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Volumn 7, Issue 12, 1999, Pages 2877-2889

Synthesis and biological activity of 22-iodo- and (E)-20(22)-dehydro analogues of 1α,25-dihydroxyvitamin D3

Author keywords

Antiproliferative agents; Molecular modeling mechanics; Receptor binding; Vitamin D3 analogues

Indexed keywords

20(22) DEHYDROCALCITRIOL; 22 IODOCALCITRIOL; CALCITRIOL; CALCITRIOL DERIVATIVE; UNCLASSIFIED DRUG; VITAMIN D RECEPTOR;

EID: 0033391499     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0968-0896(99)00249-7     Document Type: Article
Times cited : (19)

References (49)
  • 20
    • 0032230321 scopus 로고    scopus 로고
    • Some recent findings indicate that diminished VDR binding by a vitamin D analogue does not mean that it will necessarily have diminished antiproliferative/prodifferentiation potency, see
    • Some recent findings indicate that diminished VDR binding by a vitamin D analogue does not mean that it will necessarily have diminished antiproliferative/prodifferentiation potency, see Peleg, S.; Nguen, C.; Woodard, B. T.; Lee, J.-K.; Posner, G. H. Mol. Endocrinol. 1998, 12, 525.
    • (1998) Mol. Endocrinol. , vol.12 , pp. 525
    • Peleg, S.1    Nguen, C.2    Woodard, B.T.3    Lee, J.-K.4    Posner, G.H.5
  • 42
    • 0342419244 scopus 로고    scopus 로고
    • These findings are in good agreement with the published results of MM2PP calculations of the same 25-hydroxy-8-methylene derivative 14a, see ref. 27
    • These findings are in good agreement with the published results of MM2PP calculations of the same 25-hydroxy-8-methylene derivative 14a, see ref. 27.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.