554-52-9
Chemical Structure
3-Methoxytyramine
Synonym(s): 3-O-methyl Dopamine
- CAS No.: 554-52-9
- Formula:C9H13NO2
- Molecular Weight:167.21
IUPAC Name: 4-(2-aminoethyl)-2-methoxyphenol
InChIKey: DIVQKHQLANKJQO-UHFFFAOYSA-N
SMILES: OC1=CC=C(CCN)C=C1OC
Biological Activity: 3-Methoxytyramine, a well known extracellular metabolite of 3-hydroxytyramine/dopamine, is a neuromodulator.
| Cat. No. | Nom du produit | Pureté | Description | Pricing | |||||||||||||||||||
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3-Methoxytyramine | 99.07% | 3-Methoxytyramine, a well known extracellular metabolite of 3-hydroxytyramine/dopamine, is a neuromodulator. | ||||||||||||||||||||
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3-Methoxytyramine (Standard) | 93.67% | 3-Methoxytyramine (Standard) is the analytical standard of 3-Methoxytyramine. This product is intended for research and analytical applications. 3-Methoxytyramine, a well known extracellular metabolite of 3-hydroxytyramine/dopamine, is a neuromodulator. | ||||||||||||||||||||
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3-Methoxytyramine hydrochloride | 98.23% | 3-Methoxytyramine hydrochloride is an metabolite of dopamine which can activate trace amine associated receptor 1 (TAAR1). | ||||||||||||||||||||
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3-Methoxyphenylethylamine | 99.39% | 3-Methoxyphenylethylamine is an organic compound that is used as an intermediate for pharmaceuticals, dyestuffs, and liquid crystal materials. | ||||||||||||||||||||
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Dopamine | 98.56% | Dopamine is a catecholamine neurotransmitter that is produced in the substantia nigra, ventral tegmental area, and hypothalamus of the brain. Dopamine plays several important roles in the brain and body. Dopamine acts through D2 dopamine receptors to induce endocytosis of VEGFR2, which is critical for promoting angiogenesis. | ||||||||||||||||||||
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Homovanillyl alcohol (Standard) | ≥98% | Homovanillyl alcohol (Standard) is the analytical standard of Homovanillyl alcohol (HY-N7513). This product is intended for research and analytical applications. Homovanillyl alcohol is a biological metabolite of Hydroxytyrosol, and belongs to the class of phenolic organic compounds. Homovanillyl alcohol alleviates cellular oxidative stress and inflammatory responses by scavenging free radicals, inhibiting the phosphorylation of the p38 and JNK MAP kinase pathways, as well as suppressing NF-κB-driven transcription and nuclear translocation. It can be used in studies related to cardiovascular diseases and allergic asthma. | ||||||||||||||||||||
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Vanillylamine hydrochloride | 99.78% | Vanillylamine hydrochloride is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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Dihydroconiferyl alcohol | 99.78% | Dihydroconiferyl alcohol is a cell division factor. Dihydroconiferyl alcohol can be isolated from the American sycamore (Acer pseudoplatanus L.). Dihydroconiferyl alcohol inhibits the degradation of Indole-3-acetic acid (HY-18569). Dihydroconiferyl alcohol can stimulate the growth of soybean and tobacco callus tissue and synergistically enhance Indole-3-acetic acid-induced hypocotyl elongation in cucumber. Dihydroconiferyl alcohol can be used in the research of plant growth regulation. | ||||||||||||||||||||
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4-O-Methyldopamine hydrochloride | 99.46% | 4-O-Methyldopamine hydrochloride is a catecholamine compound that has an inhibitory effect on dihydropteridine reductase. | ||||||||||||||||||||
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Vanillylamine | 98.05% | Vanillylamine is an immediate precursor for capsaicinoids. Vanillylamine is a derivative of Vanillin (HY-N0098) is synthesized through a transaminase reaction in the phenylpropanoid pathway of capsaicinoid synthesis. Vanillylamine significantly alleviates myelosuppression caused by abdominal and pelvic tumor chemotherapy. | ||||||||||||||||||||
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4-Propylguaiacol | 99.95% | 4-Propylguaiacol is a phenolic lignin monomer. 4-Propylguaiacol can be isolated from plants of the Quercus genus. 4-Propylguaiacol can be used in the research of atopic dermatitis. | ||||||||||||||||||||
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4-O-Methyldopamine (Standard) | ≥98% | 4-O-Methyldopamine (Standard) is the analytical standard of 4-O-Methyldopamine. This product is intended for research and analytical applications. | ||||||||||||||||||||
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