The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
27216999 |
30 |
Protective effect of novel substituted nicotine hydrazide analogues against hypoxic brain injury in neonatal rats via inhibition of caspase. |
The Fifth Affiliated Hospital of Guangzhou Medical University |
25468037 |
76 |
Synthesis and evaluation of N-acyl-substituted 1,2-benzisothiazol-3-one derivatives as caspase-3 inhibitors. |
TBA |
25358116 |
84 |
Synthesis of 7-halogenated isatin sulfonamides: nonradioactive counterparts of caspase-3/-7 inhibitor-based potential radiopharmaceuticals for molecular imaging of apoptosis. |
Westf£Lische Wilhelms-Universit£T M£Nster |
24656804 |
44 |
1,2-benzisothiazol-3-one derivatives as a novel class of small-molecule caspase-3 inhibitors. |
Tianjin University of Science and Technology |
23685941 |
53 |
Influence of 4- or 5-substituents on the pyrrolidine ring of 5-[1-(2-methoxymethylpyrrolidinyl)sulfonyl]isatin derivatives on their inhibitory activities towards caspases-3 and -7. |
Westf£Lische Wilhelms-Universit£T M£Nster |
23656488 |
18 |
Synthesis, 18F-radiolabeling, and in vivo biodistribution studies of N-fluorohydroxybutyl isatin sulfonamides using positron emission tomography. |
Westf£Lische Wilhelms-Universit£T M£Nster |
23411396 |
60 |
Synthesis of new fluorinated, 2-substituted 5-pyrrolidinylsulfonyl isatin derivatives as caspase-3 and caspase-7 inhibitors: nonradioactive counterparts of putative PET-compatible apoptosis imaging agents. |
Westf£Lische Wilhelms-Universit£T M£Nster |
24900651 |
50 |
Irreversible inhibitors of cysteine proteases. |
Dart Neuroscience |
19715320 |
87 |
Grassystatins A-C from marine cyanobacteria, potent cathepsin E inhibitors that reduce antigen presentation. |
University of Florida |
14980679 |
30 |
Dipeptidyl aspartyl fluoromethylketones as potent caspase-3 inhibitors: SAR of the P2 amino acid. |
Maxim Pharmaceuticals |
21441025 |
147 |
Synthesis and evaluation of isatin analogs as caspase-3 inhibitors: introduction of a hydrophilic group increases potency in a whole cell assay. |
Washington University |
20541849 |
21 |
Synthesis and evaluation of vinyl sulfones as caspase-3 inhibitors. A structure-activity study. |
University of Lisbon |
19445513 |
82 |
Fluorinated isatin derivatives. Part 2. New N-substituted 5-pyrrolidinylsulfonyl isatins as potential tools for molecular imaging of caspases in apoptosis. |
Westfalische Wilhelms-Universitat |
19299147 |
60 |
Fluorinated isatin derivatives. Part 1: synthesis of new N-substituted (S)-5-[1-(2-methoxymethylpyrrolidinyl)sulfonyl]isatins as potent caspase-3 and -7 inhibitors. |
WestfäLische Wilhelms-UniversitäT |
19049429 |
70 |
Design, synthesis, and biological characterization of a caspase 3/7 selective isatin labeled with 2-[18F]fluoroethylazide. |
Imperial College |
18387304 |
4 |
Structure-based discovery of a novel non-peptidic small molecular inhibitor of caspase-3. |
Tokyo University of Science |
17889532 |
23 |
Dipeptidyl aspartyl fluoromethylketones as potent caspase inhibitors: peptidomimetic replacement of the P(2) amino acid by 2-aminoaryl acids and other non-natural amino acids. |
Epicept |
17585855 |
65 |
Isatin sulfonamide analogs containing a Michael addition acceptor: a new class of caspase 3/7 inhibitors. |
Washington University |
17251019 |
30 |
Solid-phase analogue synthesis of caspase-3 inhibitors via palladium-catalyzed amination of 3-bromopyrazinones. |
Merck Frosst Centre For Therapeutic Research |
17181147 |
10 |
Synthesis of novel caspase inhibitors for characterization of the active caspase proteome in vitro and in vivo. |
University of Edinburgh |
17154501 |
121 |
5-pyrrolidinylsulfonyl isatins as a potential tool for the molecular imaging of caspases in apoptosis. |
University Hospital of The WestfäLische Wilhelms-UniversitäT |
16891117 |
5 |
Synthesis, radiolabeling, and in vivo evaluation of an 18F-labeled isatin analog for imaging caspase-3 activation in apoptosis. |
Washington University |
15713391 |
19 |
Dipeptidyl aspartyl fluoromethylketones as potent caspase inhibitors: peptidomimetic replacement of the P2 alpha-amino acid by a alpha-hydroxy acid. |
Maxim Pharmaceuticals |
15686936 |
210 |
Novel pyrazinone mono-amides as potent and reversible caspase-3 inhibitors. |
Merck Frosst Centre For Therapeutic Research |
15454214 |
26 |
Dipeptidyl aspartyl fluoromethylketones as potent caspase inhibitors: SAR of the N-protecting group. |
Maxim Pharmaceuticals |
12270186 |
99 |
Acyl dipeptides as reversible caspase inhibitors. Part 2: further optimization. |
Idun Pharmaceuticals |
12270185 |
257 |
Acyl dipeptides as reversible caspase inhibitors. Part 1: initial lead optimization. |
Idun Pharmaceuticals |
27563406 |
128 |
Discovery of Fluoromethylketone-Based Peptidomimetics as Covalent ATG4B (Autophagin-1) Inhibitors. |
Roche Pharma Research and Early Development |
10978183 |
40 |
Caspases as targets for anti-inflammatory and anti-apoptotic drug discovery. |
Basf Bioresearch |
28615111 |
24 |
Synthesis and antitumor activities of 1,2,3-triazines and their benzo- and heterofused derivatives. |
Universit£ |
29648825 |
47 |
Rational Drug Design of Topically Administered Caspase 1 Inhibitors for the Treatment of Inflammatory Acne. |
Nestl� |
12757844 |
9 |
In vitro characterization of [3H]MethoxyPyEP, an mGluR5 selective radioligand. |
Merck Research Laboratories |
9108306 |
17 |
Molecular cloning and characterization of a new receptor for galanin. |
Merck Research Laboratories |
18812261 |
8 |
The molecular interactions of buspirone analogues with the serotonin transporter. |
National Medicines Institute |
18307303 |
75 |
Discovery of selective aminothiazole aurora kinase inhibitors. |
Novartis |
18800762 |
61 |
Inhibition of geranylgeranyl diphosphate synthase by bisphosphonates: a crystallographic and computational investigation. |
National Taiwan University |
18308563 |
39 |
Probing the elusive catalytic activity of vertebrate class IIa histone deacetylases. |
Irbm/Merck Research Laboratories |
17685602 |
33 |
Discovery of 3,3'-(2,4-diaminopteridine-6,7-diyl)diphenol as an isozyme-selective inhibitor of PI3K for the treatment of ischemia reperfusion injury associated with myocardial infarction. |
Targegen |
18754654 |
19 |
The identification of 2-(1H-indazol-4-yl)-6-(4-methanesulfonyl-piperazin-1-ylmethyl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidine (GDC-0941) as a potent, selective, orally bioavailable inhibitor of class I PI3 kinase for the treatment of cancer . |
Piramed Pharma |
14698155 |
68 |
Synthesis and evaluation of indenopyrazoles as cyclin-dependent kinase inhibitors. Part 4: Heterocycles at C3. |
Bristol-Myers Squibb |