Review Inchemical Structures of Drugs
Abstract
Our review concerned with chemical structures of some drugs in pharmaceutical fields ,some of them used in synthetic field and in synthesis of many drugs and antibiotics.
About this article
Keywords
- structures
- common.
References
[1] Kubinyi H, “Chance favors the prepared mind--from serendipity to rational drug design”, J. Recept. Signal Transduct. Res., Vol.19, No.1-4, (1999), pp.15-39.
[2] Mayr LM &Bojanic D, “Novel trends in high-throughput screening”, Current Opinion in Pharmacology, Vol.9, No.5, (2009), pp.580-588.
[3] Ertl P, “Cheminformatics analysis of organic substituents: identification of the most common substituents, calculation of substituent properties, and automatic identification of drug-like bioisosteric groups”, Journal of chemical information and computer sciences, Vol.43, No.2, (2003), pp.374-380.
[4] Bohacek RS, McMartin C &Guida WC, “The art and practice of structure‐based drug design: a molecular modeling perspective”, Medicinal research reviews, Vol.16, No.1, (1996), pp.3-50.
[5] Leiter DP, Morgan HL &Stobaugh RE, “Installation and Operation of a Registry for Chemical Compounds”, Journal of Chemical Documentation, Vol.5, No.4, (1965), pp.238-242.
[6] LednicerD, The organic chemistry of drug synthesis, John Wiley & Sons, (2007).
[7] NaghamMAljamali, Experimental Methods for Preparation of Mannich Bases, Formazan, Normal and Cyclic Sulfur Compounds, 1 Edt., Evince pub Publishing house, (2018).
[8] NaghamMAljamali, Reactions and Mechanisms, 1 Edt., IJMRA Publication, (2018).
[9] Fink T &Reymond JL, “Virtual exploration of the chemical universe up to 11 atoms of C, N, O, F: assembly of 26.4 million structures (110.9 million stereoisomers) and analysis for new ring systems, stereochemistry, physicochemical properties, compound classes, and drug discovery”, Journal of chemical information and modeling, Vol.47, No.2, (2007), pp.342-353.
[10] Wright GD, “The antibiotic resistome: the nexus of chemical and genetic diversity”, Nature Reviews Microbiology, Vol.5, No.3, (2007), pp175-186.
[11] Nagham MAljamali, “Synthesis and chemical identification of macro compounds of (Thiazol and Imidazol)”, Research J. Pharm. and Tech, Vol.8, No.1, (2015), pp.78-84.
[12] Hegazi A, Abdou AM, El-Moez S & Allah FA, “Evaluation of the antibacterial activity of bee venom from different sources”, World Applied Sciences Journal, Vol.30, No.3, (2014), pp.266-270.
[13] Intisar OA, Nuha SS, ZainabMJ &Nagham MAljamali, “Synthesis of New Organic Compounds Via Three Components Reaction with Studying of (Identification,Thermal Behavior, Bioactivity on Bacteria of Teeth)”, Journal of Global Pharma Technology, Vol.11, No.9, (2017), pp.157-164.
[14] Eman HS&Nagham MAljamali, “New Azo-Thiadiazole Ligands (Preparation, Spectral, Thermal, Biochemical, Physical properties)-Studying”, Journal of Global Pharma Technology, Vol.11, No.9, (2017), pp.165-173.
[15] Nagham MAljamali, “Preparation, Spectral Investigation, Thermal Analysis, Biochemical Studying of New (Oxadiazole-Five Membered Ring)-Ligands”, Journal of Global Pharma Technology, Vol.10, No.1, (2018), pp.20-29.
[16] Intisar Obaid A, Eman HS &Nagham MAljamali, “Synthesis of (Tetrazole, Oxazepine, Azo, Imine) Ligands and Studying of Their (Organic Identification, Chromatography, Solubility, Physical, Thermal Analysis, Bio-Study)”, Research J. Pharm. and Tech., Vol.11, No.7, (2018).
[17] Mohammed M, Nagham MAljamali, Shubber WA &Abdalrahman SA, “New Azomethine-Azo heterocyclic ligands via cyclization of ester”, Research Journal of Pharmacy and Technology, Vol.11, No.6, (2018), pp.2555-2560.
[18] Benecke C, Grund R, Hohberger R, Kerber A, Laue R & Wieland T, “MOLGEN+, a generator of connectivity isomers and stereoisomers for molecular structure elucidation”, AnalyticaChimicaActa, Vol.314, No.3, (1995), pp.141-147.