Literature DB >> 32183683

Copanlisib: Novel PI3K Inhibitor for the Treatment of Lymphoma.

Anshul Kumar1, Rohit Bhatia1, Pooja Chawla1, Durgadas Anghore1, Vipin Saini2, Ravindra K Rawal3.   

Abstract

Lymphoma refers to a specialized category of blood cancers, which is characterized by lymph node enlargement, reduced body weight, prolonged tiredness, and fever associated with sweats. Traditional treatment strategies involve chemotherapy, radiation therapy, targeted therapy, and surgery. Copanlisib has emerged as a very potent drug which acts through inhibiting PI3K enzyme. The FDA has approved it for specific treatment of follicular Lymphoma in September 2017. Copanlisib induces tumor cell death along with the prevention of proliferation of dominant malignant β-cells. Copanlisib has a large volume of distribution i.e., 871L (%CV 47.4), plasma protein binding up to 15.8%, plasma half-life(t1/2) of 39.1h and the mean systemic plasma clearance 18.9 L/h (%CV 51.2). In the present review, various aspects related to Copanlisib have been summarized, which include pathophysiology, synthetic strategy, pharmacokinetics, pharmacodynamics and clinical studies. A special emphasis is paid on various reported adverse effects and in silico/in vivo studies conducted on Copanlisib. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

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Keywords:  Lymphoma; PI3K; blood cancer; copanlisib; lymph node enlargement; systemic plasma clearance

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Year:  2020        PMID: 32183683     DOI: 10.2174/1871520620666200317105207

Source DB:  PubMed          Journal:  Anticancer Agents Med Chem        ISSN: 1871-5206            Impact factor:   2.505


  1 in total

1.  Copanlisib promotes growth inhibition and apoptosis by modulating the AKT/FoxO3a/PUMA axis in colorectal cancer.

Authors:  Ji Yan; Shida Yang; Hong Tian; Yang Zhang; Hongmei Zhao
Journal:  Cell Death Dis       Date:  2020-11-02       Impact factor: 8.469

  1 in total

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