Cardiogen

AEDR tetrapeptide research reference · Khavinson-lineage cardiac literature

Lot-specific · Batch COACAS 857267-11-9RUO
Batch COA
MOQ1 kit (10 vials) per SKU
Supplied formLinear tetrapeptide; H-Ala-Glu-Asp-Arg-OH (AEDR)
Lead time14–21 days
Cardiogen — Lot-specific lyophilized research peptide; confirm colour and cake condition on the released-lot COA
Cardiogen — Lot-specific lyophilized research peptide; confirm colour and cake condition on the released-lot COA · Representative packaging image · verify the ordered lot
Representative packaging image · verify the ordered lot

Decision summary

Key benefits

  • Research applications include AEDR identity and sequence qualification, myocardial or fibroblast cell models, cytoskeletal/nuclear-matrix readouts and replication of peptide-histone interaction findings
  • Reported tumour-model findings are a separate preclinical context and do not establish cardiovascular or anticancer efficacy.
Published research context is presented for literature orientation only. It is not a dosing, treatment or human-use instruction.

Qualification data

Specifications to confirm against the released lot

CAS
857267-11-9
Formula
C18H31N7O9
Molecular weight
489.5 g/mol
Appearance
Lot-specific lyophilized research peptide; confirm colour and cake condition on the released-lot COA
Purity
Lot-specific chromatographic purity and quantitative peptide content; confirm both on the released-lot COA · target, verify batch COA
Storage
Follow the released-lot COA, SDS and formulation-specific stability statement. Temperature, light protection, shipping range, container and any prepared-solution hold time require evidence for the exact AEDR form, matrix and concentration.
MOQ
1 kit (10 vials) per SKU
Lead time
14–21 days
PubChem CID 11583989

Qualification matrix

Identity, purity and content are separate release questions.

Identity

Confirm the stated molecule and supplied form. Start with the matching batch COA; request sequence-level evidence only when the buyer's written procedure requires it and availability or a separate scope has been agreed.

Purity

Review RP-HPLC method conditions, wavelength, integration and related-peak handling. A percentage without the method is not enough.

Content

Net peptide content is not the same as gross lyophilized powder weight. Ask which assay supports the stated amount and whether water/counter-ion is addressed.

Stability

Follow the storage condition stated on the batch COA or label from receipt onward.

Research context

What researchers study about Cardiogen

Cardiogen is specified as the linear tetrapeptide H-Ala-Glu-Asp-Arg-OH, abbreviated AEDR from its four residues. PubChem CID 11583989 independently supports that full residue sequence, formula C₁₈H₃₁N₇O₉ and molecular weight 489.5 Da. Research from the Khavinson network includes a rat myocardial-explant study, a mouse-embryonic-fibroblast study, a senescent-rat M-1 sarcoma model and a wheat-histone interaction study. No sequence-confirmed human clinical trial or pharmacokinetic programme was identified. CAS 857267-11-9 is consistently mapped by several supplier catalogues but is not displayed in the accessible PubChem synonyms, so sequence-resolved batch evidence remains primary.

  • Sequence and identity qualification; myocardial-tissue, fibroblast, cytoskeletal/nuclear-matrix and histone-interaction assays; and carefully controlled preclinical replication
  • These are research applications, not clinical indications.

Mechanism context

The question the literature is testing

PMID 20210190 reports that 10⁻¹² M Cardiogen increased the outgrowth zone in organotypic myocardial explants from 3- and 24-month-old rats and was associated with lower p53 expression; this was an ex-vivo tissue-culture experiment, not an in-vivo efficacy or dose study. PMID 22977870 separately reports 2-5-fold increases in cytoskeletal proteins and 2-3-fold increases in lamin A/C in cultured mouse embryonic fibroblasts; its claim that these changes explain cardioprotection is the authors' interpretation. PMID 23581987 reports in-vitro binding of AEDR and five other short peptides to FITC-labelled wheat histones and histone-deoxyribooligonucleotide complexes. No direct causal chain from those findings to human cardiac outcomes or tissue targeting has been established.

Evidence map

Research routes and exposure context

Evidence tierMixed evidence context
Routes reported in sources
No administration route applies
Dose / exposure contextProtocol-specific; verify the cited primary source
Routes and exposure contexts summarize cited studies or approved finished-product labels. They are not instructions for administering this RUO material; no customer dose is provided.

Evidence boundaries

Compatibility, limitations and decision context

  • Not for human or veterinary use
  • Preclinical proliferation, apoptosis and tumour-model observations do not establish human safety or a contraindication framework
  • The M-1 sarcoma study cannot be generalized to human cancer or other tumour types
  • Follow the SDS and institutional controls; chemical purity does not establish sterility or injectable suitability.

Interactions reported in the literature

  • No controlled combination or drug-interaction studies were identified
  • Pairings with Vesugen, BPC-157, TB-500 or other Khavinson peptides are vendor/community hypotheses, not validated compatibility or safety guidance.
Literature context is not a supplier release result or human-use instruction. Follow your institution's approved laboratory risk assessment.

Batch documentation

Cardiogen batch COAs

Laboratory: Manufacturer's QC laboratoryTests: HPLC purity · MS identity · endotoxin · fill amount

  • Blurred preview of a Cardiogen 20 mg batch COA20 mg

Previews are blurred on purpose so the documents cannot be reused; third-party reports show their first page only. Sales sends the clear full version for the product and strength you ask about.

Independent test fails? Full refund.

Representative records, refreshed periodically

Published COAs show recent representative batches and may not be the newest. For a quote or shipment, sales confirms the lot and sends its COA.

Third-party reports, added progressively

Previews of the first page of third-party reports are on our Quality page and on the matching product pages; sales sends the full report on request. You can also send any vial from your order to an independent laboratory of your choice. Unless agreed otherwise in writing, the buyer pays for optional testing.

Help reviewing your COA

Need help reading a batch COA or third-party report? Sales can explain the test items, specifications and how the results relate to the lot under discussion.

On every batch COA: HPLC purity · MS identity · endotoxin · fill amount · Verify LyoPep

Ask for the current packet, not a generic certificate

  • Require exact AEDR sequence and termini, supplied form/counterion, theoretical and observed high-resolution intact mass, sequence evidence, stability-indicating HPLC purity and impurity profile, quantitative peptide content, water/counterion/residuals and lot-specific stability
  • Sterility, bacterial endotoxin and bioburden are independent attributes
  • A white appearance, clear solution or “>97%” area result alone is insufficient.
Batch COA for the released lotHPLC purity with method contextMS identity resultEndotoxin resultFill amount (measured content per vial)SDS and handling statement

Available fills

Quote the fill and pack configuration you need

Reference SKUFillBase pack
CAR2020 mg10 vials

Handling

Plan storage before the parcel arrives

Follow the released-lot COA, SDS and formulation-specific stability statement. Temperature, light protection, shipping range, container and any prepared-solution hold time require evidence for the exact AEDR form, matrix and concentration.

State the destination and timing so receipt can be planned, then move the material into its stated storage condition on arrival.

Buyer FAQ

Terms to settle before the purchase order

Can a buyer arrange third-party testing?+

Yes. You can send any vial from your order to an independent laboratory of your choice. If you want the laboratory, specification, sampling, method and acceptance rule agreed with us before testing, sales confirms them in writing. Unless otherwise agreed in writing, the buyer pays the cost of this optional testing.

What if my own lab test shows the product is out of specification?+

Send any vial from your order to an independent laboratory of your choice. If the report shows the product does not meet the specification on its COA — purity below the stated minimum, or an identity that does not match — share the report with our sales team and we refund that product in full.

Does HPLC purity prove peptide content?+

No. Chromatographic purity describes the relative peak profile under a stated method. Identity, water, counter-ion, residual solvents and assay/content may require separate methods.

How should material be stored after delivery?+

Move it into the storage condition stated on the batch COA or label as soon as it arrives, and record the package condition on receipt.

How are payment terms handled?+

Available methods and milestones depend on order value, destination and project type. The pro forma invoice should state currency, bank details, fees, payment milestones and the release condition.

Why must the testing laboratory understand peptide chemistry?+

Free-base and salt forms, hydrophilic and hydrophobic sequences, aggregation and adsorption can change sample preparation and method suitability. Use a laboratory experienced with the molecule class.

These are buyer-qualification references, not claims that this RUO material is regulated, certified or released under those frameworks. Applicability depends on the buyer's workflow and jurisdiction.

Selected sources

Literature behind the research context

  • Identity: PubChem CID 11583989. Myocardial explant and p53 study: PMID 20210190. Cytoskeletal/nuclear-matrix study: PMID 22977870. Senescent-rat M-1 sarcoma model: PMID 20396706. Wheat-histone-complex interaction: PMID 23581987. A 2023 Cells review in PMC9818427 provides same-network secondary synthesis. These records support a limited preclinical research context, not human dosing, efficacy or safety.
  1. 01

    Tetrapeptide H-Ala-Glu-Asp-Arg-OH stimulates expression of cytoskeletal and nuclear matrix proteins

    Bulletin of Experimental Biology and Medicine · 2012 · peer-reviewed original research

    Open source
  2. 02

    The effect of the amino acids and cardiogen on the development of myocard tissue culture from young and old rats

    Advances in Gerontology · 2009 · peer-reviewed original research (Russian article with English abstract)

    Open source
  3. 03

    Tumor-modifying effect of cardiogen peptide on M-1 sarcoma in senescent rats

    Bulletin of Experimental Biology and Medicine · 2009 · peer-reviewed original research

    Open source
  4. 04

    Interaction of short peptides with FITC-labeled wheat histones and their complexes with deoxyribooligonucleotides

    Biochemistry (Moscow) · 2013 · peer-reviewed original in-vitro research

    Open source
  5. 05

    Senescence-Associated Secretory Phenotype of Cardiovascular System Cells and Inflammaging: Perspectives of Peptide Regulation

    Cells (MDPI) · 2023 · peer-reviewed review article

    Open source
  6. 06

    Peptide substance restoring myocardium function (US Patent 7,662,789 B2)

    United States Patent and Trademark Office / Google Patents · 2010 · regulatory document (granted patent)

    Open source
  7. 07

    Peptide compound recovering function of myocardium (RU Patent 2255756 C1)

    Russian Federal Service for Intellectual Property / Google Patents · 2005 · regulatory document (granted patent)

    Open source
  8. 08

    Peptide medicines: past, present, future

    Clinical Medicine (Russian Journal) / Klinicheskaya Meditsina · 2020 · peer-reviewed review article (author overview)

    Open source

Product FAQ

Questions buyers ask about Cardiogen

What is established about Cardiogen identity?+

PubChem CID 11583989 supports the full H-Ala-Glu-Asp-Arg-OH residue sequence, AEDR residue abbreviation, formula C₁₈H₃₁N₇O₉ and molecular weight approximately 489.5 Da. The quote and COA should also specify termini, salt/counterion, theoretical and observed intact mass, sequence evidence and quantitative peptide content. CAS 857267-11-9 is a secondary catalogue mapping and should not replace those controls.

How strong is the cardiac evidence?+

Published work includes a rat myocardial-explant study reporting proliferation and lower p53 expression, a mouse-embryonic-fibroblast study reporting cytoskeletal/nuclear-matrix protein changes, and a separate senescent-rat M-1 sarcoma model. Another in-vitro paper reports AEDR interaction with wheat histones. These findings come from a concentrated research lineage and do not establish a sequence-confirmed human cardiovascular benefit, pharmacokinetic profile or clinical safety; histone binding has not been causally linked to cardioprotection.

What should a Cardiogen lot-release package contain?+

Require exact N-to-C AEDR sequence and termini, salt/counterion and theoretical mass; high-resolution intact mass and sequence evidence; stability-indicating HPLC method and impurity profile; quantitative peptide content; water, counterion and relevant residuals; and lot-specific storage evidence. Sterility, bacterial endotoxin and bioburden are separate tests and cannot be inferred from appearance or chemical purity.

Evidence before order

Buyer intelligence