BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

127 related articles for article (PubMed ID: 28033541)

  • 1. Rhodamine B conjugates of triterpenoic acids are cytotoxic mitocans even at nanomolar concentrations.
    Sommerwerk S; Heller L; Kerzig C; Kramell AE; Csuk R
    Eur J Med Chem; 2017 Feb; 127():1-9. PubMed ID: 28033541
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Homopiperazine-rhodamine B adducts of triterpenoic acids are strong mitocans.
    Wolfram RK; Fischer L; Kluge R; Ströhl D; Al-Harrasi A; Csuk R
    Eur J Med Chem; 2018 Jul; 155():869-879. PubMed ID: 29960206
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Targeting mitochondria: Esters of rhodamine B with triterpenoids are mitocanic triggers of apoptosis.
    Wolfram RK; Heller L; Csuk R
    Eur J Med Chem; 2018 May; 152():21-30. PubMed ID: 29684707
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rhodamine 101 Conjugates of Triterpenoic Amides Are of Comparable Cytotoxicity as Their Rhodamine B Analogs.
    Heise NV; Major D; Hoenke S; Kozubek M; Serbian I; Csuk R
    Molecules; 2022 Mar; 27(7):. PubMed ID: 35408619
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mitocanic Di- and Triterpenoid Rhodamine B Conjugates.
    Hoenke S; Serbian I; Deigner HP; Csuk R
    Molecules; 2020 Nov; 25(22):. PubMed ID: 33233650
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mitochondria-Targeting 1,5-Diazacyclooctane-Spacered Triterpene Rhodamine Conjugates Exhibit Cytotoxicity at Sub-Nanomolar Concentration against Breast Cancer Cells.
    Heise N; Becker S; Mueller T; Bache M; Csuk R; Güttler A
    Int J Mol Sci; 2023 Jun; 24(13):. PubMed ID: 37445874
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Urea derivates of ursolic, oleanolic and maslinic acid induce apoptosis and are selective cytotoxic for several human tumor cell lines.
    Sommerwerk S; Heller L; Kuhfs J; Csuk R
    Eur J Med Chem; 2016 Aug; 119():1-16. PubMed ID: 27149037
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Selective killing of cancer cells with triterpenoic acid amides - The substantial role of an aromatic moiety alignment.
    Sommerwerk S; Heller L; Kuhfs J; Csuk R
    Eur J Med Chem; 2016 Oct; 122():452-464. PubMed ID: 27416552
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Synthesis of Rhodamine-Conjugated Lupane Type Triterpenes of Enhanced Cytotoxicity.
    Denner TC; Heise NV; Hoenke S; Csuk R
    Molecules; 2024 May; 29(10):. PubMed ID: 38792206
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Asiatic acid as a leading structure for derivatives combining sub-nanomolar cytotoxicity, high selectivity, and the ability to overcome drug resistance in human preclinical tumor models.
    Kraft O; Hartmann AK; Brandt S; Hoenke S; Heise NV; Csuk R; Mueller T
    Eur J Med Chem; 2023 Mar; 250():115189. PubMed ID: 36780832
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Developing an Amide-Spacered Triterpenoid Rhodamine Hybrid of Nano-Molar Cytotoxicity Combined with Excellent Tumor Cell/Non-Tumor Cell Selectivity.
    Heise NV; Denner TC; Becker S; Hoenke S; Csuk R
    Molecules; 2023 Sep; 28(17):. PubMed ID: 37687233
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Synthesis and cytotoxic activity of pentacyclic triterpenoid sulfamates.
    Sommerwerk S; Heller L; Csuk R
    Arch Pharm (Weinheim); 2015 Jan; 348(1):46-54. PubMed ID: 25581678
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Incorporation of a Michael acceptor enhances the antitumor activity of triterpenoic acids.
    Heller L; Schwarz S; Perl V; Köwitsch A; Siewert B; Csuk R
    Eur J Med Chem; 2015 Aug; 101():391-9. PubMed ID: 26177446
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cytotoxic triterpenoid-safirinium conjugates target the endoplasmic reticulum.
    Kraft O; Kozubek M; Hoenke S; Serbian I; Major D; Csuk R
    Eur J Med Chem; 2021 Jan; 209():112920. PubMed ID: 33049606
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Esters and amides of maslinic acid trigger apoptosis in human tumor cells and alter their mode of action with respect to the substitution pattern at C-28.
    Siewert B; Pianowski E; Csuk R
    Eur J Med Chem; 2013; 70():259-72. PubMed ID: 24161703
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The presence of a cationic center is not alone decisive for the cytotoxicity of triterpene carboxylic acid amides.
    Brandes B; Koch L; Hoenke S; Deigner HP; Csuk R
    Steroids; 2020 Nov; 163():108713. PubMed ID: 32795453
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Betulinic acid derived hydroxamates and betulin derived carbamates are interesting scaffolds for the synthesis of novel cytotoxic compounds.
    Wiemann J; Heller L; Perl V; Kluge R; Ströhl D; Csuk R
    Eur J Med Chem; 2015 Dec; 106():194-210. PubMed ID: 26547057
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Synthesis of some steroidal mitocans of nanomolar cytotoxicity acting by apoptosis.
    Serbian I; Hoenke S; Csuk R
    Eur J Med Chem; 2020 Aug; 199():112425. PubMed ID: 32422522
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Platanic acid: A new scaffold for the synthesis of cytotoxic agents.
    Kahnt M; Heller L; Grabandt P; Al-Harrasi A; Csuk R
    Eur J Med Chem; 2018 Jan; 143():259-265. PubMed ID: 29197730
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Betulinic acid derived amides are highly cytotoxic, apoptotic and selective.
    Hoenke S; Heise NV; Kahnt M; Deigner HP; Csuk R
    Eur J Med Chem; 2020 Dec; 207():112815. PubMed ID: 32956968
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.