Synthesis and Anti-HIV-1 Activity Evaluation for Novel 3a,6a-Dihydro-1H-pyrrolo[3,4-c]pyrazole-4,6-dione Derivatives.

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Design, synthesis and antiviral evaluation of novel heteroarylcarbothioamide derivatives as dual inhibitors of HIV-1 reverse transcriptase-associated RNase H and RDDP functions.

P2860

Q40062788-C8F9B8F1-BD5C-450B-A417-9611AEEE7A29

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Synthesis and Anti-HIV-1 Activity Evaluation for Novel 3a,6a-Dihydro-1H-pyrrolo[3,4-c]pyrazole-4,6-dione Derivatives.

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http://www.wikidata.org/entity/Q38746848

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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2016年论文

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2016年论文

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name

Synthesis and Anti-HIV-1 Activ ...... yrazole-4,6-dione Derivatives.

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type

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Synthesis and Anti-HIV-1 Activ ...... yrazole-4,6-dione Derivatives.

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Synthesis and Anti-HIV-1 Activ ...... yrazole-4,6-dione Derivatives.

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P1476

Synthesis and Anti-HIV-1 Activ ...... pyrazole-4,6-dione Derivatives

@en

P2093

Guan-Nan Liu

http://www.w3.org/2001/XMLSchema#string

Hong Liu

http://www.w3.org/2001/XMLSchema#string

Jian Li

http://www.w3.org/2001/XMLSchema#string

Liu-Meng Yang

http://www.w3.org/2001/XMLSchema#string

Rong-Hua Luo

http://www.w3.org/2001/XMLSchema#string

Xing-Jie Zhang

http://www.w3.org/2001/XMLSchema#string

Yong-Tang Zheng

http://www.w3.org/2001/XMLSchema#string

Yu Zhou

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P2860

Broad antiretroviral activity and resistance profile of the novel human immunodeficiency virus integrase inhibitor elvitegravir (JTK-303/GS-9137)

Differential inhibition of HIV-1 preintegration complexes and purified integrase protein by small molecules

DB-02, a C-6-cyclohexylmethyl substituted pyrimidinone HIV-1 reverse transcriptase inhibitor with nanomolar activity, displays an improved sensitivity against K103N or Y181C than S-DABOs

Azvudine, a novel nucleoside reverse transcriptase inhibitor showed good drug combination features and better inhibition on drug-resistant strains than lamivudine in vitro

Impact of Y143 HIV-1 integrase mutations on resistance to raltegravir in vitro and in vivo.

Resistance to integrase inhibitors.

Integrase inhibitors to treat HIV/AIDS.

4-amino-1-hydroxy-2-oxo-1,8-naphthyridine-containing compounds having high potency against raltegravir-resistant integrase mutants of HIV-1

Examination of halogen substituent effects on HIV-1 integrase inhibitors derived from 2,3-dihydro-6,7-dihydroxy-1H-isoindol-1-ones and 4,5-dihydroxy-1H-isoindole-1,3(2H)-diones

Bicyclic 1-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxamide-containing HIV-1 integrase inhibitors having high antiviral potency against cells harboring raltegravir-resistant integrase mutants.

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scholarly article

P356

10.3390/MOLECULES21091198

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English

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2016-09-08T00:00:00Z

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27617994

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6274355

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Synthesis and Anti-HIV-1 Activity Evaluation for Novel 3a,6a-Dihydro-1H-pyrrolo[3,4-c]pyrazole-4,6-dione Derivatives.

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P2860

P2860

Synthesis and Anti-HIV-1 Activity Evaluation for Novel 3a,6a-Dihydro-1H-pyrrolo[3,4-c]pyrazole-4,6-dione Derivatives.

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P1433

P1476

P2093

P2860

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P356

P407

P433

P478

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P31

P356

P407

P433

P478

P577

P698

P932