Drug intelligence / Profile preview

cyclo-(histidyl-proline)

Development stage
Unknown
Modality
Peptides, Small Molecules
Administration
Oral
01

Overview

Cyclo-(histidyl-proline) (CHP) is an endogenous, blood-brain barrier-permeable cyclic dipeptide derived from the proteolytic cleavage of thyrotropin-releasing hormone (TRH). It acts as a neuroprotective and anti-inflammatory agent by modulating key cellular signaling pathways. Specifically, CHP activates the Nuclear factor erythroid 2-related factor 2 (Nrf2) pathway, which enhances the antioxidant response, and inhibits the nuclear accumulation of Nuclear factor-kappa B (NF-κB), thereby reducing pro-inflammatory cytokine production. While it has demonstrated potential in preclinical models of neurodegeneration, metabolic disorders, and inflammation, it is currently utilized primarily as a research reagent and has no established clinical development program or commercial sponsor.

Other names
Cyclo(His-Pro)histidyl-proline diketopiperazinecyclo-L-histidyl-L-proline
02

Targets

NFE2L2 (Nuclear factor (erythroid-derived 2)-like 2)

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