Abstract
A new structural class of DGAT1 inhibitors was discovered and the structure-activity relationship was explored. The pyrrolotriazine core of the original lead molecule was changed to a pyrrolopyridazine core providing an increase in potency. Further exploration resulted in optimization of the propyl group at C7 and the discovery that the ester at C6 could be replaced by five-membered heterocyclic rings. The analogs prepared have DGAT1 IC(50) values ranging from >10 μM to 48 nM.
Copyright © 2010 Elsevier Ltd. All rights reserved.
MeSH terms
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Cell Line
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Diacylglycerol O-Acyltransferase / antagonists & inhibitors*
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Diacylglycerol O-Acyltransferase / metabolism*
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Enzyme Inhibitors / chemical synthesis
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Enzyme Inhibitors / chemistry*
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Enzyme Inhibitors / pharmacology*
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Humans
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Inhibitory Concentration 50
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Pyridazines / chemical synthesis
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Pyridazines / chemistry*
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Pyridazines / pharmacology*
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Pyrroles / chemical synthesis
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Pyrroles / chemistry*
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Pyrroles / pharmacology*
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Sterol O-Acyltransferase / antagonists & inhibitors
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Sterol O-Acyltransferase / metabolism
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Structure-Activity Relationship
Substances
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Enzyme Inhibitors
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Pyridazines
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Pyrroles
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Pyrrolopyridazine
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DGAT1 protein, human
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Diacylglycerol O-Acyltransferase
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Sterol O-Acyltransferase
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sterol O-acyltransferase 1