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Volumn 21, Issue 9, 2011, Pages 2616-2620

Probing the isoprenylcysteine carboxyl methyltransferase (Icmt) binding pocket: Sulfonamide modified farnesyl cysteine (SMFC) analogs as Icmt inhibitors

Author keywords

Anti cancer agents; Enzymes; Inhibitor; Isoprenoid; Methyltransferase; Signal transduction

Indexed keywords

METHYLTRANSFERASE INHIBITOR; PROTEIN S ISOPRENYLCYSTEINE O METHYLTRANSFERASE; SULFONAMIDE; SULFONAMIDE MODIFIED FARNESYL CYSTEINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 79955479634     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2011.01.078     Document Type: Conference Paper
Times cited : (15)

References (19)
  • 14
    • 14844337433 scopus 로고    scopus 로고
    • 14C]SAM) (50-60 mCi/mmol) (60 μM) is added and the solution is incubated at 30 °C in a water bath for 30 min. After 30 min the reaction is stopped by the addition 50 μL of 1 M NaOH/1% SDS. The reaction mixture is vortexed and spotted on to a pleated filter paper. The filter paper is lodged into the neck of a scintillation vial filled with 10 mL of scintillation fluid and capped. The filter papers were removed after 2.5 h and the radioactivity was measured using a Packard 1600CA Liquid Scintillation Analyzer.
    • (2005) J. Biol. Chem. , vol.280 , pp. 7336
    • Anderson, J.L.1    Frase, H.2    Michaelis, S.3    Hrycyna, C.A.4
  • 15
    • 0001755383 scopus 로고
    • M.D. Armstrong , and J.D. Lewis J. Org. Chem. 16 1951 749 About racemization at the alpha carbon, this Letter states that, 'Some concern was felt when it was noted that many of the derivatives of cysteine had very small numerical values for their rotations when they were measured in acid solution, since derivatives of cysteine and serine are known to racemize easily in alkaline solution. Measurement of the rotations of these compounds in water or in alkaline solutions gave much larger numerical rotations, however, and it was firmly established that, once freed of cystine, no further change in their rotation could be observed after repeated treatments with ammonia and sodium cyanide.'
    • (1951) J. Org. Chem. , vol.16 , pp. 749
    • Armstrong, M.D.1    Lewis, J.D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.