Examples of 'represented by formula' in a sentence

Meaning of "represented by formula"

Represented by formula means that a concept, idea, or relationship is expressed or symbolized using a specific mathematical or symbolic formula. It suggests that the formula is used to represent or depict the particular concept or relationship in a concise and standardized way

How to use "represented by formula" in a sentence

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represented by formula
A tetrazoyloxime derivative represented by formula.
Rivaroxaban represented by formula A was used as the comparison drug.
The phloroglucinol unit can be represented by formula III below.
Compound represented by formula I for use in preventing or treating cerebral infarction.
The copolymer obtained may be represented by formula VIII given above.
The use of a mixture of isophthaloyl and terephthaloyl dichlorides is conveniently represented by Formula VII.
The preparation of compounds represented by formula II will be discussed below.
This chloride is further reacted with pentaerythritol to give polyhydroxylated naphthol represented by formula IC.
The description of sulfo compounds represented by formula III is hereby incorporated.
Some of these inhibitors are cyclic amidine and sulfonyl amidine derivatives represented by formula C.
All of the compounds represented by Formula Ib contain a benzodioxan.
The magnesium salt of esomeprazole is represented by formula I.
The compounds represented by formula I may exist in unsolvated or solvate forms.
The whole sequence of the fragment is represented by formula III above.
The amide represented by Formula III contains at least one morpholinyl group.

See also

Examples of specific embodiments of the elements of compounds represented by formula I include the following.
The concept is represented by Formula II which describes the length of the boards.
Preferred compounds of the invention are represented by Formula II.
In one aspect the compounds represented by Formula I are used to treat a subject with cancer.
An ophthalmic solution containing a loratadine metabolite represented by formula I.
Solvates of the compounds represented by formula I are also contemplated herein.
Examples of the peptides of the present invention are represented by formula I.
The invention relates to compounds represented by Formula VI which are inhibitors of LAP proteins.
The resulting mesogen containing compound corresponds to a structure represented by Formula II.
The composition represented by Formula.
The polydiorganosiloxane oligourea segmented copolymers of the present invention are represented by Formula I.
The preparation of the compounds represented by Formula XVIII is known.
The present invention concerns enantiomers and enantiomeric mixtures of compounds represented by Formula I.
It is also contemplated that the compound represented by formula I embraces deuterated analogs.
Compounds represented by Formula I can be optically active or racemic.
The resulting product is a compound represented by Formula III.
The compositions represented by Formula I may be prepared by techniques well known in the art.
The preparation of the compounds represented by Formula XIX is known.
The monomer represented by Formula II is preferably a monomer represented by the following Formula III.
The sequence of this peptide is represented by Formula III below.
The compound represented by formula 1 can be exemplified by the following compounds.
Other preferred compounds of the invention are represented by Formula III.
A compound represented by Formula III wherein.
All doses described above relate to the amount of the parent compound represented by Formula I.
The starting material represented by Formula V is known in the art.
An example of a particular species within Formula II is represented by Formula III.
A compound represented by Formula II is described.
A method of making the organopolysiloxane diamine represented by Formula II is also provided.
The compounds represented by formula ( ) can be resolved optically by the following method.
The polyorthoesters suitable for the invention are represented by formula I and formula II below.
The compound represented by formula ( IIa ) may be synthesized according to the following scheme.
The diimines formed are represented by Formula VII.
These protecting groups are subsequently removed to form the corresponding nucleophilic amines represented by formula ( 2 ).
Another embodiment is represented by Formula III.
A compound represented by formula ( II ) can be exemplified by the following compounds.

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