Investigations of possible prodrug structures for 2-(2-mercaptophenyl)tetrahydropyrimidines: reductive conversion from anti-HIV agents with pyrimidobenzothiazine and isothiazolopyrimidine scaffolds.

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Potent and Selective Non-hydroxamate Histone Deacetylase 8 Inhibitors.Synthesis of Some Benzofuran Derivatives Containing Pyrimidine Moiety as Potent Antimicrobial Agents.

P2860

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P2860

Investigations of possible prodrug structures for 2-(2-mercaptophenyl)tetrahydropyrimidines: reductive conversion from anti-HIV agents with pyrimidobenzothiazine and isothiazolopyrimidine scaffolds.

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年論文

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Investigations of possible pro ...... othiazolopyrimidine scaffolds.

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Investigations of possible pro ...... othiazolopyrimidine scaffolds.

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Investigations of possible pro ...... othiazolopyrimidine scaffolds.

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P1476

Investigations of possible pro ...... othiazolopyrimidine scaffolds.

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P2093

Hiroaki Ohno

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Hiroto Murayama

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Nobutaka Fujii

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Shiho Okazaki

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Tsukasa Mizuhara

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P2860

Inhibition of HIV-1 replication by a bis-thiadiazolbenzene-1,2-diamine that chelates zinc ions from retroviral nucleocapsid zinc fingers

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Structure, Biochemistry, and Inhibition of Essential 4′-Phosphopantetheinyl Transferases from Two Species of Mycobacteria

Protection of a single-cysteine redox switch from oxidative destruction: On the functional role of sulfenyl amide formation in the redox-regulated enzyme PTP1B.

The central role of glutathione in the pathophysiology of human diseases.

PD 404,182 is a virocidal small molecule that disrupts hepatitis C virus and human immunodeficiency virus.

Biophysical characterization of zinc ejection from HIV nucleocapsid protein by anti-HIV 2,2'-dithiobis[benzamides] and benzisothiazolones.

A novel and potent inhibitor of dimethylarginine dimethylaminohydrolase: a modulator of cardiovascular nitric oxide.

Enfuvirtide: the first therapy to inhibit the entry of HIV-1 into host CD4 lymphocytes.

Dual-reporter phenotypic assay for human immunodeficiency viruses

P304

4706-4713

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scholarly article

P356

10.1039/C5OB00301F

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P433

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P478

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Masao Matsuoka

Shinya Oishi

Kazuya Shimura

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2015-04-01T00:00:00Z

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25800792

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Investigations of possible prodrug structures for 2-(2-mercaptophenyl)tetrahydropyrimidines: reductive conversion from anti-HIV agents with pyrimidobenzothiazine and isothiazolopyrimidine scaffolds.

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P2860

P2860

Investigations of possible prodrug structures for 2-(2-mercaptophenyl)tetrahydropyrimidines: reductive conversion from anti-HIV agents with pyrimidobenzothiazine and isothiazolopyrimidine scaffolds.

description

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type

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698