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SYNTHESIS AND EVALUATION OF NEW IMIDAZO[2,1-b]THIAZOLES AS ANTITUBERCULOSIS AGENTS

Year 2017, Volume: 21 Issue: 1, 102 - 109, 20.09.2016
https://doi.org/10.12991/marupj.259887

Abstract

New N’-(arylidene)-2-[6-(4-bromophenyl)imidazo[2,1-b]thiazol-3-yl]acetohydrazides (3a-i) were synthesized by reacting 2-[6-(4-bromophenyl)imidazo[2,1-b]thiazol-3-yl]acetohydrazide with different aromatic aldehydes. The structures of the title compounds were established by spectral data (IR, 1H NMR, 13C NMR) and  elemental  analyses.  The   synthesized  compounds  were  evaluated  for  in vitro antimycobacterial activity   against  Mycobacterium tuberculosis  H37Rv  employing  the  BACTEC 460 radiometric system. The   compounds  exhibited  varying  degrees  of   inhibition  in  the  in vitro primary screening  that  was conducted  at  a  concentration  of  6.25 mg/ml.  Among  the  synthesized compounds  [6-(4-bromophenyl) imidazo[2,1-b]thiazol-3-yl]acetic acid  2,4-dinitrobenzylidenehydrazide (3e)  was  found to be the most active compound in vitro with MIC of 6.25 mg/ml.

References

  • REFERENCES
  • Tuberculosis; World Health Organization: Geneva, 2014; http://www.who.int/tb/research/en/.
  • Singh MM. XDR-TB-Danger ahead. Indian J Tuberc 2007; 54: 1-2.
  • Remers WA. Antineoplastic Agents. In: Wilson and Gisvold's Textbook of Organic Medicinal and Pharmaceutical Chemistry. 10th ed. Delgado JN and Remers WA. eds. Lippincott-Raven: Philadelphia, 1998; p. 391.
  • Andreani A, Granaiola M, Leoni A, Locatelli A, Morigi R, Rambaldi M. Synthesis and antitubercular activity of imidazo[2,1-b]thiazoles. Eur J Med Chem 2001; 36: 743-46.
  • Cesur Z, Güner H, Ötük G. Synthesis and antimycobacterial activity of new imidazo[2,1-b]thiazole derivatives. Eur J Med Chem 1994; 29: 981-83.
  • Park JH, El-Gamal MI, Lee YS, Oh CH. New imidazo[2,1-b]thiazole derivatives: Synthesis, in vitro anticancer evaluation, and in silico studies. Eur J Med Chem 2011; 46: 5769-77.
  • Andreani A, Granaiola M, Guardigli M, Leoni A, Locatelli A, Morigi R, Rambaldi M, Roda A. Synthesis and chemiluminescent high throughput screening for inhibition of acetylcholinesterase activity by imidazo[2,1-b]thiazole derivatives. Eur J Med Chem 2005; 40: 1331-34.
  • Budriesi R, Ioan P, Locatelli A, Cosconati S, Leoni A, Ugenti MP, Andreani A, Di Toro R, Bedini A, Spampinato S, Marinelli L, Novellino E, Chiarini A. Imidazo[2,1-b]thiazole system: A scaffold endowing dihydropyridines with selective cardiodepressant activity. J Med Chem 2008; 51: 1592-1600.
  • Shetty NS, Khazi IAM, Ahn C. Synthesis, anthelmintic and anti-inflammatory activities of some novel imidazothiazole sulfides and sulfones. Bull Korean Chem Soc 2010; 31: 2337-40.
  • Juspin T, Laget M, Terme T, Azas N, Vanelle P. TDAE-assisted synthesis of new imidazo[2,1-b]thiazole derivatives as anti-infectious agents. Eur J Med Chem 2010; 45: 840-45.
  • Wang NY, Xu Y, Zuo WQ, Xiao KJ, Liu L, Zeng XX, You XY, Zhang LD, Gao C, Liu ZH, Ye TH, Xia Y, Xiong Y, Song XJ, Lei Q, Peng CT, Tang H, Yang SY, Wei YQ, Yu LT. Discovery of imidazo[2,1-b]thiazole HCV NS4B inhibitors exhibiting synergistic effect with other direct-acting antiviral agents. J Med Chem 2015; 58; 2764-78.
  • Sah PPT, Peoples SA. Isonicotinyl hydrazones as antitubercular agents and derivatives for identification of aldehydes and ketones. J Am Pharm Ass Sci Ed 1954; 43: 513–24.
  • Isler O, Gutmann H, Straub O, Fust B, Böhni E, Studer A. Chemotherapie der experimentellen Tuberkulose III. Derivate des 2-Methyl-isonicotinsäurehydrazids. Helv Chim Acta 1955; 38: 1046-60.
  • Chakravarty D, Bose A, Bose S. Synthesis and antitubercular activity of isonicotinoyl and cyanoacetyl hydrazones. J Pharm Sci 1964; 53: 1036-39.
  • Thomas KD, Adhikari AV, Telkar S, Chowdhury IH, Mahmood R, Pal NK, Row G, Sumesh E. Design, synthesis and docking studies of new quinoline-3-carbohydrazide derivatives as antitubercular agents. Eur J Med Chem 2011; 46: 5283-92.
  • Küçükgüzel ŞG, Rollas S, Küçükgüzel İ, Kiraz M, Synthesis and antimycobacterial activity of some coupling products from 4-aminobenzoic acid antimycobacterial activity of some coupling products from 4-aminobenzoic acid hydrazones. Eur J Med Chem 1999; 34: 1093-1100.
  • Cui Z, Li Y, Ling Y, Huang J, Cui J, Wang R, Yang X. New class of potent antitumor acylhydrazone derivatives containing furan. Eur J Med Chem 2010; 45: 5576-84.
  • Ulusoy N, Çapan G, Ötük G, Kiraz M. Synthesis and antimicrobial activity of new 6-phenylimidazo[2,1-b]thiazole derivatives. Boll Chim Farmac 2000; 139: 167-72.
  • Ulusoy, N. Synthesis and antituberculosis activity of cycloalkylidenehydrazide and 4- aza-1-thiaspiro[4.5]decan-3-one derivatives of imidazo[2,1-b]thiazole. Arzneim- Forsch/Drug Res 2002; 52: 565-71.
  • Ulusoy N, Kiraz M, Küçükbasmacı Ö. New 6-(4-bromophenyl)-imidazo[2,1-b]thiazole derivatives: Synthesis and antimicrobial activity. Monatsh Chem 2002; 133: 1305-15.
  • Ulusoy N, Küçükbasmacı Ö. Synthesis and antimicrobial activity evaluation of new 1,2,4- triazoles and 1,3,4-thiadiazoles bearing imidazo[2,1-b]thiazole moiety. Eur J Med Chem 2010; 45: 63-68.
  • Robert JF, Boukraa S, Panouse JJ, Loppinet V, Chaumont JP. Dérivés de l’imidazo[2,1-b]thiazole X. Propriétés fongistatiques de 2-aminothiazoles et de 6- aryl imidazo[2,1-b]thiazoles substitués respectivement en 4 et en 3 par un reste aryléthyle, aroylméthyle, β-hydroxy β-aryléthyle et et éthoxycarbonylméthyle. Eur J Med Chem 1990; 25: 731-36.
  • Kühmstedt H, Kottke K, Knoke D, Robert JF, Panouse JJ. Synthesis of amides and heterocyclic acylhydrazides with potential immunomodulator properties. Ann Pharm Fr 1983; 40: 425-29.
  • Collins L, Franzblau SG. Microplate alamar blue assay versus BACTEC 460
  • system for high-throughput screening of compounds against Mycobacterium tuberculosis
  • and Mycobacterium avium. Antimicrob Agents Chemother 1997; 41: 1004-9.
  • Inderleid CB.; in: Lorian V. (ed.), Antibiotics in Laboratory Medicine, 3rd ed.,
  • Williams  Wilkins, Baltimore 1991, p. 134.
  • Robert JF., Xicluna A, Panouse JJ. Advances in heterocyclic chemistry. Eur J Med Chem
  • Chim Ther 1975; 10: 59-64.
  • Harraga S, Nicod L, Drouhin JP, Xicluna A, Panouse JJ, Seilles E, Robert JF.
  • Imidazo[2,1-b]thiazole derivatives. XI. Modulation of the CD2-receptor of
  • human T trypsinized lymphocytes by several imidazo[2,1-b]thiazoles. Eur J Med
  • Chem 994; 29: 309-15.
  • Gürsoy E, Ulusoy Güzeldemirci N. Synthesis and primary cytotoxicity evaluation of
  • new imidazo[2,1-b]thiazole derivatives. Eur J Med Chem 2007; 42: 320-26.
  • Çapan G, Ulusoy N, Ergenç N, Kiraz M. New 6-phenylimidazo[2,1-b]thiazole
  • derivatives: Synthesis and antifungal activity. Monatsh Chem 1999; 130: 1399-1407.
  • Gürsoy A, Demirayak Ş, Cesur Z, Reisch J, Ötük G. Synthesis of some
  • hydrazide-hydrazones, thiosemicarbazides, thiadiazoles, triazoles and their derivatives
  • as possible antimicrobiales. Pharmazie 1990; 45: 246-250.

Yeni imidaz o[2,1-b]tiyazol türevlerinin sentezi ve antitüberküler etkilerinin değerlendirilmesi

Year 2017, Volume: 21 Issue: 1, 102 - 109, 20.09.2016
https://doi.org/10.12991/marupj.259887

Abstract

2-[6-(4-Bromofenil)imidazo[2,1-b]tiyazol-3-il]asetohidrazit  ile farklı aromatik aldehitlerin
reaksiyonundan yeni N’-  (ariliden)-2-[6-(4-bromofenil)imidazo[2,1-b]tiyazol-3-il]  asetohidrazitler (3a-i) elde edilmiştir. Elde
edilen bileşiklerin  yapıları spektral
veriler (IR, 1H NMR, 13C NMR) ve elementel 
analiz ile saptanmıştır. Sentezlenen bileşiklerin Mycobacterium  tuberculosis H37Rv’ye karşı
antimikobakteriyel aktiviteleri  BACTEC
460 radyometrik sistem kullanılarak tayin edilmiştir.  Bileşikler, 6.25 mg/ml konsantrasyonda
gerçekleştirilen  in vitro primer tarama
testlerinde değişik derecelerde  inhibisyon
göstermişlerdir. Sentezlenen bileşikler arasında  [6-(4-bromofenil)imidazo[2,1-b]tiyazol-3-il]asetik
asit  2,4-dinitrobenzilidenhidrazit (3e),
in vitro 6.25 mg/ml MIC  değeri ile
aktivitesi en yüksek bileşik olarak bulunmuştur.  

References

  • REFERENCES
  • Tuberculosis; World Health Organization: Geneva, 2014; http://www.who.int/tb/research/en/.
  • Singh MM. XDR-TB-Danger ahead. Indian J Tuberc 2007; 54: 1-2.
  • Remers WA. Antineoplastic Agents. In: Wilson and Gisvold's Textbook of Organic Medicinal and Pharmaceutical Chemistry. 10th ed. Delgado JN and Remers WA. eds. Lippincott-Raven: Philadelphia, 1998; p. 391.
  • Andreani A, Granaiola M, Leoni A, Locatelli A, Morigi R, Rambaldi M. Synthesis and antitubercular activity of imidazo[2,1-b]thiazoles. Eur J Med Chem 2001; 36: 743-46.
  • Cesur Z, Güner H, Ötük G. Synthesis and antimycobacterial activity of new imidazo[2,1-b]thiazole derivatives. Eur J Med Chem 1994; 29: 981-83.
  • Park JH, El-Gamal MI, Lee YS, Oh CH. New imidazo[2,1-b]thiazole derivatives: Synthesis, in vitro anticancer evaluation, and in silico studies. Eur J Med Chem 2011; 46: 5769-77.
  • Andreani A, Granaiola M, Guardigli M, Leoni A, Locatelli A, Morigi R, Rambaldi M, Roda A. Synthesis and chemiluminescent high throughput screening for inhibition of acetylcholinesterase activity by imidazo[2,1-b]thiazole derivatives. Eur J Med Chem 2005; 40: 1331-34.
  • Budriesi R, Ioan P, Locatelli A, Cosconati S, Leoni A, Ugenti MP, Andreani A, Di Toro R, Bedini A, Spampinato S, Marinelli L, Novellino E, Chiarini A. Imidazo[2,1-b]thiazole system: A scaffold endowing dihydropyridines with selective cardiodepressant activity. J Med Chem 2008; 51: 1592-1600.
  • Shetty NS, Khazi IAM, Ahn C. Synthesis, anthelmintic and anti-inflammatory activities of some novel imidazothiazole sulfides and sulfones. Bull Korean Chem Soc 2010; 31: 2337-40.
  • Juspin T, Laget M, Terme T, Azas N, Vanelle P. TDAE-assisted synthesis of new imidazo[2,1-b]thiazole derivatives as anti-infectious agents. Eur J Med Chem 2010; 45: 840-45.
  • Wang NY, Xu Y, Zuo WQ, Xiao KJ, Liu L, Zeng XX, You XY, Zhang LD, Gao C, Liu ZH, Ye TH, Xia Y, Xiong Y, Song XJ, Lei Q, Peng CT, Tang H, Yang SY, Wei YQ, Yu LT. Discovery of imidazo[2,1-b]thiazole HCV NS4B inhibitors exhibiting synergistic effect with other direct-acting antiviral agents. J Med Chem 2015; 58; 2764-78.
  • Sah PPT, Peoples SA. Isonicotinyl hydrazones as antitubercular agents and derivatives for identification of aldehydes and ketones. J Am Pharm Ass Sci Ed 1954; 43: 513–24.
  • Isler O, Gutmann H, Straub O, Fust B, Böhni E, Studer A. Chemotherapie der experimentellen Tuberkulose III. Derivate des 2-Methyl-isonicotinsäurehydrazids. Helv Chim Acta 1955; 38: 1046-60.
  • Chakravarty D, Bose A, Bose S. Synthesis and antitubercular activity of isonicotinoyl and cyanoacetyl hydrazones. J Pharm Sci 1964; 53: 1036-39.
  • Thomas KD, Adhikari AV, Telkar S, Chowdhury IH, Mahmood R, Pal NK, Row G, Sumesh E. Design, synthesis and docking studies of new quinoline-3-carbohydrazide derivatives as antitubercular agents. Eur J Med Chem 2011; 46: 5283-92.
  • Küçükgüzel ŞG, Rollas S, Küçükgüzel İ, Kiraz M, Synthesis and antimycobacterial activity of some coupling products from 4-aminobenzoic acid antimycobacterial activity of some coupling products from 4-aminobenzoic acid hydrazones. Eur J Med Chem 1999; 34: 1093-1100.
  • Cui Z, Li Y, Ling Y, Huang J, Cui J, Wang R, Yang X. New class of potent antitumor acylhydrazone derivatives containing furan. Eur J Med Chem 2010; 45: 5576-84.
  • Ulusoy N, Çapan G, Ötük G, Kiraz M. Synthesis and antimicrobial activity of new 6-phenylimidazo[2,1-b]thiazole derivatives. Boll Chim Farmac 2000; 139: 167-72.
  • Ulusoy, N. Synthesis and antituberculosis activity of cycloalkylidenehydrazide and 4- aza-1-thiaspiro[4.5]decan-3-one derivatives of imidazo[2,1-b]thiazole. Arzneim- Forsch/Drug Res 2002; 52: 565-71.
  • Ulusoy N, Kiraz M, Küçükbasmacı Ö. New 6-(4-bromophenyl)-imidazo[2,1-b]thiazole derivatives: Synthesis and antimicrobial activity. Monatsh Chem 2002; 133: 1305-15.
  • Ulusoy N, Küçükbasmacı Ö. Synthesis and antimicrobial activity evaluation of new 1,2,4- triazoles and 1,3,4-thiadiazoles bearing imidazo[2,1-b]thiazole moiety. Eur J Med Chem 2010; 45: 63-68.
  • Robert JF, Boukraa S, Panouse JJ, Loppinet V, Chaumont JP. Dérivés de l’imidazo[2,1-b]thiazole X. Propriétés fongistatiques de 2-aminothiazoles et de 6- aryl imidazo[2,1-b]thiazoles substitués respectivement en 4 et en 3 par un reste aryléthyle, aroylméthyle, β-hydroxy β-aryléthyle et et éthoxycarbonylméthyle. Eur J Med Chem 1990; 25: 731-36.
  • Kühmstedt H, Kottke K, Knoke D, Robert JF, Panouse JJ. Synthesis of amides and heterocyclic acylhydrazides with potential immunomodulator properties. Ann Pharm Fr 1983; 40: 425-29.
  • Collins L, Franzblau SG. Microplate alamar blue assay versus BACTEC 460
  • system for high-throughput screening of compounds against Mycobacterium tuberculosis
  • and Mycobacterium avium. Antimicrob Agents Chemother 1997; 41: 1004-9.
  • Inderleid CB.; in: Lorian V. (ed.), Antibiotics in Laboratory Medicine, 3rd ed.,
  • Williams  Wilkins, Baltimore 1991, p. 134.
  • Robert JF., Xicluna A, Panouse JJ. Advances in heterocyclic chemistry. Eur J Med Chem
  • Chim Ther 1975; 10: 59-64.
  • Harraga S, Nicod L, Drouhin JP, Xicluna A, Panouse JJ, Seilles E, Robert JF.
  • Imidazo[2,1-b]thiazole derivatives. XI. Modulation of the CD2-receptor of
  • human T trypsinized lymphocytes by several imidazo[2,1-b]thiazoles. Eur J Med
  • Chem 994; 29: 309-15.
  • Gürsoy E, Ulusoy Güzeldemirci N. Synthesis and primary cytotoxicity evaluation of
  • new imidazo[2,1-b]thiazole derivatives. Eur J Med Chem 2007; 42: 320-26.
  • Çapan G, Ulusoy N, Ergenç N, Kiraz M. New 6-phenylimidazo[2,1-b]thiazole
  • derivatives: Synthesis and antifungal activity. Monatsh Chem 1999; 130: 1399-1407.
  • Gürsoy A, Demirayak Ş, Cesur Z, Reisch J, Ötük G. Synthesis of some
  • hydrazide-hydrazones, thiosemicarbazides, thiadiazoles, triazoles and their derivatives
  • as possible antimicrobiales. Pharmazie 1990; 45: 246-250.
There are 42 citations in total.

Details

Subjects Health Care Administration
Journal Section Articles
Authors

Nuray Ulusoy

Elif Gürsoy This is me

Publication Date September 20, 2016
Published in Issue Year 2017 Volume: 21 Issue: 1

Cite

APA Ulusoy, N., & Gürsoy, E. (2016). SYNTHESIS AND EVALUATION OF NEW IMIDAZO[2,1-b]THIAZOLES AS ANTITUBERCULOSIS AGENTS. Marmara Pharmaceutical Journal, 21(1), 102-109. https://doi.org/10.12991/marupj.259887
AMA Ulusoy N, Gürsoy E. SYNTHESIS AND EVALUATION OF NEW IMIDAZO[2,1-b]THIAZOLES AS ANTITUBERCULOSIS AGENTS. J Res Pharm. September 2016;21(1):102-109. doi:10.12991/marupj.259887
Chicago Ulusoy, Nuray, and Elif Gürsoy. “SYNTHESIS AND EVALUATION OF NEW IMIDAZO[2,1-b]THIAZOLES AS ANTITUBERCULOSIS AGENTS”. Marmara Pharmaceutical Journal 21, no. 1 (September 2016): 102-9. https://doi.org/10.12991/marupj.259887.
EndNote Ulusoy N, Gürsoy E (September 1, 2016) SYNTHESIS AND EVALUATION OF NEW IMIDAZO[2,1-b]THIAZOLES AS ANTITUBERCULOSIS AGENTS. Marmara Pharmaceutical Journal 21 1 102–109.
IEEE N. Ulusoy and E. Gürsoy, “SYNTHESIS AND EVALUATION OF NEW IMIDAZO[2,1-b]THIAZOLES AS ANTITUBERCULOSIS AGENTS”, J Res Pharm, vol. 21, no. 1, pp. 102–109, 2016, doi: 10.12991/marupj.259887.
ISNAD Ulusoy, Nuray - Gürsoy, Elif. “SYNTHESIS AND EVALUATION OF NEW IMIDAZO[2,1-b]THIAZOLES AS ANTITUBERCULOSIS AGENTS”. Marmara Pharmaceutical Journal 21/1 (September 2016), 102-109. https://doi.org/10.12991/marupj.259887.
JAMA Ulusoy N, Gürsoy E. SYNTHESIS AND EVALUATION OF NEW IMIDAZO[2,1-b]THIAZOLES AS ANTITUBERCULOSIS AGENTS. J Res Pharm. 2016;21:102–109.
MLA Ulusoy, Nuray and Elif Gürsoy. “SYNTHESIS AND EVALUATION OF NEW IMIDAZO[2,1-b]THIAZOLES AS ANTITUBERCULOSIS AGENTS”. Marmara Pharmaceutical Journal, vol. 21, no. 1, 2016, pp. 102-9, doi:10.12991/marupj.259887.
Vancouver Ulusoy N, Gürsoy E. SYNTHESIS AND EVALUATION OF NEW IMIDAZO[2,1-b]THIAZOLES AS ANTITUBERCULOSIS AGENTS. J Res Pharm. 2016;21(1):102-9.

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