Metabolomics Analysis
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Phillyrin is a natural compound extracted from plants, primarily found in *Forsythia suspensa*, a plant commonly used in traditional medicine. It is a flavonoid glycoside and belongs to the class of phenylpropanoid glycosides. Phillyrin has attracted considerable attention due to its diverse biological activities, including potential therapeutic applications in antioxidant, anti-inflammatory, and antiviral fields. The analysis of Phillyrin is typically conducted using high-performance liquid chromatography
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• Taxifolin-7-O-Rhamnoside Analysis Service
Taxifolin-7-O-rhamnoside is a flavonoid glycoside predominantly found in various plants, including those from the family Pinaceae. This compound is characterized by a flavonoid core, taxifolin, which is linked to a rhamnose sugar molecule at the 7-O position. Taxifolin-7-O-rhamnoside exhibits a variety of bioactivities, such as antioxidant, anti-inflammatory, anti-cancer, and cardiovascular protective effects. Its antioxidant properties help in scavenging free radicals, thus preventing cellular damage and c
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• Persicogenin Analysis Service
Persicogenin is a naturally occurring flavonoid compound, specifically a flavonol, extracted from certain plants such as Silybum marianum (milk thistle) and Myrtaceae family plants. Persicogenin belongs to the polyhydroxyflavonoid compounds, with a chemical structure that typically includes two benzene rings (A and B rings) and a three-carbon bridge (C ring) connected through an oxidized pyran ring, bearing multiple hydroxyl (-OH) groups. These groups determine its bioactivity and antioxidant capacity. Pers
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• Eriodictyol Analysis Service
Eriodictyol is a natural flavonoid compound that belongs to the flavanone family, commonly found in citrus fruits and certain plants, such as lemons, oranges, and some traditional herbs. The chemical structure of Eriodictyol is 2-(3,4-dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-4-benzopyrone. It possesses a typical flavonoid structure, including two aromatic rings and a heterocyclic benzopyran ring. The molecular formula of Eriodictyol is C15H12O6. It has poor solubility in water but dissolves well in organi
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• Xanthohumol Analysis Service
Xanthohumol is a natural flavonoid compound that belongs to the chalcone family, commonly found in hops (Humulus lupulus) and certain other plants. The chemical structure of xanthohumol is (E)-1-(2,4-Dihydroxy-6-methoxy-3-(3-methylbut-2-en-1-yl)phenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one. It possesses a typical chalcone structure, including two aromatic rings connected by a three-carbon α,β-unsaturated carbonyl system. The molecular formula of xanthohumol is C21H22O5. It has limited solubility in water but d
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Phlorizin is a natural compound belonging to the dihydrochalcone class, which is a type of flavonoid. Phlorizin is primarily found in the bark, roots, and leaves of apple trees (Malus species) and other fruit trees such as pear and cherry trees. Phlorizin is a glucoside compound, consisting of a glucose molecule linked to a dihydrochalcone aglycone, specifically phloretin. Its molecular formula is C21H24O10. Phlorizin exhibits various bioactivities and pharmacological effects, such as anti-diabetic effects,
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Nobiletin is a polymethoxylated flavonoid widely found in citrus fruits, predominantly present in the peels of citrus fruits such as oranges, grapefruits, and tangerines. Its chemical structure is characterized by a flavonoid core with multiple methoxy groups, typically positioned at the 5, 6, 7, 8, 3′ and 4′ locations. Nobiletin has been proven to possess various bioactivities, including anti-cancer, anti-inflammatory, antioxidant, neuroprotective, anti-obesity, anti-diabetic, and cardiovascular protective
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• 3-Indole Acetamide Analysis Service
3-Indole Acetamide (IAM) is an important intermediate in the biosynthesis of indole-3-acetic acid (IAA). IAM consists of an indole ring attached to an acetamide group, making it a key precursor in the tryptophan-dependent pathway of IAA biosynthesis. The metabolic conversion of tryptophan (Trp) to IAA involves several enzymatic steps, with IAM serving as a pivotal intermediate. The pathway begins with the conversion of Trp to IAM by the enzyme tryptophan monooxygenase.
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• Indole-3-acetyl-L-tryptophan Analysis Service
Indole-3-acetyl-L-tryptophan (IAA-Trp) is an indole-3-acetic acid (IAA) conjugate with essential amino acid tryptophan. It is known to play a crucial role in the regulation of plant growth and development, acting as a storage form of the primary auxin, IAA. Despite its significance in plant physiology, IAA-Trp is a relatively under-studied compound due to its low abundance and the complexity of its analysis.
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• Indole-3-acetyl-L-phenylalanine Methyl Ester Analysis Service
Indole-3-acetyl-L-phenylalanine Methyl Ester is a complex organic compound that combines the bioactive indole ring with an acetyl group, L-phenylalanine, and a methyl ester. While specific metabolic pathways for Indole-3-acetyl-L-phenylalanine Methyl Ester are not as extensively documented as those for simpler indole derivatives like indole-3-acetic acid (IAA), it has crucial roles in plant physiology, particularly in the growth and development processes.
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