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Synthesis of new phosphate derivative of benzothiazole and its inhibiting effect on two series of human neuroblastoma cell growth
Authors:Mahshid Nikpour Nezhati  Gholam Hossein Riazi  Homayon Ahmad Panahi  Elham Moniri  Nasir Ahmad Rajabi  Mohammad Mehdi Sadughi  Natasha Rahmani Zaker  Robab Ardekani  Reihaneh Kooshkestani
Affiliation:1191. Department of Chemistry, Islamic Azad University, Central Tehran Branch, Tehran, Iran
2191. Department of Pharmacology, Tehran University, Tehran, Iran
3191. Department of Chemistry, Islamic Azad University, Varamin Branch (Pishva), Iran
4191. Department of Chemistry, Imam Khomeini International University (IKIU), Qazvine, Iran
5191. Young Researchers Club, Islamic Azad University, Central Tehran Branch, Tehran, Iran
6191. Young Researchers Club, Islamic Azad University, Ghaemshahr Branch, Tehran, Iran
7191. Department of Microbiology, Islamic Azad University, Science and Research Campus, Tehran, Iran
8191. Department of Biochemistry, Alzahra University, Tehran, Iran
Abstract:The sodium salt of di ((1-hydroxy-2-benzothiazolium-1-yl) ethyliden-1,1-H-bisphosphonic acid) orthophosphate was synthesized and its toxicity and viability effects screened on two different human neuroblastoma cell lines. This novel derivative of benzothiazole provides a new compound in connection with research and therapeutic application for tumor cell growth inhibition. Benzothiazole was alkylated in reaction with bromoacetic acid and then converted to its H-bisphosphonic acid derivative in presence of H3PO3/POCl3. The procedure led to formation of two molecules of corresponding H-bisphosphonic acid which attached together via a phosphate bridge. The investigated compound exhibits activities (IC50 value) ranging from 14–23 μM (corresponding to human neuroblastoma SK-BE (2) and SK-NM-C cells).
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