KLK6-IN-2
KLK6-IN-2 is a reversible non-covalent and selective KLK6 inhibitor, with an IC50 of 2.1 μM against hKLK6. KLK6-IN-2 acts as a reversible competitive inhibitor of boar Spermatozoa acrosin, with a Ki of 2.6 μM against porcine acrosin. KLK6-IN-2 exhibits trypanocidal activity against Trypanosoma brucei rhodesiense, with an IC50 of 3.71 μM.
For research use only. We do not sell to patients.
- CAS No.: 57323-76-9
- Formula: C14H14N2O
- Molecular Weight:226.27
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
All Parasite Isoforms
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Biological Activity
Description
IC50 & Target
[1]|
Trypanosoma |
KLK6 2.1 μM (IC50) |
In Vitro
KLK6-IN-2 (Compound 69) (range of concentrations; 15 min) acts as a reversible, competitive inhibitor of recombinant human KLK6 with an IC50 of 2.1 μM, a ligand efficiency of 0.43, and a Ki of 7.5 μM[1].
KLK6-IN-2 shows a favorable selectivity window for KLK6 over most tested kallikreins and trypsin-like serine proteases, with ~4- to ~9-fold selectivity relative to KLK5, KLK14, plasmin, and matriptase, but similar potency toward trypsin 3[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.
Chemical Information
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CAS No. 57323-76-9
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Molecular Weight 226.27
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Formula C14H14N2O
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SMILES
NC(C1=CC=C(COC2=CC=CC=C2)C=C1)=N
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Protocols
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Cell Cytotoxicity Assay
Cytotoxicity assays are usually based on the assessment of cell membrane damage, which can also be indirectly detected by measuring cell viability. Detection methods include MTT assay, CKK-8 assay, LDH assay and ATP assay, etc.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)