Structure‐based discovery of ( S )‐2‐amino‐6‐(4‐fluorobenzyl)‐5,6,11,11a‐tetrahydro‐1H‐imidazo[1′,5′:1,6]pyrido[3,4‐b]indole‐1,3(2H)‐dione as low nanomolar, orally bioavailable autotaxin inhibitor

Author:

Roy Ashis1,Sarkar Tonmoy1,Datta Sebak1,Maiti Arup1,Chakrabarti Monali1,Mondal Trisha1,Mondal Chaitali1,Banerjee Apurba1,Roy Subhasis1,Mukherjee Soumen1,Muley Pragati1,Chakraborty Sabyasachi1,Banerjee Manish1,Kundu Mrinalkanti1ORCID,Roy Kuldeep K.2ORCID

Affiliation:

1. TCG Lifesciences Pvt. Ltd. Kolkata India

2. Department of Pharmaceutical Sciences School of Health Sciences UPES Dehradun India

Publisher

Wiley

Subject

Molecular Medicine,Biochemistry,Drug Discovery,Pharmacology,Organic Chemistry

Reference35 articles.

1. Involvement of lysophospholipase D in the production of lysophosphatidic acid in rat plasma;Akira T.;Biochimica Et Biophysica Acta (BBA) ‐ Lipids and Lipid Metabolism,1986

2. Structure‐based design of novel boronic acid‐based inhibitors of autotaxin;Albers H. M. H. G.;Journal of Medicinal Chemistry,2011

3. Chemical evolution of autotaxin inhibitors;Albers H. M. H. G.;Chemical Reviews,2012

4. Autotaxin, a secreted lysophospholipase D, as a promising therapeutic target in chronic inflammation and cancer;Barbayianni E.;Progress in Lipid Research,2015

5. Autotaxin inhibitors: A patent review;Barbayianni E.;Expert Opinion on Therapeutic Patents,2013

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