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Loretin

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  • Inhibitors & Agonists
    6
    TargetMol | Inhibitors_Agonists
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    TargetMol | Natural_Products
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    TargetMol | Inhibitors_Agonists
Chiniofon
quiniophen, Loretin, Ferron, 8-hydroxy-7-iodo-5-quinolinesulfonate
T9549547-91-1
Chiniofon (Ferron), a halogenated 8-hydroxyquinoline, is used as an antiamebic drug. This type of anti-amebic drug exerts an anti-amebic effect by inhibiting intestinal commensal bacteria and affects amoebic dysentery, but has no effect on extra-intestinal amoebic parasites.
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Phloretin
RJC 02792, NSC 407292, Dihydronaringenin
T292460-82-2
Phloretin (NSC-407292) is a well-known inhibitor of eukaryotic urea transporters, blocks VacA-mediated urea and ion transport. Phloretin is a dihydrochalcone, a type of natural phenols. It can be found in apple tree leaves and the Manchurian apricot. It promotes potent antioxidative activities in peroxynitrite scavenging and the inhibition of lipid peroxidation. It has been found to inhibit the growth of several cancer cells and induce apoptosis of B16 melanoma and HL60 human leukemia cells.
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TargetMol | Citations Cited
Phloretin 3',5'-Di-C-glucoside
T124963
Phloretin 3',5'-Di-C-glucoside is a useful organic compound for research related to life sciences and the catalog number is T124963.
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4'-O-(6-O-Feruloylglucopyranosyl)phloretin
T1253892058292-99-0
4'-O-(6-O-Feruloylglucopyranosyl)phloretin is a useful organic compound for research related to life sciences. The catalog number is T125389 and the CAS number is 2058292-99-0.
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2′-O-Methylphloretin
T83401111316-17-7
2′-O-Methylphloretin (compound 3), a flavonoid derivative, extracted from Melodorum siamensis leaves, has demonstrated the ability to inhibit tumor cell line replication [1].
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4′-O-(β-D-2″,3″,4″,6″-Tetraacetyl-glucopyranosyl)-4-nitrophloretin
TSW-0056182628-87-3
4′-O-(β-D-2″,3″,4″,6″-Tetraacetyl-glucopyranosyl)-4-nitrophloretin is a biochemical reagent employed in glycoscience research. The study of glycoscience involves the examination of carbohydrate structures, synthesis, biological roles, and evolution. This field encompasses carbohydrate chemistry, the enzymology of glycan formation and degradation, protein-glycan interactions, and the functions of glycans in biological systems. It is intricately linked with fundamental research, biomedicine, and biotechnology.
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