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Volumn 18, Issue 2, 2008, Pages 571-575

Corrigendum to "Synthesis and structure-activity relationship studies of tyrosine-based antagonists at the human P2X7 receptor" [Bioorg. Med. Chem. Lett. 18 (2008) 571-575] (DOI:10.1016/j.bmcl.2007.11.077);Synthesis and structure-activity relationship studies of tyrosine-based antagonists at the human P2X7 receptor

Author keywords

Ethidium bromide uptake; IL 1 release; P2X7 receptor; Tyrosine based antagonists

Indexed keywords

1 [N,O BIS(5 ISOQUINOLINESULFONYL) N METHYLTYROSYL] 4 PHENYLPIPERAZINE; ETHIDIUM BROMIDE; INTERLEUKIN 1BETA; PIPERAZINE; PURINERGIC P2X7 RECEPTOR; PURINERGIC RECEPTOR BLOCKING AGENT; TYROSINE DERIVATIVE;

EID: 38149132392     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2008.05.108     Document Type: Erratum
Times cited : (19)

References (29)
  • 28
    • 38149125417 scopus 로고    scopus 로고
    • note
    • + was determined by measuring fluorescence with a fluorescent plate reader (excitation filter of 530/20 and emission filter of 590/20).
  • 29
    • 38149079635 scopus 로고    scopus 로고
    • note
    • Inhibition effects of BzATP-mediated IL-1β release by ELISA measurements. IL-1β release was measured in differentiated THP-1 cells primed for 3 h with 25 ng/ml LPS and 10 ng/ml IFNγ, and then was stimulated with 1 mM BzATP for 30 min. Synthesized tyrosine-based derivatives at 1 μM were treated for 30 min prior to BzATP. Supernatants were collected by centrifugation at 1000 rpm for 5 min and assayed for the presence of mature human IL-1β using an ELISA kit.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.