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The reported compounds can be reversibly reduced up to the trianionic state.
The reported compounds were designed as bioisosteric analogues of GABA semicarbazones.
The activity of the reported compounds warrants further optimization as novel members in cancer treatment protocols.
Previously reported compounds 1 3 were potent human KLK7 inhibitors; however, they did not exhibit inhibitory activity against mouse KLK7.
Besides, the reported compounds were screened for their antibacterial and antifungal activities against a spectrum of microbial organisms.
It is proposed that the RA patients should use reported compounds for the prescription of RA by targeting TNF-α.
They also predict a few unreported compounds in additional systems and indicate that some reported compounds may actually be unstable at low temperatures.
3, 3'-sulfonyldipropionitrile (SDPN) is structurally different from previously reported compounds and was studied as a film-forming additive for the LiMn2O4 cathode at elevated temperature.
These analogues were designed on the basis of the results obtained with our previously reported compounds S and Bt, in order to define a structure stability relationship.
We describe the design, synthesis and pharmacological evaluation of a series of biphenyl-4-carboxylic acid-type hPPARδ antagonists, including previously reported compounds, as candidate anti-HCV agents.
In the previous work, we reported compounds I and II as novel topoisomerase IIα catalytic inhibitors targeting for ATP binding site of human topoisomerase IIα ATP-binding domain.
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