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160 related items for PubMed ID: 32785022

  • 1. Chemistry of Renieramycins. Part 19: Semi-Syntheses of 22-O-Amino Ester and Hydroquinone 5-O-Amino Ester Derivatives of Renieramycin M and Their Cytotoxicity against Non-Small-Cell Lung Cancer Cell Lines.
    Chamni S, Sirimangkalakitti N, Chanvorachote P, Suwanborirux K, Saito N.
    Mar Drugs; 2020 Aug 10; 18(8):. PubMed ID: 32785022
    [Abstract] [Full Text] [Related]

  • 2. Chemistry of Renieramycins. 17. A New Generation of Renieramycins: Hydroquinone 5-O-Monoester Analogues of Renieramycin M as Potential Cytotoxic Agents against Non-Small-Cell Lung Cancer Cells.
    Chamni S, Sirimangkalakitti N, Chanvorachote P, Saito N, Suwanborirux K.
    J Nat Prod; 2017 May 26; 80(5):1541-1547. PubMed ID: 28459574
    [Abstract] [Full Text] [Related]

  • 3. Chemistry of Renieramycins. 15. Synthesis of 22-O-Ester Derivatives of Jorunnamycin A and Their Cytotoxicity against Non-Small-Cell Lung Cancer Cells.
    Sirimangkalakitti N, Chamni S, Charupant K, Chanvorachote P, Mori N, Saito N, Suwanborirux K.
    J Nat Prod; 2016 Aug 26; 79(8):2089-93. PubMed ID: 27487087
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  • 4. Semisynthesis of 5-O-ester derivatives of renieramycin T and their cytotoxicity against non-small-cell lung cancer cell lines.
    Buaban K, Innets B, Petsri K, Sinsook S, Chanvorachote P, Chansriniyom C, Suwanborirux K, Yokoya M, Saito N, Chamni S.
    Sci Rep; 2023 Dec 06; 13(1):21485. PubMed ID: 38057385
    [Abstract] [Full Text] [Related]

  • 5. Light-Mediated Transformation of Renieramycins and Semisynthesis of 4'-Pyridinecarbonyl-Substituted Renieramycin-Type Derivatives as Potential Cytotoxic Agents against Non-Small-Cell Lung Cancer Cells.
    Sinsook S, Buaban K, Iksen I, Petsri K, Innets B, Chansriniyom C, Suwanborirux K, Yokoya M, Saito N, Pongrakhananon V, Chanvorachote P, Chamni S.
    Mar Drugs; 2023 Jul 13; 21(7):. PubMed ID: 37504931
    [Abstract] [Full Text] [Related]

  • 6. Apoptosis-inducing Effect of Hydroquinone 5-O-Cinnamoyl Ester Analog of Renieramycin M on Non-small Cell Lung Cancer Cells.
    Maiuthed A, Pinkhien T, Chamni S, Suwanborirux K, Saito N, Petpiroon N, Chanvorachote P.
    Anticancer Res; 2017 Nov 13; 37(11):6259-6267. PubMed ID: 29061809
    [Abstract] [Full Text] [Related]

  • 7. Chemistry of renieramycins. Part 8: synthesis and cytotoxicity evaluation of renieramycin M-jorunnamycin A analogues.
    Charupant K, Daikuhara N, Saito E, Amnuoypol S, Suwanborirux K, Owa T, Saito N.
    Bioorg Med Chem; 2009 Jul 01; 17(13):4548-58. PubMed ID: 19457672
    [Abstract] [Full Text] [Related]

  • 8. Asymmetric Synthesis and Cytotoxicity Evaluation of Right-Half Models of Antitumor Renieramycin Marine Natural Products.
    Matsubara T, Yokoya M, Sirimangkalakitti N, Saito N.
    Mar Drugs; 2018 Dec 20; 17(1):. PubMed ID: 30577460
    [Abstract] [Full Text] [Related]

  • 9. 22-O-(N-Boc-L-glycine) ester of renieramycin M inhibits migratory activity and suppresses epithelial-mesenchymal transition in human lung cancer cells.
    Oo Y, Nealiga JQL, Suwanborirux K, Chamni S, Ecoy GAU, Pongrakhananon V, Chanvorachote P, Chaotham C.
    J Nat Med; 2021 Sep 20; 75(4):949-966. PubMed ID: 34287745
    [Abstract] [Full Text] [Related]

  • 10. Synthesis and cytotoxicity of (-)-renieramycin G analogs.
    Liu W, Dong W, Liao X, Yan Z, Guan B, Wang N, Liu Z.
    Bioorg Med Chem Lett; 2011 Mar 01; 21(5):1419-21. PubMed ID: 21295980
    [Abstract] [Full Text] [Related]

  • 11. Chemistry of renieramycins. Part 5. Structure elucidation of renieramycin-type derivatives O, Q, R, and S from thai marine sponge Xestospongia species pretreated with potassium cyanide.
    Amnuoypol S, Suwanborirux K, Pummangura S, Kubo A, Tanaka C, Saito N.
    J Nat Prod; 2004 Jun 01; 67(6):1023-8. PubMed ID: 15217287
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  • 16. Renieramycin-type alkaloids from marine-derived organisms: Synthetic chemistry, biological activity and structural modification.
    Fang Y, Li H, Ji B, Cheng K, Wu B, Li Z, Zheng C, Hua H, Li D.
    Eur J Med Chem; 2021 Jan 15; 210():113092. PubMed ID: 33333398
    [Abstract] [Full Text] [Related]

  • 17. Asymmetric Total Syntheses of (-)-Fennebricin A, (-)-Renieramycin J, (-)-Renieramycin G, (-)-Renieramycin M, and (-)- Jorunnamycin A via C-H Activation.
    Zheng Y, Li XD, Sheng PZ, Yang HD, Wei K, Yang YR.
    Org Lett; 2020 Jun 05; 22(11):4489-4493. PubMed ID: 32437173
    [Abstract] [Full Text] [Related]

  • 18. Microarray-based transcriptional profiling of renieramycin M and jorunnamycin C, isolated from Thai marine organisms.
    Charupant K, Suwanborirux K, Daikuhara N, Yokoya M, Ushijima-Sugano R, Kawai T, Owa T, Saito N.
    Mar Drugs; 2009 Oct 19; 7(4):483-94. PubMed ID: 20098592
    [Abstract] [Full Text] [Related]

  • 19. Bishydroquinone Renieramycin M Induces Apoptosis of Human Lung Cancer Cells Through a Mitochondria-dependent Pathway.
    Pinkhien T, Maiuthed A, Chamni S, Suwanborirux K, Saito N, Chanvorachote P.
    Anticancer Res; 2016 Dec 19; 36(12):6327-6333. PubMed ID: 27919953
    [Abstract] [Full Text] [Related]

  • 20. Renieramycin M Attenuates Cancer Stem Cell-like Phenotypes in H460 Lung Cancer Cells.
    Sirimangkalakitti N, Chamni S, Suwanborirux K, Chanvorachote P.
    Anticancer Res; 2017 Feb 19; 37(2):615-621. PubMed ID: 28179308
    [Abstract] [Full Text] [Related]

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