Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2020 2
2021 2
2026 0

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

2 results

Results by year

Filters applied: . Clear all
Your search was processed without automatic term mapping because it retrieved zero results.
Page 1
Exploring 3-hydroxyflavone scaffolds as mushroom tyrosinase inhibitors: synthesis, X-ray crystallography, antimicrobial, fluorescence behaviour, structure-activity relationship and molecular modelling studies.
Ashraf J, Mughal EU, Sadiq A, Bibi M, Naeem N, Ali A, Massadaq A, Fatima N, Javid A, Zafar MN, Khan BA, Nazar MF, Mumtaz A, Tahir MN, Mirzaei M. Ashraf J, et al. J Biomol Struct Dyn. 2021 Nov;39(18):7107-7122. doi: 10.1080/07391102.2020.1805364. Epub 2020 Aug 17. J Biomol Struct Dyn. 2021. PMID: 32799758
In due course and our approach to synthesize bioactive compounds, a series of varyingly substituted 3-hydroxyflavone derivatives (1-23) were synthesized in one-pot reaction and screened for in vitro against mushroom tyrosinase enzyme. ...Remarkably, the compound 2 (IC(50) …
In due course and our approach to synthesize bioactive compounds, a series of varyingly substituted 3-hydroxyflavone derivatives (1-2 …
Exploring 3-Benzyloxyflavones as new lead cholinesterase inhibitors: synthesis, structure-activity relationship and molecular modelling simulations.
Mughal EU, Sadiq A, Ayub M, Naeem N, Javid A, Sumrra SH, Zafar MN, Khan BA, Malik FP, Ahmed I. Mughal EU, et al. J Biomol Struct Dyn. 2021 Oct;39(16):6154-6167. doi: 10.1080/07391102.2020.1803136. Epub 2020 Aug 5. J Biomol Struct Dyn. 2021. PMID: 32752941
The findings showed that all the synthesized target compounds (1-10) are potent dual inhibitors of acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) enzymes with varying IC(50) values. ...[Formula: see text]HIGHLIGHTS3-benzyloxyflavone analogues were designed, s …
The findings showed that all the synthesized target compounds (1-10) are potent dual inhibitors of acetylcholinesterase (AChE) and bu …