Publication Cover
Natural Product Research
Formerly Natural Product Letters
Volume 38, 2024 - Issue 8
141
Views
0
CrossRef citations to date
0
Altmetric
Research Articles

Glabraquinone A and B, new bisanthraquinones from Prismatomeris glabra (Korth.) Valeton

, ORCID Icon, ORCID Icon & ORCID Icon
Pages 1406-1413 | Received 09 Feb 2022, Accepted 07 Nov 2022, Published online: 23 Nov 2022

References

  • Adnan NE, Mohd Nasuha NA, Abdullah Z, Choo YM, Tajuddin HA. 2018. Isolation and photophysical properties of Di- and Tri-substituted natural anthraquinones from Malaysian Morinda citrifolia. JSM. 47(5):903–908.
  • Alkadi KAA, Ashraf K, Adam A, Shah SAA, Taha M, Hasan MH, John C, Salleh RM, Ahmad W. 2021. In vitro cytotoxicity and anti-inflammatory cytokinine activity study of three isolated novel compounds of Prismatomeris glabra. J Pharm Bioallied Sci. 13(1):116–122.
  • Demagos GP, Baltus W, Höfle G. 1981. New anthraquinones and anthraquinone glycosides from Morinda lucida. Z. Naturforsch. B. 36(9):1180–1184.
  • Ford L, Rayner CM, Blackburn RS. 2018. Degradation of lucidin: new insights into the fate of this natural pigment present in Dyer’s madder (Rubia tinctorum L.) during the extraction of textile artefacts. Dyes Pigm. 154:290–295.
  • Greengard EG. 2018. Molecularly targeted therapy for neuroblastoma. Children 5(10):142.
  • Kiss LE, Soares-da-Silva P. 2014. Medicinal chemistry of catechol O-methyltransferase (COMT) inhibitors and their therapeutic utility. J Med Chem. 57(21):8692–8717.
  • Krohn K, Gehle D, Dey SK, Nahar N, Mosihuzzaman M, Sultana N, Sohrab MH, Stephens PJ, Pan JJ, Sasse F. 2007. Prismatomerin, a new iridoid from Prismatomeris tetrandra. Structure elucidation, determination of absolute configuration, and cytotoxicity. J Nat Prod. 70(8):1339–1343.
  • London WB, Castleberry RP, Matthay KK, Look AT, Seeger RC, Shimada H, Thorner P, Brodeur G, Maris JM, Reynolds CP, et al. 2005. Evidence for an age cutoff greater than 365 days for neuroblastoma risk group stratification in the Children’s Oncology Group. J Clin Oncol. 23(27):6459–6465.
  • Madrid Villegas A, Espinoza Catalán L, Montenegro Venegas I, Villena García J, Carrasco Altamirano H. 2011. New catechol derivatives of safrole and their antiproliferative activity towards breast cancer cells. Molecules 16(6):4632–4641.
  • Maris JM, Hogarty MD, Bagatell R, Cohn SL. 2007. Neuroblastoma. Lancet 369(9579):2106–2120.
  • Mohamad TAST, Naz H, Jalal RS, Hussin K, Rahman MRA, Adam A, Weber JFF. 2013. Chemical and pharmacognostical characterization of two Malaysian plants both known as Ajisamat. Rev Bras Farmacogn. 23(5):724–730.
  • Osman CP, Ismail NH, Ahmad R, Ahmat N, Awang K, Jaafar FM. 2010. Anthraquinones with antiplasmodial activity from the roots of Rennellia elliptica Korth. (Rubiaceae). Molecules. 15(10):7218–7226.
  • Paduraru PM, Popoff RTW, Nair R, Gries R, Gries G, Plettner E. 2008. Synthesis of substituted alkoxy benzene minilibraries, for the discovery of new insect olfaction or gustation inhibitors. J Comb Chem. 10(1):123–134.
  • Primus PS, Ismail MH, Adnan NE, Wu CH, Kao CL, Choo YM. 2022a. Chemical constituents and anti-neuroblastoma activity from Boesenbergia stenophylla. JSM 51(4):1075–1084.
  • Primus PS, Ismail MH, Adnan NE, Wu CH, Kao CL, Choo YM. 2022b. Stenophyllols A-C, new compounds from Boesenbergia stenophylla. J Asian Nat Prod Res. 24(2):146–152.
  • Rusia K, Srivastava SK. 1989. A new anthraquinone from the roots of Morinda citrifolia Linn. Curr Sci. 58:249–251.
  • Salleh RM, Hasan MH, Adam A. 2015a. Phenolic compound and antioxidant levels of Prismatomeris glabra. J Pharmacogn Phytochem. 3(5):5–11.
  • Salleh RM, Hasan MH, Adam A. 2015b. Prismatomeris glabra increases forced swimming time in mice. Int J Pharmacogn Phytochem Res. 7(3):473–479.
  • SciFinder. 2022. 1,2-dimethoxy-7-methyl-9,10-Anthracenedione. CAS RN: 121051-84-1. NMR spectral data calculated using Advanced Chemistry Development, Inc. (ACD/Labs) Software V11.01 (© 1994-2022 ACD/Labs). [accessed 2022 April 14]. https://scifinder-n-cas-org.ezproxy.um.edu.my/.
  • Son NT. 2017. An overview of the genus Prismatomeris: phytochemistry and biological activity. Bull Fac Pharm Cairo Univ. 55(1):11–18.
  • Tikhomirov AS, Shtil AA, Shchekotikhin AE. 2018. Advances in the discovery of anthraquinone-based anticancer agents. Recent Pat Anticancer Drug Discov. 13(2):159–183.
  • Tuntiwachwuttikul P, Butsuri Y, Sukkoe P, Prawa U, Taylor WC. 2008. Anthraquinones from the roots of Prismatomeris malayana. Nat Prod Res. 22(11):962–968.
  • Wang C, Ding X, Feng SX, Guan Q, Zhang XP, Du C, Di YT, Chen T. 2015. Seven new tetrahydroanthraquinones from the root of Prismatomeris connata and their cytotoxicity against lung tumor cell growth. Molecules 20(12):22565–22577.
  • Wong K, Turner I, Wang R, Harwood R, Seah W, Ng X, Lim R, Lua H, Mahyuni R. 2019. Rubiaceae. In: middleton D, Leong-Škorničková J, Lindsay S, editors. Flora of Singapore. Singapore: National Parks Board; p. 1–358.

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.