Carboxylic acid amides
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Filtered Search Results
eMolecules 107-91-5 | Cyanoacetamide | Key Organics/BIONET | MFCD00008024 | 84.078 | C3H4N2O | 90.000 | NC(=O)CC#N | 30mg | 629237834
Cyanoacetamide | Key Organics/BIONET | 107-91-5 | MFCD00008024 | 84.078 | C3H4N2O | 90.000 | NC(=O)CC#N | 30mg | 629237834
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eMolecules 683-57-8 | 2-Bromoacetamide | Synthonix | MFCD00008025 | 137.964 | C2H4BrNO | 96.000 | NC(=O)CBr | 1g | 649423418
2-Bromoacetamide | Synthonix | 683-57-8 | MFCD00008025 | 137.964 | C2H4BrNO | 96.000 | NC(=O)CBr | 1g | 649423418
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eMolecules 683-57-8 | 2-BROMOACETAMIDE | AstaTech | MFCD00008025 | 137.964 | C2H4BrNO | 98.000 | NC(=O)CBr | 5g | 410717042
2-BROMOACETAMIDE | AstaTech | 683-57-8 | MFCD00008025 | 137.964 | C2H4BrNO | 98.000 | NC(=O)CBr | 5g | 410717042
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eMolecules 1261676-58-7 | 2-AMINO-6-NITROBENZAMIDE | MFCD18389900 | 1g
Medchem Express | LEO 39652 | 5mg | 587658661 | HY-131707 | 1445656-91-6 | 421.453 | C23H23N3O5
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Medchemexpress LLC 2-ETHOXYBENZAMIDE 5G
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2-ETHOXYBENZAMIDE 5G
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Chem Service Inc 3.5-DINITROBENZAMIDE
NC3859395 3.5-DINITROBENZAMIDE
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Medchemexpress LLC N-BROMOACETAMIDE 10G
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N-BROMOACETAMIDE 10G
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Medchemexpress LLC N-BROMOACETAMIDE 5G
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N-BROMOACETAMIDE 5G
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Apexbio Technology LLC 2-BROMOACETAMIDE-500MG
2-Bromoacetamide (CAS No 683-57-8) is utilized primarily in biomedical research as an electrophilic reagent Originating from chemical synthesis this compound acts by alkylating thiol groups in proteins and enzymes interfering with their function Often studied in the context of enzyme inhibition pathways its activity is generally observed in the nanomolar to low micromolar range In vitro it is used to investigate the modification of cysteine residues in proteins while typical applications include diverse cell models and animal studies aimed at understanding biochemical pathways and potential therapeutic targets 2-Bromoacetamide is also employed in drug screening assays to evaluate the effects of protein modification Experimental concentrations typically depend on the specific research design ensuring applicability across various experimental setups
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Apexbio Technology LLC 2-BROMOACETAMIDE-1G
2-Bromoacetamide (CAS No 683-57-8) is utilized primarily in biomedical research as an electrophilic reagent Originating from chemical synthesis this compound acts by alkylating thiol groups in proteins and enzymes interfering with their function Often studied in the context of enzyme inhibition pathways its activity is generally observed in the nanomolar to low micromolar range In vitro it is used to investigate the modification of cysteine residues in proteins while typical applications include diverse cell models and animal studies aimed at understanding biochemical pathways and potential therapeutic targets 2-Bromoacetamide is also employed in drug screening assays to evaluate the effects of protein modification Experimental concentrations typically depend on the specific research design ensuring applicability across various experimental setups
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Medchemexpress LLC ISOBUTYRAMIDE 100G
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ISOBUTYRAMIDE 100G
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5000745871 IODOACETAMIDE-PEG5-A 10MG
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Chemscene CHEMSCENE
5000579479 2-IODOACETAMIDE 10G
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Medchemexpress LLC OXAMIC ACID SODIUM 500 mg
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OXAMIC ACID SODIUM 500MG
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Medchemexpress LLC Acetohydroxamic acid | 546-88-3 | 98.7% | 500 MG
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Acetohydroxamic acid (N-Hydroxyacetamide) is a chemical compound that acts as an inhibitor for bacterial and plant urease, commonly used for treating chronic urinary tract infections. It also exhibits selective inhibition of arachidonic acid 5-lipoxygenase, making it useful in asthma research. Beyond these, it inhibits the formation of advanced glycation end products and effectively reduces oxidative stress and inflammatory responses. This compound also demonstrates antiviral activity against HIV.
- Inhibits bacterial and plant urease
- Used for chronic urinary tract infections
- Selectively inhibits arachidonic acid 5-lipoxygenase
- Useful in asthma research
- Inhibits advanced glycation end products formation
- Reduces oxidative stress
- Reduces inflammatory responses
- Exhibits antiviral activity against HIV
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