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Dulla, Balakrishna ; Kirla, Krishna T. ; Rathore, V. ; Deora, G. S. ; Kavela, S. ; Maddika, S. ; Chatti, K. ; Reiser, Oliver ; ;

Synthesis and evaluation of 3-amino/guanidine substituted phenyl oxazoles as a novel class of LSD1 inhibitors with anti-proliferative properties

Dulla, Balakrishna, Kirla, Krishna T. , Rathore, V., Deora, G. S. , Kavela, S., Maddika, S., Chatti, K. , Reiser, Oliver , make_name_string expected hash reference and make_name_string expected hash reference (2013) Synthesis and evaluation of 3-amino/guanidine substituted phenyl oxazoles as a novel class of LSD1 inhibitors with anti-proliferative properties. Organic & Biomolecular Chemistry 11, 3103- 3107.

Date of publication of this fulltext: 04 Aug 2016 11:21
Article
DOI to cite this document: 10.5283/epub.34243


Abstract

A series of functionalized phenyl oxazole derivatives was designed, synthesized and screened in vitro for their activities against LSD1 and for effects on viability of cervical and breast cancer cells, and in vivo for effects using zebrafish embryos. These compounds are likely to act via multiple epigenetic mechanisms specific to cancer cells including LSD1 inhibition.



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Details

Item typeArticle
Journal or Publication TitleOrganic & Biomolecular Chemistry
Publisher:ROYAL SOC CHEMISTRY
Open Access Type:Alliance-/National licence
Place of Publication:CAMBRIDGE
Volume:11
Page Range:3103- 3107
Date2013
InstitutionsChemistry and Pharmacy > Institut für Organische Chemie > Lehrstuhl Prof. Dr. Oliver Reiser
Identification Number
ValueType
10.1039/c3ob40217gDOI
KeywordsHISTONE DEMETHYLASE LSD1; ANALOGS; RECEPTOR; REEXPRESSION; INACTIVATOR; CHROMATIN; GENES;
Dewey Decimal Classification500 Science > 540 Chemistry & allied sciences
StatusPublished
RefereedYes, this version has been refereed
Created at the University of RegensburgYes
URN of the UB Regensburgurn:nbn:de:bvb:355-epub-342433
Item ID34243

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