دورية أكاديمية

Cytotoxic Effects of Compounds Isolated from Ricinodendron heudelotii .

التفاصيل البيبلوغرافية
العنوان: Cytotoxic Effects of Compounds Isolated from Ricinodendron heudelotii .
المؤلفون: Yakubu OF; Department of Biochemistry, College of Science and Technology, Covenant University, Canaan Land, Ota PMB 1023, Ogun State, Nigeria. omolara.yakubu@covenantuniversity.edu.ng.; State Key Laboratory of Phytochemistry and Plant Resources of West China, Kunming Institute of Botany, Chinese Academy of Sciences. #132, Lanhei Road, Heilongtan, Kunming 650201, China. omolara.yakubu@covenantuniversity.edu.ng., Adebayo AH; Department of Biochemistry, College of Science and Technology, Covenant University, Canaan Land, Ota PMB 1023, Ogun State, Nigeria. abiodun.adebayo@covenantuniversity.edu.ng., Dokunmu TM; Department of Biochemistry, College of Science and Technology, Covenant University, Canaan Land, Ota PMB 1023, Ogun State, Nigeria. titilope.dokunmu@covenantuniversity.edu.ng., Zhang YJ; State Key Laboratory of Phytochemistry and Plant Resources of West China, Kunming Institute of Botany, Chinese Academy of Sciences. #132, Lanhei Road, Heilongtan, Kunming 650201, China. zhangyj@mail.kib.ac.cn., Iweala EEJ; Department of Biochemistry, College of Science and Technology, Covenant University, Canaan Land, Ota PMB 1023, Ogun State, Nigeria. emeka.iweala@covenantuniversity.edu.ng.
المصدر: Molecules (Basel, Switzerland) [Molecules] 2019 Jan 02; Vol. 24 (1). Date of Electronic Publication: 2019 Jan 02.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: MDPI Country of Publication: Switzerland NLM ID: 100964009 Publication Model: Electronic Cited Medium: Internet ISSN: 1420-3049 (Electronic) Linking ISSN: 14203049 NLM ISO Abbreviation: Molecules Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Basel, Switzerland : MDPI, c1995-
مواضيع طبية MeSH: Antineoplastic Agents, Phytogenic/*pharmacology , Euphorbiaceae/*chemistry , Plant Extracts/*pharmacology, Antineoplastic Agents, Phytogenic/isolation & purification ; Cell Line, Tumor ; Cell Survival/drug effects ; Drug Screening Assays, Antitumor ; Gallic Acid/chemistry ; Glucosides/chemistry ; Humans ; Hydrolyzable Tannins/chemistry ; Molecular Structure ; Phytochemicals/isolation & purification ; Phytochemicals/pharmacology ; Plant Extracts/isolation & purification ; Plant Leaves/chemistry ; Solvents/chemistry ; Structure-Activity Relationship
مستخلص: This study was designed to explore the in vitro anticancer effects of the bioactive compounds isolated from Ricinodendron heudelotii on selected cancer cell lines. The leaves of the plant were extracted with ethanol and partitioned in sequence with petroleum ether, ethyl acetate, and n -butanol. The ethyl acetate fraction was phytochemically studied using thin layer chromatography (TLC) and column chromatography (CC). Structural elucidation of pure compounds obtained from the ethyl acetate fraction was done using mass spectra, ¹H-NMR, and 13 C-NMR analysis. The isolated compounds were subsequently screened using five different cancer cell lines: HL-60, SMMC-7721, A-549, MCF-7, SW-480, and normal lung epithelial cell line, BEAS-2B, to assess their cytotoxic effects. Nine compounds were isolated and structurally elucidated as gallic acid, gallic acid ethyl ester, corilagin, quercetin-3- O -rhamnoside, myricetin-3- O -rhamnoside, 1,4,6-tri- O -galloyl glucose, 3,4,6-tri- O -galloyl glucose, 1,2,6-tri- O -galloyl glucose, and 4,6-di- O -galloyl glucose. Corilagin exhibited the most cytotoxic activity with an IC 50 value of 33.18 μg/mL against MCF-7 cells, which were comparable to cisplatin with an IC 50 value of 27.43 µg/mL. The result suggests that corilagin isolated from R. heudelotii has the potential to be developed as an effective therapeutic agent against the growth of breast cancer cells.
References: Cell Cycle. 2002 May-Jun;1(3):156-61. (PMID: 12429925)
Planta Med. 2005 Mar;71(3):237-43. (PMID: 15770544)
Biochem Biophys Res Commun. 2006 Jan 13;339(2):463-8. (PMID: 16298333)
Phytother Res. 2006 Feb;20(2):160-1. (PMID: 16444672)
J Hepatol. 2007 Feb;46(2):222-9. (PMID: 17069924)
Phytomedicine. 2007 Nov;14(11):755-62. (PMID: 17293097)
Cell. 2007 Jun 29;129(7):1337-49. (PMID: 17604722)
Pharmacogn Mag. 2010 Jan;6(21):62-6. (PMID: 20548938)
Cell. 2011 Mar 4;144(5):646-74. (PMID: 21376230)
Int J Cancer. 2012 Jan 15;130(2):245-50. (PMID: 21796634)
Int Immunopharmacol. 2012 Jul;13(3):308-15. (PMID: 22561123)
Clin Biochem. 2012 Nov;45(16-17):1519-21. (PMID: 22776359)
BMC Complement Altern Med. 2013 Feb 15;13:33. (PMID: 23410205)
J Appl Microbiol. 2013 Aug;115(2):390-7. (PMID: 23683054)
Cell Biol Int. 2013 Oct;37(10):1046-54. (PMID: 23686743)
AAPS J. 2014 Jan;16(1):151-63. (PMID: 24307610)
Sci Rep. 2014 Jun 24;4:5411. (PMID: 24958333)
BMC Cancer. 2014 Jul 24;14:535. (PMID: 25060700)
Nutr Cancer. 2014;66(8):1304-14. (PMID: 25264855)
CA Cancer J Clin. 2015 Mar;65(2):87-108. (PMID: 25651787)
Chem Pharm Bull (Tokyo). 1989 Aug;37(8):2063-70. (PMID: 2598308)
Molecules. 2015 Jun 26;20(7):11808-29. (PMID: 26132906)
Toxins (Basel). 2016 May 13;8(5):. (PMID: 27187472)
Evid Based Complement Alternat Med. 2016;2016:1418309. (PMID: 27247607)
Molecules. 2016 Aug 04;21(8):. (PMID: 27527135)
Biomed Res Int. 2016;2016:9729275. (PMID: 27777954)
BMC Complement Altern Med. 2017 Jan 5;17(1):18. (PMID: 28056977)
Biol Pharm Bull. 1993 Aug;16(8):787-90. (PMID: 8220326)
Can J Physiol Pharmacol. 1995 Oct;73(10):1425-9. (PMID: 8748933)
J Nat Prod. 1997 Jan;60(1):52-60. (PMID: 9014353)
معلومات مُعتمدة: 3240287315 Organization for Women in Science for the Developing World
فهرسة مساهمة: Keywords: Ricinodendron heudelotii; anticancer; chemoprevention
المشرفين على المادة: 0 (Antineoplastic Agents, Phytogenic)
0 (Glucosides)
0 (Hydrolyzable Tannins)
0 (Phytochemicals)
0 (Plant Extracts)
0 (Solvents)
13186-19-1 (6-O-galloylglucose)
62LOS9TW6D (corilagin)
632XD903SP (Gallic Acid)
تواريخ الأحداث: Date Created: 20190106 Date Completed: 20191024 Latest Revision: 20200225
رمز التحديث: 20221213
مُعرف محوري في PubMed: PMC6337108
DOI: 10.3390/molecules24010145
PMID: 30609707
قاعدة البيانات: MEDLINE
الوصف
تدمد:1420-3049
DOI:10.3390/molecules24010145