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Technology mapping and retargeting for field-programmable analog arrays

Sree Ganesan, Ranga Vemuri
2000 Proceedings of the conference on Design, automation and test in Europe - DATE '00  
Rapid prototyping followed by technology retargeting provides a fast and cost-effective approach to analog system synthesis.  ...  Field-programmable analog arrays (FPAAs) enable rapid implementation of a function-compliant prototype, while technology retargeting converts the functional FPAA prototype to an ASIC.  ...  Acknowledgments: The authors would like to thank Adrian Nunez, Nagu Dhanwada and Alex Doboli of the VASE team, and special thanks to Satish Ganesan.  ... 
doi:10.1145/343647.343700 fatcat:fxpp23va5vawhpkhwnh3fqsm2m

System-level design automation tools for digital microfluidic biochips

Krishnendu Chakrabarty, Fei Su
2005 Proceedings of the 3rd IEEE/ACM/IFIP international conference on Hardware/software codesign and system synthesis - CODES+ISSS '05  
Analogous to classical VLSI synthesis, a top-down system-level design automation approach can shorten the biochip design cycle and reduce human effort.  ...  Current full-custom design techniques for digital microfluidic biochips do not scale well for increasing levels of system integration.  ...  As in the case of high-level synthesis for integrated circuits, resource binding in the biochip synthesis flow refers to the mapping from bioassay operations to available functional resources.  ... 
doi:10.1145/1084834.1084887 dblp:conf/codes/ChakrabartyS05 fatcat:swxbvv2wsbfejb2yyrpsfyjbsq

High-level Synthesis [article]

Issam Damaj
2019 arXiv   pre-print
The chained synthesis tasks at each level of the design process include system synthesis, register-transfer synthesis, logic synthesis, and circuit synthesis.  ...  High-level synthesis (HLS) could be defined as the translation from a behavioral description of the intended hardware circuit into a structural description similar to the compilation of programming languages  ...  The chained synthesis tasks at each level of the design process include system synthesis, register-transfer synthesis, logic synthesis, and circuit synthesis.  ... 
arXiv:1905.02076v1 fatcat:ffzc23yqevauji7hc42lazlila

Discovery and Development of a Potent and Highly Selective Small Molecule Muscarinic Acetylcholine Receptor Subtype I (mAChR 1 or M1) Antagonist In Vitro and In Vivo Probe

C. Weaver, Douglas Sheffler, L. Lewis, Thomas Bridges, Richard Williams, Natalia Nalywajko, J. Kennedy, Matthew Mulder, Satyawan Jadhav, Leslie Aldrich, Carrie Jones, Joy Marlo (+5 others)
2009 Current Topics in Medicinal Chemistry  
An iterative parallel synthesis approach was employed to optimize all three series in parallel, which led to the development of novel microwave-assisted chemistry and provided important take home lessons  ...  for probe development projects.  ...  Therefore, we quickly explored multiple parameters and developed general, high yielding microwave-assisted protocols to accelerate the synthesis of analogs of HTS lead 6.  ... 
doi:10.2174/156802609789753635 pmid:19807667 pmcid:PMC4765323 fatcat:m3hiuqvcijbp7cchbauu755fji

Synthetic Compound Libraries Displayed on the Surface of Encoded Bacteriophage

Thomas F. Woiwode, Jill E. Haggerty, Rebecca Katz, Mark A. Gallop, Ronald W. Barrett, William J. Dower, Steven E. Cwirla
2003 Chemistry and Biology  
Encoded phage serve these libraries are a useful tool for sorting through large pools of synthetic compounds for molecules binding to as extremely robust reporters of the presence of each compound, providing  ...  To evaluate this approach, we constructed a library of 980 analogs of folic acid dis-studies of cellular uptake and transport, and for most in vivo applications. played on T7 phage, and demonstrated rapid  ...  for attachment of nicotinic acid derivatives.  ... 
doi:10.1016/j.chembiol.2003.08.005 pmid:14522055 fatcat:affv7xylazeglohszlm5jo2zkq

ADVANCES IN CHEMICAL GENETICS

Inese Smukste, Brent R. Stockwell
2005 Annual review of genomics and human genetics (Print)  
■ Abstract Chemical genetics is an emerging approach for studying biological systems using chemical tools.  ...  This strategy aims to reveal the macromolecules responsible for regulating biological systems; thus, the approach shares much in common with genetics.  ...  Thus, SLIMS provides a framework for analyzing high-throughput assay data both as a laboratory information management system and as a platform for experimental analysis.  ... 
doi:10.1146/annurev.genom.6.080604.162136 pmid:16124862 fatcat:r26ihyhqijgvtnhduyudkigkuu

Design, synthesis, and biological evaluation of abiotic, non-lactone modulators of LuxR-type quorum sensing

Christine E. McInnis, Helen E. Blackwell
2011 Bioorganic & Medicinal Chemistry  
This study reports the design and synthesis of two libraries of new, non-hydrolyzable AHL mimics.  ...  The libraries were screened for QS modulatory activity using LasR, LuxR, and TraR bacterial reporter strains, and several new, abiotic agonists and antagonists of these receptors were identified.  ...  We also thank Karla Camancho for her assistance in purifying members of Library A.  ... 
doi:10.1016/j.bmc.2011.06.072 pmid:21798749 pmcid:PMC3152649 fatcat:l4dgzunsqvaa5iyvxzxyqqtvoy

Combinatorial Chemistry Online Volume 17, Issue 4, April 2015

N.K. Terrett
2015 Combinatorial Chemistry  
The synthesis of the key compound involved using a molecular diversity approach, to rapidly advance a library of compounds for biological testing.  ...  The method is straightforward, high-yield, easy to operate, and shows a broad substrate scope, thus potentially useful for diversity-oriented synthesis [4] .  ... 
doi:10.1016/j.comche.2015.03.001 fatcat:35hxog5fo5ghrbobbaugb24d4q

Behavioral partitioning in the synthesis of mixed analog-digital systems

Sree Ganesan, Ranga Vemuri
2001 Proceedings of the 38th conference on Design automation - DAC '01  
Synthesis of mixed-signal designs from behavioral specifications must address analog-digital partitioning.  ...  We present techniques for analog-digital behavioral partitioning of the MSFG, and performance estimation of the technology-mapped analog and digital circuits.  ...  In this paper, we address the problem of analog-digital partitioning for synthesis of mixed-signal systems from behavior-level specifications.  ... 
doi:10.1145/378239.378373 dblp:conf/dac/GanesanV01 fatcat:n7vsartmhrdkzefsml45rmphdi

Comprehensive Survey of Chemical Libraries for Drug Discovery and Chemical Biology: 2009

Roland E. Dolle, Bertrand Le Bourdonnec, Karin Worm, Guillermo A. Morales, Craig J. Thomas, Wei Zhang
2010 Journal of combinatorial chemistry  
Solution-phase methodology accounted for ca. 85% of chemical library synthesis.  ...  , 366,367,369 review of Ellman's libraries, 374 solid-phase resin specifications, 359 microelectrode arrays for monitoring ligand-receptor binding events, 364 yactoliter-scale DNA reactor for small molecule  ...  Allosteric binding sites, as opposed to traditional orthosteric binding sites, offer unparalleled opportunities for drug discovery by providing high levels of selectivity, mimicking physiological conditions  ... 
doi:10.1021/cc100128w pmid:20923157 pmcid:PMC4140011 fatcat:aqvuxwobprbkfbofh2bspbygnm

Light directed massively parallel on-chip synthesis of peptide arrays with t-Boc chemistry

Xiaolian Gao, Xiaochuan Zhou, Erdogan Gulari
2003 Proteomics  
Examples are given from synthesis of metal ion binding peptides and epitope binding assys.  ...  Light directed massively parallel on-chip synthesis of peptide arrays with t-Boc chemistry Peptide and peptidomimetic molecule arrays are emerging powerful tools for parallel screening of binding in proteomics  ...  This, coupled with high-throughput synthesis, has the potential to bring the cost of the peptide chips to the level of DNA chips and make them economically viable for everyday use in research.  ... 
doi:10.1002/pmic.200300597 pmid:14595812 fatcat:4nutujestnb2dbf6dffxquddai

Chemical Dimerizers and Three-Hybrid Systems

Nikolai Kley
2004 Chemistry and Biology  
characterization of small small molecule ligand binding proteins.  ...  Traditionally, the molecule-protein interactions and proteome-wide identification of receptors for small molecules has relied identification of drug receptors. on in vitro biochemical methods, such as  ...  For example, it was chor moiety" with known binding affinity for the LBD of shown that library screens can be performed at high the DBD-fusion protein, a "test compound" moiety, for complexity and redundancy  ... 
doi:10.1016/j.chembiol.2003.09.017 pmid:15157871 fatcat:xwkyzbvvnfb5bbqgt5ktzbxkni

Chemical Dimerizers and Three-Hybrid SystemsScanning the Proteome for Targets of Organic Small Molecules

N KLEY
2004 Chemistry and Biology  
characterization of small small molecule ligand binding proteins.  ...  Traditionally, the molecule-protein interactions and proteome-wide identification of receptors for small molecules has relied identification of drug receptors. on in vitro biochemical methods, such as  ...  For example, it was chor moiety" with known binding affinity for the LBD of shown that library screens can be performed at high the DBD-fusion protein, a "test compound" moiety, for complexity and redundancy  ... 
doi:10.1016/s1074-5521(04)00119-x fatcat:inw42qxzezdedk3bhsf7qmm2by

Screening for Diguanylate Cyclase (DGC) Inhibitors Mitigating Bacterial Biofilm Formation

Kyu Hong Cho, R Grant Tryon, Jeong-Ho Kim
2020 Frontiers in Chemistry  
synthesis activity of DGCs have been performed in order to inhibit bacterial biofilm formation.  ...  This review describes currently identified chemical inhibitors that disturb the activity of DGCs and the methods of screening and assay for their discovery.  ...  An ideal high throughput screening for chemical inhibitors of DGCs would incorporate a system that monitors the changes of cellular c-di-GMP concentration in situ.  ... 
doi:10.3389/fchem.2020.00264 pmid:32373581 pmcid:PMC7186502 fatcat:a5usk2g65jexxb5ctdq52wmpoq

Novel Long-Acting Somatostatin Analog with Endocrine Selectivity: Potent Suppression of Growth Hormone But Not of Insulin

Michel Afargan, Eva Tiensuu Janson, Garry Gelerman, Rakefet Rosenfeld, Offer Ziv, Olga Karpov, Amnon Wolf, Moshe Bracha, Dvira Shohat, George Liapakis, Chaim Gilon, Amnon Hoffman (+2 others)
2001 Endocrinology  
We employed an integrated approach consisting of screening of backbone cyclic peptide libraries constructed on the basis of molecular modeling of known SRIF agonists and of high throughput receptor binding  ...  Its long-acting analogs are in clinical use for treatment of various endocrine syndromes and gastrointestinal anomalies.  ...  These SRIF analogs all have similar binding affinities for four of the five human SRIF receptor subtypes (hsst): high affinity for hsst2 and hsst5, moderate affinity for hsst3, and very low affinity for  ... 
doi:10.1210/endo.142.1.7880 pmid:11145612 fatcat:e27mfvwrgve27is4rtel2j3eda
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