Design and synthesis of 3-arylbenzopyran based non-steroidal vitamin-D3 mimics as osteogenic agents

被引:7
|
作者
Ahmad, Mohd. Imran [1 ]
Raghuvanshi, Dushyant Singh [1 ]
Singh, Sarita [1 ]
John, Aijaz A. [3 ]
Prakash, Ravi [3 ]
Nainawat, Kripa Shankar [1 ]
Singh, Divya [3 ]
Tripathi, Shubhandra [2 ]
Sharma, Ashok [2 ]
Gupta, Atul [1 ]
机构
[1] CSIR, Cent Inst Med & Aromat Plants, Dept Med Chem, Lucknow 226015, Uttar Pradesh, India
[2] CSIR, Cent Inst Med & Aromat Plants, Div Biotechnol, Lucknow 226015, Uttar Pradesh, India
[3] CSIR, Cent Drug Res Inst, Div Endocrinol, Sec 10, Lucknow, Uttar Pradesh, India
关键词
ESTROGEN-RECEPTORS ALPHA; BONE; BETA; EXPRESSION; CELLS; DERIVATIVES; OSTEOCLAST; MECHANISMS; CALCIUM;
D O I
10.1039/c6md00469e
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
3-Arylbenzopyran based non-steroidal osteogenic agents have been explored as structural templates of estrogen and vitamin-D-3. The target molecules 18a-c, 19a-c, 26a-c, 27a-c and intermediates 17a-c and 25a-c were studied for their osteogenic activity in an osteoblast differentiation assay in vitro using mouse calvarial osteoblast cells. Compounds 25c, 26b, 27b and 27c effectively increased ALP activity at 1 pM concentration compared to the untreated cells. The active compounds were devoid of inherent toxicity at 1 pM concentration in osteoblast cells. The most active compound, 27b, was studied for mineralization of osteoblast cells and expression of marker genes, viz. BMP-2, RUNX-2 & Osx, involved in osteogenesis. Molecular docking analysis performed for 27b showed its possible interactions with estrogen receptor-a and -beta (ER-alpha and ER-beta) as well as the vitamin-D receptor (VDR).
引用
收藏
页码:2381 / 2394
页数:14
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