Examples of 'pyridinyl' in a sentence
Meaning of "pyridinyl"
Pyridinyl refers to a chemical compound or group containing a pyridine ring structure. It is commonly used in organic chemistry and pharmaceutical research
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- A univalent C- radical derived from pyridine or a pyridinol
How to use "pyridinyl" in a sentence
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pyridinyl
Pyridinyl ring fused to the morpholine ring.
Examples may include pyridinyl and pyrimidinyl.
Pyridinyl is the most preferred heterocyclic radical.
Preferred heteroaryl groups are isoxazolyl and pyridinyl.
Pyridinyl and fused pyridinyl triazolone derivatives.
Especially the term refers to pyridinyl.
Z preferably denotes pyridinyl or pyrimidinyl.
Particular example of heteroaryl includes pyridinyl.
Z may represent pyridinyl or thienyl.
B is a substituted or unsubstituted phenyl or pyridinyl group.
Represents pyridinyl substituted with one substituent selected from the group consisting of.
The heteroatomic ligand is selected from pyridinyl or quinolinyl.
A substantial number of pyridinyl imidazole CSAIDs were tested in the radiolabel competitive binding assay.
Preferred heteroaromatic rings include pyridinyl and thiazolyl.
Suitably Ra is pyridinyl or pyrimidinyl optionally substituted with one trifluoromethyl.
See also
These compounds are bicyclic benzyl and pyridinyl derivatives.
Pyridinyl refers to the pyridyl radical as defined by IUPAC nomenclature.
Particular heteroaryl group is pyridinyl.
Suitably Ra is optionally substituted pyridinyl or optionally substituted pyrimidinyl.
Preferred heteroaryl group is pyridinyl.
Pyridinyl group substituted by a heteroaryl group, or.
A preferred ring system is pyridinyl.
Pyridinyl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors.
Exemplary heteroaryl groups in this embodiment are pyridinyl and pyrimidinyl.
Is preferably pyridinyl and pyrimidinyl ; more preferably pyridinyl.
A preferred heteroaromatic ring is pyridinyl.
Het is selected from pyridinyl and pyrazolyl ;.
Rb is a member selected from unsubstituted phenyl and unsubstituted pyridinyl.
Binding is highly specific for the pyridinyl imidazole CSAIDs.
For example in some embodiments the heteroaryl is substituted or unsubstituted pyridinyl.
Examples include phenyl, pyridinyl and furanyl.
In another aspect of the invention A is phenyl or pyridinyl.
More particularly oxazolyl, pyridinyl and pyrazolyl.
In one embodiment, monocyclic heteroaryl is pyrazolyl or pyridinyl.
A pyridinyl acetonitrile according to claims 1 selected in the group consisting of,.
Most preferred heteroaryl is pyridinyl.
R1 preferably is a pyridinyl or pyrimidinyl moiety optionally substituted as defined above.
More preferably heteroaryl is pyridinyl.
R ² is preferably pyridinyl and pyrimidinyl and more preferably pyridinyl.
An example of a suitable heteroaryl is pyridinyl.
Is preferably pyridinyl and pyrimidinyl and benzodioxolyl ; more preferably pyridinyl.
Most preferred are thiazolyl or pyridinyl.
Preferred heteroaryl groups are pyridinyl, oxazolyl and triazolyl, particularly pyridinyl.
Preferred are phenyl and pyridinyl.
The pyridinyl moiety may be synthesized according to the general scheme 1 shown below.
Y may be an optionally substituted pyridinyl.
Demethylation of the pyridinyl ether can be accomplished utilizing a procedure analogous to step 3 of example 1.
Especially preferred amongst these preferred heteroaryls are pyridinyl and purinyl.
For example, hydroxy substituted pyridinyl groups can also exists in their keto form,.
A preferred heteroaryl is pyridinyl.
