Erectcyanthins A-C from marine sponge Hyrtios erectus: anti-dyslipidemic agents attenuate hydroxymethylglutaryl coenzyme A reductase

References

• Anusree M, Chakraborty K, Makkar F. 2016. Pharmacological activities of brown seaweed Sargassum wightii (family Sargassaceae) using different in vitro models. Int J Food Prop. 20(4):931–945.
   Web of Science ®Google Scholar
• Anusree M, Chakraborty K. 2017. Unprecedented antioxidative and anti-inflammatory aryl polyketides from the brown seaweed Sargassum wightii. Food Res Int. 100:640–649.
   PubMed Web of Science ®Google Scholar
• Aoki S, Ye Y, Higuchi K, Takashima A, Tanaka Y, Kitagawa I, Kobayashi M. 2001. Novel neuronal nitric oxide synthase (nNOS) selective inhibitor, aplysinopsin-type indole alkaloid, from marine sponge Hyrtios erecta. Chem Pharm Bull (Tokyo). 49(10):1372–1374.
   PubMed Web of Science ®Google Scholar
• Basil MC, Levy BD. 2016. Specialized pro-resolving mediators: endogenous regulators of infection and inflammation. Nat Rev Immunol. 16(1):51–67.
   PubMed Web of Science ®Google Scholar
• Bhatnagar D, Soran H, Durrington PN. 2008. Hypercholesterolaemia and its management. BMJ. 337:a993.
   PubMed Web of Science ®Google Scholar
• Blunt JW, Copp BR, Keyzers RA, Munro MHG, Prinsep MR. 2017. Marine natural products. Nat Prod Rep. 34(3):235–294.
   PubMed Web of Science ®Google Scholar
• Chakraborty K, Francis P. 2020. Hyrtioscalaranes A and B, two new scalarane-type sesterterpenes from Hyrtios erectus with anti-inflammatory and antioxidant effects [advanced online publication]. Nat Prod Res. 2020 Jul 27:1–12.
   Google Scholar
• Chakraborty K, Maneesh A. 2020. Marine-derived polygalactofucan and its β-2-deoxy-amino substituted glucopyranan composite attenuate 3-hydroxy-3-methylglutaryl-CoA reductase: prospective natural anti-dyslipidemic leads. Med Chem Res. 29(10):281–300.
   Google Scholar
• El-Desoky AH, Kato H, Tsukamoto S. 2017. Ceylonins G-I: spongian diterpenes from the marine sponge Spongia ceylonensis. J Nat Med. 71(4):765–769.
   PubMed Web of Science ®Google Scholar
• Endo A. 1992. The discovery and development of HMG-CoA reductase inhibitors. J Lipid Res. 33(11):1569–1582.
   PubMed Web of Science ®Google Scholar
• Francis P, Chakraborty K. 2020. Antioxidant and anti-inflammatory cembrane-type diterpenoid from Echinoidea sea urchin Stomopneustes variolaris attenuates pro-inflammatory 5-lipoxygenase. Med Chem Res. 29(5):656–664.
   Google Scholar
• González Y, Torres-Mendoza D, Jones GE, Fernandez PL. 2015. Marine diterpenoids as potential anti-inflammatory agents. Mediators Inflamm. 2015:263543.
   PubMed Web of Science ®Google Scholar
• Han GY, Sun DY, Liang LF, Yao LG, Chen KX, Guo YW. 2018. Spongian diterpenes from Chinese marine sponge Spongia officinalis. Fitoterapia. 127:159–165.
   PubMed Web of Science ®Google Scholar
• Hayton J, Grant GD, Carroll AR. 2019. Three new spongian diterpenes from the marine Sponge Dendrilla rosea. Aust J Chem. 72(12):964–968.
   Web of Science ®Google Scholar
• He WF, Xue DQ, Yao LG, Li JY, Li J, Guo YW. 2014. Hainanerectamines A-C, alkaloids from the Hainan sponge Hyrtios erecta. Mar Drugs. 12(7):3982–3993.
   PubMed Web of Science ®Google Scholar
• Holmquist B, Bunning P, Riordan JF. 1979. A continuous spectrophotometric assay for angiotensin converting enzyme. Anal Biochem. 95(2):540–548.
   PubMed Web of Science ®Google Scholar
• Istvan ES, Deisenhofer J. 2000. The structure of the catalytic portion of human HMG-CoA reductase. Biochim Biophys Acta. 1529(1–3):9–18.
   PubMed Web of Science ®Google Scholar
• Istvan ES, Palnitkar M, Buchanan SK, Deisenhofer J. 2000. Crystal structure of the catalytic portion of human HMG-CoA reductase: insights into regulation of activity and catalysis. Embo J. 19(5):819–830.
   PubMed Web of Science ®Google Scholar
• Keller C. 1889. Die Spongienfauna des rothen Meeres (I. Hälfte). Z Wiss Zool. 48:311–405.
   Google Scholar
• Kobayashi M, Aoki S, Sakai H, Kawazoe K, Kihara N, Sasaki T, Kitagawa I. 1993. Altohyrtin A, a potent anti-tumor macrolide from the Okinawan marine sponge Hyrtios altum. Tetrahedron Lett. 34(17):2795–2798.
   Web of Science ®Google Scholar
• Lipinski C, Hopkins A. 2004. Navigating chemical space for biology and medicine. Nature. 432(7019):855–861.
   PubMed Web of Science ®Google Scholar
• Lunder M, Drevenšek G, Hawlina S, Sepčić K, Ziberna L. 2012. Cardiovascular effects induced by polymeric 3-alkylpyridinium salts from the marine sponge Reniera sarai. Toxicon. 60(6):1041–1048.
   PubMed Web of Science ®Google Scholar
• Maneesh A, Chakraborty K. 2017. Previously undescribed fridooleanenes and oxygenated labdanes from the brown seaweed Sargassum wightii and their protein tyrosine phosphatase-1B inhibitory activity. Phytochemistry. 144:19–32.
   PubMed Web of Science ®Google Scholar
• Naci H, Brugts JJ, Fleurence R, Tsoi B, Toor H, Ades AE. 2013. Comparative benefits of statins in the primary and secondary prevention of major coronary events and all-cause mortality: a network meta-analysis of placebo-controlled and active-comparator trials. Eur J Prev Cardiol. 20(4):641–657.
   PubMed Web of Science ®Google Scholar
• Peng J, Avery MA, Hamann MT. 2003. Cyanthiwigin AC and AD, two novel diterpene skeletons from the Jamaican sponge Myrmekioderma styx. Org Lett. 5(24):4575–4578.
   PubMed Web of Science ®Google Scholar
• Peng J, Walsh K, Weedman V, Bergthold JD, Lynch J, Lieu KL, Braude IA, Kelly M, Hamann MT. 2002. The new bioactive diterpenes cyanthiwigins E–AA from the Jamaican sponge Myrmekioderma styx. Tetrahedron. 58(39):7809–7819.
   Web of Science ®Google Scholar
• Pettit GR, Tan R, Cichacz ZA. 2005. Antineoplastic agents. 542. Isolation and structure of sesterstatin 6 from the Indian Ocean sponge Hyrtios erecta. J Nat Prod. 68(8):1253–1255.
   PubMed Web of Science ®Google Scholar
• Qiu Y, Deng Z, Pei Y, Fu H, Li J, Proksch P, Lin W. 2004. Sesterterpenoids from the marine sponge Hyrtios erectus. J Nat Prod. 67(5):921–924.
   PubMed Web of Science ®Google Scholar
• Rungprom W, Chavasiri W, Kokpol U, Kotze A, Garson MJ. 2004. Bioactive chromodorolide diterpenes from an Aplysillid sponge. Mar Drugs. 2(3):101–107.
   Google Scholar
• Shady NH, El-Hossary EM, Fouad MA, Gulder TAM, Kamel MS, Abdelmohsen UR. 2017. Bioactive natural products of marine sponges from the genus Hyrtios. Molecules. 22(5):781.
   Web of Science ®Google Scholar
• Tabernero L, Bochar DA, Rodwell VW, Stauffacher CV. 1999. Substrate-induced closure of the flap domain in the ternary complex structures provides insights into the mechanism of catalysis by 3-hydroxy-3-methylglutaryl-CoA reductase. Proc Natl Acad Sci USA. 96(13):7167–7171.
   PubMed Web of Science ®Google Scholar
• Tian YQ, Gu BB, Jiao WH, Lin HW. 2020. Four homoverrucosane-type diterpenes from the marine sponge Halichondria sp. Tetrahedron. 76(50):131697.
   Web of Science ®Google Scholar
• Tirapelli CR, Ambrosio SR, de Oliveira AM, Tostes RC. 2010. Hypotensive action of naturally occurring diterpenes: a therapeutic promise for the treatment of hypertension. Fitoterapia. 81(7):690–702.
   PubMed Web of Science ®Google Scholar
• Vo QV, Tam NM, Hieu LT, Van Bay M, Thong NM, Le Huyen T, Hoa NT, Mechler A. 2020. The antioxidant activity of natural diterpenes: theoretical insights. RSC Adv. 10(25):14937–14943.
   PubMed Web of Science ®Google Scholar