Sentence examples for bridge compound from inspiring English sources

A novel bridge compound having hetero-bi-functional reactive groups was synthesized.

According to the structure analysis, compounds 1 and 2 are three-dimensional microporous frameworks constructed by Cu dps Cu and Cu dca Cu bridges; compound 3 shows a zigzag chain constructed by a Cu dps Cu bridge; compounds 4 and 5 show double-stranded chains constructed by a Cu dps)2 Cu bridge while thiocyanate anions act as terminal groups; compound 6 is a mononuclear compound.

It retains inhibitory potency for DHFR and TS compared to the two atom bridged analog 5. Compound 13 is a poor inhibitor of purified DHFR and TS, and both 13 and 14 are poor inhibitors of the growth of CCRF-CEM human leukemia cells in culture, indicating that single carbon bridged compounds in these series though conducive to FPGS substrate activity were not potent inhibitors.

The Kβ″ peak of the PS II S1 state is relatively intense compared to other Mn2III,IV di-μ-oxo bridged compounds.

In order to examine whether as a bridge the compound could combine dyes containing amino groups with cellulosic substrates, a disperse dye containing amino group was tried to dye the cotton fibers pretreated with the reactive compound.

The second peak (0.27 V) can therefore be attributed to the reduction of the second –N=N– bridge of compound A. The last peak (0.936 V) may be attributed to the catalytic hydrogen reduction of the carbonyl group (C=O) of the intermediate B to give compound E (scheme 3).

-Ganoapplanin (122) feartured an unprecedented dioxaspirocyclic skeleton, which was constructed from a 2,4-dihydroxy benzoic acid and a bridge-ring compound 102 [48].

A series of bridge-ring compounds were formed through the free radical reactions.

This paper investigates a flexure-based compound bridge-type (CBT) displacement amplifier for piezoelectric drives.

In order to slightly modify the orientation of the pharmacophoric structural elements of the potent κ agonists 7 and 8, the three-membered bridge of these compounds was enlarged to four carbon atoms.

The presence of two binding pockets enabled us to explore a novel method of inhibition by compounds that bridge the adjacent phosphate and glycerol binding sites.