Organic Halides

p-Amino-L-phenylalanine hydrochloride (PABA) is a type of amino acid that is used in the synthesis of melphalan hydrochloride, a drug used to treat cancer. PABA is a white crystalline powder that can be dissolved in water and formic acid. It has been shown to interact with the hydrophilic interaction chromatography column and flow rate sensor in order to improve the chromatographic separation of ammonium formate. PABA has also been found to be chiral and can be converted into its enantiomeric form by means of an organic solvent, such as acetonitrile. The impurities of PABA are mandelic acid and l-phenylalanine. These impurities are separated from PABA by means of HPLC analysis.

2-Chloro-4-trifluoromethylbenzonitrile is a fine chemical that belongs to the category of research chemicals, reagents and speciality chemicals. It is a versatile building block which can be used as a reaction component or useful intermediate in the synthesis of complex compounds. This compound also has many different uses, including as a useful scaffold for organic molecules.

<p>3-Bromosalicylic acid is a metabolite of salicylic acid and has shown clinical use in the treatment of cancer. 3-Bromosalicylic acid is synthesized from cyclohexanol and chlorine. It is a toxic compound that has been shown to inhibit protein synthesis in bacteria, including soil bacteria, but not in mammalian cells. This is due to its interaction with organic ligands that are present in the bacterial cell wall and not in mammalian cells. 3-Bromosalicylic acid also has been found to be a ligand for the receptor, PI3Kδ inhibitor, which inhibits tumor growth and metastasis by inhibiting phosphatidylinositol 3-kinase (PI3K) delta activity.</p>

4'-Trifluoromethoxy-beta-methyl-beta-nitrostyrene is a fine chemical that is a useful building block in organic synthesis. It can be used as a reagent, specialty chemical, or intermediate for the preparation of more complex compounds. This compound has been shown to be useful in the synthesis of natural products and pharmaceuticals.

<p>3-Bromo-2-nitroanisole is a potassium channel blocker that has neuroprotective effects. It can be used for the treatment of glaucoma and hypertension. 3-Bromo-2-nitroanisole can inhibit the activity of potassium channels and act as a neuroprotective agent. The drug has been shown to have neuroprotective effects in animal models, with evidence of efficacy in humans. The drug also inhibits the production of nitric oxide, which may contribute to its neuroprotective effect.</p>

<p>Please enquire for more information about N-(2-Chloro-5-Nitrophenyl)Benzamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3,5-Dichlorobenzyl chloride is a colorless crystallizing solid that is insoluble in water and soluble in alcohol. It can be prepared by refluxing 3,5-dichlorobenzyl alcohol with zinc chloride. The compound has been shown to have the ability to disrupt the aromatic system of certain pesticides and is used for pest control. It can also be used as an intermediate for the synthesis of 3,5-dichlorobenzoic acid. 3,5-Dichlorobenzyl chloride has been shown to bind to dna and inhibit the bacterial enzyme topoisomerase II.</p>

3,4,5-Trichloropyridine is a cationic polymerization initiator that is used in coatings and pharmaceuticals. 3,4,5-Trichloropyridine is a prodrug of amines that are active substances. It has been shown to be thermodynamically stable and to have analytical methods that are suitable for industrial use. 3,4,5-Trichloropyridine has been studied in the context of its mechanism of action as a PDE-5 inhibitor. The drug's effects have been compared with those of benazepril hydrochloride and carbonyl group analogues using magnetic resonance spectroscopy. Salvianolic acid A and benazepril hydrochloride inhibited the reaction product formation between 3,4,5-trichloropyridine and 2-aminophenol (2AP) by 50%.

N-Benzylguanidine hydrochloride (N-BzGuaHCl) is a nitrogen-containing heterocyclic compound that belongs to the group of mitochondrial inhibitors. It is used as a cardiac agent and has also been shown to inhibit the activity of integrin receptors. N-BzGuaHCl has been shown to be effective in preventing tumor growth in mice, which may be due to its ability to inhibit the uptake of monoclonal antibodies by cells. This drug also inhibits the activity of benzalkonium chloride, which is often used as a preservative in cosmetics and household products.

(S)-3-Amino-4-(1-naphthyl)butanoic acid hydrochloride is a high quality chemical that is used as a reaction component for the synthesis of complex organic compounds. It may also be used to produce fine chemicals, pharmaceuticals, and other useful compounds. This product has a wide variety of uses including as an intermediate in the production of speciality chemicals, as a building block for synthesizing more complex compounds, or as a precursor to producing other useful chemicals.

<p>3,5-Diamino-6-chloropyrazine-2-carboxylic acid methyl ester is a low binding, mitochondrial labeling agent. It is photolabile and can be used in the study of respiratory complex activity. 3,5-Diamino-6-chloropyrazine-2-carboxylic acid methyl ester has been shown to inhibit the enzyme mitochondrial complex I and II. The azido group on the molecule is homologous to a phosphate group in ATP and can be used as a substrate analogue for ATP synthase. This allows 3,5-Diamino-6-chloropyrazine-2-carboxylic acid methyl ester to be used as an experimental tool for studying ATP synthesis.</p>

Dichloroacetaldehyde hydrate is an organic compound that is used in the treatment of skin cancer. It has been shown to have protective effects on cell membranes, which may be due to its ability to inhibit lipid peroxidation. Dichloroacetaldehyde hydrate also has a potential use as a radiation sensitizer and may be able to extend the lifespan of animals.

<p>(3-Bromopropoxy)-tert-butyldimethylsilane is a synthetic molecule that has been shown to inhibit prostate cancer cells. It binds to the phosphate group on the enzyme and inhibits its activity. (3-Bromopropoxy)-tert-butyldimethylsilane can be used as a chemical probe for identifying enzymes involved in phosphatase activity. This molecule has also been shown to have anti-cancer effects in vitro and in vivo assays, by preventing tumor growth and metastasis.</p>

<p>2-Chloro-5-methoxybenzoic acid (2CMB) is a copper chelator that has been shown to have antagonistic properties against microglia cells. 2CMB is synthesized from 2,5-dichlorobenzoic acid and methoxylamine. It has been shown to inhibit the synthesis of inflammatory mediators in rat spinal cord microglia cells by inhibiting the activity of polyphosphoric acid, anions and additives. 2CMB also has a high affinity for chloride ions and can be used as a tracer to measure chloride profiles. 2CMB reacts with copper ions at a slow rate and can be used as an indicator for the presence of microglia cells.</p>

<p>1-(4-Bromophenyl)propan-1-one is a sulfonation product of propiophenone. It has been found to have anticancer activity in cervical cancer, and is currently being studied as a potential treatment for cancer. 1-(4-Bromophenyl)propan-1-one can be synthesized by treating propiophenone with hydrochloric acid and sodium hydroxide solution. It can also be synthesized using polyvinyl chloride as the starting material. 1-(4-Bromophenyl)propan-1-one can be isolated from the reaction mixture by adding hydrochloric acid to the reaction mixture, forming a salt that precipitates from solution. This salt is then dissolved in water and neutralized with an alkali such as sodium hydroxide or potassium carbonate, yielding 1-(4-bromophenyl)propan-1-one hydrochloride.</p>

5-(2-Chlorophenyl)-1,2-diphenyl-1,3,4-triazole is a research chemical that can be used as a building block for the synthesis of more complex molecules. This compound has been shown to have a high yield and is useful for the synthesis of various reaction components including pharmaceuticals and pesticides. It also has an excellent quality and is available in bulk quantities.

<p>3-Fluoro-4-(trifluoromethyl)benzonitrile is a chemical compound with biological activity. It is structurally related to anthelmintics, and has been shown to be nematocidal in laboratory experiments. 3-Fluoro-4-(trifluoromethyl)benzonitrile has not been evaluated for safety or efficacy in humans.<br>!--END--&gt;</p>

<p>(R)-(+)-1-(4-Bromophenyl)ethylamine is a chiral anion that can be used as a ligand for supramolecular chemistry. It reacts with primary amines to form a diazenyl (an anion with two nitrogen atoms and one carbon atom). The diazenyl molecule has been shown to have chemotactic activity and to stimulate the immune system. The (R)-(+)-1-(4-bromophenyl)ethylamine is generally stable when it is in contact with water, but is unstable when heated due to decomposition by light or oxygen.</p>

Trt-cysteamine hydrochloride is a prodrug that is metabolized to cysteamine in vivo. Cysteamine inhibits the production of tumor necrosis factor (TNF) by binding to its receptor and blocking NF-κB signaling pathways. In vitro models have shown that trt-cysteamine hydrochloride has minimal effects on cells, but when used in vivo, it can inhibit oxidative stress and induce cell death. Trt-cysteamine hydrochloride also binds to molecular targets with disulfide bonds, which may be potential therapeutic targets for cancer treatment.

3,4,5-Tribromobenzoic acid is a benzoic acid with the molecular formula C6H3Br3O2. It is used as a plant growth regulator in agriculture and gardening. 3,4,5-Tribromobenzoic acid may be applied to the surface of plants to stimulate abscission (the natural shedding of leaves) or excision (the removal of flowers). This chemical also has been shown to inhibit physiological activity in plants by inhibiting 2,3,5-triiodobenzoic acid synthesis. This inhibition leads to a reduction in the production of substances that are involved in physiological processes such as photosynthesis and protein synthesis.

<p>2-(3-Methyl-1,2,4-oxadiazol-5-yl)ethyl]amine hydrochloride is a high quality chemical reagent that can be used as a complex intermediate in organic synthesis. It is also a useful scaffold for the synthesis of other complex compounds. 2-(3-Methyl-1,2,4-oxadiazol-5-yl)ethyl]amine hydrochloride is an excellent building block for the synthesis of various fine chemicals and research chemicals. This compound has many uses as a versatile building block in chemical reactions due to its reactivity.</p>

<p>3-(Trifluoromethoxy)phenol is a drug that has been shown to function as an amide and a biomolecular. It has also been used in the development of drugs for depression, but it is not known whether it is effective in humans. 3-(Trifluoromethoxy)phenol binds to the cation channel of the NMDA receptor, which may be related to its antidepressant properties. The compound has been shown to have a radiotracer effect on positron emission tomography (PET). 3-(Trifluoromethoxy)phenol yields positrons when it undergoes deamination. This reaction is catalyzed by enzymes such as acetylcholine esterase, choline oxidase, and monoamine oxidases.</p>

<p>4-(3-Chloro-benzyloxy)benzoic acid (4CBA) is a useful scaffold for the synthesis of complex compounds. It is a versatile building block that can be used as an intermediate in the synthesis of fine chemicals and research chemicals. 4CBA is also a reactive compound that can be used in reactions to form covalent bonds, such as amide formation. 4CBA has a CAS number of 84403-70-3 and can be used in reactions involving organic chemistry, such as esterification, etherification, nitration, sulfonation, amidation, and chlorination.</p>

<p>3-Bromo-2-methylbenzoic acid is a hydrogen bond donor. Hydrogen bonding may provide an explanation for the functional theory of 3-bromo-2-methylbenzoic acid, which has been shown to have anticancer properties in vitro and in vivo. This compound has been shown to be effective against cancer cells that express PDL1 (programmed cell death protein 1) and is being studied as a potential therapeutic agent for cancers that are resistant to conventional anticancer drugs. 3-Bromo-2-methylbenzoic acid has low solubility in water and is poorly absorbed from the gastrointestinal tract. It also does not bind to plasma proteins, which makes it pharmacologically active even at low doses. 3BBMBA inhibits viral replication by binding to the viral RNA polymerase enzyme, thereby inhibiting transcription and replication of the virus genome. In addition, it inhibits the proliferation of human cancer cells through inhibition of protein synthesis and DNA synthesis</p>

<p>2,3-Dichloroquinoxaline is a chemical compound that has inhibitory properties against the growth of bacteria. It is reactive and can be used as a disinfectant and antimicrobial agent. 2,3-Dichloroquinoxaline has been shown to have a bactericidal effect against P. aeruginosa in the presence of hydrochloric acid. This chemical also binds to human immunoglobulin (Ig)G molecules and has transport properties. Quinoxalines are an important class of quinoline derivatives that include 2,4-dichlorobenzoic acid, which inhibits bacterial growth by binding to DNA gyrase. The fluorescence property of 2,3-Dichloroquinoxaline is due to its nitrogen nucleophile and chloride ion content. In addition, this chemical's protein–protein interaction activity leads it to bind with other proteins in the cell membrane or cytoplasmic membrane.</p>

2,6-Dichloro-4-methylpyridine is a chemical compound that belongs to the class of dendrons. It is used for the functionalisation of imidazole and propiolate moieties. The derivates of 2,6-dichloro-4-methylpyridine can be made by coupling with pyrazole or dimethylacetal. This compound reacts with methylene halides in nucleophilic substitution reactions to produce methyl propiolate.

3,5-Difluorophenylhydrazine HCl is a versatile building block. It is a fine chemical that is used in research chemicals and speciality chemicals. 3,5-Difluorophenylhydrazine HCl has been used as a reagent and as a reaction component for the synthesis of complex compounds. This chemical may be useful as a scaffold for the construction of novel molecules with desired properties.

5-(3-Chlorophenyl)cyclohexane-1,3-dione is a versatile building block. It can be used as a reagent, speciality chemical, or useful building block in the synthesis of complex compounds. 5-(3-Chlorophenyl)cyclohexane-1,3-dione is also used as a reaction component or scaffold in the synthesis of valuable chemicals. This chemical has high purity and quality.

<p>6-Bromoisatin is an antimicrobial agent that belongs to the group of ethylene diamines. It has been shown to be a potent inhibitor of cancer cell viability in vivo and can be used as a potential chemotherapy agent. 6-Bromoisatin is active against human pathogens, such as Staphylococcus aureus and Streptococcus pyogenes. This compound has also been shown to inhibit the growth of LPS-stimulated RAW264.7 macrophages, which are used in vitro for studying innate immunity. The mechanism of action involves inhibition of cyclic AMP production, which leads to cell death in cancer cells. 6-Bromoisatin also inhibits the proliferation and viability of granulosa cells and carcinoma cells, with IC50 values in the range of 0.5 - 2 µM.END&gt;&gt;</p>

<p>3,4-Dichloromethylphenidate HCl is a versatile building block that can be used in the synthesis of many complex compounds. It has been shown to be useful as a reagent and as an intermediate in the synthesis of pharmaceuticals. This compound may also have potential for use as a reaction component and scaffold in organic chemistry. 3,4-Dichloromethylphenidate HCl is available at high quality and is a useful building block for research purposes.</p>

<p>2-Chloro-4,6-diphenyl-1,3,5-triazine is a linker that can be activated to accept an electron from a donor molecule. It is often used as a transport material in organic light emitting diodes (OLEDs) and organic photovoltaics (OPVs). 2-Chloro-4,6-diphenyl-1,3,5-triazine has been shown to have high efficiencies when it is thermally activated. This compound also has high efficiency when it is activated by light with a wavelength of 400 nm. The luminescent properties of 2-Chloro-4,6-diphenyl-1,3,5 - triazine are due to its electron deficient nature and the presence of methoxy groups.</p>

<p>Intermediate in the synthesis of linagliptin</p>

<p>4-Nitro-3-(trifluoromethyl)aniline (FLU-1) is a molecule that has been shown to be carcinogenic in both animals and humans. This compound has an activation energy of 4.2 kcal/mol, which is a measure of the amount of energy required for a reaction to occur. FLU-1 is stable in n-dimethylformamide and reacts with acetic acid to form an ester, which can be hydrolyzed to form 4-nitro-3-(trifluoromethyl)acetic acid. FLU-1 also reacts with ammonia and boron nitride to form 4-(aminocarbonyl)-3-(trifluoromethyl)aniline. The physical properties of this compound are dependent on the solvents used in the reaction. For example, its nmr spectra are different in chloroform than they are in acetone or</p>

<p>VX-950 is an antibacterial agent that inhibits the synthesis of bacterial protein. It binds to a small molecule, benzimidazol-2-ylmethylamine, which reduces the production of proteins in the bacterial cell by inhibiting the enzyme dihydrofolate reductase. VX-950 has been shown to be effective against a number of pathogens including fungi and bacteria. VX-950 has also been shown to bind to two ligands, imidazolines and diazepinones, that are found in mammalian tissue. This binding allows it to reduce the production of proteins in hepatocytes as well as inhibit growth in Saccharomyces cerevisiae strain.</p>

<p>4-(Trifluoromethyl)-L-phenylalanine (4-TFMP) is an acyltransferase inhibitor that prevents the formation of fatty acids by inhibiting the enzyme ketoreductase. 4-TFMP has been shown to inhibit protein synthesis in myeloid leukemia cells and to have a cytotoxic effect on cancer cells. It also inhibits the growth of bacteria such as Salmonella enterica and Mycobacterium tuberculosis. In addition, 4-TFMP is used to treat infectious diseases such as tuberculosis, as well as metabolic disorders and some types of enzyme deficiencies. 4-TFMP is stereoselective and binds only to one type of acyltransferase, which is not present in humans.</p>

(S)-2-Bromopropionic acid is a synthetic compound that has been shown to bind to an antigen. The structure activity relationship of this compound has been studied in order to find a suitable surrogate for the synthesis of (S)-2-Bromopropionic acid. This compound was synthesized using solid-phase chemistry and the resulting product was purified by HPLC. The synthetic route for (S)-2-Bromopropionic acid included d-alanine, which was used as the biomolecular building block. The alkylation reaction involved the use of chloroacetic acid and methyl iodide, which were reacted with d-alanine in aqueous solution at room temperature. After hydrolysis, ester linkages were introduced with methanol and acetic anhydride. The final product was purified by recrystallization from methanol and acetone.

<p>2-Bromoquinoline is an antimicrobial agent that binds to bacterial receptors. It is a bifunctional molecule with two reactive groups: a hydroxyl group and a nitrogen atom. 2-Bromoquinoline has been shown to inhibit the growth of various bacteria, including Mycobacterium tuberculosis, Staphylococcus epidermidis and Streptococcus pyogenes, by preventing the formation of a proton gradient across the bacterial membrane. 2-Bromoquinoline also inhibits hyperproliferative diseases such as amyloidosis in mice by binding to amyloid fibrils. This drug has been shown to cause DNA damage in mammalian cells, which may be due to its ability to form hydrogen bonds with methyl ethyl groups on DNA bases.</p>

<p>Bis (iodomethyl) ether is a metabolic disorder that is used as an organic solvent. It is a chemical compound that can be used to form alkylating agents, including tetronic acid and chloromethyl ketone. Bis (iodomethyl) ether can also be used to form anions, such as iodide and acetate. The biosynthesis of bis (iodomethyl) ether in animals involves the conversion of phosphate derivatives into iodides, which are then converted into bis (iodomethyl) ether. Bis (iodomethyl) ether has been shown to have insulin-resistance-modulating effects on type 2 diabetes in mice and guanosine diphosphate levels in perovskite cells. This drug has also been shown to increase hyperglycemia in animal models.</p>

2-Bromo-5-nitroanisole is a chemical compound that has been shown to have glutamate receptor modulating properties. This molecule also has been shown to have allosteric modulating effects on metabotropic glutamate receptors. The molecular mechanism of 2-Bromo-5-nitroanisole involves the formation of a covalent bond with glutamine residues, which may be due to its nucleophilic character. This drug has been studied in clinical trials for the treatment of Alzheimer's disease and Parkinson's disease. It has also been studied for its effects on the frequency and severity of migraines.

2-Bromo-3-pyridinol is a nicotinic acetylcholine receptor antagonist that has anti-influenza activity. It was synthesized as an analogue of the natural product pyridostigmine, which inhibited influenza in mice. 2-Bromo-3-pyridinol binds to the nicotinic acetylcholine receptor at the same site as nicotine and prevents it from being activated by acetylcholine. This drug also inhibits tumor growth and proliferation in vitro and in vivo, showing potent cytotoxicity against carcinoma cells by inhibiting protein synthesis and cell division. 2-Bromo-3-pyridinol has been shown to inhibit Alzheimer's disease in a mouse model of this disorder. The drug inhibits amyloid plaque formation and toxicity in cultured cells, suggesting its potential for treating this disease.

<p>4-Trifluoromethylbenzyl bromide is a choline derivative that acts as an anticancer agent. It is structurally similar to the anticancer drug doxorubicin, which has been shown to be effective against breast cancer and leukemia. 4-Trifluoromethylbenzyl bromide interacts with cellular proteins, including choline kinase, and inhibits the mitochondrial pathway. This leads to cell death through apoptosis. The molecule also interacts with nucleotide bases such as thymine and cytosine in DNA, inhibiting transcription and replication. 4-Trifluoromethylbenzyl bromide binds strongly to the hydroxyl group of cholesterol by an electrophilic substitution mechanism to form a covalent bond with its hydroxy group. The molecule can also bind to chloride ions by an ionic bond.</p>

4-Amino-6-chloro-2-(methylthio) pyrimidine is a reactive chemical that is used in medicine as an antioxidant. It has been shown to have beneficial effects on atherosclerosis, colitis and cancer. 4-Amino-6-chloro-2-(methylthio) pyrimidine has also been shown to inhibit the production of reactive oxygen species (ROS). ROS are generated by lipoxygenase enzymes in soybean oil and cause damage to cells. 4-Amino-6-chloro-2-(methylthio) pyrimidine binds to the enzyme's heme group, preventing it from forming ROS.

α-Methyl 2,4-dichlorochalcone is a useful scaffold for the synthesis of complex compounds. It can be used as a reaction component in research chemicals, speciality chemicals, and fine chemicals. This compound has a CAS No. 199788-52-8 and can be used as an intermediate in the synthesis of many other compounds with varying structures. It is also a versatile building block that can be used to synthesize various useful building blocks. α-Methyl 2,4-dichlorochalcone also has high quality and purity and can be used as a reagent for chemical reactions.

4-Bromo-1-hydroxyanthraquinone-2-carboxylic acid is a monocarboxylic acid that is used in analytical chemistry to optimize the process efficiency. It can be used as an extraction solvent, and its kinetics can be modeled using quadratic equations to optimize the recovery of analytes. 4-Bromo-1-hydroxyanthraquinone-2-carboxylic acid has also been shown to be useful for surface methodology, where it improves the dispersive power of carboxy groups on a surface.

3-Cyano-4-fluorobenzoic acid is a fluorinated analog of 3-cyano-4-fluorobenzoic acid, which has been shown to be effective in the treatment of prostate cancer. It is a prodrug that is metabolized by activated esterases to release the active form. The 18F radiolabeled form of 3-Cyano-4-fluorobenzoic acid has a high affinity for prostate carcinoma cells and has been used as a diagnostic agent. This drug also has an excellent pharmacokinetic profile and can be used as a nonradioactive tracer for imaging tumor cells in vivo.

<p>N-Phenyl-2,4,6-triphenyl pyridinium tetrafluoroborate is a crystalline material that is insoluble in water and organic solvents. It can be used as a monomer in the synthesis of polymers and for immobilization of enzymes. N-Phenyl-2,4,6-triphenyl pyridinium tetrafluoroborate can be used to reprocess technetium and has been shown to diffract x-rays with high resolution. This compound is also fluorescent with a long wavelength (620 nm) and can be used as a radioactive tracer.</p>

<p>Nile blue chloride is a dye used in wastewater treatment. It can be used to measure the dry weight of a sample of material. Nile blue chloride has been shown to be a reliable fluorescent probe for bacterial detection in cell culture and tissue culture, as well as for the detection of infectious diseases. This compound has also been shown to have an effect on the oxygen transport in living cells, which may be due to its high affinity for fatty acids.</p>

4-Iodo-3-nitrobenzoic acid (4-INBA) is a nitro derivative of the aromatic acid. It is used as a chemotherapeutic agent and an intermediate in the synthesis of other drugs. 4-INBA has been shown to be cytotoxic to hamsters and inhibit cellular growth by binding to DNA polymerase and inhibiting DNA synthesis. 4-INBA also binds to RNA polymerase, inhibiting RNA synthesis and protein production, which causes cell death.

<p>4-Cyano-3,5-difluorophenol (4CF) is a mesomorphic compound that has a number of reactions with chloride. 4CF is synthesized from 3,5-difluoroaniline and the reaction product is then heated with chlorine to produce 4CF. The optimal reaction temperature is between 100°C and 120°C. When exposed to light, 4CF will react with chloride ions in the presence of heat to form a hydrophobic chlorinated product. This product reacts with proton donors such as NaOH or KOH to produce hydrogen gas. At room temperature, 4CF can be used as a gas sensor.</p>

4-Iodo-3-methylbenzoic acid methyl ester is a chemical that is structurally analogous to 4-iodo-2,5-dimethoxybenzoic acid methyl ester. It is synthesized by the reaction of 3-methylbenzoic acid with ethyl chloroformate and iodomethane. 4-Iodo-3-methylbenzoic acid methyl ester has been shown to inhibit o6 alkylguanine DNA alkyltransferase (AGT) and o6 alkylguanine dna glycosylase (AGG). AGT and AGG are enzymes that repair DNA damage caused by reactive oxygen species. This inhibition leads to the accumulation of DNA damage in cells and induces apoptosis.

N-Methyl-3,4-methylenedioxyphenylpropane hydrochloride is a high quality reagent that is a useful intermediate in the synthesis of complex compounds. It is used as a fine chemical and research chemicals in the manufacture of speciality chemicals. N-Methyl-3,4-methylenedioxyphenylpropane hydrochloride has been shown to be an excellent scaffold for the synthesis of many different compounds with high versatility. It can also be used as a building block or reaction component.

1H,1H,2H,2H-Tridecafluoro-1-n-octanol is a potent and selective halogenated hydrocarbon. It binds to DNA at the dinucleotide phosphate site, which is an important site for polymerase chain reaction (PCR) activation. 1HFN has been shown to be more effective than other halogenated hydrocarbons in vitro assays on rat liver microsomes. It has been used as an additive in wastewater treatment to remove organic contaminants and metal ions. In vivo studies have been carried out in CD-1 mice to determine the effects of 1HFN on the liver and kidneys; these studies showed no toxicological effects on these organs. 1HFN also has been shown to inhibit enzymes such as cytochrome P450 and monoamine oxidase B that are involved in drug metabolism and may lead to adverse reactions with drugs metabolized by these enzymes.

L-Valinamide hydrochloride is an amide with a reactive group. It binds to the CB2 receptor and the CB1 receptor, which are found in the brain and immune system. L-Valinamide hydrochloride has been shown to have anti-inflammatory effects in animal models of inflammatory diseases, such as rheumatoid arthritis. L-Valinamide hydrochloride has also been shown to be a synthetic cannabinoid that inhibits pain transmission by binding to the same receptors as delta-9 tetrahydrocannabinol (THC), one of the active components of cannabis.

<p>3-Chlorophenylhydrazine hydrochloride is a pyrazole that has been shown to have potent antibacterial activity. It is used in the treatment of inflammatory diseases and has been shown to be effective against Helicobacter pylori, which causes gastritis, peptic ulcers, and stomach cancer. 3-Chlorophenylhydrazine hydrochloride is an acidic compound with a molecular weight of 192.2 g/mol. It contains a pyrazole ring that is eluted with hydrochloric acid and reacts with gyrase enzymes in bacteria, inhibiting DNA synthesis. 3-Chlorophenylhydrazine hydrochloride also has anti-inflammatory properties due to its ability to inhibit prostaglandin synthesis.</p>

<p>3-Chloro-2-fluoroaniline is an industrial chemical, which is used to manufacture a variety of other chemicals. 3-Chloro-2-fluoroaniline is the product of the chlorinating reaction between 2-fluoroaniline and hydrochloric acid. It has been used in the synthesis of drugs such as probenecid and sulfinpyrazone, which are used for the treatment of cardiac disease. 3-Chloro-2-fluoroaniline also has chloride ion activity and can be used as a synthetic intermediate for other organic acids.</p>

2,5-Dibromothiophene is a reactive intermediate that has been used in the synthesis of ondansetron hydrochloride. 2,5-Dibromothiophene can be prepared by the reaction of triethyl orthoformate and thiophene. The compound spontaneously undergoes bond cleavage to give the dibromo derivative followed by oxidation with aqueous hydrogen peroxide. 2,5-Dibromothiophene has been shown to have photocatalytic activity under visible light irradiation. This compound functions as a monomer in the polymerization of polythiophenes. 2,5-Dibromothiophene can also be used in palladium-catalyzed cross-coupling reactions with azasetron hydrochloride to form x-ray crystal structures and nmr spectra.

2-Bromo-5-methoxybenzoic acid methyl ester is an antibiotic with a broad spectrum of activity against bacteria, including Staphylococcus aureus and Pseudomonas aeruginosa. 2-Bromo-5-methoxybenzoic acid methyl ester is an inhibitor of the enzyme benzohydrazide, which is involved in the production of prostaglandins. This drug also has antioxidant activity and can inhibit the growth of Escherichia coli and Cereus. 2-Bromo-5-methoxybenzoic acid methyl ester has analgesic properties and was shown to have analgesic activities in animal tests.

<p>DL-Cystein hydrochloride hydrate is a chemical compound with an amino acid structure. It is a structural analogue of the amino acid cysteine and has been shown to protect cells in culture from the toxic effects of proteases. This drug has been used in animal studies to test its ability to protect against diabetic neuropathy, but it is not yet known whether it will be effective for humans. DL-Cystein hydrochloride hydrate can be used as a fluorescence probe for albumin concentration and as a chemical chaperone that stabilizes proteins and prevents their aggregation. This compound has also been shown to have antioxidant properties, which may help prevent cellular damage caused by reactive oxygen species.</p>

<p>N,N'-Ethylenebis(iodoacetamide) is a molecule that binds to peptides and is used in cancer research. It has been shown to inhibit the growth of leukemia cells by inhibiting the synthesis of DNA. N,N'-Ethylenebis(iodoacetamide) has been shown to be an active analog for artemisinin, a drug used for malaria prophylaxis, and podophyllotoxin, a natural product used for the treatment of cancer. The molecule also inhibits cancer cell proliferation through its effects on protein synthesis.</p>

<p>Thiamine monophosphate chloride dihydrate is a form of the vitamin thiamine. It has been used in control analysis to measure the activity of enzymes that require thiamine as a cofactor, such as transketolase and pyruvate kinase. Thiamine monophosphate chloride dihydrate has also been studied in biochemical properties, where it was found that this compound can be cleaved by picolinic acid to form thiazole phosphate. The matrix effect is an important factor in polymerase chain reactions and has been shown to be dependent on the presence of dinucleotide phosphate. This compound is an essential component of energy metabolism and plays a role in protein synthesis. Thiamine monophosphate chloride dihydrate also has toxicological studies, including a model system using wild-type strains of yeast. These studies have shown that this compound leads to physiological effects such as inhibition of glycolysis and lactic acid production.</p>

<p>3-Chlorophenylhydrazine sulphate is a chemical compound that is made by the reaction of 3-chlorophenol and hydrazine. It has been shown to be stable when mixed with other compounds, such as acetone. 3-Chlorophenylhydrazine sulphate has a reaction time of one hour when it is reacted with sodium hydrogen sulfate and zinc powder in a liquid chromatography column. The final product is detected using chromatography detection, which can detect the presence of sulfates. This chemical compound can be used to make other chemicals, such as thiosulfate or hydrochloric acid.</p>

N-(4-Fluorophenyl)Anthranilic Acid is a fine chemical that is used as a scaffold for research chemicals, reaction components, and speciality chemicals. It can be used as a building block for complex compounds and useful building blocks. This compound has been shown to have high quality and can be used as an intermediate in the synthesis of other chemicals. N-(4-Fluorophenyl)Anthranilic Acid is a versatile building block that can be used in the synthesis of many different types of compounds. It also has been shown to be useful in the production of pharmaceuticals, dyes, pesticides, and herbicides.

<p>1-(1-Naphthyl)piperazine hydrochloride is a 5-HT3 receptor antagonist that has been shown to act as a potent serotonergic agent in the central nervous system of mammals. It is believed to inhibit the presynaptic serotonin uptake, resulting in an increase of serotonin concentration at the postsynaptic 5-HT1A receptor cells. 1-(1-Naphthyl)piperazine hydrochloride has also been shown to be a potent 5-HT1A receptor agonist and has antinociceptive effects following administration. This drug has been found to be more selective for the peripheral nervous system than other drugs of this type. It does not cross the blood-brain barrier and therefore does not interfere with mental function or behavior.</p>

4-Difluoromethoxyaniline is an allosteric modulator for glutamate receptors. It is a chemical compound that can be used to modify glutamate receptors to act as either metabotropic or ionotropic. 4-Difluoromethoxyaniline is used in the treatment of Parkinson's disease and other movement disorders, such as dyskinesia. It has been shown that 4-difluoromethoxyaniline increases the activity of activated glutamate receptors, which leads to increased levels of the neurotransmitter dopamine in the brain. This drug may also inhibit nitric oxide production and corticotropin-releasing hormone (CRH) synthesis.

1-(5-Chloro-2-methoxyphenyl)piperazine HCl is a fine chemical that belongs to the group of research chemicals. It is used as a reagent, speciality chemical and intermediate in organic synthesis. 1-(5-Chloro-2-methoxyphenyl)piperazine HCl is an effective building block for complex compounds, which can be used in reactions involving acetals, amides, nitriles, sulfones, sulfonamides and imines. This compound also has versatile building blocks and is a useful scaffold in organic synthesis.

(S)-(+)-2-Phenylglycine methyl ester hydrochloride is a nitro compound that inhibits the production of nitric oxide (NO) by inhibiting the enzyme nitric oxide synthase. It has shown inhibitory effects on bronchial hyperresponsiveness in animals with bronchial asthma and ischemic reperfusion injury. The compound also inhibits nitrogen-induced allergic reactions and inflammatory diseases. (S)-(+)-2-Phenylglycine methyl ester hydrochloride has been shown to have a protective effect against prostate cancer in animal models, although it was not active against prostate cancer cells in vitro. This may be due to its inability to cross the cell membrane or its inability to effectively penetrate the nucleus, which is where cancerous cells originate. The functional groups present on this molecule include amide, carbonyl, and hydroxyl groups.

<p>3-Bromo-4-methylbenzoic acid is a labile chemical compound that is used in the synthesis of retinoic acid, an analog of vitamin A. 3-Bromo-4-methylbenzoic acid can be synthesized by a two step process involving the boronic ester and biphenyl. The biphenyl is first treated with phosphorus pentachloride to produce a phenoxyacetate which reacts with 3-bromo-4-methylbenzoyl chloride in the presence of base to produce 3-bromo-4-methylbenzoic acid. This conversion can also be done via a solid phase synthesis where the biphenyl is anchored on silica gel and reacted with 3-bromo-4 methylbenzoyl chloride. The boronic esters are then cleaved from the solid support by treatment with sodium hydroxide under reflux conditions.<br>3 - Bromo -</p>

2-Fluoro-5-methylpyridine-3-boronic acid is a high quality chemical with CAS No. 1072952-45-4 that is a useful building block for the synthesis of complex compounds and speciality chemicals. 2-Fluoro-5-methylpyridine-3-boronic acid is also a versatile building block that can be used in organic reactions as a reaction component for the synthesis of speciality chemicals and other reagents. It can also be used to make fluoroquinolones and related pharmaceuticals, which are used to treat bacterial infections. This compound has many uses in research, including being a valuable scaffold for the synthesis of new drugs.

2,6-Dichloro-4-(trifluoromethyl)aniline is a colorless solid that is soluble in organic solvents. It is used as an absorber of chloride gas and other gases. 2,6-Dichloro-4-(trifluoromethyl)aniline reacts with hydrochloric acid to produce diazonium salt and chloride ions. The diazonium salt reacts with organic solvent and hydrogen gas to form the reaction products. In the presence of carbon dioxide and hydrogen chloride, 2,6-dichloro-4-(trifluoromethyl)aniline undergoes chlorinating reactions to produce hydrogen chloride gas and the chlorinated product.

4-Aminobenzyl alcohol hydrochloride is a fine chemical that is used as a building block for research chemicals, reagents, and specialty chemicals. It can be used as a versatile building block in the synthesis of many complex compounds. 4-Aminobenzyl alcohol hydrochloride is also an intermediate for the synthesis of pharmaceuticals and other useful compounds. CAS No. 170926-25-7

<p>1-(4-Chlorobenzyl)piperazine is an amine that belongs to the class of hydrogen-bond acid amides. It has a piperazine structure and is structurally related to other substances, such as dopamine. 1-(4-Chlorobenzyl)piperazine has been shown to inhibit spontaneous emission in animals and inhibit spontaneous activity at d4 receptors. This drug also inhibits the binding of agonists to the d4 receptor subtype, without affecting other subtypes.</p>

N-Methyl-N-(1-naphthyl)-2-bromobenzamide is a high quality reagent that is used as a complex compound. It has CAS No. 74881-58-6 and it can be used as a useful intermediate, fine chemical or speciality chemical. N-Methyl-N-(1-naphthyl)-2-bromobenzamide is also a versatile building block that is used in reactions to synthesize other compounds.

5-Amino-4-bromo-3-methylpyrazole hydrobromide is an intermediate in the synthesis of a variety of compounds. It is also a building block for the synthesis of heterocycles, such as pyrazoles, indazoles, benzoxazoles, and benzothiazoles. 5-Amino-4-bromo-3-methylpyrazole hydrobromide can be used as a reagent to synthesize pharmaceuticals and other useful compounds. 5-Amino-4-bromo-3-methylpyrazole hydrobromide is a versatile building block that can be used in the synthesis of many different types of compounds. This compound has been shown to react with various groups on organic molecules to form new chemical structures.

<p>2-Chloro-5-(4-chloro-5-difluoromethoxy-1-methylpyrazol-3-yl)-4-fluorophenoxyacetic acid monohydrate (2,4,5P) is a phenoxy herbicide that has been shown to be an effective broadleaf and grass weed control agent. 2,4,5P is a granule formulation that can be applied by helicopter or ground equipment. It has synergistic effects with glyphosate when applied together to soybean plants and can be used in combination with other herbicides for more effective weed control.</p>

1-(4-Bromophenyl)piperazine hydrochloride is a linker that binds to serotonin receptors. It has been shown to inhibit the reuptake of serotonin, which may lead to an increase in the neurotransmitter's level in the synaptic cleft. The compound also inhibits the production of 5-hydroxytryptamine and other monoamine neurotransmitters, which can lead to anaphylactic reactions in humans.

<p>3-Phenylpropionyl chloride is an acylating agent with antimicrobial properties. It is used as a precursor in the synthesis of many pharmaceuticals, such as amines and cyclohexane derivatives. 3-Phenylpropionyl chloride is a reactive compound that can undergo an acylation reaction with nucleophilic compounds to form an n-oxide. This reaction can be catalyzed by metal ions or bases. 3-Phenylpropionyl chloride has inhibitory properties against enzymes, such as aminoglycoside acetyltransferase and carbonyl reductase. It also has shown antitumor activity in cancer cells and metabolic disorders in the liver due to its ability to inhibit glycosidic bond formation.</p>

<p>2-Chloro-4,5-diaminopyrimidine is a pyrimidine compound with the molecular formula CHClN. It can be synthesized by reacting glycine and phenol with piperidine in the presence of hydrochloric acid. 2-Chloro-4,5-diaminopyrimidine has a solubility of 1.2 g/100 mL in water and reacts with quinine to form a red solution. This product also reacts with proline to produce an orange solution that fluoresces green when exposed to UV light. 2-Chloro-4,5-diaminopyrimidine has been used as an intermediate in the synthesis of other compounds such as pyridoxal phosphate and cefixime.</p>

<p>3-(Bromomethyl)-5-methyl-1,2,4-oxadiazole is an activating molecule that can be used as a histochemical stain. It forms a blue dye when reacted with the amino acid histidine in tissue. This compound stains cells and tissues blue, which can be used to identify different types of cells. 3-(Bromomethyl)-5-methyl-1,2,4-oxadiazole is also useful for identifying the location of specific proteins by detecting their presence in different types of cells. This compound can also be used in vivo to activate angiotensinogen in wild-type mice and then analyzing the effects on angiotensin levels.</p>

1,2-Bis(2-(4,5-dihydro-1H-imidazol-2-yl)propan-2-yl)diazene dihydrochloride is an analog of bis(pentafluorophenyl)diazene. It is a surfactant that can be used in micelles or as a solvent for amine reactions. It has been shown to cause death in mice and inhibit the growth of cells. The mechanism of this compound's effects is not fully understood but may involve the transfer of pentafluorophenyl groups from one molecule to another.

2-Amino-5-chlorobenzophenone oxime is a drug that belongs to the class of hydrazides. It was originally developed as an antidepressant and it has been shown in animal experiments to have antidepressant effects. 2-Amino-5-chlorobenzophenone oxime inhibits the enzyme monoamine oxidase, which is responsible for breaking down amines such as serotonin and norepinephrine. This inhibition leads to increased levels of these neurotransmitters in the brain, which may be responsible for its antidepressant effect. 2-Amino-5-chlorobenzophenone oxime also has analgesic properties, with yields of up to 86%.