Literature DB >> 11045447

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

N Arai1, K Shiomi, Y Yamaguchi, R Masuma, Y Iwai, A Turberg, H Kölbl, S Omura.   

Abstract

A new chitinase inhibitor, designated as argadin (1), was isolated from the cultured broth of a fungal strain FO-7314. The strain was identified as Clonostachys sp. from the morphological characteristics. Argadin was purified from the cultured mycelium by a combination of cation exchange, adsorption and gel filtration chromatographic methods. The structure of argadin was elucidated as cyclo(Nomega-acetyl-L-arginyl-D-prolyl-homoseryl-histidyl-L- 2-aminoadipyl) in which homoseryl gamma-methylene bonded to histidyl alpha-amino residue. The IC50 value of argadin against Lucilia cuprina (blowfly) chitinase was 150 nM at 37 degrees C and 3.4 nM at 20 degrees C. Argadin arrested the moult of cockroach larvae upon injection into the ventral abdominal part.

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Year:  2000        PMID: 11045447     DOI: 10.1248/cpb.48.1442

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN: 0009-2363            Impact factor:   1.645


  21 in total

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

Authors:  Douglas R Houston; Kazuro Shiomi; Noriko Arai; Satoshi Omura; Martin G Peter; Andreas Turberg; Bjørnar Synstad; Vincent G H Eijsink; Daan M F van Aalten
Journal:  Proc Natl Acad Sci U S A       Date:  2002-07-01       Impact factor: 11.205

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

Authors:  Gleb Andryianau; Michal Kowalski; Michal C Piotrowicz; Adam A Rajkiewicz; Barbara Dymek; Piotr L Sklepkiewicz; Elzbieta Pluta; Filip Stefaniak; Wojciech Czestkowski; Sylwia Olejniczak; Marzena Mazur; Piotr Niedziejko; Robert Koralewski; Krzysztof Matyszewski; Mariusz Gruza; Agnieszka Zagozdzon; Magdalena Salamon; Aleksandra Rymaszewska; Mikolaj Welzer; Karolina Dzwonek; Jakub Golab; Jacek Olczak; Agnieszka Bartoszewicz; Adam Golebiowski
Journal:  ACS Med Chem Lett       Date:  2020-04-24       Impact factor: 4.345

3.  Fully deacetylated chitooligosaccharides act as efficient glycoside hydrolase family 18 chitinase inhibitors.

Authors:  Lei Chen; Yong Zhou; Mingbo Qu; Yong Zhao; Qing Yang
Journal:  J Biol Chem       Date:  2014-05-14       Impact factor: 5.157

4.  Potent family-18 chitinase inhibitors: x-ray structures, affinities, and binding mechanisms.

Authors:  Supansa Pantoom; Ingrid R Vetter; Heino Prinz; Wipa Suginta
Journal:  J Biol Chem       Date:  2011-04-29       Impact factor: 5.157

5.  Direct arginine modification in native peptides and application to chemical probe development.

Authors:  Verena Grundler; Karl Gademann
Journal:  ACS Med Chem Lett       Date:  2014-10-27       Impact factor: 4.345

6.  Structural dissection reveals a general mechanistic principle for group II chitinase (ChtII) inhibition.

Authors:  Wei Chen; Yong Zhou; Qing Yang
Journal:  J Biol Chem       Date:  2019-05-03       Impact factor: 5.157

7.  Observation of the controlled assembly of preclick components in the in situ click chemistry generation of a chitinase inhibitor.

Authors:  Tomoyasu Hirose; Nobuo Maita; Hiroaki Gouda; Jun Koseki; Tsuyoshi Yamamoto; Akihiro Sugawara; Hirofumi Nakano; Shuichi Hirono; Kazuro Shiomi; Takeshi Watanabe; Hisaaki Taniguchi; K Barry Sharpless; Satoshi Omura; Toshiaki Sunazuka
Journal:  Proc Natl Acad Sci U S A       Date:  2013-09-16       Impact factor: 11.205

Review 8.  Novel methylxanthine derivative-mediated anti-inflammatory effects in inflammatory bowel disease.

Authors:  In-Ah Lee; Alan Kamba; Daren Low; Emiko Mizoguchi
Journal:  World J Gastroenterol       Date:  2014-02-07       Impact factor: 5.742

9.  The cyclic dipeptide CI-4 [cyclo-(l-Arg-d-Pro)] inhibits family 18 chitinases by structural mimicry of a reaction intermediate.

Authors:  Douglas R Houston; Ian Eggleston; Bjørnar Synstad; Vincent G H Eijsink; Daan M F van Aalten
Journal:  Biochem J       Date:  2002-11-15       Impact factor: 3.857

10.  Bisdionin C-a rationally designed, submicromolar inhibitor of family 18 chitinases.

Authors:  Alexander W Schüttelkopf; Ole A Andersen; Francesco V Rao; Matthew Allwood; Christina L Rush; Ian M Eggleston; Daan M F van Aalten
Journal:  ACS Med Chem Lett       Date:  2011-03-23       Impact factor: 4.345

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