Research Article
BibTex RIS Cite
Year 2019, Volume: 6 Issue: 3, 429 - 432, 20.10.2019
https://doi.org/10.18596/jotcsa.583845

Abstract

References

  • 1. Venkatesh P. Synthesis, characterization and antimicrobial activity of various schiff bases complexes of Zn(II) and Cu(II) ions. Asian J Pharm. Hea. Sci. 2011; 1: 8-11.
  • 2. Hussein MA, Omar RH, Farghaly HS. Design, synthesis, structure elucidation and biochemical evaluation of some schiff’s base derivatives bearing pyrazolo [3,4-D] pyrimidine-4-ones. Int. J. Acad Res. 2011; 3/2: 454-462.
  • 3. Nair R, Shah A, Baluja S, Chanda S. Synthesis and antibacterial activity of some schiff base complexes. J. Serb. Chem. Soc. 2006; 71: 733-44.
  • 4. Sathe BS, Jaychandran E, Jagtap VA, Sreenivasa GM. Synthesis characterization and anti-inflammatory evaluation of new fluorobenzothiazole schiff’s bases. Int. J. Pharm. Res. Dev. 2011; 3: 164-69.
  • 5. Pandey A, Dewangan D, Verma S, Mishra A, Dubey RD. Synthesis of schiff bases of 2-amino-5-aryl-1, 3, 4-thiadiazole and its analgesic, antiinflammatory, antibacterial and antitubercular activity. Int. J. Chem. Tech. Res. 2011; 3: 178-84.
  • 6. Fahmy HH, El-Eraky W, (2001) Synthesis and evaluation of analgesic and anti-inflammatory activities of O- substituted salicylamides. Arch. Pharm. Res. 24, 171-179.
  • 7. Chinnasamy RP, Sundararagan R, Govindaraj S, (2010) Synthesis, characterization and analgesic activity of novel Schiff base isatin derivatives. J. Adv. Pharm. Technol. Res. 1, 342-347.
  • 8. Ali MM, Jesmin M, Salam SMA, Khanam JA, Islam MF, Islam MN, (2009) Pesticidal activities of some schiff bases derived from benzoin, salicylaldehde, aminophenol and 2, 4- dinitrophenylhydrazine. J. Sci. Res. 1, 641-646.
  • 9. Jesmin M, Ali MM, Islam MN, (2008) Pesticidal Activity of some Schiff Base Complexes Derived from some Divalent Metal Acetates, Glycine and Salicylaldehyde. J. Sci. Found. 6, 49-56.
  • 10. Jon JK, Swieczkowski DM, Anthony JC, Truant JP, (1972) Fatty Acids and Derivatives as Antimicrobial Agents. Antimicrob. Agents Chemother. 2/1, 23-28.
  • 11. Maag H, (1984) Fatty acid derivatives: Important surfactants for household, cosmetic and industrial purposes. J. Am. Oil Chem. Soc. 61, 259-267.
  • 12. Pasha MA, Nanjundaswamy HM, (2004) Reductive fission of azoarenes to aminoarenes by aluminium/hydrazine hydrate. J. Chem. Res. 750-752.
  • 13. Hartley D, Kidd H, (1987) The Agrochemicals Hand Book, 2nd ed.; Royal Society of Chemistry: Nottingham, p 215.
  • 14. Maurer EW, Smith FD, (1980) Fatty acid amides and anilides, syntheses and antimicrobial properties. J. Am. Oil Chem. Soc. 57, 98-103.
  • 15. Shaikh MMA, Azad MAK, Jesmin M, Ahsan S, Rahman MM, Kraham JA, Islam MN, Shahria SMS, (2012) In vivo anticancer activity of vanillin semicarbazone. Asian Pac. J. Trop. Biomed. 438-442.
  • 16. Çelik H, Özeriş S, (1996) Synthesis of Even Numbered of (2-12) Monohydroxy Eicosanoic Acid Isomers. Chim. Acta Turc. 24, 23-27.

ANTICANCER ACTIVITIES OF EVEN NUMBERED MONOKETO EICOSANOIC ACID ANILIDES AND SEMICARBAZONES

Year 2019, Volume: 6 Issue: 3, 429 - 432, 20.10.2019
https://doi.org/10.18596/jotcsa.583845

Abstract

This study was undertaken to examine the possible
cytotoxic effect of anilide and semicarbazone derivatives of (4-12) monoketo eicosanoic
acids (3.125 – 100 µM)
on canine mammary tumour cell line (CMT-U27) as compared with doxorubicin.
Among these compounds, 8-semicarbazone eicosanoic acid (3) and 10-keto eicosanoic acid anilide (9) displayed effective cytotoxic potential against CMT-U27 and IC50
concentrations were recorded at 1.952
µM and 54.00 µM, respectively. 

References

  • 1. Venkatesh P. Synthesis, characterization and antimicrobial activity of various schiff bases complexes of Zn(II) and Cu(II) ions. Asian J Pharm. Hea. Sci. 2011; 1: 8-11.
  • 2. Hussein MA, Omar RH, Farghaly HS. Design, synthesis, structure elucidation and biochemical evaluation of some schiff’s base derivatives bearing pyrazolo [3,4-D] pyrimidine-4-ones. Int. J. Acad Res. 2011; 3/2: 454-462.
  • 3. Nair R, Shah A, Baluja S, Chanda S. Synthesis and antibacterial activity of some schiff base complexes. J. Serb. Chem. Soc. 2006; 71: 733-44.
  • 4. Sathe BS, Jaychandran E, Jagtap VA, Sreenivasa GM. Synthesis characterization and anti-inflammatory evaluation of new fluorobenzothiazole schiff’s bases. Int. J. Pharm. Res. Dev. 2011; 3: 164-69.
  • 5. Pandey A, Dewangan D, Verma S, Mishra A, Dubey RD. Synthesis of schiff bases of 2-amino-5-aryl-1, 3, 4-thiadiazole and its analgesic, antiinflammatory, antibacterial and antitubercular activity. Int. J. Chem. Tech. Res. 2011; 3: 178-84.
  • 6. Fahmy HH, El-Eraky W, (2001) Synthesis and evaluation of analgesic and anti-inflammatory activities of O- substituted salicylamides. Arch. Pharm. Res. 24, 171-179.
  • 7. Chinnasamy RP, Sundararagan R, Govindaraj S, (2010) Synthesis, characterization and analgesic activity of novel Schiff base isatin derivatives. J. Adv. Pharm. Technol. Res. 1, 342-347.
  • 8. Ali MM, Jesmin M, Salam SMA, Khanam JA, Islam MF, Islam MN, (2009) Pesticidal activities of some schiff bases derived from benzoin, salicylaldehde, aminophenol and 2, 4- dinitrophenylhydrazine. J. Sci. Res. 1, 641-646.
  • 9. Jesmin M, Ali MM, Islam MN, (2008) Pesticidal Activity of some Schiff Base Complexes Derived from some Divalent Metal Acetates, Glycine and Salicylaldehyde. J. Sci. Found. 6, 49-56.
  • 10. Jon JK, Swieczkowski DM, Anthony JC, Truant JP, (1972) Fatty Acids and Derivatives as Antimicrobial Agents. Antimicrob. Agents Chemother. 2/1, 23-28.
  • 11. Maag H, (1984) Fatty acid derivatives: Important surfactants for household, cosmetic and industrial purposes. J. Am. Oil Chem. Soc. 61, 259-267.
  • 12. Pasha MA, Nanjundaswamy HM, (2004) Reductive fission of azoarenes to aminoarenes by aluminium/hydrazine hydrate. J. Chem. Res. 750-752.
  • 13. Hartley D, Kidd H, (1987) The Agrochemicals Hand Book, 2nd ed.; Royal Society of Chemistry: Nottingham, p 215.
  • 14. Maurer EW, Smith FD, (1980) Fatty acid amides and anilides, syntheses and antimicrobial properties. J. Am. Oil Chem. Soc. 57, 98-103.
  • 15. Shaikh MMA, Azad MAK, Jesmin M, Ahsan S, Rahman MM, Kraham JA, Islam MN, Shahria SMS, (2012) In vivo anticancer activity of vanillin semicarbazone. Asian Pac. J. Trop. Biomed. 438-442.
  • 16. Çelik H, Özeriş S, (1996) Synthesis of Even Numbered of (2-12) Monohydroxy Eicosanoic Acid Isomers. Chim. Acta Turc. 24, 23-27.
There are 16 citations in total.

Details

Primary Language English
Journal Section Articles
Authors

Hülya Çelik Onar 0000-0003-2573-5751

Fatma Ceren Anlaş This is me 0000-0002-7997-016X

Hasniye Yaşa 0000-0003-3171-9096

Fulya Üstün Alkan 0000-0003-1782-9467

Belma Hasdemir 0000-0002-1071-1127

Tülay Bakırel 0000-0001-5805-2178

Publication Date October 20, 2019
Submission Date June 28, 2019
Acceptance Date September 27, 2019
Published in Issue Year 2019 Volume: 6 Issue: 3

Cite

Vancouver Çelik Onar H, Anlaş FC, Yaşa H, Üstün Alkan F, Hasdemir B, Bakırel T. ANTICANCER ACTIVITIES OF EVEN NUMBERED MONOKETO EICOSANOIC ACID ANILIDES AND SEMICARBAZONES. JOTCSA. 2019;6(3):429-32.