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Phenylpropaniods are organic compounds characterized by having an aromatic ring and a three-carbon propene tail. Polyketides are compounds characterized by having two or more carbonyl functional groups connected with a single carbon atom.
A lipophilic derivative of ferulic acid, with increased ability to cross cell membranes; less DPPH radical scavenging capacity than ferulic acid (IC50 = 66.7 μM for FAEE vs. 44.6 μM for ferulic acid); increases the expression of HO-1, Hsp70, and Hsp72, providing neuroprotection against amyloid β-peptide
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m-Carboxycinnamic acid bishydroxamide (CBHA) is a small-molecule histone deacetylase (HDAC) inhibitor supplied for research use. It inhibits HDAC1 and HDAC3 with reported ID50 values of approximately 10 nM and 70 nM, respectively, and has been reported to induce apoptosis and suppress tumor growth in experimental models.
Potent HDAC inhibitor with reported ID50 ≈ 10 nM (HDAC1) and ≈ 70 nM (HDAC3).
High purity (98.0%).
Molecular formula C10H10N2O4 and molecular weight 222.20 g·mol⁻¹.
Suitable for biochemical and cell-based assays.
Demonstrated induction of apoptosis and tumor-growth suppression in studies.
Supplied as a research-grade chemical for laboratory use.
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If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link: eMolecules Building Block Tool
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Ferulic acid methyl ester is the methyl ester derivative of ferulic acid used in biochemical and pharmacological research. It functions as a lipophilic antioxidant with reported activity in pathways such as p38 MAPK and autophagy, and is commonly used in in vitro and cell-based studies.
High purity suitable for research applications.
Lipophilic antioxidant and cell-permeable compound.
Solid, off-white to pink appearance for easy handling.
Available in multiple pack sizes, including 25 g.
Stable when stored according to supplier recommendations (powder: -20°C or 4°C).
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If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link: eMolecules Building Block Tool
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Trans-Cinnamic acid is a natural antimicrobial with a minimal inhibitory concentration (MIC) of 250 μg/mL against the fish pathogen A. sobria, SY-AS1. It exhibits broad antimicrobial activity against various fish pathogens and is more effective on bacteria when the pH of the culture media is not neutralized.
Targeted activity against bacterial and endogenous metabolites
Inhibits various fish pathogens
Stable for 3 years at room temperature
Stable in solvent for 2 years at -80°C or 1 year at -20°C
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4-Chlorocinnamic acid is a derivative of Cinnamic acid (HY-N0610A) 4-Chlorocinnamic acid inhibits the monophenolase and diphenolase activities of mushroom tyrosinase with IC50 values of 0 477 mM and 0 229 mM respectively 4-Chlorocinnamic acid inhibits the mycelial growth of Colletotrichum gloeosporioides 4-Chlorocinnamic acid exhibits anticonvulsant activity against acute epilepsy induced by pentylenetetrazol[1][2][3][4]
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trans-Cinnamic acid-d7 is the deuterium-labeled analogue of trans-cinnamic acid, used as an internal standard and tracer in analytical chemistry and metabolic studies. It is supplied as a high-purity white to off-white solid intended for research applications.
Deuterium-labeled for use as an internal standard in mass spectrometry and tracer studies.
High reported purity (99.98%).
White to off-white solid, stable under standard storage conditions.
Suitable for analytical and metabolic research applications.
Available in a 10 mg analytical-scale quantity.
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