In continuation of our endeavours to synthesize immunosuppressive agents from α-santonin, we report herein the design and synthesis of a new series of α-santonin derived O-aryl/aliphatic ether, ester and amide analogs and the evaluation of their immunosuppressive activities. The in vitro studies led to several analogs with significant immunosuppressive effects by inhibiting ConA and LPS stimulated T- and B-cell proliferation in a dose dependent manner. The more significant compounds 4d, 4e, 4f, 4h, 6a and 6b displayed potent inhibitory activity on the mitogen-induced T- and B-cell proliferation in comparison to α-santonin 1. Compound 4e displayed stupendous in vitro immunosuppressive effects with â¼80% suppression of B and â¼75% suppression of T lymphocyte proliferation, respectively. The in vivo investigation on BALB/c mice revealed that non-cytotoxic compound 4e suppresses both humoral and cellular immunity.
T- and B-cell immunosuppressive activity of novel α-santonin analogs with humoral and cellular immune response in Balb/c mice.
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作者:Dangroo Nisar A, Singh Jasvinder, Gupta Nidhi, Singh Shashank, Kaul Anapurna, Khuroo Mohmmed A, Sangwan Payare L
| 期刊: | Medchemcomm | 影响因子: | 0.000 |
| 时间: | 2017 | 起止号: | 2016 Nov 11; 8(1):211-219 |
| doi: | 10.1039/c6md00527f | ||
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