PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
32759765-3	2020	We herein present a new methodology based on the synergic combination of experimental 19F-based saturation transfer difference (STD) NMR data with computational protocols, applied to analyze the interaction between DC-SIGN, a key lectin involved in inflammation and infection events with the trifluorinated glycomimetic of the trimannoside core, ubiquitous in human glycoproteins.	Methyl 3,6-di-O-(A-D-mannopyranosyl)-A-D-mannopyranoside	327-339	CD209 molecule	Homo sapiens	215-222	
17150970-3	2007	Although the trimannoside binds to DC-SIGN or DC-SIGNR more strongly than mannose, additional affinity enhancements are observed in the presence of one or more Manalpha1-2Manalpha moieties on the nonreducing termini of oligomannose structures.	Methyl 3,6-di-O-(A-D-mannopyranosyl)-A-D-mannopyranoside	13-25	CD209 molecule	Homo sapiens	35-42	
20085340-0	2010	Inhibition of DC-SIGN-mediated HIV infection by a linear trimannoside mimic in a tetravalent presentation.	Methyl 3,6-di-O-(A-D-mannopyranosyl)-A-D-mannopyranoside	57-69	CD209 molecule	Homo sapiens	14-21