Two new indolo-glycyrrhetic acid derivatives containing cyano-substitutent at C30 have been synthesized, and their anti-influenza activity has been evaluated in vitro. The resulting data demonstrated moderate inhibitory activity against the H1N1 virus with IC50 29 and 23 μM, respectively. The value of SI 18 and 21 confirm low toxicity and potential of new compounds for following research and development of new biological agents
A novel series of cyclopentane derivatives have been found to exhibit potent and selective inhibitor...
A furanosic derivative has been identified as a simple sialylmimetic and synthesized, representing t...
Influenza virus is estimated to cause 3-5 million severe complications and about 250-500 thousand de...
This Letter describes the synthesis and antiviral activity study of some glycyrrhizic acid (GL) deri...
Copyright © 2014 Dalya Al-Saad et al. This is an open access article distributed under the Creative ...
A series of aminoglucoglycerolipids derivatives had been synthesized, including 6′-acylamido-glucogl...
Influenza viruses cause considerable morbidity and mortality, whether in the context of annual epide...
The influenza virus neuraminidase (NA) is an enzyme essential for viral infection and offers a poten...
AbstractA series of novel indole-2-carboxylate derivatives were synthesized and assayed to determine...
Influenza A viruses (IAVs) have caused worldwide epidemics and pandemics by reassortment and generat...
The influenza virus neuraminidase (NA) is essential for viral infection and offers a potential targe...
© 2015 Institute of Chemistry, Slovak Academy of Sciences. In order to promote attachment of the ris...
A series of substituted aryl glycoside analogues of gastrodin have been identified as potential anti...
Influenza neuraminidase (NA) is the enzyme that releases influenza virions from infected cells, clea...
Divalent inhibitors of the neuraminidase enzyme (NA) of the Influenza A virus were synthesized with ...
A novel series of cyclopentane derivatives have been found to exhibit potent and selective inhibitor...
A furanosic derivative has been identified as a simple sialylmimetic and synthesized, representing t...
Influenza virus is estimated to cause 3-5 million severe complications and about 250-500 thousand de...
This Letter describes the synthesis and antiviral activity study of some glycyrrhizic acid (GL) deri...
Copyright © 2014 Dalya Al-Saad et al. This is an open access article distributed under the Creative ...
A series of aminoglucoglycerolipids derivatives had been synthesized, including 6′-acylamido-glucogl...
Influenza viruses cause considerable morbidity and mortality, whether in the context of annual epide...
The influenza virus neuraminidase (NA) is an enzyme essential for viral infection and offers a poten...
AbstractA series of novel indole-2-carboxylate derivatives were synthesized and assayed to determine...
Influenza A viruses (IAVs) have caused worldwide epidemics and pandemics by reassortment and generat...
The influenza virus neuraminidase (NA) is essential for viral infection and offers a potential targe...
© 2015 Institute of Chemistry, Slovak Academy of Sciences. In order to promote attachment of the ris...
A series of substituted aryl glycoside analogues of gastrodin have been identified as potential anti...
Influenza neuraminidase (NA) is the enzyme that releases influenza virions from infected cells, clea...
Divalent inhibitors of the neuraminidase enzyme (NA) of the Influenza A virus were synthesized with ...
A novel series of cyclopentane derivatives have been found to exhibit potent and selective inhibitor...
A furanosic derivative has been identified as a simple sialylmimetic and synthesized, representing t...
Influenza virus is estimated to cause 3-5 million severe complications and about 250-500 thousand de...