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Anti-Cancer AgentsKOZIKOWSKI, Alan P; BARALDI, Pier G.Current pharmaceutical design. 1999, Vol 5, Num 3, issn 1381-6128, 190 p.Serial Issue

Chemical Origins of Isoform Selectivity in Histone Deacetylase Inhibitors : Histone Deacetylase InhibitorsBUTLER, Kyle V; KOZIKOWSKI, Alan P.Current pharmaceutical design. 2008, Vol 14, Num 6, pp 505-528, issn 1381-6128, 24 p.Article

The dolastatins, a family of promising antineoplastic agentsPONCET, J.Current pharmaceutical design. 1999, Vol 5, Num 3, pp 139-162, issn 1381-6128Article

A short and efficient synthesis of the pharmacological research tool GW501516 for the peroxisome proliferator-activated receptor δWEI, Zhi-Liang; KOZIKOWSKI, Alan P.Journal of organic chemistry. 2003, Vol 68, Num 23, pp 9116-9118, issn 0022-3263, 3 p.Article

Anti-cancer agentsKOZIKOWSKI, Alan P; BARALDI, Pier G.Current pharmaceutical design. 2001, Vol 7, Num 17, issn 1381-6128, 163 p.Serial Issue

Fused azepinones with antitumor activityKUNICK, C.Current pharmaceutical design. 1999, Vol 5, Num 3, pp 181-194, issn 1381-6128Article

The protein kinase ABC's of signal transduction as targets for drug developmentGLAZER, R. I.Current pharmaceutical design. 1998, Vol 4, Num 3, pp 277-290, issn 1381-6128Article

CoMFA study of piperidine analogues of cocaine at the dopamine transporter: Exploring the binding mode of the 3α-substituent of the piperidine ring using pharmacophore-based flexible alignmentHONGBIN YUAN; KOZIKOWSKI, Alan P; PETUKHOV, Pavel A et al.Journal of medicinal chemistry (Print). 2004, Vol 47, Num 25, pp 6137-6143, issn 0022-2623, 7 p.Article

Cytotoxics derived from distamycin A and congenersCOZZI, P; MONGELLI, N.Current pharmaceutical design. 1998, Vol 4, Num 3, pp 181-201, issn 1381-6128Article

Novel PI analogues selectively block activation of the pro-survival serine/ threonine kinase AktKOZIKOWSKI, Alan P; HAIYING SUN; BROGNARD, John et al.Journal of the American Chemical Society. 2003, Vol 125, Num 5, pp 1144-1145, issn 0002-7863, 2 p.Article

Studies in polyphenol chemistry and bioactivity. 4. Synthesis of trimeric, tetrameric, pentameric, and higher oligomeric epicatechin-derived procyanidins having all-4β, 8-interflavan connectivity and their inhibition of cancer cell growth through cell cycle arrestsKOZIKOWSKI, Alan P; TÜCKMANTEL, Werner; BÖTTCHER, Gesine et al.Journal of organic chemistry. 2003, Vol 68, Num 5, pp 1641-1658, issn 0022-3263, 18 p.Article

Retinoids, apoptosis and cancerSIMONI, Daniele; TOLOMEO, Manlio.Current pharmaceutical design. 2001, Vol 7, Num 17, pp 1823-1837, issn 1381-6128Article

Synthesis of more potent analogues of the acetylcholinesterase inhibitor, huperzine BRAJENDRAN, V; SAXENA, Ashima; DOCTOR, Bhupendra P et al.Bioorganic & medicinal chemistry letters (Print). 2002, Vol 12, Num 11, pp 1521-1523, issn 0960-894XArticle

Design and synthesis of a potent and selective peptidomimetic inhibitor of caspase-3MICALE, Nicola; VAIRAGOUNDAR, Rajendran; YAKOVLEV, Alexander G et al.Journal of medicinal chemistry (Print). 2004, Vol 47, Num 26, pp 6455-6458, issn 0022-2623, 4 p.Article

Synthesis and pharmacological evaluation of novel 9- and 10-substituted cytisine derivatives. nicotinic ligands of enhanced subtype selectivityCHELLAPPAN, Sheela K; YINGXIAN XIAO; TUECKMANTEL, Werner et al.Journal of medicinal chemistry (Print). 2006, Vol 49, Num 9, pp 2673-2676, issn 0022-2623, 4 p.Article

Further structure-activity relationship studies of piperidine-based monoamine transporter inhibitors : Effects of piperidine ring stereochemistry on potency. identification of norepinephrine transporter selective ligands andbroad-spectrum transporter inhibitorsRONG HE; KUROME, Toru; GIBERSON, Kelly M et al.Journal of medicinal chemistry (Print). 2005, Vol 48, Num 25, pp 7970-7979, issn 0022-2623, 10 p.Article

2,3-disubstituted 6-azabicyclo[3.2.1]octanes as novel dopamine transporter inhibitorsQUIRANTE, Josefina; VILA, Xavier; BONJOCH, Josep et al.Bioorganic & medicinal chemistry. 2004, Vol 12, Num 6, pp 1383-1391, issn 0968-0896, 9 p.Article

Synthesis and pharmacological characterization of bivalent ligands of epibatidine at neuronal nicotinic acetylcholine receptorsWEI, Zhi-Liang; YINGXIAN XIAO; KELLAR, Kenneth J et al.Bioorganic & medicinal chemistry letters (Print). 2004, Vol 14, Num 8, pp 1855-1858, issn 0960-894X, 4 p.Article

Piperidine-based nocaine/modafinil hybrid ligands as highly potent monoamine transporter inhibitors: Efficient drug discovery by rational lead hybridizationJIA ZHOU; RONG HE; JOHNSON, Kenneth M et al.Journal of medicinal chemistry (Print). 2004, Vol 47, Num 24, pp 5821-5824, issn 0022-2623, 4 p.Article

Drugs acting on DNA topoisomerases : Recent advances and future perspectivesGATTO, B; CAPRANICO, G; PALUMBO, M et al.Current pharmaceutical design. 1999, Vol 5, Num 3, pp 195-215, issn 1381-6128Article

Structure-Activity Relationships for a Series of Quinoline-Based Compounds Active against Replicating and Nonreplicating Mycobacterium tuberculosisLILIENKAMPF, Annamaria; JIALIN MAO; BAOJIE WAN et al.Journal of medicinal chemistry (Print). 2009, Vol 52, Num 7, pp 2109-2118, issn 0022-2623, 10 p.Article

3-Deoxy-3-substituted-D-myo-inositol imidazolyl ether lipid phosphates and carbonate as inhibitors of the phosphatidylinositol 3-kinase pathway and cancer cell growthYOUHONG HU; MEUILLET, Emmanuelle J; BERGGREN, Margareta et al.Bioorganic & medicinal chemistry letters (Print). 2001, Vol 11, Num 2, pp 173-176, issn 0960-894XArticle

A redox pathway leading to the alkylation of nucleic acids by doxorubicin and related anthracyclines : Application to the design of antitumor drugs for resistant cancerTAATJES, D. J; FENICK, D. J; GAUDIANO, G et al.Current pharmaceutical design. 1998, Vol 4, Num 3, pp 203-218, issn 1381-6128Article

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