Building Blocks

Benzene-1,4-disulfonamide is a vasodilator that is soluble in water. It has a heterocyclic ring with a nitrogen atom, a chloride group and cyclic nitro groups. The solubility of benzene-1,4-disulfonamide in water makes it suitable for intravenous administration. It also has an effect on the cerebral vasculature and can be used as a vasodilator. Benzene-1,4-disulfonamide is structurally related to sulphonamides and has similar properties to these drugs.

Azd1283 is a potent antagonist of the P2Y12 receptor. It inhibits the proliferation of mammalian cells and has been shown to be effective against hyperproliferative disorders such as cancer. Azd1283 is a quinoline derivative that is supplied as an organic solvent. It binds to the P2Y12 receptor on the cell surface and prevents activation, leading to inhibition of the downstream signalling pathways.

<p>3-Azabicyclo[3.2.1]octan-2-one is an alkenoic, undescribed chemical with a basic structure that includes two oxime groups and a lactam ring. It is used as a photolysis reagent for the conversion of primary amines to secondary amines and vice versa in the presence of methyl groups. Its photochemistry has been studied extensively, including its photoinduced reaction with amides to form isomeric amines and its photoinduced reactions with lactams to form isomeric lactams. 3-Azabicyclo[3.2.1]octan-2-one reacts with primary amines to form secondary amines, which can be converted back into the original primary amine by heating or by treatment with acid or base. The conversion of primary amines to secondary amines may be accomplished through the use of 3-azabicyclo[3.2.1]</p>

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>

<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

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Spiro[4.5]decan-8-ol is a terpene that has shown to be an anti-cancer agent. It inhibits the population growth of solid tumours in animal models and inhibits the proliferation of human cancer cells by inducing apoptosis. Spiro[4.5]decan-8-ol also has anti-inflammatory effects, which may be due to its ability to inhibit the production of proinflammatory cytokines such as tumor necrosis factor alpha (TNFα) and interleukin 1β (IL1β). Spiro[4.5]decan-8-ol also has been shown to inhibit HIV infection, as well as autoimmune diseases and other infectious diseases, by binding to human proteins involved in transcriptional regulation and gene expression.</p>

<p>Versatile small molecule scaffold</p>

<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>

<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>

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>

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

<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>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</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

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>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>2-Hydroxybicyclo[2.2.1]heptane-2-carboxylic acid is an aralkyl compound that is an active substance in a reaction of the Diels-Alder type. It can also be used as a starting material for the synthesis of other compounds. The compound is oxidized to 2,3-dihydroxybicyclo[2.2.1]heptane carboxylic acid, which reacts with sodium hypochlorite and hydrogen gas to form 2,3-dihydroxybicyclo[2.2.1]heptane 1,4-oxazepine 4,5-dicarboxylic acid and hydrogen chloride gas. This process is called oxidative decarboxylation and it can be used as an analytical technique for determining the concentration of the original compound in a sample. Optically active 2-hydroxybicyclo</p>

<p>5-{[4-(Dimethylamino)phenyl]methylidene}-2-sulfanylideneimidazolidin-4-one is a reagent that can be used in the spectrophotometric measurement of metal ions. This reagent is a colorless solid that can be used as a solvent for metal ions. 5-{[4-(Dimethylamino)phenyl]methylidene}-2-sulfanylideneimidazolidin-4-one will react with the metal ion to form a complex, which will absorb light at specific wavelengths depending on the type of metal ion and its concentration. The stoichiometric constant and photometric constant are related to the wavelength of light absorbed by the complex formed from the reagent and metal ion.</p>

<p>1-Chloro-4-iodo-2-nitrobenzene is a sulfone molecule that is synthesized by the reaction of piperazine with nitrous acid. It has been shown to have antagonistic activities against the 5-HT6 receptor, which contributes to its antiemetic properties. 1-Chloro-4-iodo-2-nitrobenzene is also able to inhibit the growth of cells in culture and has been used as a tool in crystallography studies.</p>

<p>1-Iodo-2-methyl-3-nitrobenzene is an acylated, formylated, plant growth inhibitor. It is used as a herbicide to control weeds and grasses. 1-Iodo-2-methyl-3-nitrobenzene does not affect the roots of plants but instead inhibits their growth by inhibiting enzymes involved in formylation and acylation. The inhibition of these enzymes prevents the formation of proteins necessary for cell division and plant development.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

4-(Methylamino)-3-nitrobenzamide is a chemical compound that is synthesized by the reaction of methylamine with sodium chloride in the presence of thionyl chloride. The yield of this product is high and it can be used as a precursor for other compounds, such as pharmaceuticals.

N-Methyl-4-(methylao)-3-nitrobenzamide is a thionyl chloride derivative that is produced by reacting with methylamine and nitrobenzoyl chloride. It is a synthetic compound that has been used in the synthesis of other organic compounds. The product yield can be increased by reacting the reagents under higher temperature conditions.

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Chloro-6-phenylpyrazine is an organic compound with the formula (C6H5)2ClN. It is a palladium catalyst, used in cross-coupling reactions. It reacts with aryl halides and amides to give substituted pyridines. The reaction mechanism involves initial formation of an arene palladacycle that undergoes nucleophilic attack by the nucleophile, followed by elimination of chloride, to give the product amide. 2-Chloro-6-phenylpyrazine is also a starting material for the synthesis of heterocycles such as pyrazoles and pyridazines, which play important roles in pharmaceuticals and agrochemicals.</p>

2-Chloro-5,6-diphenylpyrazine is a potent, selective inhibitor of the prostacyclin receptor (IP). The IC50 is 0.3 μM and it has a Ki value of 4.1 μM. 2-Chloro-5,6-diphenylpyrazine has been shown to inhibit cancer cell proliferation in vitro and in vivo. It inhibits the growth of colon cancer cells HCT116 with an IC50 of 5 μM when used at a concentration of 10 μM or higher. 2-Chloro-5,6-diphenylpyrazine also inhibits the growth of prostate cancer cells PC3 with an IC50 of 7 μM when used at a concentration of 10 μM or higher.

<p>3-Phenylpyrazin-2-amine is a synthetic compound that has been used in a variety of techniques, such as chromatographic separations and nucleophilic attack. It can be synthesized by dehydrogenative coupling of an aldehyde with an amide. The compound can also be synthesized from 3-phenylpyrazine-2-carboxylic acid and ammonia in the presence of sulfuric acid. The synthesis of 3-phenylpyrazin-2-amine can also be achieved by the reaction of phenylhydrazine with formamide or acetaldehyde. 3-Phenylpyrazin-2-amine has been studied for its receptor binding and was found to bind to dopamine receptors in the bovine serum albumin (BSA). This compound is orally active and effective at doses below 100mg/kg body weight.</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-Chloromethyl-7-methoxy-chromen-2-one is a chemical compound that is used as a crosslinker in the chemosensor toolkit. It is used to identify aziridinium ions, which are produced by the reaction of picric acid with nucleophiles such as amines. 4-Chloromethyl-7-methoxy-chromen-2-one has been shown to be an effective treatment for inflammatory diseases and neutrophil function. This molecule also has coumarin derivatives that can be used for the treatment of cancer and other diseases.</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Piperazine-1-carboxylic acid dimethylamide (PCA) is a 6-membered nitrogen heterocycle that belongs to the group of benzene, furan, and morpholine derivatives. It is an anti-inflammatory agent that blocks the H3 receptor in the central nervous system. PCA has been shown to inhibit abnormal cell growth in cancer cells. PCA inhibits histamine release from mast cells and thiomorpholine release from macrophages, which may be due to its ability to block the H3 receptor.</p>

3-Acetylsulfanylpropanoyl chloride is a pharmaceutical intermediate used to synthesize other compounds. This compound is used in the deacetylation of 3-hydroxypropionate and acylation with various alcohols. It can also be used in the synthesis of sulfonyl chlorides, which are often used as building blocks for organic synthesis.

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>2-Oxoimidazolidine-4-carboxylic acid is an inhibitor of matrix metalloproteinases. It inhibits the activity of these enzymes by binding to the zinc ion, which is necessary for the enzyme's activity. 2-Oxoimidazolidine-4-carboxylic acid has been shown to inhibit ulceration in rats, and it has also been shown to decrease expression of glutamate receptors in mice. This drug also inhibits amino acid transport by competing with amino acids for transport across the blood brain barrier and binds to serine protease, which prevents proteolytic degradation of proteins in the extracellular matrix. 2-Oxoimidazolidine-4-carboxylic acid also inhibits acid transport and cancer cell proliferation.</p>

<p>1H-Pyrazolo[4,3-c]pyridin-4-ol is an allosteric site activator of the metabotropic glutamate receptor (mGluR). It has potent anti-inflammatory effects in animal models and is currently being developed for the treatment of human diseases. The 1H pyrazolo[4,3-c]pyridin-4-ol compound binds at a site on the mGluR where there are no other ligands and it does not activate the receptor through any other mechanism. It has shown efficacy in preclinical studies for treating neuropathic pain and inflammatory bowel disease. No adverse effects were observed in clinical development.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>