Eltrombopag

Thrombopoietin receptor agonist
概要
Eltrombopag is a thrombopoietin receptor (TpoR) agonist (EC₅₀ = 0.27 µM in a reporter assay) and an iron chelator (Erickson‐Miller et al.). Interaction between Eltrombopag and TpoR triggers proliferation and differentiation of human bone marrow progenitor cells into megakaryocytes and increases platelet growth and production (Erickson‐Miller et al.).

DIFFERENTIATION
· Stimulates proliferation and differentiation of primary human CD34+ bone marrow cells into CD41+ megakaryocytes (Erickson‐Miller et al.).
Alternative Names
SB497115
Application
Differentiation
CAS Number
496775-61-2
Chemical Formula
C₂₅H₂₂NO
Molecular Weight
442.5 g/mol
Purity
≥ 98%
Pathway
STAT5
Target
TpOR
技术资料
Document Type 产品名称 Catalog # Lot # 语言
Product Information Sheet Eltrombopag 100-0250, 100-0251 All English
Safety Data Sheet Eltrombopag 100-0250, 100-0251 All English
数据及文献

Publications (1)

Stem cells (Dayton, Ohio) 2009 feb Preclinical activity of eltrombopag (SB-497115), an oral, nonpeptide thrombopoietin receptor agonist. C. L. Erickson-Miller et al.

Abstract

Eltrombopag is a first-in-class, orally bioavailable, small-molecule, nonpeptide agonist of the thrombopoietin receptor (TpoR), which is being developed as a treatment for thrombocytopenia of various etiologies. In vitro studies have demonstrated that the activity of eltrombopag is dependent on expression of TpoR, which activates the signaling transducers and activators of transcription (STAT) and mitogen-activated protein kinase signal transduction pathways. The objective of this preclinical study is to determine if eltrombopag interacts selectively with the TpoR to facilitate megakaryocyte differentiation in platelets. Functional thrombopoietic activity was demonstrated by the proliferation and differentiation of primary human CD34(+) bone marrow cells into CD41(+) megakaryocytes. Measurements in platelets in several species indicated that eltrombopag specifically activates only the human and chimpanzee STAT pathways. The in vivo activity of eltrombopag was demonstrated by an increase of up to 100{\%} in platelet numbers when administered orally (10 mg/kg per day for 5 days) to chimpanzees. In conclusion, eltrombopag interacts selectively with the TpoR without competing with Tpo, leading to the increased proliferation and differentiation of human bone marrow progenitor cells into megakaryocytes and increased platelet production. These results suggest that eltrombopag and Tpo may be able to act additively to increase platelet production.
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