Difference between revisions of "Alvocidib (Flavopiridol)"

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m (Text replacement - "Chronic lymphocytic leukemia (CLL) and Small lymphocytic lymphoma (SLL)" to "Chronic lymphocytic leukemia (CLL/SLL)")
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==Mechanism of action==
 
==Mechanism of action==
Flavonoid alkaloid CDK9 kinase inhibitor
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From the [https://www.cancer.gov/publications/dictionaries/cancer-drug?cdrid=42068 NCI Drug Dictionary]: A synthetic N-methylpiperidinyl chlorophenyl flavone compound. As an inhibitor of cyclin-dependent kinase, alvocidib induces cell cycle arrest by preventing phosphorylation of cyclin-dependent kinases (CDKs) and by down-regulating cyclin D1 and D3 expression, resulting in G1 cell cycle arrest and apoptosis.
 
<br>Route: PO
 
<br>Route: PO
  
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*4/13/2007: Granted orphan status for treatment of [[Chronic lymphocytic leukemia (CLL/SLL) | B-cell chronic lymphocytic leukemia (B-CLL)]] or prolymphocytic leukemia arising from CLL.
 
*4/13/2007: Granted orphan status for treatment of [[Chronic lymphocytic leukemia (CLL/SLL) | B-cell chronic lymphocytic leukemia (B-CLL)]] or prolymphocytic leukemia arising from CLL.
 
*4/23/2014: Granted orphan designation for the treatment of patients with [[Acute myeloid leukemia | acute myeloid leukemia (AML)]]
 
*4/23/2014: Granted orphan designation for the treatment of patients with [[Acute myeloid leukemia | acute myeloid leukemia (AML)]]
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==Also known as==
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*'''Code names:''' HMR 1275, L-868275
  
 
[[Category:Drug index]]
 
[[Category:Drug index]]
[[Category:Chemotherapy]]
 
 
[[Category:Oral medications]]
 
[[Category:Oral medications]]
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[[Category:Kinase inhibitors]]
 
[[Category:Kinase inhibitors]]
 
[[Category:CDK inhibitors]]
 
[[Category:CDK inhibitors]]
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[[Category:Chronic lymphocytic leukemia (CLL/SLL) medications]]
 
[[Category:Chronic lymphocytic leukemia (CLL/SLL) medications]]
  
[[Category:Drugs FDA approved in 2007]]
 
 
[[Category:Orphan drug]]
 
[[Category:Orphan drug]]
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[[Category:Investigational]]

Revision as of 18:28, 29 October 2017

Mechanism of action

From the NCI Drug Dictionary: A synthetic N-methylpiperidinyl chlorophenyl flavone compound. As an inhibitor of cyclin-dependent kinase, alvocidib induces cell cycle arrest by preventing phosphorylation of cyclin-dependent kinases (CDKs) and by down-regulating cyclin D1 and D3 expression, resulting in G1 cell cycle arrest and apoptosis.
Route: PO

Diseases for which it is used

History of changes in FDA indication

Also known as

  • Code names: HMR 1275, L-868275