21 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 34953094 | Engineering Enzyme-Cleavable Oligonucleotides by Automated Solid-Phase Incorporation of Cathepsin B Sensitive Dipeptide Linkers. | 2022 Mar 21 | 2 |
2 | 32798638 | Controlled loading of albumin-drug conjugates ex vivo for enhanced drug delivery and antitumor efficacy. | 2020 Dec 10 | 1 |
3 | 31184188 | Preparation of a Multiple-Targeting NIR-Based Fluorogenic Probe and Its Application for Selective Cancer Cell Imaging. | 2019 Jun 21 | 1 |
4 | 29473076 | Impact of cathepsin B-sensitive triggers and hydrophilic linkers on in vitro efficacy of novel site-specific antibody-drug conjugates. | 2018 Mar 14 | 1 |
5 | 31156276 | Improved Methodology for the Synthesis of a Cathepsin B Cleavable Dipeptide Linker, Widely Used in Antibody-Drug Conjugate Research. | 2018 Oct 3 | 1 |
6 | 29123088 | A water-soluble nucleolin aptamer-paclitaxel conjugate for tumor-specific targeting in ovarian cancer. | 2017 Nov 9 | 2 |
7 | 23903896 | Preclinical studies of targeted therapies for CD20-positive B lymphoid malignancies by Ofatumumab conjugated with auristatin. | 2014 Feb | 1 |
8 | 23712251 | Toward very potent, non-covalent organophosphonate inhibitors of cathepsin C and related enzymes by 2-amino-1-hydroxy-alkanephosphonates dipeptides. | 2013 Aug | 1 |
9 | 24900316 | Design, Synthesis, and Antitumor Activity of 4-Halocolchicines and Their Pro-drugs Activated by Cathepsin B. | 2011 May 12 | 1 |
10 | 19131246 | Development of dual-acting prodrugs for circumventing multidrug resistance. | 2009 Feb 1 | 1 |
11 | 19199576 | Development of protein-binding bifunctional linkers for a new generation of dual-acting prodrugs. | 2009 Feb | 1 |
12 | 11802791 | S2' substrate specificity and the role of His110 and His111 in the exopeptidase activity of human cathepsin B. | 2002 Feb 1 | 2 |
13 | 12121142 | Cathepsin B-labile dipeptide linkers for lysosomal release of doxorubicin from internalizing immunoconjugates: model studies of enzymatic drug release and antigen-specific in vitro anticancer activity. | 2002 Jul-Aug | 1 |
14 | 10841792 | Peptide and peptide mimetic inhibitors of antigen presentation by HLA-DR class II MHC molecules. Design, structure-activity relationships, and X-ray crystal structures. | 2000 Jun 1 | 1 |
15 | 9873731 | Cathepsin B-sensitive dipeptide prodrugs. 1. A model study of structural requirements for efficient release of doxorubicin. | 1998 Dec 1 | 1 |
16 | 9873732 | Cathepsin B-sensitive dipeptide prodrugs. 2. Models of anticancer drugs paclitaxel (Taxol), mitomycin C and doxorubicin. | 1998 Dec 1 | 2 |
17 | 8754751 | The combined action of two thyroidal proteases releases T4 from the dominant hormone-forming site of thyroglobulin. | 1996 Aug | 2 |
18 | 8230139 | Peptide alpha-keto ester, alpha-keto amide, and alpha-keto acid inhibitors of calpains and other cysteine proteases. | 1993 Oct 29 | 1 |
19 | 1797709 | Synthesis of histidine-containing dipeptide affinity-labelling agents. Relative inactivation rates of cathepsins B and L. | 1991 Oct | 1 |
20 | 3318115 | [Brain cathepsin as dipeptidylcarboxypeptidase transforming provasopressor, pro-opioid and model peptides]. | 1987 Sep-Oct | 2 |
21 | 666735 | The specificity of cathepsin B. Hydrolysis of glucagon at the C-terminus by a peptidyldipeptidase mechanism. | 1978 Jun 1 | 1 |