154 related articles for article (PubMed ID: 28457127)
1. Microbial Secondary Metabolite, Phlegmacin B
Chen L; Liu T; Duan Y; Lu X; Yang Q
J Agric Food Chem; 2017 May; 65(19):3851-3857. PubMed ID: 28457127
[TBL] [Abstract][Full Text] [Related]
2. Glycoside hydrolase family 18 and 20 enzymes are novel targets of the traditional medicine berberine.
Duan Y; Liu T; Zhou Y; Dou T; Yang Q
J Biol Chem; 2018 Oct; 293(40):15429-15438. PubMed ID: 30135205
[TBL] [Abstract][Full Text] [Related]
3. Glycosyl triazoles as novel insect β-N-acetylhexosaminidase OfHex1 inhibitors: Design, synthesis, molecular docking and MD simulations.
Dong L; Shen S; Chen W; Lu H; Xu D; Jin S; Yang Q; Zhang J
Bioorg Med Chem; 2019 Jun; 27(12):2315-2322. PubMed ID: 30528165
[TBL] [Abstract][Full Text] [Related]
4. Synthesis, Optimization, and Evaluation of Glycosylated Naphthalimide Derivatives as Efficient and Selective Insect β- N-Acetylhexosaminidase OfHex1 Inhibitors.
Shen S; Dong L; Chen W; Wu R; Lu H; Yang Q; Zhang J
J Agric Food Chem; 2019 Jun; 67(22):6387-6396. PubMed ID: 31090403
[TBL] [Abstract][Full Text] [Related]
5. Fully deacetylated chitooligosaccharides act as efficient glycoside hydrolase family 18 chitinase inhibitors.
Chen L; Zhou Y; Qu M; Zhao Y; Yang Q
J Biol Chem; 2014 Jun; 289(25):17932-40. PubMed ID: 24828498
[TBL] [Abstract][Full Text] [Related]
6. Structural determinants of an insect beta-N-Acetyl-D-hexosaminidase specialized as a chitinolytic enzyme.
Liu T; Zhang H; Liu F; Wu Q; Shen X; Yang Q
J Biol Chem; 2011 Feb; 286(6):4049-58. PubMed ID: 21106526
[TBL] [Abstract][Full Text] [Related]
7. Pocket-based Lead Optimization Strategy for the Design and Synthesis of Chitinase Inhibitors.
Dong Y; Hu S; Jiang X; Liu T; Ling Y; He X; Yang Q; Zhang L
J Agric Food Chem; 2019 Apr; 67(13):3575-3582. PubMed ID: 30865442
[TBL] [Abstract][Full Text] [Related]
8. Structural dissection reveals a general mechanistic principle for group II chitinase (ChtII) inhibition.
Chen W; Zhou Y; Yang Q
J Biol Chem; 2019 Jun; 294(24):9358-9364. PubMed ID: 31053640
[TBL] [Abstract][Full Text] [Related]
9. A modeling study for structure features of β-N-acetyl-D-hexosaminidase from Ostrinia furnacalis and its novel inhibitor allosamidin: species selectivity and multi-target characteristics.
Wang Y; Liu T; Yang Q; Li Z; Qian X
Chem Biol Drug Des; 2012 Apr; 79(4):572-82. PubMed ID: 22177554
[TBL] [Abstract][Full Text] [Related]
10. Design of Inhibitors Targeting Chitin-Degrading Enzymes by Bioisostere Substitutions and Scaffold Hopping for Selective Control of
Liang P; Li J; Chen W; Zhou H; Lai X; Li J; Xu Z; Yang Q; Zhang J
J Agric Food Chem; 2024 May; 72(19):10794-10804. PubMed ID: 38711396
[TBL] [Abstract][Full Text] [Related]
11. Synthesis of ureido thioglycosides as novel insect β‑N‑acetylhexosaminidase OfHex1 inhibitors.
Shen S; Dong L; Lu H; Dong Y; Yang Q; Zhang J
Bioorg Med Chem; 2020 Aug; 28(15):115602. PubMed ID: 32631559
[TBL] [Abstract][Full Text] [Related]
12. Structure-Based Virtual Screening, Compound Synthesis, and Bioassay for the Design of Chitinase Inhibitors.
Dong Y; Jiang X; Liu T; Ling Y; Yang Q; Zhang L; He X
J Agric Food Chem; 2018 Apr; 66(13):3351-3357. PubMed ID: 29554796
[TBL] [Abstract][Full Text] [Related]
13. Structural analysis of group II chitinase (ChtII) catalysis completes the puzzle of chitin hydrolysis in insects.
Chen W; Qu M; Zhou Y; Yang Q
J Biol Chem; 2018 Feb; 293(8):2652-2660. PubMed ID: 29317504
[TBL] [Abstract][Full Text] [Related]
14. Design and synthesis of thiazolylhydrazone derivatives as inhibitors of chitinolytic N-acetyl-β-d-hexosaminidase.
Yang H; Liu T; Qi H; Huang Z; Hao Z; Ying J; Yang Q; Qian X
Bioorg Med Chem; 2018 Nov; 26(20):5420-5426. PubMed ID: 30274940
[TBL] [Abstract][Full Text] [Related]
15. Active-pocket size differentiating insectile from bacterial chitinolytic β-N-acetyl-D-hexosaminidases.
Liu T; Zhang H; Liu F; Chen L; Shen X; Yang Q
Biochem J; 2011 Sep; 438(3):467-74. PubMed ID: 21692744
[TBL] [Abstract][Full Text] [Related]
16. A sperm-plasma β-N-acetyl-D-hexosaminidase interacting with a Chitinolytic β-N-Acetyl-D-hexosaminidase in insect molting fluid.
Qu M; Liu T; Chen P; Yang Q
PLoS One; 2013; 8(8):e71738. PubMed ID: 23951233
[TBL] [Abstract][Full Text] [Related]
17. A Potential Multitarget Insect Growth Regulator Candidate: Design, Synthesis, and Biological Activity of Novel Acetamido Derivatives Containing Hexacyclic Pyrazole Carboxamides.
Guo B; Chen L; Luo S; Wang C; Feng Y; Li X; Cao C; Zhang L; Yang Q; Zhang X; Yang X
J Agric Food Chem; 2024 May; 72(18):10271-10281. PubMed ID: 38655868
[TBL] [Abstract][Full Text] [Related]
18. Structure, Catalysis, and Inhibition of
Liu T; Chen L; Zhou Y; Jiang X; Duan Y; Yang Q
J Biol Chem; 2017 Feb; 292(6):2080-2088. PubMed ID: 28053084
[TBL] [Abstract][Full Text] [Related]
19. Proteomic analysis of insect molting fluid with a focus on enzymes involved in chitin degradation.
Qu M; Ma L; Chen P; Yang Q
J Proteome Res; 2014 Jun; 13(6):2931-40. PubMed ID: 24779478
[TBL] [Abstract][Full Text] [Related]
20. Identification of novel insect β-N-acetylhexosaminidase OfHex1 inhibitors based on virtual screening, biological evaluation, and molecular dynamics simulation.
Dong L; Shen S; Xu Y; Wang L; Yang Q; Zhang J; Lu H
J Biomol Struct Dyn; 2021 Mar; 39(5):1735-1743. PubMed ID: 32193983
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
