Syntheses of C-13 and C-14-labeled versions of the investigational proteasome inhibitor MLN9708-Reference-Cited by-同舟云学术

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Syntheses of C-13 and C-14-labeled versions of the investigational proteasome inhibitor MLN9708

Published:2013-07 Issue:9-10 Volume:56 Page:464-470
ISSN:0362-4803
Container-title:Journal of Labelled Compounds and Radiopharmaceuticals
language:en
Short-container-title:J. Label Compd. Radiopharm

Author:

Plesescu Mihaela¹,Elliott Eric L.¹,Li Yuexian¹,Prakash Shimoga R.¹

Affiliation:

1. Department of Drug Metabolism and Pharmacokinetics; Millennium Pharmaceuticals, Inc.; 40 Landsdowne Street; Cambridge; MA; 02139; USA

Publisher

Wiley

Subject

Organic Chemistry,Spectroscopy,Drug Discovery,Radiology, Nuclear Medicine and imaging,Biochemistry,Analytical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/jlcr.3079/fullpdf

Reference13 articles.

1. In Vitro and In Vivo Selective Antitumor Activity of a Novel Orally Bioavailable Proteasome Inhibitor MLN9708 against Multiple Myeloma Cells

2. Antitumor Activity of the Investigational Proteasome Inhibitor MLN9708 in Mouse Models of B-cell and Plasma Cell Malignancies

3. Building on bortezomib: second-generation proteasome inhibitors as anti-cancer therapy

4. Next-generation proteasome blockers promise safer cancer therapy

5. Evaluation of the Proteasome Inhibitor MLN9708 in Preclinical Models of Human Cancer

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