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Proteases—From Basic Structure to Function to Drug Design as Targeted Therapy
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In the two last decades, proteases have constituted one of the primary and important targets in drug discovery. The U.S. FDA has approved more than 12 protease therapies in the last 10 years, and a number of next-generation or completely new proteases are under clinical development. Protease inhibition strategies are one of the fastest expanding areas in the field of of drugs that show considerable promise. This Special Issue will focus on the recent advances in the discovery and development of protease inhibitors, covering the synthesis of protease inhibitors, the design of new chemical entities acting as inhibitors of special/particular types of proteases, and their mode of actions (Frolova et al. 2020; Slapak et al. 2020; Künnapuu et al. 2021). In addition, the new applications of these interesting compounds/biomolecules and their limitations have been discussed and described (Wang et al. 2020; Bartošová-Sojková et al. 2021).
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Keywords
- ADAMTS3
- Angiogenesis
- Apoptosis
- Bowman–Birk inhibitor
- Cancer
- cathepsin D
- CCBE1
- cysteine protease inhibitor
- diversification
- Extracellular matrix
- gentamicin
- Immune response
- KLK3
- lymphangiogenesis
- lymphedema
- matrix metalloproteases
- matrix metalloproteinase
- metastasis
- MMP
- MMP14
- MMP2
- MMP7
- MMP9
- nuclei
- Pancreatic Cancer
- parasite
- PDAC
- phylogenetic analysis
- plasmin
- PlGF
- prostate-specific antigen (PSA)
- Proteases
- protein structure
- proteolytic activation
- ranacyclin
- Reference, information & interdisciplinary subjects
- Research & information: general
- signal peptide
- stefin
- structure–activity relationship
- synergistic effect
- thema EDItEUR::G Reference, Information and Interdisciplinary subjects::GP Research and information: general
- thrombin
- trypsin inhibitor
- vascular biology
- vascular endothelial growth factors (VEGFs)
- VEGF-A
- VEGF-B
- VEGF-C
- VEGF-D
- Wound healing
Links
DOI: 10.3390/books978-3-0365-2574-7Editions