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NORTHVERITY / CH20

Chonluten

20 mg × 10 vials

For laboratory procurement

Chonluten 20 mg × 10 vials · CH20 · Catalog illustration—not an actual packaging photo.
Catalog illustration—not an actual packaging photo.
Procurement details
Catalog number
CH20
Listed specification
20 mg
Vials per pack
10 vials
Current supply lot
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Compound profile

Chonluten is a synthetic Glu-Asp-Gly tripeptide described in THP-1 monocyte and macrophage signalling experiments.

Identity

Sequence
H-EDG-OH
Residues
3
Molecular formula
C11H17N3O8
Average molecular weight
319.27 g/mol
Monoisotopic mass (calculated)
319.1016 Da
CAS number
75007-24-8
PubChem CID
194641
Other names
EDG

The full cited paper explicitly identifies Chonluten as Glu-Asp-Gly; the database verifies free EDG. Direct literature is limited, so one paper is cited. The research is connected to the originating group. UniProt is inapplicable; SMILES and 2D coordinates were not transcribed.

Identity data from: PubChem CID 194641: properties, biologic line notation and synonyms · PubMed PMID 35408963: Chonluten sequence in the full paper Peptides section

Residue diagram of Chonluten
Drawn from the verified identity data on this page.

Research overview

Chonluten is the tripeptide Glu-Asp-Gly, abbreviated EDG. In the full text of the cited study, investigators identify it as a synthetic peptide based on information from a tissue-derived counterpart. Its terminal glycine and two preceding acidic residues distinguish the sequence from other short peptides in the same paper. That investigation compared Chonluten with several defined peptides and a peptide complex, so their identities and individual observations should remain separate [1].

The experiments used the THP-1 monocytic cell line and cells differentiated toward a macrophage phenotype. They assessed proliferation-related kinase phosphorylation, including ERK1/2 and JNK, together with cytokine measurements under lipopolysaccharide stimulation. The paper reported lower TNF production in monocytes exposed to Chonluten in that experimental context [1]. It also examined cytokine patterns in differentiated cells and adhesion to activated endothelial-cell layers. Those assays connect intracellular signals with a cell-interaction readout, but the shared panel design does not mean that all peptides produced identical changes. A cell line, a differentiation condition and a particular inflammatory stimulus define the observation; they do not establish a specific molecular receptor for EDG or an organ-level response [1].

The cited biological literature is limited and mainly comes from one connected research group. These experiments describe particular cell or tissue systems. Their readouts do not establish a general mechanism across organs, and independent replication remains important when assessing the proposed molecular interactions [1].

Laboratory storage and handling

Follow the storage conditions stated in the documentation supplied with the lot. Keep the sealed vial cold, dry and protected from light. Let it reach room temperature before opening to reduce moisture condensation on the material. Avoid repeated freezing and thawing of laboratory stocks, record lot identifiers with experiments and wear standard laboratory protective equipment. Published biological observations do not establish storage stability for a particular lot.

Questions about Chonluten

What sequence does this profile describe?

Chonluten is the free peptide Glu-Asp-Gly, written EDG in one-letter notation. The identity record specifies an unmodified N terminus and a free carboxyl terminus; a salt form would be a separate chemical description.

Which experimental systems appear in the cited work?

The paper uses THP-1 monocytes, macrophage-like differentiated THP-1 cells and activated endothelial-cell layers. Kinase, cytokine and adhesion assays describe different aspects of that in vitro model [1].

How should the evidence be interpreted?

The paper provides observations in defined experimental models and is connected to an originating research network. It does not establish that the same molecular response occurs in unrelated systems. Independent comparisons and careful identification of the material remain necessary.

References

  1. Peptides Regulating Proliferative Activity and Inflammatory Pathways in the Monocyte/Macrophage THP-1 Cell Line. Int J Mol Sci 2022. PMID 35408963

Identity data checked on 2026-10-03. Literature summaries describe published research models and are not specifications of any product lot.

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