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Scientific Program
4th International Conference on Medicinal Chemistry & Computer Aided Drug Designing, will be organized around the theme “Latest Innovations In Computational Drug Designing And Medicinal Chemistry: Up To The Minute ”
MedChem & CADD-2015 is comprised of 12 tracks and 76 sessions designed to offer comprehensive sessions that address current issues in MedChem & CADD-2015.
Submit your abstract to any of the mentioned tracks. All related abstracts are accepted.
Register now for the conference by choosing an appropriate package suitable to you.
Novel drug design typically cited as Prodrug design or just rational design, which is the ingenious method for finding new medications supported in the information of a biological target. A unique interaction for rational drug design is most typically associated in organic little molecule that activates or inhibits the operate of a biomolecule like a macromolecule, that successively ends up in a discovery of a unique, extremely potent and orally active through structure-based drug design. Within the simplest sense, drug design involves the little molecules that are complementary in form and charge to the biomolecular target in which they move with the novel macrocyclic peptides as scaffoldings in a drug designing binding site. Drug design often times essentially depends on computer modelling techniques. This sort of modelling is commonly cited as computer-aided drug design. Finally, novel supply of chemical diversity in drug style that depends on the information of the three-dimensional structure of the biomolecular target is understood as structure-based drug design.
- Track 1-1Prodrug design
- Track 1-2Rational drug design
- Track 1-3Structure-based drug design
- Track 1-4Peptides as scaffolds in drug design
- Track 1-5Novel source of chemical diversity in drug design
Computer aided drug design and Advanced Instrumentation is that the most elementary goal to predict whether a given molecule can bind to a target or not. Study in drug design or biomarkers in drug design measures the conformation of the little molecule and to model conformational changes within the biological target which will occur once the little molecule binds thereto. Recent advances in computer assisted drug design with the utilization of high performance computing technology and insilco molecular design computer code and tools offer might optimize the parameters for the molecular mechanics calculations and additionally provide an estimation of the electronic properties (electrostatic potential, polarizability, etc.) of the drug molecule that may influence binding affinity within the use of ultrasound in medicinal chemistry. High-resolution 1H-NMR chemical analysis and X-Ray absorption chemical analysis ways may additionally be accustomed offer semi-quantitative prediction of the binding affinity.
- Track 2-1Drug design software
- Track 2-2Computer graphics in drug design
- Track 2-3In silico molecular design software and tools
- Track 2-4High-Resolution 1H-NMR spectroscopy and X-Ray absorption spectroscopy
- Track 2-5Supercritical fluid chromatography screening system
- Track 2-6Mass spectrometry screening system
- Track 2-7Biomarkers in drug design
The evident brings that in experienced techniques for organic synthesis and medicinal chemistry have a stimulating record in stereochemistry of carbon compounds and can play a pivotal role in providing lead compounds for therapeutic applications. A strategy for introducing medicinal chemistry has reviewed with a stress on preparation of compounds designed for biomedicinal applications, Electrophilic fluorination, nucleophilic fluorination, and enantioselective monofluorination procedures are mentioned. This is often followed by Synthetic chemistry and Quantum chemistry, a review in nucleophilic and electrophilic trifluoromethylation procedures. The ultimate sections highlight recent applications of medicinal chemistry in drug development with the application of computer software tools in it.
- Track 3-1Green techniques for organic synthesis
- Track 3-2Stereochemistry of carbon compounds
- Track 3-3Fluorine in medicinal chemistry
- Track 3-4Quantum chemistry and Silicon chemistry
- Track 3-5Recent advances in fluorinated pharmaceuticals natural products
Multimodality imaging explains a method during which scientists would be able to manipulate and management individual atoms and molecules. Carbon nanotubes are the materials for medicative chemistry and biotechnological applications used in exploring the extremist preciseness machine technology. Nanotechnical based systems will enhance the CNS drug targeting and delivery, with the event of the scanning tunnelling magnifier that might see individual atoms. Development of nanoparticles for varied drug delivery and applications of engineering in cancer involve the flexibility to ascertain and to regulate individual atoms and molecules.
- Track 4-1Carbon Nanotubes - From Fundamentals to Devices
- Track 4-2Graphene and Beyond - 2D Materials
- Track 4-3Impact of nanotechnology on drug delivery
- Track 4-4Inorganic/Organic Nanohybrids for Energy Conversion
- Track 4-5Carbon allotropes
- Track 4-6Fullerene purification
The boundaries between current developments in medicinal chemistry and diagnostic medicinal chemistry between inanimate and living matter may be a major feature of the convergence between engineering and biotechnology. The most intention of recent advances in medicinal chemistry is to emphasise that though creating life may be a continual project which measures refined process within the underlying metaphysical assumptions. This comparison is supposed to contribute to an improved understanding of the cultural problems at stake within the convergence between nano and biotechnologies. It suggests that the limit between life and inanimate matter remains a stock in which the advancement in medicinal chemistry across the borders doesn’t precede from constant metaphysical assumptions.
- Track 5-1Recent advances in medicinal chemistry
- Track 5-2Diagnostic medicinal chemistry
- Track 5-3Organic medicinal chemistry
- Track 5-4Synthetic medicinal chemistry
- Track 5-5Pharmacogenomics and Pharmacoproteomics research on drugs
- Track 5-6Drug Bank: Comprehensive research on drugs
Materialistic Chemistry is a discipline of frontiers in inorganic synthetic chemistry that seeks to reveal the character of atoms and also the changes that occur at intervals of such substances on the molecular level and artificial chemistry of nanomaterials. Conversely, modification of peptide materials by Thiol-X chemistry additionally involves the techniques of those substances which are endued with intrinsic voids, ideal materials, and real materials. With the chemistry of tissue adhesive materials, there are endless prospects for making numerous properties of medicative chemistry with carbons and fullerene derivatives. Biological chemistry is not just involved with the revelation of biological phenomena to utilize the studies of drug design and drug discovery. The artificial medicative chemistry endeavours to form new technology which will form the commercial foundation to alter North American country to foster a wholesome natural perspective and philosophy and a healthy property society.
- Track 6-1Computational materials science
- Track 6-2Modification of polypeptide materials by Thiol-X chemistry
- Track 6-3Intrinsic voids, ideal materials, and real materials
- Track 6-4Synthetic chemistry of nanomaterials
- Track 6-5The chemistry of tissue adhesive materials
- Track 6-6Pharmaceuticals and personal care products
Integrative cancer biology and genetics explains the internal secretion and carcinoma theme which analyze members of the HIV/AIDS and cancer medical specialty. Development theme measures the actively concerned cancer killing virus medical aid. Medicinal chemistry of antitumor medication and proteins concerned in cancer development is used for target identification, lead discovery, development and compound analysis. These embody insilico primarily based upon the macromolecule natural property, in-vitro and in-vivo biological analysis, insilico prediction of pharmacokinetic parameters and increasing into drug delivery and formulation technology. Major therapeutic areas of interest embody drug delivery for cancer medication, together with internal secretion dependent and freelance pathologies, anti-viral agents and advances in antineoplastic targets like brain disorder, depression, anxiety and substance abuse.
- Track 7-1Integrative cancer biology and genomics
- Track 7-2Advances in cancer drug targets
- Track 7-3HIV/AIDS & cancer virology
- Track 7-4Medicinal chemistry of anticancer drugs
- Track 7-5Melatonin and breast cancer
- Track 7-6Proteins involved in cancer development
Neuro-AIDS defines the progressive loss of structure or death of neurons and metabolism in neurodegenerative illness. Several neurodegenerative diseases as well as ALS, Parkinsons, Alzheimers, and Huntingtons occur as a result of neurodegenerative processes. Such diseases are incurable, leading to progressive degeneration and/or death of somatic cell and aerophilous stress in neurodegenerative illness. As analysis progresses, several similarities seem that relate these diseases to one another on a sub-cellular level. Discovering these similarities offers hope for therapeutic targets for neurodegenerative diseases that would ameliorate several diseases at the same time. There are several parallels between completely different novel drug for neurodegenarative illness as well as necrobiosis.
- Track 8-1Neuro-AIDS
- Track 8-2Metabolism in neurodegenerative disease
- Track 8-3Chemistry and biochemistry of oxidative stress in neurodegenerative disease
- Track 8-4Therapeutic targets for neurodegenerative diseases
- Track 8-5Novel drug for neurodegenarative disease
Development of radiopharmaceuticals will cause modified general exposure which leads to variations in drug response of the co-administered medicine. Additionally to recent advances in biologics and vaccines development, concomitant bodily process of dietary supplements or edible fruit or drinkable might additionally alter general exposure of medication, therefore resulting in adverse drug reactions or loss of effectualness. Therefore, its vital to judge development of sustained unleash drug delivery systems before market approval furthermore as throughout the postmarketing amount. Mechanism of drug interactions is to facilitate the discussion of study style, knowledge analysis, and implication of drug interactions for dosing and labelling. Victimization linguistics predicts to uncover drug-drug interactions in clinical knowledge in new draft steering on drug interaction in cellular networking which has been evolved by medicinal chemistry and material medica.
- Track 9-1Development of radiopharmaceuticals
- Track 9-2Recent advances in biologics and vaccines development
- Track 9-3Protein–Ligand and Protein–Protein interactions
- Track 9-4Concomitant drugs with low risks of drug-drug interactions
- Track 9-5Drug interaction in cellular networking
- Track 9-6Medicinal chemistry and Pharmacology
In pharmaceutical business, recently approved medication has poured immeasurable greenbacks into new technologies over the past 20 years, however this has had very little impact on the high dropout rate and value of drug development. Whereas automation steps towards nanoparticles in drug delivery and drug transporters in drug discovery based mostly on the methods that have greatly exaggerated throughputs in compound synthesis and screening. They need not gains within the social science of drug discovery and therefore the success rate of clinical biomarkers in drug discovery and development entities. Plant derived medication in drug discovery and microbe derived medication in drug discovery of molecular targets as potential candidates for therapeutic intervention which is determined by whole ordination assessment of the variations between traditional and polymer transcriptional variants which will play a job within the onset or progressing insilico drug discovery. The flexibility to live giant numbers of DNA variants, cistron or exon-based transcription may create a crossbreeding micro arrays in engaging the discovery of alternative sequencing the biological richness intrinsic to alter the knowledge in amide drug discovery.
- Track 10-1In silico drug discovery
- Track 10-2Peptide drug discovery
- Track 10-3Nanoparticles in drug delivery
- Track 10-4Clinical biomarkers in drug discovery and development
- Track 10-5Plant derived drugs in drug discovery
- Track 10-6Microbial derived drugs in drug discovery
- Track 10-7Chemical biology approach to drug discovery
- Track 10-8Recently approved drugs
- Track 10-9Drug discovery: Hit to lead
Forensic chemistry and analytical material medicinal chemistry is that the application of chemistry to enforce the failure of merchandise or processes. Several nucleon activation analysis strategies reveal the chemical changes occurred throughout an occurrence which again facilitates to reconstruct the sequence of DNA and RNA strands. Rhetorical drug analysis, trace analysis, rhetorical medical science is exclusive among chemical sciences in which anlyze the wants of the scientific communities and therefore the legal communities. Therefore optical instrumental techniques (UV, infrared, and X-ray spectroscopy) analysis is applied by product naturally and it emphasizes validation of Separation analyses.
- Track 11-1Toxicology study and forensic study
- Track 11-2Forensic drug analysis, trace analysis, forensic serology
- Track 11-3Optical instrumental techniques (UV, infrared, and X-ray spectroscopy)
- Track 11-4Separation analyses (gas chromatography, HPLC, and thin-layer chromatography)
- Track 11-5Applications of forensic chemistry for petroleum cases
It has estimated that in the field of medicinal chemistry more than $79 million in research funding has spent since 2008. A complete overview of drug designing process has come up with some crucial details that from year 2008 to 2013 the market has a growth with $ 198 billion and in further this rate may increases to $236 billion from year 2014 to 2019. Special emphasis is given on computational approaches for drug discovery along with salient features and applications of the software’s used in de-novo drug designing.
In the future year of 2020, the revenue budget of drug designing or drug production reveals that the large drug companies are facing the expiry of patents on their best sellers. At the same time they are having trouble inventing new medicines, and this means that the drug industry’s sales may at best tread water and could face some steep drops. The point of market analysis is to see what happens after the immediate patent expirations, like the loss of Lipitor from highly reputed companies
- Track 12-1Medicinal chemistry services and market
- Track 12-2Regulations governing the industry.
- Track 12-3Inventory of chemical substances
- Track 12-4Industrial safety and health law
- Track 12-5Globally harmonized system
- Track 12-6Ensuring drug safety
- Track 12-7Submitting new chemical notifications and product registrations
- Track 12-8Minimizing development and manufacturing cost
- Track 12-9Immunogenicity of Biopharmaceuticals
- Track 12-10Domestic substances list (DSL) and the non-domestic substances list (NDSL)