Building Blocks

<p>(S)-(-)-1-Phenylpropylamine is a compound that can be synthesized by the asymmetric synthesis of 1-phenylethylamine. It is an amine that is used in the production of other compounds and has been shown to be reactive with a number of different compounds. The chemical profile of (S)-(-)-1-Phenylpropylamine consists mainly of aldehydes, amides, amines, and alkylating agents. This chiral molecule can be used for the production of drugs or as a precursor for other chemicals.</p>

<p>2,2-Dimethyl-1,3-dioxan-5-ol is a chemical compound that has been shown to have catalytic properties. It has also been used as an additive in organic synthesis reactions to activate carboxylic acids. 2,2-Dimethyl-1,3-dioxan-5-ol is an oxygenated compound that can be synthesized by the reaction of pyridine and formaldehyde. This substance can be used in acidic conditions and must be activated by solketal or dioxane before use. The physical properties of this chemical are shown using FTIR spectroscopy on corncob samples and physicochemical parameters were determined using standard techniques.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Bromo-5-fluoro-4-nitroaniline can be synthesized in a reaction system of ammonium chloride, hydrochloric acid, and water vapor. The reaction is carried out at a temperature of 190°C under reflux. The efficiency of this synthesis is high, and the chemical yield is about 90%.</p>

<p>(1H-Indazol-4-yl)acetic acid is a cation that has been shown to have pharmacological activity. It is hydrolyzable and is used as an anti-inflammatory agent. This compound also decarboxylates and hydrolyzes, which are processes that produce carboxyl and fluoro groups. (1H-Indazol-4-yl)acetic acid has been shown to be an anti-inflammatory agent, with effects against inflammation in the central nervous system. This drug also inhibits the production of inflammatory cytokines, including tumor necrosis factor alpha (TNFα), interleukin 1β (IL1β), and IL6.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Oxohexanoic acid (2-OHBA) is a fatty acid that is synthesized from the amino acids lysine and methionine. It is involved in mitochondrial metabolism and has been found to be necessary for spermatozoa motility. 2-OHBA has been shown to inhibit the activity of glutamate dehydrogenase, an enzyme that catalyzes the conversion of glutamate to α-ketoglutarate, which is required for energy production. This inhibition leads to a decrease in ATP levels, which may cause a variety of symptoms, including fatigue and weight loss. Furthermore, 2-OHBA inhibits protein synthesis by blocking the incorporation of amino acids into proteins. The inhibition of this process can lead to high ammonia levels in the blood and accumulation of other nitrogenous wastes in tissues such as liver or muscle tissue. Analysis of urine samples has shown that 2-OHBA is excreted unchanged in urine.</p>

<p>Versatile small molecule scaffold</p>

<p>4-Hydroxy-5-methoxy-2-nitrobenzaldehyde (4HMN) is a proton donor that can be used as a crosslinking agent. It is an acidic compound that binds to the substrate, usually via hydrogen bonds. 4HMN has been shown to have good binding affinity for tumour cell lines and can be used as a crosslinking agent in bioconjugation reactions. It is also a reversible chemical reaction, which means it can be hydrolyzed under certain conditions. 4HMN has been shown to be capable of enhancing the rate of enzymatic reactions by acting as a cofactor or coenzyme, such as degradable enzymes and enzymes with low turnover rates. The kinetic process of these reactions are measured by fluorescence techniques and gel permeation chromatography.</p>

<p>GSK'547 is a small molecule that can interact with the ferroptosis pathway, which is involved in both acute and chronic kidney injury. GSK'547 has been shown to inhibit ischemia reperfusion-induced renal dysfunction by suppressing inflammation and oxidative stress. GSK'547 also inhibits cancer cell proliferation and acts as an anti-inflammatory agent. In addition, GSK'547 has been shown to be beneficial for treating tuberculosis infections and cavity diseases. The mechanism of action of GSK'547 involves inhibiting bacterial cell wall synthesis by binding to the beta-subunit of DNA gyrase. This binding prevents the formation of an antibiotic-inhibitor complex with the enzyme cell wall synthesis that is required for cell wall biosynthesis, inhibiting protein synthesis and cell division.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Dimethyl pyridine-3,4-dicarboxylate is an organic compound that is used as a precursor to make other chemicals. It is a pyridinedicarboxylic acid and it can be synthesized from the reduction of pyridine with sodium borohydride in ethanol. Dimethyl pyridine-3,4-dicarboxylate is also used in the production of acetaldehyde by way of hydrosilylation with chloride and chloroform. This chemical has been found to be useful for the synthesis of various drugs such as antiepileptics, antihistamines, antipsychotics, and antidepressants.</p>

<p>Nerol oxide is a natural compound and fragrance ingredient that has been shown to have anti-aging effects. Nerol oxide is an ester of citronellal, nerolic acid and ethyl decanoate. It is found naturally in orange blossoms and other citrus plants, as well as in lavender oil. Nerol oxide can be extracted from the plant material using solid phase microextraction. The chemical analyses of this extract reveal the presence of various fatty acids, including ethyl esters, fatty acids and their corresponding alcohols. These compounds are used to produce nerol oxide by polymerization with an initiator such as potassium hydroxide or sodium hydroxide at a neutral pH.</p>

<p>3,6-Dichloropicolinonitrile is a peroxide that is used in the synthesis of organic compounds. It is produced by the reaction of sodium carbonate and hydrochloric acid with nitric acid as a catalyst. 3,6-Dichloropicolinonitrile has been shown to be more selective than other oxidizing agents such as hydrogen peroxide and potassium permanganate. The product can then be purified by adding diacetate, which selectively reacts with the chlorine to form acetyl chloride and glycolic acid. The resulting mixture can then be distilled to produce 3,6-dichloropicolinonitrile in high purity. 3,6-Dichloropicolinonitrile can also be used in electrochemical methods for the synthesis of cyanides or biochemically for virulent products such as pesticides and organic solvents.</p>

<p>(Chloromethyl)cyclohexane is a synthase gene that is responsible for synthesizing the enzyme chloromethyl cyclohexane, which is used as a solid catalyst. The synthesis of (chloromethyl)cyclohexane from phenyl groups and liquid crystal composition has been demonstrated using expression plasmids and active oxygen. The compound inhibits inflammatory diseases by preventing the production of arachidonic acid, which is an inflammatory agent. This compound also inhibits the production of prostaglandins, which are involved in the release of histamine from mast cells. Pharmaceutical preparations that contain this compound are primarily used to treat rheumatoid arthritis and other inflammatory diseases.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3,3,5-Trimethylcyclohexanone is an intermediate in the synthesis of polymers and polyesters. This compound is a reactive hydrogenation product which can be used to produce polymers with desired properties. The unsaturated side chain of 3,3,5-trimethylcyclohexanone reacts with borohydride to form a ketal. After being converted to the corresponding acid chloride, the 3,3,5-trimethylcyclohexanone can be used for the synthesis of polyesters. This compound has also been shown to be an effective catalyst for producing β-unsaturated ketones from aldehydes and dienes.</p>

<p>2-Octyldecanoic acid is a fatty acid that is used as a stabilizer in detergent compositions. This stabilizer is also utilizable at high alkali metal concentrations, which makes it suitable for use in hard water conditions. 2-Octyldecanoic acid has a low viscosity at room temperature, and the nature of its hydrocarbon chain leads to increased stability against decomposition when heated or exposed to carbon tetrachloride. It can be synthesized from an aliphatic hydrocarbon, such as octane, to form a macrocyclic ring structure. 2-Octyldecanoic acid also has optical properties that depend on the configuration of the carbon atoms. The molecule has two chiral centers and can exist in four different forms: erythro (E), threo (T), dithreo (D) and meso (M). The optical activity of 2-octyldecanoic acid depends</p>

<p>1-Phenyl-1-butanol (1PB) is a chiral compound that forms hydrogen bonds with itself. It is a colorless liquid that is soluble in organic solvents and has a boiling point of 61 °C. 1PB has been found to inhibit the growth of Pseudomonas aeruginosa by inhibiting fatty acid synthesis, which may be due to its ability to inhibit β-hydroxylase activity. 1PB also inhibits the growth of some bacteria (e.g., Staphylococcus aureus) by blocking the synthesis of fatty acids, which are important for bacterial cell membrane integrity. The hydroxyl group in 1PB helps it form hydrogen bonds with other molecules, including proteins and DNA strands, which makes it useful for chromatographic separation and as an antioxidant in food preservation.</p>

<p>Timonacic is an analog of nicotinamide that has been shown to be an effective inhibitor of energy metabolism in the mitochondria. It has antioxidative properties and can protect against the development of heart disease by inhibiting the production of reactive oxygen species. Timonacic's anti-inflammatory properties may be due to its ability to inhibit prostaglandin synthesis. It also has a high affinity for fatty acids, which may contribute to its inhibitory effects on lipid peroxidation. This drug has a carboxy terminal and is used as a sodium salt, which may play a role in its enzyme inhibition activity. Timonacic inhibits the activities of enzymes such as carnitine acetyltransferase and pyruvate dehydrogenase kinase, which are involved in the biosynthesis of fatty acids. The intramolecular hydrogen bonds formed with timonacic may contribute to its inhibitory effect on these enzymes.</p>

<p>4-Acetamidobenzenesulfonamide is a drug that inhibits the activity of several enzymes and is used in wastewater treatment. It has been shown to have a beneficial effect on metabolic disorders, such as insulin resistance, obesity, and type 2 diabetes. 4-Acetamidobenzenesulfonamide also regulates transcriptional activity by inhibiting the interaction between DNA and RNA polymerases. This drug has been shown to be active in treating autoimmune diseases, such as multiple sclerosis, rheumatoid arthritis, lupus erythematosus and Crohn's disease. It also aids in HIV infection by acting as an inhibitor of toll-like receptor signalling pathways. The drug binds to hydrogen bonds and hydrophobic interactions with water molecules to form a hydrophobic layer on the surface of cells in order to reduce water permeability. The drug also reduces bowel diseases such as ulcerative colitis and liver lesions caused by alcohol consumption or congestive</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>tert-Butyl 2-(hydroxymethyl)azetidine-1-carboxylate is a versatile compound that has various applications across different industries. It is commonly used as a building block in the synthesis of shikimic acid, which is a key intermediate in the production of inhibitors and herbicides. Additionally, this compound can be utilized in electrode fabrication and is often sought after by researchers for their chemical studies. Another notable application of tert-Butyl 2-(hydroxymethyl)azetidine-1-carboxylate is its use in the pharmaceutical industry. It serves as an important starting material for the synthesis of cetirizine, an antihistamine medication used to alleviate allergy symptoms. Furthermore, it has been studied for its potential therapeutic effects on conditions such as psoriasis and photocatalytic reactions. In addition to its pharmaceutical applications, tert-Butyl 2-(hydroxymethyl)azetidine-1-carboxylate</p>

<p>6-Bromo-2-methoxyquinoline is a versatile compound with various applications. It is commonly used as a disinfectant in ceramic compositions and research chemicals. Additionally, it has been found to have potential therapeutic benefits. Studies have shown that 6-Bromo-2-methoxyquinoline exhibits antioxidant properties and can inhibit the production of inflammatory mediators such as arachidonic acid and prostaglandins. Furthermore, it has been found to modulate potassium channels, which play a crucial role in cellular function. This compound also shows promise in the development of copolymers and other materials due to its unique chemical structure. With its wide range of applications, 6-Bromo-2-methoxyquinoline is an essential compound for various industries.</p>

<p>Versatile small molecule scaffold</p>

<p>Doxazosin is a research chemical that has shown potential in various fields. It is a water-soluble compound that has been studied for its effects on microcystins, cytidine, and vitamins. Doxazosin has also been found to have aldehyde and particulate properties, making it a versatile compound for different applications. In the field of medicine, Doxazosin has been researched for its potential in treating certain conditions. Studies have shown that Doxazosin can interact with 1-hydroxy-2-naphthoic acid and glutamate, which are important molecules involved in various biological processes. Additionally, Doxazosin has shown promising results in inhibiting the growth of e. cloacae bacteria, making it a potential candidate for antibacterial treatments. Furthermore, Doxazosin has been studied in the field of chemistry due to its unique properties. It can undergo derivatization reactions with fatty acids and z</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>FG-2216 is a peptide that activates the G protein-coupled receptor, leading to increased intracellular calcium. FG-2216 is a potent agonist of the GPRC6A receptor and has been shown to inhibit pain perception in animal models. FG-2216 has been shown to have no effect on ion channels and does not affect cellular proliferation or migration. FG-2216 may be useful as a research tool for studying the function of the GPRC6A receptor in animal models.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>(1R,2S)-2-Phenylcyclopropane-1-carboxylic acid is a dicarboxylic acid that is produced from the decarboxylation of benzyne. This compound has been shown to be a precursor of benzene and ozonolysis. The stereospecifically of (1R,2S)-2-Phenylcyclopropane-1-carboxylic acid has been determined using lead tetraacetate as the substrate. (1R,2S)-2-Phenylcyclopropane-1-carboxylic acid is an asymmetric molecule.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>tert-Butyl 2-bromo-2-methylpropanoate is a versatile compound with various applications. It is commonly used as a cytotoxic agent in the pharmaceutical industry and as an amide intermediate in organic synthesis. This compound has also been studied for its potential therapeutic effects, such as its ability to inhibit the growth of cancer cells. tert-Butyl 2-bromo-2-methylpropanoate is often utilized in research settings to study the efficacy of drugs like rabeprazole and tripterygium. Additionally, it finds applications in the production of polymers, catalysts, and hydrogen atom transfer reactions. With its wide range of uses, tert-Butyl 2-bromo-2-methylpropanoate is a valuable compound for researchers and industries alike.</p>

<p>2,3-Dihydro-1H-pyrrolo[3,2-c]pyridine is an alkaloid compound that has various applications in research and chemical studies. It has been found to interact with dopamine receptors and exhibit photothermal properties. This compound has been studied in the context of G. lucidum (also known as Reishi mushroom) and its potential therapeutic effects. Additionally, it has shown interactions with quinpirole, lithium, ergovaline, efrotomycin, and other compounds. The photocatalytic and fatty acid properties of 2,3-Dihydro-1H-pyrrolo[3,2-c]pyridine make it a versatile compound for various research purposes.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Amino-5-cyano-3-methylbenzoic acid is a diester of methylamine. It is an acid ester that has been used in the synthesis of other compounds. 2-Amino-5-cyano-3-methylbenzoic acid is an intermediate in the synthesis of some pharmaceuticals, such as carbamazepine and methylphenidate. This compound has not been shown to have any biological activity.</p>

<p>Versatile small molecule scaffold</p>

<p>Bromo-PEG3-azide is a PEG compound with two different functional groups (also known as heterobifunctional). Unlike homobifunctional PEG compounds (same functional group on both ends), this type of compounds are more versatile as have two different anchor points. Bromo-PEG3-azide is used as a linker and spacer to add a PEG moiety, via pegylation (a bioconjugation technique) to proteins, peptides, oligonucleotides, small molecules and nanoparticles.</p>

<p>2-Bromo-3-hydroxy-benzaldehyde is a nitrate that has been shown to have anti-cancer properties. It inhibits the growth of cancer cells by binding to bromodomains in their DNA, thereby preventing transcription and replication. 2-Bromo-3-hydroxy-benzaldehyde also inhibits the production of nitric oxide, which may lead to an inhibitory effect on tumour angiogenesis. The stereoisomers of this compound are used as precursors for the synthesis of ammonium nitrate, which is used as a fertilizer and explosive. 2-Bromo-3-hydroxy-benzaldehyde is also used in organic synthesis as a precursor for acetylation or halide reactions with palladium complexes or halides.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Imidazolidone-4-carboxylic acid is a potent inhibitor of matrix metalloproteinases, which are enzymes that break down proteins in the extracellular matrix. 2-Imidazolidone-4-carboxylic acid inhibits the activity of both serine protease and matrix metalloproteinase, two enzymes involved in the inflammation process. 2-Imidazolidone-4-carboxylic acid has been shown to inhibit the transport of amino acids, leading to decreased protein synthesis and cell growth. It also inhibits cancer cells by disrupting their ability to grow new blood vessels and invade other tissues.</p>

<p>Versatile small molecule scaffold</p>

<p>Hexahydro-1H-pyrrolizin-1-amine is a synthetic compound that is used to control endophytic fungi and fungal diseases in plants. The activity of this molecule is due to the acid molecules that are released when it reacts with plant tissue, which prevents the growth of fungi by inhibiting their cell membranes. Hexahydro-1H-pyrrolizin-1-amine also has an antibacterial effect, which may be due to its ability to bind to bacterial 16S ribosomal RNA and inhibit protein synthesis. This product can be used on plants that are infected with endophytic fungi or fungal diseases. It can also be applied as a preventative measure against future infections.<br><br>The following table summarizes the information for each product:<br><br>Product Name <br>Characteristics <br>Description</p>

<p>Versatile small molecule scaffold</p>

<p>2,6-Dimethylphenylacetic acid is a hydrogen phosphate that is soluble in solvents such as acetonitrile. It has been used in the synthesis of lidocaine with high sensitivity and specificity. It can be used to detect phosphoric compounds, which are often present in pharmaceuticals and food supplements. This compound has also been shown to have a solvent effect on the conditions of the reaction, making it a useful additive for optimizing processes. The main impurities of this compound are 2-methylbenzoic acid and benzoic acid.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>(1-Pyridin-2-yl)piperidin-4-amine is a drug that acts as an anorexiant. It binds to the serotonin 5HT3 receptor, which is involved in the regulation of appetite and mood. It also blocks the action of serotonin at the 5HT4 receptor, which is involved in mediating intestinal motility. This agent has been shown to have a potent antagonist effect on the 1-4c alkyl group of serotonin receptors. The phenoxy group and methyl group are also responsible for binding with serotonin receptors and blocking their activity.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about 8-Methylnonan-1-ol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Versatile small molecule scaffold</p>

<p>Pentanimidamide hydrochloride is a drug that belongs to the group of aromatic hydrocarbon drugs. It is a potent antihypertensive agent with a rapid onset and long duration of action. Pentanimidamide hydrochloride has been shown to inhibit the production of reactive oxygen species, which are generated by the respiratory chain in mitochondria, and to prevent the formation of pyrazinoic acid, an inhibitor of blood vessel relaxation. This drug also has been shown to reduce blood pressure in animal models by binding to specific receptors on cells in the cardiovascular system. The active form is bound to plasma proteins such as albumin and alpha-1-acid glycoprotein, which are found in high concentrations in erythrocytes. Pentanimidamide hydrochloride also binds to alkynyl groups and phenyl groups, which may be due to its ability to form covalent bonds with these functional groups.</p>

<p>Versatile small molecule scaffold</p>

<p>Iridium(III) bis-(2-phenylpyridine) (Ir{dFCF3ppy}2(bpy)) is a monomeric amido ligand that can be used in polymerization processes. It has an average molecular weight of 185.8 and a transition temperature of -55°C. Ir{dFCF3ppy}2(bpy) is soluble in organic solvents such as chloroform and acetone and will react with amines, anionic sites, and cycloalkyl groups to form polymers. The yields of the polymerization process are dependent on the starting materials used.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Cabozantinib is a small molecule that is the first to target VEGFR-2, which is a receptor tyrosine kinase involved in the development of fibrosis. Cabozantinib inhibits the activity of VEGFR-2 by binding to its ATP-binding site and blocking the phosphorylation of downstream signaling pathways. Cabozantinib has been shown to have antifibrotic properties in both preclinical and clinical models. The drug candidate has been shown to reduce kidney fibrosis in animal models. The standard dose for cabozantinib was found to be 5 mg/kg, with a maximum tolerated dose of 20 mg/kg. In vitro studies have indicated that cabozantinib binds with high affinity to the ATP-binding pocket of VEGFR-2, exhibiting competitive inhibition against other kinases such as PDGFR-beta and cKit, as well as diaryliodonium (a specific inhibitor). Caboz</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-(Isopropylamino)butanol is a colorless liquid with an alkaline reaction. It reacts easily with acids and is soluble in water. The boiling point of this substance is 242°C. In the presence of ammonium chloride, the solution becomes acidic. 4-(Isopropylamino)butanol is used as a solvent for paints, varnishes, and lacquers.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>DSP-4 hydrochloride is a neurotoxin that inhibits the synthesis of norepinephrine. It binds to neurons and prevents the uptake of dopamine, which can lead to neuronal death. DSP-4 hydrochloride affects brain functions by decreasing the concentration of serotonin in the cortex and increasing the concentrations of norepinephrine in the coeruleus. DSP-4 hydrochloride also has estrogenic effects by binding to estrogen receptors and increasing estradiol benzoate concentrations.</p>

<p>Versatile small molecule scaffold</p>

<p>5-Chloro-2-ethoxy-phenylamine is an enzyme inhibitor that binds to the active site of glucocerebrosidase, the enzyme that catalyzes the hydrolysis of glucocerebroside to glucose and ceramide. This compound has been shown to be a selective inhibitor against this enzyme and not affect other hydrolases or chaperones. It was also found that 5-chloro-2-ethoxy-phenylamine can act as a chemical chaperone by stabilizing protein folding in vitro. 5-Chloro-2-ethoxy phenylamine is a new analogue of 3-(3,4,-dichlorophenyl)-1-[(1R,2S)-2-(5,6,-dichloropyridin-3 yl)ethenyl]-1H-pyrazole. It is an inhibitor of Gaucher disease caused by glu</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>