Proteases—From Basic Structure to Function to Drug Design as Targeted Therapy

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 inhibit...

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Year of Publication:2021
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spelling Kwok, Hang Fai edt
Proteases—From Basic Structure to Function to Drug Design as Targeted Therapy
Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute 2021
1 electronic resource (93 p.)
text txt rdacontent
computer c rdamedia
online resource cr rdacarrier
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).
English
Research & information: general bicssc
MMP
MMP2
MMP9
MMP7
MMP14
matrix metalloproteases
PDAC
pancreatic cancer
Bowman–Birk inhibitor
ranacyclin
trypsin inhibitor
structure–activity relationship
synergistic effect
Gentamicin
matrix metalloproteinase
extracellular matrix
nuclei
cancer
apoptosis
immune response
cysteine protease inhibitor
stefin
signal peptide
parasite
phylogenetic analysis
diversification
protein structure
vascular endothelial growth factors (VEGFs)
VEGF-A
PlGF
VEGF-B
VEGF-C
VEGF-D
angiogenesis
lymphangiogenesis
CCBE1
proteases
ADAMTS3
plasmin
cathepsin D
KLK3
prostate-specific antigen (PSA)
thrombin
wound healing
metastasis
proteolytic activation
vascular biology
lymphedema
3-0365-2575-0
3-0365-2574-2
Shaw, Christopher edt
Walker, Brian edt
Kwok, Hang Fai oth
Shaw, Christopher oth
Walker, Brian oth
language English
format eBook
author2 Shaw, Christopher
Walker, Brian
Kwok, Hang Fai
Shaw, Christopher
Walker, Brian
author_facet Shaw, Christopher
Walker, Brian
Kwok, Hang Fai
Shaw, Christopher
Walker, Brian
author2_variant h f k hf hfk
c s cs
b w bw
author2_role HerausgeberIn
HerausgeberIn
Sonstige
Sonstige
Sonstige
title Proteases—From Basic Structure to Function to Drug Design as Targeted Therapy
spellingShingle Proteases—From Basic Structure to Function to Drug Design as Targeted Therapy
title_full Proteases—From Basic Structure to Function to Drug Design as Targeted Therapy
title_fullStr Proteases—From Basic Structure to Function to Drug Design as Targeted Therapy
title_full_unstemmed Proteases—From Basic Structure to Function to Drug Design as Targeted Therapy
title_auth Proteases—From Basic Structure to Function to Drug Design as Targeted Therapy
title_new Proteases—From Basic Structure to Function to Drug Design as Targeted Therapy
title_sort proteases—from basic structure to function to drug design as targeted therapy
publisher MDPI - Multidisciplinary Digital Publishing Institute
publishDate 2021
physical 1 electronic resource (93 p.)
isbn 3-0365-2575-0
3-0365-2574-2
illustrated Not Illustrated
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