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5NRF

Crystal structure of human chitotriosidase-1 (hCHIT) catalytic domain in complex with compound 7i

Summary for 5NRF
Entry DOI10.2210/pdb5nrf/pdb
DescriptorChitotriosidase-1, 1-(3-azanyl-1~{H}-1,2,4-triazol-5-yl)-~{N}-[2-(4-chlorophenyl)ethyl]-~{N}-(phenylmethyl)piperidin-4-amine, GLYCEROL, ... (4 entities in total)
Functional Keywordschitotriosidase-1 (hchit) catalytic domain in complex with compound 7i, hydrolase
Biological sourceHomo sapiens (Human)
Cellular locationSecreted: Q13231
Total number of polymer chains1
Total formula weight42727.33
Authors
Primary citationMazur, M.,Olczak, J.,Olejniczak, S.,Koralewski, R.,Czestkowski, W.,Jedrzejczak, A.,Golab, J.,Dzwonek, K.,Dymek, B.,Sklepkiewicz, P.L.,Zagozdzon, A.,Noonan, T.,Mahboubi, K.,Conway, B.,Sheeler, R.,Beckett, P.,Hungerford, W.M.,Podjarny, A.,Mitschler, A.,Cousido-Siah, A.,Fadel, F.,Golebiowski, A.
Targeting Acidic Mammalian chitinase Is Effective in Animal Model of Asthma.
J. Med. Chem., 61:695-710, 2018
Cited by
PubMed Abstract: This article highlights our work toward the identification of a potent, selective, and efficacious acidic mammalian chitinase (AMCase) inhibitor. Rational design, guided by X-ray analysis of several inhibitors bound to human chitotriosidase (hCHIT1), led to the identification of compound 7f as a highly potent AMCase inhibitor (IC values of 14 and 19 nM against human and mouse enzyme, respectively) and selective (>150× against mCHIT1) with very good PK properties. This compound dosed once daily at 30 mg/kg po showed significant anti-inflammatory efficacy in HDM-induced allergic airway inflammation in mice, reducing inflammatory cell influx in the BALF and total IgE concentration in plasma, which correlated with decrease of chitinolytic activity. Therapeutic efficacy of compound 7f in the clinically relevant aeroallergen-induced acute asthma model in mice provides a rationale for developing AMCase inhibitor for the treatment of asthma.
PubMed: 29283260
DOI: 10.1021/acs.jmedchem.7b01051
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.447 Å)
Structure validation

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