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Original Article

Syntheses and evaluation of multicaulin and miltirone-like compounds as antituberculosis agents

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Pages 878-884 | Received 14 Mar 2017, Accepted 23 May 2017, Published online: 29 Jun 2017

References

  • Tiwari R, Moraski GC, Krchňák V, et al. Thiolates chemically induce redox activation of BTZ043 and related potent nitroaromatic anti-tuberculosis agents. J Am Chem Soc 2013;135:3539–49.
  • WHO Global Tuberculosis Report. (2016). Available from: http://who.int/tb/publications/global_report/en/ [last accessed 14 May 2017].
  • Addla D, Jallapally A, Gurram D, et al. Design, synthesis and evaluation of 1,2,3-triazoleadamantylacetamide hybrids as potent inhibitors of Mycobacterium tuberculosis. Bioorg Med Chem Lett 2014;24:1974–9.
  • Naik M, Ghorpade S, Jena LK, et al. Phenylindole and arylsulphonamide: novel scaffolds bactericidal against Mycobacterium tuberculosis. ACS Med Chem Lett 2014;5:1005–9.
  • Cappoen D, Jacobs J, Nguyen Van T, et al. Straightforward palladium-mediated synthesis and biological evaluation of benzo[j]phenanthridine-7,12-diones as anti-tuberculosis agents. Eur J Med Chem 2012;48:57–68.
  • Claes P, Cappoen D, Mbala BM, et al. Synthesis and antimycobacterial activity of analogues of the bioactive natural products sampangine and cleistopholine. Eur J Med Chem 2013;67:98–110.
  • Cappoen D, Claes P, Jacobs J, et al. 1,2,3,4,8,9,10,11-octahydrobenzo[j]phenanthridine-7,12-diones as new leads against Mycobacterium tuberculosis. J Med Chem 2014;57:2895–907.
  • Claes P, Cappoen D, Uythethofken C, et al. 2,4-Dialkyl-8,9,10,11-tetrahydrobenzo[g]pyrimido[4,5-c]isoquinoline-1,3,7,12(2H,4H)-tetraones as new leads against Mycobacterium tuberculosis. Eur J Med Chem 2014;77:409–21.
  • Dias DA, Urban S, Roessner U. A historical overview of natural products in drug discovery. Metabolites 2012;2:303–36.
  • Strohl WR. The role of natural products in a modern drug discovery program. Drug Discov Today 2000;5:39–41.
  • Ulubelen A. Cardioactive and antibacterial terpenoids from some Salvia species. Phytochemistry 2003;64:395–9.
  • Somer NU, Sarikaya B, Erac B, et al. Chemical composition and antimicrobial activity of essential oils from the aerial parts of Salvia pinnata L. Rec Nat Prod 2015;9:614–8.
  • Ulubelen A, Topcu G, Johansson CB. Norditerpenoids and diterpenoids from Salvia multicaulis with antituberculous activity. J Nat Prod 1997;60:1275–80.
  • Wu YB, Ni ZY, Shi QW, et al. Constituents from Salvia species and their biological activities. Chem Rev 2012;112:5967–6026.
  • Hatipoglu S, Zorlu D, Dirmenci NT, et al. Determination of volatile organic compounds in fourty five Salvia species by thermal desorption-GC-MS technique. Rec Nat Prod 2016;10:659–700.
  • Wang X, Wei Y, Yuan S, et al. Potential anticancer activity of tanshinone IIA against human breast cancer. Int J Cancer 2005;116:799–807.
  • Chang HM, Chui KY, Tan FW, et al. Structure-activity relationship of miltirone, an active central benzodiazepine receptor ligand isolated from Salvia miltiorrhiza Bunge (Danshen). J Med Chem 1991;34:1675–92.
  • Seçinti H, Burmaoğlu S, Altundaş R, Seçen H. Total syntheses of multicaulins via oxidative photocyclization of stilbenes. J Nat Prod 2014;77:2134–7.
  • Sengupta SK, Biswas RN, Bhattacharyya BK. Friedel–Crafts reaction. IV. Synthesis of 7-isopropyl-3-oxo-6-methoxy-1,2,3,9,10,10a-hexahydrophenanthrene. J Indian Chem Soc 1959;36:659–68.
  • Holzgrabe U. Quantitative NMR spectroscopy in pharmaceutical applications. Prog Nucl Magn Reson Spectrosc 2010;57:229–40.
  • Malz F, Jancke H. Validation of quantitative NMR. J Pharm Biomed Anal 2005;38:813–23.
  • Saito T, Ihara T, Koike M, et al. New traceability scheme for the development of international system-traceable persistent organic pollutant reference materials by quantitative nuclear magnetic resonance. Accredit Qual Assur 2009;14:79–86.
  • Bostan MS, Senol M, Cig T, et al. Controlled release of 5-aminosalicylicacid from chitosan based pH and temperature sensitive hydrogels. Int J Biol Macromol 2013;52:177–83.
  • Burnell RH, Caron S. Approach to the synthesis of candelabrone and synthesis of 3,7-diketo-12-hydroxyabieta-8,11,13-triene. Can J Chem 1992;70:1446–54.
  • Smith MB. March’s advanced organic chemistry, 6th ed. New Jersey: Wiley; 2007.
  • Caronna T, Ferrario F, Servi S. Intermolecular and intramolecular phenol phenylation: regioselective synthesis of unsymmetrically substituted biphenyls and 9,10-dihydrophenanthrenes. Tetrahedron Lett 1979;20:657–60.
  • Sokmen A, Gulluce M, Akpulat HA, et al. The in vitro antimicrobial and antioxidant activities of the essential oils and methanol extracts of endemic Thymus spathulifolius. Food Control 2004;15:627–34.