138 related articles for article (PubMed ID: 31330447)
1. 2-O-(2-chlorobenzoyl) maslinic acid triggers apoptosis in A2780 human ovarian carcinoma cells.
Serbian I; Siewert B; Al-Harrasi A; Csuk R
Eur J Med Chem; 2019 Oct; 180():457-464. PubMed ID: 31330447
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. Tormentic acid derivatives: synthesis and apoptotic activity.
Csuk R; Siewert B; Dressel C; Schäfer R
Eur J Med Chem; 2012 Oct; 56():237-45. PubMed ID: 22995818
[TBL] [Abstract][Full Text] [Related]
7. The chemical and biological potential of C ring modified triterpenoids.
Siewert B; Wiemann J; Köwitsch A; Csuk R
Eur J Med Chem; 2014 Jan; 72():84-101. PubMed ID: 24361521
[TBL] [Abstract][Full Text] [Related]
8. Cytotoxic and Apoptosis-inducing Activities of Taraxastane-type Triterpenoid Derivatives in Human Cancer Cell Lines.
Ukiya M; Ohkubo C; Kurita M; Fukatsu M; Suzuki T; Akihisa T
Chem Biodivers; 2016 Aug; 13(8):1018-29. PubMed ID: 27389784
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. An access to a library of novel triterpene derivatives with a promising pharmacological potential by Ugi and Passerini multicomponent reactions.
Wiemann J; Heller L; Csuk R
Eur J Med Chem; 2018 Apr; 150():176-194. PubMed ID: 29529499
[TBL] [Abstract][Full Text] [Related]
12. Synthesis and antitumor activity of ring A modified 11-keto-β-boswellic acid derivatives.
Csuk R; Niesen-Barthel A; Schäfer R; Barthel A; Al-Harrasi A
Eur J Med Chem; 2015 Mar; 92():700-11. PubMed ID: 25618017
[TBL] [Abstract][Full Text] [Related]
13. Maslinic Acid Inhibits Cervical Intraepithelial Neoplasia by Suppressing Interleukin- 6 and Enhancing Apoptosis in a Mouse Model.
Chen J; Wang L
Anticancer Agents Med Chem; 2022; 22(3):579-585. PubMed ID: 34477530
[TBL] [Abstract][Full Text] [Related]
14. Targeting cancer cells with oleanolic and ursolic acid derived hydroxamates.
Wiemann J; Heller L; Csuk R
Bioorg Med Chem Lett; 2016 Feb; 26(3):907-909. PubMed ID: 26750249
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Membrane damaging activity of a maslinic acid analog.
Siewert B; Csuk R
Eur J Med Chem; 2014 Mar; 74():1-6. PubMed ID: 24440377
[TBL] [Abstract][Full Text] [Related]
18. Synthesis of β-boswellic acid derivatives as cytotoxic and apoptotic agents.
Kumar A; Qayum A; Sharma PR; Singh SK; Shah BA
Bioorg Med Chem Lett; 2016 Jan; 26(1):76-81. PubMed ID: 26608550
[TBL] [Abstract][Full Text] [Related]
19. Synthesis and in vitro antitumor evaluation of betulin acid ester derivatives as novel apoptosis inducers.
Yang SJ; Liu MC; Xiang HM; Zhao Q; Xue W; Yang S
Eur J Med Chem; 2015 Sep; 102():249-55. PubMed ID: 26280921
[TBL] [Abstract][Full Text] [Related]
20. Synthesis and biological evaluation of celastrol derivatives as anti-ovarian cancer stem cell agents.
Li X; Ding J; Li N; Liu W; Ding F; Zheng H; Ning Y; Wang H; Liu R; Ren S
Eur J Med Chem; 2019 Oct; 179():667-679. PubMed ID: 31279299
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]