Cartalax

კარტალაქსი

კარტალაქსი

Cartalax is a short-chain synthetic peptide with the amino acid sequence Ala-Glu-Asp.

 

 

გააზიარე შენი სიყვარული

Cartalax is a short-chain synthetic peptide with the amino acid sequence Ala-Glu-Asp. Derived from a natural protein fragment present within healthy cartilage, it is a carefully designed synthetic molecule.

The specific sequence of amino acids mimics those of ენდოგენური signaling molecules; binding to certain cellular receptors, a subsequent cascade of cellular responses is triggered.

Rational synthetic design grants Cartalax high biological activity, specificity, low immunogenicity, and good transdermal or oral absorption.

Ongoing research details its multi-targeted, multi-level comprehensive protective and reparative potential.

Effective suppression of inflammation is one such outcome – downregulation of pro-inflammatory cytokine induced Matrix metalloproteinases (MMPs) და ADAMTS being the primary mechanisms; direct erosion and degradation of type II collagen and various proteoglycans are mitigated, articular cartilage structural integrity being preserved.

Enhancing the regenerative capacity of the უჯრედგარე მატრიქსი is another line of action suggested by more recent studies; chondrocyte specific markers are upregulated and their synthesis promoted.

Minor cartilage damage can be repaired through these means, healthy ჰომეოსტაზის maintained.

ანთების საწინააღმდეგო, immunomodulatory and anti-aging properties are all part of Cartalax’s profile; clinical trials are currently exploring all of the above.

Synthesis and application of Cartalax represents a promising direction of bioactive peptide therapy.

თანმიმდევრობა

ალა-გლუ-ასპ

CAS ნომერი

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მოლეკულური ფორმულა

C12H19N3O8

მოლეკულური წონა

333.297

Research Of Cartalax Peptide

1.Inhibition of Cartilage Catabolism

As stated, the prevention of excessive degradation is at the core of all Cartalax based research.

Abnormal pro-inflammatory factor signaling must be interrupted, and the enzymes responsible for degrading the matrix (ისევ, primarily MMPs/Matrix Metalloproteinases) either directly or indirectly inhibited.

Mechanical integrity of cartilage tissue is the end point of all this work.

2.ხელშეწყობა Cartilage Synthesis

Cartalax also demonstrates an exceptional capacity to enhance tissue anabolic metabolism.

Upregulating chondrocyte functional activity, it rapidly increases the synthesis and subsequent secretion of various extracellular matrix components; direct cartilage formation is the primary end result of this process.

In vitro studies have confirmed this effect – treated chondrocytes or stem cells show significantly elevated gene expression levels of type II collagen and aggrecan, with corresponding increases in the actual production of said proteins.

Further indirect enhancement of cellular metabolism and protein synthesis are achieved through specific intracellular signaling pathways (TGF-β/Smad being a prime example); tissue regeneration is the desired outcome.

Repairing pre-existing microdamage and constructing a functional matrix are two valuable pathways enabled by this line of action.

3.Anti-inflammatory and Immunomodulatory Effects

NF-κB serves as a key signal for activating numerous inflammatory factors.

Cartalax actively suppresses, or at least reduces, NF-κB expression – hitting the source of most inflammatory responses.

Pain, swelling and the more permanent stiffness associated with inflammation are all effectively alleviated.

The cartilage protective effects described above are intrinsically part of this anti-inflammatory process; reducing inflammation is a fundamental aspect of Cartalax’s overall mechanism of action.

COA

HPLC

MS

(1) ჩალისოვა, ნ. მე.; მიჭირს, ნ. ს.; Nichik, თ. ე.; რიჟაკი, ა. პ.; დუდკოვი, ა. ვ.; რიჟაკი, გ. ა. Peptide Regulation of Cells Renewal Processes in Kidney Tissue Cultures from Young and Old Animals. Bull Exp Biol Med 2015, 159 (1), 124-127. DOI: 10.1007/s10517-015-2906-9 From NLM Medline.

(2) ჩალისოვა, ნ. მე.; მიჭირს, ნ. ს.; Nichik, თ. ე.; რიჟაკი, ა. პ.; დუდკოვი, ა. ვ.; რიჟაკი, გ. ა. Peptide Regulation of Cells Renewal Processes in Kidney Tissue Cultures from Young and Old Animals. Bull Exp Biol Med 2015, 159 (1), 124-127. DOI: 10.1007/s10517-015-2906-9 From NLM Medline.

(3) ხავინსონი, ვ.; მიჭირს, ნ. ს.; პოლიაკოვა, ვ. ო.; Durnova, ა. ო.; Nichik, თ. ე.; კვეტნოი, მე. მ. Peptides regulate expression of signaling molecules in kidney cell cultures during in vitro aging. Bull Exp Biol Med 2014, 157 (2), 261-264. DOI: 10.1007/s10517-014-2540-y From NLM Medline.

(4) მიჭირს, ნ. ს.; Drobintseva, ა. ო.; Orlova, ო. ა.; Kuznetsova, ე. პ.; პოლიაკოვა, ვ. ო.; კვეტნოი, მე. მ.; ხავინსონი, ვ. Peptide Regulation of Skin Fibroblast Functions during Their Aging In Vitro. Bull Exp Biol Med 2016, 161 (1), 175-178. DOI: 10.1007/s10517-016-3370-x From NLM Medline.

(5) ბმულები, ნ.; ხავინსონი, ვ.; დიატლოვა, ა.; მიაკიშევა, ს.; რიჟაკი, გ. ქონდროგენული ღეროვანი უჯრედების დიფერენციაციის პეპტიდური რეგულირება. Int J Mol Sci 2023, 24 (9). DOI: 10.3390/ijms24098415 From NLM Medline.

თანმიმდევრობა:

ალა-გლუ-ასპ

CAS:

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მ.ვ:

333.297 გ/მოლ

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