ABSTRACT
A library of queuine analogues targeting the modification of tRNA isoacceptors for Asp, Asn, His and Tyr catalysed by queuine tRNA ribosyltransferase (QTRT, also known as TGT) was evaluated in the treatment of a chronic multiple sclerosis model: murine experimental autoimmune encephalomyelitis. Several active 7-deazaguanines emerged, together with a structure-activity relationship involving the necessity for a flexible alkyl chain of fixed length.
Subject(s)
Encephalomyelitis, Autoimmune, Experimental , Animals , Mice , Encephalomyelitis, Autoimmune, Experimental/drug therapy , RNA, Transfer , Structure-Activity Relationship , Pentosyltransferases/metabolismABSTRACT
Eukaryotic tRNA-guanine transglycosylase (TGT) - an enzyme recently recognised to be of potential therapeutic importance - catalyses base-exchange of guanine for queuine at the wobble position of tRNAs associated with 4 amino acids via a distinct mechanism to that reported for its eubacterial homologue. The presence of queuine is unequivocally required as a trigger for reaction between the enzyme and tRNA and exhibits cooperativity not seen using guanine as a substrate.
Subject(s)
Guanine/analogs & derivatives , Pentosyltransferases/chemistry , RNA, Transfer/chemistry , Catalysis , Guanine/chemistryABSTRACT
The synthesis of novel mecamylamine analogues is described in which one, two or three of the methyl groups of mecamylamine have been systematically replaced with ethyl groups. Assessment of the compounds highlights that simple ethyl for methyl changes changes to the parent structure can dramatically enhance activity and selectivity towards either the α4ß2 (at the expense of α3ß4) or the α3ß4 (at the expense of α4ß2) nicotinic acetylcholine receptor sub-type as compared to the parent compound.
ABSTRACT
A new synthesis of mecamylamine - a known anti-hypertensive drug with anti-addictive properties is described. The new route allowed access to two novel analogues whose activity at two nicotinic acetylcholine receptor subtypes was assessed.
Subject(s)
Antihypertensive Agents/chemical synthesis , Antihypertensive Agents/pharmacology , Behavior, Addictive/drug therapy , Mecamylamine/chemical synthesis , Mecamylamine/pharmacology , Antihypertensive Agents/chemistry , Antihypertensive Agents/therapeutic use , Chemistry Techniques, Synthetic , Mecamylamine/chemistry , Mecamylamine/therapeutic use , Methylation , Receptors, Nicotinic/metabolismABSTRACT
A new approach to 3-nitro-2-substituted thiophenes has been developed. Exposure of commercially available 1,4-dithane-2,5-diol to nitroalkenes in the presence of 20% triethylamine results in a tandem Michael-intramolecular Henry reaction to form the corresponding tetrahydrothiophene. Subsequent microwave irradiation on acidic alumina in the presence of chloranil effects the solvent free dehydration and aromatization to form 3-nitro-2-substituted thiophenes cleanly and rapidly. A simple workup procedure removes the requirement for purification by chromatography in most cases.
