Synthesis of [125I]iodoclorgyline, a selective monoamine oxidase A inhibitor, and its biodistribution in mice.

DOI: 10.1248/cpb.39.3343

Source and publish data:

Chemical and pharmaceutical bulletin p. 3343 - 3345 (1991)

Update date:2022-07-30

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Authors:

Ohmomo Ohmomo

Hirata Hirata

Murakami

Magata Magata

Tanaka Tanaka

Yokoyama

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Article abstract of DOI:10.1248/cpb.39.3343

A new radioiodinated monoamine oxidase A (MAO-A) specific inhibitor, [125I]iodoclorgyline, was synthesized from its tin precursor by iododestannylation reaction using sodium [125I]iodide and hydrogen peroxide with high yield and site specificity. The prod

Full text of DOI:10.1248/cpb.39.3343

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Article Doi

Synthesis of [125I]iodoclorgyline, a selective monoamine oxidase A inhibitor, and its biodistribution in mice.

DOI: 10.1248/cpb.39.3343

Source and publish data:

Authors:

Article abstract of DOI:10.1248/cpb.39.3343

Full text of DOI:10.1248/cpb.39.3343

Products guided by the article

R&D Labs maybe for 140163-69-5

Relevant to this article

Serum stability of selected decapeptide agonists of KISS1R using pseudopeptides

Auxiliary-Assisted Palladium-Catalyzed Direct C(sp3)-H Sulfonamidation to Afford 1,2-Amino Alcohol Derivatives

Highly sensitive sensing of volatile organic compound ethylamine

Structure-activity studies of 7-heteroaryl-3-azabicyclo[3.3.1]non-6-enes: A novel class of highly potent nicotinic receptor ligands

Ipso -Iodocyclization of ethoxyethyl ethers to alkynes at the ortho -position: An efficient synthesis of functionalized spiro compounds

Radical conjugate addition of aryl-tethered -alkoxyacrylates: Formal synthesis of (±)-Frenolicin B and (±)- epi -Frenolicin B

Auxiliary-Assisted Palladium-Catalyzed Direct C(sp³)-H Sulfonamidation to Afford 1,2-Amino Alcohol Derivatives