005. Available on line at www.amgen.com/science/pipe_AMG076. html.
    • (2005)
  • 23
    • 33745637768 scopus 로고    scopus 로고
    • (b) GlaxoSmithKline, 2005. Available on line at www.gsk.com/financial/ product_pipe-line.html.
    • (2005)
  • 25
    • 29544442936 scopus 로고    scopus 로고
    • Melanin-concentrating hormone receptor 1 antagonists for the treatment of depression and anxiety
    • (a) Chaki, S.; Yamaguchi, J.; Yamada, H.; Kanuma, K.; Sekiguchi, Y. Melanin-concentrating hormone receptor 1 antagonists for the treatment of depression and anxiety. Drug Dev. Res. 2005, 65, 278-290.
    • (2005) Drug Dev. Res. , vol.65 , pp. 278-290
    • Chaki, S.1    Yamaguchi, J.2    Yamada, H.3    Kanuma, K.4    Sekiguchi, Y.5
  • 26
    • 29544433086 scopus 로고    scopus 로고
    • Small molecule melanin-concentrating hormone receptor 1 antagonists as anxiolytic and antidepressive agents
    • (b) Dyck, B. Small molecule melanin-concentrating hormone receptor 1 antagonists as anxiolytic and antidepressive agents. Drug Dev. Res. 2005, 65, 291-300.
    • (2005) Drug Dev. Res. , vol.65 , pp. 291-300
    • Dyck, B.1
  • 27
    • 24744461364 scopus 로고    scopus 로고
    • 6-Acylamino-2-aminoquinolines as potent melanin-concentrating hormone 1 receptor antagonists. Identification, structure-activity relationship, and investigation of binding mode
    • Ulven, T.; Frimurer, T. M.; Receveur, J.-M.; Little, P. B.; Rist, O.; Norregaard, P. K.; Hogberg, T. 6-Acylamino-2-aminoquinolines as potent melanin-concentrating hormone 1 receptor antagonists. Identification, structure-activity relationship, and investigation of binding mode. J. Med. Chem. 2005, 48, 5684-5697.
    • (2005) J. Med. Chem. , vol.48 , pp. 5684-5697
    • Ulven, T.1    Frimurer, T.M.2    Receveur, J.-M.3    Little, P.B.4    Rist, O.5    Norregaard, P.K.6    Hogberg, T.7
  • 28
    • 0022915419 scopus 로고
    • Synthesis, saludiuretic, and antihypertensive activity of 6,7-disubstituted 1(2H)- and 3,4-dihydro-1(2H)-phthalazinones
    • Cherkez, S.; Herzig, J.; Yellin, H. Synthesis, saludiuretic, and antihypertensive activity of 6,7-disubstituted 1(2H)- and 3,4-dihydro-1(2H)- phthalazinones. j. Med. Chem. 1986, 29, 947-959.
    • (1986) J. Med. Chem. , vol.29 , pp. 947-959
    • Cherkez, S.1    Herzig, J.2    Yellin, H.3
  • 29
    • 0028826218 scopus 로고
    • A large scale preparation of 3-chloro-5-methoxypyridazine
    • Bryant, R. D.; Kunng, F.-A.; South, M. S. A large scale preparation of 3-chloro-5-methoxypyridazine. J. Heterocycl. Chem. 1995, 32, 1473-1476.
    • (1995) J. Heterocycl. Chem. , vol.32 , pp. 1473-1476
    • Bryant, R.D.1    Kunng, F.-A.2    South, M.S.3
  • 30
    • 0347024177 scopus 로고    scopus 로고
    • Synthetic studies on isoquinoline derivatives with multidrug resistance (MDR) modulating activity
    • Ma, C.; Cho, S.; Falck, J. R.; Shin, D. Synthetic studies on isoquinoline derivatives with multidrug resistance (MDR) modulating activity. Heterocycles 2004, 63, 75-85.
    • (2004) Heterocycles , vol.63 , pp. 75-85
    • Ma, C.1    Cho, S.2    Falck, J.R.3    Shin, D.4
  • 31
    • 0142059301 scopus 로고    scopus 로고
    • 5-Alkynyl-4-chloro- and 4-alkynyl-5-chloropyridazin-3(2H)-ones: Convenient precursors for the preparation of 2-substituted pyrrolo[2,3-d] pyridazinones
    • R'kyek, O.; Maes, B. U. W.; Lemiere, G. L. F.; Dommisse, R. A. 5-Alkynyl-4-chloro- and 4-alkynyl-5-chloropyridazin-3(2H)-ones: convenient precursors for the preparation of 2-substituted pyrrolo[2,3-d]pyridazinones. Heterocycles 2003, 60, 2471-2483.
    • (2003) Heterocycles , vol.60 , pp. 2471-2483
    • R'Kyek, O.1    Maes, B.U.W.2    Lemiere, G.L.F.3    Dommisse, R.A.4
  • 32
    • 0036843920 scopus 로고    scopus 로고
    • 5-Alkynyl-4-chloro- and 4-alkynyl-5-chloropyridazin-3(2H)-ones towards oxygen and sulfur nucleophiles
    • R'kyek, O.; Maes, B. U. W.; Lemiere, G. L. F.; Dommisse, R. A. 5-Alkynyl-4-chloro- and 4-alkynyl-5-chloropyridazin-3(2H)-ones towards oxygen and sulfur nucleophiles. Heterocycles 2002, 57, 2115-2128.
    • (2002) Heterocycles , vol.57 , pp. 2115-2128
    • R'Kyek, O.1    Maes, B.U.W.2    Lemiere, G.L.F.3    Dommisse, R.A.4
  • 33
    • 0034794463 scopus 로고    scopus 로고
    • A general and efficient copper catalyst for the amidations of aryl halides and the N-arylation of nitrogen heterocycles
    • Klapars, A.; Antilla, J. C.; Huang, X.; Buchwald, S. L. A general and efficient copper catalyst for the amidations of aryl halides and the N-arylation of nitrogen heterocycles. J. Am. Chem. Soc. 2001, 123, 7727-7729.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 7727-7729
    • Klapars, A.1    Antilla, J.C.2    Huang, X.3    Buchwald, S.L.4
  • 34
    • 0031466149 scopus 로고    scopus 로고
    • Nonspecific binding to microsomes: Impact on scale-up of in vitro intrinsic clearance to hepatic clearance as assessed through examination of warfarin, imipramine, and propanolol
    • Obach, R. S. Nonspecific binding to microsomes: impact on scale-up of in vitro intrinsic clearance to hepatic clearance as assessed through examination of warfarin, imipramine, and propanolol. Drug Metab. Dispos. 1997, 25, 1359-1369.
    • (1997) Drug Metab. Dispos. , vol.25 , pp. 1359-1369
    • Obach, R.S.1
  • 36
    • 1642276168 scopus 로고    scopus 로고
    • Darifenacin, an M3 selective receptor antagonist, is an effective and well-tolerated once-daily treatment for overactive bladder
    • Haab, F.; Stewart, L.; Dwyer, P. Darifenacin, an M3 selective receptor antagonist, is an effective and well-tolerated once-daily treatment for overactive bladder. Eur. Urol. 2004, 45, 420-429.
    • (2004) Eur. Urol. , vol.45 , pp. 420-429
    • Haab, F.1    Stewart, L.2    Dwyer, P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.