Nonsteroidal selective glucocorticoid modulators: the effect of C-5 alkyl substitution on the transcriptional activation/repression profile of 2,5-dihydro-10-methoxy-2,2,4-trimethyl-1H-[1]benzopyrano[3,4-f]quinolinesELMORE, Steven W; COGHLAN, Michael J; JACOBSON, Peer B et al.Journal of medicinal chemistry (Print). 2001, Vol 44, Num 25, pp 4481-4491, issn 0022-2623Article

Synthesis and structure-activity relationships of a novel series of tricyclic dihydropyridine-based K_ATP openers that potently inhibit bladder contractions in vitroCARROLL, William A; AGRIOS, Konstantinos A; KORT, Michael E et al.Journal of medicinal chemistry (Print). 2004, Vol 47, Num 12, pp 3180-3192, issn 0022-2623, 13 p.Article

Synthesis and characterization of non-steroidal ligands for the glucocorticoid receptor: Selective quinoline derivatives with prednisolone-equivalent functional activityCOGHLAN, Michael J; KYM, Philip R; NAKANE, Masaki et al.Journal of medicinal chemistry (Print). 2001, Vol 44, Num 18, pp 2879-2885, issn 0022-2623Article

Structure-activity studies for a novel series of tricyclic dihydropyridopyrazolones and dihydropyridoisoxazolones as K_ATP channel openersDRIZIN, Irene; ALTENBACH, Robert J; CARROLL, William A et al.Bioorganic & medicinal chemistry. 2004, Vol 12, Num 8, pp 1895-1904, issn 0968-0896, 10 p.Article

Effects of intermediate-conductance Ca²⁺-activated K⁺ channel modulators on human prostate cancer cell proliferationPARIHAR, Ashutosh S; COGHLAN, Michael J; GOPALAKRISHNAN, Murali et al.European journal of pharmacology. 2003, Vol 471, Num 3, pp 157-164, issn 0014-2999, 8 p.Article

Spontaneous phasic activity of the pig urinary bladder smooth muscle: Characteristics and sensitivity to potassium channel modulatorsBUCKNER, Steven A; MILICIC, Ivan; DAZA, Anthony V et al.British journal of pharmacology. 2002, Vol 135, Num 3, pp 639-648, issn 0007-1188Article

Effects of substitution on 9 -(3 -bromo -4 -fluorophenyl ) -5,9 -dihydro -3H,4H -2,6 -dioxa -4-azacyclopenta [b ]naphthalene -1,8 -dione, a dihydropyridine ATP-sensitive potassium channel openerALTENBACH, Robert J; BRUNE, Michael E; MILICIC, Ivan et al.Journal of medicinal chemistry (Print). 2006, Vol 49, Num 23, pp 6869-6887, issn 0022-2623, 19 p.Article

Nonsteroidal selective glucocorticoid modulators: The effect of C-10 substitution on receptor selectivity and functional potency of 5-allyl-2,5-dihydro-2,2,4-trimethyl-1H-[1]benzopyrano[3,4-f]quinolinesKYM, Philip R; KORT, Michael E; FALLS, H. Douglass et al.Journal of medicinal chemistry (Print). 2003, Vol 46, Num 6, pp 1016-1030, issn 0022-2623, 15 p.Article

Structure-activity relationship of a novel class of naphthyl amide K_ATP channel openersTURNER, Sean C; CARROLL, William A; DAZA, Anthony V et al.Bioorganic & medicinal chemistry letters (Print). 2003, Vol 13, Num 10, pp 1741-1744, issn 0960-894X, 4 p.Article

Tenidap, a novel anti-inflammatory agent, is an opener of the inwardly rectifying K⁺ channel hKir2.3YI LIU; DONG LIU; PRINTZENHOFF, David et al.European journal of pharmacology. 2002, Vol 435, Num 2-3, pp 153-160, issn 0014-2999Article