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Volumn 18, Issue 2, 2008, Pages 688-693

Optimization of the heterocyclic core of the quinazolinone-derived CXCR3 antagonists

Author keywords

Chemokine; CXCL10; CXCL11; CXCL9; CXCR3; IP10; ITAC; Mig

Indexed keywords

1,8 NAPHTHYRIDINE DERIVATIVE; 8 AZAQUINAZOLINONE DERIVATIVE; AMG 487; BENZIMIDAZOLE; CHEMOKINE RECEPTOR ANTAGONIST; CHEMOKINE RECEPTOR CXCR3; CHEMOKINE RECEPTOR CXCR3 ANTAGONIST; FUSED HETEROCYCLIC RINGS; IMIDAZOPYRIDINE DERIVATIVE; NAPHTHYRIDINE DERIVATIVE; PYRIDOPYRIMIDINE; PYRIMIDINE DERIVATIVE; QUINAZOLINONE DERIVATIVE; QUINOLINE; QUINOXALINE; UNCLASSIFIED DRUG;

EID: 38149133179     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2007.11.060     Document Type: Article
Times cited : (45)

References (24)
  • 23
    • 38149118824 scopus 로고    scopus 로고
    • note
    • 125I]-IP10 binding assay in buffer with the exception that EDTA-anti-coagulated human plasma ("plasma") was added to the assay buffer, to 50% final assay concentration. ITAC in vitro cell migration assay: 100 ng/ml of human ITAC resuspended in 100% plasma was added to the lower chamber of a migration plate. Human PBMC (prepared as above) were resuspended in 100% plasma and placed in the upper chamber of the migration plate. Compounds were measured for their ability to inhibit CXCR3 mediated migration of cells into the lower chamber, in response to ITAC.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.