The Synthesis and Anti-cancer Activities of Ferrocenyl Chalcones; Drug-Likeness Calculations
Year 2021,
Volume: 13 Issue: 2, 690 - 703, 18.06.2021
Emine Albayrak
Özer Işılar
,
Mutluhan Bıyıkoğlu
,
Ayşe Şahin Yağlıoğlu
,
Adnan Bulut
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
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,
Volume: 13 Issue: 2, 690 - 703, 18.06.2021
Emine Albayrak
Özer Işılar
,
Mutluhan Bıyıkoğlu
,
Ayşe Şahin Yağlıoğlu
,
Adnan Bulut
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.
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