148 related articles for article (PubMed ID: 23889687)
1. Structure-based design and synthesis of novel dual-target inhibitors against cyanobacterial fructose-1,6-bisphosphate aldolase and fructose-1,6-bisphosphatase.
Li D; Han X; Tu Q; Feng L; Wu D; Sun Y; Chen H; Li Y; Ren Y; Wan J
J Agric Food Chem; 2013 Aug; 61(31):7453-61. PubMed ID: 23889687
[TBL] [Abstract][Full Text] [Related]
2. A Rational Design, Synthesis, Biological Evaluation and Structure--Activity Relationship Study of Novel Inhibitors against Cyanobacterial Fructose-1,6-bisphosphate Aldolase.
Han X; Zhu X; Zhu S; Wei L; Hong Z; Guo L; Chen H; Chi B; Liu Y; Feng L; Ren Y; Wan J
J Chem Inf Model; 2016 Jan; 56(1):73-81. PubMed ID: 26669534
[TBL] [Abstract][Full Text] [Related]
3. Design and syntheses of novel N'-((4-oxo-4H-chromen-3-yl)methylene)benzohydrazide as inhibitors of cyanobacterial fructose-1,6-/sedoheptulose-1,7-bisphosphatase.
Tu QD; Li D; Sun Y; Han XY; Yi F; Sha Y; Ren YL; Ding MW; Feng LL; Wan J
Bioorg Med Chem; 2013 Jun; 21(11):2826-31. PubMed ID: 23623712
[TBL] [Abstract][Full Text] [Related]
4. Structural and biochemical characterization of fructose-1,6/sedoheptulose-1,7-bisphosphatase from the cyanobacterium Synechocystis strain 6803.
Feng L; Sun Y; Deng H; Li D; Wan J; Wang X; Wang W; Liao X; Ren Y; Hu X
FEBS J; 2014 Feb; 281(3):916-26. PubMed ID: 24286336
[TBL] [Abstract][Full Text] [Related]
5. Interaction between muscle aldolase and muscle fructose 1,6-bisphosphatase results in the substrate channeling.
Rakus D; Pasek M; Krotkiewski H; Dzugaj A
Biochemistry; 2004 Nov; 43(47):14948-57. PubMed ID: 15554702
[TBL] [Abstract][Full Text] [Related]
6. Pharmacophore-based virtual screening and experimental validation of novel inhibitors against cyanobacterial fructose-1,6-/sedoheptulose-1,7-bisphosphatase.
Sun Y; Zhang R; Li D; Feng L; Wu D; Feng L; Huang P; Ren Y; Feng J; Xiao S; Wan J
J Chem Inf Model; 2014 Mar; 54(3):894-901. PubMed ID: 24524690
[TBL] [Abstract][Full Text] [Related]
7. In silico screening of a novel scaffold for fructose-1,6-bisphosatase (FBPase) inhibitors.
Huang Y; Chi B; Xu Y; Song R; Wei L; Rao L; Feng L; Ren Y; Wan J
J Mol Graph Model; 2019 Jan; 86():142-148. PubMed ID: 30366190
[TBL] [Abstract][Full Text] [Related]
8. Structure-Based Rational Design of Novel Inhibitors Against Fructose-1,6-Bisphosphate Aldolase from Candida albicans.
Han X; Zhu X; Hong Z; Wei L; Ren Y; Wan F; Zhu S; Peng H; Guo L; Rao L; Feng L; Wan J
J Chem Inf Model; 2017 Jun; 57(6):1426-1438. PubMed ID: 28475320
[TBL] [Abstract][Full Text] [Related]
9. Discovery of novel indole derivatives as allosteric inhibitors of fructose-1,6-bisphosphatase.
Bie J; Liu S; Li Z; Mu Y; Xu B; Shen Z
Eur J Med Chem; 2015 Jan; 90():394-405. PubMed ID: 25461330
[TBL] [Abstract][Full Text] [Related]
10. A new level of regulation in gluconeogenesis: metabolic state modulates the intracellular localization of aldolase B and its interaction with liver fructose-1,6-bisphosphatase.
Droppelmann CA; Sáez DE; Asenjo JL; Yáñez AJ; García-Rocha M; Concha II; Grez M; Guinovart JJ; Slebe JC
Biochem J; 2015 Dec; 472(2):225-37. PubMed ID: 26417114
[TBL] [Abstract][Full Text] [Related]
11. Structure-guided design of AMP mimics that inhibit fructose-1,6-bisphosphatase with high affinity and specificity.
Erion MD; Dang Q; Reddy MR; Kasibhatla SR; Huang J; Lipscomb WN; van Poelje PD
J Am Chem Soc; 2007 Dec; 129(50):15480-90. PubMed ID: 18041833
[TBL] [Abstract][Full Text] [Related]
12. Design, synthesis and biological evaluation of novel inhibitors against cyanobacterial pyruvate dehydrogenase multienzyme complex E1.
Feng J; He H; Zhou Y; Guo X; Liu H; Cai M; Wang F; Feng L; He H
Bioorg Med Chem; 2019 Jun; 27(12):2413-2420. PubMed ID: 30692021
[TBL] [Abstract][Full Text] [Related]
13. Structure optimization and bioactivity evaluation of ThDP analogs targeting cyanobacterial pyruvate dehydrogenase E1.
Feng J; He H; Zhou Y; Cai M; Peng H; Liu H; Liu L; Feng L; He H
Bioorg Med Chem; 2019 Dec; 27(24):115159. PubMed ID: 31699453
[TBL] [Abstract][Full Text] [Related]
14. Synthesis and structure-activity relationship of non-phosphorus-based fructose-1,6-bisphosphatase inhibitors: 2,5-Diphenyl-1,3,4-oxadiazoles.
Liao BR; He HB; Yang LL; Gao LX; Chang L; Tang J; Li JY; Li J; Yang F
Eur J Med Chem; 2014 Aug; 83():15-25. PubMed ID: 24946215
[TBL] [Abstract][Full Text] [Related]
15. Design, synthesis and biological evaluation of 7-nitro-1H-indole-2-carboxylic acid derivatives as allosteric inhibitors of fructose-1,6-bisphosphatase.
Bie J; Liu S; Zhou J; Xu B; Shen Z
Bioorg Med Chem; 2014 Mar; 22(6):1850-62. PubMed ID: 24530031
[TBL] [Abstract][Full Text] [Related]
16. Biological evaluation and SAR analysis of novel covalent inhibitors against fructose-1,6-bisphosphatase.
Han X; Huang Y; Wei L; Chen H; Guo Y; Tang Z; Hu W; Xia Q; Wang Q; Yan J; Ren Y
Bioorg Med Chem; 2020 Sep; 28(18):115624. PubMed ID: 32828433
[TBL] [Abstract][Full Text] [Related]
17. Design, synthesis and algicides activities of thiourea derivatives as the novel scaffold aldolase inhibitors.
Xiao S; Wei L; Hong Z; Rao L; Ren Y; Wan J; Feng L
Bioorg Med Chem; 2019 Mar; 27(5):805-812. PubMed ID: 30711311
[TBL] [Abstract][Full Text] [Related]
18. A class I fructose-1,6-bisphosphate aldolase is associated with salt stress tolerance in a halotolerant cyanobacterium Halothece sp. PCC 7418.
Patipong T; Ngoennet S; Honda M; Hibino T; Waditee-Sirisattha R; Kageyama H
Arch Biochem Biophys; 2019 Sep; 672():108059. PubMed ID: 31356779
[TBL] [Abstract][Full Text] [Related]
19. Ligand-based designing, in silico screening, and biological evaluation of new potent fructose-1,6-bisphosphatase (FBPase) inhibitors.
Tayyem RF; Zalloum HM; Elmaghrabi MR; Yousef AM; Mubarak MS
Eur J Med Chem; 2012 Oct; 56():70-95. PubMed ID: 22960695
[TBL] [Abstract][Full Text] [Related]
20. Synthesis, SAR, and X-ray structure of tricyclic compounds as potent FBPase inhibitors.
Tsukada T; Takahashi M; Takemoto T; Kanno O; Yamane T; Kawamura S; Nishi T
Bioorg Med Chem Lett; 2009 Oct; 19(20):5909-12. PubMed ID: 19762234
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]