4-Iodo-2-methylphenol (CAS 60577-30-2)
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4-Iodo-2-methylphenol is a chemical compound that functions as a potent inhibitor of certain enzymatic processes. It exerts its mechanism of action by targeting and binding to the active site of the enzyme, thereby disrupting its normal function. This disruption ultimately leads to the inhibition of the enzyme′s catalytic activity, preventing the conversion of substrate molecules into products. 4-Iodo-2-methylphenol′s interaction with the enzyme at the molecular level interferes with the normal progression of biochemical pathways, making it useful for studying the specific roles of these enzymes in cellular processes. 4-Iodo-2-Methylphenol′s mechanism of action at the molecular level allows for the precise manipulation of enzymatic processes, offering insights into the fundamental biochemical processes that govern cellular function.
4-Iodo-2-methylphenol (CAS 60577-30-2) References
- Thermotropic and lyotropic liquid crystalline phases of rigid aromatic amphiphiles. | Kolbel, M., et al. 2000. Chemistry. 6: 3821-37. PMID: 11073253
- 4-(Pyrrolidinyl)methoxybenzoic acid derivatives as a potent, orally active VLA-4 antagonist. | Chiba, J., et al. 2006. Chem Pharm Bull (Tokyo). 54: 1515-29. PMID: 17077548
- Dimerization of dendrimeric lanthanide complexes: thermodynamic, thermal, and liquid-crystalline properties. | Jensen, TB., et al. 2010. Inorg Chem. 49: 8601-19. PMID: 20718488
- Selective peroxisome proliferator-activated receptor δ isosteric selenium agonists as potent anti-atherogenic agents in vivo. | Chin, J., et al. 2010. Bioorg Med Chem Lett. 20: 7239-42. PMID: 21074432
- Development of an enzyme-linked immunosorbent assay (ELISA) for residue analysis of the fungicide azoxystrobin in agricultural products. | Kondo, M., et al. 2012. J Agric Food Chem. 60: 904-11. PMID: 22224459
- Synthesis and biological evaluation of phosphonate analogues of nevirapine. | Parrish, J., et al. 2013. Bioorg Med Chem Lett. 23: 1493-7. PMID: 23375792
- Fundamental understanding of chemical processes in extreme ultraviolet resist materials. | Kostko, O., et al. 2018. J Chem Phys. 149: 154305. PMID: 30342450
- Formation of Iodinated Disinfection Byproducts (I-DBPs) in Drinking Water: Emerging Concerns and Current Issues. | Dong, H., et al. 2019. Acc Chem Res. 52: 896-905. PMID: 30919613
- Application of (LC/)MS/MS precursor ion scan for evaluating the occurrence, formation and control of polar halogenated DBPs in disinfected waters: A review. | Yang, M., et al. 2019. Water Res. 158: 322-337. PMID: 31051377
- High Sensitivity Resists for EUV Lithography: A Review of Material Design Strategies and Performance Results. | Manouras, T. and Argitis, P. 2020. Nanomaterials (Basel). 10: PMID: 32823865
- Occurrence, influencing factors, toxicity, regulations, and abatement approaches for disinfection by-products in chlorinated drinking water: A comprehensive review. | Kali, S., et al. 2021. Environ Pollut. 281: 116950. PMID: 33819670
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
4-Iodo-2-methylphenol, 5 g | sc-232779 | 5 g | $92.00 |