Metabolomics Analysis
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• 8-Aminooctanoic Acid Analysis Service
8-Aminooctanoic acid, also known as 8-amino-caprylic acid, is an organic compound featuring an aliphatic chain with eight carbon atoms and an amino group (-NH₂) attached to the eighth position, along with a carboxylic acid group (-COOH) at the first position. This structure classifies it as an amino acid, specifically a long-chain aliphatic amino acid. The amino group imparts basic properties, while the carboxylic acid group confers acidity, allowing the molecule to participate in both acid-base interaction
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• Quinoline-2-Carboxylic Acid Analysis Service
Quinoline-2-carboxylic acid, also known as quinaldic acid, is an organic compound featuring a quinoline ring system with a carboxylic acid group (-COOH) attached at the second position. Quinoline is an aromatic heterocyclic compound with a structure consisting of a benzene ring fused to a pyridine ring. The carboxylic acid group at the 2-position increases polarity and has the potential to form hydrogen bonds, thereby affecting its chemical reactivity and biological activity. The aromatic nature of quinolin
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• 3-(2-Hydroxyphenyl)Propanoic Acid Analysis Service
3-(2-Hydroxyphenyl)propanoic acid, also known as homovanillic acid, is an organic compound characterized by a phenyl ring with a hydroxyl group (-OH) at the ortho position (2-position) and a three-carbon propanoic acid chain attached to the phenyl ring. This structure classifies it as a hydroxy-substituted aromatic acid. The hydroxyl group imparts hydrophilic properties and potential for hydrogen bonding, while the carboxylic acid group confers acidity, enabling the molecule to participate in a range of che
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Ala-Phe is a dipeptide composed of the amino acids alanine (Ala) and phenylalanine (Phe). Alanine is a non-polar, aliphatic amino acid with a simple methyl side chain, while phenylalanine contains an aromatic side chain with a phenyl group. The unique molecular structure formed by the peptide bond between the carboxyl group of alanine and the amino group of phenylalanine retains the hydrophobic characteristics of alanine and the aromatic properties of phenylalanine. Due to its constituent components, Ala-Ph
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Leu-Ala is a dipeptide composed of two amino acids: leucine (Leu) and alanine (Ala). In this dipeptide, the carboxyl group of leucine is linked to the amino group of alanine through a peptide bond. Leu-Ala combines the hydrophobic nature of leucine, a branched-chain amino acid, with the simpler, smaller structure of alanine, an amino acid that plays a key role in glucose metabolism and protein synthesis.
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Aniline is an aromatic amine with the molecular formula C₆H₇N. It consists of a benzene ring attached to an amino group (-NH₂), which contributes to its aromaticity and electron-rich nature. The lone pair of electrons on the nitrogen atom can participate in the π-electron cloud of the benzene ring, slightly decreasing the basicity of the amino group while making aniline more reactive toward electrophilic substitution reactions compared to benzene. Due to its aromatic structure and electron-donating properti
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• Ritalinic Acid Analysis Service
Ritalinic acid is a monocarboxylic acid that is phenylacetic acid substituted by a piperidin-2-yl group at position 2. It is a metabolite of the drug methylphenidate. It has a molecular formula of C₁₃H₁₇NO₂ and a molecular weight of 2219.28 g/mol. As the primary active metabolite of methylphenidate, ritalinic acid is directly involved in the drug’s mechanism by contributing to its pharmacological effects. The accurate quantification of ritalinic acid and its metabolites in biological fluids, such as serum a
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Oxypurinol is a pyrazolopyrimidine that is 4,5,6,7-tetrahydro-H-pyrazolo[3,4-d]pyrimidine substituted by oxo groups at positions 4 and 6, with a molecular formula of C₅H₄N₄O₂ and a molecular weight of 152.11 g/mol. Oxypurinol is the primary active metabolite of allopurinol, directly involved in inhibiting xanthine oxidase (XO), thereby reducing uric acid production. Accurate quantification of oxypurinol and its metabolites in serum and urine is essential for evaluating the therapeutic efficacy of allopurino
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• 16α-Hydroxy Estrone Analysis Service
16α-Hydroxy estrone is a steroid compound with an aromatic ring structure and is a hydroxylated derivative of estrone (E1) at the 16th carbon position. Its structure contains a phenolic hydroxyl group (-OH) and a hydroxyl group at the 16th position, giving it high polarity and biological activity. 16α-Hydroxy estrone has strong estrogenic activity and is more potent than estrone. It can bind to estrogen receptors (ERα and ERβ), thereby exerting its hormonal effects. Its high estrogenic activity makes it pla
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• H-Phe-Trp-OH Analysis Service
G: H-Phe-Trp-OH Analysis Service T: H-Phe-Trp-OH Analysis Service | MtoZ Biolabs A: h-phe-trp-oh-analysis-service Figure 1. The Structure of H-Phe-Trp-OH MtoZ Biolabs offers a state-of-the-art H-Phe-Trp-OH Analysis Service, utilizing our advanced liquid chromatography-mass spectrometry (LC-MS) platform and experienced metabolomics team. Our service ensures a comprehensive H-Phe-Trp-OH analysis, guaranteeing high sensitivity and precision. Analysis Workflow Service Advantages Applications Identifi......
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