The set of chemical compounds shared by two or more chemical libraries is assessed routinely as means of comparing these libraries for various applications. Traditionally this is achieved by comparing the members of the chemical libraries individually for identity. This approach becomes impractical when operating on chemical libraries exceeding billions or even trillions of compounds in size. As a result, no such analysis exists for ultralarge chemical spaces like the Enamine REAL Space containing over 20 billion compounds. In this work, we present a novel tool called SpaceCompare for the overlap calculation of large, nonenumerable combinatorial fragment spaces. In contrast to existing methods, SpaceCompare utilizes topological fingerprints and the combinatorial character of these chemical spaces. The tool is able to determine the exact overlap of prominent spaces like Enamine's REAL Space, WuXi's GalaXi Space, and Otava's CHEMriya for the first time.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.jcim.1c01378 | DOI Listing |
RSC Adv
January 2025
Department of Chemical Engineering, National Cheng Kung University Tainan 70101 Taiwan
The functions of peptides often emerge upon their self-assembly or binding with other co-factors. However, the synthetic complexity makes these functional peptides intractable. Here, we utilize the ester-amide exchange reaction in deep eutectic solvents to generate peptide libraries from unactivated amino acids.
View Article and Find Full Text PDFJ Proteome Res
January 2025
Department of Chemistry "Ugo Schiff", University of Florence, Sesto Fiorentino 50019, Italy.
A combination of pathway enrichment and metabolite clustering analysis is used to interpret untargeted H NMR metabolomics data, enabling a biochemically informative comparison of the effects induced by a panel of known cytotoxic gold(I) and gold(III) compounds in A2780 ovarian cancer cells. The identification of the most dysregulated pathways for the major classes of compounds highlights specific chemical features that lead to common biological effects. The proposed approach may have broader applicability to the screening of metal-based drug candidate libraries, which is always complicated by their multitarget nature, and support the comprehensive interpretation of their metabolic actions.
View Article and Find Full Text PDFRecent Pat Anticancer Drug Discov
January 2025
Department of Biochemistry and Molecular Biology, Shantou University Medical College, Shantou, 515041, PR China.
Background: Lysyl oxidase-like 2 (LOXL2) is a metalloenzyme that catalyzes oxidative deamination ε-amino group of lysine. It has been found that LOXL2 is a promotor for the metastasis and invasion in kinds of tumors. Previous studies show that disulfide bonds are important components in LOXL2, and their bioactivity can be regulated by those bonds.
View Article and Find Full Text PDFBMC Bioinformatics
January 2025
MOE Key Laboratory for Industrial Biocatalysis, Institute of Biochemical Engineering, Department of Chemical Engineering, Tsinghua University, Beijing, 100084, China.
Background: CRISPRi screening has become a powerful approach for functional genomic research. However, the off-target effects resulting from the mismatch tolerance between sgRNAs and their intended targets is a primary concern in CRISPRi applications.
Results: We introduce Guide Library Designer (GLiDe), a web-based tool specifically created for the genome-scale design of sgRNA libraries tailored for CRISPRi screening in prokaryotic organisms.
J Am Soc Mass Spectrom
January 2025
Mass Spectrometry Data Center, Biomolecular Measurement Division, National Institute of Standards and Technology (NIST), Gaithersburg, Maryland, 20899, United States.
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!