MEDISunday, August 19, 2007

7:00 PM-9:00 PM BCEC -- Exhibit Hall - B2, Poster
Poster Session
Organizer:James R. McCarthy
3-(Amino)alkoxy indoles: Novel class of centrally acting anti-obesity agents
Ramakrishna V. S. Nirogi, Anand V Daulatabad, Narendra Varma Gaddiraju, Parandhama Gudla, Mallesh Junnuri, Srinivasulu Kota, Rama Sastry Kambhampati, Anil K. Shinde
Nonpsychotropic biaryl cannabinoid agonists
Karin Worm, Q. Jean Zhou, Gabriel Stabley, Robert N. DeHaven, Nathalie C. Conway-James, Christopher J LaBuda, Michael Koblish, Patrick J Little, Roland E. Dolle
Synthesis of (-)-Δ9-tetrahydrocannabinol and (-)-Δ9-tetrahydrocannabivarin metabolites and their regiospecifically deuterated analogs
Spyros P. Nikas, Ganesh A. Thakur, Damon Parish, Shakiru O. Alapafuja, Marilyn A Huestis, Alexandros Makriyannis
Deuterated and tritiated enantiomers of CP55,940 as novel probes of cannabinoid receptors
Kejun Cheng, Klaus Gawrisch, Kenner C. Rice
Synthesis of isotopically labeled 2-pyridinyloxyisobubanoic acid, a building block for CB-1 inhibitors as drug candidates for obesity treatment
Jonathan Z. Ho, Matthew P Braun
Synthesis and biological evaluations of carbamoyl oxime analogs of the cannabinoid receptor-1 (CB1) anatagonist SR141716
Sung-Hwa Yoon, Hee-yeon Kim, Hyun-Ji Kim, Hyo-jae Jung
Synthesis and SAR of Diaryl cyclohexene carboxamides as potent and orally active CB1 antagonists
Charles L. Jayne, Yan Xia, H. Vaccaro, Samuel Chackalamannil, William Greenlee, George Boykow, Ruth A. Duffy, Timothy Kowalski, Xiaoming Cui
Synthesis and SAR of derivatives from 2, 3-dihydro-1H-spiro [isoquinoline-4, 4'-piperidine] as MC4R agonists for the treatment of obesity
Jian Liu, Tianying Jian, Iyassu K. Sebhat, Rui Tang, David H. Weinberg, Tanya MacNeil, Angeles Cabello, Airu S. Chen, Howard Y. Chen, Cherrie A. Shepherd, Alison Strack, R. Miller, Ralph Stearns, Zhesheng Chen, Tom Holt, Tung M. Fong, Matthew J. Wyvratt, Ravi P. Nargund
Optimization of privileged structures for selective and potent melanocortin subtype-4 receptor ligands
Qingmei Hong, Raman K. Bakshi, James Dellureficio, Rui Tang, Rubana N. Kalyani, Tanya MacNeil, Aurawan Vongs, Charles I. Rosenblum, David H. Weinberg, Qianping Peng, Constantin Tamvakopoulos, Randy R. Miller, Ralph A. Stearns, Doreen Cashen, William J. Martin, Airu S. Chen, Joseph M. Metzger, Howard Y. Chen, Alison M. Strack, Tung M. Fong, D. Euan MacIntyre, Lex H. T. Van der Ploeg, Arther A. Patchett, Matthew J. Wyvratt, Ravi P. Nargund
Potent and orally bioavailable nonpeptidyl melanocortin subtype-4 receptor modulators: Syntheses, SAR and pharmacokinetics
Liangqin Guo, Zhixiong Ye, Iyassu K. Sebhat, Feroze Ujjainwalla, Heather L. Sings, David H. Weinberg, Rui Tang, Tanya MacNeil, Constantin Tamvakopoulos, Qianping Peng, Euan MacIntyre, Lex H. T. Van der Ploeg, Mark T. Goulet, Matthew J. Wyvratt, Ravi P. Nargund
Aminobenzimidazoles as potent Melanin Concentrating Hormone (MCH)-R1 antagonists
T K Sasikumar, Li Qiang, Duane A Burnett, William J Greenlee, Brian E Hawes, Timothy J Kowalski, Kim O'Neill, Brian D Spar, Blair Weig
Tetrahydro carbazoles: Novel, potent and selective 5-HT6 receptor antagonists
Rama Sastry Kambhampati, Jagadish B. Konda, Prabhakar Kothmirkar, Trinath R. Bandyala, Sivasekhar NK. Yarra, Sobhanadri Arepalli, Anil K. Shinde, Ramakrishna V. S. Nirogi
Novel 1-(arylsulfonyl)-3-(piperidinylmethyl)-1H-indoles as potent and selective 5-HT6 antagonists
Ping Zhou, Yanfang Li, Boyd L. Harrison, Guo Ming Zhang, Deborah Smith, Michael G. Kelly, Lee Schechter, Albert J Robichaud
SUVN-504: Potent and selective high brain penetrating 5-HT6 receptor antagonist
Gopinadh Bhyrapuneni, Nageswararao Muddana, Koteshwara Mudigonda, Vishwottam N. Kandikere, Ramakrishna V. S. Nirogi
Aminoalkyl indoles: Novel, potent and highly selective 5-HT6 receptor antagonists
Anil K. Shinde, Amol D. Deshpande, Anil K. Chindhe, Rajesh Kumar Badange, Kameswara R. Karuturi, Narasimha Reddy P. Gangadasari, Raja Rajeswari Katta, Ramakrishna V. S. Nirogi
Conformationally restricted piperazines: Novel class of potent and selective 5-HT6 receptor ligands
Ramakrishna V. S. Nirogi, Amol D. Deshpande, Adi R. Dwarampudi, Venugopala Rao Bhatta, Laxman Kota, Ravichandra R. V. Vangavarugu, Rama Sastry Kambhampati, Anil K. Shinde
Small-molecule Y2 receptor antagonists: Identification of a novel and potent series using pharmacophore-based virtual screening
Mark Seierstad, Pascal Bonaventure, Lisa Dvorak, Brian Lord, Kirsten L. Miller, S. Timothy Motley, Diane H. Nepomuceno, Wenying Chai, Curt A. Dvorak, Jill A. Jablonowski, Dale A. Rudolph, Chandra Shah, Devin M. Swanson, Victoria D. Wong, Frank U. Axe, Timothy W. Lovenberg, Nicholas I. Carruthers
Discovery and optimization of imidazoline derivatives, a potent, orally active neuropeptide Y Y5 receptor antagonist
Makoto Ando, Nagaaki Sato, Shiho Ishikawa, Makoto Jitsuoka, Keita Nagai, Tsuyoshi Nagase, Hirobumi Takahashi, Aya Sakuraba, Hiroyasu Tsuge, Mioko Hirayama, Junko Ito, Hisashi Iwaasa, Hiroko Matsushita, Akira Gomori, Satoshi Mashiko, Akane Ishihara, Naoko Fujino, Sachiko Tanaka, Tomoyuki Ohe, Kiyoshi Tadano, Takahiro Fukuroda, Yasuyuki Ishii, Akio Kanatani, Takehiro Fukami
Synthesis and SAR of thiophene acid-mimetics as PTP1B inhibitors
Eva Binnun, Zhao-Kui Wan, Bruce Follows, Steven J. Kirincich, Douglas Wilson, Wei-Xin Xu, Diane Joseph-McCarthy, Junjun Wu, Michael J. Smith, Yanling Zhang, May Tam, Dave Erbe, Steve Tam, Eddine Saiah, Jinbo Lee
Discovery and synthesis of nipecotic amide as novel, potent and selective 11ß-HSD-1 inhibitors
Jincong Zhuo, Meizhong Xu, Colin Zhang, Dingquan Qian, Yanlong Li, Reid Huber, Maryanne Covington, Cindy Marando, Brian Metcalf, Wenqing Yao
Novel analogs as 11β-HSD1 inhibitors
Unmesh Shah, Craig D. Boyle, Samuel Chackalamannil, Hana Baker, Timothy Kowalski, Lili Zhang, Giuseppe Terracina
B-keto sulfonamides as selective inhibitors of the 11b-HSD1
Manus Ipek, Jason Xiang, Lihren Chen, Nelson Huang, Jim Li, Wei Li, Tarek Mansour, John C McKew, Jill Nunez, Vipin Suri, Tam May, Steve Tam, James F Tobin, Charlie Wu, Yuzhe Xing, Xin Xu, Yanling Zhang
Discovery and biological evaluation of novel benzamide derivatives as potent 11b-HSD1 inhibitors for the treatment of type II diabetes
Lisa D. Julian, Tracy Bostick, Sebastien Caille, Hon Chan, Michael Degraffenreid, Xiao He, Randall W. Hungate, Juan Jaen, Ben Jiang, Jacob Kaizerman, Jinsong Liu, Dustin McMinn, Jay P. Powers, Yosup Rew, Athena Sudom, Daqing Sun, Hua Tu, Stefania Ursu, Zhulun Wang, Xuelei Yan, Qiuping Ye
Discovery and SAR of novel derivatives as 11β-hydroxysteroid dehydrogenase type 1 inhibitors
Claire M. Lankin, Craig D. Boyle, Samuel Chackalamannil, Unmesh Shah, Hana Baker, Timothy Kowalski, Lili Zhang, Giuseppe Terracina
Synthesis and biologic evaluation of selective inhibitors of 11β-HSD1 as a potential treatment for metabolic disorders
Santhosh F. Neelamkavil, Craig D. Boyle, Samuel Chackalamannil, Hana Baker, Timothy Kowalski, Lili Zhang, Giuseppe Terracina
Syntheses and SAR of piperidin-3-yl ureas as potent and selective 11β-HSD-1 inhibitors
Yun-Long Li, Lori Bostrom, Jincong Zhuo, Yanlong Li, Maryanne Covington, Reid Huber, Brian Metcalf, Wenqing Yao
Discovery and optimization of arysulfonamide as a novel class of 11beta-HSD1 inhibitors
Daqing Sun, Michael DeGraffenreid, Xiao He, Juan Jaen, Jay P. Powers, Xuelei Yan, Yongmei Di, Hua Tu, Stefania Ursu, Ji Ma, Shichang Miao, Liang Tang, Qiuping Ye, Athena Sudom, Zhulun Wang
Azapaullones: GSK-3 inhibitors activating beta cell protection and proliferation
Hendrik Stukenbrock, Rainer Mussmann, Matthias Austen, Marcus Geese, Simone Kegel, Olivier Lozach, Laurent Meijer, Conrad Kunick
Synthesis, SAR and evaluation of C-aryl glucosides as sodium-glucose cotransporter inhibitors for the treatment of type 2 diabetes
Wei Meng, William N. Washburn, Bruce A. Ellsworth, Ravindar N. Girotra, Peggy J. McCann, Prashant P. Deshpande, Annie J. Pullockaran, Manorama Patel, Philip M. Sher, Gang Wu, Scott A. Biller, Deborah L. Hagan, Songping Han, Ashish Khanna, Joseph R. Taylor, Li Xin, John R. Wetterau, Jean M. Whaley
Influence of selective fluorination on the biological activity and proteolytic stability of glucagon-like peptide 1
He Meng, Krishna Kumar
Synthesis and biological evaluation of 3-aryl-3-(4-phenoxy)-propionic acid as a novel series of G protein-coupled receptor 40 (GPR40) agonists
Fengbin Song, Songfeng Lu, Joe Gunnet, Jun Z. Xu, Pam Wines, Yin Liang, Chris Baumann, Jim Lenhard, William V. Murray, Keith T. Demarest, Gee-Hong Kuo
Dipeptidyl peptidase IV inhibitors incorporating fused azoles as effective amide isosteres
Hong Dong, Wallace T. Ashton, Rosemary M. Sisco, Kathryn A. Lyons, Huaibing He, Barbara Leiting, Reshma A. Patel, Joseph K. Wu, Xiaoping Zhang, Nancy A. Thornberry, Ann E. Weber
Paper Withdrawn
Synthesis, SAR, and in vivo efficacy of novel GPR119 agonists with a 4-[3-(4-methanesulfinylphenoxy)propyl]-1-Boc-piperidine core
Matthew C. T. Fyfe, Adam J. Babbs, Lisa S. Bertram, Stuart E. Bradley, Sheila M. Doel, Smita Gadher, William T. Gattrell, Revathy P. Jeevaratnam, John F. Keily, James G. McCormack, Hilary A. Overton, Chrystelle M. Rasamison, Christine Reynet, Philip J. Rushworth, Colin P. Sambrook Smith, Vilas K. Shah, David F. Stonehouse, Simon A. Swain, Jonathan R. White, Peter S. Widdowson, Geoffrey M. Williams, Martin J. Procter
Nε-methanesulfonyl-lysine as a nonhydrolyzable functional surrogate for Nε-acetyl-lysine
Nuttara Jamonnak, David G. Fatkins, Lanlan Wei, Weiping Zheng
Design, synthesis and bioactivity of novel inhibitors of E. coli Aspartate Transcarbamoylase
Joby Eldo, Sabrina Heng, Evan R. Kantrowitz
Thermal stability and activity of fluorinated single-isoleucine mutants of chloramphenicol acetyltransferase
Natalya Voloshchuk, Man Xia Lee, Wan Wen Zhu, Ismet Caglar Tanrikulu, Jin K. Montclare
Analogs of orotidine monophosphate (OMP): Their effect on the activity of OMP decarboxylase
Srinath Thirumalairajan, Stephen L. Bearne
Assessing the role of tyrosine 190 in the catalytic mechanism of hamster N-acetyltransferase 2 by site-directed mutagenesis, pre-steady state and steady state kinetic studies
Xin Zhou, Li Liu, Patrick E. Hanna, Carston R. Wagner
Development of C2-symmetric, active site-directed inhibitors for Cystathionine beta-Synthase
Christopher D. McCune, Weijun Shen, Woo Jin Chung, David B. Berkowitz
Discrimination of carbonic anhydrase isozymes by the excited-state lifetimes of polymerized liposome incorporated lanthanide ions
Adekunle Elegbede, Manas Haldar, Sumathra Manokaran, Sanku Mallik, D. K. Srivastava
Design, synthesis and chemical reactivity of 1,4-naphtoquinone derivatives as cysteine protease irreversible inhibitors
Claudia Valente, Rui Moreira, Rita C. Guedes, Jim Iley, Mohammed Jaffar, Kenneth T. Douglas
Synthetic approaches to amino acid cyclobutanone derivatives
Preeti Kataria, Nick Armoush, Daniel P. Becker
Phosphonosulfonates are potent inhibitors of dehydrosqualene synthase and staphyloxanthin biosynthesis in Staphylococcus aureus
Yongcheng Song, George Liu, Fenglin Yin, Victor Nizet, Eric Oldfield
Modeling, synthetic, crystallographic, and activity studies of novel bisphosphonates as inhibitors of farnesyl pyrophosphate synthase
James M. Hogan, Sylvine Deprele, Boris A. Kashemirov, BL Barnett, Artem Evdokimov, Jim Dunford, R. Graham G. Russell, Frank H. Ebetino, Charles E. McKenna
Structure-based design of reversible peptides inhibitors of Factor VII-a
Cristina C. Clement, Lisa Gingold, Manfred Philipp
7-Fluoroindazoles as potent and selective factor Xa inhibitors
Yu-Kai Lee, Tianbao Lu, Daniel J. Parks, Tho V. Thieu, Thomas Markotan, Wenxi Pan, David F. McComsey, Karen L. Milkiewicz, Carl Crysler, Nisha Ninan, Marta C. Abad, Edward C. Giardino, Bruce E. Maryanoff, Bruce P. Damiano, Mark R. Player
Discovery of N-{(1R,2S,5S)-2-{[(5-chloroindol-2-yl)carbonyl]amino}-5-[(dimethylamino)carbonyl]cyclohexyl}-5-methyl-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridine-2-carboxamide hydrochloride (DT-831j): A novel, potent and orally active direct inhibitor of factor Xa
Tsutomu Nagata, Toshiharu Yoshino, Noriyasu Haginoya, Kenji Yoshikawa, Masatoshi Nagamochi, Shozo Kobayashi, Satoshi Komoriya, Aki Yokomizo, Ryo Muto, Mitsuhiro Yamaguchi, Ken Osanai, Makoto Suzuki, Hideyuki Kanno
Induced polarization in drug-receptor binding: Contribution to the binding affinity of a meta-chlorobenzyl side chain in the S1 pocket of thrombin
Menshawy Mohamed, Bernhard Baum, Marek Freindorf, Gerhard Klebe, David G. Hangauer
Drug target validation using transcription profiling and reverse-engineered gene networks
Melissa M. Dominguez, Elissa Cosgrove, Yingchun Zhou, Eric D. Kolaczyk, Scott E. Schaus, Timothy S. Gardner
Imidazole-acetamide substituted piperazinylbenzimidazole antagonists of the Gonadotropin Releasing Hormone receptor
Joseph T. Lundquist IV, John F. Mehlmann, Lloyd Garrick, Jeffrey C. Pelletier, Jay Wrobel, Joshua E. Cottom, Linda Shanno, Murty V. Chengalvala, Christine Huselton, Irene B. Feingold
Simultaneous biological optimization and structural simplification of a pendant heterocyclic thiobenzimidazolone on a series of 2-phenyl-4-(piperazin-1-yl)benzimidazole antagonists of the Gonadotropin Releasing Hormone Receptor
Jeffrey C. Pelletier, Murty V. Chengalvala, Joshua E. Cottom, Lloyd Garrick, James Jetter, Wenling Kao, Linda Shanno, Jay Wrobel
Design, synthesis and SAR of uracil diamines as potent GnRH receptor antagonists
Charles Huang, Warren Wade, Yun-Fei Zhu, Chen Chen, Zack Guo, Yongsheng Chen, Scott Struthers, Martin W. Rowbottom, Jamie Rueter, Duncan Wu, Joann Xie, John Saunders
Parallel synthesis of substituted pyridones for use as Gonadotropin Releasing Hormone (GnRH) antagonists
Daniel Green, Jeffrey C. Pelletier, Murty V. Chengalvala, Joshua E. Cottom, Linda Shanno
Substituted 5-oxopyrazoles as HCV polymerase inhibitors
Tong Wang, Dansu Li, Gerald W. Shipps Jr., Kristin E. Rosner, Patrick Curran, Yongqi Deng, Janeta Popovici-Muller, Alan B Cooper, Viyyoor Girijavallabhan
HCV NS3 serine protease inhibitors: Discovery of carbamate derived new P4 capping moieties with improved profile
A. Arasappan, A. I. Padilla, F. Bennett, S. L. Bogen, Kevin X Chen, S. Hendrata, Y. Huang, Edwin Jao, W. Pan, R. E. Pike, S. Ruan, M. Sannigrahi, S. Venkatraman, B. Vibulbhan, Wanli Wu, W. Yang, A. K. Saksena, V. Girijavallabhan, Xiao Tong, K-C. Cheng, N-Y. Shih, F. G. Njoroge
Molecular docking and 3-D-QSAR studies on benzimidazole series of Hepatitis C virus NS5B polymerase inhibitors
Pallav D Patel, Tanaji T Talele
Discovery of new P4 (esters, acids, ketones) extended ketoamide inhibitors of the HCV NS3 serine protease with improved potency and PK profile
Stephane L Bogen, Weidong Pan, S. Ruan, Ashok Arasappan, Frank Bennett, Kevin Chen, S. Hendrata, Y. Huang, Edwin Jao, Y-T. Liu, R. Lovey, Latha Nair, A. I. Padilla, R. Pike, Patrick Pinto, M. Sannigrahi, Francisco Velazquez, S. Venkatraman, B. Vibulbhan, Wanli Wu, W. Yang, A. K. Saksena, Viyyoor Girijavallabhan, Xiao Tong, K-C. Cheng, N-Y. Shih, F. George Njoroge
Novel HCV protease inhibitors: Using acyl-sulfamides to form P1-P1′ macrocycles
Jason P Shanley, Hui-Ju Chen, Charles W Hutchins, Dale J. Kempf, Larry L. Klein, Kevin Kurtz, Alex Konstantinidis, Keith F. McDaniel
Discovery of Novel P4 capped sulfonamide derived inhibitors of HCV NS3 protease
Srikanth Venkatraman, Wanli Wu, Melissa Blackman, Ashok Arasappan, Frank Bennett, Stephane L Bogen, Kevin X Chen, Siska Hendrata, Yuhua Huang, Edwin Jao, Latha Nair, A. I. Padilla, Weidong Pan, R. Pike, Patrick Pinto, S. Ruan, Mousumi Sannigrahi, Francisco Velazquez, Bancha Vibulbhan, Weiying Yang, Anil Saksena, Viyyoor Girijvallabhan, Xiao Tong, K-C. Cheng, Neng-Yang Shih, F. George Njoroge
Synthesis and anti-HIV-RT activity of a series of indole alkyl sulfones
Xufang Zhang, Vandna Munshi, Dan diStefano, Linda Ecto, Peter J. Felock, Meizhen Feng, Jessica A. Flynn, MingTain Lai, Yuexia Liang, Meiquing Lu, Mike Miller, Greg Moyer, Rebecca A. Poehnelt, Sridhar Prasad, Rosa I. Sanchez, William Schleif, Maricel Torrent, Sinoeun Touch, BangLin Wan, Theresa M. Williams
Design and synthesis of HIV-1 protease inhibitors incorporating oxazolidinones as P2/P2' ligands in pseudosymmetric dipeptide isosteres
G. S. Kiran Kumar Reddy, Akbar Ali, Madhavi N. L. Nalam, Saima Ghafoor Anjum, Hong Cao, Robin S. Nathan, Celia A. Schiffer, Tariq M. Rana
Potent HIV integrase inhibitor with excellent pharmacokinetics
Melissa Egbertson, Michelle Kuo, Debra Perlow, Marie Langford, Jeffrey Melamed, John Wai, Joseph Vacca, Audrey Wallace, Yvonne Leonard, Daria J. Hazuda, Peter J. Felock, Kara Stillmock, William Schleif, Lori J. Gabryelski, Gregory Moyer, Joan Ellis, Lixia Jin, Steven D. Young
Molecular modeling, synthesis, and in vitro/in vivo evaluation of 1,4-dihydropyridine, pyrrole, and benzopyran analogs as HIV-1 RT inhibitors
Tanaji T Talele, Dinesh Manvar, Kena Raval, Virendra N Pandey, Anamik Shah
Phthalimide-containing hydrazides and amides as diketo acid-class HIV-1 integrase inhibitors
Xue Zhi Zhao, Elena A. Semenova, B. Christie Vu, Chenzhong Liao, Marc C Nicklaus, Stephen H. Hughes, Yves Pommier, Terrence R. Burke Jr.
Design, synthesis, and biological evaluation of HIV-1 protease inhibitors incorporating phenyloxazolidines as novel P2 ligands
Akbar Ali, G. S. Kiran Kumar Reddy, Hong Cao, Saima Ghafoor Anjum, Madhavi N. L. Nalam, Celia A. Schiffer, Tariq M. Rana
Discovery of novel HIV-1 integrase inhibitors by pharmacophore search
Chenzhong Liao, Christophe Marchand, Yves Pommier, Marc C. Nicklaus
Synthesis and anti-HIV activities of fatty acyl derivatives of 2',3'-dideoxy-3'-thiacytidine
Hitesh Kumar Agarwal, Michael Hanley, Gustavo F. Doncel, Keykavous Parang
Synthesis and evaluation of bis(fatty acyl-glycol)phosphate triester derivatives of 3'-fluoro-2',3'-dideoxythymidine
Hitesh Kumar Agarwal, Gustavo F. Doncel, Keykavous Parang
Water-soluble prodrugs of lopinavir, ritonavir and new investigational HIV PIs
David A. DeGoey, William J. Flosi, David J. Grampovnik, Kennan C. Marsh, Larry L. Klein, Michelle A. Long, Dale J. Kempf
Non-hydrolysable glycosylated porphyrins and chlorins: Potential new photodynamic therapy agents and applications in vivo imaging
Sebastian A. Thompson, Diana Samaroo, Mikki Vinodu, Charles Michael Drain
Gd(III)-based bile acid conjugates for dual magnetic resonance and fluorescence imaging
Sooyoun Lim, Xiang Ma, Hyun-Soon Chong
pH-Sensitive cyanine dyes for optical imaging of acidic environments
Scott A. Hilderbrand, Ralph Weissleder
The preparation of the stable substrate for imaging HSV1-TK expression and its biological study
gwangil An, kyochul Lee, Taehyun Choi, Hakjune Rhee, Hyunseok Ahn, Kwonsoo Chun, gijeong Cheon, sangmoo Lim, Byungseok Moon
Synthesis of novel technetium-99m-PIB complex as SPECT imaging agent for CNS disease
Kuanqiang Gao, Chunying Wu, Yanming Wang
Peptide nucleic acid (PNA) FRET agents for imaging gene expression
Bereket Y. Oquare, Huafeng Fang, John-Stephen Taylor
Decaprenyl diphosphate synthase inhibitors activate gamma delta T cells
Fenglin Yin, Yonghui Zhang, Rong Cao, Craig T Morita, Eric Oldfield
Impact of secondary structure of agonists of Toll-like receptor 9 on immune stimulatory activity
Dong Yu, Mallikarjuna R Putta, Lakshmi Bhagat, Daqing Wang, Meiru Dai, Jimmy X. Tang, Ekambar R. Kandimalla, Sudhir Agrawal
Synthetic agonists of Toll-like receptor 9: Impact of linkers
Mallikarjuna R. Putta, Dong Yu, Daqing Wang, Lakshmi Bhagat, Meiru Dai, Jimmy X. Tang, Ekambar R. Kandimalla, Sudhir Agrawal
Synthetic oligoribonucleotides containing secondary structures activate Toll-like receptor 8 and induce immune responses
Tao Lan, Lakshmi Bhagat, Meiru Dai, Jimmy X. Tang, Ekambar R. Kandimalla, Sudhir Agrawal
Synthesis and biological evaluation of NETA and NETA analogs as iron depletion agents
Xiang Ma, Hyun-Soon Chong
Synthesis of a reactive linker for the construction of antibody-drug hybrid molecules
Joshua D. Thomas, Thomas Hofer, Christoph Rader, Terrence R. Burke Jr.
Synthesis and use of cocaine-based MRI contrasting agents to detect the concentration of DAT
Gregory R Naumiec, Brenton DeBoef
Noncovalent cellular delivery of phosphopeptides by amphipathic peptides
Guofeng Ye, Nguyen H. Nam, Anil Kumar, Keykavous Parang
Bisphosphonates targeting geranylgeranyl diphosphate synthase: A QSAR investigation
Rong Cao, Yonghui Zhang, Fenglin Yin, Michael P. Hudock, Eric Oldfield
Study of solvent interactions in solvolytic reactions of several common pharmaceutical intermediates
Malcolm J. D'Souza, Zoon H. Ryu, Dennis N. Kevill, Byoung-Chun Park
Drug-receptor binding affinity: The strength of hydrophobic binding can be increased by adding hydrogen bonds
Laveena Muley, Michael Smolinski, Bernhard Baum, Christof Gerlach, Marek Freindorf, Gerhard Klebe, David G. Hangauer
Hemostatic effects of liposomes carrying fibrinogen gamma-chain dodecapeptide and encapsulating adenosine 5'-diphosphate as a platelet substitute
Yosuke Okamura, Ippei Maekawa, Makoto Handa, Yasuo Ikeda, Shinji Takeoka
From SAMs to drugs: Application of the Pharmacomer Technology Platform to small molecule drug discovery
Bridget M Cole, Paul Sweetnam, Enoch Kim, David Duffy, James Ellis, Dominick Casalena, Alessandra Bartolozzi, Yingfei Yang, Hope Foudoulakis, Brian Kirk, Elsa Mak, Eric Wong, Sharon McGonigle, Stewart Campbell, Olivier Schueller, John Ferkany, William Prince
Conjugated porphyrin dimers with large two-photon absorption cross section for photodynamic therapy
Milan Balaz, Hazel A. Collins, Marina K. Kuimova, Emma Dahlstedt, Klaus Suhling, David Phillips, Harry L. Anderson
Review of various classes of organic compounds for optimal purification on RediSep Rf Diol media
Veronica D. Thomason
Examination of secondary conformational constraint in the design of macrocyclic Grb2-SH2 domain-binding ligands
Fa Liu, Karen M. Worthy, Lakshman Bindu, Robert J Fisher, Terrence R. Burke Jr.
Synthetic efforts toward the development of Shc SH2 domain-binding peptides
Won Jun Choi, Andrew G. Stephen, Robert J Fisher, Terrence R. Burke Jr.
Multimodal nanoagent for the diagnosis and treatment of atherosclerosis
Jason R. McCarthy, Ethan Korngold, Farouc Jaffer, Ralph Weissleder
Paper Withdrawn
Anodized nanotubular titanium as novel drug eluting orthopedic implants
Chang Yao, Thomas J. Webster
A structure- and NMR-based approach for the discovery of novel agents against Influenza A virus
William H. Bisson, Maurizio Pellecchia
Inhibition of inducible nitric oxide synthase expression by structural analogs of pterostilbene
Cassia S Mizuno, Shiby Paul, Nanjoo Suh, Agnes M. Rimando
Design and synthesis of novel cyclic oxyguanidines as potential iNOS inhibitors
Guo-Hua Chu, Minghua Gu, Bertrand Le Bourdonnec, Christopher W. Ajello, Lara K. Leister, Joel A. Cassel, Robert N. DeHaven, Roland E. Dolle
Design and synthesis of novel imidazolepyrimidines as potent iNOS dimerization inhibitors - Part I
Guo-Hua Chu, Bertrand Le Bourdonnec, Minghua Gu, Christopher W. Ajello, Lara K. Leister, Paul A. Tuthill, Ian Sellitto, Heather O'Hare, Joel A. Cassel, Robert N. DeHaven, Roland E. Dolle
Releasing of nitric oxide from elastic electrospun nanofibers
Piyaporn Kampeerapappun, Marcos Lopez, Patricio Lopez-Jaramillo, Daniel J. Smith
Design and synthesis of novel imidazolepyrimidines as potent iNOS dimerization inhibitors
Ian F Sellitto, Betrand LeBourdennec, Guo-Hua Chu, Minghua Gu, Christopher W. Ajello, Lara K. Leister, Paul A. Tuthill, Heather O'Hare, Joel A. Cassel, Robert N. DeHaven, Ronald E. Dolle
Potential applications of fendiline NONa in coronary health
Melinda K. Carnahan, Wilmarie Flores, Daniel J. Smith
Synthesis, pharmacological and toxicological studies of nitric oxide releasing analog of acetaminophen
Tilak Raj Bhardwaj, Manoj Kumar, Neeraj Mehta, Neelima Dhingra
Preclinical pharmacokinetic study of Zaltoprofen in rats
Nageswararao Muddana, Gopinadh Bhyrapuneni, Koteshwara Mudigonda, Vishwottam N. Kandikere, Ramakrishna V. S. Nirogi
Discovery of orally active mGluR1 receptor antagonists for the treatment of chronic pain
Stephanie Cooke, Peter Korakas, Lisa S. Silverman, Julius Matasi, Deen Tulshian, Duane Burnett, William J Greenlee, A. Reggiani, A. Veltri, R. Bertorelli, P Downey, S. Fredduzzi, M. Grilli, E. Nicolussi, G. Lozza, G Forlani, R Petrò, V Liporati, G. Tarozzo, S Contib, C. Foglia
The SAR and discovery of tricyclic mGluR1 antagonists for the treatment of chronic pain
Julius Matasi, Stephanie Cooke, Peter Korakas, Lisa S. Silverman, Deen Tulshian, Duane A. Burnett, William J Greenlee, A. Reggiani, A. Veltri, R. Bertorelli, P Downey, S. Fredduzzi, M. Grilli, E. Nicolussi, G. Lozza, A Forlani, R Petrò, V Liporati, G. Tarozzo, S. Conti, C. Foglia
Discovery of piperidine carboxamide TRPV1 antagonists
Raul R. Calvo, Wing S Cheung, Sui Po Zhang, Tasha Hutchinson, Mark R. Player
Pyrazolo-pyrimidines as selective and potent p38 inhibitors
Robert V. Moquin, Jagabandhu Das, Gary Schieven, Sidney Pitt, Rosemary Zhang, Ding Ren Shen, Kim W McIntyre, Kathleen M Gillooly, Jack Sack, Arthur Doweyko, Hongjian Zhang, Susan E. Kiefer, Kevin Kish, Joel Barrish, John H. Dodd, Katerina Leftheris
Calcitonin gene-related peptide (CGRP) receptor antagonists: Development of the pyridinone series
Diem N. Nguyen, Anthony W. Shaw, Daniel V. Paone, Christopher S. Burgey, Samuel L. Graham, Scott D. Mosser, Christopher A Salvatore, Yvonne M Leonard, Cynthia Miller-Stein, Stefanie A. Kane, Kenneth S. Koblan, Theresa M. Williams, Joseph P Vacca
Synthesis and biological evaluation of novel 5-(3-indolyl)-1-(4-sulfamylphenyl)-3-trifluoromethyl pyrazolines as dual inhibitors of COX/LOXs
Vinaykumar Billa, Venkat R Pallela, Rengasamy Boominathan, Muralidhar R Mallireddigari, Balaiah Akula, Revathi Patti, Stanley C Bell, E. Premkumar Reddy, MV. Ramana Reddy
Syntheses and opioid receptor binding affinities of conformationally restricted analogs of Cyclazocine
Rakesh R Ganorkar, Qun Lu, Mark P. Wentland, Jean M. Bidlack
Design, synthesis of a new chiral sigma-1 receptor ligand and validation as a potential anticocaine agent
Marion Toussaint, Brice Delair, Catherine Foulon, Alexandre Lebeau, Nadège Lempereur, Claude Vaccher, Tangui Maurice, Patricia Melnyk
Tricyclic mluR1 antagonists for the treatment of chronic pain
Chad Knutson, Chad Bennett, Peter Korakas, Duane A. Burnett, Deen Tulshian, William J Greenlee, A. Reggiani, Rosalia Bertorreli, M. Grilli, C. Foglia, S. Fredduzzi, G. Lozza, G. Tarozzo
Novel biaryl pyrazinone amides as hNav1.7 blockers for the treatment of neuropathic pain
Feng Ye, Pengcheng Shao
Synthesis and structure-activity relationships of 3-substituted 8-benzhydryl-nortropane analogs as nociceptin receptor ligands
Shu-Wei Yang, Deen Tulshian, Ginny D Ho, William J Greenlee, Stephen Eckel, John Anthes
Design of trisubstituted pyrimidines as vanilloid receptor 1 (TRPV1) antagonists with improved solubility
Xianghong Wang, Partha Chakrabarti, Narender Gavva, Vassil I. Ognyanov, Liping H. Pettus, Rami Tamir, Helming Tan, Phi Tang, James JS. Treanor, Mark H. Norman
Synthesis of carbon-11 labeled benzoxazole derivatives as new potential PET radioligands for imaging of 5-HT3 receptor
Mingzhang Gao, Min Wang, Qi-Huang Zheng
Synthesis of (S)-[18F]-fluoro-Exaprolol, via [18F]-1-fluoro-2-propanamine, for imaging cerebral beta-adrenergic receptors with PET
Karin A. Stephenson, Erik M. van Oosten, Alan A. Wilson, Andrei K. Yudin, Jeffrey H. Meyer, Sylvain Houle, Neil Vasdev
Synthesis of carbon-11 labeled 7-aroyl-aminoindoline-1-sulfonamides as new potential PET agents for imaging cancer tubulin polymerization
Min Wang, Mingzhang Gao, Qi-Huang Zheng
Synthesis of radiolabeled 2-oxoquinoline derivatives as new potential PET agents for imaging of CB2 receptor
Mingzhang Gao, Min Wang, Qi-Huang Zheng
Discovery and biological evaluation of novel 2-acetamido-indoles as potent and selective openers of Kv7/KCNQ potassium channels
Thomas E Christos, Grant McNaughton-Smith, Robert N. Atkinson, Matthew E. Secrest, Aaron C. Gerlach, Scott D. Conary, Brett M. Antonio, Sally J. Stoehr, Rosemarie Roeloffs
Classifcation QSAR modeling of the imbalanced dataset of hERG K+ channel blockers and openers
Kun Wang, Alexander Golbraikh, Bryan R. Roth, Alexander Tropsha
Synthesis and SAR of thiadiazolone dioxides as selective androgen receptor modulators
Mark Manfredi, Yingzhi Bi, Alexandra Nirschl, James Sutton, Ramakrishna Seethala, Rajasree Golla, Blake Beehler, Paul Sleph, Gary Grover, Jacek Ostrowski, Lawrence Hamann
Design of potent and selective LXR agonists from a series of indazole aniline core compounds
Stephen Marc Bowen, Robert J. Steffan, Edward Matelan, Raymond Unwalla, Ponnal Nambi, Elaine Quinet, Anita Halpern, Dawn Savio, Anna Wilhelmsson, Annika Goos Nilsson, Crina Ursu, Erik Arnelof, Johnny Sandberg, Christopher Enroth, Tomas Bonn, Mathias Farnegardh, Jay Wrobel
Quinoline biarylethers as high affinity, potent LXR agonists
Ronald C. Bernotas, Robert R. Singhaus Jr., David Kaufman, John W. Ullrich, Robert L. Morris, Horace Fletcher III, Li Di, Ray J Unwalla, Ponnal Nambi, Elaine Quinet, Dawn Savio, Anita Halpern, Irene B. Feingold, Anna Wihelmsson, Annika Goos Nilsson, Crina Ursu, Erik Arnelof, Johnny Sandberg, Christopher Enroth, Jay Wrobel
Quinoline biarylether amides as liver X receptor modulators
David Kaufman, Ronald C. Bernotas, Robert R. Singhaus Jr., Michael Collini, John W. Ullrich, Ray J Unwalla, Li Di, Ponnal Nambi, Elaine Quinet, Anita Halpern, Dawn Savio, Irene Feingold, Anna Wihelmsson, Annika Goos Nilsson, Crina Ursu, Erik Arnelof, Johnny Sandberg, Christopher Enroth, Jay Wrobel
Discovery and structure-activity relationship studies of indole derivatives as Liver X receptor (LXR) agonists
Madhavi Pannala, Farid Bakir, Sunil Kher, Norma Wilson, Trang Nguyen, Ila Sircar, Kei Takedomi, Chiaki Fukushima, James Zapf, Kui Xu, Shao-Hui Zhang, Juping Liu, Morera Lisa, Lisa Schneider, Naoki Sakurai, Rick Jack, Jie-Fei Cheng
Synthesis, hypolipidemic activity and computational studies of phenoxyacetic acid derivatives related to α-asarone and clofibrate
Nancy Argüelles, José Luis Medina-Franco, Aaron Mendieta, Fabiola Jiménez, Leticia Garduño, Maria del Carmen Cruz, Germán Chamorro, Joaquín Tamariz
Identification of highly potent and subtype-selective PPARalpha agonists: Synthesis, SAR and in vivo efficacy
Yukiyoshi Yamazaki, Kazutoyo Abe, Tsutomu Tohma, Masahiro Nishikawa, Hidefumi Ozawa, Ayumu Okuda, Takaaki Araki, Soichi Oda, Keisuke Inoue, Kimiyuki Shibuya, Bart Staels, Jean-Charles Fruchart
Design, synthesis and structure-activity relationships of piperidine and dehydropiperidine carboxylic acids as novel, potent PPARalpha/gamma dual activators
Xiang-Yang Ye, Yi-Xin Li, Shung Wu, Arthur Doweyko, Dennis Farrelly, Neil Flynn, Liqun Gu, Kenneth T. Locke, Jonathan Lippy, Kevin O'Malley, Celeste Twamley, Litao Zhang, Denis E. Ryono, Narayanan Hariharan, Robert Zahler, Peter T. W. Cheng
Discovery and structure-activity relationships of BMS-711939, a potent and highly selective PPARalpha activator
Yan Shi, Jun Li, Lawrence J. Kennedy, Hiwei Tao, Xiang-Yang Ye, Stephanine Chen, Hao Zhang, Andres Hernandez, Sean Chen, Zhi Lai, Wei Wang, Pratik Devasthale, Rebecca Smirk, Shung Wu, Scott A. Bolton, Denis Ryono, Ying Wang, Kenneth T Locke, Kevin M. O'Malley, Litao Zhang, Raiajit Srivastava, Bowman Miao, Daniel Meyers, Hossain Monshizadegan, Debra Search, Denise Grimm, Rongan Zhang, Thomas Harrity, Lori Kunselman, Henry Wong, Juliang Zhu, Ashok Trehan, Ngiap-Kie Lim, Huiping Zhang, Bang-Chi Chen, Michael Cap, Jodi Muckelbauer, Chiehying Chang, Stanley Krystek, Yi-Xin Li, Vinayak Hosagrahara, Lisa Zhang, Pathanjali Kadiyala, Carrie Xu, Michael Blanar, Robert Zahler, Ranjan Mukherjee, Peter T. Cheng, Joseph A. Tino
Novel zwitterionic phenoxyacetic acid derivatives as potent PPAR agonist
Mitsuhiro Yamaguchi, Yoshihiro Shibata, Masahiro Ohta, Katsuji Kagechika, Hiroyuki Usui, Toshiharu Ohta
Structure activity relationship studies of phenethylglycine PPARa/g dual activators for the treatment of metabolic diseases
Shung Wu, Rebecca Smirk, Hao Zhang, Sean Chen, Dennis Farrelly, Liqun Gu, Andrew Peters, Thomas Harrity, Michael Cap, C Chu, Lori Kunselman, Nathan Morgan, Randolph Ponticiello, Rachel Zebo, Litao Zhang, Kenneth T Locke, Jonathan Lippy, Kevin M. O'Malley, Vinayak Hosagrahara, Lisa Zhang, Pathanjali Kadiyala, Carrie Xu, Arthur Doweyko, Jodi Muckelbauer, Robert Zahler, Narayanan Hariharan, Peter T. Cheng
Discovery of para-alkylthiophenoxyacetic acids as a novel series of potent and selective PPAR delta agonists
Rui Zhang, Aihua Wang, Alan DeAngelis, Patricia Pelton, Jun Xu, Peifang Zhu, Lubing Zhou, Keith Demarest, William V Murray, Gee-Hong Kuo
Novel bisphosphonates targeting prenyltransferases
Yonghui Zhang, Fenglin Yin, Rong Cao, Michael P Hudock, Kilannin Krysiak, Annette Leon, Craig T Morita, Eric Oldfield
Design, synthesis, and biological evaluation of 17-thiazole-4-azasteroids as tissue-selective androgen receptor modulators
Mildred L. Kaufman, Helen J. Mitchell, George D. Hartman, Thomayant Prueksaritanont, Azriel Schmidt, Chang Bai, Fang Chen, Donald B. Kimmel, Mark E. Duggan, Robert S. Meissner
Synthesis, structure-activity relationship, in vitro/in vivo profiles and molecular modeling of novel oxa-steroids as potent and selective progesterone receptor antagonists
Fu-An Kang, Jihua Guan, Nareshkumar Jain, George Allan, Olivia Linton, Pamela Tannenbaum, Jun Xu, Peifang Zhu, Joseph W Gunnet, Xin Chen, Keith Demarest, Scott Lundeen, Zhihua Sui
Preparation of diverse array of imidazoles for general screening
David J. Malwitz, Pawel Nowak
Rapid SAR against functional Cardiac Ion Channels using an automated patch clamp system
Nathan J Lautermilch, Adam Bishop, Teddy Lin, Shimin Wang, James Baumgartner
Selection of compounds in discovery stage based on the novel HTS solubility measurement and parallel artificial membrane permeability assay
Katsuya Akimoto, Kyosuke Suzuki, Shinsaku Tsukamoto, Kenichi Sudo, Osamu Okazaki
Design and synthesis of site-selective fluorescent naphthalimide probes for microscopy
Leah L. Groess, Ashley M. Dreis, Kyle M. Kopidlansky, David E. Lewis
Microarray screening of antithrombin interactions on the high affinity heparin glycan chips
Tae-Joon Park, Moo-Yeal Lee, Moon Il Kim, Jeffrey G. Martin, Jonathan S. Dordick, Robert J. Linhardt
Studies on the ligand selectivity and economics of metal scavenging polymers
Paul A Boguszewski, Andrew F Coffey, Aubrey J Mendonca, John W Davies, Frank P Warner
New techniques for salt and polymorph screening of new drug candidates
Carl H Behrens, Hui-Yin Harry Li
Open access mass-directed purification: Adaptation to diverse loading scales and compound polarities
Leonard O Hargiss, Weiqun Wang
NCI60 screening data: A versatile tool for in silico models predicting substrate properties for ABC-transporter
Gerhard F Ecker, Barbara Zdrazil, Chakguy Prakasvudhisarn
Virtual screening of the inhibitors into Tyrosyl-DNA Phoshodiesterase (Tdp1) active sites
Iwona E Weidlich, Thomas Dexheimer, Yves Pommier, Christophe Merchand, Marc C Nicklaus
Molecular docking and 3-D-QSAR studies on a series of 6,7-dimethoxy-4-pyrrolidylquinazoline as PDE10A inhibitors
Shridhar Kulkarni, Tanaji T Talele
Predicting modifications to the inhibitor of InhA, the M.tb enoyl reductase enzyme to stabilize inhibitor-active site loop interactions using computational chemistry tools
Salma Banu Rafi, Peter J. Tonge, Carlos L. Simmerling
Chemical modifications to improve pharmacokinetic properties of siRNA: Probing the tolerance of phosphorothioate modifications on siRNA activity
Thazha P. Prakash, Garth A. Kinberger, Charles R. Allerson, Andrew T. Watt, Andreas Berdeja, Hans J. Gaus, Eric G. Marcusson, Eric E. Swayze, Balkrishen Bhat
Polyconjugates: A new synthetic vehicle for in vivo delivery of siRNA to hepatocytes
Darren H. Wakefield, David Rozema, So C. Wong, Jason J. Klein, Dave L. Lewis, Stepanie Bertin, Tom Reppen, Paula L. Roesch, James E. Hagstrom, Jon A. Wolff
Studies toward the synthesis of fluorescent and isotopically labeled discodermolide analogs
Chao Yang, Abhijit Banerjee, Susan Bane, David G. I. Kingston
Stereoselective total synthesis of soybean flavonoids Glyceollin I, II
Rahul S Khupse, Paul W Erhardt
Stereoselective synthesis of (2S,3S,4S)-3,4-dihydroxy-L-glutamic acid via intramolecular nucleophilic epoxidation
Young Gyu Kim, Hyeonjeong Kim, Dongwon Yoo, Myeong Hak Kim, Suk-Koo Hong
Improved asymmetric synthesis of the alose reductase inhibitor 2-methyl sorbinil
Hongxia Jin, James M. Randazzo, Peter F. Kador
Study for total synthesis of antibiotic pestalone and its analog
Yudao Ma, Yong Dai, Zhijun Sun, Xi Fang, Changqin Ma, Chun Song
An efficient and operationally convenient general synthesis of tertiary amines by direct N-alkylation of secondary amines and heterocycles with alkyl halides in the presence of CsOH
Ralph Nicholas Salvatore, Jason Hovland
Synthesis of fluorine-containing heterocycles for medicinal chemistry
Mark J. Penny, Adrian P Dobbs, Levan Pivnevi, Peter Jones
Synthesis of novel fluorinated carbohydrate and pipecolic acid analogs and C-aryl glycosides via a common methodology
Adrian P Dobbs, Diluar Khan, Robert J Parker
Applications of polymeric reagents and SPE in the synthesis and purification of reductive amination reactions
Paul A Boguszewski, Andrew F Coffey, John W Davies, Aubrey J Mendonca, Frank P Warner
Selective N-alkylation of aromatic amines
Ralph N. Salvatore, Jason Hovland
Synthesis of N-9-substituted 2,8-diaminopurines
Gulzar Ahmed, Andrew G. Cole, Marc-Raleigh Brescia, Ian Henderson, Lan-Ying Qin, Axel Metzger, James Wen, Ray J. Chan, Linda O'Brien
From a polymer crosslinker to soluble epoxide hydrolase (sEH) inhibitors: The quest for lower cost drug intermediates
James R. Sanborn, Christophe Morisseau, Paul D. Jones, Hsing-Ju Tsai, Sung Hee Hwang, Bruce D. Hammock
Production of different structural analogs of sophorolipids through modification of fermentation medium
Vishal Shah, Dan Badia
Versatile photosensitizers based on photon upconverting nanoparticles for photodynamic therapy
Peng Zhang, Wim Steelant, Manoj Kumar, Matthew Scholfield
Allosteric modulation of mGluR1 and mGluR5
Tanja Weil, Gisbert Schneider, Steffen Renner, Swetlana Derksen, Mirko Hechenberger, Christopher G. Parsons
Benzamide inhibitors of soluble epoxide hydrolase
Steven J Taylor, Stéphane DeLombaert, Anne Eldrup, Neil Farrow, Ingo Mugge, Fariba Soleymanzadeh
Paper Withdrawn
In vitro metabolic studies of a bivalent KOR agonist, MOR mixed agonist
Brian S. Fulton, Jennifer L. Mathews, Jean M. Bidlack, John L. Neumeyer
Paper Withdrawn
Paclitaxel (Taxol®) binding to human serum albumin: Insights from computational studies
Krisztina Paal, Aliaksei Shkarupin, Laura Beckford
Paper Withdrawn
Structural dynamics of the cooperative binding of organic molecules in the human Cytochrome P450 3A4 (CYP3A4)
Dan Fishelovitch, Carina Hazan, Sason Shaik, Haim Wolfson, Ruth Nussinov
High affinity InhA inhibitors with activity against drug-resistant strains of Mycobacterium tuberculosis
Todd J. Sullivan, Christopher am Ende, James J. Truglio, Francis Johnson, Ann Lenaerts, Richard A. Slayden, Caroline Kisker, Peter J Tonge
Structure-based design, synthesis, and biological evaluation of novel inhibitors of Mycobacterium tuberculosis malate synthase
Justin P. Roberts, Inna Kriger, Qingan Sun, Eric McKee, Thomas R. Ioerger, Joel S. Freundlich, James C. Sacchettini
Synthesis and optimization of a library of novel benzimidazole leads for antituberculosis drug discovery
Kunal Kumar, Seung-Yub Lee, Ilaria Zanardi, Richard A. Slayden, Iwao Ojima
Synthesis of novel optically active 2-aminobenzothiazole derivatives as antitubercular agents
Bhoomendra A. Bhongade, Malleshappa N. Noolvi, Andanappa K. Gadad, Gurdial Singh

Symposium Grid -- Division of Medicinal Chemistry -- Session Listing

The 234th ACS National Meeting, Boston, MA, August 19-23, 2007