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AT 406
Known as:
AT406 cpd
, IAP Inhibitor AT-406
, Pyrrolo(1,2-a)(1,5)diazocine-8-carboxamide, n-((1,1'-biphenyl)-2-ylmethyl)decahydro-5-(((2s)-2-(methylamino)-1-oxopropyl)amino)-3-(3-methyl-1-oxobutyl)-6-oxo-, (5s,8s,10ar)
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An orally bioavailable inhibitor of IAP (Inhibitor of Apoptosis Protein) family of proteins with potential apoptotic inducing and antineoplastic…
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National Institutes of Health
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2 relations
NCIt Antineoplastic Agent Terminology
SM 406
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
IAPs protect host target tissues from graft-versus-host disease in mice.
T. Toubai
,
Corinne Rossi
,
+13 authors
P. Reddy
Blood Advances
2017
Corpus ID: 33304984
Inhibitors of apoptosis proteins (IAPs) regulate apoptosis, but little is known about the role of IAPs in the regulation of…
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2016
2016
IAP antagonists Birinapant and AT-406 efficiently synergise with either TRAIL, BRAF, or BCL-2 inhibitors to sensitise BRAFV600E colorectal tumour cells to apoptosis
P. Perimenis
,
A. Galaris
,
A. Voulgari
,
M. Prassa
,
A. Pintzas
BMC Cancer
2016
Corpus ID: 255828087
High expression levels of Inhibitors of Apoptosis Proteins (IAPs) have been correlated with poor cancer prognosis and block the…
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2016
2016
Acquired cisplatin resistance in malignant pleural mesothelioma cells is reversed by both BH3-mimetic obatoclax and IAP-inhibitor AT-406
A. Tyler
,
C. Sandberg
,
+4 authors
K. Grankvist
2016
Corpus ID: 90900843
Background Cisplatin is used for treatment of malignant pleural mesothelioma (MPM) and non-small cell lung cancer (NSCLC) but…
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2015
2015
Inhibition of Bcl-2 or IAP proteins does not provoke mutations in surviving cells.
Tanmay M. Shekhar
,
Maja Green
,
D. Rayner
,
Mark A. Miles
,
S. Cutts
,
C. Hawkins
Mutation research
2015
Corpus ID: 19159190
2015
2015
Discovery of Novel, Potent, and Specific Cell‐Death Inducers in the Jurkat Acute Lymphoblastic Leukemia Cell Line
E. Carosati
,
Natascha van den Höfel
,
+7 authors
C. Mahotka
ChemMedChem
2015
Corpus ID: 11455506
The limited clinical efficacy of many cancer therapeutics has initiated intense research efforts toward the discovery of novel…
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2014
2014
Phase I study of Debio1143 (AT406) in combination with daunorubicin (D) and cytarabine (C) in patients with poor-risk acute myeloid leukemia (AML).
J. Dipersio
,
H. Erba
,
+8 authors
J. M. Sorensen
2014
Corpus ID: 74792268
7029 Background: Treatment of AML remains difficult due to the development of treatment resistance. Inhibitors of apoptosis…
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2014
2014
First-in-human, pharmacokinetic (PK), and pharmacodynamics (PD) phase I study of Debio1143 (AT-406) in patients with advanced cancer: Final results.
H. Hurwitz
,
Henry C. Pitot
,
+5 authors
J. M. Sorensen
2014
Corpus ID: 78648430
2532 Background: Inhibitors of apoptosis proteins (IAPs) modulate multiple processes, including caspases activation and NF-κB…
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2013
2013
Physiologically based pharmacokinetic and pharmacodynamic modeling of an antagonist (SM‐406/AT‐406) of multiple inhibitor of apoptosis proteins (IAPs) in a mouse xenograft model of human breast…
Tao Zhang
,
Yanyan Li
,
+4 authors
Duxin Sun
Biopharmaceutics & drug disposition
2013
Corpus ID: 10911353
The inhibitors of apoptosis proteins (IAPs) are a class of key apoptosis regulators overexpressed or dysregulated in cancer. SM…
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2012
2012
76 Preliminary Report of a First-in-human, Open-label, Multicenter, Phase I Study of AT-406 (Debio 1143), an Oral Small Molecule Multi-IAP Inhibitor, in Solid Tumors and Lymphomas
H. Hurwitz
,
H. Pitot
,
+4 authors
David C. Smith
2012
Corpus ID: 71633546
2009
2009
Abstract #1917: Synergistic effect of AT-406, a small molecule inhibitor of XIAP, with chemotherapy and tyrosine kinase inhibitors
Hengbang Wang
,
Guangfeng Wang
,
+12 authors
Dajun Yang
2009
Corpus ID: 80151650
X-linked inhibitor of apoptosis protein (XIAP) suppresses apoptosis in cells by inhibiting the apoptosis caspase-9 and caspase-3…
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