These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 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.