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The Synthesis and Anti-cancer Activities of Ferrocenyl Chalcones; Drug-Likeness Calculations

Year 2021, , 690 - 703, 18.06.2021
https://doi.org/10.29137/umagd.927358

Abstract

A series of 1-8 different ferrocenyl chalcones were synthesized through the Claisen–Schmidt condensation and the Friedel−Crafts acylation. Their structures were confirmed by means of 1H, 13C NMR and FT-IR. The cytotoxic and antiproliferative activities of the chalcones were screened against HeLa (cervix cancer) and PC3 (prostate cancer) cell lines. They showed excellent anti-cancer activities especially against PC3 cell even at very low concentration (5 µM). Also, their physicochemical properties, drug-likeness calculations and the rule of five (RO5) were investigated.

Supporting Institution

Scientific Research Projects Coordination Unit of Kırıkkale University

Project Number

2018/85

References

  • Baba, K., Nakata, K., Taniguchi, M., Kido, T., & Kozawa, M. (1990). Chalcones from Angelica keiskei. Phytochemistry, 29, 3907-3910. https://doi.org/10.1016/0031-9422(90)85357-L
  • Boumendjel, A., Ronot, X., & Boutonnat, J. (2009). Chalcones Derivatives Acting as Cell Cycle Blockers: Potential Anti Cancer Drugs?. Current Drug Targets, 10, 363-371. https://doi.org/10.2174/138945009787846416
  • Dogan, Ö., Şenol, V., Zeytinci, H., Koyuncu, H., & Bulut, A. (2005). Efficient synthesis of ferrocenylenones by Friedel-Crafts acylation with EtAlCl2-Me3Al. Journal of Organometallic Chemistry, 690, 430-434. https://doi:10.1016/j.jorganchem.2004.09.055
  • Hano, Y., Ichikawa, K., Okuyama, M., Yamanaka, J., Miyoshi, T., & Nomura, T. (1995). Sanggenons R, S, and T, three new isoprenylated phenols from the Chinese crude drug Sang-Bai-Pi (Morus root bark). Heterocycles, 2, 953–965. http://doi.org/10.3987/COM-94-S96
  • Harborne, J. B., Mabry, T. J., & Mabry, H. (1975). The flavonoids. Chapman and Hall, London. https://doi.org/10.1007/978-1-4899-2909-9
  • Janka, V., Zatko, D., Ladislav, V., Pal, P., & Gabriela, M. (2015). Some ferrocenyl chalcones as useful candidates for cancer treatment. In Vitro Cellular & Development Biology-Animal, 51, 964–974. http://doi.org/10.1007/s11626-015-9919-6
  • Kakati, D., & Sarma, J. C. (2011). Microwave-assisted solvent free synthesis of 1, 3-diphenyl propenones. Chemistry Central Journal, 5(1), 8. https://doi.org/10.1186/1752-153X-5-8
  • Li, Y., Ishibashi, M., Chen, X., & Ohizumu, Y. (2003). Littorachalcone, a new enhancer of NGF-mediated neurite outgrowth, from Verbena littoralis. Chemical & Pharmaceutical Bulletin, 51, 872-874. https://doi.org/10.1248/cpb.51.872
  • Lopez, J.A., Barillas, W, Gomez-Laurito, J, Martin, G.E., Lin, F.T., Al-Rehaily, A.J., Zemaitis, M.A., & Schiff, P.L. (1998). Galiposin: a new β-hydroxy chalcone from Galipea granulosa. Planta Medica, 64, 76–77. http://doi.org/10.1055/s-2006-957373
  • Masesane, I.B., Yeboah, S.O., Liebscher, J., Mügge, C., & Abegaz, B.M. (2000). A bichalcone from the twigs of Rhus pyroides. Phytochemistry, 53, 1005–1008. . https://doi.org/10.1016/S0031-9422(99)00553-1
  • Muskinja, J., Burmudzija, A., Ratkovic, Z., Rankovic, B., Kosanic, M., Bogdanovic, G.A., & Novakovic, S.B. (2016). Ferrocenyl chalcones with O-alkylated vanillins: synthesis, spectral characterization, microbiological evaluation, and single-crystal X-ray analysis. Medicinal Chemistry Research, 25, 1744–1753. https://doi.org/10.1007/s00044-016-1609-8
  • Parkin, D.M., Bray, F., Felay, J., & Pisani, B. (2005). Global Cancer Statistics 2002, CA. Cancer Journal for Clinicians, 55, 74-108. https://doi.org/10.3322/canjclin.55.2.74
  • Petignat, P., & Roy, M. (2007). Diagnosis and management of cervical cancer. BMJ, 335, 765-768. http://doi:10.1136/bmj.39337.615197.80
  • Prakash, O., Kumar, A., Sadana, A., Prakash, R., Singh, S.P., Claramunt, R.M., Sanz, D., Alkorta, I., & Elguero, J. (2005). Study of the reaction of chalcone analogs of dehydroacetic acid and o-aminothiophenol: synthesis and structure of 1,5-benzothiazepines and 1,4-benzothiazines. Tetrahedron, 61, 6642-6651. https://doi.org/10.1016/j.tet.2005.03.035
  • Shotter, R. G., Johnston, K. M., & Jones, J. F. (1978). Reactions of unsaturated acid halides IV1: Competitive Friedel-Crafts acylation and alkylations of monohalogenobenzenes by the bifunctional cinnamoyl chloride. Tetrahedron, 34, 741−746. https://doi.org/10.1016/0040-4020(78)88113-7
  • Smith, H. E., & Paulson, M. C. (1954). The preparation of chalcones from hydroxy and methoxy aldehydes and ketones. Journal of American Chemical Society, 76, 4486–4487. https://doi.org/10.1021/ja01646a072
  • Tanaka, T., Iınuma, M., Yuki, K., Fujii, Y., & Mizuno, M. (1991). Two New β-Hydroxychalcones from the Root Bark of Pongamia pinnata. Chemical and Pharmaceutical Bulletin, 39, 1473-1475. https://doi.org/10.1248/cpb.39.1473
  • Tomasch, M., Schwed, J. S., & Stark, H. (2012). Novel chalcone based fluorescent human histamine h(3) receptor ligands as pharmacological tools. Frontiers in Systems Neuroscience, 6, 14. https://doi.org/10.3389/fnsys.2012.00014
  • Yadav, D.K., Kaushik, P., Pankaj, Rana V.S., Kamil, D., Khatri, D., & Shakil, N.A. (2019). Microwave Assisted Synthesis, Characterization and Biological Activities of Ferrocenyl Chalcones and Their QSAR Analysis. Frontiers in Chemistry, 7, 814. http://doi:10.3389/fchem.2019.00814
  • Zhuang, C., Zhang, W., Sheng, C., Zhang, W., Xing, C., & Miao, Z. (2017). Chalcone: A Privileged Structure in Medicinal Chemistry. Chemical Reviews, 117, 7762−7810. https://doi.org/10.1021/acs.chemrev.7b00020
  • Zou, G., Guo, J. P., Wang, Z. Y., Huang, W., & Tang, J. (2007). Heck type coupling vs. conjugate addition in phosphine-rhodium catalyzed reactions of aryl boronic acids with α,β-unsaturated carbonyl compounds: a systematic investigation. Dalton Transactions, 28, 3055-3064. https://doi.org/10.1039/B615473E

Ferrosenil Kalkonların Sentezi ve Anti-kanser Aktiviteleri; İlaç Benzerlik Hesaplamaları

Year 2021, , 690 - 703, 18.06.2021
https://doi.org/10.29137/umagd.927358

Abstract

Claisen - Schmidt kondenzasyonu ve Friedel - Crafts açilleme tepkimeleri ile 1-8 farklı ferrosenil çalkon sentezlendi. Yapıları 1H NMR, 13C NMR and FT-IR ile aydınlatılmıştır. Çalkonların sitotoksik ve antiproliferatif aktiviteleri, HeLa (rahim kanseri) ve PC3 (prostat kanseri) hücre hatlarına karşı tarandı. Çok düşük konsantrasyonda (5 µM) bile özellikle PC3 hücresine karşı mükemmel anti-kanser aktivite gösterdiler. Ayrıca fizikokimyasal özellikleri, ilaç benzerliği hesaplamaları ve beş kuralı (RO5) araştırıldı.

Project Number

2018/85

References

  • Baba, K., Nakata, K., Taniguchi, M., Kido, T., & Kozawa, M. (1990). Chalcones from Angelica keiskei. Phytochemistry, 29, 3907-3910. https://doi.org/10.1016/0031-9422(90)85357-L
  • Boumendjel, A., Ronot, X., & Boutonnat, J. (2009). Chalcones Derivatives Acting as Cell Cycle Blockers: Potential Anti Cancer Drugs?. Current Drug Targets, 10, 363-371. https://doi.org/10.2174/138945009787846416
  • Dogan, Ö., Şenol, V., Zeytinci, H., Koyuncu, H., & Bulut, A. (2005). Efficient synthesis of ferrocenylenones by Friedel-Crafts acylation with EtAlCl2-Me3Al. Journal of Organometallic Chemistry, 690, 430-434. https://doi:10.1016/j.jorganchem.2004.09.055
  • Hano, Y., Ichikawa, K., Okuyama, M., Yamanaka, J., Miyoshi, T., & Nomura, T. (1995). Sanggenons R, S, and T, three new isoprenylated phenols from the Chinese crude drug Sang-Bai-Pi (Morus root bark). Heterocycles, 2, 953–965. http://doi.org/10.3987/COM-94-S96
  • Harborne, J. B., Mabry, T. J., & Mabry, H. (1975). The flavonoids. Chapman and Hall, London. https://doi.org/10.1007/978-1-4899-2909-9
  • Janka, V., Zatko, D., Ladislav, V., Pal, P., & Gabriela, M. (2015). Some ferrocenyl chalcones as useful candidates for cancer treatment. In Vitro Cellular & Development Biology-Animal, 51, 964–974. http://doi.org/10.1007/s11626-015-9919-6
  • Kakati, D., & Sarma, J. C. (2011). Microwave-assisted solvent free synthesis of 1, 3-diphenyl propenones. Chemistry Central Journal, 5(1), 8. https://doi.org/10.1186/1752-153X-5-8
  • Li, Y., Ishibashi, M., Chen, X., & Ohizumu, Y. (2003). Littorachalcone, a new enhancer of NGF-mediated neurite outgrowth, from Verbena littoralis. Chemical & Pharmaceutical Bulletin, 51, 872-874. https://doi.org/10.1248/cpb.51.872
  • Lopez, J.A., Barillas, W, Gomez-Laurito, J, Martin, G.E., Lin, F.T., Al-Rehaily, A.J., Zemaitis, M.A., & Schiff, P.L. (1998). Galiposin: a new β-hydroxy chalcone from Galipea granulosa. Planta Medica, 64, 76–77. http://doi.org/10.1055/s-2006-957373
  • Masesane, I.B., Yeboah, S.O., Liebscher, J., Mügge, C., & Abegaz, B.M. (2000). A bichalcone from the twigs of Rhus pyroides. Phytochemistry, 53, 1005–1008. . https://doi.org/10.1016/S0031-9422(99)00553-1
  • Muskinja, J., Burmudzija, A., Ratkovic, Z., Rankovic, B., Kosanic, M., Bogdanovic, G.A., & Novakovic, S.B. (2016). Ferrocenyl chalcones with O-alkylated vanillins: synthesis, spectral characterization, microbiological evaluation, and single-crystal X-ray analysis. Medicinal Chemistry Research, 25, 1744–1753. https://doi.org/10.1007/s00044-016-1609-8
  • Parkin, D.M., Bray, F., Felay, J., & Pisani, B. (2005). Global Cancer Statistics 2002, CA. Cancer Journal for Clinicians, 55, 74-108. https://doi.org/10.3322/canjclin.55.2.74
  • Petignat, P., & Roy, M. (2007). Diagnosis and management of cervical cancer. BMJ, 335, 765-768. http://doi:10.1136/bmj.39337.615197.80
  • Prakash, O., Kumar, A., Sadana, A., Prakash, R., Singh, S.P., Claramunt, R.M., Sanz, D., Alkorta, I., & Elguero, J. (2005). Study of the reaction of chalcone analogs of dehydroacetic acid and o-aminothiophenol: synthesis and structure of 1,5-benzothiazepines and 1,4-benzothiazines. Tetrahedron, 61, 6642-6651. https://doi.org/10.1016/j.tet.2005.03.035
  • Shotter, R. G., Johnston, K. M., & Jones, J. F. (1978). Reactions of unsaturated acid halides IV1: Competitive Friedel-Crafts acylation and alkylations of monohalogenobenzenes by the bifunctional cinnamoyl chloride. Tetrahedron, 34, 741−746. https://doi.org/10.1016/0040-4020(78)88113-7
  • Smith, H. E., & Paulson, M. C. (1954). The preparation of chalcones from hydroxy and methoxy aldehydes and ketones. Journal of American Chemical Society, 76, 4486–4487. https://doi.org/10.1021/ja01646a072
  • Tanaka, T., Iınuma, M., Yuki, K., Fujii, Y., & Mizuno, M. (1991). Two New β-Hydroxychalcones from the Root Bark of Pongamia pinnata. Chemical and Pharmaceutical Bulletin, 39, 1473-1475. https://doi.org/10.1248/cpb.39.1473
  • Tomasch, M., Schwed, J. S., & Stark, H. (2012). Novel chalcone based fluorescent human histamine h(3) receptor ligands as pharmacological tools. Frontiers in Systems Neuroscience, 6, 14. https://doi.org/10.3389/fnsys.2012.00014
  • Yadav, D.K., Kaushik, P., Pankaj, Rana V.S., Kamil, D., Khatri, D., & Shakil, N.A. (2019). Microwave Assisted Synthesis, Characterization and Biological Activities of Ferrocenyl Chalcones and Their QSAR Analysis. Frontiers in Chemistry, 7, 814. http://doi:10.3389/fchem.2019.00814
  • Zhuang, C., Zhang, W., Sheng, C., Zhang, W., Xing, C., & Miao, Z. (2017). Chalcone: A Privileged Structure in Medicinal Chemistry. Chemical Reviews, 117, 7762−7810. https://doi.org/10.1021/acs.chemrev.7b00020
  • Zou, G., Guo, J. P., Wang, Z. Y., Huang, W., & Tang, J. (2007). Heck type coupling vs. conjugate addition in phosphine-rhodium catalyzed reactions of aryl boronic acids with α,β-unsaturated carbonyl compounds: a systematic investigation. Dalton Transactions, 28, 3055-3064. https://doi.org/10.1039/B615473E
There are 21 citations in total.

Details

Primary Language English
Subjects Engineering
Journal Section Articles
Authors

Emine Albayrak This is me 0000-0003-4022-0860

Özer Işılar 0000-0001-7547-2537

Mutluhan Bıyıkoğlu 0000-0003-0752-2242

Ayşe Şahin Yağlıoğlu 0000-0002-7668-6286

Adnan Bulut 0000-0001-9322-0325

Project Number 2018/85
Publication Date June 18, 2021
Submission Date April 27, 2021
Published in Issue Year 2021

Cite

APA Albayrak, E., Işılar, Ö., Bıyıkoğlu, M., Şahin Yağlıoğlu, A., et al. (2021). The Synthesis and Anti-cancer Activities of Ferrocenyl Chalcones; Drug-Likeness Calculations. International Journal of Engineering Research and Development, 13(2), 690-703. https://doi.org/10.29137/umagd.927358

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