Synthesis of Novel Succinamide Derivatives Having a 5,11-Dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one Skeleton as Potent and Selective M 2 Muscarinic Receptor Antagonists. Part 2. -Among the screened compounds derivative (IIIe) exhibits the highest affinity for M 2 muscarinic receptors and (III
ChemInform Abstract: Discovery and Synthesis of [6-Hydroxy-3-[4-[2-(1-piperidinyl)ethoxy]phenoxy]- 2-(4-hydroxyphenyl)]benzo[b]thiophene: A Novel, Highly Potent, Selective Estrogen Receptor Modulator.
โ Scribed by A. D. PALKOWITZ; A. L. GLASEBROOK; K. J. THRASHER; K. L. HAUSER; L. L. SHORT; D. L. PHILLIPS; B. S. MUEHL; M. SATO; P. K. SHETLER; G. J. CULLINAN; T. R. PELL; H. U. BRYANT
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 32 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
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โฆ Synopsis
Discovery and Synthesis of [6-Hydroxy-3-[4-[2-(1-piperidinyl)ethoxy]phenoxy]-2-(4hydroxyphenyl)]benzo[b]thiophene: A Novel, Highly Potent, Selective Estrogen Receptor Modulator.
-The title compound (V) displays greater estrogen antagonist potency in vitro in a human MCF-7 breast cancer cell proliferation assay and in vivo in uterine tissue than any known agent. In addition, (V) retains beneficial estrogen agonist actions on bone and lipid metabolism. -(PALKOWITZ, A. D.; GLASEBROOK, A.
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