The Absolute Best Science Experiment for 18331-34-5

If you are interested in 18331-34-5, you can contact me at any time and look forward to more communication. Application In Synthesis of 5-Benzylidene-3-ethyl-2-thioxothiazolidin-4-one

Application In Synthesis of 5-Benzylidene-3-ethyl-2-thioxothiazolidin-4-one, Career opportunities within science and technology are seeing unprecedented growth across the world, and those who study chemistry or another natural science at university now have increasingly better career prospects. In a article, 18331-34-5, molcular formula is C12H11NOS2, introducing its new discovery.

We have designed and synthesized three novel compounds, 5-isopropylidiene derivatives of 3-dimethyl-2-thio-hydantoin (ITH-1), 3-ethyl-2-thio-2,4- oxazolidinedione (ITO-1), and 5-benzilidene-3-ethyl rhodanine (BTR-1), and have tested their chemotherapeutic properties. Our results showed that all three compounds induced cytotoxicity in a time- and concentration-dependent manner on leukemic cell line, CEM. Among the compounds tested, BTR-1 was 5- to 7-fold more potent than ITH-1 and ITO-1 when compared by trypan blue and MTT assays. IC50 value of BTR-1 was estimated to be <10 muM. Both cell cycle analysis and tritiated thymidine assays revealed that BTR-1 affects DNA replication by inducing a block at S phase. BTR-1 treatment led to increased level of ROS production and DNA strand breaks suggesting activation of apoptosis for induction of cell death. If you are interested in 18331-34-5, you can contact me at any time and look forward to more communication. Application In Synthesis of 5-Benzylidene-3-ethyl-2-thioxothiazolidin-4-one

Reference:
Quinuclidine – Wikipedia,
Quinuclidine | C7H826N | ChemSpider