331-39-5
331-39-5
Chemical Structure
Caffeic acid
- CAS No.: 331-39-5
- Formula:C9H8O4
- Molecular Weight:180.16
IUPAC Name: (E)-3-(3,4-dihydroxyphenyl)acrylic acid
InChIKey: QAIPRVGONGVQAS-DUXPYHPUSA-N
SMILES: O=C(O)/C=C/C1=CC=C(O)C(O)=C1
Biological Activity: Caffeic acid is an inhibitor of both TRPV1 ion channel and 5-Lipoxygenase (5-LO).
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Caffeic acid | 99.92% | Caffeic acid is an inhibitor of both TRPV1 ion channel and 5-Lipoxygenase (5-LO). | ||||||||||||||||||||
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Caffeic acid (Standard) | 99.29% | Caffeic acid (Standard) is the analytical standard of Caffeic acid. This product is intended for research and analytical applications. Caffeic acid is an inhibitor of both TRPV1 ion channel and 5-Lipoxygenase (5-LO). | ||||||||||||||||||||
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Caffeic acid-13C3 | 98.75% | Caffeic acid-13C3 is an 13C labeled caffeic acid. Caffeic acid is a phytonutrient belonging to the flavonoids. Caffeic acid and its derivatives, are potential antimicrobial agents, chronic infection induced by microbes such as bacteria, fungi, and viruses. | ||||||||||||||||||||
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trans-Caffeic acid (Standard) | 99.52% | trans-Caffeic acid (Standard) is the analytical standard of trans-Caffeic acid (HY-121231). This product is intended for research and analytical applications. trans-Caffeic acid is a hydroxycinnamic acid widely distributed in coffee, propolis, and Lamiaceae herbs. trans-Caffeic acid exhibits significant antioxidant and photoprotective activities, and can be used in cancer-related research. trans-Caffeic acid readily undergoes reversible isomerization to form its cis-isomer in protic solvents, under high temperature, ultraviolet radiation, and stress conditions. Binding of trans-Caffeic acid with aluminum, lead, or copper ions attenuates isomerization and inhibits the formation of vinylcatechol, while complexation with lead or copper ions also promotes the formation of aesculetin. | ||||||||||||||||||||
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trans-2,3-Dihydroxycinnamate | trans-2,3-Dihydroxycinnamate, a derivative of Cinnamic acid (HY-N0610A), is a metabolite of cannabidiol. trans-2,3-Dihydroxycinnamate possesses antioxidizing activity. | |||||||||||||||||||||
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Ferulic acid (Standard) | 99.98% | Ferulic acid (Standard) is the analytical standard of Ferulic acid. This product is intended for research and analytical applications. Ferulic acid is a novel fibroblast growth factor receptor 1 (FGFR1) inhibitor with IC50s of 3.78 and 12.5 μM for FGFR1 and FGFR2, respectively. | ||||||||||||||||||||
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Ferulic acid-13C3 | 98.3% | Ferulic acid-13C3 is the 13C-labeled Ferulic acid. Ferulic acid is a novel fibroblast growth factor receptor 1 (FGFR1) inhibitor with IC50s of 3.78 and 12.5 μM for FGFR1 and FGFR2, respectively. | ||||||||||||||||||||
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Isoferulic acid | 99.91% | Isoferulic acid (3-Hydroxy-4-methoxycinnamic acid) is an orally active cinnamic acid derivative. Isoferulic acid exhibits hypoglycemic, antiviral, and antioxidant activities. Isoferulic acid can also inhibit fructose- and glucose-mediated protein glycation. Isoferulic acid can be used in the research of diseases such as diabetes. | ||||||||||||||||||||
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(E)-Osmundacetone (Standard) | ≥98% | (E)-Osmundacetone (Standard) is the analytical standard of (E)-Osmundacetone (HY-N1966). This product is intended for research and analytical applications. (E)-Osmundacetone is an inhibitor of the MAPK pathway. (E)-Osmundacetone inhibits the activation of the MAPK signaling pathway and restores the expression of PPARα/ACOX1. (E)-Osmundacetone abrogates abnormal cell proliferation, migration and liver metastasis induced by PTPRO silencing in colorectal cancer cells. (E)-Osmundacetone blocks OA-RD17-mediated activation of the MAPK signaling pathway, thereby reducing macrophage proliferation and migration. (E)-Osmundacetone is applicable to relevant research on colorectal cancer. | ||||||||||||||||||||
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Methyl caffeate | 99.89% | Methyl caffeate is a phenylpropanoid, antibacterial agent, and Apoptosis-inducing agent. Methyl caffeate can be isolated from the flowers of peach Prunus persica (L.). Methyl caffeate upregulates the expression of pro-apoptotic proteins Bid, Bax and p53, and downregulates the expression of anti-apoptotic protein BCL-2. Methyl caffeate downregulates SASP factors. Methyl caffeate enhances glucose-stimulated insulin secretion. Methyl caffeate inhibits the growth of Gram-positive bacteria, Gram-negative bacteria, fungi, and Mycobacterium tuberculosis strains. Methyl caffeate can be used in studies related to breast cancer, type 2 diabetes, and tuberculosis. | ||||||||||||||||||||
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(E)-Methyl caffeate | (E)-Methyl caffeate is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | |||||||||||||||||||||
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2,5-Dihydroxycinnamic acid | 2,5-Dihydroxycinnamic acid is a phenolic acid. 2,5-Dihydroxycinnamic acid can be found in the leaves of Grevillea robusta A. Cunn. | |||||||||||||||||||||
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