A Review on Pharmacological Aspects of Pyrimidine Derivatives
Abstract
Pyrimidine is an aromatic heterocyclic organic compound similar to pyridine. One of the three diazines (six-membered heterocyclics with two nitrogen atoms in the ring), it has the nitrogens at positions 1 and 3 in the ring. Pyrimidines are typically synthesized by the “Principal Synthesis” involving cyclization of beta-dicarbonyl compounds with N-C-N compounds. Reaction of the former with amidines to give 2-substituted pyrimidines, with urea to give 2-pyrimidiones, and guanidines to give 2-aminopyrimidines are typical. Pyrimidines can be prepared via the biginelli reaction. Many other methods rely on condensation of carbonyls with diamines for instance the synthesis of 2-Thio-6-methyluracil from thiouria and ethyl acetoacetate or the synthesis of 4-methylpyrimidine with 4, 4-dimethoxy-2-butanone and formamide. Pyrimidine derivatives show antimicrobial activity, anticancer activity, anti-inflammatory activity, antidiabetic, and analgesic activity.1.
Keywords: Pyrimidine derivatives, Synthesis, derivatives and pharmacological activities.
Keywords:
Pyrimidine derivatives, Synthesis, derivatives and pharmacological activitiesDOI
https://doi.org/10.22270/jddt.v10i5.4295References
Delgado JN and Remers WA; Wilson and Giswold’s Textbook of Organic Chemistry Medicinal and Pharmaceutical Chemistry; 10th ed. Philadelphia:Lippincott Raven; 1998.
Miller D; Remington- The Science and Practice of Pharmacy; 19th ed. Pennsylvania: MACK Publishing Company; 1995; 425.
Amir M, Javed SA and Kumar H; Indian J. Pharm. Sciences; 2007; 69(3):337-343.
Cox RA; Quart. Rev.; 1968; 22:499.
Jain MK, Sharnevas SC; Organic Chem.; 2008; 3:997-999.
Eussell JA; Annu. Rev. Biochem.; 1945; 14:309.
Hitchings GH, Elion GB, Wanderers H and Falco EA; J. Biol. Chem.; 1948; 174:765.
Futterman S; J. Biol. Chem.; 1957, 228:1031.
Cheng CC and Roth B; In Progress in Medicinal Chem. (eds Ellis GP and West GB), Butterworths London; 1982; 19:267.
Kompis I and Wick A; Helv. Chim. Acta; 1977; 60; 3025.
Polak A. and Scholer HJ; Chemotherapy; 1975; 21:113.
Padamshari B, Vaidya VP and Vijayayakumar ML; Indian J.Hetero. Chem.; 2002; 12:89-94.
Naik TA and Chikhalia KH; E-Journal of Chem.; 2007; 4(1):60-66.
Aly and AA, Chinese J. of Chem.; 2005; 23:211-217.
Mogilaiah K and Sudhakar GR; Indian J. Hetero. Chem.; 2003; 42B:636-640.
Mishra A and Singh DV; Indian J. Hetero. Chem.; 2004; 14:43-46.
Russo F, Romeo G, Caruso A, Cutuli V, Amore D and Santagati NA; Eur. J. Med. Chem.; 1999; 29:569.
Cenicola, Donnoli D, Stella L, Paola CD, Constantino M, Anignente E, Arena F, Luraschi E and Saturnino C, Pharmacology Res.; 1990; 22:80.
Nargund LVG, Badiger VV and Yarnal SM; J. Pharm. Sci.; 1992; 81:365.39. Rashand.
Honkanen E, Pipuri A, Kairisalo P, Nore P, Karppaness H and Paakari I; J. Med. Chem.;1983; 26:143.
Mery Press B, James Mc Nally J, Joan Keisher A, Steve Offord J, Laurence Katz B, Robert Falotico and Alfonso Tobaia J; Eur. J. Med Chem.; 1989; 24:627.
Ronald Russell K, Jeffery Press B, Richard Rampulla A, James Mcnally J, Robert Falotico, Joan Keiser A, David Bright A and Alfonso Tobia; J. Med. Chem.; 1988; 31:1786.
Ganzevoort W, Rep A, Bonsel G.J, De Vries JI and Wolf H; Hypertension; 2004; 22:1235–1242.
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