Cardiogen 20mg (Bioregulator)

Cardiogen is a short peptide investigated as a bioregulator with reported effects on fibroblast activity and extracellular matrix dynamics. Fibroblasts are central to tissue repair, scar formation, and long-term structural remodeling following injury. In experimental settings, Cardiogen is used to explore how small peptides may influence gene-expression programs related to cellular differentiation, apoptosis regulation, and fibrosis-associated signaling.

Although frequently studied in cardiovascular research frameworks, Cardiogen has also been examined in prostate aging models and select oncology-related systems. Experimental endpoints often include apoptosis markers, proliferation indices, fibrosis-related gene expression, and tissue remodeling metrics. Observations remain model-dependent and are interpreted strictly within preclinical and mechanistic research settings.

Molecular Formula: C₁₈H₃₁N₇O₉
Molecular Weight: 489.5 g/mol
PubChem CID: 11583989
Alternative Names: SCHEMBL3194515

Source: PubChem

Cardiogen is utilized in cardiovascular research models to investigate mechanisms of myocardial remodeling following experimental injury. Laboratory endpoints typically include measurements of cardiomyocyte viability, fibroblast proliferation rates, extracellular matrix deposition markers, and apoptosis-regulatory signaling (including p53-associated pathways). These studies aim to characterize how peptide-mediated modulation may influence structural remodeling dynamics in controlled environments.

In oncology-focused preclinical research, Cardiogen has been explored in tumor models to assess potential effects on apoptosis signaling and tumor microenvironment regulation. Investigations may include dose-response analyses, tumor-cell apoptosis markers, and fibroblast-derived signaling factors that influence epithelial–stromal interactions, particularly in aging-related prostate tissue models. These applications are exploratory and intended solely for laboratory and scientific investigation.

Experimental models describe Cardiogen-associated modulation of gene-expression networks involved in fibroblast proliferation, cardiomyocyte development, and apoptosis regulation. In myocardial tissue cultures derived from rodents, Cardiogen has been studied for its association with altered growth patterns and differentiation states of cardiac-supporting cell populations.

Mechanistic analyses further implicate transcriptional pathways linked to p53-associated signaling, extracellular-matrix remodeling, and stromal–parenchymal cell interactions. These pathways are commonly evaluated in vitro and in vivo using molecular readouts such as apoptosis markers, proliferation indices, and transcriptomic profiling.

In oncology-related experimental systems, Cardiogen has been examined for differential apoptosis signaling in tumor versus non-tumor cell populations, with interpretation confined strictly to molecular and cellular observations in rodent models.

Additional in-vitro studies investigate peptide-associated regulation of fibroblast-derived signaling factors within prostate tissue cultures, emphasizing age-associated changes in stromal gene-expression profiles rather than organism-level outcomes.

The peer-reviewed literature on Cardiogen consists primarily of:

• Rodent myocardial tissue culture studies evaluating peptide effects on cardiac cell development
• Rat tumor models assessing apoptosis-related molecular endpoints
• In-vitro fibroblast culture studies examining differentiation-associated signaling molecules
• Age-associated stromal-cell gene-expression analyses

All findings are interpreted strictly within the constraints of the experimental systems described and do not imply translational, therapeutic, or clinical relevance.

Cardiogen is supplied as a synthetic research peptide. Standard analytical characterization methods for peptide identity and purity may include chromatographic and mass-spectrometric techniques, as documented in supplier-specific quality-control materials where applicable.

The above literature was researched, edited and organized by Dr. E. Logan, M.D. Dr. E. Logan holds a doctorate degree from Case Western Reserve University School of Medicine and a B.S. in molecular biology.

Vladimir Khavinson is a Professor, President of the European region of the International Association of Gerontology and Geriatrics; Member of the Russian and Ukrainian Academies of Medical Sciences; Main gerontologist of the Health Committee of the Government of Saint Petersburg, Russia; Director of the Saint Petersburg Institute of Bioregulation and Gerontology; Vice-president of Gerontological Society of the Russian Academy of Sciences; Head of the Chair of Gerontology and Geriatrics of the North-Western State Medical University, St-Petersburg; Colonel of medical service (USSR, Russia), retired. Vladimir Khavinson is known for the discovery, experimental and clinical studies of new classes of peptide bioregulators as well as for the development of bioregulating peptide therapy. He is engaged in studying of the role of peptides in regulation of the mechanisms of ageing. His main field of actions is design, pre-clinical and clinical studies of new peptide geroprotectors. A 40-year-long investigation resulted in a multitude of methods of application of peptide bioregulators to slow down the process of ageing and increase human life span. Six peptide-based pharmaceuticals and 64 peptide food supplements have been introduced into clinical practice by V. Khavinson. He is an author of 196 patents (Russian and international) as well as of 775 scientific publications. His major achievements are presented in two books: “Peptides and Ageing” (NEL, 2002) and “Gerontological aspects of genome peptide regulation” (Karger AG, 2005). Vladimir Khavinson introduced scientific specialty “Gerontology and Geriatrics” in the Russian Federation on the governmental level. Academic Council headed by V. Khavinson has oversighted over 200 Ph.D. and Doctorate theses from many different countries.

Prof. Vladimir Khavinson is being referenced as one of the leading scientists involved in the research and development of Cardiogen. In no way is this doctor/scientist endorsing or advocating the purchase, sale, or use of this product for any reason. There is no affiliation or relationship, implied or otherwise, between Peptide Sciences and this doctor. The purpose of citing the doctor is to acknowledge, recognize, and credit the exhaustive research and development efforts conducted by the scientists studying this peptide.

1. N. I. Chalisova et al., “[The effect of the amino acids and cardiogen on the development of myocard tissue culture from young and old rats],” Adv. Gerontol. Uspekhi Gerontol., vol. 22, no. 3, pp. 409–413, 2009.
2. N. V. Levdik and I. V. Knyazkin, “Tumor-modifying effect of cardiogen peptide on M-1 sarcoma in senescent rats,” Bull. Exp. Biol. Med., vol. 148, no. 3, pp. 433–436, Sep. 2009, doi: 10.1007/s10517-010-0730-9.
3. L. Begley, C. Monteleon, R. B. Shah, J. W. Macdonald, and J. A. Macoska, “CXCL12 overexpression and secretion by aging fibroblasts enhance human prostate epithelial proliferation in vitro,” Aging Cell, vol. 4, no. 6, pp. 291–298, Dec. 2005, doi: 10.1111/j.1474-9726.2005.00173.x.
4. O. V. Kheĭfets, V. O. Poliakova, and I. M. Kvetnoĭ, “[Peptidergic regulation of the expression of signal factors of fibroblast differentiation in the human prostate gland in cell aging],” Adv. Gerontol. Uspekhi Gerontol., vol. 23, no. 1, pp. 68–70, 2010.

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The products offered on this website are furnished for in-vitro studies only. In-vitro studies (Latin: in glass) are performed outside of the body. These products are not medicines or drugs and have not been approved by the FDA to prevent, treat or cure any medical condition, ailment or disease. Bodily introduction of any kind into humans or animals is strictly forbidden by law.

For Laboratory Research Only. Not for human use, medical use, diagnostic use, or veterinary use.