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Shin-Shay Tian

Researcher at GlaxoSmithKline

Publications -  7
Citations -  664

Shin-Shay Tian is an academic researcher from GlaxoSmithKline. The author has contributed to research in topics: Receptor & Signal transduction. The author has an hindex of 7, co-authored 7 publications receiving 604 citations.

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Journal ArticleDOI

Preclinical activity of eltrombopag (SB-497115), an oral, nonpeptide thrombopoietin receptor agonist.

TL;DR: 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.
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Discovery and characterization of a selective, nonpeptidyl thrombopoietin receptor agonist.

TL;DR: SB 394725, a small molecule with a molecular weight of 452 Da, is capable of activating Tpo-specific signal transduction, proliferation, and differentiation responses similar to the responses and functions of the protein growth factor, Tpo.
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Hydrazinonaphthalene and azonaphthalene thrombopoietin mimics are nonpeptidyl promoters of megakaryocytopoiesis.

TL;DR: Modification of the core structure and adjustment of unwanted functionality resulted in the development of (5-oxo-1,5-dihydropyrazol-4-ylidene)hydrazines which exhibited efficacies equivalent to those of TPO in several cell-based assays designed to measure thrombopoietic activity.
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Species Specificity and Receptor Domain Interaction of a Small Molecule TPO Receptor Agonist.

TL;DR: In this article, a series of chimeric TpoR chimeric receptors were constructed in which the complement receptor homology region 1 (CRH1), CRH2 and the transmembrane (TM) and cytoplasmic domains were interchanged.
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Biological Activity and Selectivity for Tpo Receptor of the Orally Bioavailable, Small Molecule Tpo Receptor Agonist, SB-497115.

TL;DR: SB-497115 is the first non-peptide small molecule TpoR agonist to demonstrate activity in human in vitro bone marrow assays and demonstrate pharmacological activity in humans.