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Volumn 18, Issue 13, 2008, Pages 3814-3818

Synthesis of 5″-branched derivatives of cyclic ADP-carbocyclic-ribose, a potent Ca2+-mobilizing agent: The first antagonists modified at the N1-ribose moiety

Author keywords

Ca2+ mobilization; cADPR; Nucleotide; Second messenger

Indexed keywords

CYCLIC ADENOSINE DIPHOSPHATE RIBOSE; RIBOSE; ADENINE; ADENOSINE DIPHOSPHATE RIBOSE; CALCIUM; CYCLIC ADP CARBOCYCLIC RIBOSE; CYCLIC ADP-CARBOCYCLIC-RIBOSE; DRUG DERIVATIVE; PHOSPHATE;

EID: 44849127953     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2008.04.083     Document Type: Article
Times cited : (5)

References (35)
  • 8
    • 0027313269 scopus 로고
    • Examples of synthetic study of cADPR analogues:
    • Examples of synthetic study of cADPR analogues:. Walseth T.F., and Lee H.C. Biochim. Biophys. Acta 1178 (1993) 235
    • (1993) Biochim. Biophys. Acta , vol.1178 , pp. 235
    • Walseth, T.F.1    Lee, H.C.2
  • 26
    • 44849099656 scopus 로고    scopus 로고
    • Morgan, A. J.; Galione, A. In Ref. 2a, pp 167-197.
    • Morgan, A. J.; Galione, A. In Ref. 2a, pp 167-197.
  • 29
    • 44849134546 scopus 로고    scopus 로고
    • note
    • The stereochemistry was determined by the modified Mosher's method.
  • 34
    • 44849128639 scopus 로고    scopus 로고
    • note
    • -].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.