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24 articles for thisTarget


The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Data
Article Title
Organization
Wortmannilactones I-L, new NADH-fumarate reductase inhibitors, induced by adding suberoylanilide hydroxamic acid to the culture medium of Talaromyces wortmannii.EBI
Dalian University of Technology
Design and application of a rigid quinazolone scaffold based on two-face Bima-helix mimicking.EBI
Dalian University of Technology
Novel soluble myeloid cell leukemia sequence 1 (Mcl-1) inhibitor (E,E)-2-(benzylaminocarbonyl)-3-styrylacrylonitrile (4g) developed using a fragment-based approach.EBI
Dalian University of Technology
Fragment-based design, synthesis, and biological evaluation of N-substituted-5-(4-isopropylthiophenol)-2-hydroxynicotinamide derivatives as novel Mcl-1 inhibitors.EBI
Dalian University of Technology
3-Thiomorpholin-8-oxo-8H-acenaphtho [1,2-b] pyrrole-9-carbonitrile (S1) derivatives as pan-Bcl-2-inhibitors of Bcl-2, Bcl-xL and Mcl-1.EBI
Dalian University of Technology
An anthraquinone scaffold for putative, two-face Bim BH3a-helix mimic.EBI
Dalian University of Technology
A novel series of l-2-benzyloxycarbonylamino-8-(2-pyridyl)-disulfidyloctanoic acid derivatives as histone deacetylase inhibitors: design, synthesis and molecular modeling study.EBI
Dalian University of Technology
Nitrogen-containing flavonoid analogues as CDK1/cyclin B inhibitors: synthesis, SAR analysis, and biological activity.EBI
Dalian University of Technology
Discovery of novel selective inhibitors for EGFR-T790M/L858R.EBI
Dalian University of Technology
Probing the difference between BH3 groove of Mcl-1 and Bcl-2 protein: Implications for dual inhibitors design.EBI
Dalian University of Technology
3-Thiomorpholin-8-oxo-8H-acenaphtho[1,2-b]pyrrole-9-carbonitrile (S1) based molecules as potent, dual inhibitors of B-cell lymphoma 2 (Bcl-2) and myeloid cell leukemia sequence 1 (Mcl-1): structure-based design and structure-activity relationship studies.EBI
Dalian University of Technology
A novel Hsp70 inhibitor specifically targeting the cancer-related Hsp70-Bim protein-protein interaction.EBI
Dalian University of Technology
Total synthesis and biological evaluation of 7-hydroxyneolamellarin A as hypoxia-inducible factor-1α inhibitor for cancer therapy.EBI
Dalian University of Technology
Synthesis and structure-activity relationship of coumarins as potent Mcl-1 inhibitors for cancer treatment.EBI
Dalian University of Technology
Targeting the Allosteric Pathway That Interconnects the Core-Functional Scaffold and the Distal Phosphorylation Sites for Specific Dephosphorylation of Bcl-2.EBI
Dalian University of Technology
Small-Molecule Antagonist Targeting Exportin-1 via Rational Structure-Based Discovery.EBI
Dalian University of Technology
A Series of Compounds Bearing a Dipyrido-Pyrimidine Scaffold Acting as Novel Human and Insect Pest Chitinase Inhibitors.EBI
Dalian University of Technology
De Novo Molecular Design of a Novel Octapeptide That Inhibits In Vivo Melanogenesis and Has Great Transdermal Ability.EBI
Dalian University of Technology
Bcl-2/MDM2 Dual Inhibitors Based on Universal Pyramid-Like α-Helical Mimetics.EBI
Dalian University of Technology
Synthesis and quantitative structure-activity relationships of fluorine-containing 4,4-dihydroxylmethyl-2-aryliminooxazo(thiazo)lidines as trehalase inhibitors.EBI
Dalian University of Technology
Selective inhibition of β-N-acetylhexosaminidases by thioglycosyl-naphthalimide hybrid molecules.EBI
Dalian University of Technology
Varic acid analogues from fungus as PTP1B inhibitors: Biological evaluation and structure-activity relationships.EBI
Dalian University of Technology
Pentacyclic triterpenes asα-glucosidase andα-amylase inhibitors: Structure-activity relationships and the synergism with acarbose.EBI
Dalian University of Technology