PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
9377092-2	1997	When the substituent at C-4 of the tetrahydropyridine moiety is a carbamoyloxy functionality, the resulting dihydropyridinium metabolite undergoes spontaneous hydrolytic cleavage to yield 1-methyl-5,6-dihydro-4-pyridone, CO2, and the corresponding secondary amine.	Pyrrolidines	35-53	complement C4A (Rodgers blood group)	Homo sapiens	24-27	
19421309-2	2008	Reaction of electrophiles with 3-oxo pyrrolidine dianions readily introduces substituents, regioselectively at C-4 in these pyrrolidines.	Pyrrolidines	124-136	complement C4A (Rodgers blood group)	Homo sapiens	111-114	
31508886-1	2019	Amino-acid-derived phosphine catalyzed [4+2] cycloaddition leading to chiral tetrahydropyridines, making use of alpha-substituted allenic ketones as "C4 synthons" and N-sulfonyl cyclic ketimines, has been developed.	Pyrrolidines	77-96	complement C4A (Rodgers blood group)	Homo sapiens	149-152	
1447747-5	1992	In this paper we report the results of synthetic and metabolic studies on a series of tetrahydropyridine analogs of MPTP with oxygen, sulfur, and carbamoyloxy derivatives on C-4 which serve as model compounds to evaluate the scope of this prodrug concept.	Pyrrolidines	86-104	complement C4A (Rodgers blood group)	Homo sapiens	174-177