Thales Kronenberger
Overview
Explore the profile of Thales Kronenberger including associated specialties, affiliations and a list of published articles.
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Articles
91
Citations
384
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Recent Articles
1.
Wang M, Medarametla P, Kronenberger T, Deingruber T, Brear P, Figueroa W, et al.
Nat Commun
. 2025 Mar;
16(1):2334.
PMID: 40057486
Fatty acids are a primary source of carbon for Pseudomonas aeruginosa (PA) in the airways of people with cystic fibrosis (CF). Here, we use tandem mass-tag proteomics to analyse the...
2.
Dusek J, Mejdrova I, Dohnalova K, Smutny T, Chalupsky K, Krutakova M, et al.
Nat Commun
. 2025 Feb;
16(1):1418.
PMID: 39915454
Constitutive androstane receptor (CAR) and pregnane X receptor (PXR) are closely related nuclear receptors with overlapping regulatory functions in xenobiotic clearance but distinct roles in endobiotic metabolism. Car activation has...
3.
Rudalska R, Harbig J, Forster M, Woelffing P, Esposito A, Kudolo M, et al.
Nat Cancer
. 2025 Jan;
6(2):259-277.
PMID: 39820127
Colorectal cancer (CRC) constitutes the second leading cause of cancer-related death worldwide and advanced CRCs are resistant to targeted therapies, chemotherapies and immunotherapies. p38α (Mapk14) has been suggested as a...
4.
Flury P, Kruger N, Sylvester K, Breidenbach J, Al Hamwi G, Qiao J, et al.
J Med Chem
. 2025 Jan;
68(3):3626-3652.
PMID: 39813204
The main protease (M) of SARS-CoV-2 is a key drug target for the development of antiviral therapeutics. Here, we designed and synthesized a series of small-molecule peptidomimetics with various cysteine-reactive...
5.
Waitman K, Martin H, Carlos J, Braga R, Souza V, Melo-Filho C, et al.
bioRxiv
. 2024 Dec;
PMID: 39677737
Highlights: Novel kinase/HDAC inhibitors for cancer treatment were found using machine learning61 QSAR models for hematological cancers and its targets were built and validatedK562, MV4-11, MM1S, NB-4, U937, and HDAC6...
6.
Liu L, Francisco K, Sun Y, Serafim M, Amarasinghe D, Teixeira T, et al.
ACS Infect Dis
. 2024 Nov;
10(12):4182-4193.
PMID: 39589805
The proteasome is essential for eukaryotic cell proteostasis, and inhibitors of the 20S proteasome are progressing preclinically and clinically as antiparasitics. We screened, the causative agent of human and animal...
7.
Engelhardt M, Zimmermann M, Dammann M, Stahlecker J, Poso A, Kronenberger T, et al.
J Chem Theory Comput
. 2024 Sep;
20(23):10716-10730.
PMID: 39291905
Halogen bonding is a valuable interaction in drug design, offering an unconventional way to influence affinity and selectivity by leveraging the halogen atoms' ability to form directional bonds. The present...
8.
da Silva Oliveira D, Paz F, Ferreira Brito N, Kruger A, Cassiano Martinho A, Jacques Dit Lapierre T, et al.
Eur J Med Chem
. 2024 Jun;
275:116621.
PMID: 38944935
An optimization of the pyridylpiperazine series against Plasmodium falciparum has been performed, exploring a structure-activity relationship carried out on the toluyl fragment of hit 1, a compound with low micromolar...
9.
Flury P, Breidenbach J, Kruger N, Voget R, Schakel L, Si Y, et al.
ACS Pharmacol Transl Sci
. 2024 Apr;
7(4):1195-1196.
PMID: 38633592
[This corrects the article DOI: 10.1021/acsptsci.3c00313.].
10.
Rashidian A, Dusek J, Drastik M, Smutna L, Fritsche K, Braeuning A, et al.
Environ Sci Technol
. 2024 Apr;
58(16):6913-6923.
PMID: 38593436
4-Nonylphenol (4-NP), a -substituted phenolic compound with a straight or branched carbon chain, is a ubiquitous environmental pollutant and food contaminant. 4-NP, particularly the branched form, has been identified as...