Premium
Selenium‐Containing Heterocycles: Synthesis and Pharmacological Activities of Some New 4‐Methylquinoline‐2(1 H ) Selenone Derivatives
Author(s) -
AbdelHafez Shams H.,
Hussein Mostafa A.
Publication year - 2008
Publication title -
archiv der pharmazie
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.468
H-Index - 61
eISSN - 1521-4184
pISSN - 0365-6233
DOI - 10.1002/ardp.200700202
Subject(s) - chemistry , acetic anhydride , antifungal , acute toxicity , organic chemistry , proton nmr , stereochemistry , toxicity , catalysis , medicine , dermatology
Several selenolo[2,3‐ b ]quinolines and pyrimido[4′,5′:4,5]selenolo[2,3 ‐b ]quinolines were prepared by annulations via reaction of NaSeH with 2‐chloro‐3‐cyano‐4‐methylquinoline 1 followed by reactions with aromatic aldehydes, cycloalkanones, and acetic anhydride. Spectroscopic (IR, 1 H‐NMR, and MS) properties of the synthesized compounds are reported. Some selected compounds 5a , 7b , 7c , 8b–d , 9a , 11b , and 11d were investigated for their anti‐inflammatory and analgesic activities; in addition, the most active compounds were tested for their ulcerogenicity and acute toxicity. Moreover, some of the test compounds 7c , 9a , 11b , and 11d were screened for their antibacterial and antifungal activities.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom