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Barbara Francis

Researcher at Merck & Co.

Publications -  12
Citations -  373

Barbara Francis is an academic researcher from Merck & Co.. The author has contributed to research in topics: In vivo & Receptor. The author has an hindex of 9, co-authored 12 publications receiving 371 citations.

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Journal Article

Receptor-Binding Radiotracers: A Class of Potential Radiopharmaceuticals

TL;DR: Theoretical calculations showed that derivatives binding to the estrogen receptor, the beta adrenoceptor, or the cholinergic receptor are capable of achieving satisfactory target-to-blood ratios.
Journal Article

[I-125] 17 alpha-Iodovinyl 11 beta-methoxyestradiol: in vivo and in vitro properties of a high-affinity estrogen-receptor radiopharmaceutical.

TL;DR: By in vivo competition studies with nonradioactive estradiol, it is found that 95% of the [I-125]MIVE2 bound in the uterus is specifically bound to estrogen receptors.
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Synthesis and evaluation of radioiodinated derivatives of 1-azabicyclo[2.2.2]oct-3-yl .alpha.-hydroxy-.alpha.-(4-iodophenyl)-.alpha.-phenylacetate as potential radiopharmaceuticals

TL;DR: Preliminary distribution studies indicate that 1b localizes in the organs known to have a large concentration of muscarinic receptors and that this localization is due to binding to those receptors.
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Synthesis and evaluation of (17.alpha.,20E)-21-[125I]iodo-19-norpregna-1,3,5(10),20-tetraene-3,17-diol and (17.alpha.,20E)-21-[125I]iodo-11.beta.-methoxy-19-norpregna-1,3,5(10),20-tetraene-3,17-diol [17.alpha.-iodovinyl)estradiol derivatives] as high specific activity potential radiopharmaceuticals

TL;DR: Preliminary distribution studies indicate that although both 4b and 4d localize in the tissues known to have a large concentration of estrogen receptors, 4d accumulates in higher amounts in target tissues and provides a high target to nontarget ratio.
Journal Article

Use of 3-quinuclidinyl 4-iodobenzilate as a receptor binding radiotracer.

TL;DR: 3-Quinuclidinyl 4-iodobenzilate was shown to bind to the muscarinic acetylcholine receptor (mAChR) by testing the saturability and the stereoselectivity in the corpus striatum, cerebellum, and the heart, but the ratio of radioactivity in tissues containing different concentrations of mAChR was less than the ratio in vitro saturation assay.