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Volumn 127, Issue 24, 2005, Pages 8846-8855

Synthesis of stable and cell-type selective analogues of cyclic ADP-ribose, a Ca2+-mobilizing second messenger. Structure-activity relationship of the N1-ribose moiety

Author keywords

[No Author keywords available]

Indexed keywords

CARBOXYLIC ACIDS; CELLS; CONDENSATION; CONFORMATIONS; MOLECULAR STRUCTURE; PROTEINS; REACTION KINETICS; SYNTHESIS (CHEMICAL);

EID: 20944431987     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja050732x     Document Type: Article
Times cited : (43)

References (81)
  • 3
    • 0027452685 scopus 로고
    • (a) Galione, A. Science 1993, 259, 325-326.
    • (1993) Science , vol.259 , pp. 325-326
    • Galione, A.1
  • 6
    • 0345609814 scopus 로고    scopus 로고
    • (d) Lee, H. C. Physiol. Rev. 1997, 77, 1133-1164.
    • (1997) Physiol. Rev. , vol.77 , pp. 1133-1164
    • Lee, H.C.1
  • 74
    • 20944436074 scopus 로고    scopus 로고
    • note
    • Calculations were performed using SYBYL ver. 6.5 software (Tripos. Inc.).
  • 77
    • 20944431506 scopus 로고    scopus 로고
    • note
    • 1/2 value of 60 h under the same conditions.
  • 81
    • 20944449815 scopus 로고    scopus 로고
    • note
    • In the Jurkat T-cell system, cADPR (1) was roughly 3-fold more potent in inducing calcium release than cADPcR (2) at 100 μM (see ref 7g), indicating that 3′-deoxy-cADPcR (4) was slightly less effective than cADPcR.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.