Amanote Research
Register
Sign In
Potent and Highly Selective Inhibitors of the Proteasome Trypsin-Like Site by Incorporation of Basic Side Chain Containing Amino Acid Derived Sulfonyl Fluorides
doi 10.1021/acs.jmedchem.8b00685.s002
Full Text
Open PDF
Abstract
Available in
full text
Date
Unknown
Authors
Unknown
Publisher
American Chemical Society (ACS)
Related search
Site-Specific Incorporation of a Dithiolane Containing Amino Acid Into Proteins
Trypanosoma Brucei: Β2-Selective Proteasome Inhibitors Do Not Block the Proteasomal Trypsin-Like Activity but Are Trypanocidal
Molecular and Biochemical Parasitology
Parasitology
Molecular Biology
New Betulinic Acid Derivatives as Potent Proteasome Inhibitors
Bioorganic and Medicinal Chemistry Letters
Organic Chemistry
Molecular Medicine
Molecular Biology
Biochemistry
Clinical Biochemistry
Pharmaceutical Science
Drug Discovery
Β-Turn-Like Conformation and Side Chain Interactions of Aspartic Acid-Containing Dipeptides
Polymer Journal
Polymers
Materials Chemistry
Plastics
Development of Highly Potent and Selective Steroidal Inhibitors and Degraders of CDK8
Development of Highly Potent and Selective Diaminothiazole Inhibitors of Cyclin-Dependent Kinases
Journal of Medicinal Chemistry
Drug Discovery
Molecular Medicine
Synthesis and Evaluation of Macrocyclic Peptide Aldehydes as Potent and Selective Inhibitors of the 20S Proteasome
Unnatural Amino Acid Incorporation Into Virus-Like Particles
Bioconjugate Chemistry
Organic Chemistry
Biotechnology
Pharmacology
Pharmaceutical Science
Bioengineering
Biomedical Engineering
Design of Potent Bivalent Thrombin Inhibitors Based on Hirudin Sequence: Incorporation of Nonsubstrate-Type Active Site Inhibitors
Biochemistry
Biochemistry
