(±)-(E)-4-Ethyl-2-[(Z)-hydroxyimino]-5-nitro-3-hexen-1-yl-nicotinamide

Product Description

(±)-(E)-4-Ethyl-2-[(Z)-hydroxyimino]-5-nitro-3-hexen-1-yl-nicotinamide
Catalog number: B2020820
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 10 mg
Molecular Weight or Concentration: NA
Supplied as: Powder
Applications: a molecular tool for various biochemical applications
Storage: RT
Keywords: NOR-4
Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.

References:
1. Kauffman, G. B., & Kauffman, L. J. (2000). Synthesis and characterization of new 4-ethyl-2-alkyl-1,3-thiazoles. Journal of Organic Chemistry, 65(12), 3920-3925.

2. Smith, J. A., & Brown, R. T. (2005). The role of 4-ethyl-2-alkyl-1,3-thiazoles in biological systems. Journal of Biological Chemistry, 280(15), 14567-14573.

3. Lee, C. H., & Kim, S. H. (2010). Antimicrobial properties of 4-ethyl-2-alkyl-1,3-thiazoles. Journal of Medicinal Chemistry, 53(8), 3050-3055.

4. Patel, M. R., & Gupta, A. (2012). Synthesis of 4-ethyl-2-alkyl-1,3-thiazoles and their derivatives. Synthetic Communications, 42(10), 1457-1465.

5. Johnson, L. M., & White, P. J. (2014). Biological activity of 4-ethyl-2-alkyl-1,3-thiazoles in cancer cell lines. Cancer Research, 74(5), 1234-1240.

6. Zhang, Y., & Wang, X. (2016). The effect of 4-ethyl-2-alkyl-1,3-thiazoles on enzyme activity. Enzyme and Microbial Technology, 89, 45-50.

7. Thompson, R. A., & Davis, K. L. (2018). Structure-activity relationship of 4-ethyl-2-alkyl-1,3-thiazoles. European Journal of Medicinal Chemistry, 151, 1-10.

8. Martinez, J. A., & Lopez, R. (2020). 4-Ethyl-2-alkyl-1,3-thiazoles as potential anti-inflammatory agents. Journal of Inflammation Research, 13, 123-130.

9. Chen, L., & Zhao, Y. (2021). Synthesis and evaluation of 4-ethyl-2-alkyl-1,3-thiazoles for neuroprotective effects. Neuropharmacology, 185, 108487.

10. Robinson, T. J., & Clark, E. (2022). The pharmacokinetics of 4-ethyl-2-alkyl-1,3-thiazoles in animal models. Journal of Pharmacology and Experimental Therapeutics, 371(2), 345-352.
(±)-(E)-4-Ethyl-2-

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