Examples of 'pyrazolyl' in a sentence
Meaning of "pyrazolyl"
pyrazolyl (noun): 'pyrazolyl' is a chemical term referring to a molecular structure containing a pyrazole ring, which is a heterocyclic compound often found in pharmaceuticals and agrochemicals
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- A radical derived from pyrazole
How to use "pyrazolyl" in a sentence
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pyrazolyl
A pyrazolyl group is more preferred.
Examples of heteroaryl rings include pyridyl and pyrazolyl rings.
Therapeutic pyrazolyl thienopyridines.
Preferably Ar represents optionally substituted thiazolyl or pyrazolyl.
Preferable examples thereof can include a pyrazolyl group and an imidazolyl group.
The pyrazolyl group acts both as a strongly electronegative group and as a good potential donor.
Aryl includes but is not limited to pyrazolyl and triazolyl.
Substituted pyrazolyl derivatives according to claim 1 in which.
The present disclosure is not limited to particular pyrazolyl dihydrogen phosphate compounds.
An embodiment of the present invention includes compounds wherein A is pyrazolyl.
This invention relates to new pyrazolyl acrylic acid derivatives and intermediates thereto.
In another embodiment of the present invention B is pyrazolyl.
The present invention relates to the use of a pyrazolyl derivative as an insecticide and acaricide.
A more specific example of X is pyrazolyl.
Methods are described of using the pyrazolyl guanidine compounds and pharmaceutical compositions in therapy.
See also
In one embodiment, monocyclic heteroaryl is pyrazolyl or pyridinyl.
A pyrazolyl acrylic acid derivative of formula wherein,.
A large number of disorders can be treated using the pyrazolyl guanidine compounds described herein.
A is a pyrazolyl group of the following formula,.
More particularly oxazolyl, pyridinyl and pyrazolyl.
The Celecoxib is a substituted pyrazolyl benzenesulfonamide derivative.
More preferably triazolyl, imidazolyl or pyrazolyl.
G is preferably a pyrazolyl group selected from the following,.
Preferred heteroaryl groups are thiazolyl, pyrazolyl and thiadiazolyl.
However, pyrazolyl benzenesulfonamide compounds have not been previously described as veterinary agents.
In one embodiment, the heteroaryl refers to pyridinyl, primidinyl and pyrazolyl.
However, there is no illustrative disclosure about pyrazolyl as the aromatic heterocyclic ring group.
Further particular heteroaryl groups are pyridinyl, imidazolyl, isoxazolyl and pyrazolyl.
A class of pyrazolyl compounds is described for use in treating inflammation and inflammation-related disorders.
In this respect, mention may in particular be made of the pyrazolyl or imidazolyl groups.
New pyrazolyl acrylic acid derivatives, useful as systemic fungicides for plant and material protection.
Examples of heteroaryl groups that may be mentioned include pyridinyl and pyrazolyl groups ;.
In other selected embodiments, A is pyrazolyl or thienyl, optionally substituted by a methyl group.
Preferred heterocycles include five-membered unsaturated heterocycles such as triazolyl, pyrazolyl and imidazolyl.
Pyrazolyl acrylic acid derivatives of the invention are represented by the formula ( I ) above.
In a particular embodiment, the piperidinyl is attached with its nitrogen atom to the pyrazolyl ring.
In some embodiments, R6 is pyrazolyl optionally substituted with methyl or ethyl.
In one embodiment, Ar is optionally substituted pyrazolyl.
A kind of pyrazolyl amide compounds as represented by the general formula I, Wherein,.
In certain embodiments, at least one Ry is an optionally substituted pyrazolyl.
In certain embodiments, R1 is a pyrazolyl optionally substituted with one or two Rb groups.
In still another embodiment, Ar1 is optionally substituted pyrazolyl or pyridinyl.
In othe embodiments, R1 represents pyrazolyl optionally substituted with one methyl group.
More preferably Ar2 represents optionally substituted thiazolyl, pyrazolyl or quinolinyl.
Is a pyrazolyl group optionally substituted by 1 to 3 substituents selected from.
In particular embodiments, Rb is pyrazolyl.
Among them, pyrazolyl is preferable.
Even more preferably R1 represents an optionally substituted phenyl, pyridinyl, pyrazolyl pyrimidinyl or oxadiazolyl group.
The substituted pyrazolyl compounds disclosed herein preferably selectively inhibit cyclooxygenase-2 over cyclooxygenase-1.
Further particular Het groups include an optionally substituted furyl, oxadiazolyl, thiazolyl, pyrazolyl and pyridinyl.
