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Volumn 18, Issue 4, 2008, Pages 1318-1322

Synthesis and structure-activity relationships of heteroaryl substituted-3,4-diamino-3-cyclobut-3-ene-1,2-dione CXCR2/CXCR1 receptor antagonists

Author keywords

3,4 Diaminocyclobut 3 ene 1,2 dione class of CXCR2 CXCR1 receptor antagonists; CXCR1 receptor; CXCR2 receptor; Interleukin 8

Indexed keywords

3,4 DIAMINO 3 CYCLOBUT 3 ENE 1,2 DIONE; CHEMOKINE RECEPTOR ANTAGONIST; CHEMOKINE RECEPTOR CXCR1; CHEMOKINE RECEPTOR CXCR2; HETEROCYCLIC COMPOUND; UNCLASSIFIED DRUG;

EID: 38949192884     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2008.01.024     Document Type: Article
Times cited : (19)

References (38)
  • 28
    • 38949173333 scopus 로고    scopus 로고
    • Kanniess, F.; Khalilieh, S.; Ludwig-Sengiel, A.; Stryszak, P.; Soni, P.; Holz, O. In Abstract of Papers, 17th European Respiratory Society Annual Congress, Stockholm, Sweden, September 15-19, 2007; p 1292.
    • Kanniess, F.; Khalilieh, S.; Ludwig-Sengiel, A.; Stryszak, P.; Soni, P.; Holz, O. In Abstract of Papers, 17th European Respiratory Society Annual Congress, Stockholm, Sweden, September 15-19, 2007; p 1292.
  • 29
    • 38949123817 scopus 로고    scopus 로고
    • Work presented in part: Dwyer, M. P.; Yu, Y.; Chao, J.; Aki, C.; Chao, J.; Purakkattle, B.; Rindgen, D.; Bond, R.; Jakway, J.; Hipkin, R. W.; Fossetta, J.; Gonsiorek,W.; Bian, H.; Fine, J.; Merritt, J. R.; Rokosz, L. L.; Kaiser, B.; Li, G.; Wang, W.; Stauffer, T.; Ozgur, L.; Taveras, A. In Abstract of Papers, 231st National Meeting of the American Chemical Society, Atlanta, GA, United States, March 26-30, 2006; American Chemical society: Washington, DC, 2006; MEDI-019.
    • Work presented in part: Dwyer, M. P.; Yu, Y.; Chao, J.; Aki, C.; Chao, J.; Purakkattle, B.; Rindgen, D.; Bond, R.; Jakway, J.; Hipkin, R. W.; Fossetta, J.; Gonsiorek,W.; Bian, H.; Fine, J.; Merritt, J. R.; Rokosz, L. L.; Kaiser, B.; Li, G.; Wang, W.; Stauffer, T.; Ozgur, L.; Taveras, A. In Abstract of Papers, 231st National Meeting of the American Chemical Society, Atlanta, GA, United States, March 26-30, 2006; American Chemical society: Washington, DC, 2006; MEDI-019.
  • 31
    • 38949154643 scopus 로고    scopus 로고
    • Full experimental details have appeared elsewhere: Taveras, A. G.; Aki, C. J.; Bond, R. W.; Chao, J.; Dwyer, M.; Ferreira, J. A.; Chao, J.; Yu, Y.; Baldwin, J. J.; Kaiser, B.; Li, G.; Merritt, J. R.; Nelson, K. H.; Rokosz, L. L. WO 2002083624.
    • Full experimental details have appeared elsewhere: Taveras, A. G.; Aki, C. J.; Bond, R. W.; Chao, J.; Dwyer, M.; Ferreira, J. A.; Chao, J.; Yu, Y.; Baldwin, J. J.; Kaiser, B.; Li, G.; Merritt, J. R.; Nelson, K. H.; Rokosz, L. L. WO 2002083624.
  • 34
    • 38949131291 scopus 로고    scopus 로고
    • note
    • The enantiomeric (S)-ethyl derivative of 45 was prepared accordingly to Scheme 3 except using (S)-valinol as an auxiliary according to Ref. 13. The enantiomeric (S) derivative of 45 was found to have poorer affinity for both the CXCR2 and CXCR1 receptor versus the corresponding (R)-ethyl derivative which is consistent with previously reported trends reported in Ref. 11b.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.