Challenges and Opportunities in the Discovery of New Therapeutics Targeting the Kynurenine Pathway

Journal of Medicinal Chemistry - Tập 58 Số 22 - Trang 8762-8782 - 2015
Amy B. Dounay1, Jamison B. Tuttle2, Patrick R. Verhoest2
1Department of Chemistry and Biochemistry, Colorado College, 14 E. Cache La Poudre Street, Colorado Springs, Colorado 80903, United States
2Worldwide Medicinal Chemistry, Pfizer Worldwide Research & Development, Cambridge, Massachusetts 02139, United States

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Tài liệu tham khảo

10.1038/nrd3793

Kotake Y., 1936, Z. Physiol. Chem., 243, 237, 10.1515/bchm2.1936.243.6.237

Yamamoto S., 1967, J. Biol. Chem., 242, 5260, 10.1016/S0021-9258(18)99420-2

10.1016/j.gene.2007.04.010

10.1158/0008-5472.CAN-07-1872

10.1007/s00239-007-9049-1

10.1073/pnas.0610007104

10.1186/1756-6606-2-8

10.1016/j.biocel.2007.01.004

10.1007/s00702-011-0681-y

10.1084/jem.189.9.1363

10.1046/j.1365-2567.2002.01526.x

10.1084/jem.20020121

10.1038/sj.cdd.4401073

10.4049/jimmunol.176.11.6752

10.1038/ni.2077

10.1126/science.281.5380.1191

10.1158/0008-5472.CAN-12-0569

10.1016/S0065-2776(08)60911-6

10.1038/nm934

10.1016/0003-9861(91)90142-6

10.1038/nm1196

1-Methyl-D-tryptophan and docetaxel in treating patients with metastatic solid tumors.http://clinicaltrials.gov/show/NCT01191216(accessed June 17, 2015) .

1-Methyl-D-tryptophan in treating patients with metastatic or refractory solid tumors that cannot be removed by surgery.http://clinicaltrials.gov/show/NCT00567931(accessed June 17, 2015) .

Multiple ongoing clinical trials.https://clinicaltrials.gov/ct2/results?term=indoximod&Search=Search(accessed June 17, 2005) .

10.1158/0008-5472.CAN-08-2106

10.1007/s00262-008-0513-6

10.1158/0008-5472.CAN-06-2925

10.1007/s00726-014-1766-3

10.1371/journal.pone.0044797

10.1371/journal.pone.0019823

10.1038/cdd.2012.151

10.1038/nchembio.83

10.1038/nm.2438

10.1021/acs.jmedchem.5b00326

10.1021/bi00439a012

10.1517/13543776.2013.827662

10.1073/pnas.0508996103

10.1021/jm800512z

Mautino, M.; Kumar, S.; Jaipuri, F.; Waldo, J.; Kesharwani, T.; Zhang, X.Imidazole derivatives as IDO inhibitors. WO2011056652, 2011.

Mautino, M.; Kumar, S.; Waldo, J.; Jaipuri, F.; Kesharwani, T.Fused imidazole derivatives useful as IDO inhibitors. WO2012142237, 2012.

Kumar, S.; Waldo, J.; Jaipuri, F.; Mautino, M.Tricyclic compounds as inhibitors of immunosuppression mediated by tryptophan metabolization. WO2014159248, 2014.

Newlink Genetics. NLG919, a novel indoleamine-2,3-dioxygenase (IDO)-pathway inhibitor drug candidate for cancer therapy.http://newlinkgenetics.com/assets/pdfs/AACR_2013_-_NLG919_and_Indoximod.pdf(accessed June 17, 2015) .

IDO inhibitor in advanced solid tumors.https://clinicaltrials.gov/ct2/show/NCT02048709?term=NLG919&rank=1’(accessed June 17, 2015) .

10.1021/jm300260v

10.1021/jm900518f

Combs, A. P.; Zhu, W.; Sparks, R. B.Preparation of N-hydroxyamidinooxadiazoles and related analogs as modulators of indoleamine 2,3-dioxygenase. WO2008058178A1, 2008.

Combs, A. P.; Yue, E. W.; Sparks, R. B.; Zhu, W.; Zhou, J.; Lin, Q.; Weng, L.; Yue, T.Y.; Liu, P.Preparation of 1,2,5-oxadiazoles as inhibitors of indoleamine 2,3-dioxygenase. WO2010005958A2, 2010.

10.1182/blood-2009-09-246124

Pharmacodynamic assessment of INCB024360, an inhibitor of indoleamine 2,3-dioxygenase 1 (IDO1) in advanced cancer patients.http://www.incyte.com/sites/default/files/ASCO%202012%20-%20INCB024360%20oral%20presentation%20-%20FINAL%20sec.pdf(accessed June 22, 2015) .

Bristol-Myers Squibb and Incyte enter into a clinical collaboration agreement to evaluate combination regimen of two novel immunotherapies.http://news.bms.com/press-release/partnering-news/bristol-myers-squibb-and-incyte-enter-clinical-collaboration-agreement(accessed June 17, 2015) .

A phase 1/2 randomized, blinded, placebo controlled study of ipilimumab in combination with INCB024360 or placebo in subjects with unresectable or metastatic melanoma.https://www.clinicaltrials.gov/ct2/results?term=A+Phase+1%2F2+Randomized%2C+Blinded%2C+Placebo+Controlled+Study+of+Ipilimumab+in+Combination+With+INCB024360+or+Placebo+in+Subjects+With+Unresectable+or+Metastatic+Melanoma&Search=Search(accessed June 17, 2015) .

A phase 2 study of the IDO inhibitor INCB024360 versus tamoxifen for subjects with biochemical-recurrent-only EOC, PPC or FTC following complete remission with first-line chemotherapy.https://www.clinicaltrials.gov/ct2/results?term=A+Phase+2+Study+of+the+IDO+Inhibitor+INCB024360+Versus+Tamoxifen+for+Subjects+With+Biochemical-recurrent-only+EOC%2C+PPC+or+FTC+Following+Complete+Remission+With+First-line+Chemotherapy+&Search=Search(accessed June 17, 2015) .

Incyte announces clinical trial collaboration with Merck to evaluate combination of two novel immunotherapies.http://investor.incyte.com/phoenix.zhtml?c=69764&p=irol-newsArticle&ID=1897007(accessed June 17, 2015) .

10.1016/j.bbapap.2011.07.023

10.1021/ml500247w

10.1016/j.ejmech.2014.06.078

10.1093/jnci/djs152

10.1002/eji.200939535

10.1038/nature10491

10.1073/pnas.1113873109

10.1016/0028-3908(94)00147-K

10.1016/0006-2952(95)00006-L

10.1016/0960-894X(96)00124-2

10.1021/jm2006782

10.1111/febs.12036

10.1016/j.bmcl.2012.10.010

10.1038/nrc2639

10.1158/0008-5472.CAN-12-0569

10.4049/jimmunol.171.4.1652

10.3390/toxins6030914

10.1016/B978-0-12-396492-2.00004-7

10.1016/j.imlet.2008.08.008

10.4137/IJTR.S4294

10.1007/978-1-60761-720-4_19

10.1096/fj.04-3228fje

10.4049/jimmunol.1001628

10.1136/jnnp.42.7.640

10.1007/s00702-007-0667-y

10.1016/S0304-3940(02)00710-3

10.1038/nrn3257

10.1002/jlac.18530860115

10.1007/s00702-011-0763-x

10.4137/IJTR.S12536

10.1369/jhc.2010.955955

10.1093/intimm/dxt011

10.1038/nrc3846

Dolwick K. M., 1993, Mol. Pharmacol., 44, 911

10.1093/toxsci/kfq024

10.1007/s10354-014-0321-x

10.1111/all.12346

10.1016/j.tips.2011.02.002

10.1002/hep.25977

10.1074/jbc.M603503200

10.1038/nrd3793

10.3389/fnins.2014.00012

10.4137/IJTR.S16800

10.1002/glia.20432

10.1016/j.biopsych.2010.08.006

10.1016/j.schres.2014.04.037

10.1093/schbul/sbs076

10.1186/1756-6606-6-5

10.1016/j.bcp.2012.12.014

10.2174/138161210790170094

10.1007/s00213-013-3275-6

Hilmas C., 2001, J. Neurosci., 21, 7463, 10.1523/JNEUROSCI.21-19-07463.2001

10.1371/journal.pone.0041108

10.1016/j.neuropharm.2009.06.003

10.1007/s00109-013-1046-9

10.1038/nn.3540

10.1007/s007020050149

10.1016/j.neuint.2006.08.012

10.1097/00001756-200312190-00005

10.1002/hbm.22055

10.1111/j.1471-4159.2009.06442.x

10.1016/j.nbd.2004.07.006

10.1016/j.nbd.2006.02.011

10.1016/S0014-5793(97)00627-3

10.1002/glia.20090

10.1523/JNEUROSCI.4101-07.2007

10.1016/0003-2697(92)90432-7

10.1038/nature12039

10.1046/j.1471-4159.1996.67020692.x

10.1007/978-1-4615-0135-0_71

Dominguez, C. L. A.; Toledo-Sherman, L. M.; Courtney, S. M.; Prime, M.; Mitchell, W.; Brown, C. J.; De Aguiar, P. C.; Johnson, P.Certain kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof. WO2013016488, 2013.

10.1021/jm970467t

10.1139/y94-025

10.1016/j.cell.2011.05.020

10.1124/dmd.112.046532

Mucke L., 2000, J. Neurosci., 20, 4050, 10.1523/JNEUROSCI.20-11-04050.2000

10.1016/S0092-8674(00)81369-0

10.1007/s00018-009-0166-4

10.1146/annurev.biochem.73.011303.074021

10.1523/JNEUROSCI.5631-03.2004

10.1038/npp.2010.39

10.1111/j.1742-4658.2011.08106.x

10.1021/jm100464k

10.1002/cmdc.200500095

10.1093/schbul/sbt157

10.1021/ml200204m

10.1016/j.neuropharm.2014.03.004

10.3389/fpsyt.2011.00014

10.1523/JNEUROSCI.1107-14.2014

10.1074/jbc.C200303200

10.1074/jbc.M409291200

10.1016/j.brainres.2006.05.082

10.1016/j.bmcl.2011.12.138

10.2174/156802612803989264

10.1074/jbc.M113.474908