34433-31-3 Purity
98%
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Specification
Chronic administration of 4-iodopyrazole provides a unique experimental approach to probe ethanol metabolism in vivo. In controlled mouse studies, the compound was delivered continuously via drinking water, enabling sustained systemic exposure. Unlike acute dosing, which primarily reduced alcohol dehydrogenase activity without altering aldehyde dehydrogenase, chronic ingestion resulted in a marked suppression of hepatic aldehyde dehydrogenase activity. This metabolic blockade was validated by the accumulation of acetaldehyde in blood following ethanol challenge, confirming impaired enzymatic clearance. Experimental protocols demonstrated reproducibility across multiple treatment cycles, with enzymatic assays from excised livers confirming activity modulation. Additionally, behavioral studies revealed reduced ethanol preference in C57BL mice, directly correlating biochemical inhibition with altered consumption behavior. These findings position 4-iodopyrazole as a valuable tool for mechanistic investigations of alcohol metabolism and aldehyde dehydrogenase-dependent pathways in pharmacological research.
The molecular formula of 4-iodopyrazole is C3H3IN2.
The molecular weight of 4-iodopyrazole is 193.97 g/mol.
Some synonyms for 4-iodopyrazole include 4-Iodo-1H-pyrazole and 4-iodo pyrazole.
The IUPAC name for 4-iodopyrazole is 4-iodo-1H-pyrazole.
The InChIKey of 4-iodopyrazole is LLNQWPTUJJYTTE-UHFFFAOYSA-N.
The CAS number of 4-iodopyrazole is 3469-69-0.
4-iodopyrazole has 1 hydrogen bond donor count.
The topological polar surface area of 4-iodopyrazole is 28.7Ų.
Yes, 4-iodopyrazole is a canonicalized compound.
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