Fu HG - Search Results

1

Synthesis and antibacterial evaluation against resistant Gram-negative bacteria of monobactams bearing various substituents on oxime residue.

Li ZW, Lu X, Wang YX, Hu XX, Fu HG, Gao LM, You XF, Tang S, Song DQ. Li ZW, et al. Among authors: fu hg. Bioorg Chem. 2020 Jan;94:103487. doi: 10.1016/j.bioorg.2019.103487. Epub 2019 Dec 2. Bioorg Chem. 2020. PMID: 31831161

2

Synthesis and structure-activity relationship of 8-substituted protoberberine derivatives as a novel class of antitubercular agents.

Li YH, Fu HG, Su F, Gao LM, Tang S, Bi CW, Li YH, Wang YX, Song DQ. Li YH, et al. Among authors: fu hg. Chem Cent J. 2013 Jul 10;7(1):117. doi: 10.1186/1752-153X-7-117. Chem Cent J. 2013. PMID: 23837573 Free PMC article.

3

Synthesis and biological evaluation of sophoridinol derivatives as a novel family of potential anticancer agents.

Bi C, Zhang C, Li Y, Tang S, Wang S, Shao R, Fu H, Su F, Song D. Bi C, et al. ACS Med Chem Lett. 2014 Sep 22;5(11):1225-9. doi: 10.1021/ml500289h. eCollection 2014 Nov 13. ACS Med Chem Lett. 2014. PMID: 25408835 Free PMC article.

4

Design, synthesis and biological evaluation of monobactams as antibacterial agents against gram-negative bacteria.

Fu HG, Hu XX, Li CR, Li YH, Wang YX, Jiang JD, Bi CW, Tang S, You XF, Song DQ. Fu HG, et al. Eur J Med Chem. 2016 Mar 3;110:151-63. doi: 10.1016/j.ejmech.2016.01.024. Epub 2016 Jan 20. Eur J Med Chem. 2016. PMID: 26827160

5

Synthesis and Biological Evaluation of Quinoline Derivatives as a Novel Class of Broad-Spectrum Antibacterial Agents.

Fu HG, Li ZW, Hu XX, Si SY, You XF, Tang S, Wang YX, Song DQ. Fu HG, et al. Molecules. 2019 Feb 2;24(3):548. doi: 10.3390/molecules24030548. Molecules. 2019. PMID: 30717338 Free PMC article.

6

Evolution and development of potent monobactam sulfonate candidate IMBZ18g as a dual inhibitor against MDR Gram-negative bacteria producing ESBLs.

Li Z, Guo Z, Lu X, Ma X, Wang X, Zhang R, Hu X, Wang Y, Pang J, Fan T, Liu Y, Tang S, Fu H, Zhang J, Li Y, You X, Song D. Li Z, et al. Acta Pharm Sin B. 2023 Jul;13(7):3067-3079. doi: 10.1016/j.apsb.2023.03.002. Epub 2023 Mar 7. Acta Pharm Sin B. 2023. PMID: 37521870 Free PMC article.

7

Atroposelective Synthesis of Axial Biaryls by Dynamic Kinetic Resolution Using Engineered Imine Reductases.

Hao X, Tian Z, Yao Z, Zang T, Song S, Lin L, Qiao T, Huang L, Fu H. Hao X, et al. Angew Chem Int Ed Engl. 2024 Oct 7;63(41):e202410112. doi: 10.1002/anie.202410112. Epub 2024 Sep 6. Angew Chem Int Ed Engl. 2024. PMID: 39016184

8

From Ground-State to Excited-State Activation Modes: Flavin-Dependent "Ene"-Reductases Catalyzed Non-natural Radical Reactions.

Fu H, Hyster TK. Fu H, et al. Acc Chem Res. 2024 May 7;57(9):1446-1457. doi: 10.1021/acs.accounts.4c00129. Epub 2024 Apr 11. Acc Chem Res. 2024. PMID: 38603772 Review.

9

Development and validation of a novel nomogram for predicting good neoangiogenesis after encephaloduroarteriosynangiosis in patients with moyamoya disease and type 2 diabetes mellitus: a case-control study.

Li JJ, Ren B, Wang XP, Wang QN, Bao XY, Guo QB, Kong ZQ, Liu JQ, Gao G, Wang MJ, Liu SM, Fu HG, Tong HY, Duan L. Li JJ, et al. Among authors: fu hg. J Neurosurg. 2024 May 17;141(5):1177-1186. doi: 10.3171/2024.2.JNS24208. Print 2024 Nov 1. J Neurosurg. 2024. PMID: 38759234

10

Development and validation of a novel nomogram for predicting long-term rebleeding risk among patients with hemorrhagic moyamoya disease: a 10-year multicenter retrospective cohort study.

Li JJ, Wang XP, Bao XY, Wang QN, Kong ZQ, Guo QB, Liu JQ, Gao G, Wang MJ, Liu SM, Fu HG, Tong HY, Duan L. Li JJ, et al. Among authors: fu hg. J Neurosurg. 2024 May 10;141(4):1000-1010. doi: 10.3171/2024.2.JNS232744. Print 2024 Oct 1. J Neurosurg. 2024. PMID: 38728755

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