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1.
Org Biomol Chem ; 12(29): 5331-45, 2014 Aug 07.
Article in English | MEDLINE | ID: mdl-24947937

ABSTRACT

The Nazarov cyclization, a well-known method for the formation of cyclopentenones, mechanistically involves the 4π electrocyclization of a 1,4-pentadienyl cation, generated from cross-conjugated divinyl ketones. Recently, advances related to this cyclization, such as the incorporation of heteroatoms as well as the use of cyclopropanes as double bond equivalents have extended the scope of the original reaction. The modifications discussed in this review, which covers the years 2009-2013, have allowed the realization of both heteroatom- and homo-Nazarov cyclizations.

2.
Bioorg Med Chem Lett ; 20(1): 398-402, 2010 Jan 01.
Article in English | MEDLINE | ID: mdl-19939680

ABSTRACT

Two classes of compounds, thiocarbamates 1 and triazoles 2, have been identified as HIV RT RNase H inhibitors using a novel FRET-based HTS assay. The potent analogs in each series exhibited selectivity and were active in cell-based assays. In addition, saturable, 1:1 stoichiometric binding to target was established and time of addition studies were consistent with inhibition of RT-mediated HIV replication.


Subject(s)
Anti-HIV Agents/chemistry , Enzyme Inhibitors/chemistry , Ribonuclease H, Human Immunodeficiency Virus/antagonists & inhibitors , Thiocarbamates/chemistry , Triazoles/chemistry , Amino Acid Sequence , Anti-HIV Agents/chemical synthesis , Anti-HIV Agents/pharmacology , Cell Line , Enzyme Inhibitors/chemical synthesis , Enzyme Inhibitors/pharmacology , Fluorescence Resonance Energy Transfer , High-Throughput Screening Assays , Humans , Molecular Sequence Data , Ribonuclease H, Human Immunodeficiency Virus/metabolism , Structure-Activity Relationship , Thiocarbamates/chemical synthesis , Thiocarbamates/pharmacology , Triazoles/chemical synthesis , Triazoles/pharmacology , Virus Replication/drug effects
3.
Bioorg Med Chem Lett ; 19(24): 6957-61, 2009 Dec 15.
Article in English | MEDLINE | ID: mdl-19875283

ABSTRACT

A novel series of pyrazolo[1,5-a]pyrimidines bearing a 3-hydroxyphenyl group at C(3) and substituted tropanes at C(7) have been identified as potent B-Raf inhibitors. Exploration of alternative functional groups as a replacement for the C(3) phenol demonstrated indazole to be an effective isostere. Several compounds possessing substituted indazole residues, such as 4e, 4p, and 4r, potently inhibited cell proliferation at submicromolar concentrations in the A375 and WM266 cell lines, and the latter two compounds also exhibited good therapeutic indices in cells.


Subject(s)
Antineoplastic Agents/chemistry , Enzyme Inhibitors/chemistry , Proto-Oncogene Proteins B-raf/antagonists & inhibitors , Pyrazoles/chemistry , Pyridines/chemistry , Pyrimidines/chemistry , Antineoplastic Agents/pharmacology , Cell Line, Tumor , Cell Proliferation/drug effects , Enzyme Inhibitors/pharmacology , Humans , Pyrazoles/pharmacology , Pyridines/pharmacology , Pyrimidines/pharmacology
4.
Bioorg Med Chem Lett ; 14(16): 4157-60, 2004 Aug 16.
Article in English | MEDLINE | ID: mdl-15261261

ABSTRACT

The preparation of alpha-methylbenzyl thioureas and their biological activity against varicella zoster virus is described. Several analogs demonstrated IC50s<0.1 microM and their SAR are discussed. These compounds represent a novel class of potent and selective nonnucleoside inhibitors of varicella zoster virus.


Subject(s)
Antiviral Agents/pharmacology , Herpesvirus 3, Human/drug effects , Thiourea/pharmacology , Antiviral Agents/chemistry , Microbial Sensitivity Tests , Structure-Activity Relationship , Thiourea/chemistry
5.
Bioorg Med Chem Lett ; 13(20): 3483-6, 2003 Oct 20.
Article in English | MEDLINE | ID: mdl-14505653

ABSTRACT

The synthesis and biological activity of pyrimidotetrazin-6-ones against HCMV protease is described. The mechanism of action for these inhibitors is the oxidation of several cysteine residues to generate cross-linked enzyme.


Subject(s)
Cytomegalovirus/enzymology , Endopeptidases/drug effects , Flavins/chemistry , Protease Inhibitors/pharmacology , Pyrimidines/pharmacology , Endopeptidases/metabolism , Oxidation-Reduction , Protease Inhibitors/chemistry , Pyrimidines/chemistry
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