Identification of a Potent Phosphoinositide 3‐Kinase Pan Inhibitor Displaying a Strategic Carboxylic Acid Group and Development of Its Prodrugs. (31st August 2017)
- Record Type:
- Journal Article
- Title:
- Identification of a Potent Phosphoinositide 3‐Kinase Pan Inhibitor Displaying a Strategic Carboxylic Acid Group and Development of Its Prodrugs. (31st August 2017)
- Main Title:
- Identification of a Potent Phosphoinositide 3‐Kinase Pan Inhibitor Displaying a Strategic Carboxylic Acid Group and Development of Its Prodrugs
- Authors:
- Pirali, Tracey
Ciraolo, Elisa
Aprile, Silvio
Massarotti, Alberto
Berndt, Alex
Griglio, Alessia
Serafini, Marta
Mercalli, Valentina
Landoni, Clarissa
Campa, Carlo Cosimo
Margaria, Jean Piero
Silva, Rangel L.
Grosa, Giorgio
Sorba, Giovanni
Williams, Roger
Hirsch, Emilio
Tron, Gian Cesare - Abstract:
- Abstract: Activation of the phosphoinositide 3‐kinase (PI3K) pathway is a key signaling event in cancer, inflammation, and other proliferative diseases. PI3K inhibitors are already approved for some specific clinical indications, but their systemic on‐target toxicity limits their larger use. In particular, whereas toxicity is tolerable in acute treatment of life‐threatening diseases, this is less acceptable in chronic conditions. In the past, the strategy to overcome this drawback was to block selected isoforms mainly expressed in leukocytes, but redundancy within the PI3K family members challenges the effectiveness of this approach. On the other hand, decreasing exposure to selected target cells represents a so‐far unexplored alternative to circumvent systemic toxicity. In this manuscript, we describe the generation of a library of triazolylquinolones and the development of the first prodrug pan‐PI3K inhibitor. Abstract : Pro drugs : Starting from LY294002, a potent pan‐phosphoinositide 3‐kinase (PI3K) inhibitor was identified through a straightforward click‐chemistry approach. The pivotal carboxylic acid was esterified to give prodrugs useful as topical treatments for chronic inflammation conditions such as psoriasis and asthma.
- Is Part Of:
- ChemMedChem. Volume 12:Number 18(2017)
- Journal:
- ChemMedChem
- Issue:
- Volume 12:Number 18(2017)
- Issue Display:
- Volume 12, Issue 18 (2017)
- Year:
- 2017
- Volume:
- 12
- Issue:
- 18
- Issue Sort Value:
- 2017-0012-0018-0000
- Page Start:
- 1542
- Page End:
- 1554
- Publication Date:
- 2017-08-31
- Subjects:
- click chemistry -- inflammation -- nitrogen heterocycles -- phosphoinositide 3-kinases -- prodrugs
Pharmaceutical chemistry -- Periodicals
615.19005 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1860-7187 ↗
http://www3.interscience.wiley.com/cgi-bin/jhome/110485305 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cmdc.201700340 ↗
- Languages:
- English
- ISSNs:
- 1860-7179
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3172.254000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 8303.xml