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Diethyl 1,4-dihydro-2,4,6-trimethyl-3,5-pyridinedicarboxylate blocks heme synthesis and prevents hepatic heme oxygenase-1 induction. It contributes to the formation of Mallory bodies in the liver. Diethyl 1,4-dihydro-2,4,6-trimethyl-3,5-pyridinedicarboxylate plays a role in studying diverse aspects such as enzyme kinetics, metabolic pathways, and cell signaling. Furthermore, it serves as useful for investigating the intricate structure and function of proteins and nucleic acids. Diethyl 1,4-dihydro-2,4,6-trimethyl-3,5-pyridinedicarboxylate effectively targets enzymes like protein kinases and phosphatases by binding to their active sites, impeding substrate binding and hindering enzymatic catalysis. Additionally, Diethyl 1,4-dihydro-2,4,6-trimethyl-3,5-pyridinedicarboxylate exhibits the ability to interact with other proteins and nucleic acids, potentially disrupting their structure and impinging on their functionality.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Diethyl 1,4-dihydro-2,4,6-trimethyl-3,5-pyridinedicarboxylate, 25 g | sc-239721 | 25 g | $151.00 |