Skip to content
2000
Volume 10, Issue 4
  • ISSN: 1573-4064
  • E-ISSN: 1875-6638

Abstract

Diels-Alder reaction between furan and maleic anhydride resulted in 5,6-dehydro norcantharidin, then norcantharidin was obtained by reduction. The substituted-carboxylic acid was condensed with N-aminothiourea in presence of phosphorus oxychloride, yielding 2-amino-1,3,4-thiadiazole derivatives. Novel norcantharidin derivatives were synthesized with acylation, then intramolecular condensation using norcantharidin (or 5,6-dehydro norcantharidin) and 2-amino- 1,3,4-thiadiazole derivatives. All the target compounds were confirmed by IR, 1HNMR, ESI-MS and were reported for the first time. Norcantharidin derivatives antiproliferative assay was tested by MTT method against A549 and PC-3 cell lines. The results showed that all the norcantharidin derivatives displayed moderate inhibitory activities.

Loading

Article metrics loading...

/content/journals/mc/10.2174/15734064113099990037
2014-06-01
2025-05-19
Loading full text...

Full text loading...

/content/journals/mc/10.2174/15734064113099990037
Loading

  • Article Type:
    Research Article
Keyword(s): antiproliferative activity; Norcantharidin; synthesis
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test