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Chonluten

Bioregulator

Also known as: EDG, Glu-Asp-Gly

Tier 3, Preclinical only

Evidence is limited to animal or in-vitro work. No human pharmacokinetics. Any human dose in circulation is extrapolated, and extrapolation across species routinely fails.

Half-life
Not established

No pharmacokinetic data found on allowed hosts.

Dosing
No established dose

A Khavinson-affiliated narrative review (PMC7583759) states Chonluten is given orally for bronchopulmonary pathology, but the accessible text gives no dose, frequency, or duration, and no primary controlled trial could be located.

Regulatory status
Not approved by FDA/EMA. Sold in Russia as a registered peptide bioregulator/parapharmaceutical, not equivalent to drug approval.
Evidence base
mixed · confidence: low

Single Russian lineage. Allowed-host evidence: (1) an in-vitro THP-1 human monocyte/macrophage study (Avolio et al. 2022, PMC8999041) showing Chonluten inhibits LPS-induced TNF at 100 ng/mL; (2) a Khavinson-authored narrative review (PMC7583759) asserting oral clinical use without retrievable trial methodology, sample size, or dose. No independent non-Russian replication, no RCT. Sequence Glu-Asp-Gly and MW 319.27 Da confirmed on PubChem (CID 194641).

Safety

No human safety/toxicology data with dosing detail found on allowed hosts. No adverse-event reporting located for Chonluten specifically. Absence of reported harm is not evidence of safety.