New acylated sulfoglycolipids and digalactolipids and related known glycolipids from cyanobacteria with a potential to inhibit the reverse transcriptase of HIV-1
V Reshef, E Mizrachi, T Maretzki… - Journal of natural …, 1997 - ACS Publications
Five novel diacylated sulfoglycolipids (1− 5) were isolated from the cyanobacterium
Scytonema sp.(TAU strain SL-30-1-4) and four novel acylated diglycolipids (6− 9) were …
Scytonema sp.(TAU strain SL-30-1-4) and four novel acylated diglycolipids (6− 9) were …
Sulfoquinovosyldiacylglycerol, KM043, a new potent inhibitor of eukaryotic DNA polymerases and HIV-reverse transcriptase type 1 from a marine red alga, Gigartina …
K Ohta, Y MIZUSHIMA, N Hirata… - Chemical and …, 1998 - jstage.jst.go.jp
抄録 A new sulfolipid, KM043, which belongs to the 6-sulfo-α-D-quinovopyranosyl-(1→ 3')-1',
2'-diacylglycerol (SQDG) class of compounds, has been isolated from a marine red alga …
2'-diacylglycerol (SQDG) class of compounds, has been isolated from a marine red alga …
Polycitone A, a novel and potent general inhibitor of retroviral reverse transcriptases and cellular DNA polymerases
S LOYA, A RUDI, Y KASHMAN, A HIZI - Biochemical Journal, 1999 - portlandpress.com
Polycitone A, an aromatic alkaloid isolated from the ascidian Polycitor sp. exhibits potent
inhibitory capacity of both RNA-and DNA-directed DNA polymerases. The drug inhibits …
inhibitory capacity of both RNA-and DNA-directed DNA polymerases. The drug inhibits …
Bioactive marine prenylated quinones/quinols
S de Rosa, G Tommonaro - Studies in Natural Products Chemistry, 2012 - Elsevier
Prenylated hydroquinones and related metabolites have been isolated from marine
organisms with a terpenoid portion that ranges from one to nine isoprene units. Triprenyl …
organisms with a terpenoid portion that ranges from one to nine isoprene units. Triprenyl …
[PDF][PDF] Review of natural products from marine organisms in the Red Sea
R Abou El-Ezz, A Ibrahim, E Habib… - International journal …, 2017 - researchgate.net
The marine environment is a rich source of both biological and chemical diversity. This
diversity has been the source of unique chemical compounds with potential for drug …
diversity has been the source of unique chemical compounds with potential for drug …
De Novo Parallel Design, Synthesis and Evaluation of Inhibitors against the Reverse Transcriptase of Human Immunodeficiency Virus Type-1 and Drug-Resistant …
A Herschhorn, L Lerman, M Weitman… - Journal of medicinal …, 2007 - ACS Publications
We used molecular modeling to design de novo broad-range inhibitors against wild type
and drug-resistant variants of the reverse transcriptase (RT) of human immunodeficiency …
and drug-resistant variants of the reverse transcriptase (RT) of human immunodeficiency …
Mode of inhibition of HIV-1 reverse transcriptase by polyacetylenetriol, a novel inhibitor of RNA-and DNA-directed DNA polymerases
S Loya, A Rudi, Y Kashman, A Hizi - Biochemical Journal, 2002 - portlandpress.com
Polyacetylenetriol (PAT), a natural marine product from the Mediterranean sea sponge
Petrosia sp., was found to be a novel general potent inhibitor of DNA polymerases. It inhibits …
Petrosia sp., was found to be a novel general potent inhibitor of DNA polymerases. It inhibits …
Virtual screening, identification, and biochemical characterization of novel inhibitors of the reverse transcriptase of human immunodeficiency virus type-1
A Herschhorn, A Hizi - Journal of medicinal chemistry, 2008 - ACS Publications
The reverse transcriptase (RT) of human immunodeficiency virus type-1 (HIV-1) is a leading
target in current antiretroviral therapy. Unfortunately, drug-resistant RT mutants evolve under …
target in current antiretroviral therapy. Unfortunately, drug-resistant RT mutants evolve under …
A novel mechanism for inhibition of HIV-1 reverse transcriptase
AG Skillman, KW Maurer, DC Roe, MJ Stauber… - Bioorganic …, 2002 - Elsevier
The human immunodeficiency virus (HIV) epidemic is an important medical problem.
Although combination drug regimens have produced dramatic decreases in viral load …
Although combination drug regimens have produced dramatic decreases in viral load …
Quantitative analysis of the interactions between HIV-1 integrase and retroviral reverse transcriptases
A Herschhorn, I Oz-Gleenberg, A Hizi - Biochemical Journal, 2008 - portlandpress.com
The RT (reverse transcriptase) of HIV-1 interacts with HIV-1 IN (integrase) and inhibits its
enzymatic activities. However, the molecular mechanisms underling these interactions are …
enzymatic activities. However, the molecular mechanisms underling these interactions are …