An overview of the latest outlook of sulfamate derivatives as anticancer candidates (2020-2024).
Esra M MustafaAfnan I ShahinAishah S AlrashedAesheh H BahaaddinAljawhra A AlajmiOmar HashemHanan S AnbarMohammed I El-GamalPublished in: Archiv der Pharmazie (2024)
Considering the emergence of new anticancer drugs, in this review we emphasized and highlighted the recent reports and advances related to sulfamate-incorporating compounds with potential anticancer activity during the last 5 years (2020-2024). Additionally, we discussed their structure-activity relationship, clarifying their potent bioactivity as anticancer agents. Sulfamate derivatives hold promise as effective therapeutic candidates against cancer. By targeting biological targets associated with the development of cancer, such as steroid sulfatases (STS), carbonic anhydrases (CAs), microtubules, NEDD8-activating enzyme, small ubiquitin-like modifiers (SUMO)-activating enzyme (SAE), cyclin-dependent kinases (CDKs), breast cancer susceptibility gene 1 (BRCA1), and so on, this can furnish small molecules as anticancer lead candidates serving the drug discovery field. For example, compound 2, an STS inhibitor, demonstrated superior activity compared to its reference, irosustat, by fivefold. In addition, compound 21, an SAE, is under phase I clinical trials. Continued research into sulfamate derivatives holds potential for the development of novel therapeutic agents targeting various diseases.
Keyphrases
- structure activity relationship
- drug discovery
- papillary thyroid
- clinical trial
- squamous cell
- signaling pathway
- crispr cas
- human health
- childhood cancer
- risk assessment
- small molecule
- genome editing
- machine learning
- big data
- young adults
- squamous cell carcinoma
- emergency department
- drug delivery
- cell proliferation
- gene expression
- genome wide
- study protocol
- open label
- drug induced
- electronic health record
- climate change
- phase iii
- recombinant human