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>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>3-[(4-Butylphenyl)sulfamoyl]benzoic acid is a sulfonamide that inhibits the activity of antibodies by binding to the antibody molecule. 3-[(4-Butylphenyl)sulfamoyl]benzoic acid is used as a research tool in cell biology, pharmacology, and immunology. It has been shown to inhibit the activity of ion channels by binding to the channel protein. The drug also binds to ligands and activates them, which may be due to its ability to bind with high affinity and specificity. 3-[(4-Butylphenyl)sulfamoyl]benzoic acid also binds with high affinity and specificity to receptors that are involved in cellular signaling.</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>Methyl 2-bromo-6-(bromomethyl)benzoate is a pharmacological agent that belongs to the group of dopamine D2-like receptor ligands. It has been shown to bind to the dopamine D2-like receptor in rat brain tissue, and has affinity for this receptor. Methyl 2-bromo-6-(bromomethyl)benzoate may induce behavioral effects by interacting with the dopamine system in the central nervous system. This compound binds to dopamine receptors, especially those with affinity for D2-like subtypes. The binding of this compound induces conformational changes in the receptor, which leads to changes in downstream signal transduction and ultimately influences behavior.</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-[(2-Methyl-2,3-dihydro-1H-indol-1-yl)sulfonyl]benzoic acid is a synthetic sulfonamide that has been used as an inhibitor of the protein tyrosine phosphatase SHP2. In cell biology, it has been used as a research tool to study the cellular functions of proteins such as ion channels and receptors. 3-[(2-Methyl-2,3-dihydro-1H-indol-1-yl)sulfonyl]benzoic acid can be used in pharmacology to study the effects of ligands on cells or tissue. It is also known to activate certain receptors in the brain and central nervous system. This compound is highly pure with a CAS number of 326619-13-0, and it has an ionization constant (pKa) of 7.6 at pH 7.4.</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>(2R)-3-[(Carboxymethyl)sulfanyl]-2-acetamidopropanoic acid is a metabolite of the drug sulfapyridine. It is formed by conjugation with glutathione in the liver to form 3-glutathione-2-sulfapyridine, and then excreted into bile. (2R)-3-[(Carboxymethyl)sulfanyl]-2-acetamidopropanoic acid has been found to be genotoxic in mice, which may be due to its ability to form reactive metabolites that bind to DNA. This compound also possesses cytotoxic properties, which may be due to its ability to inhibit protein synthesis.</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-(3-Chlorophenyl)-1H-pyrazole-4-carbaldehyde is a pesticide that acts as a selective insecticide. It is effective against the larval stage of insects, such as the cabbage moth, Plutella xylostella. This compound has been shown to have biological activity against mites and insects with hydrazine hydrochloride and cinnabarinus. 1-(3-Chlorophenyl)-1H-pyrazole-4-carbaldehyde has also been shown to be able to cyclize with hydrazine to form an insecticidal compound.</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>tert-Butyl 5-nitroisoindoline-2-carboxylate is a platelet inhibitor that belongs to the group of antagonists. It has been shown to inhibit human platelets and inhibit the aggregation of fibrinogen. Tert-butyl 5-nitroisoindoline-2-carboxylate has also been shown to have high potency in animal models, but it is not yet known whether it will be effective in humans. The drug has been shown to be a potent antagonist at the platelet P2Y12 receptor, which mediates platelet aggregation and activation, as well as inhibiting ADP-, collagen-, thrombin-, and epinephrine-induced aggregation. Tert-butyl 5-nitroisoindoline-2-carboxylate may also act as a surrogate for agonists or mimetics of the P2Y12 receptor.</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>2-Methyl-4,6-bis(trichloromethyl)-1,3,5-triazine is a triazine with an ionic structure. It is used as a precursor to benzene and acetonitrile. The yields of 2-methyl-4,6-bis(trichloromethyl)-1,3,5-triazine are higher in the presence of benzene compared to acetonitrile. The quantum yield for 2-methyl-4,6-bis(trichloromethyl)-1,3,5-triazine has been found to be 0.2 from the photophysical properties of its emission spectrum. This technique has been used to detect small amounts of singlet oxygen that are generated by photolysis or irradiation with lasers.</p>

<p>2,3-Dihydro-1lambda6,2-benzothiazole-1,1-dione is a plant growth regulator that is used in horticultural applications. It is an anion that can be used as an additive to prevent corrosion and rusting of metals. 2,3-Dihydro-1lambda6,2-benzothiazole-1,1-dione reacts with chloride ions to form the corresponding chromatographic product. This compound also forms reaction products with other compounds such as pyrrole, amide and carbonyl group.</p>

<p>Versatile small molecule scaffold</p>

<p>Glyoxal bis(sodium hydrogen sulfite) adduct hydrate is a reactive compound that has been shown to react with quinoxaline derivatives. The nitrogen atoms in the amide and nitrogen atoms in the quinoxaline derivative are oxidized by oxidation catalyst, such as sodium carbonate, to form an amide-quinone. This reaction leads to the formation of a polyvinyl polymer that can be used for sample preparation. In addition, this compound has been shown to have receptor activity and detergent compositions. Glyoxal bis(sodium hydrogen sulfite) adduct hydrate also has antimicrobial properties and can be used for plant physiology studies and pharmacokinetic properties.</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>