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BindingDB contains 3.2M data for 1.4M Compounds and 11.4K Targets. Of those, 1.5M data for 728K Compounds and 4.7K Targets were curated by BindingDB curators. BindingDB is a FAIRsharing resource.

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16 articles for thisTarget


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

PMID
Data
Article Title
Organization
Human acidic mammalian chitinase as a novel target for anti-asthma drug design using in silico screening.EBI
Kitasato University
Identification and characterization of acidic mammalian chitinase inhibitors.EBI
Pfizer
Molecular modeling of human acidic mammalian chitinase in complex with the natural-product cyclopentapeptide chitinase inhibitor argifin.EBI
Kitasato University
Acetazolamide-based fungal chitinase inhibitors.EBI
University of Dundee
Discovery and Optimization of a Novel Macrocyclic Amidinourea Series Active as Acidic Mammalian Chitinase Inhibitors.EBI
University of Siena
An insight into the medicinal attributes of berberine derivatives: A review.EBI
Isf College of Pharmacy
Discovery of EBI
Oncoarendi Therapeutics
Benzoxazepine-Derived Selective, Orally Bioavailable Inhibitor of Human Acidic Mammalian Chitinase.EBI
Oncoarendi Therapeutics
A Series of Compounds Bearing a Dipyrido-Pyrimidine Scaffold Acting as Novel Human and Insect Pest Chitinase Inhibitors.EBI
Dalian University of Technology
Development of Dual Chitinase Inhibitors as Potential New Treatment for Respiratory System Diseases.EBI
Oncoarendi Therapeutics
Targeting Acidic Mammalian chitinase Is Effective in Animal Model of Asthma.EBI
Oncoarendi Therapeutics
Substituted amino triazoles useful as chitinase inhibitorsBDB
Molecure
Substituted amino triazoles useful as human chitinase inhibitorsBDB
Oncoarendi Therapeutics
Substituted amino triazoles useful as human chitinase inhibitorsBDB
Oncoarendi Therapeutics
Substituted amino triazoles useful as human chitinase inhibitorsBDB
Oncoarendi Therapeutics
Analyzing airway inflammation with chemical biology: dissection of acidic mammalian chitinase function with a selective drug-like inhibitor.BDB
University of Edinburgh