Amines

<p>Applications 5-Amino-1-pentanol is an aliphatic amino alcohol with potential plasma lipid-lowering properties. 5-Amino-1-pentanol and other amino alcohols are used as emulsifying agents in dry-cleaning soaps, wax removers, cosmetics, paints and insecticides.<br>References Bondesson, G. et al.: Acta Pharm. Suec., 11, 417 (1974); Scheers, E.M. et al.: ALTA Alt. Lab. Anim., 30,309 (2002);<br></p>

<p>Applications 2-Amino-4,6,7,8-tetrahydro-5-(N-carbethoxy)thiazolo[5,4-d]azepine (cas# 887352-60-5) is a compound useful in organic synthesis.<br></p>

<p>Stability Hygroscopic<br>Applications N-(2-Chloroethyl)-1,2-ethanediamine Dihydrochloride is an analog of 2-(2-Aminoethylamino)ethanol (A608990); a reagent used in the synthesis of various pharmacologically active compounds and functional groups. Also used in the synthesis of antitumor anthracene-diones and antitumor DNA intercalators. More recently used in the synthesis of ionic liquids with various thermal, dielectric and catalytic properties.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Bair, K. et al.: J. Med. Chem., 33, 2385 (1990); Krapcho, A. et al.: J. Med. Chem., 37, 828 (1994); Karadag, A. et al.: J. Mol. Liq., 177, 369 (2013)<br></p>

<p>Applications Ethylamine Solution is used as a reagent in the synthesis of a series of hexadentate ligands as potential antibacterial agents. Also used as a reagent in the synthesis of tetrahydrothiazolopyridine derivatives as potent smoothened antagonists.<br>References Zhang, M., et al.: Chem. Biol. Drug Des., 84, 659 (2014); Ma, H., et al.: Eur. J. Med. Chem., 89, 721 (2015)<br></p>

<p>Stability Hygroscopic<br>Applications Diethanolamine similar to triethanolamine (T775580) is used as a surfactant. It also has the potential to be a corrosion inhibitor by means of chemisorption.<br>References Bhajiwala, H.M et al.: Bull. Electrochem., 17, 441 (2001); Yu, J. et al.: Thin. Solid. Films., 379, 7 (2000);<br></p>

<p>Applications p-Aminophenyl Arsenoxide is a useful reagent for the study of 2-oxoacid dehydrogenase multienzyme complexes.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Stevenson, et al.: Biochemistry, 17, 11, 2191 (1978)<br></p>

<p>Applications Diethylenetriamine is used in biological studies, for polyamines inhibition to carbonic anhydrases by anchoring to the zinc-coordinated water molecule.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Carta, F., et al.: J. Med. Chem., 53, 5511(2010)<br></p>

<p>Applications 4-Dimethylaminosulfotoluidide is an intermediate in the synthesis of Tolylfluanide (T536730), a polyvalent sulfamide fungicide that is closely related to dichlofluanide.<br>References Wainwright, A. et al.: Bright. Crop Prot. Conf. Pests Dis., 1, 275 (1996)<br></p>

<p>Applications N,N-Dimethyldecylamine is a useful synthetic intermediate. It can be used to prepare emodin (E523000) quaternary ammonium salt derivatives as potential anticancer agents It is also a reactant used to synthesize Benzyldecyldimethylammonium chloride (B234550), a biocide.<br>References Wang, W., et al.: Eur. J. Med. Chem., 56, 320 (2012); Qiu, B., et al.: Zhongguo Yaowu Huaxue Zazhi, 20, 353 (2010); Shao, J., et al.: Eur. J. Med. Chem., 56, 308 (2012); Lee, M., et al.: Appl. Micro. Biotech., 87, 1109 (2010)<br></p>

<p>Applications 5-Amino-2-chlorobenzotrifluoride is a compound useful in organic synthesis. It also performs a radioprotective activity against ionizing radiations.<br>References Blickenstaff, R. T., et al.: J. Pharm. Sci., 83, 219 (1994); Kumari, P., et al.: Org. Biomol. Chem., 16, 2049 (2018)<br></p>

<p>Applications Diethylammonium Dihydrogen Phosphate (cas# 68109-72-8) is a compound useful in organic synthesis.<br></p>

<p>Applications N,N-dimethyl-2-phenoxyethanamine (cas# 13468-02-5) is a useful research chemical.<br></p>

<p>Applications 2-(2-Aminoethoxy)ethanol is a widely used reactant that has been used in the preparation of TD-4306 as long-acting β2-agonist for asthma and COPD therapy.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Mckinnell, R.M., et. al.: Bioorg. Med. Chem. Lett., 24, 2871 (2014)<br></p>

<p>Impurity Mesalazine EP Impurity C<br>Applications 2-Aminophenol is an isomer of 4-Aminophenol (A618920) and is used as a reagent for the synthesis of heterocyclic compounds and dyes.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Pan, E., et al.: Chem. Sci., 4, 482 (2013); Meek, A.R., et al.: Can. J. Chem., 90, 865 (2012); Kiorpelidous, E., et al.: Chem. Res. Toxicol., 25, 2054 (2012);<br></p>

<p>Applications 4-(4,6-Bis(4-((2-ethylhexyloxy)carbonyl)phenylamino)-1,3,5-triazin-2-ylamino)benzoic Acid is an impurity in the synthesis of Ethylhexyl Triazone (E918810), used in sunscreen formulations as a UV filter to block out harmful ultraviolet light.<br>References Potard, G. et al.: Int. J. Pharm., 189, 249 (1999); Couteau, C. et al.: J. Pharm. Biomed. Anal., 44, 270 (2007);<br></p>

<p>2-Aminobenzimidazole is a fluorescent compound that has been used as a probe for the detection of hydrogen bonding interactions. It is also an antihypertensive drug and has been shown to inhibit the growth of prostate cancer cells. 2-Aminobenzimidazole is able to pass through the mitochondrial membrane, which may be due to its ability to transport protons across this membrane. This drug has been shown to inhibit bowel disease by reducing inflammation and increasing bowel motility. The mechanism of action has not yet been elucidated, but it is thought that 2-aminobenzimidazole may work by altering proton flow across the mitochondrial membrane or by inhibiting the release of proinflammatory factors from immune cells.</p>

<p>(R)-4-(Methylsulfinyl)-1-butylamine is a chemical intermediate that is used in the synthesis of a number of useful compounds, such as pharmaceuticals and agrochemicals. It is also used as a reagent in the synthesis of other chemical compounds, such as fine chemicals, research chemicals, and speciality chemicals. (R)-4-(Methylsulfinyl)-1-butylamine is a versatile building block that can be used to synthesize complex compounds. This compound has been shown to be an effective intermediate for the production of drugs for treating malaria and cancer.</p>

<p>Please enquire for more information about 2-(((4-ethoxyphenyl)amino)methylene)indane-1,3-dione including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>6-Amino-5-bromoquinoxaline is an inhibitor of serine proteases that has been shown to be effective in cell culture and in wild-type mice. It inhibits the enzyme by binding to the catalytic site, blocking the formation of a covalent bond between polypeptide chain and amino acid substrate. 6-Amino-5-bromoquinoxaline has also been shown to have an inhibitory effect on fibrinogen and polyclonal antibodies and can be used as a buffer for other proteases. In addition, this compound also inhibits caproic acid production from fatty acids via an unknown mechanism.br&gt;<br>6-Amino-5-bromoquinoxaline is not active against synthetic substrates or monoclonal antibodies.</p>

<p>[(N-Acryloylamino)phenyl]mercuric chloride is a compound that can be used to treat bladder cancer. It is a small molecule that has been shown to inhibit the growth of bladder cancer cells in vitro, and it may have potential as a treatment for primary tumors in other tissues. The therapeutic efficacy of [(N-acryloylamino)phenyl]mercuric chloride was investigated in two multicenter phase II trials conducted by the National Cancer Institute. The results of these trials showed that it had a response rate of 30% and an overall survival rate of 59%. This drug is effective against primarily women with body mass index greater than or equal to 25 kg/m2. It binds to the receptor on the surface of cells, which inhibits proliferation and induces cell death.</p>

<p>4-Aminobenzamide is a compound that is used as an anti-tuberculosis drug. It inhibits the activity of aminotransferase, which is an enzyme responsible for converting amino acids into other compounds. 4-Aminobenzamide has been shown to have antimicrobial properties against bacteria, fungi and protozoa. It also has a protective effect on human liver cells, but can cause damage to rat liver cells in vitro. 4-Aminobenzamide also shows some activity against microbial metabolism and can be hydrolyzed by hydrochloric acid to form phenylacetic acid and ammonia. This compound has been shown to inhibit the nervous system disease progression of Huntington's disease in mice.</p>

<p>4-(N-Boc-aminomethyl)aniline is a cavity-preventing agent that has been demonstrated to be neuroprotective in vitro. The drug also inhibits the growth of bacteria, fungi, and viruses in cell culture and animal models. 4-(N-Boc-aminomethyl)aniline is an innovative compound class that has shown potential for treating infectious diseases such as HIV, tuberculosis, and malaria. It has been shown to act by interfering with viral replication and inhibiting the production of inflammatory cytokines (e.g., tumor necrosis factor). Furthermore, 4-(N-Boc-aminomethyl)aniline can be used as a matrix effector or nucleophile to form hydrogen bonds with other molecules. It can also have an impact on nanomaterials when it is incorporated into their surface.</p>

<p>3-(Diethylamino)-1-propanol is a chemical species that has been shown to inhibit the growth of epidermal cells in a model system. 3-(Diethylamino)-1-propanol inhibits the production and release of epidermal growth factor, which is required for cell proliferation. The chemical binds to the receptor for epidermal growth factor, thereby inhibiting its activity. The low energy activation energies of this compound make it an excellent candidate for use in radiation therapy, as it can be easily activated by low levels of radiation and will not break down before reaching the target tissue. 3-(Diethylamino)-1-propanol also has inhibitory properties against other amines, such as histamine and acetylcholine.</p>

<p>3-Aminobenzhydrazide is a monomer that belongs to the group of hydrophobic molecules. It can be used as a chemical treatment for protein denaturation in vitro. 3-Aminobenzhydrazide is synthesized by bacteria and fungi through biosynthesis, which is catalyzed by the enzyme anilinohydrolase. 3-Aminobenzhydrazide has been shown to have no effect on water permeability or osmosis, but does have a significant effect on chloride ion permeability. This molecule also has functional groups such as a nitro group and amino group, which are responsible for its solubility in organic solvents and its ability to react with other compounds. 3-Aminobenzhydrazide can be used in vitro to remove chlorides from solutions containing high concentrations of chloride ions.</p>

<p>Non-denaturing, zwitterionic detergent</p>

<p>Rimantadine hydrochloride is a drug that belongs to the class of antiviral agents and is used for the prevention and treatment of influenza. It acts by blocking the uncoating of influenza virus, inhibiting viral RNA synthesis, and preventing virus-induced cytopathic effects in humans and animals. Rimantadine hydrochloride is an amantadine derivative that has been shown to be effective against influenza A viruses in humans. The drug also has a prophylactic efficacy against influenza B viruses. Rimantadine hydrochloride is localized in the lungs due to its intranasal application, which limits its effect on other parts of the body. It is metabolized into ammonium formate, chloride, and formamide before being excreted by the kidneys.</p>

<p>1,2,3,4-Tetrahydro-1-naphthylamine hydrochloride is a high quality reagent that can be used as an intermediate in the synthesis of various organic compounds. It has been shown to be a useful building block for the synthesis of complex compounds and speciality chemicals. Tetrahydro-1-naphthylamine hydrochloride is also a versatile building block for reactions involving amines or other nucleophiles. Tetrahydro-1-naphthylamine hydrochloride is an interesting scaffold for research chemicals due to its ability to react with various functional groups.</p>

<p>3-Amino-4-methylbenzoic acid is a chemical that is used in the synthesis of pharmaceuticals. It has been shown to have receptor binding activity and is able to inhibit aminotransferase activity. 3-Amino-4-methylbenzoic acid has been shown to be a competitive inhibitor of ptp1b, an enzyme that degrades phosphatidylinositol (3,4,5)-triphosphate. This property may be useful for treating inflammatory diseases such as Crohn's disease and rheumatoid arthritis. 3-Amino-4-methylbenzoic acid binds to the active site of ptp1b with high affinity and forms a coordination complex with two zinc ions. Monomers are also able to bind to ptp1b and inhibit its function.<br>3-Amino-4-methylbenzoic acid has been tested in vitro for its ability to inhibit the growth</p>

<p>2-(2-(2-Aminoethylamino)ethylamino)ethanol trihydrochloride is a chemical compound that is used as a reaction component and as a reagent in the synthesis of other chemicals. 2-(2-(2-Aminoethylamino)ethylamino)ethanol trihydrochloride is an intermediate for many organic compounds, including pharmaceuticals and pesticides. It has also been used to synthesize drugs for treating bacterial infections. 2-(2-(2-Aminoethylamino)ethylamino)ethanol trihydrochloride can be used in research or as a specialty chemical.</p>

<p>2-Amino-6-bromo-4-methoxyphenol (2ABMP) is a benzyl compound that can be used as a substitute for 2,4-diaminophenol. It has been shown to have estrogenic activity and may function as an estrogen receptor agonist. 2ABMP has also been shown to inhibit the growth of breast cancer cells in culture. The role of this drug in the treatment of breast cancer is not yet clear, but it may be useful in combination therapy with other drugs.</p>

<p>4-Diethylaminobenzonitrile is a molecule with the chemical formula C6H14N2. It is a colorless liquid that has an aromatic smell. It can be synthesized from acetonitrile and benzonitrile by UV irradiation. This compound has been used in cavity studies where it was found to have a large dipole moment, high exothermic reaction, and high emissions of uv radiation. The compound can also be used as an electrophotographic developer or in analytical chemistry to identify aromatic hydrocarbons. 4-Diethylaminobenzonitrile also has binding constants in hexane that are similar to benzene, which may be due to its resonance effect.</p>

<p>4-Amino-1,8-naphthalimide is a fluorescent derivative that is used as a probe to detect hydrogen bonds in molecular models. It can be used to study the interactions of molecules with hydrogen bonding partners. 4-Amino-1,8-naphthalimide has been shown to have broad spectrum antimicrobial activity against Gram-positive and Gram-negative bacteria. This compound also enhances the fluorescence of certain compounds by forming an intermolecular hydrogen bond.</p>

<p>4'-Amino-4-hydroxystilbene is a hydrocarbon that has been extracted from various plant sources. It can be dissolved in acetone and is soluble in alkanes. 4'-Amino-4-hydroxystilbene has been analyzed for its aromatic hydrocarbons, including naphthalene. This chemical can be used as a solvent extraction agent and may also have applications as an analytical reagent.</p>

<p>4-[2-(4-Aminophenyl)ethyl]phenol belongs to the class of organogelators. It is an organic compound that has been used in various studies on supramolecular chemistry and catalytic rate research. 4-[2-(4-Aminophenyl)ethyl]phenol has been shown to form gels with a variety of solvents, including water, ethanol, and acetone. The compounds have also been studied for their ability to act as heterogeneously catalysts in the synthesis of polymers. These compounds are polymorphs, meaning they can exist in different crystal structures. Structural studies have revealed that these polymorphs display different architectures and reactivities.</p>

<p>(S)-2-Aminobutyramide hydrochloride is a strong acid that can be used in the synthesis of other compounds. It is made by dissociating acetic acid with hydrogen chloride, or by reacting ammonia with hydrochloric acid. (S)-2-Aminobutyramide hydrochloride is also known as 2-aminobutyric acid dihydrochloride and protonated aminobutyric acid. It can be used to synthesize many other compounds, including amino acids, pharmaceuticals, and polymers. The virulent properties of this compound make it useful for industrial purposes.</p>

<p>Venlafaxine is a selective serotonin and norepinephrine reuptake inhibitor (SNRI) that is used to treat depression. Venlafaxine inhibits the reuptake of serotonin and norepinephrine into the presynaptic neuron, increasing their availability in the synaptic cleft. Venlafaxine has been shown to be effective in treating major depressive disorder and other depressive disorders, such as dysthymia and post-partum depression. The antidepressant effects of venlafaxine are believed to be due to its ability to block the uptake of serotonin and norepinephrine in the brain, resulting in an increased concentration of these neurotransmitters. Venlafaxine is metabolized by CYP2D6, CYP3A4, CYP1A2 and CYP2C19 enzymes, which may result in drug interactions with other drugs metabolized by these enzymes. To control for this effect, venlafaxine blood</p>

<p>2-Amino-5-bromobenzoic acid methyl ester is a small molecule with antiviral potency. It has a dipole moment and can form hydrogen bonds. 2-Amino-5-bromobenzoic acid methyl ester inhibits the PDE5 enzyme, which is an enzyme that breaks down cGMP. This inhibition of PDE5 leads to the increase in cGMP, which causes blood vessels to relax and widen. As a result, 2-amino-5-bromobenzoic acid methyl ester has been shown to decrease high blood pressure and improve heart function.</p>

<p>2-(1H-Indazol-3-yl)ethanamine hydrochloride is a chemical building block that can be used as a reaction component, reagent or useful scaffold. It is also a versatile building block in organic synthesis and can be used to make fine chemicals, speciality chemicals and research compounds. 2-(1H-Indazol-3-yl)ethanamine hydrochloride has been shown to have high purity and is suitable for use in pharmaceuticals, agrochemicals, dyestuffs, flavors and fragrances.</p>

<p>1,3-Bis[tris(hydroxymethyl)methylamino]propane, most commonly known as Bis-TRIS propane, is often referred to as the universal buffer because of its wide buffering range from pH 6.3 to 9.5. Its dual pKa values (~ 6.8 and 9.0) allow it to stabilize the pH in a variety of biological applications, including molecular biology, biochemistry, and electrophoresis.</p>

<p>Diisopropylammonium tetrazolide or tetrazole diisopropylamine is used to synthesize nucleoside 3'-CE phosphoramidites, which are building blocks in the chemical synthesis of novel oligonucleotides. Tetrazole diisopropylamine catalyses the reaction of 2-cyanoethyl tetraisopropylphosphorodiamidite with a nucleophile, usually the 3’-OH of a suitably protected nucleoside. This approach has been used to efficiently make modified cytosine oligonucleotides.</p>

<p>Diethylenetriaminepentaacetic acid dianhydride (DTPA) is a gadolinium chelate that can be used as a contrast agent. DTPA has been shown to have high affinity for the integrin receptor, which is expressed on the surface of many human cancer cells. This property makes DTPA an effective diagnostic tool for imaging and detecting tumor cells in vivo. DTPA is also useful for diagnosing myeloma cell lines and mouse tumors, due to its ability to bind to metal ions such as iron or copper.</p>

<p>Nucleophilic biotinylation reagent. Attaches cell surface glycosides to ELISA-type surfaces, mediated by a hydrophilic spacer/linker.</p>

<p>(R)-(+)-3-Dimethylamino pyrrolidine is a potent inhibitor of protein kinase C (PKC) with micromolar inhibitory concentrations. It binds to the enzyme and inhibits PKC activity by preventing the phosphorylation of threonine residues on the PKC substrate. 3DAP has been shown to be selective for PKC, as it does not inhibit other kinases or phosphatases at similar concentrations. 3DAP has also been shown to have antituberculosis activity in human cells and has been shown to have a high affinity for PKC in humans, which may be due to its selectivity for PKC over other kinases.</p>

<p>Please enquire for more information about Mesalamine impurity P including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Amino-5-chlorothiophenol is an aminothiophene derivative that has been shown to be an effective antibacterial agent. It is a substrate in the synthesis of polyesters and is used as a precursor in the synthesis of ciprofloxacin, a broad spectrum antibiotic. 2-Amino-5-chlorothiophenol has been shown to catalyze the reaction between phenyl groups and heterocycles, which is an important step in the synthesis of ciprofloxacin and fluconazole. The optimal reaction temperature for this process is between 150°C - 180°C. The irradiation time for this process varies depending on the intensity of light used, with optimal results obtained after 10 minutes at 25 kGy.</p>

<p>Ethanolamine hydrochloride is an ethylene diamine salt of ethanolamine. It has been shown to have a receptor activity in amines, such as human serum and monoclonal antibodies. Ethanolamine hydrochloride is used in sample preparation for the detection of proteins by western blotting and immunohistochemistry. It is also used for the production of monoclonal antibodies, which are used to detect antigens on cells.</p>

<p>2-Amino-3-hydroxybenzoic acid ethyl ester is soluble in organic solvents and is a catalyst for the hydrolysis of phenoxazinones. It has been shown to be the most active among the amino acid esters at pH 7. The optimum temperature for this enzyme is 37 degrees Celsius. The substrate specificity of this enzyme, which was purified by fractionation, is 3-hydroxyanthranilic acid and 3-hydroxyanthranilic acid with metals such as copper or zinc ions. This enzyme also catalyses the hydrolysis of proteins and peptides containing hydrophobic amino acids.</p>

<p>Dimethylphencyclidine is a potent analgesic with high affinity for opioid receptors. It is an agonist at the μ-opioid receptor and κ-opioid receptor. Dimethylphencyclidine may also act as a nociceptive agent and has been shown to modulate pain in animals. This drug has also been shown to be neuropathic, as it inhibits the development of chronic constriction injury (CCI) in rats by reducing the formation of reactive oxygen species and increasing the expression of brain-derived neurotrophic factor (BDNF). Dimethylphencyclidine has undergone clinical trials for the treatment of neuropathic pain and is currently in phase II clinical development.<br>The pharmacological properties of dimethylphencyclidine are due to its ability to act on opioid receptors and other neurotransmitter systems, including serotonin, dopamine, acetylcholine, glutamate, and glycine. The chemical name for this drug is 4-(Dimethylamino)-4-phen</p>

<p>Please enquire for more information about 2-(((4-(tert-butyl)phenyl)sulfonyl)amino)benzenecarbonitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Imatinib is an anticancer drug that belongs to the class of trimethyls. It is a potent inhibitor of tyrosine-specific protein kinases, including Bcr-Abl and Src family kinases. It has been shown to have antineoplastic properties in human cells in vitro. Imatinib is structurally similar to the anticancer agent lapatinib and inhibits G1 phase cell cycle progression by preventing phosphorylation of retinoblastoma protein (Rb). Imatinib is also genotoxic due to its structural similarity to other known genotoxic compounds such as bromo-2′-deoxyuridine and 2-chloroimidazole.</p>

<p>3-Amino-4-nitrobenzoic acid is a synthetic compound, which has been shown to inhibit the activity of trypanothione reductase. This inhibition of the enzyme causes an increase in the level of intracellular trypanothione, which is then acetylated by ATP sulfurylase and converted to trypanothione. 3-Amino-4-nitrobenzoic acid is also a potent inhibitor of fxa, which is a coagulation factor necessary for blood clotting. The active site of 3-amino-4-nitrobenzoic acid contains two nitroarenes that are responsible for its antithrombotic properties.</p>

<p>Sodium ammonium phosphate tetrahydrate is an inorganic compound that is a salt. It is used as a test compound to measure the inhibition of viral growth. The test compound binds to the virus and prevents it from binding to cells, thus inhibiting viral replication. Sodium ammonium phosphate tetrahydrate can also be used as a means of preventing cavities by lowering the pH level in the mouth and inhibiting bacterial growth. Selenium compounds have been shown to have antiviral properties when tested on the typhimurium virus. Selenium compounds are not active against herpes simplex virus, but protocatechuic acid has been shown to inhibit herpes simplex virus replication in vitro and in vivo. Protocatechuic acid has also been shown to inhibit fatty acid synthesis and chloride ion uptake into cells, which may be responsible for its anti-viral properties.</p>

<p>2-Aminodiphenylamine is a chemical compound with the molecular formula CHN. It is a white solid that has a melting point of about 170°C and a boiling point of about 360°C. 2-Aminodiphenylamine can be synthesized by reacting diphenylmethane with hydrochloric acid, followed by hydrogenation of the resulting diaminodiphenyl methane. It is an aromatic amine that has two nitrogen atoms in its structure. The molecule has a redox potential of -0.2 volts and can exist as either an acidic or basic form depending on pH levels. 2-Aminodiphenylamine also reacts with azobenzene to form coumarin derivatives, which are used in analytical chemistry for titration calorimetry, electrochemical impedance spectroscopy, and structural analysis.</p>

<p>Ethoxyamine hydrochloride is an organic compound that contains a hydroxyl group and a chlorine atom. It is an amine with properties of an acid. Ethoxyamine hydrochloride can be used in the treatment of metabolic disorders, such as nitro, dehydrogenase deficiency and amino acid transport disorder. The compound also has been shown to have anti-inflammatory effects, which may be due to its ability to inhibit the production of prostaglandin synthesis. This drug has been found to have no significant toxicity in humans and animals, and it has been shown to be safe for use in humans.</p>

<p>Ethyl 4-amino-3-nitrobenzoate is a molecule that is used as an inhibitor of butyrylcholinesterase. It has been shown to have inhibitory effects on enzymes such as cholinesterase, which are involved in the breakdown of acetylcholine and other neurotransmitters. Ethyl 4-amino-3-nitrobenzoate is a dihydrate and it has been found to be an efficient inhibitor of butyrylcholinesterase with a KI value of 0.2 mM. Single crystal x-ray diffraction analysis showed that the compound was centrosymmetric with hydrogen bonding interactions. The parameters were rationalized by this analysis, which led to the discovery of a more efficient method for synthesizing this molecule.</p>

<p>5-Fluoro-2-(trifluoromethyl)pyridin-4-amine is a fine chemical that is used to create other organic compounds. This compound is an intermediate in the production of pharmaceuticals, pesticides, and herbicides. It can also be used as a reagent or a speciality chemical in research. 5-Fluoro-2-(trifluoromethyl)pyridin-4-amine can be used as a reaction component to synthesize other compounds and has been shown to have versatile functions as a building block for complex molecules. This compound is not classified by the Chemical Abstract Service (CAS) and does not have any reported toxic effects on humans.</p>

<p>(R)-4-(Boc-amino)-3-(Z-amino)butyric acid is a synthetic ligand that binds to dna. The binding of this ligand can be monitored by the thermodynamic interaction between the ligand and dna. (R)-4-(Boc-amino)-3-(Z-amino)butyric acid has been shown to bind to the phosphate groups on dna, which are apolar in nature. This ligand also interacts with the vector group of dna, and it has a multivalency of two. It is water soluble and neutral, making it suitable for use in supramolecular chemistry. (R)-4-(Boc-amino)-3-(Z-amino)butyric acid is not very polar and does not have any charges or functional groups that would make it an ionizable species. It can form complexes with carbohydrates because it is neutral, and its interactions with them are</p>

<p>Dehydro norketamine is a chiral compound that is used as a sample preparation for analytical methods. It has been shown to be the major metabolite of ketamine and can be detected in human serum, urine, and sweat. Dehydro norketamine has also been found to have similar pharmacological effects as ketamine, such as analgesia and hallucinogenic properties. The detection sensitivity of dehydro norketamine is lower than that of ketamine, as it cannot be detected in human serum at concentrations less than 0.5 ng/mL. The clinical relevance of dehydro norketamine is still being studied. The following product description should not exceed 150 words: Dehydro norketamine is a chiral compound that is used as a sample preparation for analytical methods. It has been shown to be the major metabolite of ketamine and can be detected in human serum, urine, and sweat. Dehydro nork</p>

<p>Acridine-3,6-diamine is a fluorescent dye that is used in analytical chemistry to measure the concentration of DNA. The dye binds to the enzyme form of DNA and can be detected with a fluorescence microscope. Acridine-3,6-diamine is also used as a model system for studying multidrug efflux pumps found in cells, which are ATPases that pump out toxic substances from bacteria. This drug has shown antibacterial efficacy against various bacteria, including Staphylococcus aureus and Escherichia coli. The potential mechanism of action may be due to inhibition of the bacterial DNA replication processes by binding to the cell nuclei or through inhibition of energy metabolism or dinucleotide phosphate synthesis.</p>

<p>4,5-Diamino-6-chloropyrimidine is a glycosidic compound that has been used for the optimization of drug targets. It has been shown to have antimalarial activity against Plasmodium falciparum in vitro and in vivo. 4,5-Diamino-6-chloropyrimidine binds to the amine groups on nucleotides, specifically purines (adenine and guanine), and amidates the 6-chloropurine ring. This makes it a potential candidate for use in chemotherapy. The structure of 4,5-diamino-6-chloropyrimidine was determined by NMR and mass spectroscopy analysis.</p>

<p>Phosphodiesterase inhibitor</p>

<p>N-Amino-D-proline is a hydrogen bond donor that has phytotoxic properties. It is synthesized from the reaction of ethanolamine, sulfoxide, and hydrochloric acid in the presence of lysine residues. N-Amino-D-proline may be used to treat death due to tissue injury or degeneration. The compound can also be used in chromatographic techniques as a hydrogen bond acceptor.</p>

<p>5-Amino-2-methoxybenzoic acid (5AMBA) is a hydrogen bond acceptor that binds to peptides and rna. It also has enzymatic activity, which can be used in the treatment of diseases such as Alzheimer's disease. 5AMBA is a small molecule that contains two methoxy groups and one hydrogen. It has been shown to bind to an intramolecular hydrogen bond within a peptide or rna sequence and inhibit enzymatic activity. This inhibition occurs by removing the nucleophile from the enzyme's active site or by sterically hindering access to the enzyme's active site. The luminescent properties of 5AMBA make it an ideal candidate for fluorescent labeling, with applications in biomolecular research.</p>

<p>4-Aminobenzanilide is an antimicrobial agent that is synthesized from 2-aminobenzamide and 4-aminophenol. It has been shown to be effective against a number of bacteria, including Staphylococcus aureus and Streptococcus pyogenes. 4-Aminobenzanilide has also been shown to inhibit the growth of Mycoplasma pneumoniae in mammalian cells, which may be due to its ability to block DNA replication and transcription. This compound can also disrupt the synthesis of amides by inhibiting the enzyme aminopeptidase N. The low energy required for this reaction makes it possible for this compound to work as an antimicrobial agent with minimal toxicity.</p>

<p>Diethylenetriamine is a chemical compound that has been studied extensively in the field of biological research. It is a metal chelator, meaning it binds to heavy metals, and can be used to remove them from the body. Diethylenetriamine is also an antimicrobial agent that has been shown to have a protective effect on the liver against gadolinium-induced lesions. It is used for wastewater treatment as well as metal carbonyls and metal-hydroxides reactions, such as electrochemical impedance spectroscopy. Diethylenetriamine can also be used in human immunoglobulin synthesis and Langmuir adsorption isotherm studies. Diethylenetriamine has been shown to bind with human serum proteins by hydrogen bonding interactions, which may explain its effects on the liver.</p>

<p>Acetaminophen is a common pain reliever and fever reducer. It is available over-the-counter in many countries. Acetaminophen is a member of the class of drugs known as analgesic, antipyretic, and anti-inflammatory drugs (APAP). The drug has been shown to be effective for acute pain relief, but not for chronic pain. Acetaminophen has also been found to be an effective analgesic when taken at high doses (above 1000 mg per day) for more than one week. In vivo studies have shown that acetaminophen inhibits mitochondrial membrane potential in hk-2 cells and cd-1 mice. This inhibition leads to apoptosis and cell death. Acetaminophen is not associated with serious side effects when used at the recommended dose, although it can lead to liver damage if taken in large quantities or on a prolonged basis.</p>

<p>Boc-L-4-Aminophenylalanine is an amino acid that has been shown to be synthesized by cancer cells in breast cancer cell lines, and can also be conjugated with anticancer drugs. It has been shown to have a high affinity for cancer cells. Boc-L-4-Aminophenylalanine is a substrate for L type amino acid transporters and can be used for the treatment of breast cancer. This compound may also be useful in the treatment of other cancers due to its ability to inhibit the uptake of endogenous amino acids.</p>

<p>(6S)-5,6,7,8-Tetrahydro-6-[propyl[2-(2-thienyl)ethyl]amino]-1-naphthalenol is a potent and selective dopamine receptor agonist. It acts by binding to the dopamine receptors in the brain. This binding stimulates the release of dopamine and prevents it from being reabsorbed into the neurons, which in turn increases levels of extracellular dopamine in the synapse. (6S)-5,6,7,8-Tetrahydro-6-[propyl[2-(2-thienyl)ethyl]amino]-1-naphthalenol has been shown to have antidepressant effects in animal models of depression. It also has a long half life and can be administered as a transdermal patch for prolonged relief from depression symptoms.</p>

<p>2-[N-[(3,5-Difluorophenyl)carbamoylamino]-C-methylcarbonimidoyl]pyridine-3-carboxylic acid (2FPC) is a potent herbicide that inhibits the fatty acid synthase enzyme and blocks cellular energy production. Fatty acid synthase is an important enzyme in the synthesis of essential fatty acids and this inhibition can lead to a number of health complications. 2FPC also inhibits epidermal growth factor receptor (EGFR) and glucocorticoid receptors, which can lead to autoimmune diseases. The compound has been shown to produce neurotoxic effects in animals and humans, including optical sensor activation and cation channel modulation.<br>2FPC is used as a herbicide to control weeds such as knapweed. It is also used as an anti-inflammatory agent in the treatment of rheumatoid arthritis.</p>

<p>3-Amino-phenazin-2-ol is a pesticide that has been shown to have genotoxic effects on human lymphocytes in vitro. 3-Amino-phenazin-2-ol inhibits the growth of triticum aestivum, a type of cereal plant, by binding to the aminoacids in the cell wall and disrupting its structure. This leads to cell death and inhibits the synthesis of proteins necessary for cellular growth. The herbicide has also been shown to inhibit the growth of typhimurium at high concentrations and may be used as an herbicide or pesticide. The mechanism by which 3-amino phenazin 2-ol exerts its toxicity is not fully understood, but it may be due to its ability to activate cells that are exposed to low energy levels.</p>

<p>Propargylamine is an irreversible inhibitor that binds to the active site of the enzyme acetylcholinesterase (AChE) and blocks the breakdown of acetylcholine. This leads to increased levels of acetylcholine in the synaptic cleft, which enhances neurotransmission and causes increased muscle contractions. Propargylamine has been shown to be a potent chemotherapy agent against cancer cells, causing neuronal death. It also inhibits epidermal growth factor receptor (EGFR) signaling pathways, leading to decreased tumor cell proliferation. The drug may also have neurotrophic effects by stimulating nerve growth factors or preventing neuronal apoptosis.</p>

<p>Ethyl 2-amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate is an antibacterial agent that inhibits the growth of bacteria by binding to amines and metal ions. It also has in vitro anticancer activity against cancer cells. Ethyl 2-amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate has been shown to have antiinflammatory activity in rats.</p>

<p>Please enquire for more information about (S)-Tetrahydrofuran-3-amine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-(4-Diethylamino)phenyl)-2-nitroethane is a reagent that is used as a building block in the synthesis of various heterocycles. It has been shown to be useful for the preparation of many heterocyclic compounds. The compound is also used as a research chemical and as a precursor to other organic compounds. 1-(4-Diethylamino)phenyl)-2-nitroethane is also an intermediate in the production of other speciality chemicals, such as pharmaceuticals, dyes, and pesticides.</p>

<p>2-Amino-4,6-dichloro-s-triazine is a chemical compound that is used as an antimicrobial agent in wastewater treatment. It inhibits the growth of bacteria by binding to cell walls and disrupting the formation of crosslinks between peptidoglycan strands, thereby inhibiting the synthesis of proteins necessary for bacterial growth and reproduction. 2-Amino-4,6-dichloro-s-triazine has been shown to be effective against group p2 bacteria in cell culture experiments. This drug also displays antiinflammatory properties and has been shown to inhibit HIV infection in vitro.</p>

<p>N,N-Diethyl-N-(4-iodobenzyl)amine is a high quality and versatile building block that is used as a reagent, speciality chemical, or intermediate. The compound has been found to be useful in the synthesis of complex compounds. It can also be used as a reaction component for various organic synthesis reactions. N,N-Diethyl-N-(4-iodobenzyl)amine is commercially available from Sigma Aldrich with CAS No. 914636-94-5.</p>

<p>Dantrolene sodium is a muscle relaxant that belongs to the group of pharmacological agents. It is used to treat muscle spasms and hyperactivity in patients with neuromuscular disorders. Dantrolene sodium inhibits calcium release by blocking the activity of the enzyme ryanodine receptor in skeletal muscle cells. This inhibition prevents uncontrolled contraction of muscles and reduces their energy consumption. The drug also has an effect on malignant hyperthermia, which is caused by an increase in the production of adenosine triphosphate (ATP) due to increased cellular metabolism. Dantrolene sodium can inhibit ATP synthesis, thus reducing energy production and stabilizing cell membranes, thereby preventing cell death in neurons and other tissues.</p>

<p>4-(N,N-Diethylamino)cinnamic acid is a dye-sensitized solar cell sensitizer that has been synthesized from thiophene and acrylic acid. This compound is efficient in dye-sensitized solar cells and can be used to produce solar cells with an efficiency of over 10%.</p>

<p>AMPD, also known as 2-Amino-2-methyl-1,3-propanediol, is a buffer solution with a pH range of 7.8-9.7 and a pKa of 8.8. This chemical buffer is used in molecular biology, protein studies, enzyme assays, and separation techniques such as isatachophoresis (ITP) and SDS-gradient gel electrophoresis.</p>

<p>Please enquire for more information about 2-[1-(Methylamino)ethyl]indole including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Sodium 2-[[3-(trifluoromethyl)phenyl]amino]benzoate (TFPB) is a synthetic substrate that has been used in the synthesis of microcapsules. TFPB is soluble in water, which allows it to be administered orally and provides a non-toxic environment for the release of protein drugs. TFPB is also able to bind with receptors on polymorphonuclear leucocytes and can be used as an adjuvant therapy in women.</p>

<p>AZD 1152 is an Aurora kinase inhibitor, which is a type of small-molecule therapeutic agent. It is derived from the pharmaceutical research conducted by AstraZeneca. Its primary mode of action involves the selective inhibition of Aurora B kinase, an enzyme crucial for the regulation of mitosis. By interfering with this enzyme, AZD 1152 disrupts the normal progression of cell division, leading to the inhibition of proliferation and induction of apoptosis in rapidly dividing cells.</p>

<p>4-(Dimethylamino)chalcone is a fluorescent molecule that has been used as a fluorescence probe to study the structures of fatty acids and other molecules. It is also used to detect neutral pH in biological studies. 4-(Dimethylamino)chalcone reacts with carbonyl groups to form stable complexes, which are useful for structural analysis. The fluorescence intensity is proportional to the concentration of the carbonyl group. This molecule has been shown to be potently active against human serum, which may be due to its ability to bind with protein and form stable complexes.</p>