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Volumn 14, Issue 21, 2004, Pages 5389-5394

Novel, potent and selective anilinoquinazoline and anilinopyrimidine inhibitors of p38 MAP kinase

Author keywords

p38 MAP kinase inhibitors

Indexed keywords

ENZYME INHIBITOR; MITOGEN ACTIVATED PROTEIN KINASE P38; PYRIMIDINE DERIVATIVE; QUINAZOLINE DERIVATIVE;

EID: 5444244504     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2004.08.007     Document Type: Article
Times cited : (64)

References (33)
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    • see Ref. 7
    • For in vitro assay experimental procedures see Ref. 7
  • 16
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    • Cumming, J. G. WO 0020402, 2000
    • Cumming, J.G.1
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    • Chem. Abstr. 132 2000 265207
    • (2000) Chem. Abstr. , vol.132 , pp. 265207
  • 19
    • 84888980829 scopus 로고    scopus 로고
    • WO 0127089, 2000
    • Cumming, J. G. WO 0127089, 2000
    • Cumming, J.G.1
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    • Chem. Abstr. 134 2000 295834
    • (2000) Chem. Abstr. , vol.134 , pp. 295834
  • 23
    • 84888962925 scopus 로고    scopus 로고
    • Work carried out on behalf of AstraZeneca by Sir Philip Cohen, Division of Signal Transduction Therapy, University of Dundee, Dundee, UK. The kinase panel used was the Core panel shown in Table 1 of Ref. 11
    • Work carried out on behalf of AstraZeneca by Sir Philip Cohen, Division of Signal Transduction Therapy, University of Dundee, Dundee, UK. The kinase panel used was the Core panel shown in Table 1 of Ref. 11
  • 25
    • 84888944328 scopus 로고    scopus 로고
    • note
    • Procedure for rat in vivo LPS model: Female Alderley Park rats (five per group) were dosed orally with the test compound (10 mg/kg; formulated in 1:1 v/v PEG/water; 0.2 mL per 100 g body weight) 60 min prior to challenge with LPS administered intravenously [LPS E.Coli 0111:B4; Sigma L-4130; 30 μg in 0.2 mL sterile physiological saline (Phoenix Pharma Ltd)]. Control animals received vehicle alone prior to LPS challenge. Blood was obtained 60 min after LPS challenge and plasma isolated and stored at -80°C. TNFα concentration was measured by ELISA (R&D Systems rat TNF-α Quantikine kit, catalogue no. SRTA00). For each compound/dose the percentage inhibition of TNFα was calculated as a percentage of controls


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.