KN-62

Catalog No.S7422 Batch:S742201

Print

Technical Data

Formula

C38H35N5O6S2
Molecular Weight 721.84 CAS No. 127191-97-3
Solubility (25°C)* In vitro DMSO 100 mg/mL (138.53 mM)
Water Insoluble
Ethanol Insoluble
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.
* Room temperature shipping (Stability testing shows this product can be shipped without any cooling measures.)

Preparing Stock Solutions

Biological Activity

Description KN-62 is a potent and specific inhibitor of Ca2+/calmodulin-dependent protein kinase II (CaMKII) with Ki of 0.9 μM; also a non-competitive antagonist of the purinergic receptor P2RX7 (IC50 = 15 nM). It is selective for CaMKII relative to PKA, PKC and MLCK, but inhibits CaMKI and CaMKIV equally well, The Ki value of KN-62 for CaMK V is 0.8 μM.
Targets
CaMKⅠ [5] CaMKⅣ [6] P2RX7 [8] CaMKⅤ [7] CaMKII [1]
0.8 μM(Ki) 0.9 μM(Ki)
In vitro KN-62 suppresses the A23187-induced autophosphorylation of Ca2+/CaM kinase in PC12 D cells. [1] KN-62 (10 μM) inhibits carbachol and potassium-stimulated insulin secretion from rat pancreatic islets. [2] KN-62 also inhibits growth of K562 cells and blocks cell cycle progression. [3]
In vivo KN-62 inhibits seizure-induced expression of brain-derived neurotrophic factor mRNA in adult rat brain. [4]

Protocol (from reference)

Kinase Assay:

[1]
  • Kinase assay

    Total kinase activity of CaMKII, determined in a standard 2 min assay (100 μL), contained 35 mM HEPES, 10 mM MgCl2, 1 mM CaCl2, 10 μg of chicken gizzard myosin 20-kD light chain, 0.1 μM calmodulin, and 10 μM [γ-33]ATP at 30 °C. The kinase reaction is halted by adding 1 mL of 10% trichloroacetic acid.

Cell Assay:

[3]
  • Cell lines

    K562 cells

  • Concentrations

    10 μM

  • Incubation Time

    48 hours

  • Method

    For cell growth analysis, K562 cells are plated in a 3-cm dish with 5 mL of culture medium containing various concentration of KN-62. After two days in these condition cell numbers are counted.
Animal Study:

[4]
  • Animal Models

    Sprague Dawley Rats

  • Dosages

    2 pmol

  • Administration

    i.c.v.

Customer Product Validation

Data from [Data independently produced by , , Front Cell Neurosci, 2017, https://doi.org/10.3389/fncel.2017.00281]

Selleck's KN-62 has been cited by 19 publications

Selective nitration of Hsp90 acts as a metabolic switch promoting tumor cell proliferation [ Redox Biol, 2024, 75:103249] PubMed: 38945076
Hydrogen Sulfide Exerted a Pro-Angiogenic Role by Promoting the Phosphorylation of VEGFR2 at Tyr797 and Ser799 Sites in Hypoxia-Reoxygenation Injury [ Int J Mol Sci, 2024, 25(8)4340] PubMed: 38673925
Single-cell transcriptomics of NRAS-mutated melanoma transitioning to drug resistance reveals P2RX7 as an indicator of early drug response [ Cell Rep, 2023, 42(7):112696] PubMed: 37379213
Capsaicin ameliorates intermittent high glucose-mediated endothelial senescence via the TRPV1/SIRT1 pathway [ Phytomedicine, 2022, 100:154081] PubMed: 35405615
Non-catalytic allostery in α-TAT1 by a phospho-switch drives dynamic microtubule acetylation [ J Cell Biol, 2022, 221-11e202202100] PubMed: 36222836
Terfenadine resensitizes doxorubicin activity in drug-resistant ovarian cancer cells via an inhibition of CaMKII/CREB1 mediated ABCB1 expression [ Front Oncol, 2022, 12:1068443] PubMed: 36439493
Derivation and Characterization of Murine and Amphibian Müller Glia Cell Lines [ Transl Vis Sci Technol, 2022, 11(4):4] PubMed: 35377941
TLR4 signalling via Piezo1 engages and enhances the macrophage mediated host response during bacterial infection [ Nat Commun, 2021, 12(1):3519] PubMed: 34112781
CAMK2/CaMKII activates MLKL in short-term starvation to facilitate autophagic flux [ Autophagy, 2021, 1-19] PubMed: 34282994
A phospho-regulated ensemble signal motif of α-TAT1 drives dynamic microtubule 1 acetylation 2 [ HAL open science, 2021, 10.1101/2020.09.23.310235] PubMed: None

RETURN POLICY
Selleck Chemical’s Unconditional Return Policy ensures a smooth online shopping experience for our customers. If you are in any way unsatisfied with your purchase, you may return any item(s) within 7 days of receiving it. In the event of product quality issues, either protocol related or product related problems, you may return any item(s) within 365 days from the original purchase date. Please follow the instructions below when returning products.

SHIPPING AND STORAGE
Selleck products are transported at room temperature. If you receive the product at room temperature, please rest assured, the Selleck Quality Inspection Department has conducted experiments to verify that the normal temperature placement of one month will not affect the biological activity of powder products. After collecting, please store the product according to the requirements described in the datasheet. Most Selleck products are stable under the recommended conditions.

NOT FOR HUMAN, VETERINARY DIAGNOSTIC OR THERAPEUTIC USE.