Design, synthesis of some 2,6,9-trisubstituted purinyl thioureido derivatives and evaluation of antimicrobial activity

被引:0
作者
Jigisha A. Modi
K. C. Patel
机构
[1] V. N. S. G. University,Department of Chemistry
来源
Medicinal Chemistry Research | 2012年 / 21卷
关键词
Purine; Thioureido linkage; Minimum inhibitory concentration (MIC);
D O I
暂无
中图分类号
学科分类号
摘要
Some new trisubstituted purinyl thioureido were synthesized and evaluated for their in vitro antimicrobial activity against Gram positive and Gram negative strains and antifungal strain using a micro dilution procedure. Synthesized compounds 6a–j prove to be effective with minimum inhibitory concentration (MIC) (mg ml−1), among them 6a, 6d, and 6e showed excellent activity against a panel of microorganisms. The newly synthesized compounds were characterized using IR, 1H-NMR, and elemental analysis.
引用
收藏
页码:1660 / 1664
页数:4
相关论文
共 48 条
  • [1] Fathalla WM(2002)Synthesis of heterocyclic skeletons by the reaction of N1-(2-cyanophenyl)-benzimidoyl chloride with thioamides Molecules 7 96-103
  • [2] Pazdera P(2003)Identification of a new chemical class of potent angiogenesis inhibitors based on conformational considerations and database searching Bioorg Med Chem Lett 13 2967-2971
  • [3] Furet P(2006)The purines: potent and versatile small molecule inhibitors and modulators of key biological targets Bioorg Med Chem 14 3987-4006
  • [4] Bold G(2004)Synthesis and anti-inflammatory, analgesic, ulcerogenic and lipid peroxidation activities of some new 2-[(2,6-dichloroanilino) phenyl]acetic acid derivatives Eur J Med Chem 39 535-545
  • [5] Hofmann F(2004)Sensible improvements induced by ionic liquids in the reaction of modified carbasugars with bases for the building of constrained carbanucleosides J Org Chem 69 2881-2883
  • [6] Manley P(2004)Effect of stereochemistry on the anti-HIV activity of chiral thiourea compounds Bioorg Med Chem 12 4275-4284
  • [7] Meyer T(1998)Rational design and synthesis of phenethyl-5-bromopyridyl thiourea derivatives as potent non-nucleoside inhibitors of HIV reverse transcriptase Bioorg Med Chem 6 1789-1797
  • [8] Altmann K-H(2004)Synthesis and evaluation of indenopyrazoles as cyclin-dependent kinase inhibitors. Part 4. Heterocycles at C3 Bioorg Med Chem Lett 14 343-346
  • [9] Legraverend M(2008)Synthesis and antimicrobial activity of some derivatives of acylhydrazine including novel benzenediazasulfonamides ARKIVOC 2 141-152
  • [10] Grierson DS(2007)Synthesis and anti-tumor activities of novel [1,2,4]triazolo[1,5-a]pyrimidines Molecules 12 1136-1146