Molecular structure of 4-Nitrobenzyl chloride, CAS Number: 100-14-1
4-Nitrobenzyl chloride (CAS 100-14-1)
Alternate Names:
alpha-Chloro-4-nitrotoluene
Application:
4-Nitrobenzyl chloride is a GST Substrate
CAS Number:
100-14-1
Molecular Weight:
171.58
Molecular Formula:
C7H6ClNO2
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
4-Nitrobenzyl chloride is a GST Substrate.
4-Nitrobenzyl chloride (CAS 100-14-1) References
- Fast product formation and slow product release are important features in a hysteretic reaction mechanism of glutathione transferase T2-2. | Jemth, P. and Mannervik, B. 1999. Biochemistry. 38: 9982-91. PMID: 10433705
- Protease inhibitors. Part 12. Synthesis of potent matrix metalloproteinase and bacterial collagenase inhibitors incorporating sulfonylated N-4-nitrobenzyl-beta-alanine hydroxamate moieties. | Scozzafava, A., et al. 2000. Eur J Pharm Sci. 11: 69-79. PMID: 10913755
- Purification and characterization of a glutathione S-transferase from the fungus Cunninghamella elegans. | Cha, CJ., et al. 2001. FEMS Microbiol Lett. 203: 257-61. PMID: 11583857
- Identification and expression of a novel class of glutathione-S-transferase from amphioxus Branchiostoma belcheri with implications to the origin of vertebrate liver. | Fan, C., et al. 2007. Int J Biochem Cell Biol. 39: 450-61. PMID: 17084657
- Bioaccumulation kinetics of organic xenobiotic pollutants in the freshwater invertebrate Gammarus pulex modeled with prediction intervals. | Ashauer, R., et al. 2010. Environ Toxicol Chem. 29: 1625-36. PMID: 20821614
- Acute toxicity of organic chemicals to Gammarus pulex correlates with sensitivity of Daphnia magna across most modes of action. | Ashauer, R., et al. 2011. Aquat Toxicol. 103: 38-45. PMID: 21392493
- Significance of xenobiotic metabolism for bioaccumulation kinetics of organic chemicals in Gammarus pulex. | Ashauer, R., et al. 2012. Environ Sci Technol. 46: 3498-508. PMID: 22321051
- Hydrolysis of S-aryl-cysteinylglycine conjugates catalyzed by porcine kidney cortex membrane dipeptidase. | Poon, JC. and Josephy, PD. 2012. Xenobiotica. 42: 1178-86. PMID: 22742779
- Identification and functional characterization of an epsilon glutathione S-transferase from the beet armyworm (Spodoptera exigua). | Wan, H., et al. 2016. Pestic Biochem Physiol. 132: 81-8. PMID: 27521917
- Toxic Mixtures in Time-The Sequence Makes the Poison. | Ashauer, R., et al. 2017. Environ Sci Technol. 51: 3084-3092. PMID: 28177231
- [Molecular characteristics of two Phi glutathione S-transferases in Selaginella moellendorffii]. | Zhang, Y., et al. 2016. Sheng Wu Gong Cheng Xue Bao. 32: 927-936. PMID: 29019214
- Effects of Substrate-Binding Site Residues on the Biochemical Properties of a Tau Class Glutathione S-Transferase from Oryza sativa. | Yang, X., et al. 2019. Genes (Basel). 11: PMID: 31878175
- Target-Site Mutations and Glutathione S-Transferases Are Associated with Acequinocyl and Pyridaben Resistance in the Two-Spotted Spider Mite Tetranychus urticae (Acari: Tetranychidae). | Choi, J., et al. 2020. Insects. 11: PMID: 32784738
- Evidence that human class Theta glutathione S-transferase T1-1 can catalyse the activation of dichloromethane, a liver and lung carcinogen in the mouse. Comparison of the tissue distribution of GST T1-1 with that of classes Alpha, Mu and Pi GST in human. | Sherratt, PJ., et al. 1997. Biochem J. 326 (Pt 3): 837-46. PMID: 9307035
Substrate of:
GST.Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
4-Nitrobenzyl chloride, 25 g | sc-254711 | 25 g | $56.00 |