Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Hugo Alejandro Garro"'
Publikováno v:
Medicinal Chemistry Research. 27:1432-1442
Using a feasible method, we generated a small focused library of structurally related alkenylcoumarins. These compounds were evaluated as potential antitumoral agents against Taq DNA polymerase. 6-(pent-4-enyloxy)-coumarin (7) IC50 = 48.33 ± 2.85 μ
Publikováno v:
Current drug targets. 20(1)
Background:The discovery of new chemotherapeutic agents still remains a continuous goal to achieve. DNA polymerases and topoisomerases act in nucleic acids metabolism modulating different processes like replication, mitosis, damage repair, DNA topolo
Human Immunodeficiency Virus (HIV) is the viral agent of Acquired Immunodeficiency Syndrome (AIDS), and at present, there is no effective vaccine against HIV. Reverse Transcriptase (RT) is an essential enzyme for retroviral replication, such as HIV a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6e3e7951526c27b3f95c532b73818f8
http://www.eurekaselect.com/133277/article
http://www.eurekaselect.com/133277/article
Publikováno v:
Bioorganicmedicinal chemistry letters. 25(4)
DNA polymerases are enzymes that play a crucial role in DNA metabolism such as replication, repair, transcription, recombination, and chromosome segregation during mitosis. Herein we report the isolation of a new iridoid (6-epi-catalpol, 2) and per-O
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Several natural and synthetic coumarins were assayed against different cancer cell lines. Four of them have shown cytotoxicity against a panel of three human solid tumor cell lines (HeLa, T-47D, and WiDr) and a clearly activity/hydrophobicity relatio
Autor:
Osvaldo A. Martin, Hugo Alejandro Garro, Marcela B. Kurina Sanz, Carlos R. Pungitore, Carlos E. Tonn
Publikováno v:
Journal of molecular modeling. 17(10)
In this work, a novel catalpol derivative (6,10,2′,6′-tetraacetyl-O-catalpol), which was previously obtained by our group and shown experimentally to inhibit a type of Taq DNA polymerase, was studied in silico. Studies of the interaction of 6,10,