Abstract
The advancement of a series of ligand efficient 2-amino-[1,2,4]triazolo[1,5-a]pyridines, initially identified from high-throughput screening, to a JAK2 inhibitor with pharmacodynamic activity in a mouse xenograft model is disclosed.
Keywords:
JAK2; Janus kinase; Triazolopyridine.
Copyright © 2013 Elsevier Ltd. All rights reserved.
MeSH terms
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Amitrole / chemistry*
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Amitrole / pharmacology
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Amitrole / therapeutic use*
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Animals
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Antineoplastic Agents / chemistry*
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Antineoplastic Agents / pharmacology
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Antineoplastic Agents / therapeutic use*
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Crystallography, X-Ray
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Humans
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Janus Kinase 2 / antagonists & inhibitors*
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Janus Kinase 2 / chemistry
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Janus Kinase 2 / metabolism
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Mice
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Models, Molecular
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Neoplasms / drug therapy
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Neoplasms / enzymology
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Neoplasms / pathology
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Pyrimidines / chemistry*
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Pyrimidines / pharmacology
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Pyrimidines / therapeutic use*
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Structure-Activity Relationship
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Triazoles / chemistry*
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Triazoles / pharmacology
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Triazoles / therapeutic use*
Substances
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1,2,4-triazolo(1,5-c)pyrimidine
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Antineoplastic Agents
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Pyrimidines
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Triazoles
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Janus Kinase 2
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Amitrole