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Design and synthesis of a novel series of cyclohexyloxy-pyridyl derivatives as inhibitors of diacylglycerol acyl transferase 1

Plowright, Alleyn T. (author)
Barton, Peter (author)
Bennett, Stuart (author)
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Birch, Alan M. (author)
Birtles, Susan (author)
Buckett, Linda K. (author)
Butlin, Roger J. (author)
Davies, Robert D. M. (author)
Ertan, Anne (author)
Gutierrez, Pablo Morentin (author)
Kemmitt, Paul D. (author)
Leach, Andrew G. (author)
Svensson, Per H. (author)
KTH,Tillämpad fysikalisk kemi
Turnbull, Andrew V. (author)
Waring, Michael J. (author)
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 (creator_code:org_t)
2013
2013
English.
In: MedChemComm. - : Royal Society of Chemistry (RSC). - 2040-2503 .- 2040-2511. ; 4:1, s. 151-158
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • A novel series of potent diacylglycerol acyl transferase 1 inhibitors was developed from the clinical candidate AZD3988. Replacement of the phenyl cyclohexyl-ethanoate side chain with substituted oxy-linked side chains to introduce changes in shape and polarity, reduce lipophilicity and mask the hydrogen bond donors with internal hydrogen bond acceptors led to improvements in solubility, unbound clearance and excellent selectivity over the related enzyme acyl-coenzyme A:cholesterol acyltransferase 1. A comparison of the small molecule crystal structures of compound 4 and compound 28 is described. Compounds in this series have good ADMET properties and provide an exposure-dependent decrease in circulating plasma triglyceride levels in a rat oral lipid tolerance test.

Subject headings

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Keyword

Potent
Acyltransferase
Discovery
Obesity
Dgat-1

Publication and Content Type

ref (subject category)
art (subject category)

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