Publication Cover
Archives of Physiology and Biochemistry
The Journal of Metabolic Diseases
Volume 123, 2017 - Issue 4
357
Views
11
CrossRef citations to date
0
Altmetric
Original Article

Natural product inhibitors of carbonic anhydrase I and II isoenzymes: osajin and pomiferin

, , , ORCID Icon &
Pages 219-224 | Received 31 Jan 2017, Accepted 04 Mar 2017, Published online: 24 Mar 2017

References

  • Arslan, O., et al., 1997. A new method for the purification of carbonic anhydrase izozymes by affinity chromatography. Turkish journal of medical sciences, 27, 559–563.
  • Balaydin, H.T., et al., 2012. Synthesis and carbonic anhydrase inhibitory properties of novel bromophenols including natural products. Journal of enzyme inhibition and medicinal chemistry, 27, 43–50.
  • Bayram, E., et al., 2008. In vitro inhibition of salicylic acid derivatives on human cytosolic carbonic anhydrase isozymes I and II. Bioorganic & medicinal chemistry, 6, 9101–9105.
  • Burmaoğlu, S., et al., 2016. Synthesis of two phloroglucinol derivatives with cinnamyl moieties as inhibitors of the carbonic anhydrase isozymes I and II: an in vitro study. Journal of enzyme inhibition and medicinal chemistry, 13, 1–5.
  • Çağlar, S., et al., 2016. New metal complexes with diclofenac containing 2-pyridineethanol or 2-pyridinepropanol: synthesis, structural, spectroscopic, thermal properties, catechol oxidase and carbonic anhydrase activity. Journal of coordination chemistry, 69, 3321–3335.
  • Carroll, J., et al., 2010. Elemol and amyris oil repel the ticks Ixodes scapularis and Amblyomma americanum (Acari: Ixodidae) in laboratory bioassays. Experimental and applied acarology, 51, 383–392.
  • Casey, J.R., 2006. Why bicarbonate? Biochemistry and cell biology, 84, 930–939.
  • Chatterjee, A., et al., 2013. Polysaccharide-rich fraction of Termitomyces eurhizus accelerate healing of indomethacin induced gastric ulcer in mice. Glycoconjugate journal, 30, 759–768.
  • Dilek, E.B., Küfrevioğlu, O.I., and Beydemir, S., 2013. Impacts of some antibiotics on human serum paraoxonase 1 activity. Journal of enzyme inhibition and medicinal chemistry, 28, 758–776.
  • Dilek, E. and Caglar, S., 2015. Effects of mono and dinuclear copper (II) complexes derived from non-steroidal anti-inflammatory drug naproxen on human serum paraoxanase1 (PON1) activity. International journal of pharmaceutical chemistry, 5, 189–195.
  • Dilek, E. and Polat, M.F., 2016. In vitro inhibition of three different drugs used in rheumatoid arthritis treatment on human serum paraoxanase 1 enzyme activity. Protein & peptide letters, 23 (1), 3–8.
  • Durdagi, S., et al., 2011. Kinetic and docking studies of phenol-based inhibitors of carbonic anhydrase isoforms I, II, IX and XII evidence a new binding mode within the enzyme active site. Bioorganic & medicinal chemistry, 19, 1381–1389.
  • Ekinci, D., Beydemir, S., and Kufrevioglu, O.I., 2007. In vitro inhibitory effects of some heavy metals on human erythrocyte carbonic anhydrases. Journal of enzyme inhibition and medicinal chemistry, 22, 745–750.
  • Florian, T., et al., 2006. Effects of prenylated isoflavones osajin and pomiferin in premedication on heart ischemia reperfusion. Biomedical papers of the medical faculty of the university Palacky, Olomouc, Czechoslovakia, 150, 93–100.
  • Hassan, M.I., et al., 2013. Structure, function and applications of carbonic anhydrase isozymes. Bioorganic & medicinal chemistry, 21, 1570–1582.
  • Innocenti, A., et al., 2008. Carbonic anhydrase inhibitors: inhibition of the new membrane-associated isoform XV with phenols. Bioorganic & medicinal chemistry letters, 18, 3593–3596.
  • Innocenti, A., et al., 2008a. Investigations of the esterase, phosphatase, and sulfatase activities of the cytosolic mammalian carbonic anhydrase isoforms I, II, and XIII with 4-nitrophenyl esters as substrates. Bioorganic & medicinal chemistry letters, 18, 2267–2271.
  • Innocenti, A., et al., 2008b. Carbonic anhydrase inhibitors: interactions of phenols with the 12 catalytically active mammalian isoforms (CA I-XIV). Bioorganic & medicinal chemistry letters, 18, 1583–1587.
  • Kupeli, E., et al., 2006. Anti-inflammatory and antinociceptive potential of Maclura pomifera (Rafin.) Schneider fruit extracts and its major isoflavonoids, scandenone and auriculasin. Journal of ethnopharmacology, 107, 169–174.
  • Lineweaver, H. and Burk, D., 1934. The determination of enzyme dissociation constants. Journal of the American chemical society, 56, 658–666.
  • Nair, S.K., Ludwig, P.A., and Christianson, D.W., 1994. Two-site binding of phenol in the active site of human carbonic anhydrase II: structural implications for substrate association. Journal of the American chemical society, 116, 3659.
  • Orhan, I., et al., 2009. Cholinesterase inhibitory effects of the extracts and compounds of Maclura pomifera (Rafin.) Schneider. Food and chemical toxicology, 47, 1747–1751.
  • Ozcelik, B., Orhan, I., and Toker, G., 2006. Antiviral and antimicrobial assessment of some selected flavonoids. Zeitschrift für naturforschung, 61c, 632–638.
  • Ozensoy, O., Arslan, O., and Oznur Sinan, S., 2004. A new method for purification of carbonic anhydrase isozymes by affinity chromatography. Biochemistry (Moscow), 69, 216–219.
  • Pastorekova, S., et al., 2004. Carbonic anhydrases: current state of the art, therapeutic applications and future prospects. Journal of enzyme inhibition and medicinal chemistry, 19, 199–229.
  • Sarıkaya, S.B.O., Gülcin, I., and Supuran, C.T., 2010. Carbonic anhydrase inhibitors: inhibition of human erythrocyte isozymes I and II with a series of phenolic acids. Chemical biology & drug design, 75, 515–520.
  • Sarikaya, S.B.O., et al., 2011. In vitro inhibition of α-carbonic anhydrase isozymes by some phenolic compounds. Bioorganic & medicinal chemistry letters, 21, 4259–4262.
  • Senturk, M., et al., 2009. Carbonic anhydrase inhibitors. Inhibition of human erythrocyte isozymes I and II with a series of antioxidant phenols. Bioorganic & medicinal chemistry, 17, 3207–3211.
  • Sly, W.S. and Hu, P.Y., 1995. Human carbonic anhydrases and carbonic anhydrase deficiencies. Annual review of biochemistry, 64, 375–401.
  • Son, I.H., et al., 2007. Pomiferin, histone deacetylase inhibitor isolated from the fruits of Maclura pomifera. Bioorganic & medicinal chemistry letters, 17, 4753–4755.
  • Supuran, C.T., 2008. Carbonic anhydrases: novel therapeutic applications for inhibitors and activators. Nature reviews drug discovery, 7, 168–181.
  • Supuran, C.T., 2008. Diuretics: from classical carbonic anhydrase inhibitors to novel applications of the sulfonamides. Current pharmaceutical design, 14, 641–648.
  • Supuran, C.T. and Scozzafava, A., 2007. Carbonic anhydrases as targets for medicinal chemistry. Bioorganic & medicinal chemistry, 15, 4336–4350.
  • Supuran, C.T., et al., 2004. Designing of novel carbonic anhydrase inhibitors and activators. Current medicinal chemistry – cardiovascular & hematological agents, 2, 49–68.
  • Teixeira, D.M. and Costa, C., 2005. Novel methods to extract flavanones and xanthones from the root bark of Maclura pomifera. Journal of chromatography A, 1062, 175–181.
  • Thiry, A., et al., 2007. Carbonic anhydrase inhibitors as anticonvulsant agents. Current topics in medicinal chemistry, 7, 855–864.
  • Tran, V.H., et al., 2011. Modulation of P-glycoprotein-mediated anticancer drug accumulation, cytotoxicity, and ATPase activity by flavonoid interactions. Nutrition and cancer, 63, 435–443.
  • Verpoorte, J.A., Mehta, S., and Edsall, J.T., 1967. Esterase activities of human carbonic anhydrases B and C. Journal of biological chemistry, 242, 4221–4229.
  • Yang, R., et al., 2011. Antiproliferative activity of pomiferin in normal (MCF-10A) and transformed (MCF-7) breast epithelial cells. Journal of agricultural and food chemistry, 59, 13328–13336.
  • Zengin Kurt, B., et al., 2016a. Synthesis, antioxidant and carbonic anhydrase I and II inhibitory activities of novel sulphonamide-substituted coumarylthiazole derivatives. Journal of enzyme inhibition and medicinal chemistry, 31 (6), 991–998.
  • Zengin Kurt, B., et al., 2016b. In vitro inhibition effects on erythrocyte carbonic anhydrase I and II and structure–activity relationships of cumarylthiazole derivatives. Russian journal of bioorganic chemistry, 42 (5), 506–511.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.