Results 251 to 260 of about 75,606 (303)
Reviewing Glycosyl‐Inositols: Natural Occurrence, Biological Roles, and Synthetic Techniques
Overall, this comprehensive review underscores the significance of glycosyl inositols as versatile molecules with diverse biological functions and promising applications in scientific research and industry. Methods for their chemical and enzymatic synthesis are also reviewed, highlighting recent advances and challenges in the field.
Alfonso Miranda‐Molina+3 more
wiley +1 more source
Proteome‐Wide Profiling of Olaparib Interactors Using a Biotinylated Photoaffinity Probe
Novel interactors found for olaparib: Olaparib is an important anti‐cancer drug in BRCA‐mutated cancers. In this study, we identified novel interactors for olaparib using photoaffinity labeling. We designed a biotinylated photoaffinity probe and used it in a proteomic screening to discover a broad range of olaparib interactors, including previously ...
Femke L. A. M. van der Heijden+5 more
wiley +1 more source
Chondroitin Sulfate‐Coated Heteroduplex‐Molecular Spherical Nucleic Acids
[60]fullerene‐based molecular spherical nucleic acids (MSNAs) were used as hybridization‐mediated carriers for an antisense oligonucleotide, suppressing Tau protein, and its conjugates with chondroitin sulfate (CS) tetrasaccharides. The impact of the MSNA‐carriers and the CS‐halo on the cellular uptake and suppression of Tau‐protein was studied with ...
Toni Laine+4 more
wiley +1 more source
Synthesis and Preliminary Evaluation of Tanshinone Mimic Conjugates for Mechanism of Action Studies
A small array of Tanshinone Mimics (TM) probes with a detection‐promoting moiety (either a photoaffinity probe ‐ PAP or biotin) has been synthesized for mechanism of action (MoA) studies on Human antigen R (HuR). Biological and biochemical assays were used to characterize the novel TM conjugates.
Giulia Assoni+5 more
wiley +1 more source
This study reports the synthesis of five tetrazine‐coordinated, half‐sandwich iridium complexes and extensively describe their reactivity. Live cell fluorescent bioorthogonal labeling reveals the nuclear tropism of the most cytotoxic complex. Intracellular imaging of anticancer metallodrugs often relies on prelabeling with organic fluorophores, which ...
Alfonso Annunziata+6 more
wiley +1 more source
FtsZ is the only target protein that has been biochemically confirmed to be hydrolyzed both in vitro and in bacterial cells. Coupled with activity‐based protein profiling of nonribosomal peptide synthetases, the ClpP‐ADEP1 proteolytic complex that degrades the surfactin synthetases SrfAA and SrfAB in cell lysates and bacterial cells is demonstrated ...
Fumihiro Ishikawa+4 more
wiley +1 more source
L‐Leu‐AMS‐based adenylation domain inhibitors with the modification of 2′‐OH in the adenosine skeleton are synthesized. Coupled with affinity‐based protein profiling of nonribosomal peptide synthetases (NRPSs), their activities toward surfactin‐NRPSs in Bacillus subtilis are evaluated.
Fumihiro Ishikawa+3 more
wiley +1 more source
Leishmaniasis poses a global health challenge with limited treatment options and rising drug resistance. Activity‐based protein profiling using fluorophosphonate probes is employed to profile serine hydrolases, key virulence factors in Leishmania mexicana.
Jaime A. Isern+7 more
wiley +1 more source
Chromenone derivatives as CRM1 Inhibitors for Targeting Glioblastoma
Glioblastoma (GBM) is one of the most aggressive and deadly cancers. Due to the complexity and redundancy within signaling networks in GBM, targeted inhibitors of specific pathways have shown only limited success. The nuclear export receptor Chromosome Region Maintenance 1 (CRM1) has recently emerged as a promising therapeutic target, as its inhibition
Wolfgang Link+10 more
wiley +1 more source
A series of adenosine triphosphate derivatives bearing chloro, fluoro, amino, methyl, vinyl and ethynyl groups at position 2 were synthesized and tested as substrates for RNA and DNA polymerases. The modified nucleotides worked well in in vitro transcription with T7 polymerase and primer extension (PEX) using engineered DNA polymerases (TGK, 2M) except
Ugnė Šinkevičiūtė+5 more
wiley +1 more source