Building Blocks

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-(2-Dimethylamino-ethylamino)-ethanol is an organogold compound that has been synthesized by irradiating 2-(2-dimethylamino-ethyl)aminopyridine with gamma rays. This compound is a ligand for the phthalocyanine axial coordination complex and is cationic in nature. It reacts with sulfur to form a sulfide, which can be used as a reagent for the synthesis of other compounds. 2-(2-Dimethylamino-ethylamino)-ethanol has shown hydrophilicity and can be used as an additive in cosmetic products.<br>2-(2-Dimethylamino-ethylamino)-ethanol has been found to have high reactivity with ammonium ions and may be useful in the preparation of amides.</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>

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>2,5-Dimethylpyrrolidine hydrochloride is a chiral compound that is used to prepare cyclopropanes. It can be used in enantioselective reductions of diazoacetates and cyclopropanations. It is an efficient reagent for the synthesis of styrene derivatives with high enantioselectivity. 2,5-Dimethylpyrrolidine hydrochloride has been used to synthesize the binaphthyl system using dinitrogen as the source of chirality. The configuration of the binaphthyl system was determined by the configuration of the nitrogen atom on 2,5-dimethylpyrrolidine hydrochloride.</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>6-Methylpyridine-2-carboxamide is a nitrogenous compound that contains a metal ion. It has an amide group and a carboxylate group, which are both protonated at physiological pH. The compound is soluble in water and alcohols. 6-Methylpyridine-2-carboxamide can be used as an amplifier in the measurement of magnetic resonance imaging (MRI) spectra and nuclear magnetic resonance (NMR) spectra. It has been shown to have transistor properties, which may be due to its ability to transfer an electron from one side of the molecule to the other. 6-Methylpyridine-2-carboxamide also has a high melting point, which makes it suitable for use in high temperature environments such as in the production of semiconductors.</p>

<p>2-{[(Pyridin-2-ylmethyl)amino]methyl}phenol is a ligand that crystallizes in the monoclinic space group P21/c. The compound crystallizes with two molecules per asymmetric unit, and contains one water molecule per molecule. It has been shown to have cyclic voltammetry, which includes cyclic voltammetry and linear sweep voltammetry. 2-{[(Pyridin-2-ylmethyl)amino]methyl}phenol binds to the perchlorate ion and oxygen atoms coordinate to the nitrogen atoms of the ligand.</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>R(+)-Baclofen.Hydrochloride is a GABA analogue that stimulates the GABA-benzodiazepine receptor complex and produces antinociception. It has been shown to be effective against diabetic neuropathy in rats, with no observed side effects. R(+)-Baclofen.Hydrochloride is used for the treatment of trigeminal neuralgia, butyric acid induced hyperalgesia and chronic constriction injury in rats. The main mechanism of action of R(+)-Baclofen.Hydrochloride is its ability to activate the benzodiazepine receptor by binding to it, which leads to mitochondrial membrane potential depolarization and an increase in the release of gamma-aminobutyric acid (GABA) from neurons.</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>6-Amino-1H-pyrazolo[3,4-b]pyridine is a cholesterol inhibitor that belongs to the pyridine derivative class. It has been shown to decrease the level of total cholesterol and low density lipoprotein (LDL) cholesterol in rats with atherosclerosis. This drug inhibits protein synthesis by binding to the active site of HMG-CoA reductase and preventing it from forming an enzyme-substrate complex with cholesteryl ester. 6-Amino-1H-pyrazolo[3,4-b]pyridine is an enantiomeric mixture of two stereoisomers, R and S. The R isomer has been shown to be more potent than the S isomer in inhibiting HMG CoA reductase activity.</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>6-chloro-5-methoxy-1H-indole is an aromatic compound that can be synthesized by the amination of acetyl chloride. This reaction is followed by a borohydride reduction of the imine, and then an acetylation of the resulting alcohol. The synthesis method involves two steps: first, a borohydride reduction of the imine using sodium borohydride; and second, an acetylation with chloral. The final product is purified by distillation and elemental analysis to determine yields.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-(bromomethyl)-6-chloropyridine is a ligand that binds to metal atoms. It forms a complex with the metal atom by coordinating with two or more bromine atoms and one or two hydrogens. 2-(Bromomethyl)-6-chloropyridine has been shown to interact with pyridine, x-ray diffraction studies, crystal x-ray diffraction, and ligands in crystal x-ray diffraction studies. The conformation of this compound can be deformed by substituting the methyl group on the chloro group for other moieties. These interactions have been shown using X-Ray diffraction studies and crystal x-ray diffraction studies.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Oxa-7-azaspiro[4.5]decane is a compound that is structurally related to the neurotransmitter substance P and has been shown to be a potent, selective antagonist of neurokinin (NK) receptors. Oxa-7-azaspiro[4.5]decane inhibits the release of dopamine from rat brain synaptosomes and depresses synapses in the rat hippocampus, an effect that can be reversed by administration of an NK receptor antagonist. This drug also has anti-cancer activity against chemotherapy-induced depression in rats and has been shown to inhibit proliferation in rat hepatocytes. The oxygen atom on the molecule is responsible for its oxidative properties, which are due to its ability to form reactive oxygen species such as superoxide and hydroxyl radicals when it reacts with water or hydrogen peroxide. These reactive oxygen species are able to damage DNA, RNA, enzymes, or other molecules by oxidation.</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>Propane-2-sulfonyl fluoride is a fluorinating agent that has been used to study the structure of nucleic acids. It is also used in the preparation of sulfones and sulfuryls. In Alzheimer's disease, Propane-2-sulfonyl fluoride has been shown to crosslink the amyloid beta peptide and inhibit the formation of fibrils. The effective dose is determined by its therapeutic value as a treatment for Alzheimer's disease.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>5-Methylthiophen-2-yl)methanol is a furan that contains a sulfo group. It is an electrophilic compound with mechanisms and exchangers that are still being studied. 5-Methylthiophen-2-yl)methanol reacts with thiophene to form the sulfone, which is then converted to the methylene by alkylation. The reaction of 5-methylthiophen-2-yl)methanol with pyrrole leads to the formation of the heterocycle, which can be oxidized to form the corresponding carboxylic acid. This compound also has been shown to react with formalin and acidic conditions, as well as being able to be oxidized into formaldehyde.</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-Methoxypyrazine-2-carbaldehyde (3MP) is a synthetic, biomimetic molecule that can be produced through a biomimetic synthesis. It has been shown to be an effective inhibitor of the enzyme schischkiniin. 3MP also has bidirectional reactivity and can act as both a nucleophile and electrophile. 3MP thermally reacts with dicarbaldehydes to form the natural product pyrazinyl and it can also react with amides to form amidations. 3MP has been shown to have antimicrobial properties against Staphylococcus aureus, Bacillus subtilis, Streptococcus pneumoniae, and Pseudomonas aeruginosa. The sequence of this molecule is shown below:</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>2-(2-Hydroxyethoxy)benzamide is a dopamine receptor agonist that inhibits 5-HT3 receptors in vitro. It is an orally active drug that has been shown to have a good safety profile in humans. 2-(2-Hydroxyethoxy)benzamide has also been shown to be a 5-HT4 receptor antagonist, which may account for the lack of serotonin syndrome in animal studies. This drug can cause intestinal contractions and nausea, and may also cause symptoms such as headache, dizziness, and insomnia. Levosulpiride is a selective 5-HT4 receptor agonist that may be more effective than 2-(2-Hydroxyethoxy)benzamide at alleviating the gastrointestinal side effects of this drug.</p>