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FAP-PID: sourced facts only. name: "FAP-binding affinities of [natIn]-In-FAP-PID and [natIn]-In-FAP-ID were comparable to or higher than those of the monomeric counterparts." [PMID:42312172]; target: "FAP-binding affinities of [natIn]-In-FAP-PID and [natIn]-In-FAP-ID were comparable to or higher than those of the monomeric counterparts." [PMID:42312172]; developer: "Department of Patho-Functional Bioanalysis, Graduate School of Pharmaceutical Sciences, Kyoto University, 46-29 Yoshida, Shimoadachi-cho, Sakyo-Ku, Kyoto 606-8501, Japan." [PMID:42312172]; modality: "In this study, we newly designed and synthesized three types of FAP-targeting dimers based on FAPI-46 and FAP-2286: heterodimer FAP-PID, small molecule-based homodimer FAP-ID, and cyclic peptide-based homodimer FAP-PD." [PMID:42312172]
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