An internal standard for the quantification of camostat
Related Products
Unlabeled Version(s)
16018Camostat (mesylate)
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Camostat-d6 (hydrochloride)

Item No. 30984

Technical Information
Formal Name
4-[[4-[(aminoiminomethyl)amino]benzoyl]oxy]-benzeneacetic acid, 2-(di(methyl-d3)amino)-2-oxoethyl ester, monohydrochloride
CAS Number
2930627-60-2
Molecular Formula
C20H16D6N4O5 • HCl
Formula Weight
Purity
≥99% deuterated forms (d1-d6)
A solid
DMSO: SolubleMethanol: SolubleWater: Soluble
SMILES
NC(NC1=CC=C(C(OC2=CC=C(CC(OCC(N(C([2H])([2H])[2H])C([2H])([2H])[2H])=O)=O)C=C2)=O)C=C1)=N.Cl
InChi Code
InChI=1S/C20H22N4O5.ClH/c1-24(2)17(25)12-28-18(26)11-13-3-9-16(10-4-13)29-19(27)14-5-7-15(8-6-14)23-20(21)22;/h3-10H,11-12H2,1-2H3,(H4,21,22,23);1H/i1D3,2D3;
InChi Key
LJMUBVFXGFAKKZ-TXHXQZCNSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Camostat-d6 is intended for use as an internal standard for the quantification of camostat (Item No. 16018) by GC- or LC-MS. Camostat (50 µM) inhibits entry of vesicular stomatitis virus (VSV) particles pseudotyped with severe acute respiratory syndrome coronavirus (SARS-CoV) and SARS-CoV-2 spike glycoprotein in Calu-3 cells and primary human lung epithelial cells.1 It reduces the number of SARS-CoV-2 genomic equivalents, a marker of infection, in Calu-3 cells. Camostat inhibits sodium channel function in human airway epithelial cells (IC50 = 50 nM) and enhances mucociliary clearance in sheep.2 Dietary administration of camostat (1 mg/kg) inhibits the production of TNF-α and chemokine (C-C motif) ligand 2 (CCL2) by monocytes, as well as proliferation of pancreatic stellate cells in a rat model of pancreatic fibrosis.3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Hoffmann, M., Kleine-Weber, H., Schroeder, S., et alSARS-CoV-2 cell entry depends on ACE2 and TMPRSS2 and is blocked by a clinically proven protease inhibitor. Cell 181(2), 271-280 (2020).

    2. Maianti, J.P., McFedries, A., Foda, Z.H., et alAnti-diabetic activity of insulin-degrading enzyme inhibitors mediated by multiple hormones. Nature 511(7507), 94-98 (2014).

    3. Gibo, J., Ito, T., Kawabe, K., et alCamostat mesilate attenuates pancreatic fibrosis via inhibition of monocytes and pancreatic stellate cells activity. Lab Invest. 85(1), 75-89 (2005).