Reactions catalyzed within inorganic and organic materials and at electrochemical interfaces commonly occur at high coverage and in condensed media, causing turnover rates to depend strongly on interfacial structure and composition, 653-37-2, Name is 2,3,4,5,6-Pentafluorobenzaldehyde, SMILES is FC1=C(F)C(F)=C(C=O)C(F)=C1F, in an article , author is Yamakuma, Michiko, once mentioned of 653-37-2, Application In Synthesis of 2,3,4,5,6-Pentafluorobenzaldehyde.
1-HYDROXYETHYLHALENAQUINONE: A NEW PROTEASOME INHIBITOR FROM THE MARINE SPONGE XESTOSPONGIA SP.
A new halenaquinone derivative, 1-hydroxyethylhalenaquinone (1), was isolated from the marine sponge Xestospongia sp. as a proteasome inhibitor together with three known compounds, halenaquinone (2) and 3-ketoadociaquinones A (3) and B (4). 1-Hydroxyethylhalenaquinone (1) was the first halenaquinone derivative containing an alkyl group at the keto-furan C-1 position. Compounds 1 and 2 inhibited the chymotrypsin-like activity of the proteasome with IC50 values of 0.19 and 0.63 mu M, respectively, whereas 3 or 4, each containing a thiomorpholine 1,1-dioxide moiety, scarcely inhibited its activity, even at a concentration of 5 mu M.
But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! 653-37-2, you can contact me at any time and look forward to more communication. Application In Synthesis of 2,3,4,5,6-Pentafluorobenzaldehyde.
Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem