𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of 123I- and 131I-labelled derivatives of low-density lipoprotein for radiopharmaceutical use

✍ Scribed by S. S. Moerlein; K. K. Dalal; Y. Yano


Publisher
John Wiley and Sons
Year
1987
Tongue
French
Weight
564 KB
Volume
24
Category
Article
ISSN
0022-2135

No coin nor oath required. For personal study only.

✦ Synopsis


The syntheres of two analogues of lowdensity lipoprotein (LDL) labelled with 123i Rabbit LDL was employed or l3'I was optimized for radbpharmaceutlcal application.

due to its uoefulness in pre-cliniml experimentation, although the parameters which were optlmlzed also pertain to human LDL. LDL was iodinated directly with exchange-labelled rpl]lCl to produce Injectable Val]LDL in 40% radiochemical yield within 30 min. A derlvatized version of LDL, ral]TC-LDL, radiochemical yield within 75 min by radioiodination of tyraminecellobiose (TC) via h . c & oxidation of 9followed by cross-linking to LDL using cyanuric chloride. Quality control tests Indicated that both radloiodinated LDL and TC-LDL were very similar in character to the native LDL molecule.

was produced In about 30% 0362-4803/87/111325-15W S O @ 1987 by John Wiley & Sons, Ltd.


📜 SIMILAR VOLUMES


Synthesis and biological evaluation of 1
✍ Jacob Madsen; Betina Elfving; Vibe G. Frokjaer; Birgitte R. Kornum; Gerda Thomse 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 French ⚖ 199 KB

## Abstract Two novel radioligands for the serotonin transporter (SERT), [^125^I]{3‐[5‐iodo‐1‐[4‐fluorophenyl)‐1,3‐dihydroisobenzofuran‐1‐yl]‐propyl}‐dimethylamine ([^125^I]‐2) and __S__‐[^125^I]{3‐[5‐iodo‐1‐(4‐fluorophenyl)‐1,3‐dihydroisobenzofuran‐1‐yl]‐propyl}‐dimethylamine ([^125^I]‐(__S__)‐2)

Synthesis of a novel 123I-labelled deriv
✍ Xiao-Shu He; Kan Sam Lee; Daniel Weinberger; Brian R. de Costa 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 French ⚖ 408 KB 👁 1 views

## Abstract [^123^I]1‐[2‐(Diphenylmethoxy)ethyl]‐4‐[3‐(__m__‐iodophenyl)‐2‐propenyl]piperazine ([^123^I]2), a potential SPECT imaging agent for dopamine reuptake sites was efficiently synthesized in 4 steps from 1‐[2‐(diphenylmethoxy)ethyl]piperazine (3). A key step in the synthesis was the selecti