Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 148-51-6, is researched, Molecular C8H12ClNO2, about Inhibition of ruminal degradation of L-tryptophan to 3-methylindole in vitro, the main research direction is tryptophan metabolism pulmonary emphysema; antibiotic tryptophan metabolism emphysema.COA of Formula: C8H12ClNO2.
A closed-system, in vitro ruminal fermentation technique was used to screen 27 compounds for their ability to reduce the conversion of L-tryptophan (TRP) [73-22-3] to 3-methylindole (3MI) [83-34-1] in order to inhibit acute bovine pulmonary edema and emphysema. 20-Desoxysalinomycin [64003-50-5], X-206 [36505-48-3], chloral hydrate [302-17-0], nigericin [28380-24-7], lasalocid [11054-70-9], monensin [17090-79-8], narasin [55134-13-9], and salinomycin [53003-10-4] all reduced 3MI production by >80% at 5 μg/mL without reducing total volatile fatty acid production All of these compounds, except chloral hydrate, are polyether antibiotics. At least part of the inhibition due to monensin and narasin occurs at the level of TRP conversion to IAA [87-51-4].
If you want to learn more about this compound(5-(hydroxymethyl)-2,4-dimethylpyridin-3-ol hydrochloride)COA of Formula: C8H12ClNO2, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(148-51-6).
Reference:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia