Cover Picture: Identification and Optimization of the First Highly Selective GLUT1 Inhibitor BAY-876 (ChemMedChem 20/2016)

The front cover picture shows a railway track symbolizing the transport of glucose as energy supply into a tumor cell by the GLUT1‐transporter. This import through the GLUT1‐transporter is blocked by a quinolinedicarboxamide, a compound series inhibiting the glucose transport in a competitive, rever...

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Veröffentlicht in:ChemMedChem 2016-10, Vol.11 (20), p.2240-2240
Hauptverfasser: Siebeneicher, Holger, Cleve, Arwed, Rehwinkel, Hartmut, Neuhaus, Roland, Heisler, Iring, Müller, Thomas, Bauser, Marcus, Buchmann, Bernd
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container_issue 20
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container_title ChemMedChem
container_volume 11
creator Siebeneicher, Holger
Cleve, Arwed
Rehwinkel, Hartmut
Neuhaus, Roland
Heisler, Iring
Müller, Thomas
Bauser, Marcus
Buchmann, Bernd
description The front cover picture shows a railway track symbolizing the transport of glucose as energy supply into a tumor cell by the GLUT1‐transporter. This import through the GLUT1‐transporter is blocked by a quinolinedicarboxamide, a compound series inhibiting the glucose transport in a competitive, reversible, and very selective manner against GLUT2, 3, and 4. The structure–activity relationship (SAR) and in vitro pharmacokinetics (PK) of the quinolinedicarboxamides presented in this work ended in the shown lead compound BAY‐876, a chemical probe with an appropriate in vivo PK profile for efficacy studies. More information can be found in the Full Paper by Bernd Buchmann et al. on page 2261 in Issue 20, 2016 (DOI: 10.1002/cmdc.201600276).
doi_str_mv 10.1002/cmdc.201600503
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subjects GLUT1 inhibitors
medicinal chemistry
Optimization
quinoline carboxamides
structure-activity relationships
Warburg effect
title Cover Picture: Identification and Optimization of the First Highly Selective GLUT1 Inhibitor BAY-876 (ChemMedChem 20/2016)
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