PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
15652990-8	2005	Activation of mGluR3 with DCG-IV (but not of mGluR5 with DHPG) enhanced, in the presence of IL-1beta, the release of IL-6 in a dose dependent manner in astrocytes cultured under conditions (+EGF) in which the mGluR expression is known to be upregulated.	dcg	26-29	glutamate receptor, ionotropic, AMPA3 (alpha 3)	Mus musculus	14-20	
16674916-3	2006	[(3)H]Quisqualic acid binding to mGluR1 required the presence of calcium (or magnesium) ions but not sodium or chloride ions while [(3)H]DCG-IV binding to mGluR3 was dependent upon both cations and anions.	dcg	137-140	glutamate receptor, ionotropic, AMPA3 (alpha 3)	Mus musculus	155-161	
8556329-5	1995	Application of DCG-IV, a novel mGluR2/mGluR3-selective agonist, suppressed field EPSPs only slightly even at a high dose (3 microM).	dcg	15-18	glutamate receptor, ionotropic, AMPA3 (alpha 3)	Mus musculus	38-44	
8782108-4	1996	Application of a novel and potent mGluR2/mGluR3-specific agonist (2S,1"R,2"R,3"R)-2-(2,3-dicarboxycyclopropyl)glycine (DCG-IV, 0.1 microM) reversibly suppressed field excitatory postsynaptic potentials evoked by mossy fibre stimulation.	dcg	119-122	glutamate receptor, ionotropic, AMPA3 (alpha 3)	Mus musculus	41-47	
15178451-1	2004	In this study, 10 truncated constructs encompassing all or part of the extracellular ligand binding domain of the mGluR3 subtype of metabotropic glutamate receptor were generated, expressed in human embryonic kidney cells, and tested for secretion and binding of the high affinity agonist [(3)H]DCG-IV.	dcg	295-298	glutamate receptor, ionotropic, AMPA3 (alpha 3)	Mus musculus	114-120	
12614345-10	2003	In OPCs the group II mGluR agonist (2S,2"R,3"R)-2-(2",3"-dicarboxycyclopropyl)glycine (DCG-IV) decreased forskolin-stimulated cAMP synthesis, indicating the presence of functional mGluR3.	dcg	87-90	glutamate receptor, ionotropic, AMPA3 (alpha 3)	Mus musculus	180-186	
7472317-8	1995	The compound (2S,1"R,2"R,3"R)-2-(2.3-dicarboxycyclopropyl)glycine (DCG-IV) activates both mGluR2 and mGluR3 at submicromolar concentrations, whereas it is inactive at mGluR4 and mGluR1, suggesting that this compound may be selective for group II mGluRs.	dcg	67-70	glutamate receptor, ionotropic, AMPA3 (alpha 3)	Mus musculus	101-107