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Ethylenethiourea is a degradation product of the ethylenebisthiocarbamate group of fungicides. It is recognized as tumorigenic and teratogenic, and is orally active.
Degradation product of ethylenebisthiocarbamate fungicides.
Tumorigenic and teratogenic agent.
Orally active.
Stable at elevated temperatures over a wide pH range.
For research use only.
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AHL modulator-1 is a compound that modulates N-acylated L-homoserine lactone (AHL) activity. It exhibits both agonism and antagonism in cellulase activity and potato maceration. This product is suitable for laboratory research applications.
Soluble in DMSO
Stable as powder at -20°C for 3 years
Stable as powder at 4°C for 2 years
Stable in solvent at -80°C for 6 months
Stable in solvent at -20°C for 1 month
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Tetrahydrothiophen-3-one is an endogenous metabolite and a pharmaceutical intermediate used to synthesize thiazole compounds. It is found in natural food and has good safety.
Endogenous metabolite
Pharmaceutical intermediate for synthesizing thiazole compounds
Exists in natural food with good safety
Appearance: Liquid
Color: Colorless to light yellow
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CB2R/FAAH modulator-3 is a dual-targeting modulator that acts as a CB2R agonist and FAAH inhibitor. It has potential applications in studies related to cancer, neurodegenerative diseases, and COVID-19 infection.
Acts as a dual-targeting modulator
Functions as a CB2R agonist and FAAH inhibitor
Exhibits Ki values of 20.1 nM for CB2R and 67.6 nM for CB1R
Has an IC50 value of 3.4 μM for FAAH
Reduces pro-inflammatory cytokines such as TNFα, IFN-γ, IL-1β, and IL6 in unstimulated monocytes and macrophages at 10 μM
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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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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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CSTSMLKAC (peptide 2) is a cyclic 9 amino acid sequence that mimics endogenous peptide sequences. CSTSMLKAC homes to cardiomyocytes in the ischemic myocardium.
Cyclic 9 amino acid sequence
Mimics endogenous peptide sequences
Homes to cardiomyocytes in the ischemic myocardium
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2,6-Dichlorodiphenylamine is an analogue of Diclofenac Sodium and exhibits anti-Candida albicans activity. Diclofenac Sodium is described as a potent and nonselective anti-inflammatory agent that acts as a COX inhibitor, with IC50s of 4 and 1.3 nM for human COX-1 and COX-2 in CHO cells.
Analogue of Diclofenac Sodium.
Exhibits anti-Candida albicans activity.
Potent and nonselective anti-inflammatory agent.
Acts as a COX inhibitor.
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