Amines

<p>Applications Tetrabutylammonium tetrafluoroborate (cas# 429-42-5) is a useful research chemical.<br></p>

<p>Applications 2-(3-Aminophenyl)ethanol is a useful compound for the synthesis of indolines and dihydrobenzofurans via iron and copper-catalyzed iodination and cyclization.<br>References Henry, M. C., et al.: J. Org. Chem., 84, 346 (2019)<br></p>

<p>Applications Pyrimidine with the ability to form complexes with heavy metal ions.<br>References Iltzsch, M., et al.: Biochem. Pharmacol., 48, 781 (1994),<br></p>

<p>Applications 1,4-Diaminobutane is an amino acid degradation product. Used in the preparation of hexahydropyrimidines as novel hepatitis C virus inhibitors. Also a reagent in the synthesis of antibacterial castor oil-based polyurethane membranes.<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 Hwang, J. et al.: Eur. J. Med. Chem., 70, 315 (2013); Yari, A. et al.: J. Biomed. Mat. Res., 102A, 84 (2014);<br></p>

<p>Applications 5-(Aminomethyl)-2,3-dihydro-1H-inden-1-one Hydrochloride is a useful research chemical for organic synthesis.<br></p>

<p>Applications 2-(bis(2-(tert-butoxy)-2-oxoethyl)amino)acetic acid (cas# 171557-31-6) is a useful research chemical.<br></p>

<p>Applications 2-amino-6-hydroxybenzoic acid (cas# 567-62-4) is a useful research chemical.<br></p>

<p>Stability Light Sensitive, Temperature Sensitive<br>Applications 4-(2-Aminophenyl)-4-oxo-2-butenoic Acid is a novel human lens metabolite from normal and cataractous human lenses. A UV filter.<br>References Mizdrak, J., et al.: Tetrahedron, 63, 4990 (2007); Taylor, L. M., et al.: Exp. Eye Res., 75, 165 (2002)<br></p>

<p>Applications Methyl 2-Aminothiazole-5-carboxylate (cas# 6633-61-0) is a compound useful in organic synthesis.<br></p>

<p>Applications 4'-Dimethylaminophenyl acetylene<br></p>

<p>Applications trans-4-(Dimethylamino)-3-buten-2-one is an reagent used in the synthetic preparation of various substances.<br>References Maggiulli, C.A., et al.: Org. Prep. Pro. Int., 16, 31 (1984); Afarinkia, K., et al.: Sci. Syn., 14, 275 (2003);<br></p>

<p>Applications 5-Amino-2-chlorobenzenesulfonamide (cas# 2015-19-2) is a compound useful in organic synthesis.<br>References Somers, F., et al.: Pharm. Pharmacol. Commun., 6, 89 (2000), D'Ambrosio, K., et al.: J. Med. Chem., 51, 3230 (2008),<br></p>

<p>Applications 1-(2-Phenylethynyl)cyclohexanamine is a reactant that functions as a catalyst in the cyclization of propargylamines.<br>References Zhao, D. et al.: ChemCatChem., 9, 4598 (2017); Yuan, R. et al.: J. Org. Chem., 82, 3639 (2017);<br></p>

<p>Applications (1R)-2,3-Dihydro-N-2-propen-1-yl-1H-inden-1-amine Ethanedioate is an intermediate used in the synthesis of propargylated aminoindan derivatives via allylation, bromination, dehalogenation sequence.<br>References Phull, M., et al.: PCT Int. Appl., WO 2009081148 A1 20090702 (2009)<br></p>

<p>Applications Used for the preparation of dihydrouracils as anti-ictogenic or anti-epileptogenic agents.<br>References Akoulitchev, S., et al.: Nature, 377, 557 (1995), Marshall, N., et al.: J. Biol. Chem., 270, 12335 (1995), Marshall, N., et al.: J. Biol. Chem., 271, 27176 (1996), Shapiro, G., et al.: J. Clin. Oncol., 24, 1770 (2006),<br></p>

<p>Applications 2-(3-Aminopropylamino)ethanol is the hydroxy analogue of WR-1065 (A576820), a metabolite of Amifostine (A576810). Amifostine is an organic thiophosphate that has the ability to protect a broad range of tissues from cytotoxicity (e.g. from chemotherapeutic agents) without inducing an antitumour response. 2-(3-Aminopropylamino)ethanol is also used as an nucleophilic tag in the detection of human butyrylcholinesterase adducts.<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 Antonadou, D., et al.: Int. J. Rad. Oncol. Biol. Phys., 52, 739 (2002); Kemp, G., et al.: J. Clin. Oncol., 14, 2101 (1996)<br></p>

<p>Applications 5-Chloropyridazin-3-amine is an intermediate used to prepare aminopyrazines as novel, potent Nav1.7 antagonists.<br>References Bregman, H., et al.: Bioorg. Med. Chem. Lett., 22, 2033 (2012)<br></p>

<p>Applications 1,4-Phenylenediamine-13N2 is the isotope labelled analogue of 1,4-Phenylenediamine (P319845), an organic compound that is a derivative of aniline and a main ingredient for the production of polymers and hair 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 Chugh, K., et al.: J. Med., 13, 131 (1982), Baud, F., et al.: J. Toxicol. Med., 4, 279 (1984), Ashraf, W., et al.: Human Exp. Toxicol., 13, 167 (1994),<br></p>

<p>Applications 2-(Tributylstannyl)-2-propen-1-amine (cas# 155258-22-3) is a compound useful in organic synthesis.<br></p>

<p>Applications 2-[(7-Nitro-2,1,3-benzoxadiazol-4-yl)amino]ethanethiol is used in the preparation of fluorescent N/S acyl derivatives.<br>References 2-[(7-Nitro-2,1,3-benzoxadiazol-4-yl)thio]ethanamine<br></p>

<p>Applications 4-(Aminomethyl)-Cyclohexanecarboxylic Acid (cas# 701-54-2) is a useful research chemical.<br></p>

<p>Applications N-Ethyl-3-phenylpropylamine is an intermediate in the synthesis of 4-Hydroxy Alverine (H827950), a metabolite of Alverine (A575780) in plasma.<br>References Bouvier, M., et al.: Gastroenterol. Clin. Biol., 16, 334 (1992), Mitchell, S., et al.: Aliment. Pharmacol. Ther., 16, 1187 (2002), Hayase, M., et al.: Br. J. Pharmacol., 152, 1228 (2007),<br></p>

<p>Applications 4-amino-N-(2,6-dimethylphenyl)benzamide (cas# 787-93-9) is a useful research chemical.<br></p>

<p>Applications ethyl 2-(methylamino)-2-oxoacetate (cas# 18522-95-7) is a useful research chemical.<br></p>

<p>Applications (2R)-1-(9H-Purin-6-ylamino)-2-propanol is a reagent for the synthesis of tenofovir disoproxil fumarate, a medication for the treatment of hepatitis B and to prevent and treat HIV/AIDS.<br>References Yan, N., et al.: Jingxi Huagong, 31, 983 (2014); Ripin, D. H. B., et al.: Org. Process Res. Dev., 14, 1194 (2010)<br></p>

<p>Applications 2-[6-(Acetylphenylamino)-1,3,5-hexatrienyl]-1,1-dimethyl-3-sulfobutyl-1H=-benz[e]indolium Inner Salt is a reactant used in the preparation of indocyanine green as an infrared probe.<br>References Suganami, A. et al.: Bioorg. Med. Chem. Lett., 22, 7481 (2012); Doi, T. et al.: Synlett., 23, 306 (2012);<br></p>

<p>Applications N-(Trifluoroacetyl)hexanolamine (cas# 40248-34-8) is a compound useful in organic synthesis.<br></p>

<p>Applications B-[3-[[2-Hydroxy-3-[3-(triethoxysilyl)propoxy]propyl]amino]phenyl]boronic acid was prepared for the use as porous polymeric monolith for the specific capture of cis-​diol-​containing flavone under neutral condition.<br>References Pan, J., et al.: Chem. Eng. J., 317, 317-330 (2017);<br></p>

<p>Applications Ammonium Bicarbonate is a useful reagent in the synthesis of double-shelled CoMn2O5 hollow microcubes used as anode material for lithium-ion batteries.<br>References Zhou, L., et al.: Adv. Mater., 24, 745 (2012);<br></p>

<p>Applications 4-Amino-2-ethynylphenol is a disubstituted phenol.<br></p>

<p>Applications o-Chloramine T (cas# 110076-44-3) is a useful research chemical.<br></p>

<p>Applications (1-ethylcyclohexyl)methanamine (cas# 143689-16-1) is a useful research chemical.<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></p>

<p>Applications Ecamsule Triethanolamine is used in the preparation of sunscreens providing a UV filter.<br>References Salvador, A. et al.: Anal. Achim. Acta., 537, 15 (2005);<br></p>

<p>Applications 5-Aminononane-5-carboxylic Acid is a reagent used in the synthesis of Fmoc-α-​dialkylamino acids.<br>References Suresh B. et al.: Indian J. Chem. Section B: Chem. Inc. Med., 40B, 70 (2001);<br></p>

<p>Applications Diethyl 3-(N-Hydroxyamino)propylphosphate (cas# 66508-19-8) is a compound useful in organic synthesis.<br></p>

<p>Applications N-Hydroxybenzylamine Hydrochloride, is a versatile intermediate for the synthesis of various pharmaceutical compounds. It is used for the preparation of Ticagrelor (T437700) derivatives as novel antiplatelet agents.<br>References Zhang, H., et al.: Bioorg. Med. Chem. Lett., 22, 3598 (2012); Jakubowski, J., et al.: Cardiovasc. Drug Rev., 25, 357 (2007);<br></p>

<p>Stability Hygroscopic<br>Applications [3-(3,4-dimethoxyphenyl)propyl](methyl)amine hydrochloride (cas# 83979-31-1) is a useful research chemical.<br></p>

<p>Applications 4-(dimethylamino)benzenesulfonamide (cas# 6162-21-6) is a useful research chemical.<br></p>

<p>2-Amino-4,6-dimethylpyrimidine is a molecule that contains a hydroxyl group, copper chloride, nitrogen atoms, sodium carbonate, and hydroxybenzoic acid. The antimicrobial properties of 2-amino-4,6-dimethylpyrimidine are due to the presence of the hydroxyl group and copper chloride in its structure. This compound has been shown to have bactericidal activity against Pseudomonas aeruginosa and other gram-negative bacteria. It also inhibits the growth of these bacteria by interfering with their ability to synthesize proteins. 2-Amino-4,6-dimethylpyrimidine is a molecule that has an octahedral coordination geometry and forms hydrogen bonds with water molecules. It binds to the surface of minerals such as calcite or quartz and can be used for gravimetric analysis.</p>

<p>Please enquire for more information about N-[3-Fluoro-4-[(methylamino)carbonyl]phenyl]-2-methylalanine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Methylcyclohexylamine is a compound that is used as an inhibitor of the enzyme ornithine decarboxylase. It also has been shown to have anti-inflammatory properties in cell culture and in animal models of inflammatory bowel disease. 4-Methylcyclohexylamine binds to the active site of the enzyme, preventing it from converting ornithine into putrescine. Ornithine decarboxylase inhibitors are a new class of drugs for the treatment of inflammatory bowel disease, which are effective against both ulcerative colitis and Crohn's disease.</p>

<p>Pyridin-4-ylmethanamine is a chemical compound that contains a pyridine ring and an amine (-NH2) group. It is usually used as a building block for the synthesis of other compounds. Pyridin-4-ylmethanamine can be synthesized from picolinic acid, which is obtained through a reaction with sodium hydrochloride in an alkaline solution. This reaction proceeds via two steps: first, the formation of a pyridinecarboxylic acid ester and then the addition of ammonia to form pyridin-4-ylmethanamine. The transfer reactions that occur during this process are highly dependent on temperature and pH. The frequency shift effect can be observed when pyridin-4-ylmethanamine interacts with amines, which changes its absorption spectrum.</p>

<p>Please enquire for more information about E-3-(Tributylstannyl)-2-propen-1-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Diethyl[2-(4-nitrophenoxy)ethyl]amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Eltrombopag olamine is an orally active drug that belongs to the class of thiazolidinones. It has been used for the treatment of thrombocytopenia in patients with chronic liver disease and myelodysplastic syndrome. Eltrombopag olamine inhibits platelet aggregation by binding to glycoprotein IIb/IIIa receptors on the surface of platelets. The drug is a prodrug that is metabolized in vivo to its active form, eltrombopag. This conversion is catalysed by CYP3A4 and CYP2D6 enzymes and can be inhibited by drugs that inhibit these enzymes, such as trifluoroacetic acid and hydroxyl group-containing compounds. Eltrombopag olamine binds to erythrocytes, which may be due to its ability to form intramolecular hydrogen bonds with nitrogen atoms. The synthesis of elt</p>

<p>1-(4-Aminophenyl)-1H-pyridin-2-one is a synthetic chemical that is used in the manufacturing of 8-hydroxyquinoline. It is an industrial chemical that is used to produce potassium carbonate by a reflux reaction with potassium and carbonate. 1-(4-Aminophenyl)-1H-pyridin-2-one is a gas at room temperature and pressure and has been shown to be stable under these conditions.</p>

<p>Trans-4-aminocyclohexanol is a cell signaling molecule that belongs to the class of heterocyclic compounds. It has been shown to have an anti-inflammatory effect and inhibit the production of pro-inflammatory cytokines in vitro. Trans-4-aminocyclohexanol also inhibits cyclooxygenase (COX) activity, which is responsible for the conversion of arachidonic acid into prostaglandins. This inhibition leads to decreased inflammation and pain. Trans-4-aminocyclohexanol is orally bioavailable and can be detected in the blood plasma within one hour after administration. The compound has been shown to bind to the enzyme protein kinase C, which is involved in cell signaling pathways, and inhibit its activity.</p>

<p>Please enquire for more information about N-Boc-amino-(4-N-fmoc-piperidinyl)carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about [(1-Benzyl-1H-pyrazol-4-yl)methyl]amine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(4-methoxyphenyl)ethyl]methylamine is a pharmacological agent that inhibits protein synthesis. It has been shown to have an optimum concentration of 1 μM, with maximal inhibition at 10 μM. 2-(4-methoxyphenyl)ethyl]methylamine binds to the basic amino acid residues of proteins and inhibits the activity of eosinophil cationic protein, which is responsible for histamine release. 2-(4-Methoxyphenyl)ethyl]methylamine has also been shown to reduce the activity of epidermal growth factor, which is responsible for cell proliferation and differentiation. The drug has been demonstrated to be an effective inhibitor of activated eosinophils, but not normal cells. 2-(4-Methoxyphenyl)ethyl]methylamine may be used as a treatment for chronic asthma patients who suffer from eosinophilic inflammation in their</p>

<p>Dimethyl-p-phenylenediamine sulfate (DMPD) is a response element that is involved in the regulation of physiological function and energy metabolism. DMPD is found in prostate cancer cells, which may be due to its ability to regulate the apoptosis pathway. The clinical relevance of DMPD has been shown by a low dose study on rats with myocardial infarcts. Rats were given doses of 0.5, 1, or 2 mg/kg DMPD for 3 weeks before being subjected to an occlusive coronary artery ligation procedure. The results showed that the rats given DMPD had significantly lower systolic blood pressure than those not given DMPD, but there was no difference in diastolic blood pressure.</p>

<p>Please enquire for more information about 2-Hydroxy-2-(3,4-dimethoxyphenyl)ethylamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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

<p>Please enquire for more information about 4'-Methyl aminorex including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Tetraethylenepentamine is a cell-signaling agent that binds to the MCL-1 protein and inhibits its function as a cell factor. This inhibition prevents the induction of apoptosis, which is important for the development of bowel disease. Tetraethylenepentamine can be used in wastewater treatment to remove glycol ethers from industrial effluent. It also has been shown to adsorb at acidic pH levels, making it an ideal candidate for use in solid phase microextraction (SPME) experiments. Tetraethylenepentamine interacts with fluorescence probes such as hydroxycoumarin, which makes it useful for surface methodology studies.</p>

<p>1-Methylhexylamine is a chemical compound that has been shown to be an effective treatment for inflammatory bowel disease. It works by activating the H1 receptor, which blocks the production of proinflammatory cytokines and reduces inflammation. 1-Methylhexylamine also has anti-inflammatory effects and can inhibit the growth of bacteria in vitro. This compound can be used as an analog for histamine in sample preparation, where it is used to reduce hydrochloric acid from acidic samples. The uptake of 1-methylhexylamine into cells is pH dependent and can be enhanced by adding sodium citrate or redox potential. 1-Methylhexylamine has been shown to cause symptoms such as headache, nausea, vomiting, dizziness, and depression when it is injected or ingested at high doses. Toxicity studies have shown that this drug may cause liver damage and kidney failure at high doses.</p>

<p>Please enquire for more information about 3-Aminopropyl Silica Gel (0.6-1.3mmol/g) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 3-Amino-6-hydroxy-2-methylquinazolin-4(3H)-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Methylphenethylamine is a synthetic amine that is used in the production of 3-methylphenethylamine hydrochloride. It has been shown to have a wide range of pharmacological effects, including increasing blood pressure, heart rate, and respiration. This drug also has an antitussive effect and can be used to treat asthma symptoms. 3-Methylphenethylamine can be synthesized by reacting phenylethylamine with formaldehyde and hydrogen chloride gas in the presence of alcohol or sodium hydroxide solution.</p>

<p>5-Amino-8-hydroxyquinoline dihydrochloride (5-AQDH) is an anticancer drug that inhibits the activity of survivin, a protein that is overexpressed in cancer cells. It has been shown to be effective in vivo against melanoma tumor growth. 5-AQDH binds to the unpaired cysteine residues of the survivin molecule and inhibits its function by binding to the active site, blocking access to ATP and preventing DNA synthesis. The efficacy of 5-AQDH has been confirmed in vitro by studying the effect on cell viability and DNA synthesis, as well as by measuring plasma mass spectrometry data from melanoma patients. This drug is currently being investigated for its potential use as an anticancer agent.</p>

<p>Please enquire for more information about [2-(5-Fluoro-1-methyl-1H-indol-3-yl)ethyl]amine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about (5-Amino-1H-1,2,4-triazol-3-yl)methanol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>(S)-(-)-1-Boc-3-aminopyrrolidine is an inhibitor that inhibits the activity of phosphoinositide 3-kinase (PI3K) by binding to the ATP binding site and inhibiting PI3K. It has been shown to inhibit the activation of PI3Kδ, which plays a key role in tumorigenesis and metastasis. The drug also has metabolic stability and selectivity for PI3Kδ over other kinases, as well as high affinity for this enzyme. The drug was found to have low toxicity in vitro, but its effects on humans are unknown.</p>

<p>4-Amino-5-methoxy-2-methyl-N-methylbenzenesulfonamide is a surfactant that is used in the chemical industry to dissolve diazotized aromatic amines. It is also used in the preparation of coupling agents, such as naphthol, and hydrochloric acid. 4-Amino-5-methoxy-2-methylbenzenesulfonamide can be prepared by the diazotization of aniline followed by coupling with hydrochloric acid and sodium phosphate. The product can then be purified by recrystallization from a salt solution containing sodium acetate.</p>

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

<p>Please enquire for more information about 5-Bromo-2-methoxyphenethylamine hydrobromide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3,4-Diaminobenzotrifluoride is a photophysical agent that emits light of a specific wavelength when irradiated with ultraviolet light. It has been shown to inhibit the growth of human cervical carcinoma cells in vitro and to cause apoptosis in these cells. 3,4-Diaminobenzotrifluoride also inhibits the proliferation of human liver and lung cancer cells in vitro. The mechanism by which this agent causes cell death is unknown. 3,4-Diaminobenzotrifluoride is an acid catalyst and stabilizes the chloride ion. This agent may inhibit DNA synthesis or affect proteins that are involved in signal transduction pathways for cell proliferation.</p>

<p>5-Aminoorotic acid is an antimicrobial agent that has been shown to have anticancer activity. It has a nitrogen atom and two oxygen atoms in the molecule. The chemical structure of 5-aminoorotic acid can be determined using NMR spectroscopy and its biological properties are dependent on hydrogen bonding interactions with other molecules. 5-Aminoorotic acid is a chelate ring, which means it can bind to metal ions such as lanthanum (La3+). 5-Aminoorotic acid has been shown to inhibit the glycol oxidation reaction and may also be able to inhibit other enzymatic reactions. This drug is stable for use in model systems and may also be used for cancer treatment.</p>

<p>4-Aminomethylphenylacetic acid is a nonsteroidal anti-inflammatory drug that is used to treat inflammation and pain. It belongs to the class of peptidomimetics, which are compounds that mimic the structure of a natural biological molecule. 4-Aminomethylphenylacetic acid has an analog with a lactam ring at position 3, which is not present in other NSAIDs. This structural difference may contribute to its high stability and low reactivity. 4-Aminomethylphenylacetic acid has been shown to exhibit antiviral activity against viruses such as HIV or Hepatitis C virus by inhibiting viral replication.</p>

<p>5-tert-Butyl-1,3-thiazol-2-amine is an aromatic compound with the molecular formula CHN. This compound is a colorless solid that is soluble in water and alcohol. It can be used as a substitute for 2-aminothiazole, which belongs to the group of halogenated compounds. 5-tert-Butyl-1,3-thiazol-2-amine has been shown to react with alkyl halides to form alkylated products. The reaction with alkyl halides may be due to its primary amino group and amino group. 5-tert-Butyl-1,3-thiazol-2-amine also reacts with sulfuric acid and sulfuric acid salts to form thiazoles and thiazolones.</p>

<p>Gamma-aminobutyric acid (GABA) is a neurotransmitter that inhibits the transmission of nerve impulses in the brain. GABA binds to specific receptors and blocks voltage-dependent calcium channels, which are ion channels that allow the passage of calcium ions into cells. GABA also has a number of other functions, including biochemical properties, its role in brain function and drug interactions. The GABA receptor is found on neurons and is subject to modulation by drugs that interact with GABA receptors. In addition, GABA can react with water vapor to produce hydrogen bonding interactions. This reaction is used in electrochemical impedance spectroscopy as an analytical tool for determining the concentration of free water in a sample.</p>

<p>2-(trifluoromethyl)pyridin-3-amine is an industrial chemical that is used as a reagent in the synthesis of other chemicals. It is synthesized from benzene and an acid ethyl ester in a complex reaction. 2-(trifluoromethyl)pyridin-3-amine is toxic, with industrial uses such as the synthesis of dyes and pesticides.</p>

<p>Please enquire for more information about 2-(1H-Indol-5-yl)ethanamine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Aminobenzooxazole is a cox-2 inhibitor that has been shown to inhibit the growth of cervical cancer cells. It acts by inhibiting ubiquitin ligases, which are enzymes that regulate protein degradation. 5-Aminobenzooxazole has shown anticancer activity in vitro and in vivo and induces cell cycle arrest and apoptosis (cell death) of cervical cancer cells. The mechanism for this effect may be due to the ability of 5-aminobenzooxazole to disrupt the acidic environment of the tumor microenvironment. This drug also inhibits glutamate neurotransmitter release, leading to neuronal death. 5-Aminobenzooxazole is not active against normal cells because they lack the enzyme needed for this reaction.</p>