Chonluten

Compound Overview

Research Use Only. Not for Human Consumption.

Chonluten is supplied by Nexus as a sequence-defined short peptide bioregulator for controlled in-vitro research and analytical workflows. The provided chemistry record identifies Chonluten as Glu-Asp-Gly, abbreviated EDG, a 3-residue synthetic peptide associated with respiratory and lung-tissue research models.

Chonluten is categorized in the Nexus catalog under Russian Bioregulators. The current Nexus variant is a 20mg research-size vial under SKU CH20. The available source record supports its peptide sequence, classification, molecular formula, calculated molecular weight, physical form, intended use, and storage guidance. It does not provide a confirmed CAS number, lot-specific purity value, salt or counter-ion assignment, batch number, or Certificate of Analysis values.

Because the supplied source data is limited, this page is intentionally limited as well. It does not infer therapeutic properties, dosing information, biological outcomes, mechanism-specific findings, reconstitution instructions, or compound-specific stability windows beyond the facts included in the research record.

• Product: Chonluten
• SKU: CH20
• Available Research Size: 20mg
• Class: Khavinson short peptide bioregulator
• Sequence: EDG
• Sequence Display: Glu-Asp-Gly
• Physical Form: Lyophilized powder
• Use: For in-vitro research use only. Not for human consumption.

Research Background & Published Literature

The available literature for Chonluten is concentrated in Russian and Eastern European bioregulator research. For this product record, the strongest usable chemistry anchor is the defined amino-acid sequence: Glu-Asp-Gly. That sequence provides the basis for the calculated molecular formula and molecular weight listed in the technical specifications below.

Chonluten is identified in the supplied research data as a Khavinson short peptide bioregulator associated with respiratory and lung-tissue research models. The provided record does not include detailed experimental abstracts, assay protocols, validated mechanism-specific findings, study conditions, or lot-level release analytics. For that reason, this page avoids unsupported statements about biological effects and treats the EDG sequence, classification, physical form, and computed chemistry values as the primary verified descriptors.

Researchers reviewing the literature around this compound can use the peer-reviewed resources below for additional context on mechanism of action, signaling pathways, and controlled laboratory research applications:

• Khavinson et al. (2021) — Molecules
• Khavinson et al. (2020) — Stem Cell Rev Rep

Storage, Handling & Stability Guidelines

Store lyophilized Chonluten material at -20°C, desiccated, and protected from light. These are the only Chonluten-specific storage parameters included in the current research record.

After reconstitution, aliquot the material and avoid repeated freeze-thaw cycles. The source record does not specify a reconstitution solvent, target concentration, post-reconstitution hold time, validated stability window, acceptable number of freeze-thaw events, container-closure compatibility, or light-exposure tolerance after reconstitution. Those details should not be inferred from this page.

Laboratories should document handling conditions according to their own validated internal procedures and preserve traceability between aliquots, source vial, and lot-level verification records. The absence of a provided stability study means this description should be treated as a conservative storage summary rather than a complete stability protocol.

Lab Verification

Nexus maintains a Lab Verified reference area for research-compound verification records. Where current lot documentation is available, HPLC may be used to review chromatographic purity and Mass Spectrometry may be used to support molecular identity confirmation.

No exact Chonluten COA values are included in the current product record. This page therefore does not list a batch number, purity percentage, chromatographic retention time, measured mass, salt form, counter-ion, or release-test result. The current research warning is to confirm final CAS, salt or counter-ion, purity, and mass values against the supplier COA before relying on a specific batch for analytical work.