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Volumn 55, Issue 12, 2007, Pages 1758-1761

A study of the calcium complex of a glucosylceramide, soya-cerebroside II

Author keywords

Calcium ion binding affinity; Calcium ion chelator; Continuous variation method; Endogenous ionophore; Sphingoglycolipid

Indexed keywords

CALCIUM DERIVATIVE; CALCIUM ION; GLUCOSYLCERAMIDE; O (3,6 DIDEOXY BETA DEXTRO GLUCOPYRANOSYL) (1-1) 2 (2' HYDROXYACTANAMIDO) OCT 4 ENE 1 OL; O (BETA DEXTRO GLUCOPYRANOSYL) (1-1) 2 (2' HYDROXYACTANAMIDO) OCT 4 ENE 1 OL; SOYA CEREBROSIDE 2; UNCLASSIFIED DRUG;

EID: 36849013922     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.55.1758     Document Type: Article
Times cited : (5)

References (37)
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    • The C4″-equatrial hydroxy group should be an important functional group to lock the pyran moiety to be the 4C1 chair conformation. Thus, the C4″-OH in the designed molecule was retained
    • 1 chair conformation. Thus, the C4″-OH in the designed molecule was retained.
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    • The detailed syntheses of 6 will be reported elsewhere.
    • The detailed syntheses of 6 will be reported elsewhere.
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    • 2+ were ca. 0.01 M.
    • 2+ were ca. 0.01 M.
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    • see a web site
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    • +).
    • +).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.