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Volumn 18, Issue 7, 2008, Pages 2399-2403

Aryl-indolyl maleimides as inhibitors of CaMKIIδ. Part 3: Importance of the indole orientation

Author keywords

Calmodulin; Inhibitors; Kinase; Maleimides

Indexed keywords

ADENOSINE TRIPHOSPHATE; AMINE; FUNCTIONAL GROUP; INDOLE; INDOLYLMALEIMIDE DERIVATIVE; MALEIMIDE DERIVATIVE; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; PROTEIN KINASE (CALCIUM,CALMODULIN); UNCLASSIFIED DRUG;

EID: 41149139078     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2008.02.057     Document Type: Article
Times cited : (8)

References (14)
  • 11
    • 41149170966 scopus 로고    scopus 로고
    • note
    • 2, 8.3μg/ml calmodulin, 25 μM [His 5] Autocamtide-2, 120 nM [g-33P]ATP) and the reaction mixture incubated at rt for 3 minutes. Reactions were terminated by transferring 25 μl to a UNIFILTER 96-well P81microplate (Whatman, UK), pre-wet with 15 μl 1% phosphoric acid. After 10 min, the plate was washed 3 times with 1% phosphoric acid and 1 time with 95% ethanol on a BiomekFX (Beckman Coulter, CA) equipped with a vacuum manifold. Plates were dried for approximately 60 min, scintillant was added to the wells, and the plates were read on a TopCount NXT Microplate Scintillation and Luminescence Counter (Perkin-Elmer, MA).
  • 13
    • 41149158362 scopus 로고    scopus 로고
    • http://www.upstate.com/features/kp_reference.asp#.
    • http://www.upstate.com/features/kp_reference.asp#.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.