PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 17035026-0 2007 Modifications of the pyroglutamic acid and histidine residues in thyrotropin-releasing hormone (TRH) yield analogs with selectivity for TRH receptor type 2 over type 1. Pyrrolidonecarboxylic Acid 21-38 thyrotropin releasing hormone Homo sapiens 65-94 17035026-0 2007 Modifications of the pyroglutamic acid and histidine residues in thyrotropin-releasing hormone (TRH) yield analogs with selectivity for TRH receptor type 2 over type 1. Pyrrolidonecarboxylic Acid 21-38 thyrotropin releasing hormone Homo sapiens 96-99 17035026-0 2007 Modifications of the pyroglutamic acid and histidine residues in thyrotropin-releasing hormone (TRH) yield analogs with selectivity for TRH receptor type 2 over type 1. Pyrrolidonecarboxylic Acid 21-38 thyrotropin releasing hormone Homo sapiens 136-139 17035026-3 2007 For example, the most selective agonist of the series 13, in which pGlu is replaced with the pAad and histidine residue is substituted at the N-1 position with an isopropyl group, was found to activate TRH-R2 with a potency (EC(50)=1.9microM) but did not activate TRH-R1 (potency>100 microM); that is, exhibited >51-fold greater selectivity for TRH-R2 versus TRH-R1. Pyrrolidonecarboxylic Acid 67-71 thyrotropin releasing hormone Homo sapiens 202-205