Design of noncovalent inhibitors of human cathepsin L. from the 96-residue proregion to optimized tripeptidesCHOWDHURY, Shafinaz F; SIVARAMAN, J; SULEA, Traian et al.Journal of medicinal chemistry (Print). 2002, Vol 45, Num 24, pp 5321-5329, issn 0022-2623, 9 p.Article

Pulmonary and blood enzyme kinetics as predictors of pulmonary metabolism of estersDICKINSON, P. A; TAYLOR, G.International journal of pharmaceutics. 1995, Vol 116, Num 2, pp 231-236, issn 0378-5173Article

Structure-based design of COX-2 selectivity into flurbiprofenBAYLY, C. I; BLACK, W. C; LEGER, S et al.Bioorganic & medicinal chemistry letters (Print). 1999, Vol 9, Num 3, pp 307-312, issn 0960-894XArticle

Simple and rapid analysis of pefloxacin, fenbufen and felbinac in human plasma using high performance liquid chromatographyCARLUCCI, G; PALUMBO, G; MAZZEO, P et al.Journal of liquid chromatography & related technologies. 1996, Vol 19, Num 7, pp 1107-1115, issn 1082-6076Article

Enhanced rectal absorption and reduced local irritation of the anti-inflammatory drug ethyl 4-biphenylylacetate in rats by complexation with water-soluble β-cyclodextrin derivatives and formulation as oleaginous suppositoryARIMA, H; KONDO, T; IRIE, T et al.Journal of pharmaceutical sciences. 1992, Vol 81, Num 11, pp 1119-1125, issn 0022-3549Article

Possible enhancing mechanism of the cutaneous permeation of 4-biphenylylacetic acid by β-cyclodextrin derivatives in hydrophilic ointmentARIMA, H; MIYAJI, T; IRIE, T et al.Chemical and pharmaceutical bulletin. 1996, Vol 44, Num 3, pp 582-586, issn 0009-2363Article

Crystal structure of heptakis(2,3,6-tri-O-methyl)-β-cyclodextrin complexes with m-iodophenol and 4-biphenylacetic acid. Guest-induced conformational change of a pyranose ringHARATA, K; HIRAYAMA, F; ARIMA, H et al.Perkin transactions. 2. 1992, Num 7, pp 1159-1166, issn 0300-9580Article

Potent small molecule mouse CD22-inhibitors: Exploring the interaction of the residue at C-2 of sialic acid scaffoldABDU-ALLAH, Hajjaj H. M; WATANABE, Kozo; HAYASHIZAKI, Koji et al.Bioorganic & medicinal chemistry letters (Print). 2009, Vol 19, Num 19, pp 5573-5575, issn 0960-894X, 3 p.Article

Highly twisted adamantyl arotinoids: Synthesis, antiproliferative effects and RXR transactivation profilesPEREZ-RODRIGUEZ, Santiago; ORTIZ, Maria A; PEREIRA, Raquel et al.European journal of medicinal chemistry. 2009, Vol 44, Num 6, pp 2434-2446, issn 0223-5234, 13 p.Article

Novel agmatine and agmatine-like peptidomimetic inhibitors of the West Nile virus NS2B/NS3 serine proteaseHUICHANG ANNIE LIM; JOY, Joma; HILL, Jeffrey et al.European journal of medicinal chemistry. 2011, Vol 46, Num 7, pp 3130-3134, issn 0223-5234, 5 p.Article

Design, synthesis and evaluation of mutual prodrug of 4-biphenylacetic acid and quercetin tetramethyl ether (BPA-QTME) as gastrosparing NSAIDMADHUKAR, Mamta; SAWRAJ, Shruti; PRITAM DEV SHARMA et al.European journal of medicinal chemistry. 2010, Vol 45, Num 6, pp 2591-2596, issn 0223-5234, 6 p.Article

Base-catalyzed deuterium and tritium labelling of 1-biphenyl-4-ylpropane-1,2-dione and deuteration of aryl methyl ketonesBERTHELETTE, Carl; SCHEIGETZ, John.Journal of labelled compounds & radiopharmaceuticals. 2004, Vol 47, Num 12, pp 891-894, issn 0362-4803, 4 p.Article

β-Lactams Derived from a Carbapenem Chiron Are Selective Inhibitors of Human Fatty Acid Amide Hydrolase versus Human Monoacylglycerol LipaseFELEDZIAK, Marion; MICHAUX, Catherine; URBACH, Allan et al.Journal of medicinal chemistry (Print). 2009, Vol 52, Num 22, pp 7054-7068, issn 0022-2623, 15 p.Article

Scaffold hopping in the rational design of novel HIV-1 non-nucleoside reverse transcriptase inhibitorsO'MEARA, Jeff A; JAKALIAN, Araz; THAVONEKHAM, Bounkham et al.Bioorganic & medicinal chemistry letters (Print). 2007, Vol 17, Num 12, pp 3362-3366, issn 0960-894X, 5 p.Article