19 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Preparation of biotinylated allosamidins with strong chitinase inhibitory activities.

University of Tokyo
Discovery and Optimization of a Novel Macrocyclic Amidinourea Series Active as Acidic Mammalian Chitinase Inhibitors.

University of Siena
Discovery of aromatic 2-(3-(methylcarbamoyl) guanidino)-N-aylacetamides as highly potent chitinase inhibitors.

China Agricultural University
An insight into the medicinal attributes of berberine derivatives: A review.

Isf College of Pharmacy
Recent Progress in the Discovery of Antifungal Agents Targeting the Cell Wall.

Shaanxi University of Science and Technology
Discovery of

Oncoarendi Therapeutics
Benzoxazepine-Derived Selective, Orally Bioavailable Inhibitor of Human Acidic Mammalian Chitinase.

Oncoarendi Therapeutics
A Series of Compounds Bearing a Dipyrido-Pyrimidine Scaffold Acting as Novel Human and Insect Pest Chitinase Inhibitors.

Dalian University of Technology
Development of Dual Chitinase Inhibitors as Potential New Treatment for Respiratory System Diseases.

Oncoarendi Therapeutics
Targeting Acidic Mammalian chitinase Is Effective in Animal Model of Asthma.

Oncoarendi Therapeutics
Triazolo-pyrimidine compounds and uses thereof

Dizal (Jiangsu) Pharmaceutical
5-[(piperazin-1-yl)-3-oxo-propyl]-imidazolidine-2,4-dione derivatives as ADAMTS inhibitors for the treatment of osteoarthritis

Galapagos
[1,2,4]triazolo[1,5-a]pyridinyl substituted indole compounds

Bristol-Myers Squibb
Synthesis, antielastase, antioxidant and radical scavenging activities of 4-(aza substituted) methylene substituted dihydroxy coumarines.

Giresun University
Disorazoles Block Group A Streptococcal Invasion into Epithelial Cells Via Interference with the Host Factor Ezrin.

Saarland University
Novel 4-aminoquinolines active against chloroquine-resistant and sensitive P. falciparum strains that also inhibit botulinum serotype A.

University of Belgrade
SYNTHESIS AND BIOLOGICAL EVALUATION OF CONFORMATIONALLY CONSTRAINED BICYCLIC AND TRICYCLIC BALANOL ANALOGUES AS INHIBITORS OF PROTEIN KINASE C.

Sphinx Laboratories