Non-steroidal aromatase inhibitors based on a biphenyl scaffold: synthesis, in vitro SAR, and molecular modelling |
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Authors: | Jackson Toby Woo L W Lawrence Trusselle Melanie N Purohit Atul Reed Michael J Potter Barry V L |
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Affiliation: | Medicinal Chemistry, Department of Pharmacy and Pharmacology, and Sterix Ltd. University of Bath, Claverton Down, UK. |
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Abstract: | The synthesis and in vitro biological evaluation (JEG-3 cells) of a series of novel and potent aromatase inhibitors, prepared by microwave-enhanced Suzuki cross-coupling methodology, are reported. These compounds possess a biphenyl template incorporated with the haem-ligating triazolylmethyl moiety, either on its own or in combination with other substituent(s) at various positions on the phenyl rings. The most potent aromatase inhibitor reported herein has an IC(50) value of 0.12 nM, although seven of its congeners are also highly potent (IC(50)
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