He Q - Search Results

1

Design and synthesis of novel desfluoroquinolone-aminopyrimidine hybrids as potent anti-MRSA agents with low hERG activity.

Song R, Wang Y, Wang M, Gao R, Yang T, Yang S, Yang CG, Jin Y, Zou S, Cai J, Fan R, He Q. Song R, et al. Among authors: he q. Bioorg Chem. 2020 Oct;103:104176. doi: 10.1016/j.bioorg.2020.104176. Epub 2020 Aug 26. Bioorg Chem. 2020. PMID: 32891858

2

Synthesis and anti-HIV activity of 2-naphthyl substituted DAPY analogues as non-nucleoside reverse transcriptase inhibitors.

Liang YH, He QQ, Zeng ZS, Liu ZQ, Feng XQ, Chen FE, Balzarini J, Pannecouque C, Clercq ED. Liang YH, et al. Bioorg Med Chem. 2010 Jul 1;18(13):4601-5. doi: 10.1016/j.bmc.2010.05.036. Epub 2010 May 20. Bioorg Med Chem. 2010. PMID: 20570527

3

Hybrid diarylbenzopyrimidine non-nucleoside reverse transcriptase inhibitors as promising new leads for improved anti-HIV-1 chemotherapy.

Zeng ZS, He QQ, Liang YH, Feng XQ, Chen FE, De Clercq E, Balzarini J, Pannecouque C. Zeng ZS, et al. Bioorg Med Chem. 2010 Jul 15;18(14):5039-47. doi: 10.1016/j.bmc.2010.05.081. Epub 2010 Jun 4. Bioorg Med Chem. 2010. PMID: 20598556

4

Synthesis and biological evaluation of naphthyl phenyl ethers (NPEs) as novel nonnucleoside HIV-1 reverse transcriptase inhibitors.

Gu SX, Zhang X, He QQ, Yang LM, Ma XD, Zheng YT, Yang SQ, Chen FE. Gu SX, et al. Bioorg Med Chem. 2011 Jul 15;19(14):4220-6. doi: 10.1016/j.bmc.2011.05.060. Epub 2011 Jun 2. Bioorg Med Chem. 2011. PMID: 21689939

5

Synthesis and biological activity of naphthyl-substituted (B-ring) benzophenone derivatives as novel non-nucleoside HIV-1 reverse transcriptase inhibitors.

Ma XD, Zhang X, Dai HF, Yang SQ, Yang LM, Gu SX, Zheng YT, He QQ, Chen FE. Ma XD, et al. Bioorg Med Chem. 2011 Aug 1;19(15):4601-7. doi: 10.1016/j.bmc.2011.06.007. Epub 2011 Jun 15. Bioorg Med Chem. 2011. PMID: 21719299

6

Structural modifications of quinolone-3-carboxylic acids with anti-HIV activity.

He QQ, Gu SX, Liu J, Wu HQ, Zhang X, Yang LM, Zheng YT, Chen FE. He QQ, et al. Bioorg Med Chem. 2011 Aug 15;19(16):5039-45. doi: 10.1016/j.bmc.2011.06.020. Epub 2011 Jul 15. Bioorg Med Chem. 2011. PMID: 21763149

7

Synthesis and biological evaluation of (±)-benzhydrol derivatives as potent non-nucleoside HIV-1 reverse transcriptase inhibitors.

Ma XD, Zhang X, Yang SQ, Dai HF, Yang LM, Gu SX, Zheng YT, He QQ, Chen FE. Ma XD, et al. Bioorg Med Chem. 2011 Aug 15;19(16):4704-9. doi: 10.1016/j.bmc.2011.07.003. Epub 2011 Jul 13. Bioorg Med Chem. 2011. PMID: 21788138

8

Synthesis and structure-activity relationship of novel diarylpyrimidines with hydromethyl linker (CH(OH)-DAPYs) as HIV-1 NNRTIs.

Gu SX, He QQ, Yang SQ, Ma XD, Chen FE, De Clercq E, Balzarini J, Pannecouque C. Gu SX, et al. Bioorg Med Chem. 2011 Sep 1;19(17):5117-24. doi: 10.1016/j.bmc.2011.07.023. Epub 2011 Jul 26. Bioorg Med Chem. 2011. PMID: 21824782

9

Synthesis and biological evaluation of HQCAs with aryl or benzyl substituents on N-1 position as potential HIV-1 integrase inhibitors.

He QQ, Zhang X, Wu HQ, Gu SX, Ma XD, Yang LM, Zheng YT, Chen FE. He QQ, et al. Bioorg Med Chem. 2011 Sep 15;19(18):5553-8. doi: 10.1016/j.bmc.2011.07.037. Epub 2011 Jul 27. Bioorg Med Chem. 2011. PMID: 21862337

10

Synthesis and anti-HIV activity of aryl-2-[(4-cyanophenyl)amino]-4-pyrimidinone hydrazones as potent non-nucleoside reverse transcriptase inhibitors.

Ma XD, Yang SQ, Gu SX, He QQ, Chen FE, De Clercq E, Balzarini J, Pannecouque C. Ma XD, et al. ChemMedChem. 2011 Dec 9;6(12):2225-32. doi: 10.1002/cmdc.201100334. Epub 2011 Sep 8. ChemMedChem. 2011. PMID: 21990112

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