Review Inchemical Structures of Drugs

Authors

  • Nagham Mahmood Aljamali
  • . .

DOI:

https://doi.org/10.14419/ijet.v7i4.36.24216

Published:

2018-12-09

Keywords:

structures, common.

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.

 

References

[1] Kubinyi H, “Chance favors the prepared mind--from serendipity to rational drug designâ€, J. Recept. Signal Transduct. Res., Vol.19, No.1-4, (1999), pp.15-39.

[2] Mayr LM &Bojanic D, “Novel trends in high-throughput screeningâ€, 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 groupsâ€, 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 structureâ€based drug design: a molecular modeling perspectiveâ€, 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 Compoundsâ€, 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 discoveryâ€, 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 diversityâ€, Nature Reviews Microbiology, Vol.5, No.3, (2007), pp175-186.

[11] Nagham MAljamali, “Synthesis and chemical identification of macro compounds of (Thiazol and Imidazol)â€, 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 sourcesâ€, 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)â€, 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)-Studyingâ€, 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)-Ligandsâ€, 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)â€, 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 esterâ€, 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 elucidationâ€, AnalyticaChimicaActa, Vol.314, No.3, (1995), pp.141-147.

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How to Cite

Mahmood Aljamali, N., & ., . (2018). Review Inchemical Structures of Drugs. International Journal of Engineering & Technology, 7(4.36), 644–654. https://doi.org/10.14419/ijet.v7i4.36.24216

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Received 2018-12-18
Accepted 2018-12-18
Published 2018-12-09