Related Experiment Video
Updated: Mar 24, 2026

13:22
Kinase Inhibitor Screening In Self-assembled Human Protein Microarrays
Published on: October 23, 2019
8.4K
Acalabrutinib (ACP-196): a selective second-generation BTK inhibitor
Jingjing Wu1, Mingzhi Zhang1, Delong Liu2
1Department of Oncology, The first Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, China.
Journal of Hematology & Oncology
|March 10, 2016
Summary
Acalabrutinib, a potent Bruton's tyrosine kinase (BTK) inhibitor, shows promise for B cell malignancies. This review details its preclinical and clinical data, highlighting its improved selectivity over ibrutinib.
Area of Science:
- Oncology
- Pharmacology
Background:
- Targeted therapies for B cell malignancies are advancing.
- Bruton's tyrosine kinase (BTK) inhibitors like ibrutinib are established treatments.
- Newer, more selective BTK inhibitors are under investigation.
Purpose of the Study:
- To review the preclinical research and clinical data of acalabrutinib (ACP-196).
- To evaluate acalabrutinib as a second-generation BTK inhibitor.
Main Methods:
- Literature review of preclinical studies.
- Analysis of clinical trial data for acalabrutinib.
Main Results:
- Acalabrutinib demonstrates higher potency and selectivity compared to ibrutinib.
- Preclinical and clinical data support acalabrutinib's efficacy.
Conclusions:
- Acalabrutinib represents a significant advancement in BTK-targeted therapy for B cell malignancies.
- Its improved profile warrants further clinical investigation and application.
More Related Videos
Related Concept Videos
Targeted Cancer Therapies
9.1K
The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against...
There are several types of targeted therapies against...
9.1K
Targeted Cancer Therapies
1.7K
1.7K
PI3K/mTOR/AKT Signaling Pathway
6.2K
The mammalian target of rapamycin (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1 (mTORC1) and mTOR complex 2 (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast, mTORC2 consists of a...
6.2K
Inhibition of Cdk Activity
6.2K
The orderly progression of the cell cycle depends on the activation of Cdk protein by binding to its cyclin partner. However, the cell cycle must be restricted when undergoing abnormal changes. Most cancers correlate to the deregulated cell cycle, and since Cdks are a central component of the cell cycle, Cdk inhibitors are extensively studied to develop anticancer agents. For instance, cyclin D associates with several Cdks, such as Cdk 4/6, to form an active complex. The cyclin D-Cdk4/6 complex...
6.2K
Inhibition of CDK Activity
5.6K
5.6K
Treatment Resistent Cancers
1.5K
1.5K

