Examples of 'are agonists' in a sentence

Meaning of "are agonists"

are agonists - In medical or biological terms, this phrase refers to substances or drugs that mimic the action of a particular neurotransmitter or hormone in the body

How to use "are agonists" in a sentence

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are agonists
In one embodiment of the present modulators are agonists.
Triceps are agonists and biceps are antagonists.
Preferably the present modulators are agonists.
Compounds according to the invention are agonists of nicotinic acetylcholine receptors.
Another class of antibody products are agonists.
Cannabinoids are agonists that attach themselves to special receptors on your cells.
Divalent antibodies of the prior art are agonists or partial agonists.
The first two are agonists and the last a receptor antagonist.
In one embodiment of the present invention the modulators are agonists.
Among the compounds provided herein are agonists of androgen receptor.
Included are agonists or antagonists of the gene or gene products identified herein.
The cyclic dinucleotides of the invention are agonists of the receptor STING.
Agents which are agonists enhance one or more of the biological activities of the polypeptide.
Preferred PPAR activators according to the present invention are agonists of PPARa activity.
There are agonists.

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Timolol is an antagonist, the other compounds are agonists.
These compounds are agonists at muscarinic receptors in the CNS.
The present invention preferably includes compounds that are agonists of the melanocortin-4 receptor.
Further described are agonists and antagonists of an OATP of the present invention.
We have now found a series of imidazopyridinones which are agonists of TLR7.
In one aspect they are agonists or partial agonists of the relevant PPAR.
In one embodiment, the compounds provided herein are agonists of LXR.
Compounds of formula I are agonists of nicotinic acetylcholine receptors.
FGF-Rexs which are angiogenic even in the absence of FGF are agonists.
The compounds are agonists of RAR retinoid receptors.
In one embodiment, compounds of the invention are agonists of GLP-1R.
Vaptans are agonists for MAP kinase activation.
In another embodiments, Compounds of the Invention are agonists of one or more opioid receptors.
FGF-Rexs which activate autophosphorylation of the cell-associated FGF-R in the absence of FGF are agonists.
Compounds of this invention are agonists or antagonists of the histamine-H3 receptor.
In another embodiment, the modulators of CRTH2 are agonists of CRTH2.
Compounds of the invention that are agonists have several uses including as anti-cancer compounds.
In addition, the compounds are agonists of IR 1.
Many of these are agonists for the H1, H2, or both histamine receptors . Doxepin, A dibenzoxepin tricyclic compound.
The compounds of the invention are agonists of the B3 receptor.
Specific ecdysteroids are agonists for the DHR23a receptor in mammalian cells.
In further embodiments, compounds of the invention are agonists of the RUP25 receptor.
The compounds of the present invention are agonists of cAMP-linked metabotropic glutamate receptors.
Insulinotropic glucagon-like peptides are agonists of the GLP-1 receptor.
Specifically, the Formula I compounds are agonists of the negatively-coupled cAMP-linked metabotropic glutamate receptors.
Insulinotropic peptides and compounds are agonists of the GLP-1 receptor.
The agents nafarelin and triptorelin are agonists with single substitutions at position 6.
Thus the invention provides compounds of formula ( I ) which are agonists at the adenosine A1 receptor.
Each of these agents are agonists of Toll-Like Receptors ( TIR ).
The compounds of the present invention are agonists of the M-1 muscarinic receptors.
The compounds of this invention are agonists of the histamine H3 receptor.
Zaleplon and zolpidem both are agonists at the GABA A ɣ 1 subunit.
In one embodiment, the ligands are agonists to the melanocortin 4 receptor.
In one instance, the ligands are agonists to the melanocortin 4 receptor.
The invention relates to compounds which are agonists of the sphingosine 1-phosphate receptor subtype 1.

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