Tubulin inhibitor 23

Modify Date: 2025-08-26 18:18:14

Tubulin inhibitor 23 Structure
Tubulin inhibitor 23 structure
Common Name Tubulin inhibitor 23
CAS Number 170488-57-0 Molecular Weight 477.53
Density N/A Boiling Point N/A
Molecular Formula C26H23NO6S Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Tubulin inhibitor 23


Tubulin inhibitor 23 is a potent Tubulin inhibitor with an IC50 of 4.8 µM. Tubulin inhibitor 23 induces cell apoptosis. Tubulin inhibitor 23 shows antiangiogenic activity in a dose-dependent manner. Tubulin inhibitor 23 has the potential for the research of leukaemia[1].

 Names

Name Tubulin inhibitor 23

 Tubulin inhibitor 23 Biological Activity

Description Tubulin inhibitor 23 is a potent Tubulin inhibitor with an IC50 of 4.8 µM. Tubulin inhibitor 23 induces cell apoptosis. Tubulin inhibitor 23 shows antiangiogenic activity in a dose-dependent manner. Tubulin inhibitor 23 has the potential for the research of leukaemia[1].
Related Catalog
Target

IC50: 4.8 µM (Tubulin)[1]

In Vitro Tubulin inhibitor 23 (compound 29e) (0-100 µM) inhibits tubulin polymerisation (IC50=4.8 µM) and anti-angiogenesis (IC50=3.4 µM) in Zebrafish[1]. Tubulin inhibitor 23 (0-200 nM; 48 h) induces cell apoptosis in a concentration-dependent manner[1]. Tubulin inhibitor 23 (0-20 µM; 0-29 min) binds to the colchicine site of tubulin and inhibit the microtubule polymerisation[1]. Tubulin inhibitor 23 (0.1, 1, 10 µM; 1 h) shows anti-angiogenesis activity with low toxicity (IC50=58.6 µM) in Human umbilical vein endothelial cells (HUVECs)[1]. Cell Proliferation Assay[1] Cell Line: MV4-11, HL60, K562, THP-1,CCRF-CEM, Jurkat, HuT 78 cells Concentration: Incubation Time: 72 h Result: Showed potent growth inhibitory activity with IC50s of 0.25, 0.18, 0.09, 0.37, 0.84, 1.22, 0.26 µM for MV4-11, HL60, K562, THP-1,CCRF-CEM, Jurkat, HuT 78 cells, respectively. Apoptosis Analysis[1] Cell Line: K562 cells Concentration: 0, 50, 100, 200 nM Incubation Time: 48 h Result: The percentage of apoptotic cell significantly increased from 5.95% to 45.81%. Western Blot Analysis[1] Cell Line: K562 cells Concentration: 0, 50, 100, 200 nM Incubation Time: 48 h Result: Increased the expression of cleaved caspase-3 and PARP.
In Vivo Tubulin inhibitor 23 (2, 6 µM; add into embryo water) shows antiangiogenic activity in a dose-dependent manner[1]. Tubulin inhibitor 23 (2, 6 µM; add into embryo water) suppresses the proliferation and metastasis of K562 cells in zebrafish xenografts in a dose-dependent manner[1]. Animal Model: 3hpf zebrafish embryos[1] Dosage: 2.0, 6.0 µM Administration: Add into embryo water Result: Decreased the number and length of ISVs (intersegmental vessels) in a dose-dependent inhibition pattern. Animal Model: Transgenic zebrafish (fil1:EGFP) (K562 cell xenograft)[1] Dosage: 2, 6 µM Administration: Add into embryo water Result: Reduced intensities and decreased tumour area.
References

[1]. Yao Y,wt al. Angiogenesis and anti-leukaemia activity of novel indole derivatives as potent colchicine binding site inhibitors. J Enzyme Inhib Med Chem. 2022 Dec;37(1):652-665.

 Chemical & Physical Properties

Molecular Formula C26H23NO6S
Molecular Weight 477.53
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.