Identification of a novel quinoline-based DNA demethylating compound highly potent in cancer cells
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1868-7083
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Identification of a novel quinoline-based DNA demethylating compound highly potent in cancer cells ; volume:11 ; number:1 ; day:6 ; month:5 ; year:2019 ; pages:1-18 ; date:12.2019
Clinical epigenetics ; 11, Heft 1 (6.5.2019), 1-18, 12.2019
- Urheber
-
Zwergel, Clemens
Schnekenburger, Michael
Sarno, Federica
Battistelli, Cecilia
Manara, Maria Cristina
Stazi, Giulia
Mazzone, Roberta
Fioravanti, Rossella
Gros, Christina
Ausseil, Frédéric
Florean, Cristina
Nebbioso, Angela
Strippoli, Raffaele
Ushijima, Toshikazu
Scotlandi, Katia
Tripodi, Marco
Arimondo, Paola B.
Altucci, Lucia
Diederich, Marc
Mai, Antonello
Valente, Sergio
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/s13148-019-0663-8
- URN
-
urn:nbn:de:101:1-2019071919143509366223
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:31 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Zwergel, Clemens
- Schnekenburger, Michael
- Sarno, Federica
- Battistelli, Cecilia
- Manara, Maria Cristina
- Stazi, Giulia
- Mazzone, Roberta
- Fioravanti, Rossella
- Gros, Christina
- Ausseil, Frédéric
- Florean, Cristina
- Nebbioso, Angela
- Strippoli, Raffaele
- Ushijima, Toshikazu
- Scotlandi, Katia
- Tripodi, Marco
- Arimondo, Paola B.
- Altucci, Lucia
- Diederich, Marc
- Mai, Antonello
- Valente, Sergio
- SpringerLink (Online service)
Ähnliche Objekte (12)
Correction: Identification of a novel quinoline-based DNA demethylating compound highly potent in cancer cells
(Iso)Quinoline–Artemisinin Hybrids Prepared through Click Chemistry: Highly Potent Agents against Viruses
Low concentration cell painting images enable the identification of highly potent compounds
Quinoline-thiosemicarbazone-1,2,3-triazole-acetamide derivatives as new potent α-glucosidase inhibitors
Cladosporin, A Highly Potent Antimalaria Drug?
Increasing the Activity of Copper Guanidine Quinoline Catalysts: Substitution at the Quinoline Backbone Leads to Highly Active Complexes for ATRP
Potent in vivo anti-malarial activity and representative snapshot pharmacokinetic evaluation of artemisinin-quinoline hybrids
Synthesis, structure identification, antioxidant and antimicrobial activities of some novel quinoline derivatives
Pyrazole compound BPR1P0034 with potent and selective anti-influenza virus activity
Synthesis,Antidiabetic and Antitubercular Evaluation of Quinoline–pyrazolopyrimidine hybrids and Quinoline‐4‐Arylamines
OXIDATION OF INDOLO-QUINOLINE STRUCTURES
Optimized Compound Layer Design for Highly Loaded Nitrided Gears
Correction: Identification of a novel quinoline-based DNA demethylating compound highly potent in cancer cells
(Iso)Quinoline–Artemisinin Hybrids Prepared through Click Chemistry: Highly Potent Agents against Viruses
Low concentration cell painting images enable the identification of highly potent compounds
Quinoline-thiosemicarbazone-1,2,3-triazole-acetamide derivatives as new potent α-glucosidase inhibitors
Cladosporin, A Highly Potent Antimalaria Drug?
Increasing the Activity of Copper Guanidine Quinoline Catalysts: Substitution at the Quinoline Backbone Leads to Highly Active Complexes for ATRP
Potent in vivo anti-malarial activity and representative snapshot pharmacokinetic evaluation of artemisinin-quinoline hybrids
Synthesis, structure identification, antioxidant and antimicrobial activities of some novel quinoline derivatives
Pyrazole compound BPR1P0034 with potent and selective anti-influenza virus activity
Synthesis,Antidiabetic and Antitubercular Evaluation of Quinoline–pyrazolopyrimidine hybrids and Quinoline‐4‐Arylamines
OXIDATION OF INDOLO-QUINOLINE STRUCTURES
Optimized Compound Layer Design for Highly Loaded Nitrided Gears
Correction: Identification of a novel quinoline-based DNA demethylating compound highly potent in cancer cells
(Iso)Quinoline–Artemisinin Hybrids Prepared through Click Chemistry: Highly Potent Agents against Viruses
Low concentration cell painting images enable the identification of highly potent compounds
Quinoline-thiosemicarbazone-1,2,3-triazole-acetamide derivatives as new potent α-glucosidase inhibitors
Cladosporin, A Highly Potent Antimalaria Drug?
Increasing the Activity of Copper Guanidine Quinoline Catalysts: Substitution at the Quinoline Backbone Leads to Highly Active Complexes for ATRP
Potent in vivo anti-malarial activity and representative snapshot pharmacokinetic evaluation of artemisinin-quinoline hybrids
Synthesis, structure identification, antioxidant and antimicrobial activities of some novel quinoline derivatives
Pyrazole compound BPR1P0034 with potent and selective anti-influenza virus activity
Synthesis,Antidiabetic and Antitubercular Evaluation of Quinoline–pyrazolopyrimidine hybrids and Quinoline‐4‐Arylamines
OXIDATION OF INDOLO-QUINOLINE STRUCTURES