Anticancer agent 83

Modify Date: 2024-01-15 11:32:49

Anticancer agent 83 Structure
Anticancer agent 83 structure
Common Name Anticancer agent 83
CAS Number 904815-29-8 Molecular Weight 377.46
Density N/A Boiling Point N/A
Molecular Formula C20H19N5OS Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Anticancer agent 83


Anticancer agent 83 is a potent anticancer agent, inhibits LOX IMVI cells growth with a GI50 value of 0.15 mM. Anticancer agent 83 reduces mitochondrial membrane potential and induces DNA damage to induces leukemia cells apoptosis[1].

 Names

Name Anticancer agent 83

 Anticancer agent 83 Biological Activity

Description Anticancer agent 83 is a potent anticancer agent, inhibits LOX IMVI cells growth with a GI50 value of 0.15 mM. Anticancer agent 83 reduces mitochondrial membrane potential and induces DNA damage to induces leukemia cells apoptosis[1].
Related Catalog
In Vitro Anticancer agent 83 (compound 4a) (0.01-100 μM; 24 h) showing strong activity towards human colon carcinoma HCT116 p53−/− cells with deletion of P53 gene (GI50=8.4 μM), human epidermoid cervix carcinoma KB3-1 (GI50=7.4 μM), human ovarian carcinoma Skov 3 cells (GI50=10 μM), and human chronic myelogenous leukemia K562 cells (GI50=5.4 μM)[1]. Anticancer agent 83 (0.5 μM; 24 h) interrupts DNA stability and induction of apoptosis in Jurkat cells, and decreases mitochondrial membrane potential[1]. Cell Viability Assay[1] Cell Line: Human colon carcinoma HCT116 p53−/− cells with deletion of P53 gene, human epidermoid cervix carcinoma KB3-1, human ovarian carcinoma Skov 3 cells, and human chronic myelogenous leukemia K562 cells Concentration: 0.01, 0.1, 1, 10, 100 μM Incubation Time: 24 hours Result: Inhibited cell viability in different cells with GI50s of 8.4 M (HCT116 p53−/−), 7.4 M (KB3-1), 10 M (Skov 3), and 5.4 M (K562), respectively. Immunofluorescence[1] Cell Line: Jurkat cells Concentration: 0.5 μM Incubation Time: 24 hours Result: Induced morphological changes (including apoptotic bodies, membrane blebbing, chromatin condensation), and DNA fragmentation in Jurkat T-cells.
References

[1]. Pokhodylo N, et al. Novel N-(4-thiocyanatophenyl)-1H-1,2,3-triazole-4-carboxamides exhibit selective cytotoxic activity at nanomolar doses towards human leukemic T-cells. Eur J Med Chem. 2022 Nov 5;241:114633.

 Chemical & Physical Properties

Molecular Formula C20H19N5OS
Molecular Weight 377.46