Rapid Development of a Commercial Process for Linrodostat, an Indoleamine 2,3-Dioxygenase (IDO) Inhibitor

Author:

Fraunhoffer Kenneth J.1ORCID,DelMonte Albert J.1ORCID,Beutner Gregory L.1ORCID,Bultman Michael S.1ORCID,Camacho Kathryn1,Cohen Benjamin1ORCID,Dixon Darryl D.1ORCID,Fan Yu1,Fanfair Dayne1,Freitag Adam J.1,Glace Andrew W.1,Gonzalez-Bobes Francisco1ORCID,Gujjar Manjunath2,Haley Matthew W.1,Hickey Matthew R.1,Ho Jeanne1,Iyer Vidya1,Maity Prantik2,Patel Sunil1,Rosso Victor W.1,Schmidt Michael A.1ORCID,Stevens Jason M.1ORCID,Tan Yichen1,Wilbert Christopher1,Young Ian S.1ORCID,Yu Miao1ORCID

Affiliation:

1. Chemical and Synthetic Development, Bristol-Myers Squibb Global Product Development and Supply, One Squibb Drive, P.O. Box 191, New Brunswick, New Jersey 08903-0191, United States

2. Chemical and Synthetic Development, Biocon Bristol-Myers Squibb Research and Development Center, Biocon Park, Jigani Link Road, Bommasandra IV, Bangalore 560099, India

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference30 articles.

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2. Why tumours eat tryptophan

3. Immune-modulating enzyme indoleamine 2,3-dioxygenase is effectively inhibited by targeting its apo-form

4. Beck, H. P.; Jaen, J. C.; Osipov, M.; Powers, J. P.; Reilly, M. K.; Shunatona, H. P.; Walker, J. R.; Zibinsky, M.; Balog, J. A.; Williams, D. K.; Markwalder, J. A.; Cherney, E.; Shan, W.; Huang, A. Immunoregulatory Agents. WO2016073770A1, May 12, 2016.

5. Lanthanoids in organic synthesis. 5. Selective reductions of ketones in the presence of aldehydes

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