Examples of 'subject compound' in a sentence
Meaning of "subject compound"
subject compound: Refers to a topic or area of study that involves chemical compounds or elements. This phrase is commonly used in the field of chemistry or science to denote an academic subject concerning compound substances
How to use "subject compound" in a sentence
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subject compound
A subject compound can be administered rectally vía a suppository.
The solution was condensed to give the subject compound.
The subject compound may be in the form of a hydrate or a solvate.
The preferred mode of administering the subject compound is perorally.
The subject compound is useful as an intermediate to prepare substituted pyrimidines.
The invention further provides prodrug forms of the subject compound.
The subject compound combination is useful to treat proliferative disorders.
The whole was stirred to provide a suspension containing the subject compound as a crystal.
The subject compound remained as a slightly yellowish viscous liquid.
A quaternary ammonium salt of the subject compound is encompassed in the salt of the invention.
A subject compound can be utilized in aerosol formulation to be administered vía inhalation.
The following details an exemplary procedure for ascertaining chemical stability of a subject compound.
The subject compound was also obtained by the method described below.
A pharmaceutical composition will in some embodiments include a subject compound and a pharmaceutically acceptable excipient.
Necessary if the subject compound is determined to be severely irritating from other available information.
See also
In some embodiments, multiple doses of a subject compound are administered.
In some embodiments, a subject compound is administered for the lifetime of the individual.
Accordingly, the invention provides a pharmaceutical composition that improves the intestinal absorption of the subject compound.
The administration of the subject compound of the invention is useful as an antiarrhythmic agent.
Unless otherwise noted, NMR data refer to the free base of the subject compound.
As discussed above, in some embodiments, a subject compound is administered continuously.
A subject compound may be administered in a therapeutically effective amount, according to an appropriate dosing regiment.
In this case, the methyl ester of the subject compound was used as the substrate.
A subject compound may be administered in a therapeutically effective amount, according to an appropriate dosing regimen.
In many embodiments, a subject compound inhibits HCV viral replication.
Unless otherwise noted, NMR data refers to the free base of the subject compound.
In some embodiments, a subject compound can be delivered by a continuous delivery system.
Example D shows the potent inhibition of in-cell RNAPII phosphorylation by the subject compound.
As described above, the subject compound is clinically very useful compound.
The obtained crystal was dried under reduced pressure and 325g of the subject compound was prepared.
Thus, a subject compound can be incorporated into a variety of formulations for therapeutic administration.
AFRICOM, unknowns are advancing toward subject compound moving from south / southeast over open ground.
The subject compound combination can also be co-administered with a variety of other drugs.
The concentration of the solvent provides the subject compound ( 94 mg ) as a yellow solid.
The subject compound is an adenosine having an N-6 substituent that comprises an epoxide moiety.
The final vacuum distillation yielded the subject compound as a yellowish liquid having a purity of above 90 %.
The subject compound may be used as substrates for a variety of enzymes with B-galactosidase activity.
Infrared spectral analysis ( done with KBr pellet ) of the subject compound is shown in Figure 1.
Whether a subject compound inhibits HCV NS3 protease can be readily determined using any known method.
Compound of Example 139 is reduced according to the methods below to produce the subject compound.
In many embodiments, a subject compound inhibits the enzymatic activity of a hepatitis virus C ( HCV ) NS3 helicase.
Fig . 7 is a powder X-ray diffraction pattern of the Form A crystal of the subject compound.
Background Art The subject compound and its synthesis method have been already disclosed ( Non-patent Literature 1 ).
The reaction solution was concentrated to give the subject compound ( 591mg ).
The subject compound combination can be co-administered, e.g., in the same or different formulation.
The solvent was removed to give the subject compound as a colorless oil ( 651mg, quantitatively ).
The solvent was distilled away under reduced pressure to give the subject compound ( 6.6 g ).
The solvent was distilled away to give the subject compound ( 290 mg ) as a yellowish oily substance.
The solid compound was further recrystallized from ethyl ether-hexane to give the subject compound ( 515 mg ).
The concentration of the organic solvent provided the subject compound ( 6.6 g ) as a yellow solid.
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