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Synthesis and biological evaluation of indolyl bisphosphonates as anti-bone resorptive and anti-leishmanial agents
A series of indole conjugated bisphosphonate derivatives have been synthesized and evaluated for their in vitro anti-bone resorptive activity using bone marrow osteoclast culture. Two bisphosphonates 23 and 24 significantly inhibited osteoclastogenesis, 23 showed inhibition at 10 and 100 pM which wa...
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Published in: | Bioorganic & medicinal chemistry 2008-09, Vol.16 (18), p.8482-8491 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A series of indole conjugated bisphosphonate derivatives have been synthesized and evaluated for their in vitro anti-bone resorptive activity using bone marrow osteoclast culture. Two bisphosphonates
23 and
24 significantly inhibited osteoclastogenesis,
23 showed inhibition at 10 and 100
pM which was lower than the concentration of standard drug alendronate, and
24 inhibited osteoclastogenesis at 100
nM which was comparable to alendronate. Two other compounds
13 and
14 also showed inhibition comparable to alendronate, but were cytotoxic in the osteoblast cells. The two active bisphosphonates
23 and
24 induced significant osteoclast apoptosis at concentrations 100
nM for compound
24 and at 10
pM for compound
23 compared to alendronate. In vivo effect of active bisphosphonates
23 and
24 resulted in osteoclastogenesis of bone marrow cells (BMCs) to almost 40–50% (
23 showing 8.4% decrease and
24 showing 9.0%) compared to 16.5% of the ovariectomized group. Further, screening of anti-leishmanial activity, four compounds
24–
25 and
27–
28 showed more than 80% inhibition against both the promastigote and amastigote stages of the
Leishmania parasite. |
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ISSN: | 0968-0896 1464-3391 |
DOI: | 10.1016/j.bmc.2008.08.024 |