The phrase "an appropriate compound for" is correct and usable in written English.
It can be used when discussing the suitability of a specific compound in a particular context, such as chemistry, materials science, or any field where compounds are relevant.
Example: "In this experiment, we need to select an appropriate compound for the reaction to ensure optimal results."
Alternatives: "a suitable compound for" or "an ideal compound for".
Therefore, we propose the following candidate score to select an appropriate compound for the j-th intermediate compound C i n t e r (j ) (j = 1, 2, …, (k − 1 ) ) by integrating individual reaction sequence-likeness evaluation functions f 1, f 2, …, f (k − 1 ) in a recursive manner: s k (j ) (C ) = f j (C s t a r t, C ) + f k + 1 − j (C, C g o a l ).
Cells were then induced with 25 nM doxycycline for 14 hr and subsequently treated with the appropriate compounds for the indicated times.
How is the 'diversity' of a compound set defined and how is the most appropriate compound subset identified for assay when screening the entire HTS deck is not an option?
For selecting an appropriate indicator compound, the following criteria were defined: (1) the compound should be prone to oxidation in ESI, (2) the redox chemistry should be simple (only one dominant oxidation reaction should occur), (3) the compound and its oxidation product should be detectable by ESI-MS, (4) the compound should be synthetic, and (5) the reagent costs should be low.
Therefore, we developed a preprocessing stage that generates instantiated forms of generic reactions, in which appropriate compound instances have been substituted for compound classes.
The screen is useful for choosing appropriate compounds and exposure levels for subsequent in-depth studies in which complete histopathologic evaluations will be made.
Anther culture in the presence of appropriate compounds is a potent tool for obtaining complete pollen formation and for studying possible deviations from normal development (Heberle-Bors, 1989).
One of the challenges in the field of quantitative structure-activity relationship (QSAR) analysis is the correct classification of a chemical compound to an appropriate model for the prediction of activity.
Although absolute concentrations cannot be determined without generating calibration equations like those above for every NP, which would require the use of authentic standards of known concentration for all 137 appropriate compounds, the general concentration ranges for these NPs are estimated to be 1 100 nM.
On the other hand, Slc2a1, which was significantly (p ≤ 0.05) more highly expressed in the colon, might be an appropriate drug-carrier for compounds sensitive to pancreatic enzymatic degradation.
