| Literature DB >> 30108707 |
Nisar A Dangroo1, Jasvinder Singh2,3, Nidhi Gupta1, Shashank Singh2,3, Anapurna Kaul2, Mohmmed A Khuroo4, Payare L Sangwan1,3.
Abstract
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 ∼80% suppression of B and ∼75% 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.Entities:
Year: 2016 PMID: 30108707 PMCID: PMC6072515 DOI: 10.1039/c6md00527f
Source DB: PubMed Journal: Medchemcomm ISSN: 2040-2503 Impact factor: 3.597