An inhibitor of LTA4 hydrolase
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Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.

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ARM1

Item No. 15865

Technical Information
Formal Name
4-[4-(phenylmethyl)phenyl]-2-thiazolamine
CAS Number
68729-05-5
Molecular Formula
C16H16N2S
Formula Weight
Purity
≥95%
A crystalline solid
DMF: 15 mg/mlDMF:PBS(pH 7.2)(1:6): 0.1 mg/mlDMSO: 10 mg/mlEthanol: 1mg/ml
λmax
236, 285, 344 nm
SMILES
NC(N1)=SC=C1C(C=C2)=CC=C2CC3=CC=CC=C3
InChi Code
InChI=1S/C16H16N2S/c17-16-18-15(11-19-16)14-8-6-13(7-9-14)10-12-4-2-1-3-5-12/h1-9,11,18-19H,10,17H2
InChi Key
CEXYUVBVAHGQJI-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    ARM1 is a thiazolamine that inhibits LTB4 synthesis in human neutrophils (IC50 = ~0.5 µM) and conversion of LTA4 to LTB4 by purified LTA4 hydrolase (Ki = 2.3 µM).1 ARM1 does not significantly affect the hydrolysis of Pro-Gly-Pro by LTA4 hydrolase.1

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Stsiapanava, A., Olsson, U., Wan, M., et alBinding of Pro-Gly-Pro at the active site of leukotriene A4 hydrolase/aminopeptidase and development of an epoxide hydrolase selective inhibitor. Proc. Natl. Acad. Sci. USA 111(11), 4227-4232 (2014).