BK50164

Modify Date: 2025-08-26 16:07:12

BK50164 Structure
BK50164 structure
Common Name BK50164
CAS Number 2204291-78-9 Molecular Weight 405.72
Density N/A Boiling Point N/A
Molecular Formula C13H13ClFN5O7 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of BK50164


BK50164 is a potent CD73 inhibitor with an IC50 value of 13.089 µM. BK50164 binds to CD99 with a KD value of 1.5 µM. BK50164 shows antiproliferative activity. BK50164 induced Apoptosis and cell cycle arrest at Sub-G1 phase[1].

 Names

Name BK50164

 BK50164 Biological Activity

Description BK50164 is a potent CD73 inhibitor with an IC50 value of 13.089 µM. BK50164 binds to CD99 with a KD value of 1.5 µM. BK50164 shows antiproliferative activity. BK50164 induced Apoptosis and cell cycle arrest at Sub-G1 phase[1].
Related Catalog
Target

IC50: 13.089 µM (CD73)[1]

In Vitro BK50164 (0-400 µM;48 小时) 显示抗增殖活性,对 A4573, TC-32, TC-71, Saos-2, U-2 OS 细胞的 IC50 值分别为35.8, 34.28, 5.17, ≥400, ≥400 µM[2]。 BK50164 (4-16 µM; 48 h) 诱导细胞凋亡和细胞周期停滞在 Sub-G1 期[2]。 Cell Viability Assay[2] Cell Line: A4573, TC-32, TC-71, Saos-2, U-2 OS cells Concentration: 0-400 µM Incubation Time: 48 h Result: Inhibited cell viability witn IC50s of 35.8, 34.28, 5.17, ≥400, ≥400 µM for A4573, TC-32, TC-71, Saos-2, U-2 OS cells, respectively. Cell Cycle Analysis[2] Cell Line: TC-32, U-2 OS cells Concentration: 4, 8, 16 µM Incubation Time: 48 h Result: Induced apoptosis in only TC-32 ES cells but not in U-2 OS cell line and induces cell cycle arrest at Sub-G1 phase.
References

[1]. Roland Joseph Billedeau, et al. Ectonucleotidase inhibitors and methods of use thereof. WO2018119284A1.

[2]. Balaraman K, et al. Design, synthesis and biological evaluation of Nucleosidic CD99 inhibitors that selectively reduce Ewing sarcoma viability. Eur J Med Chem. 2023 May 5;251:115244.  

 Chemical & Physical Properties

Molecular Formula C13H13ClFN5O7
Molecular Weight 405.72
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