Building Blocks

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>2-Amino-1-(4-methoxyphenyl)ethanol is a lactam that is minimally reactive with biological systems. It has been shown to inhibit the binding of the linker molecule to calcitriol, which is a vital component of vitamin D synthesis. This compound can also be used in intra-articular injections for the treatment of arthritis and other inflammatory disorders. 2-Amino-1-(4-methoxyphenyl)ethanol has been synthesized from an endogenous amino acid precursor and conjugated with a fluorophore, enabling it to be tracked in vivo by fluorescence imaging. It has been demonstrated that 2-Amino-1-(4-methoxyphenyl)ethanol can be used as a traceless bioactive molecule in molecular modelling and simulations.</p>

<p>3-(4-Methoxy-phenyl)-1H-indazole is a kinase inhibitor that inhibits the activity of terminal kinases. It has been shown to inhibit the activity of indazole derivatives and may be useful in treating diseases associated with these kinases, such as cancer. 3-(4-Methoxy-phenyl)-1H-indazole is a potent inhibitor of human caspase 9, which plays an important role in apoptosis by activating downstream proteases. It also inhibits the activation of protein kinase B, which is involved in cellular signaling pathways and cell cycle regulation.</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>3-Ethylmorpholine hydrochloride is a tryptic that is used to detect fingerprints, viruses, and tissue. It reacts with amines to form a product that can be detected by chromatography. 3-Ethylmorpholine hydrochloride has been shown to react with the transition state of the enzyme trypsin and inhibit its activity. 3-Ethylmorpholine hydrochloride is also reactive towards benzene, which may be due to its ability to form sulphone or primary amine intermediates. This would allow 3-Ethylmorpholine hydrochloride to undergo reactions with other solvents in the environment, such as cellular proteins in host cells.</p>

<p>3-Benzylcyclobutanone is a chiral, cyclic, sulfoxide that is synthesized via the asymmetric synthesis of 3-benzoylcyclobutanone and benzaldehyde. It can be used in the preparation of oxazolidinones, which are synthetic drugs with anti-inflammatory, analgesic and antipyretic properties. The optical purity of 3-benzylcyclobutanone has been shown to be greater than 99% by chiral GC analysis. This compound has also been synthesized using a preparative yield of 92%.</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>4-Phenylpyridine-2-carboxaldehyde (4PA) is a crystalline compound with a molecular weight of 198.3. It has been shown to have intramolecular hydrogen bonds and intermolecular hydrogen bonds, which are responsible for the formation of the crystal structure. 4PA is most commonly found in acetone, thiourea, and other organic solvents. The diffraction data for this molecule were obtained using x-ray diffraction methods.</p>

<p>Ethyl 2-hydroxy-3-methylbenzoate is an organic compound with the chemical formula CH3COCH2CH(OH)COOH. It is a colorless liquid that is soluble in alcohol, ether, and chloroform. It has been used as a precursor to salicylic acid and other compounds with similar function. This product can be synthesized by cyclization of enol ethers with acid derivatives or by cyclization of alkyl phenols with anhydrides. Cyclization reactions are efficient, requiring only a few steps and high temperatures. Salicylic acid can also be obtained from ethyl 2-hydroxy-3-methylbenzoate via hydrolysis of the ester group, which then undergoes decarboxylation to form salicylic acid.</p>

<p>2-(2-Hydroxy-ethoxy)-benzoic acid is a semicrystalline solid with a melting point at about 220°C. It has a concentration range of 0.5 to 10% and a molecular weight of 192.2 g/mol. 2-(2-Hydroxy-ethoxy)-benzoic acid has been used as an additive in polymers and copolymers, lowering the transition temperature of the polymer or copolymer. The compound has also been used as an intermediate in the synthesis of other compounds such as amorphous polymers, polycaprolactone, and polyesters. 2-(2-Hydroxy-ethoxy)-benzoic acid is an organic compound that belongs to the group of benzoic acids and can be synthesized by reacting ethylene glycol with phthalic anhydride.</p>

<p>Versatile small molecule scaffold</p>

<p>2-(4-Formylphenyl)acetonitrile is a nucleophilic solvent that can react with benzyl alcohol in the liquid phase. It is used to produce benzaldehyde and toluene by hydrogenating benzyl alcohol. 2-(4-Formylphenyl)acetonitrile has a constant boiling point, which makes it useful for adsorption. It also reacts with hydrogen in the presence of a catalyst to produce benzylamine and hydrogen gas. The kinetic study of this reaction has shown that it follows first order kinetics.</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Phenyl-6H-1,3,4-thiadiazin-2-amine is a bidentate ligand that has been used in analyses to study the binding of various substances. It is a phenolic compound with an azomethine group and nitrogen atoms. Phenyl-6H-1,3,4-thiadiazin-2-amine can be synthesized by reacting 1,5-diaminonaphthalene with 2,6-dihydroxyphenol. This reaction can be followed by elemental analysis and elemental identification. Phenyl-6H-1,3,4-thiadiazin-2 amine also has magnetic properties and phenolic oxygen. It displays thermogravimetric properties that can be analyzed using a TGA instrument. The electronic spectra of this substance can also be analyzed using UV/Vis spectroscopy or NMR spectroscopy. Phenyl-[H]-</p>

<p>Versatile small molecule scaffold</p>

2-Bromo-3,4-dimethoxybenzaldehyde (BDMB) is a fluorescent aldehyde that can be used as an analog for 2,4-dinitrofluorobenzene. It has been shown to have cytotoxic effects on cancer cells. BDMB binds to microtubules and inhibits their polymerization and depolymerization, preventing the formation of the cytoskeleton in the cell. This leads to cell death by apoptosis. The affinity of BDMB for microtubules is much higher than its affinity for other cellular components. BDMB also has been shown to inhibit DNA synthesis in cancer cells through inhibition of RNA polymerase II transcription.

<p>5-Methyl-5-hexenoic acid is a synthetic chemical that can be used as a marker for biochemical pathways. It is synthesized from hydrochloric acid and boron trifluoride etherate, which are heated together at 130°C until all the HCI has been evaporated. 5-Methyl-5-hexenoic acid is then reacted with an amide to produce a fatty acid. Oxazolidinones are often used to synthesize this compound, although it can also be made through dehydrating and anhydrous sodium chloride. The product contains impurities and diastereomers that must be removed before it can be used in the manufacture of pharmaceuticals.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Methyl 3-methyl-4,5-dihydro-1,2-oxazole-5-carboxylate (MMDC) is a heterocyclic compound that is used as a raw material for the production of various chemicals. It can be used to produce aniline and acetaldehyde. MMDC is also used in the synthesis of other heterocyclic compounds, such as methyl 2-(3,4-dimethoxybenzoyl)-1H-imidazole-5-carboxylate. This chemical has been found to be an effective inhibitor of bacterial nitrite reductase activity.

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

1,1'-(2-Hydroxy-5-methyl-1,3-phenylene)diethanone is a dioxime ligand that binds to metal ions in a stereochemical fashion. This compound has been shown to bind to the Fe ion and to undergo an intramolecular hydrogen transfer reaction. 1,1'-(2-Hydroxy-5-methyl-1,3-phenylene)diethanone has also been used as a macrocycle that can be assembled into supramolecular structures with metal ions. This molecule is magnetic and its magnetic properties have been studied by electrochemical methods.

<p>Versatile small molecule scaffold</p>

<p>1-Bromocyclohexanecarboxylic acid is a member of the class of organic compounds known as carboxylic acids. It is an oxygenated compound that contains the carboxyl group (-COOH). It has been used to synthesize a number of other organic compounds. 1-Bromocyclohexanecarboxylic acid also reacts with metal salt to form phosphine, which can be used as a reducing agent in organic reactions. The conformation and reactivity of 1-bromocyclohexane can be predicted using theory and calculations. Hydrocarbon groups are added by diisocyanate, which react with hydrocarbon catalytically to produce benzene. This reaction can be used for analgesic or carbamate production.</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<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>

Versatile small molecule scaffold

<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>2,4-Dibromobut-1-ene is a dihedral molecule that is used as an intermediate in the synthesis of other compounds. The highest serum levels are seen in infants and rationalized to protonation of the tertiary butyl group. Dehydration leads to formation of a high yield via alkylation with long-term exposure. 2,4-Dibromobut-1-ene has been shown to be an antineoplastic drug that inhibits cell growth by binding to electron deficient positions on DNA molecules. This causes nucleic acid strand breakage and inhibition of DNA synthesis, leading to cell death.</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>4-Methyl-N-(prop-2-yn-1-yl)benzenesulfonamide is a chiral, isopropyl substituted sulfonamide that has been synthesized by a palladium-catalyzed coupling reaction. It is an example of a biomolecular catalyst that has been shown to have the ability to catalyze the formation of chlorides, terminal alkynes and formyl groups. The crystal structure of this compound has been determined by X-ray diffraction and it was found to be composed of two molecules in the asymmetric unit with one molecule being disordered. 4-Methylbenzenesulfonamide is also an alkylating agent and can react with amines and amides to form cinchona alkaloid derivatives.</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Please enquire for more information about Cefdinir related compound B including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>alpha-Cyano-3-hydroxycinnamic acid is a mitochondrial matrix analog that has been shown to inhibit the uptake of carnitine, glutamate, and branched-chain amino acids. This compound also inhibits the activity of glyceraldehyde-3-phosphate dehydrogenase and dodecyl CoA dehydrogenase, which are enzymes involved in the production of cellular energy. alpha-Cyano-3-hydroxycinnamic acid also inhibits the synthesis of mitochondrial DNA and RNA. The compound binds to the enzyme succinate dehydrogenase, inhibiting its function. This inhibition leads to a decrease in cellular energy production and an increase in oxidative stress.</p>

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

Please enquire for more information about Cinidon ethyl including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>Please enquire for more information about 2-Chloro-10-[3-[[3-(dimethylamino)propyl]methylamino]propyl]phenothiazine 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-Chloro-4-methylpyrimidine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Furo[3,2-d]pyrimidin-4(3H)-one is a heterocyclic compound that has been reported to have anticoccidial properties. This compound has been shown to inhibit the growth of Eimeria tenella and Eimeria acervulina in vitro. Furo[3,2-d]pyrimidin-4(3H)-one also inhibits the synthesis of DNA in these protozoa.</p>