Abstract
Herein, we describe the synthesis and SAR of a series of small molecule macrocycles that selectively inhibit JAK2 kinase within the JAK family and FLT3 kinase. Following a multiparameter optimization of a key aryl ring of the previously described SB1518 (pacritinib), the highly soluble 14l was selected as the optimal compound. Oral efficacy in the murine collagen-induced arthritis (CIA) model for rheumatoid arthritis (RA) supported 14l as a potential treatment for autoimmune diseases and inflammatory disorders such as psoriasis and RA. Compound 14l (SB1578) was progressed into development and is currently undergoing phase 1 clinical trials in healthy volunteers.
MeSH terms
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Animals
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Antirheumatic Agents / chemical synthesis*
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Antirheumatic Agents / pharmacokinetics
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Antirheumatic Agents / pharmacology
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Arthritis, Experimental / chemically induced
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Arthritis, Experimental / drug therapy
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Arthritis, Rheumatoid / drug therapy*
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Cell Line
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Cell Membrane Permeability
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Collagen Type II
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Dogs
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Female
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Heterocyclic Compounds, 4 or More Rings / chemical synthesis*
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Heterocyclic Compounds, 4 or More Rings / pharmacokinetics
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Heterocyclic Compounds, 4 or More Rings / pharmacology
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Humans
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Janus Kinase 2 / antagonists & inhibitors*
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Janus Kinase 2 / physiology
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Macaca mulatta
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Male
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Mice
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Mice, Nude
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Microsomes / metabolism
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Models, Molecular
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Rats
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Signal Transduction / drug effects
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Solubility
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Stereoisomerism
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Structure-Activity Relationship
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TYK2 Kinase / antagonists & inhibitors
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fms-Like Tyrosine Kinase 3 / antagonists & inhibitors*
Substances
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15-(2-(pyrrolidin-1-yl)ethoxy)-7,12,25-trioxa-19,21,24-triazatetracyclo(18.3.1.1(2,5).1(14,18))hexacosa-1(24),2,4,9,14(26),15,17,20,22-nonaene
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Antirheumatic Agents
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Collagen Type II
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Heterocyclic Compounds, 4 or More Rings
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fms-Like Tyrosine Kinase 3
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Janus Kinase 2
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TYK2 Kinase