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Synthesis and evaluation of 4-triazolylflavans as new aromatase inhibitors

Tipo de material: TextoTextoSeries ; Bioorganic & Medicinal Chemistry Letters, 14(20), p.5215-5218, 2004Trabajos contenidos:
  • Yahiaoui, S
  • Pouget, C
  • Fagnere, C
  • Champavier, Y
  • Habriouxa, G
  • Chulia, A.J
Recursos en línea: Resumen: Aromatase is a target of pharmacological interest for the treatment of estrogen-dependent cancers. Azole derivatives such as letrozole or anastrozole have been developed for aromatase inhibition and are used for the treatment of breast tumors. In this paper, four 4-triazolylflavans were synthesized and were found to exhibit moderate to high inhibitory activity against aromatase.
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Aromatase is a target of pharmacological interest for the treatment of estrogen-dependent cancers. Azole derivatives such as letrozole or anastrozole have been developed for aromatase inhibition and are used for the treatment of breast tumors. In this paper, four 4-triazolylflavans were synthesized and were found to exhibit moderate to high inhibitory activity against aromatase.

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