(Q30860139)

27 June 2017

title

Chitinase inhibitors: extraction of the active framework from natural argifin and use of in situ click chemistry (English)

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27 June 2017

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11

Satoshi Omura

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27 June 2017

10

K Barry Sharpless

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27 June 2017

Tomoyasu Hirose

1

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27 June 2017

Toshiaki Sunazuka

2

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27 June 2017

Akihiro Sugawara

3

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27 June 2017

Ayako Endo

4

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27 June 2017

Kanami Iguchi

5

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27 June 2017

Tsuyoshi Yamamoto

6

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27 June 2017

Hideaki Ui

7

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27 June 2017

Kazuro Shiomi

8

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27 June 2017

Takeshi Watanabe

9

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27 June 2017

language of work or name

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27 March 2009

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The Journal of Antibiotics

27 June 2017

published in

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27 June 2017

volume

62

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27 June 2017

issue

5

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27 June 2017

page(s)

277-282

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Oral administration of chitin down-regulates serum IgE levels and lung eosinophilia in the allergic mouse.

27 June 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

Argadin, a new chitinase inhibitor, produced by Clonostachys sp. FO-7314.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

Identification of a novel acidic mammalian chitinase distinct from chitotriosidase

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Transmission-blocking activity of a chitinase inhibitor and activation of malarial parasite chitinase by mosquito protease

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Natural product family 18 chitinase inhibitors

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Acidic mammalian chitinase in asthmatic Th2 inflammation and IL-13 pathway activation

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Argifin, a new chitinase inhibitor, produced by Gliocladium sp. FTD-0668. I. Taxonomy, fermentation, and biological activities.

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Argifin, a New Chitinase Inhibitor, Produced by Gliocladium sp. FTD-0668. II. Isolation, Physico-chemical Properties, and Structure Elucidation.

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Structure of argifin, a new chitinase inhibitor produced by Gliocladium sp.

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Chitinases A, B, and C1 of Serratia marcescens 2170 produced by recombinant Escherichia coli: enzymatic properties and synergism on chitin degradation

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Specificity and affinity of natural product cyclopentapeptide inhibitors against A. fumigatus, human, and bacterial chitinases.

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

High-resolution structures of a chitinase complexed with natural product cyclopentapeptide inhibitors: mimicry of carbohydrate substrate

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Structure-Based Dissection of the Natural Product Cyclopentapeptide Chitinase Inhibitor Argifin

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Self-assembling cytotoxins

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Synergism through direct covalent bonding between agents: a strategy for rational design of chemotherapeutic combinations

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Multisubstrate adduct inhibitors of glycinamide ribonucleotide transformylase: Synthetic and enzyme-assembled

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

10-Formyl-5,8,10-trideazafolic acid (10-formyl-TDAF): a potent inhibitor of glycinamide ribonucleotide transformylase

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Combinatorial target-guided ligand assembly: identification of potent subtype-selective c-Src inhibitors

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Target-Accelerated Combinatorial Synthesis and Discovery of Highly Potent Antibiotics Effective Against Vancomycin-Resistant Bacteria

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Unexpected formation of an epoxide-derived multisubstrate adduct inhibitor on the active site of GAR transformylase

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Using an Enzyme's Active Site To Template Inhibitors This work was supported by the Centre National de la Recherche Scientifique and by the Ecole Polytechnique (predoctoral fellowship to R.N.). We thank Prof. Jean-Marie Lehn for stimulating discussi

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Synthesis and biological evaluation of vancomycin dimers with potent activity against vancomycin-resistant bacteria: target-accelerated combinatorial synthesis.

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Tyrosylprotein sulfotransferase inhibitors generated by combinatorial target-guided ligand assembly

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

DNA-templated dimerization of hairpin polyamides

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Bcl-XL-templated assembly of its own protein-protein interaction modulator from fragments decorated with thio acids and sulfonyl azides

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

In situ click chemistry: a powerful means for lead discovery

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Click chemistry in situ: acetylcholinesterase as a reaction vessel for the selective assembly of a femtomolar inhibitor from an array of building blocks

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

In situ click chemistry: enzyme inhibitors made to their own specifications

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Freeze-frame inhibitor captures acetylcholinesterase in a unique conformation

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

In situ selection of lead compounds by click chemistry: target-guided optimization of acetylcholinesterase inhibitors

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

In situ click chemistry: enzyme-generated inhibitors of carbonic anhydrase II.

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Inhibitors of HIV-1 protease by using in situ click chemistry

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Chitinase B from Serratia marcescens BJL200 is exported to the periplasm without processing

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Inhibition of chitinolytic activities from tree species and associated fungi.

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

A stepwise huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(i)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Polytriazoles as copper(I)-stabilizing ligands in catalysis

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Ruthenium-catalyzed cycloaddition of alkynes and organic azides

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Ruthenium-catalyzed azide-alkyne cycloaddition: scope and mechanism

1 reference

https://api.crossref.org/works/10.1038%2FJA.2009.28

7 January 2021

Identifiers

DOI

10.1038/JA.2009.28

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Dimensions Publication ID

27 June 2017

1003457544

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1 reference