PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
30138624-11	2018	The docking study revealed three separate ligand binding pockets within the hOCT1 translocation pathway, defined by their interactions with three prototypical substrates: MPP+, TEA, and acyclovir.	Acyclovir	186-195	solute carrier family 22 member 1	Homo sapiens	76-81	
11861798-3	2002	Time- and concentration-dependent uptake of ACV and GCV was observed in hOAT1- and hOCT1-expressing cells.	Acyclovir	44-47	solute carrier family 22 member 1	Homo sapiens	83-88	
11861798-6	2002	The Km values of ACV uptake by hOAT1 and hOCT1 were 342.3 and 151.2 microM, respectively, whereas those of GCV uptake by hOAT1 and hOCT1 were 895.5 and 516.2 microM, respectively.	Acyclovir	17-20	solute carrier family 22 member 1	Homo sapiens	41-46	
11861798-9	2002	In conclusion, these results suggest that hOAT1 and hOCT1 mediate renal ACV and GCV transport, whereas hOAT1, hOAT2, hOAT3, and hOAT4 mediate renal AZT transport.	Acyclovir	72-75	solute carrier family 22 member 1	Homo sapiens	52-57	
34678271-3	2022	In this study, the contribution of physiology (i.e., OCT1 activity) to the oral disposition of acyclovir immediate release (IR) tablets was hypothesized to be greater than dissolution.	Acyclovir	95-104	solute carrier family 22 member 1	Homo sapiens	53-57