Halogénures organiques

<p>Please enquire for more information about 7-Fluoro-imidazo[1,2-a]pyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>N-Acetyl-S-(1,2-dichloroethenyl)-L-cysteine is a reactive compound that is formed from the metabolism of acetaminophen. It has been shown to cause oxidative injury in the mitochondria of proximal tubule cells. N-Acetyl-S-(1,2-dichloroethenyl)-L-cysteine disrupts mitochondrial membrane potential and causes ATP depletion. It also causes mitochondrial dysfunction by inhibiting respiratory chain activity and lowering cytosolic calcium levels. N-Acetyl-S-(1,2-dichloroethenyl)-L-cysteine has been shown to be toxic in animals and humans. The main analytical method used to detect this compound is the tetrazolium dye assay.</p>

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<p>2,4,6-Trichlorobenzoyl chloride is a chemical compound that forms during the synthesis of benzalkonium chloride. It can be used as an efficient method for the synthesis of fatty acids and cyclic peptides. The reaction products are chlorinated and have a hydroxyl group. The 2,4,6-trichlorobenzoyl chloride is used in the synthesis of fatty acids by reacting with acetic acid to produce a chlorinated fatty acid. Hydroxyl groups react with 2,4,6-trichlorobenzoyl chloride to form a chlorinated hydroxy fatty acid. This product has been shown to inhibit cervical cancer cell growth and reduce the incidence of cervical cancer by inhibiting DNA replication.</p>

<p>(R)-(-)-alpha-Methoxy-alpha-trifluoromethyl-phenylacetyl chloride is an enantiomer that has a chiral center. It is used in the synthesis of metoprolol and bisoprolol, which are drugs that are prescribed to treat hypertension and angina pectoris. The racemate is used in the separation of amines by high performance liquid chromatography (Hplc). This compound also has a hydroxyl group and two fatty acids, which can be identified using a chromatographic method. The compound contains a chloride as well as a transfer group.</p>

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<p>H-Pro-AMC hydrobromide salt is an enzyme that belongs to the family of proteases. H-Pro-AMC hydrobromide salt has been shown to have carboxypeptidase activity, which cleaves peptides at the C terminus of a single amino acid. It has also been shown to interact with other enzymes and proteins, such as recombinant proteins and enzymes from the ubiquitin-proteasome system. This enzyme's ability to cleave peptides at the C terminus of a single amino acid makes it useful for protein sequencing. H-Pro-AMC hydrobromide salt has also been sequenced and found to share homology with other proteases, such as subtilisin E.</p>

<p>Benzyl bromoacetate is a bicyclic heterocycle that is metabolized by the enzyme benzyl alcohol dehydrogenase. The resulting metabolites are then converted to methyl benzoate and benzyl alcohol. It has been shown to inhibit prostate cancer cells and basic fibroblasts, which may be due to its ability to inhibit enzymes involved in fatty acid synthesis. Benzyl bromoacetate also has therapeutic effects on autoimmune diseases such as bowel disease, which may be due to its ability to reduce inflammation and suppress the immune system.</p>

<p>Alfentanil is an opioid analgesic that is used for the treatment of severe or acute pain. It is a potent synthetic analog of fentanyl, which is an opioid analgesic that is used for the treatment of short-term (acute) and long-term (chronic) pain. Alfentanil has been shown to have a high affinity for α1-acid glycoprotein, which has been associated with drug interactions and blood sampling. Alfentanil also has chemical stability in experimental models and does not interact with nonsteroidal anti-inflammatory drugs. This drug may have a matrix effect on the concentration of cortisol in the blood.</p>

<p>1,3-Dichloropropene is a fumigant that inhibits the production of malonic acid by inhibiting the enzyme malonate semialdehyde dehydrogenase. 1,3-Dichloropropene has been shown to be toxic in vitro, but not in vivo. In addition, this compound has been shown to inhibit the activity of enzymes such as quillaja saponaria and polymerase chain reaction (PCR) in vitro. 1,3-Dichloropropene has been found to cause chronic exposure and site specific toxicity in rats. Chronic exposure was associated with an increased incidence of lymphomas and leukemias. The mechanism for these effects is unknown, but may be due to damage to DNA or inhibition of RNA synthesis.</p>

<p>Chloromethylated polystyrene is a polymer that contains a hydroxyl group and a disulfide bond. It can be used to synthesize an asymmetric synthesis of the borane-tetrahydrofuran complex, which is an important reagent in organic synthesis. In this reaction, trifluoroacetic acid reacts with hydrogen fluoride to produce chloromethylated polystyrene. This product has been shown to be effective in preventing cancerous tissue growth and inhibiting infectious diseases by binding to nucleophilic sites on the cell surface.</p>

<p>Please enquire for more information about Desmethyl chlorpheniramine maleate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Amino-2',5-dichlorobenzophenone (2,5-DCP) is a molecule with a chromatographic retention time of 23.8 minutes. 2,5-DCP has been detected in human urine samples using the chemical ionization technique as well as the Nova-Pak C18 column and an acetic acid/methanol mobile phase. This compound has been used as a standard for the detection of benzodiazepine drugs such as diazepam and flunitrazepam in urine samples by gas chromatography. 2,5-DCP has also been used in analytical toxicology to detect lormetazepam and lorazepam metabolites in human urine samples.</p>

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<p>3-Maleimidopropionyl chloride is a hydrophobic chemical that is often used in the synthesis of other compounds. 3-Maleimidopropionyl chloride advances transport of nutrients through cells and membranes, and also interacts with cellular parameters. It is reactive to cell membranes, and can be activated by coatings or nature techniques. 3-Maleimidopropionyl chloride is a synthetic compound that has been shown to react with cell membrane phospholipids, leading to changes in the properties of the lipid bilayer.</p>

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<p>Etifoxine hydrochloride is a drug that has been used in the treatment of asthma and other pulmonary diseases. It is a potent inhibitor of phospholipase A2, which modulates the production of inflammatory mediators. Etifoxine hydrochloride has been shown to have neurotrophic effects, with potential for clinical use in the treatment of neurodegenerative disorders such as Alzheimer's disease and Parkinson's disease. This drug also has anti-inflammatory properties due to its inhibition of prostaglandin synthesis. Etifoxine hydrochloride acts as an agonist on receptors, which may be responsible for some of its biological properties, including thermal expansion and axonal growth. In addition, this drug is a competitive inhibitor of the enzyme poly(ADP-ribose) polymerase (PARP), which is involved in DNA repair and cell division.</p>

1-Azaspiro[4.4]nonane hydrochloride is a versatile building block that is also used in research, as a reagent, and as a speciality chemical. It has been shown to be an excellent building block for complex compounds, with wide applications in the pharmaceutical industry. 1-Azaspiro[4.4]nonane hydrochloride has a CAS No. of 1417567-64-6 and can be found under the trade name Azapropynalene Hydrochloride (AP). It is soluble in water, alcohols, ethers and acetone but insoluble in most other solvents. 1-Azaspiro[4.4]nonane hydrochloride has been shown to have high quality and stability when stored under appropriate conditions; it is also resistant to degradation by light or air.

<p>N,N'-Dimethylhydrazine dihydrochloride (DMHD) is a nonsteroidal anti-inflammatory drug that inhibits the production of prostaglandins by blocking cyclooxygenase-2 (COX-2). It works by inhibiting tumor growth and inducing apoptosis. DMHD has been shown to inhibit angiogenesis and induce apoptosis in liver cells. DMHD also inhibits the mitochondrial membrane potential, which is important for regulating cell function. The molecular docking analysis has shown that DMHD binds to COX-2 protein with high affinity and specificity. DMHD also inhibits fatty acid synthesis, which may be due to its inhibition of mitochondrial beta-oxidation enzymes. DMHD has been shown to have toxic effects on colon cells in rats. This agent can cause damage to the colon lining through a number of mechanisms, including causing DNA damage and increasing oxidative stress.</p>

<p>2,5-Dichloro-4-methoxybenzoic acid is a synthetic herbicide that inhibits the enzyme 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS). This enzyme is necessary for the synthesis of aromatic amino acids. 2,5-Dichloro-4-methoxybenzoic acid is used as a selective herbicide in plants grown in vitro to eliminate weeds. It is also used to control populations of wild plants and grasses. 2,5-Dichloro-4-methoxybenzoic acid has been shown to inhibit the growth of glyphosate resistant weed species by inhibiting EPSPS activity.</p>