Building Blocks

<p>Methyl 3-oxocyclohexanecarboxylate is a chiral molecule that belongs to the class of β-unsaturated ketones. It has been shown to interact with enzymes from horse liver, dehydrogenase and carbanion. Methyl 3-oxocyclohexanecarboxylate is unreactive under most conditions and does not react with other molecules. The compound can be used as a starting material for the synthesis of olefinic compounds.</p>

<p>Cyclobutanethiol is a 1-cyclopentene-1-carboxylic acid, which is a cyclic form of the alkylthio group. It is an organic solvent with a hydroxyl group at one end and an alkyl group at the other end. Cyclobutanethiol can be used as a sealant or as a solvent in organic chemistry. The compound has been shown to inhibit insulin resistance by binding to cb1 receptors on cells, thereby inhibiting the production of glucose. Cyclobutanethiol also absorbs ultraviolet light, so it can be used in photochemistry.</p>

<p>Versatile small molecule scaffold</p>

<p>4-Amino-2,6-dimethoxypyrimidine is an organic compound that has been shown to be a methylating agent. It reacts with the hydrogen chloride present in seawater to form methyl chloride and hydrochloric acid. 4-Amino-2,6-dimethoxypyrimidine also interacts with hydrogen bonds and forms hydrogen bonds with other molecules. The molecular modeling study revealed that this compound is soluble in mineral acids such as sulfuric acid and hydrochloric acid. The solubility data also showed that 4-amino-2,6-dimethoxypyrimidine is soluble in water but not in chlorinated water. This drug has shown significant antifungal activity against Cryptococcus neoformans and Gram-negative organisms such as Escherichia coli, Salmonella typhi, Pseudomonas aeruginosa, Klebsiella pneumoniae, Proteus mirabilis, Enterobacter</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>Please enquire for more information about 6-Amino-3-pyridinethiol dihydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>4-Acetylimidazole is a histidine analogue that has been shown to have anticancer activity in breast cancer cells. It can react with amines and form imidazoles. The hydroxyl group on the 4-position of the imidazole ring is able to undergo dehydration, which leads to the formation of a chloride ion. This reaction mechanism is reversible and can be used in organic synthesis. 4-Acetylimidazole can also act as an h2 receptor antagonist, although it does not bind to the zwitterionic site of the h2 receptor. NMR spectra show that 4-acetylimidazole exists as a zwitterion in water solution, but becomes a monovalent ion when dissolved in an organic solvent such as methanol or acetone. 4-Acetylimidazole is chemically stable and does not react with poloxamer.</p>

<p>1-Bromo-4-isobutylbenzene is a ketone that can be synthesized by the reaction of benzene with acetonitrile in the presence of a catalytic amount of oxone. The synthesis is an example of an arylation, which is the addition of an aromatic group to another molecule. It has been shown experimentally that 1-bromo-4-isobutylbenzene undergoes a transition from the x-ray structure analysis to the crystal x-ray structure when dissolved in acetonitrile and heated to 100°C. The final product is then purified by recrystallization with ethylene as a solvent.</p>

<p>3-(p-tolyl)propiolic acid is a functional group that is used in organic chemistry. It is an alkynoic acid with a terminal triple bond. The compound can be synthesized by the reaction of propiolic acid with an alkyne, followed by oxidation. The 3-(p-tolyl)propiolic acid can be used as a surrogate for other functional groups in organic synthesis, and it has been shown to react as an oxidant in biomolecular systems.</p>

<p>N-(4-Aminophenyl)-N-methyl-2-(4-methylpiperazin-1-yl)acetamide is an environmental and industrial chemical that is used as a formate, benzoate, and methyl benzoate intermediate. It reacts with nitric acid to form N-(4-aminophenyl)-N-methyl-2-(4-nitrophenoxy)acetamide (NPA). NPA has been shown to have antiangiogenic properties. NPA inhibits the proliferation of endothelial cells by interfering with the cell cycle and inducing apoptosis.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3,4-Dihydroxyphenylalanine (3,4-DOPA) is a non-protein amino acid that is an intermediate in the synthesis of dopamine and norepinephrine. 3,4-DOPA is metabolized by the enzyme dopa decarboxylase to dopamine and then by catechol-O-methyl transferase to norepinephrine. 3,4-DOPA has antioxidant properties and has been shown to have anticancer effects in animals. It also has been shown to interact with other biomolecules such as proteins and nucleic acids. 3,4-DOPA binds strongly to metal ions through its carboxylic acid group and can chelate metals such as copper or iron. This property may be used for coatings on metal surfaces or for interacting with other molecules.br&gt;br&gt; 3,4-Dopa contains a chiral center due to the presence of two stereogenic carbons on the phen</p>

<p>JMJD2 is an enzyme that catalyzes the methylation of histone H3 at lysine 27. JMJD2 inhibitors are compounds that inhibit JMJD2 activity, which may be used to treat cancer. This class of drugs inhibits the activity of JMJD2 by binding to the active site and blocking the substrate from entering. The most potent compound in this class, 5-carboxy-8HQ, has been shown to have antibacterial efficacy in a squamous cell carcinoma model system and up-regulated expression in wild-type cells. Additionally, this compound has been shown to significantly inhibit tumor growth in a mouse model of atherosclerotic lesion.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Methyl 5-hexynoate is a synthetic product that can be synthesized from soybean lipoxygenase and hydrogenation reduction. This product has been shown to be a useful synthon for the synthesis of monoclonal antibodies with high binding affinity. The synthetic pathway, which involves cross-coupling and asymmetric synthesis, is outlined in the diagram below. The following are the steps involved in the production of methyl 5-hexynoate: 1) Addition of ethyl bromide to terminal alkynes 2) Addition of hydrochloric acid 3) Reaction with potassium tert-butoxide 4) Hydrogenation reduction 5) Cross-coupling reaction 6) Asymmetric synthesis</p>

<p>Versatile small molecule scaffold</p>

<p>8-Chlorotetrazolo[1,5-A]pyrazine is a chlorine-containing compound. It is a heterocyclic aromatic organic compound and an important intermediate in the synthesis of other compounds. 8-Chlorotetrazolo[1,5-A]pyrazine is not found in nature. The elimination of chlorine from 8-chlorotetrazolo[1,5-A]pyrazine produces benzotriazole and the molecule tetrazole. 8-Chlorotetrazolo[1,5-A]pyrazine is used as a raw material for many organic syntheses.</p>

<p>Versatile small molecule scaffold</p>

<p>The chemical is a palladium-based complex that inhibits the activity of α4β7 integrin. It has been shown to be effective in prophylaxis and treatment of inflammatory diseases, such as autoimmune diseases, and other conditions, such as congenital disorders. The compound has been shown to inhibit the growth of plants by causing phytotoxic effects.</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>Please enquire for more information about 2-Bromo-1-(4-chloro-3-fluorophenyl)ethanone 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>Versatile small molecule scaffold</p>

<p>Methyl 4-(2-bromoethyl)benzoate is a potent HDAC6 inhibitor. It has been shown to inhibit cancer cell growth and induce apoptosis in vitro and in vivo. Methyl 4-(2-Bromoethyl)benzoate is also an anti-cancer agent that inhibits the histone deacetylase enzyme, which then prevents the transcription of genes involved in cancer development. In addition, this agent inhibits the production of prostaglandin E2, which may contribute to its anti-cancer activity. The most common side effects are nausea and vomiting.</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-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>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Ethyl 3-formyl-1H-pyrrole-2-carboxylate is a formyl compound with the molecular formula C8H8O3. It is a colorless liquid that has a strong odor. The compound can be obtained by the reaction of ethyl acetoacetate and pyrrole in the presence of aluminum chloride. The compound has been studied for its nuclear magnetic resonance (NMR) properties. It has two conformers, which are distinguished by their different chemical shifts, and this difference can be used to study coupling between the carbonyl group and other groups in the molecule.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-chloro-4-fluoroisoquinoline is a chlorinating agent that has been used as a synthetic method for the synthesis of oxychloride. It is typically used in the presence of palladium catalyst, in the presence of phosphorus and under reductive conditions. The chlorination reaction is initiated by addition of hydrochloric acid or phosphorous oxychloride. The 1-hydroxyisoquinoline reacts with phosphorus to form a chloroformate, which reacts with fluorine gas to produce an intermediate chlorofluorinate. This intermediate then reacts with chlorine gas in the presence of palladium catalyst to generate the desired product, 1-chloro-4-fluoroisoquinoline.</p>

<p>Versatile small molecule scaffold</p>

<p>Cyclopent-2-en-1-ol is a reactive monomer that can react with chloride and hydroxyl groups. It can also undergo reaction with sodium carbonate to form a cyclic ester. Cyclopent-2-en-1-ol can be converted to an epoxide by the use of acid catalyst. This compound also has the ability to polymerize, forming polymers that are used in rayon production.</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>3-Methoxythiophene-2-carbaldehyde is a ligand that has been shown to form a stable complex with potassium chloride. This compound is also reactive, and can be stabilized in the reaction vessel. In the presence of sulfate ions, 3-methoxythiophene-2-carbaldehyde will react to form a phosphotungstic acid precipitate. The dehydrated salt can be recrystallized by adding phosphotungstic acid, which stabilizes the product.</p>

<p>Versatile small molecule scaffold</p>

<p>Thiodiglycolic anhydride is a synthetic reagent that is used in the synthesis of erdosteine. It also has been used in the synthesis of other products, such as magnetic particles for imaging and therapeutic uses. Thiodiglycolic anhydride can be used to synthesize erdosteine, which is a substrate for the enzyme hydroxylase and contains a hydroxy group in its structure. The hydroxyl group on erdosteine reacts with thiodiglycolic anhydride to form acrylonitrile, which then reacts with benzyl groups to form benzylthio-esters. These benzylthio-esters are then converted into acid transporters.</p>

<p>1H-[1,2,3]Triazolo[4,5-d]pyrimidin-5-amine is a nitro compound that binds to the receptor binding sites of certain inflammatory bowel disease and cancer cells. It also inhibits the production of adenosine in these cells. 1H-[1,2,3]Triazolo[4,5-d]pyrimidin-5-amine has been shown to be effective against bowel disease and cancer by inhibiting cyclic AMP (cAMP) degradation. This drug has also been shown to be an irreversible inhibitor of ischemia reperfusion injury in animal models. 1H-[1,2,3]Triazolo[4,5-d]pyrimidin-5-amine is a nitro compound that binds to the receptor binding sites of certain inflammatory bowel disease and cancer cells. It also inhibits the production of adenosine in these cells. 1H</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>Cucurbit[7]uril is a chemical compound that can be used as a fluorescent probe for protein target. It has been shown to produce significant cytotoxicity against cancer cell lines in vitro. Cucurbit[7]uril also exhibits hydrophobic effects, which bind to the cell nuclei of cancer cells and inhibits DNA replication. The photophysical properties of cucurbit[7]uril are stable under physiological conditions and it can be used in vivo as a styryl dye. This chemical compound is also able to form stable complexes with carbonyl oxygens, making it an interesting candidate for anti-cancer drug development.</p>

<p>BMS-986165 is a P-glycoprotein (P-gp) inhibitor that has been shown to reduce the absorption of ciclosporin, tacrolimus, and everolimus in vitro. BMS-986165 has an activity index of 100% and inhibits the inflammatory response by inhibiting the production of cytokines. It has been found to be effective for treating bowel diseases, such as ulcerative colitis and Crohn's disease. The drug also may be used for the treatment of autoimmune diseases, such as psoriasis or rheumatoid arthritis. BMS-986165 is administered orally and is rapidly absorbed. It is metabolized by CYP3A4 and excreted in urine as metabolites. END&gt;&gt; END&gt;&gt;</p>

<p>Versatile small molecule scaffold</p>

<p>This linker is chemically stable and not cleavable under standard intracellular or extracellular conditions. N-Boc-3-Azetidinol is also a versatile organic intermediate used primarily in the pharmaceutical industry for synthesizing a wide range of drugs, including antibacterials, immunosuppressants, and cancer therapies.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1,9-Nonanediol is a chemical substance that has been synthesized with the use of a constant pressure process. It is an asymmetric synthesis with light exposure. The molecule has been characterized by chromatographic methods and has the molecular formula CH3(CH2)9O. 1,9-Nonanediol is a dodecanedioic acid and an aliphatic hydrocarbon. It exists in two forms: one hydroxyl group and one hydrogen bond, which are both involved in the dehydration process. This substance does not have any chloride or magnetic resonance spectroscopy properties because it does not contain any chlorine atoms or hydrogen atoms.</p>

<p>Versatile small molecule scaffold</p>

<p>3,6-Dichlorobenzene-1,2-diol is a conjugate acid of benzene. It has two dimensions in the plane of the molecule and three dimensions in space. The molecule is composed of six carbon atoms, six hydrogen atoms, and one chlorine atom. 3,6-Dichlorobenzene-1,2-diol has a centroid at the center of the molecule that is surrounded by a ring of four hydrogen atoms. The hydrogen-bonded molecules stack on top of each other to form a hexagonal shape. 3,6-Dichlorobenzene-1,2-diol forms hydrogen bonds with other molecules through its lone pairs of electrons on both oxygen atoms as well as through its pi electron system.</p>

<p>Versatile small molecule scaffold</p>

<p>Mito-TEMPO is a mitochondrial-targeted antioxidant that scavenges reactive oxygen species (ROS) and protects against oxidative injury. It has been shown to be effective in reducing oxidative damage in the heart and liver, as well as in models of neuronal death. Mito-TEMPO is also a potent inhibitor of lipid peroxidation and is able to prevent the formation of aldehydes. This drug has minimal toxicity, which may be due to its ability to accumulate in mitochondria without disrupting mitochondrial functions. Mito-TEMPO has been tested on healthy individuals with no observed side effects.</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about (3S)-3- [4- [(2-Chlorophenyl) methyl] phenoxy] tetrahydrofuran 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>(4-(tert-Butoxy)phenyl)methanamine (BPMT) is a ligand that binds to the alpha-2 receptor and acts as an antagonist. This compound has been shown to be a molecular target for positron emission tomography imaging, which is used in the diagnosis of tumours. BPMT is also used in the treatment of neuropeptide-associated disorders such as Parkinson's disease. The chiral nature of this compound makes it useful for the production of radiopharmaceuticals and other diagnostic agents with different physical properties.</p>

<p>Methyl 2-chloro-5-iodonicotinate is a basic and yields a radioligand for use in imaging studies. It is used as a specific activity and solid-phase extraction. Methyl 2-chloro-5-iodonicotinate has been shown to be effective for radiolabeling studies of the brain following intravenous administration.</p>

<p>Please enquire for more information about Chlorpheniramine N-oxide 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>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about 6-(Chloromethyl)pteridine-2,4-diamine monohydrochloride 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>Trans-3-(Benzyloxy)cyclobutanol is a radiolabeled compound that is used as a model system for understanding the metabolism of drugs in humans. It has been shown to be metabolized by the liver to produce metabolites that are excreted in urine. Trans-3-(Benzyloxy)cyclobutanol has also been shown to have tumor cell line stability, which may be due to its ability to inhibit DNA synthesis and protein synthesis in vitro and reduce tumor cells in vivo. Trans-3-(Benzyloxy)cyclobutanol has been shown to have no effect on normal rat plasma and lung carcinoma cells, but does affect prosthetic group activity.</p>

<p>Versatile small molecule scaffold</p>

<p>Benzyl N,N,N',N'-tetraisopropylphosphorodiamidite is a reagent that reacts with hydroxybenzyl amine to form an ester. This product is used for the synthesis of phosphoramidites and benzyl esters. It is also used as a catalyst for the synthesis of diesters.</p>

<p>Please enquire for more information about Cyanidin 3-O-rutinoside 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>Versatile small molecule scaffold</p>

<p>4-Bromopyridine HCl is a chemical compound with the molecular formula C6H5BrN. It is an aromatic heterocycle and is used in organic synthesis as a coupling partner in cross-coupling reactions. The bromine atom of 4-bromopyridine is replaced by chloride, resulting in 4-chloropyridine. The chlorination reaction can be conducted using either hydrochloric acid or thionyl chloride. This process can be done on an industrial scale and the chlorinated product has been used in the manufacture of pharmaceuticals, dyes, and pesticides. The reaction mechanism for this substitution reaction involves a nucleophilic attack by chlorine on the pyridine ring at carbon atom 2 followed by displacement of hydrogen from the adjacent position on nitrogen atom 3. Acylation reactions are oxidation processes that involve conversion of carboxylic acids to acyl halides or acyl chlorides through treatment with acidified halogenating agents such</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>Please enquire for more information about Coproporphyrin III including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>