Potent norovirus inhibitors based on the acyclic sulfamide scaffoldDOU, Dengfeng; TIEW, Kok-Chuan; RAO MANDADAPU, Sivakoteswara et al.Bioorganic & medicinal chemistry. 2012, Vol 20, Num 6, pp 2111-2118, issn 0968-0896, 8 p.Article

Inhibitory effect of chloroform on fermentative hydrogen and methane production from lipid-extracted microalgaeYUN, Yeo-Myeong; CHO, Si-Kyung; JUNG, Kyung-Won et al.International journal of hydrogen energy. 2014, Vol 39, Num 33, pp 19256-19261, issn 0360-3199, 6 p.Conference Paper

Haloenol lactones: potent enzyme-activated irreversible inhibitors for α-chymotrypsinDANIELS, S. B; COONEY, E; SOFIA, M. J et al.The Journal of biological chemistry (Print). 1983, Vol 258, Num 24, pp 15046-15053, issn 0021-9258Article

Rat α₁-cysteine proteinase inhibitor: an acute phase reactant identical with α₁ acute phase globulinESNARD, F; GAUTHIER, F.The Journal of biological chemistry (Print). 1983, Vol 258, Num 20, pp 12443-12447, issn 0021-9258Article

The MUT056399 Inhibitor of FabI Is a New Antistaphylococcal CompoundESCAICH, S; PROUVENSIER, L; SOULAMA-MOUZE, C et al.Antimicrobial agents and chemotherapy. 2011, Vol 55, Num 10, pp 4692-4697, issn 0066-4804, 6 p.Article

Pheophorbide a is a specific probe for ABCG2 function and inhibitionROBEY, Robert W; STEADMAN, Kenneth; POLGAR, Orsolya et al.Cancer research (Baltimore). 2004, Vol 64, Num 4, pp 1242-1246, issn 0008-5472, 5 p.Article

Discovery of a potent small molecule IL-2 inhibitor through fragment assemblyBRAISTED, Andrew C; OSLOB, Johan D; DELANO, Warren L et al.Journal of the American Chemical Society. 2003, Vol 125, Num 13, pp 3714-3715, issn 0002-7863, 2 p.Article

Inverse type of synthetic inhibitors of trypsin, S-ω-aminoalkyl thioestersKUNIEDA, T; ISHIZUKA, T; HIROBE, M et al.Chemical and pharmaceutical bulletin. 1983, Vol 31, Num 9, pp 3360-3362, issn 0009-2363Article

A Novel, Selective, and Efficacious Nanomolar Pyridopyrazinone Inhibitor of ^V600EBRAFWHITTAKER, Steven; MENARD, Delphine; LAMBROS, Maryou et al.Cancer research (Chicago, Ill.). 2010, Vol 70, Num 20, pp 8036-8044, issn 0008-5472, 9 p.Article

New substituted triaza-benzo[cd]azulen-9-ones as promising phosphodiesterase-4 inhibitorsDEVILLERS, Ingrid; PEVET, Isabelle; JACOBELLI, Henry et al.Bioorganic & medicinal chemistry letters (Print). 2004, Vol 14, Num 12, pp 3303-3306, issn 0960-894X, 4 p.Article

Discovery and characterization of a novel potent, selective and orally active inhibitor for mammalian ELOVL6SHIMAMURA, Ken; NAGUMO, Akira; NAGASE, Tsuyoshi et al.European journal of pharmacology. 2010, Vol 630, Num 1-3, pp 34-41, issn 0014-2999, 8 p.Article

Lipophilic amines as potent inhibitors of N-acylethanolamine-hydrolyzing acid amidaseYAMANO, Yumiko; TSUBOI, Kazuhito; HOZAKI, Yuki et al.Bioorganic & medicinal chemistry. 2012, Vol 20, Num 11, pp 3658-3665, issn 0968-0896, 8 p.Article

Structure and stereochemistry of tetrahedral inhibitor complexes of papain by direct NMR observationGAMCSIK, M. P; MALTHOUSE, J. P. G; PRIMROSE, W. U et al.Journal of the American Chemical Society. 1983, Vol 105, Num 20, pp 6324-6325, issn 0002-7863Article

Adaptive response of yeasts to furfural and 5-hydroxymethylfurfural and new chemical evidence for HMF conversion to 2,5-bis-hydroxymethylfuranLIU, Z. L; SLININGER, P. J; DIEN, B. S et al.Journal of industrial microbiology & biotechnology. 2004, Vol 31, Num 8, pp 345-352, issn 1367-5435, 8 p.Article

Kinetics and Computational Docking Studies on the Inhibition of Tyrosinase Induced by OxymatrineLIU, Xiao-Xia; SUN, Shi-Qing; WANG, Yu-Jie et al.Applied biochemistry and biotechnology. 2013, Vol 169, Num 1, pp 145-158, issn 0273-2289, 14 p.Article

Chemical synthesis and biological evaluation of triazole derivatives as inhibitors of InhA and antituberculosis agentsMENENDEZ, Christophe; CHOLLET, Aurelien; RODRIGUEZ, Frederic et al.European journal of medicinal chemistry. 2012, Vol 52, pp 275-283, issn 0223-5234, 9 p.Article

Discovery and evaluation of dual CDK1 and CDK2 inhibitorsPAYTON, Marc; CHUNG, Grace; ASKEW, Ben et al.Cancer research (Baltimore). 2006, Vol 66, Num 8, pp 4299-4308, issn 0008-5472, 10 p.Article

Milbemycins: More than Efflux Inhibitors for Fungal PathogensSILVA, Luis Vale; SANGUINETTI, Maurizio; VANDEPUTTE, Patrick et al.Antimicrobial agents and chemotherapy. 2013, Vol 57, Num 2, pp 873-886, issn 0066-4804, 14 p.Article

Peptide deformylase inhibitors as potent antimycobacterial agentsTEO, Jeanette W. P; THAYALAN, Pamela; HASAN, Samiul et al.Antimicrobial agents and chemotherapy. 2006, Vol 50, Num 11, pp 3665-3673, issn 0066-4804, 9 p.Article

Synthesis and biological evaluation of quinazoline and quinoline bearing 2,2,6,6-tetramethylpiperidine-N-oxyl as potential epidermal growth factor receptor(EGFR) tyrosine kinase inhibitors and EPR bio-probe agentsSIYUAN LI; CHUNYING GUO; XIANQIANG SUN et al.European journal of medicinal chemistry. 2012, Vol 49, pp 271-278, issn 0223-5234, 8 p.Article

Overview of inhibitorsASTERMARK, Jan.Seminars in hematology. 2006, Vol 43, Num 2, issn 0037-1963, S3-S7, SUP4Conference Paper

The role of Mcl-1 downregulation in the proapoptotic activity of the multikinase inhibitor BAY 43-9006CHUNRONG YU; BRUZEK, Laura M; XUE WEI MENG et al.Oncogene (Basingstoke). 2005, Vol 24, Num 46, pp 6861-6869, issn 0950-9232, 9 p.Article

Inhibitors of amyloid aggregation: Technologies for the discovery of novel lead compoundsDOIG, Andrew J; STOTT, Kelvin; TREHERNE, J. Mark et al.Biotechnology & genetic engineering reviews. 2004, Vol 21, pp 197-212, issn 0264-8725, 16 p.Article

Application of PHSC equation of state in prediction of gas hydrate formation conditionVALAVI, Masood; REZA DEHGHANI, Mohammad.Fluid phase equilibria. 2012, Vol 333, pp 27-37, issn 0378-3812, 11 p.Article

Application of PRSV2 equation of state to predict hydrate formation temperature in the presence of inhibitorsMORADI, Gholamreza; KHOSRAVANI, Ehsan.Fluid phase equilibria. 2012, Vol 333, pp 18-26, issn 0378-3812, 9 p.Article