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Fernando Pelaez

Researcher at Merck & Co.

Publications -  124
Citations -  7806

Fernando Pelaez is an academic researcher from Merck & Co.. The author has contributed to research in topics: Integrase & Farnesyl Protein Transferase. The author has an hindex of 41, co-authored 124 publications receiving 7350 citations. Previous affiliations of Fernando Pelaez include Autonomous University of Madrid.

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Barceloneic acid A, a new farnesyl-protein transferase inhibitor from a Phoma species.

TL;DR: Three new diphenyl ethers, barceloneic acids A, B, and barcel oneic lactone were isolated from a fermentation extract of a fungus of the genus Phoma and the effect of these compounds on the inhibition of farnesyl-protein transferase (FPTase) was evaluated and results are presented.
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Antisense-guided isolation and structure elucidation of pannomycin, a substituted cis-decalin from Geomyces pannorum.

TL;DR: An extract of Geomyces pannorum was identified as providing increased activity against the sensitized strain as compared with the wild-type control, andBioassay-guided isolation of the active component from this fungal extract provided a new cis-decalin secondary metabolite, which is named pannomycin.
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Hinnuliquinone, a C2-symmetric dimeric non-peptide fungal metabolite inhibitor of HIV-1 protease.

TL;DR: Screening of microbial extracts followed by bioassay-guided isolation led to the discovery of a natural hinnuliquinone, a C(2)-symmetric bis-indolyl quinone natural product that inhibited the wild-type and a clinically resistant (A44) strain of HIV-1 protease.
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Infraspecific variation in two species of aquatic hyphomycetes assessed by RAPD analysis

TL;DR: Random amplified polymorphic DNA (RAPD) profiles were used to analyse the infraspecific variability within the populations of the two dominant species, Heliscus lugdunensis and Articulospora tetracladia, suggesting the presence of a relatively stable pool of fungal genotypes colonizing the plant substrates along the stream.
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Inhibitors of farnesylation of Ras from a microbial natural products screening program

TL;DR: Ten different families of compounds are identified, all of which selectively inhibit FPTase with a variety of mechanisms, which originated from the fermentations of a number of microorganisms, either actinomycetes or fungi, isolated from different substrates collected in tropical and temperate areas.