An enzyme, receptor, nucleic acid, hormone, ion channel, membrane protein/s, or other cellular structure that is involved in a molecular-level knowledge of a certain disease is referred to as a target. Target identification is the initial step in the drug development program's computer-aided drug design process, and it's crucial to ensure that the chosen targets are responsible for the disease. The function of a potential therapeutic target (gene/protein) and its role in the disease are the first steps in target identification and characterization. Following the identification of the target, the molecular mechanisms addressed by the target are characterised. A good target should be effective, safe, and druggable while also meeting clinical and commercial needs.
Target validation is the initial step in identifying a novel medicine and can often take 2-6 months. The method comprises the application of a set of techniques that try to demonstrate that medication effects on the target can give a therapeutic benefit with an acceptable safety window. Early in-depth target validation improves understanding of the relationship between target alteration and disease efficacy, increasing the likelihood of clinical success. The research advances onto the hit identification phase once a target has reached an acceptable level of validation and disease correlation.
Title : A qsar survey on tyrosine kinase inhibitors
Atefeh Hajiagha Bozorgi, Faculty of pharmacy, Iran (Islamic Republic of)
Title : Abbott diagnostics: COVID-19 inactivation, nucleocapsid antigen automated immunoassay development, and variant testing for automated and lateral flow assays binaxnow™ and panbio™
Philip M Hemken, Abbott Laboratories, United States
Title : Synthesis, antibacterial activity of 3-amino 5-methoxyl-2-methyl quinazolin-4(3H)-one an amino-6-methoxyl-2-methyl of 4H–benzo[d] [1,3]–oxazine–4–one
Osarumwense Peter Osarodion, Ondo State University of Sciences and Technology, Nigeria
Title : Tackling mycobacterium tuberculosis resistance with tailored isatin-pyrimidine hybrids enoyl acyl carrier protein reductase (Inha)
Amgad Albohy, The British University in Egypt (BUE), Egypt
Title : Transition metal complexes/Organometallic compounfs as anticancer drugs
Prakash kinthda, Nims university,jaipur,rajasthan, India
Title : New n-ribosides and n-mannosides of rhodanine derivatives with anticancer activity on leukaemia cell line: Design, synthesis, dft and molecular modelling studies
Ahmed, Kafrelsheikh University, Egypt