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Volumn 39, Issue 28, 1998, Pages 5065-5068

Synthesis of 1-O-[(3S,4R)-3-hydroxytetrahydrofuran-4-yl]-α-D- glucopyranoside 3,4,3'-triphosphate as a novel potent IP3 receptor ligand

Author keywords

Glycosidation; Inositols; Receptors; Structure activity

Indexed keywords

1 O [3 HYDROXYTETRAHYDROFURAN 4 YL] ALPHA DEXTRO GLUCOPYRANOSIDE 3,4,3' TRISPHOSPHATE; ADENOPHOSTIN A; ADENOPHOSTIN B; INOSITOL 1,4,5 TRISPHOSPHATE DERIVATIVE; INOSITOL 1,4,5 TRISPHOSPHATE RECEPTOR; LIGAND; UNCLASSIFIED DRUG;

EID: 0032500143     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)00954-X     Document Type: Article
Times cited : (28)

References (15)
  • 9
    • 34548296261 scopus 로고
    • [9] Ogawa investigated the regioselective benzylation of 8 by various methods and obtained 9 in the highest yield (70%) by treating the 2,3-dibutylstannylidene derivative of 8 with BnBr in DMF: Ogawa T, Kaburagi T. Carbohydr. Res. 1982;103:53-64.
    • (1982) Carbohydr. Res. , vol.103 , pp. 53-64
    • Ogawa, T.1    Kaburagi, T.2
  • 15
    • 1542501236 scopus 로고    scopus 로고
    • equation presented
    • [15] The synthesis of 3-O-(α-D-glucopyranosyl)-β-D-ribofuranoside 2,3′4′-trisphosphate 23, which was also designed to restrict the conformation of the side-chain moiety of 4, has also been reported recently: Jenkins DJ, Potter BVL. Chem. Commun. 1997:449-450. (equation presented)
    • (1997) Chem. Commun. , pp. 449-450
    • Jenkins, D.J.1    Potter, B.V.L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.