Chemicals

Protein Kinase C (19-31) CAS NO.121545-65-1

<p>Protein Kinase C (19-31) is a synthetic 13-amino acid peptide inhibitor, also known as PKC(19-31) or the PKC pseudosubstrate inhibitor. With the sequence <strong>RFARKGALRQKNV</strong>, it corresponds to the pseudosubstrate regulatory domain of conventional Protein Kinase C (cPKC) isoforms (α, β, γ). This peptide mimics the substrate recognition sequence of PKC but contains an alanine (A) residue instead of a pho…

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TECHNICAL SPECIFICATIONS


Item
Specification
Product Name
Protein Kinase C (19-31)
CAS NO.
121545-65-1
Appearance
White to off-white lyophilized powder
Molecular Formula
C67H118N26O16
Molecular Weight
1543.84g/mol 
Purity (RP-HPLC)
≥ 95.0%
Solubility

Soluble in water, 0.1% TFA, or DMSO (up to 20 mg/mL)

Endotoxin≤1.0 EU/mg
Biological Activity
 Acts as a specific substrate for Protein Kinase C; can be used to measure PKC activity in kinase assays and to validate antibody specificity
Storage Conditions
Store at -20°C; stable for 24 months when desiccated. Avoid repeated freeze-thaw cycles.
Stock Location
Stock in USA
MOQ
1g


1.MECHANISM OF ACTION

PKC(19-31) functions as a competitive, substrate-specific inhibitor of conventional Protein Kinase C (cPKC) isoforms (α, βI, βII, γ). Its mechanism is based on molecular mimicry. Inactive cPKC is autoinhibited by its own pseudosubstrate domain, which occupies the catalytic cleft. Upon activation by diacylglycerol (DAG) and calcium, this inhibitory interaction is released.


    2.PRODUCT INDICATIONS

  • PKC(19-31) functions as a competitive, substrate-specific inhibitor of conventional Protein Kinase C (cPKC) isoforms (α, βI, βII, γ). Its mechanism is based on molecular mimicry. Inactive cPKC is autoinhibited by its own pseudosubstrate domain, which occupies the catalytic cleft. Upon activation by diacylglycerol (DAG) and calcium, this inhibitory interaction is released.

    3.CLINICAL EFFICACY OF PRODUCT

  • Research Tool Efficacy: It is highly effective and widely cited for its ability to potently and selectively inhibit cPKC activity in a wide range of cellular and biochemical experiments, providing clear mechanistic insights.

  • Therapeutic Target Validation: Research using this and similar inhibitors has been instrumental in establishing the pathological roles of specific PKC isoforms in diseases such as cancer, diabetic complications, cardiovascular diseases, and central nervous system disorders.

  • Drug Development Context: The pseudosubstrate region of PKC served as the conceptual blueprint for developing ATP-competitive small-molecule PKC inhibitors. While early pan-PKC inhibitors had toxicity issues, isoform-selective inhibitors (e.g., ruboxistaurin for diabetic retinopathy) have been developed and tested in clinical trials based on the foundational knowledge gained using tools like PKC(19-31).

  • Clinical Status: No peptide-based PKC inhibitor like PKC(19-31) is used clinically due to stability and delivery challenges. However, the pathway it helps to elucidate is targeted by several investigational drugs. Its value is entirely in preclinical target validation and mechanism elucidation.


  • 4.DELIVERY & SHIPPING

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    Shipping Methods 
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