@conference { ISI:000299378301476, title = {Computer vision based chemical information extraction from digital images and streaming videos}, booktitle = {242nd National Meeting of the American-Chemical-Society (ACS)}, volume = {242}, year = {2011}, note = {242nd National Meeting of the American-Chemical-Society (ACS), Denver, CO, AUG 28-SEP 01, 2011}, month = {AUG}, publisher = {American-Chemical-Society (ACS)}, organization = {American-Chemical-Society (ACS)}, address = {1155 16th ST, NW, Washington, DC 20036 USA}, issn = {0065-7727}, author = {Karthikeyan, Muthukumarasamy} } @proceedings { ISI:000349165103353, title = {ChemInfoCloud: opensource based cloud compatible chemical textmining tools for harvesting largescale medical literature}, volume = {248}, year = {2014}, note = {248th National Meeting of the American-Chemical-Society (ACS), San Francisco, CA, AUG 10-14, 2014}, month = {AUG}, pages = {Meeting Abstract: 69-CINF}, publisher = {American Chemical Society}, type = {Meeting Abstract}, address = {1155 16th ST, NW, Washington, DC 20036 USA}, issn = {0065-7727}, author = {Karthikeyan, Muthukumarasamy} } @inbook {43325, title = {Chemoinformatics approach for the design and screening of focused virtual libraries}, booktitle = {Practical Chemoinformatics}, year = {2014}, pages = {93-131}, publisher = {Springer}, organization = {Springer}, chapter = {Chemoinformatics Approach for the Design and Screening of focused virtual libraries}, address = {India}, abstract = {

It is challenging to handle a large volume of molecular data without appropriate tools. Here, we describe the need and the approaches for the development of focussed virtual libraries to design efficient molecules and optimize them for lead generation. The experimental chemists and biologists are more interested in properties of chemicals and their response to biological system in both beneficial and adverse effects context rather than just their structures. In this chapter, the focus is to relate newly designed chemical structures to their predicted activity, property or toxicity. Property prediction tools save time, money and lives of experimental animals. They come in handy while taking informed decisions especially in certain cases involving pharmacodynamic studies of drug molecules in humans where there are inevitable ethical and safety concerns. Property prediction is an important component in virtual screening which is at the heart of drug design and the most important step where chemoinformatics plays a major role. The other fields where structure{\textendash}activity relation-based principles hold good for virtual screening are agrochemicals and environmental science, specifically the toxicity and biodegradability prediction of pollutant molecules. In this chapter, we will show how to design software tools to handle generation of focussed virtual libraries from a given set of molecules with common features, fragments or bioactivity spectrum.

}, doi = {10.1007/978-81-322-1780-0_2 }, author = {Karthikeyan, Muthukumarasamy and Vyas, Renu} } @article { ISI:000360934800005, title = {Chemoinformatics approach for building molecular networks from marine organisms}, journal = {Combinatorial Chemistry \& High Throughput Screening}, volume = {18}, number = {7}, year = {2015}, month = {JAN}, pages = {673-684}, publisher = {BENTHAM SCIENCE PUBL LTD}, address = {EXECUTIVE STE Y-2, PO BOX 7917, SAIF ZONE, 1200 BR SHARJAH, U ARAB EMIRATES}, abstract = {

Natural products obtained from marine sources are considered to be a rich and diverse source of potential drugs. In the present work we demonstrate the use of chemoinformatics approach for the design of new molecules inspired by molecules from marine organisms. Accordingly we have assimilated information from two major scientific domains namely chemoinformatics and biodiversity informatics to develop an interactive marine database named MIMMO (Medicinally Important Molecules from Marine Organisms). The database can be queried for species, molecules, scaffolds, drugs, diseases and associated cumulative biological activity spectrum along with links to the literature resources. Molecular informatics analysis of the molecules obtained from MIMMO was performed to study their chemical space. The distinct skeletal features of the biologically active compounds isolated from marine species were identified. Scaffold molecules and species networks were created to identify common scaffolds from marine source and drug space. An analysis of the entire molecular data revealed a unique list of around 2000 molecules from which ten most frequently occurring distinct scaffolds were obtained.

}, keywords = {Chemoinformatics, Drug design, marine, virtual library}, issn = {1386-2073}, doi = {10.2174/1386207318666150703112950}, author = {Karthikeyan, Muthukumarasamy and Nimje, Deepika and Pahujani, Rakhi and Tyagi, Kushal and Bapat, Sanket and Vyas, Renu and Padmakumar, Krishna Pillai} } @article { ISI:000360934400003, title = {ChemScreener: a distributed computing tool for scaffold based virtual screening}, journal = {Combinatorial Chemistry \& High Throughput Screening}, volume = {18}, number = {6}, year = {2015}, month = {JAN}, pages = {544-561}, publisher = {BENTHAM SCIENCE PUBL LTD}, address = {EXECUTIVE STE Y-2, PO BOX 7917, SAIF ZONE, 1200 BR SHARJAH, U ARAB EMIRATES}, abstract = {

In this work we present ChemScreener, a Java-based application to perform virtual library generation combined with virtual screening in a platform-independent distributed computing environment. ChemScreener comprises a scaffold identifier, a distinct scaffold extractor, an interactive virtual library generator as well as a virtual screening module for subsequently selecting putative bioactive molecules. The virtual libraries are annotated with chemophore-, pharmacophore- and toxicophore-based information for compound prioritization. The hits selected can then be further processed using QSAR, docking and other in silico approaches which can all be interfaced within the ChemScreener framework. As a sample application, in this work scaffold selectivity, diversity, connectivity and promiscuity towards six important therapeutic classes have been studied. In order to illustrate the computational power of the application, 55 scaffolds extracted from 161 anti-psychotic compounds were enumerated to produce a virtual library comprising 118 million compounds (17 GB) and annotated with chemophore, pharmacophore and toxicophore based features in a single step which would be non-trivial to perform with many standard software tools today on libraries of this size.

}, keywords = {Scaffold extraction, therapeutic category, virtual library generation, virtual screening}, issn = {1386-2073}, doi = {10.2174/1386207318666150703112242}, author = {Karthikeyan, Muthukumarasamy and Pandit, Deepak and Vyas, Renu} } @article {43400, title = {ChemEngine: harvesting 3D chemical structures of supplementary data from PDF files}, journal = {Journal of Cheminformatics}, volume = {8}, year = {2016}, month = {DEC}, pages = {Article Number: 73}, abstract = {Digital access to chemical journals resulted in a vast array of molecular information that is now available in the supplementary material files in PDF format. However, extracting this molecular information, generally from a PDF document format is a daunting task. Here we present an approach to harvest 3D molecular data from the supporting information of scientific research articles that are normally available from publisher{\textquoteright}s resources. In order to demonstrate the feasibility of extracting truly computable molecules from PDF file formats in a fast and efficient manner, we have developed a Java based application, namely ChemEngine. This program recognizes textual patterns from the supplementary data and generates standard molecular structure data (bond matrix, atomic coordinates) that can be subjected to a multitude of computational processes automatically. The methodology has been demonstrated via several case studies on different formats of coordinates data stored in supplementary information files, wherein ChemEngine selectively harvested the atomic coordinates and interpreted them as molecules with high accuracy. The reusability of extracted molecular coordinate data was demonstrated by computing Single Point Energies that were in close agreement with the original computed data provided with the articles. It is envisaged that the methodology will enable large scale conversion of molecular information from supplementary files available in the PDF format into a collection of ready-to-compute molecular data to create an automated workflow for advanced computational processes.}, doi = {10.1186/s13321-016-0175-x}, author = {Karthikeyan, Muthukumarasamy and Vyas, Renu} } @conference {44599, title = {CCCTK (Compute Cure for Cancer ToolKit) an open source drug discovery platform for design of novel anti-cancer agents}, booktitle = {255th National Meeting and Exposition of the American-Chemical-Society (ACS) - Nexus of Food, Energy, and Water}, year = {2018}, month = {MAR}, publisher = {ACS, 1155 16TH ST, NW, Washington, DC 20036 USA}, organization = {ACS, 1155 16TH ST, NW, Washington, DC 20036 USA}, address = {New Orleans, LA}, author = {Karthikeyan, Muthukumarasamy and Vyas, Renu} } @conference {45434, title = {CCCTK: High performance molecular informatics toolkit for the design of anti-cancer molecule}, booktitle = {256th National Meeting and Exposition of the American-Chemical-Society (ACS) - Nanoscience, Nanotechnology and Beyond}, year = {2018}, month = {AUG}, publisher = {American-Chemical-Society (ACS)}, organization = {American-Chemical-Society (ACS)}, address = { Boston, MA}, author = {Karthikeyan, Muthukumarasamy} } @article {49130, title = {Comprehensive molecular docking and dynamic simulations for drug repurposing of clinical drugs against multiple cancer kinase targets}, journal = {Journal of Biomolecular Structure and Dynamics}, volume = {41}, year = {2023}, month = {NOV }, pages = {7735-7743}, type = {Article}, abstract = {

Drug repurposing is a method to identify novel therapeutic agents from the existing drugs and clinical compounds. In the present comprehensive work, molecular docking, virtual screening and dynamics simulations were carried out for ten cancer types viz breast, colon, central nervous system, leukaemia, melanoma, ovarian, prostate, renal and lung (non-small and small cell) against validated eighteen kinase targets. The study aims to understand the action of chemotherapy drugs mechanism through binding interactions against selected targets via comparative docking simulations with the state-art molecular modelling suits such as MOE, Cresset-Flare, AutoDock Vina, GOLD and GLIDE. Chemotherapeutic drugs (n = 112) were shortlisted from standard drug databases with appropriate chemoinformatic filters. Based on docking studies it was revealed that leucovorin, nilotinib, ellence, thalomid and carfilzomib drugs possessed potential against other cancer targets. A library was built to enumerate novel molecules based on the scaffold and functional groups extracted from known drugs and clinical compounds. Twenty novel molecules were prioritised further based on drug-like attributes. These were cross docked against 1MQ4 Aurora-A Protein Kinase for prostate cancer and 4UYA Mitogen-activated protein kinase for renal cancer. All docking programs yielded similar results but interestingly AutoDock Vina yielded the lowest RMSD with the native ligand. To further validate the final docking results at atomistic level, molecular dynamics simulations were performed to ascertain the stability of the protein-ligand complex. The study enables repurposing of drugs and lead identification by employing a host of structure and ligand based virtual screening tools and techniques. Communicated by Ramaswamy H. Sarma

}, keywords = {chemotherapeutic drugs, Drug repurposing, Molecular docking, molecular simulation (MD), structure-based drug designing (SBDD), virtual screening}, issn = {0739-1102}, doi = {10.1080/07391102.2022.2124453}, author = {Shaikh, Nilofer and Linthoi, R. K. and Swamy, V, K. and Karthikeyan, Muthukumarasamy and Vyas, Renu} }