PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
31948828-1	2020	Pharmacological inhibition of the enzyme fatty acid amide hydrolase (FAAH), which terminates signaling of the endocannabinoid N-arachidonoylethanolamine (or anandamide, AEA), exerts favourable effects in rodent models of stress-related depression.	aea	169-172	fatty-acid amide hydrolase-like	Rattus norvegicus	69-73
31948828-8	2020	Conversely, pharmacological inhibition of FAAH activity with URB694 restored both AEA and BDNF levels within the hippocampus of socially isolated rats and prevented the development of behavioral and physiological alterations.	aea	82-85	fatty-acid amide hydrolase-like	Rattus norvegicus	42-46
31935741-8	2020	Meanwhile, serum AEA levels correlated positively with serum interleukin-6, and negatively with serum very low-density lipoprotein levels.	aea	17-20	interleukin 6	Homo sapiens	61-74
31872059-1	2019	Introduction: The cannabinoid type 1 (CB1) receptor and cannabinoid type 2 (CB2) receptor are widely expressed in the body and anandamide (AEA) and 2-arachidonoylglycerol (2-AG) are their best characterized endogenous ligands.	aea	139-142	cannabinoid receptor 1	Homo sapiens	38-41
31680861-2	2019	Indomethacin enhanced the binding of [3H]CP55940 to hCB1R and enhanced AEA-dependent [35S]GTPgammaS binding to hCB1R in Chinese hamster ovary (CHO) cell membranes.	aea	71-74	cannabinoid receptor 1	Homo sapiens	111-116
7770064-1	1995	The cationic amphiphile, cholesteryl-3 beta-carboxyamidoethylene-trimethylammonium iodide, can alter the substrate specificity of protein kinase C (PKC).	aea	25-89	proline rich transmembrane protein 2	Homo sapiens	130-146
7770064-1	1995	The cationic amphiphile, cholesteryl-3 beta-carboxyamidoethylene-trimethylammonium iodide, can alter the substrate specificity of protein kinase C (PKC).	aea	25-89	proline rich transmembrane protein 2	Homo sapiens	148-151