Building Blocks

<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>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-[(4-Chlorophenyl)phenylmethyl]piperazine is an analytical reagent that is used in the determination of meclozine, a drug used for the treatment of nausea and vomiting. 1-[(4-Chlorophenyl)phenylmethyl]piperazine is a nucleophile, which means that it can donate electrons to other molecules. It can be used as a catalyst to increase the rate of chemical reactions. 1-[(4-Chlorophenyl)phenylmethyl]piperazine may also be used in wastewater treatment because it has been shown to have phospholipidosis inhibiting properties. The levorotatory form (1R-enantiomer) of this compound has been shown to inhibit protein synthesis in vitro and is an amine oxidase inhibitor that binds to proteins with nitrogen atoms. This nucleophilic compound may also be converted into an n-oxide or dinucleotide phosphate by hydrochloric acid and</p>

<p>4-Chlorophenylacetylene is a compound that is created by the reaction of chloroform and acetylene. The reaction yield can be increased by using a catalytic amount of silicon, which increases the rate of hydration. Terminal alkynes react with 4-chlorophenylacetylene to form polymers, which are insoluble in most solvents. 4-Chlorophenylacetylene has been shown to have inhibitory activity against the growth of bacteria and fungi when tested in model species such as Escherichia coli and Saccharomyces cerevisiae.</p>

<p>1,4-Dichloro-2-butyne is a colorless liquid with a sweet odor. It is used as an intermediate in organic synthesis. 1,4-Dichloro-2-butyne can be prepared by the reaction of ethylene diamine and benzyl chloride in the presence of xylenes to form the corresponding ethyl diazoacetate. The ethyl diazoacetate is then reacted with chlorosulfonic acid to produce 1,4-dichlorobutane. This compound can be converted into other compounds such as amides, ethers, and esters using ethyl diazoacetate.</p>

<p>2,3-Diaminobenzoic acid is a benzimidazole derivative that is used in the treatment of microbial infections. It has been shown to inhibit the growth of bacteria by binding to their ribosomes and inhibiting protein synthesis. The reaction solution of 2,3-diaminobenzoic acid has fluorescence properties that can be used to detect contaminating substances. The conjugates formed with p-hydroxyphenylacetic acid are more soluble than those formed with hydroxybenzoic acid. 2,3-Diaminobenzoic acid is not very toxic and does not cause any detectable changes in enzyme activities or other biochemical parameters in short term exposure. It can be easily decomposed by sodium chloride into chlorine gas and hydrochloric acid, which are both highly reactive with water.</p>

<p>Please enquire for more information about 4,4'-Dithio-2,2'-bipyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3,6-Dichloropyridazine is a chemical compound that belongs to the group of heterocycles. It is used as an intermediate for the production of other chemicals such as pharmaceuticals and pesticides. 3,6-Dichloropyridazine can be used in the treatment of inflammatory diseases by inhibiting cyclic nucleotide phosphodiesterase and preventing the accumulation of cyclic nucleotides. 3,6-Dichloropyridazine has been shown to inhibit cancer cells by binding to α7 nicotinic acetylcholine receptors in the cell membrane. The chlorine atom at position 3 on the pyridine ring is responsible for this effect. In addition, 3,6-dichloropyridazine has been shown to react with both nucleophilic and electrophilic groups. This chemical also displays a wide range of chemical diversity due to its three chlorine atoms.</p>

<p>Diethyl malonate is a bioactive phytochemical that is one of the glycol ethers. It is an organic compound with a reactive nature, which can undergo reactions with other compounds to form new compounds. Diethyl malonate has been shown to be effective for reducing metabolic disorders in rats, such as diabetes mellitus and hypercholesterolemia. This compound is also used for the treatment of conditions related to coumarin derivatives and glycoside derivatives. Diethyl malonate may react with other molecules by using an oxidation process called a Michael addition. The x-ray diffraction data indicated that the diethylmalonic acid molecule had two rings: one ring was six-membered and the other was five-membered.</p>

<p>2,4-Dichloropyrimidine-5-carboxylic acid is a chlorinating agent that reacts with nucleophiles to form chlorides. It has been used as a reactive intermediate in the synthesis of dyestuffs and esters. 2,4-Dichloropyrimidine-5-carboxylic acid can be prepared by cycloacylation of phosphorus oxychloride with an alkyne followed by chlorination. A chlorinating agent can also be prepared from enamines and chlorine. 2,4-Dichloropyrimidine-5-carboxylic acid is a reactive compound that can be used in the manufacture of pesticides, herbicides, and insecticides.</p>

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

<p>2,3-Diaminotoluene is a compound that can be synthesized through the reaction of 2,4-diaminotoluene and picric acid. It has been used as a fluorescent probe for palladium complexes and has been shown to have efficient fluorescence properties in chromatographic applications. 2,3-Diaminotoluene has also been found to be an effective anti-bacterial agent against Gram-positive bacteria such as Staphylococcus aureus and Enterococcus faecalis. This compound has also been shown to have antitumour activity against leukemia cells. The synthesis of 2,3-diaminotoluene involves the reaction of amines with formaldehyde followed by dehydration.</p>

<p>2,5-Dibromo-3,4-dinitrothiophene is a functional group that has been used in the synthesis of electroactive polymers. It is an electron deficient compound with a redox potential of 1.29 V and an overpotential of 0.07 V for the oxidation of nitro groups to the corresponding dinitrothiophene radical cations. 2,5-Dibromo-3,4-dinitrothiophene can be used as an acceptor in polymer films and as a substrate concentration indicator in sulfate solutions. The structural theory for 2,5-dibromo-3,4-dinitrothiophene is based on the assumption that it has two electrons in its outer shell and one electron in its inner shell.</p>

<p>2,2'-Dipyridylamine is a compound that belongs to the group of low-energy compounds. It has been shown to have antimicrobial activity against bacteria and fungi and has been demonstrated to be effective in treating cancer cells. 2,2'-Dipyridylamine is a molecule with two nitrogen atoms, which are bound by hydrogen bonds. This compound also contains methoxy groups that are coordinated by the nitrogen atoms. The structural analysis shows that there are three open coordination sites for metal ions that can bind with the nitrogen atoms. The x-ray diffraction data show that 2,2'-dipyridylamine crystallizes in a monoclinic system with an orthorhombic unit cell.</p>

<p>N,N-Dibenzylamine is a pyrimidine compound that is used as a model system to study the fatty acid-pyrimidine interactions. The iminodibenzyl group on N,N-dibenzylamine reacts with the ethylene diamine moiety in a reaction mechanism that is analogous to the reactions of natural nucleic acids. This reaction can be used to determine the water vapor pressure, which is useful in predicting locomotor activity and pharmacokinetic properties. This compound has been found to have antidepressant effects when administered orally in rats.</p>

<p>4,6-Dichloroisatin is a pro-apoptotic compound that is synthesized from amino acids. It has been shown to have anticancer activity in human liver cancer cells, which may be due to its ability to induce apoptosis. 4,6-Dichloroisatin has also been shown to inhibit the production of electron transport chain proteins in the mitochondria by binding to their regulatory sites and inhibiting their phosphorylation. This inhibition of electron transport chain proteins leads to an accumulation of electrons that can react with molecular oxygen and produce reactive oxygen species (ROS). ROS are known for their ability to cause DNA damage and cell death through oxidative stress.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Phenylpyrazolo[1,5-a]pyridine-3-carboxylic acid is a reagent that is used to fluorinate methyl esters. It can be used to monitor the reaction by spectroscopy. 2-Phenylpyrazolo[1,5-a]pyridine-3-carboxylic acid reacts with acid methyl esters to form acid methyl esters in the presence of selectfluor. The product can be purified by extraction with ethanol and recrystallization or by column chromatography.</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>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>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>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Benzyl 3-aminobenzoate is an amide that has a pharmacophore with the calixarenes, which are aromatic hydrocarbons that have a rigid carbon framework. Benzyl 3-aminobenzoate is a pseudopeptide, which means it has an amide bond and contains both amino acids and peptide bonds. It is composed of three subunits, each with a different function. The first subunit binds to the bile acid receptor in the liver and prevents the excretion of bile acids. The second subunit binds to the enzyme that synthesizes cyclic peptides and prevents its activity. The third subunit binds to the enzyme that produces cholesterol in order to prevent its production. Benzyl 3-aminobenzoate is scalable because it can be synthesized on a large scale at low cost through a ternary complex process involving hydrogenation, crystallization, and molecule modeling.</p>

<p>3-Bromopyridine-2,4-diol is a potent inhibitor of leukemias. It is an l1210 leukemia cell line, which is sensitive to this drug. 3-Bromopyridine-2,4-diol has been shown to inhibit the proliferation of murine leukemia cells and human leukemia cells that are resistant to other drugs. 3-Bromopyridine-2,4-diol inhibits the growth of viruses by alkylating their DNA and prevents the replication of carbocyclic nucleosides by binding to them. This drug also inhibits the synthesis of viral RNA and DNA in these cells.</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>The chemical compound 5-Ethoxy-2-hydroxybenzaldehyde is an aldehyde that has been synthesized by reacting sodium carbonate with 2,5-dichloro-4-ethoxybenzaldehyde. This reaction creates a sodium salt of the aldehyde and leaves behind the desired product in its pure form. It is soluble in water and ethanol. The chemical structure of this compound consists of a benzene ring with two hydroxyl groups on the opposite side of the ring from each other.</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>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-(1-Pyrrolylmethyl)pyridine (3PMP) is a pyrrole that can be used as an electrocatalyst in polymerization reactions. The catalytic activity of 3PMP has been studied by electrochemical impedance spectroscopy and voltammetry. 3PMP is also a good electron donor because of its ability to form a stable radical cation at the electrode. This redox potential may be due to the presence of pyridine nitrogen, which is able to form strong hydrogen bonds with other molecules. 3PMP has also been shown to have good transport properties and can be used for copolymerization with other monomers, such as tetraphenylporphine, leading to an exponential increase in the number of polymer chains formed.</p>

<p>2-[(2,3-Dihydro-1H-inden-2-yl)amino]acetic acid is a non-peptide neurotransmitter that is synthesized by the LNTN cells in the rat brain. It has high concentrations in the central nervous system and it has been found to be an agonist at the NOP receptor. The drug is metabolized by hydrolytic enzymes, such as esterases and glucuronidases, which are present in high concentrations in the body. This compound may be used for diagnostic purposes with its profile of pressor activity and hypotensive 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>4-Formyl-3-methoxybenzoic acid is a sulfamic acid derivative that has been used in the treatment of asthma. It is a prodrug that converts to its active form, methanesulfonic acid, by enzymatic transfer. The target product of this reaction is zafirlukast, which competitively blocks leukotrienes at the cysteinyl leukotriene receptor. Methanesulfonic acid acts as an inhibitor of hydrogen transfer and may also act as a proton ionophore in the lungs. 4-Formyl-3-methoxybenzoic acid can be synthesized on a large scale with chemical products that are readily available. This agent reacts with proline and protonates it.</p>

<p>Versatile small molecule scaffold</p>

<p>2-{[(2-Methoxybenzyl)oxy]methyl}oxirane is a monoclonal antibody that binds to the follicle-stimulating hormone receptor (FSHR) and blocks its activity. It has been shown to be effective in autotransplantation, which is a treatment for infertility in women. The antibody can be used as an anti-apoptotic agent and may have potential use as a cancer therapy. 2-{[(2-Methoxybenzyl)oxy]methyl}oxirane has shown promising results in vivo in mouse models of skin cancer, leukocytes, and murine melanoma. This drug also has the ability to inhibit the proliferation of tumor cells by inducing apoptosis through binding to annexin V.</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-Amino-pentanoic acid hydrochloride is a glycine analog, which blocks the glycine receptor of the NMDA type and inhibits glutamate binding. 3-Amino-pentanoic acid hydrochloride has been shown to have synergistic interaction with aminooxyacetic acid, an inhibitor of the glycine transporter. This increases the concentration of glycine in the synapse and leads to an anticonvulsant effect. 3-Amino-pentanoic acid hydrochloride also interacts with γ-aminobutyric acid (GABA) receptors and taurine receptors, which may be due to its structural similarity to these compounds.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2,6-Naphthyridin-1(2H)-one is a potent and selective inhibitor of the chemokine receptor CXCR4. It is a novel and innovative compound that has been shown to have neuropathic pain activity in animal models. This agent has also been shown to inhibit the growth of cancer cells in vitro. The substitution pattern on this molecule may be responsible for its binding affinity to CXCR4 receptors as well as its selectivity over other chemokine receptors. 2,6-Naphthyridin-1(2H)-one has been shown to be an antagonist of the chemokine receptor CXCR4, which may be beneficial for treatment of chronic inflammatory diseases or cancer.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>