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>3-tert-Butyl-1-methyl-2-pyrazolin-5-one is an electrophilic compound with a variety of use in the medical field. The compound has been used in research as a potential therapeutic for Alzheimer's disease, cancer, and other conditions. 3-tert-Butyl-1-methyl-2-pyrazolin-5-one has also been used to treat skin diseases such as psoriasis. It is typically administered topically or orally.</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>(2S)-2-Amino-N,3-dimethylbutanamide is a trifunctional molecule with a carbocycle that belongs to the class of chemical substances. It has been shown to be an inhibitor of human serum enzymes and it can also inhibit the production of human immunodeficiency virus (HIV). It binds to the receptor molecule and prevents HIV from binding to CD4 cells. The toxicological studies for this compound have been performed in cell culture and in animals. There are no reports on its effects on humans. This compound is not metabolized in vivo, but it is rapidly hydrolyzed by esterases in vitro, forming ethyl esters.</p>

<p>Versatile small molecule scaffold</p>

<p>5,7-Dimethyl-2-phenylpyrazolo[1,5-a]pyrimidine is an aromatic heterocyclic compound. It can be prepared by the palladium-catalyzed coupling of aryl bromides with 5,7-dimethylpyrazolo[1,5-a]pyrimidines. The yield and synthesis conditions are dependent on the type of aryl bromide used in the reaction. This process has been shown to be a useful methodology for the synthesis of various heterocyclic compounds.</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-Oxa-spiro[4.5]decan-8-one is a pentafluoroethyl derivative of an odorant that has been used as a blood substitute, and it has been shown to be insoluble in solvents. 1-Oxa-spiro[4.5]decan-8-one has a strong odor and is not soluble in water or common organic solvents. It can be found in the blood of mammals, but not humans.</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-(tert-Butyldimethylsilyloxy)butanal is a molecule that has been shown to have anticancer activity. It is structurally related to paclitaxel and epothilones, which are both derived from the cyclopentenone family of compounds. 4-(tert-Butyldimethylsilyloxy)butanal was found to be effective against a number of cancer cell lines, including leukemias, lymphomas, and breast cancers. The anticancer activity of 4-(tert-Butyldimethylsilyloxy)butanal is due to its ability to stabilize the enolate form of the enzyme alkylation, leading to inhibition of protein synthesis in cancer cells.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-Hydroxymethyloxan-4-ol is a synthetic chemical that is used as a catalyst in the synthesis of citric acid. It is also used to catalyze the hydrogen peroxide oxidation of hydroxylated compounds and to produce citric acid from sugars. 4-Hydroxymethyloxan-4-ol is an acidic compound and can react with metals such as sodium, calcium, and magnesium to form metal oxides. This chemical has been shown to be a good inhibitor of peroxide formation in catalases.</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>7-Bromo-5-nitroindoline is a synthetic compound that has been shown to bind to auxin, which is a plant hormone. It has been used in photoaffinity labeling and can be used in the synthesis of other compounds. 7-Bromo-5-nitroindoline binds reversibly and covalently to auxin in the presence of light. The regiospecificity of this binding allows for the determination of specific properties of auxin binding. 7-Bromo-5-nitroindoline is also used as a tritiated label in syntheses and as a deuterated label for photoaffinity labeling.</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>Pyrimidine-2-carbohydrazide is a bioinorganic compound that has been shown to be active against bacteria, including staphylococcus. It is also effective against tuberculosis and leishmania. Pyrimidine-2-carbohydrazide binds to the bacterial cell membrane and inhibits its growth by preventing the synthesis of essential proteins. This drug's pharmacokinetic properties have been studied using techniques such as bioinorganic and electron paramagnetic resonance spectroscopy. The tetranuclear nature of pyrimidine-2-carbohydrazide makes it an excellent candidate for use with ciprofloxacin in the treatment of leishmaniasis.</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>2,3-Dihydro-1λ⁶-thiophene-1,1,3-trione is a chemical compound that has been synthesized by the reaction of two molecules of dimethyldioxirane with one molecule of thiol. It is a colorless liquid that can be oxidized to 2,3-dihydro-2λ⁶-thiophene-2,2,4(1H)-trione or reduced to 2-(2'-formylphenyl)ethanol. This chemical is an important precursor for the synthesis of sulfur and nitrogen nucleophiles. The yields are high and it is commercially available.</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-Chloro-5-methyl-2,3-dihydro-1H-indole is a 5HT receptor agonist that has been shown to be an effective antidepressant in animal models. It has a high affinity for the 5HT2A and 5HT2C receptors, but does not bind to other serotonin receptor subtypes. 6-Chloro-5-methyl-2,3-dihydro-1H-indole also possesses oral activity and is selective for the 5HT2A receptor subtype. The compound has been cloned and evolutionarily optimized to produce a more potent and selective compound.</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-Bromo-5-isopropoxybenzaldehyde is an isopropoxy analog of the natural product suzukol. It has been synthesized by a novel methodology involving oxidative bromination of the phenylacetone. This compound has been used as a model for the synthesis of 2,3,4,5-tetrahydrobenzofuran and can be used as a starting material for the synthesis of other natural products.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Amino-5-methoxyphenol is a chiral compound with two enantiomers. It has been shown to inhibit tumour growth and to have antitumour properties. 3-Amino-5-methoxyphenol has also been found to be effective against Gram-positive bacteria, such as methicillin resistant Staphylococcus aureus (MRSA). 3-Amino-5-methoxyphenol binds to the active site of bacterial ribosomes and inhibits protein synthesis. This leads to cell death by inhibiting the production of proteins vital for cell division. 3-Amino-5-methoxyphenol can also be used as an antibiotic in humans because it does not affect the metabolism of human serum.</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>