Sentence examples for moiety in this from inspiring English sources
This probe was designed based on the mechanism that H2S selectively cleaved the NBD (7-nitro-2,1,3-benzoxadiazole) ether moiety in this probe and therefore release the fluorophore, 3-hydroxyflavone.
However, the 3- pyridin-3-yl)aniline moiety in this case occupies the phosphate binding region.
On the other hand, the colocalization coefficient My describes the fluorescence contribution of the more abundant moiety (in this case α-actinin, green) to the less abundant moiety (in this case Nm, red), i.e. the proportion of red pixels that overlap with green pixels compared with the total number of red pixels.
Compound 33RE was selected for synthesis and inhibition analysis given the prominence of the P2 position in conferring N-selectivity and the presence of a non-carboxylate moiety in this position.
The numerous interactions of three arginine residues from the Cv1693 insertion domain with the 5′-phosphate of AMP suggested that the true substrate would bind an AMP-like moiety in this pocket and contribute to substrate recognition.
In other words, the lack of a core M1 structure at Thr-319 may prevent post-phosphoryl modification of core M3 at Thr-317, which would account for detection of the incomplete form of the LG-binding moiety in this mapping analysis.
Moreover, a number of patents concerning this moiety in the last few years further highlight its worth.
This was corroborated by the expanded LiverTox dataset, as there were 18 drugs with this moiety in the hepatotoxic class, 15 in the possible hepatotoxic class, and only 3 in the nonhepatotoxic class.
Aminoborane-free Ti-complex 64 was also synthesized to study the effect of boryl moiety in the polymerization, and this complex produced the polymer of the type poly -NBE vip-co-poly(E) with no poly -NBE vip-co-polyces [73].
Whereas the indanone carbonyl in these molecules was originally designed as a 'putative electrophilic head group' [ 35, 36], the crystal structure of compound 6 places this moiety in the S4 binding pocket remote from the β5 catalytic Thr residue, thereby precluding such an interaction.
To establish the role of the ferrocenyl moiety in the antiplasmodial activity of this series, purely organic parent compounds were also synthesized and tested.
