Heterocyclic compounds based on 3-(4-bromophenyl) azo-5-phenyl-2 (3H)-furanone: Anti-avian influenza virus (H5N1) activity

EM Flefel, RE Abdel-Mageid, WA Tantawy, MA Ali… - Acta …, 2012 - hrcak.srce.hr
Sažetak 3-[2-(4-Bromphenyl) hydrazono]-5-phenyl-furan-2 (3H)-one (1) was used for
preparation of some novel pyrazole, pyridazinone, oxadiazole, triazole, thiazolidine and …

Screening of some synthetic fused heterocyclic pyrimidines for anti-avian influenza virus (H5N1) activity

OR Alfarouk, AB Barakat, SA Shoman… - … Academic Journal of …, 2013 - journals.ekb.eg
Thirteen chemical compounds belonging to the fused heterocyclic pyrimidines were
synthesized and screened in order to assay their antiviral activity against the avian influenza …

Synthesis and anti-viral activities of some 3-(naphthalen-1-ylmethylene)-5-phenylfuran-2(3H)-one candidates

EM Flefel, WA Tantawy, RE Abdel-Mageid… - Research on Chemical …, 2014 - Springer
(Naphthalen-1-ylmethylene)-5-phenylfuran-2 (3 H)-one 1 was prepared and converted into
a variety of heterocyclic systems of synthetic and biological importance. Benzylamine was …

Synthesis and anti H5N1 activities of some novel fused heterocycles bearing pyrazolyl moiety

SK Ramadan, WSI Abou-Elmagd - Synthetic Communications, 2018 - Taylor & Francis
Ring transformation of the acid hydrazide, derived from 2 (3 H)-furanone, into
triazolopyridazine, triazolothiadiazole, and triazolothiadiazine derivatives, was investigated …

Synthesis and antioxidant, antimicrobial, and antiviral activity of some pyrazole-based heterocycles using a 2(3H)-furanone derivative

YM Youssef, ME Azab, GA Elsayed… - Journal of the Iranian …, 2023 - Springer
Some pyrazole-based heterocycles such as pyrrolone, pyridazinone, and imidazole
derivatives were synthesized utilizing the pyrazolyl-2 (3 H)-furanone derivative 3, which was …

A facile synthesis and anti-avian influenza virus (H5N1) screening of some novel pyrazolopyrimidine nucleoside derivatives

AE Rashad, AH Shamroukh… - … and Nucleic Acids, 2010 - Taylor & Francis
Treatment of 5-amino-1-(9-methyl-5, 6-dihydronaphtho [1′, 2′: 4, 5] thieno [2, 3-d]
pyrimidin-11-yl)-1H-pyrazole-4-carbonitrile (1) with formic acid afforded pyrazolo [3, 4-d] …

New route to the synthesis of Benzamide-Based 5-aminopyrazoles and their fused heterocycles showing remarkable antiavian influenza virus activity

AMS Hebishy, HT Salama, GH Elgemeie - ACS omega, 2020 - ACS Publications
This study describes a new route to the synthesis of novel benzamide-based 5-
aminopyrazoles and their corresponding pyrazolo [1, 5-a] pyrimidine and pyrazolo [5, 1-c][1 …

Efficient synthesis of 3H, 3′ H-spiro [benzofuran-2, 1′-isobenzofuran]-3, 3′-dione as novel skeletons specifically for influenza virus type B inhibition

Y Malpani, R Achary, SY Kim, HC Jeong, P Kim… - European journal of …, 2013 - Elsevier
An efficient and novel two step synthetic procedure to prepare various substituted 3H, 3′ H-
spiro [benzofuran-2, 1′-isobenzofuran]-3, 3′-diones A, was established from very simple …

Evaluation of some new heterocycles bearing 2‐oxoquinolyl moiety as immunomodulator against highly pathogenic avian influenza virus (H5N8)

EAE El‐Helw, ARI Morsy… - Journal of Heterocyclic …, 2021 - Wiley Online Library
The hydrazide obtained from furan‐2 (3 H)‐one integrated with a quinolin‐2 (1 H)‐one core
reported previously by our research group was utilized as a building block synthon to obtain …

Synthesis and anti-influenza virus activity of tricyclic compounds with a unique amine moiety

M Oka, Y Ishiwata, N Iwata, N Honda… - Chemical and …, 2001 - jstage.jst.go.jp
Several novel tricyclic compounds with a unique amine moiety (1, 2a—i) were designed and
prepared based on the structure of triperiden for the development of anti-influenza virus …