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Results for "

caffeic acid

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    18
    TargetMol | Inhibitors_Agonists
  • Peptide Products
    2
    TargetMol | Peptide_Products
  • Natural Products
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    TargetMol | Natural_Products
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    TargetMol | Isotope_Products
Caffeic Acid
T2807331-39-5
Caffeic Acid is an orally bioavailable, hydroxycinnamic acid derivative and polyphenol, with potential anti-oxidant, anti-inflammatory, and antineoplastic activities.
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Caffeic Acid Phenethyl Ester
Phenylethyl Caffeate, CAPE
T6429104594-70-9
Caffeic Acid Phenethyl Ester (Phenylethyl Caffeate) (CAPE) inhibits the activation of nuclear transcription factor NF-kappa B and may suppress p70S6K and Akt-driven signaling pathways, with antineoplastic, cytoprotective and immunomodulating activities. CAPE is the phenethyl alcohol ester of caffeic acid and a bioactive component of honeybee hive propolis. In addition, CAPE inhibits PDGF-induced proliferation of vascular smooth muscle cells through the activation of p38 mitogen-activated protein kinase (MAPK) and hypoxia-inducible factor (HIF)-1alpha and subsequent induction of heme oxygenase-1 (HO-1).
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Trans-caffeic acid
3,4-Dihydroxybenzeneacrylic acid
TMA0003501-16-6
Trans-caffeic acid (3,4-Dihydroxybenzeneacrylic acid) can be used as a highly sensitive fluorescent probe for the detection of laccase in food and can also stimulate the growth of germ tissue.
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Caffeic acid 4-O-glucoside
T125634166735-99-5
Caffeic acid 4-O-glucoside (Linocaffein), a glycosylation product of Caffeic acid, reverses Aβ25-35-induced axonal atrophy and induces axonal regeneration in mouse cortical neurons, and can be used in Alzheimer's disease research.
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Caffeic acid 4-O-glucuronide
T126424
Caffeic acid 4-O-glucuronide is a useful organic compound for research related to life sciences and the catalog number is T126424.
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Caffeic acid 4-O-glucopyranoside
TN859717093-82-2
Caffeic acid 4-O-glucopyranoside is a natural product that can be used in related research in the field of life sciences. Its product number is TN8597.
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7-10 days
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Caffeic acid glucoside
TN8786892501-29-0
Caffeic acid glucoside is a natural product that can be used in related research in the field of life sciences. Its product number is TN8786.
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7-10 days
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Dihydrocaffeic acid
T05391078-61-1
Dihydrocaffeic acid is a metabolite of chlorogenic acid, a well-known antioxidant component with antioxidant, anti-Alzheimer's disease, neuroprotective, arousal and lipid-lowering effects.
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3,4-Dimethoxycinnamic acid
Dimethylcaffeic acid, Caffeic acid dimethyl ether, O-Methylferulic acid
T37592316-26-9
3,4-Dimethoxycinnamic acid (O-Methylferulic acid) is a monomer found in *Securidaca inappendiculata* Hassk. It exerts anti-apoptotic effects on L-02 cells via the ROS-mediated signaling pathway.
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TargetMol | Inhibitor Sale
3-(3-Hydroxyphenyl)propionic Acid
m-Hydroxyphenylpropionic acid, 3-Hydroxyhydrocinnamic acid
T7437621-54-5
3-(3-Hydroxyphenyl)propionic Acid (m-Hydroxyphenylpropionic acid) is one of the major metabolites of ingested caffeic acid.it inhibited osteoclastogenesis and bone osteoclastic resorptive activity.
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Ethyl trans-caffeate
Ethyl caffeate, Caffeic Acid Ethyl Ester
T3S001366648-50-8
1. Ethyl trans-caffeate (Caffeic Acid Ethyl Ester) has anti-inflammatory activity. 2. Ethyl trans-caffeate may as a promising natural compound for future application in chronic liver disease. 3. Ethyl trans-caffeate is a potent chemopreventive compound against skin carcinogenesis caused by solar UV exposure. 4. Ethyl trans-caffeate is the high-resolution structures of representative inhibitors in complex with human pancreatic α-amylase. 5. Ethyl trans-caffeate strongly inhibits neoplastic transformation of JB6 Cl41 cells without toxicity. PI3K, ERK1 2, and p38 kinase activities were suppressed by direct binding with HOEC in vitro.
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Phenethyl ferulate
Caffeic Acid 3-Methyl Phenethyl Ester
TN233071835-85-3
Phenethyl ferulate (Caffeic Acid 3-Methyl Phenethyl Ester) has chemopreventive properties against chemically induced colon carcinogenesis. It enhances apoptosis in azoxymethane induced colon tumors. It shows inhibitory activity against cyclooxygenase (COX) and 5-lipoxygenase (5-LOX) with IC50 values of 4.35 μM and 5.75 μM, respectively.
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