Back Cover: Discovery of a Highly Selective PLD2 Inhibitor (ML395): A New Probe with Improved Physiochemical Properties and Broad-Spectrum Antiviral Activity against Influenza Strains (ChemMedChem 12/2014)

Further chemical optimization of the halopemide-derived family of dual phospholipaseD1/2 (PLD1/2) inhibitors afforded ML395 (VU0468809), a potent, >80-fold PLD2 selective allosteric inhibitor (cellular PLD1, IC50 >30000nM; cellular PLD2, IC50 =360nM). Moreover, ML395 possesses an attractive in...

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Published inChemMedChem Vol. 9; no. 12; p. 2820
Main Authors O'Reilly, Matthew C., Oguin III, Thomas H., Scott, Sarah A., Thomas, Paul G., Locuson, Charles W., Morrison, Ryan D., Daniels, J. Scott, Brown, H. Alex, Lindsley, Craig W.
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 01.12.2014
Wiley Subscription Services, Inc
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ISSN1860-7179
1860-7187
DOI10.1002/cmdc.201490047

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Abstract Further chemical optimization of the halopemide-derived family of dual phospholipaseD1/2 (PLD1/2) inhibitors afforded ML395 (VU0468809), a potent, >80-fold PLD2 selective allosteric inhibitor (cellular PLD1, IC50 >30000nM; cellular PLD2, IC50 =360nM). Moreover, ML395 possesses an attractive in vitro DMPK profile, improved physiochemical properties, ancillary pharmacology (Eurofins Panel) cleaner than any other reported PLD inhibitor, and has been found to possess interesting activity as an antiviral agent in cellular assays against a range of influenza strains (H1, H3, H5 and H7).
AbstractList Further chemical optimization of the halopemide-derived family of dual phospholipaseD1/2 (PLD1/2) inhibitors afforded ML395 (VU0468809), a potent, >80-fold PLD2 selective allosteric inhibitor (cellular PLD1, IC50 >30000nM; cellular PLD2, IC50 =360nM). Moreover, ML395 possesses an attractive in vitro DMPK profile, improved physiochemical properties, ancillary pharmacology (Eurofins Panel) cleaner than any other reported PLD inhibitor, and has been found to possess interesting activity as an antiviral agent in cellular assays against a range of influenza strains (H1, H3, H5 and H7).
Author O'Reilly, Matthew C.
Locuson, Charles W.
Thomas, Paul G.
Oguin III, Thomas H.
Scott, Sarah A.
Morrison, Ryan D.
Daniels, J. Scott
Brown, H. Alex
Lindsley, Craig W.
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  organization: Department of Pharmacology, Vanderbilt Center for Neuroscience Drug Discovery, Vanderbilt Specialized Chemistry Center (MLPCN), Vanderbilt University Medical Center, Nashville, TN 37232-6600 (USA)
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  givenname: Thomas H.
  surname: Oguin III
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  organization: Department of Immunology, St. Jude Children's Hospital, Memphis, TN 38105 (USA)
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  givenname: Sarah A.
  surname: Scott
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  organization: Department of Pharmacology, Vanderbilt Center for Neuroscience Drug Discovery, Vanderbilt Specialized Chemistry Center (MLPCN), Vanderbilt University Medical Center, Nashville, TN 37232-6600 (USA)
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  givenname: Paul G.
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  givenname: Ryan D.
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  givenname: J. Scott
  surname: Daniels
  fullname: Daniels, J. Scott
  organization: Department of Pharmacology, Vanderbilt Center for Neuroscience Drug Discovery, Vanderbilt Specialized Chemistry Center (MLPCN), Vanderbilt University Medical Center, Nashville, TN 37232-6600 (USA)
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  givenname: H. Alex
  surname: Brown
  fullname: Brown, H. Alex
  organization: Department of Pharmacology, Vanderbilt Center for Neuroscience Drug Discovery, Vanderbilt Specialized Chemistry Center (MLPCN), Vanderbilt University Medical Center, Nashville, TN 37232-6600 (USA)
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  givenname: Craig W.
  surname: Lindsley
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  email: craig.lindsley@vanderbilt.edu
  organization: Department of Pharmacology, Vanderbilt Center for Neuroscience Drug Discovery, Vanderbilt Specialized Chemistry Center (MLPCN), Vanderbilt University Medical Center, Nashville, TN 37232-6600 (USA)
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Snippet Further chemical optimization of the halopemide-derived family of dual phospholipaseD1/2 (PLD1/2) inhibitors afforded ML395 (VU0468809), a potent, >80-fold...
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SubjectTerms antivirals
inhibitors
lipids
Pharmacology
phospholipase D
PLD2
Title Back Cover: Discovery of a Highly Selective PLD2 Inhibitor (ML395): A New Probe with Improved Physiochemical Properties and Broad-Spectrum Antiviral Activity against Influenza Strains (ChemMedChem 12/2014)
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