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Development of a 1,2,4-Triazole-Based Lead Tankyrase Inhibi..:

Ruben G. G. Leenders (11812585) ; Shoshy Alam Brinch (11812588) ; Sven T. Sowa (9017705)...
https://figshare.com/articles/journal_contribution/Development_of_a_1_2_4-Triazole-Based_Lead_Tankyrase_Inhibitor_Part_II/17145814. , 2021

Link: https://doi.org/10.1021/acs.jmedchem.1c01264.s002

RT Journal
T1 <Title>Development of a 1,2,4-Triazole-Based Lead Tankyrase Inhibitor: Part II</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_17145814&Exemplar=1&LAN=DE
				
A1 Ruben G. G. Leenders (11812585)
A1 Shoshy Alam Brinch (11812588)
A1 Sven T. Sowa (9017705)
A1 Enya Amundsen-Isaksen (11812591)
A1 Albert Galera-Prat (161919)
A1 Sudarshan Murthy (3625238)
A1 Sjoerd Aertssen (9017714)
A1 Johannes N. Smits (11812594)
A1 Piotr Nieczypor (2729590)
A1 Eddy Damen (9017717)
A1 Anita Wegert (3832396)
A1 Marc Nazaré (2030308)
A1 Lari Lehtiö (1860307)
A1 Jo Waaler (1970758)
A1 Stefan Krauss (217340)
YR 2021
K1 Biochemistry
K1 Genetics
K1 Molecular Biology
K1 Pharmacology
K1 Biotechnology
K1 Immunology
K1 Cancer
K1 Mental Health
K1 Infectious Diseases
K1 Chemical Sciences not elsewhere classified
K1 showed picomolar ic
K1 reduced cell growth
K1 overall favorable absorption
K1 improved pharmacokinetic profile
K1 east -
K1 south
K1 dependent biomarker engagement
K1 hippo signaling pathways
K1 hybrids identified compound
K1 24 </ b
K1 50 </ sub
K1 2 also impact
K1 based lead compound
K1 1 </ b
K1 translational modification
K1 target proteins
K1 target liabilities
K1 point alterations
K1 involved pathways
K1 induced dose
K1 catalyze post
K1 1700 )
K1 153 )
JF https://figshare.com/articles/journal_contribution/Development_of_a_1_2_4-Triazole-Based_Lead_Tankyrase_Inhibitor_Part_II/17145814
LK http://dx.doi.org/https://doi.org/10.1021/acs.jmedchem.1c01264.s002
DO https://doi.org/10.1021/acs.jmedchem.1c01264.s002
SF ELIB - SuUB Bremen

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