Building Blocks

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Tert-butyl 4-hydroxybenzoate is a tyrosine kinase inhibitor. It inhibits the activity of tyrosine kinases, which play a role in cell proliferation and differentiation. The compound has been evaluated for its ability to inhibit vascular endothelial growth factor receptor 2 (VEGFR-2) and Azd2932, two proteins that are involved in tumor angiogenesis. Tert-butyl 4-hydroxybenzoate also has an affinity for reductive cleavage of esters and reductive arylsulfonates.</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2,6-Diphenylpyrazine (2,6-DPP) is a cross-linked complex that contains 4-methoxyphenylboronic acid. It has been shown to react with anions and form coordination complexes with imidazoline ligands. The coordination chemistry of 2,6-DPP is dependent on the structure of the anion. For example, in acetonitrile or nitrate solutions, 2,6-DPP coordinates to the negative charge through two nitrogen atoms and two carbon atoms. In aqueous solutions containing halides such as chloride or fluoride ions, 2,6-DPP coordinates through three nitrogen atoms and one carbon atom.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>5-Phenyl-1H-pyrazin-2-one is a potent inhibitor of tyrosine kinase, which is an enzyme that regulates the activity of cells by transferring phosphate groups from ATP to tyrosine residues. This drug binds to the ATP binding site, resulting in inhibition of the enzyme's activity and reduced cell proliferation. 5-Phenyl-1H-pyrazin-2-one has been shown to be effective in treating rheumatoid arthritis and other autoimmune diseases, with no adverse effects on bone metabolism or blood pressure. It also has no effect on platelet aggregation or erythrocytes.</p>

<p>2-Chloro-5-phenylpyrazine (2CPP) is an amide nucleophile that reacts with diphenyl to form the corresponding diphenyl amide. 2CPP is a nucleophilic compound that yields the product in high yields. The attack of the nucleophile on the electrophilic carbon atom generates a new carbon-nucleus bond, and another molecule of 2CPP or other nucleophile can attack the same carbon atom to produce a second product. 2CPP reacts with potassium to form a white solid, which is then heated to release hydrogen chloride gas.</p>

<p>Versatile small molecule scaffold</p>

<p>N-Methylpropane-1-sulfonamide (NMS) is an anti-inflammatory drug that has been shown to inhibit the production of cytokines, such as IL-6, IL-12, and TNF. It also inhibits the activation of immune cells by suppressing the production of proinflammatory cytokines, including IL-1β and TNFα. In addition, NMS has been shown to have a protective effect against rheumatoid arthritis by inhibiting inflammation in joints. NMS binds to kinases and blocks their activity by preventing phosphorylation. This prevents the formation of new inflammatory proteins and reduces the severity of rheumatoid arthritis symptoms.</p>

1-(4-Bromophenyl)-3-phenylpropane-1,3-dione is a ternary molecule that contains one electron in its ground state. It has a monochromatic emission spectrum with peaks at 468 nm and 544 nm. The fluorescence emission spectrum peaks at 488 nm and 527 nm. 1-(4-Bromophenyl)-3-phenylpropane-1,3-dione absorbs light in the visible range of the electromagnetic spectrum and emits light in the near infrared range of the electromagnetic spectrum. The ligand is connected to nitrogen atoms on one side of the molecule, while oxygen atoms are on the other side of the molecule. Luminescence occurs when electrons are transferred from an excited state to a lower energy state. The ternary complex is made up of three different parts: an organic compound, an inorganic compound and an electron donor or acceptor. This molecule's electron donor is carbon monoxide

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

1-Chlorocyclohexane-1-carboxylic acid (1CCA) is an aryl halide that is used in the synthesis of polymers. It is used as an oxidation catalyst and as a structural formula for cationic polymerization. 1CCA has been shown to efficiently initiate the polymerization of aromatic hydrocarbons, such as styrene, divinylbenzene, and vinyl toluene. The structure of 1CCA is similar to that of aminoglycosides, which are antibiotics that inhibit bacterial protein synthesis by binding to ribosomes. This similarity suggests that 1CCA may have antibiotic properties and could be useful in treating lymphocytic leukemia. However, more research would be needed to confirm this hypothesis.

<p>1,2-Dimethyl-1H-indol-5-ol is an indole with the chemical formula C8H9NO2. It is a colorless to white crystalline solid that is soluble in water and ethanol. The compound has an acidic nature and a pungent odor. It also has a nitro group and two substituents: methoxy and acetoxy. This compound is used as a precursor for the synthesis of other organic compounds, including pharmaceuticals, agrochemicals, and dyes.</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Morpholine-4-sulfonamide is a chemical compound that belongs to the class of amides. It is used as a tool in pain models and has been shown to be toxic in animal studies. Morpholine-4-sulfonamide has been shown to inhibit cancer cell growth, apoptosis, and bowel disease in mice. This drug also has anti-inflammatory properties. Morpholine-4-sulfonamide may have some therapeutic potential for the treatment of Alzheimer's disease based on its ability to inhibit nitric oxide release and lysine residues.</p>

<p>N-Propylacrylamide is an organic monomer that is used in the production of acrylate polymers. It is a reactive chemical that can be used to modify surfaces and create coatings. N-Propylacrylamide has been shown to react with ammonium persulfate in the presence of an organic solvent to form a polymer. This reaction creates particles that are then used as a phase transition temperature probe for polymerization reactions. N-Propylacrylamide also reacts with metal cations, such as copper, and can be used as fluorescent probes in sequences.</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>N'-Hydroxyfuran-2-carboximidamide is an antibacterial agent that inhibits the growth of bacteria by binding to the 50S ribosomal subunit. It is used to treat eye infections and is also used as an adjuvant in animal vaccines. N'-Hydroxyfuran-2-carboximidamide has been shown to be effective against methicillin-resistant Staphylococcus aureus (MRSA) and Clostridium perfringens, although is not active against acid-fast bacteria such as Mycobacterium tuberculosis or Mycobacterium avium complex.</p>

<p>Versatile small molecule scaffold</p>

Pyridazine-4-carboxaldehyde is a pyridine derivative that has been shown to have antiherpetic properties. It can be synthesized by reacting pyridazine with methyl iodide and anhydrous potassium carbonate. Pyridazine-4-carboxaldehyde is a potent inhibitor of human cytomegalovirus (HCMV) replication in cell culture, and its activity against the virus may be due to its ability to inhibit DNA synthesis and act as a cytotoxic agent. Pyridazine-4-carboxaldehyde has also been studied for its potential use in cancer treatment, with one study showing that it was able to inhibit tumor growth in mice.

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

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>3-Amino-2,4-dichlorobenzoic acid is a metabolite of malonate that inhibits the synthesis of fatty acids by inhibiting the activity of fatty acid synthetase. It has been shown to inhibit lipid accumulation in plants and may be used as an inhibitor in plant physiology experiments. 3-Amino-2,4-dichlorobenzoic acid can be applied to explants before or after treatment with test compounds to determine its inhibitory effect on fatty acid synthetase activity. 3-Amino-2,4-dichlorobenzoic acid is also a potent inhibitor of endogenous lipogenic enzymes.</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

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>2-(3-Aminophenoxy)ethan-1-ol is a nitro compound that has been synthesized from 3-aminophenol and ethyl chloroformate. The synthesis of this compound involves the use of a copper catalyst to form the nitro group. This chemical is an intermediate in the production of other nitro compounds, such as 2,4-dinitrophenol, which are used in explosives and dyes. 2-(3-Aminophenoxy)ethan-1-ol can be used as a stabilizing agent for nanoparticles because it contains amines that can bind to metal ions. It also has optical properties that can be exploited for various purposes, such as catalyzed reactions or optical studies. 2-(3-Aminophenoxy)ethan-1-ol is also useful when analyzing nitroarenes by using techniques such as chemoselective oxidation and hydrolysis.</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

3,5-Dichloro-2,6-dimethylpyridin-4-amine is a phytotoxic compound that belongs to the group of heterocyclic compounds. It has been used in hydroponic cultures as a carboxyl herbicide and for the control of clopidol-resistant weeds. The symptoms induced by 3,5-dichloro-2,6-dimethylpyridin-4-amine are similar to those observed in plants treated with picolinic acid. Ingestion of this substance can lead to symptoms such as vomiting and diarrhea. The chemical is toxic and ingestion can result in death.

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<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>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

This compound is an indole carboxylic acid with a tert-butoxycarbonyl group. It has a functional group of an ester at the C3 position, which is positioned at the 2-position on the indole ring. The molecule is a heterocycle and can be found in nature. This compound is bioactive and has been shown to have an affinity for human inflammatory receptors. It can also act as a surrogate for other molecules that might be too difficult to synthesize or too expensive to produce.

<p>Versatile small molecule scaffold</p>

Methyl 3-amino-4-butanamido-5-methylbenzoate is a chemical compound that has been used as a pharmacological agent. It has an affinity for acidic sites on muscle and blocks angiotensin II, which causes vasodilatation of blood vessels, increases blood flow to the heart, and lowers blood pressure. Methyl 3-amino-4-butanamido-5-methylbenzoate is also a strong blocker of angiotensin receptors in the brain. This drug is usually administered in the form of its hydrochloride salt. The physicochemical properties of this compound are determined by elemental analysis and chromatographic methods. Methyl 3-amino-4-butanamido-5-methylbenzoate can be synthesized from 4-(dimethylamino) butyric acid and methyl 3-(aminomethyl) benzoate through the following reaction:

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>

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>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-Bromo-2-iodopyridine is a chemical compound that can be used in cross-coupling reactions. It has been shown to be an emissive compound, where the emission of light is due to the electron transition from a higher energy level to a lower one. 4-Bromo-2-iodopyridine is also conjugated, meaning that it contains alternating single and double bonds. The reactivity of this compound depends on its architecture, as dimers are more reactive than monomers.</p>

<p>3-Aminobenzamide oxime is a molecular entity that is used in research to modify the phenotype of cells. 3-Aminobenzamide oxime has been shown to have synergistic effects with other drugs, such as tnf-α, which may be due to its ability to alter the nature of certain cellular devices or its ability to act as a ligand for polyvalent metals. 3-Aminobenzamide oxime is also used in the production of nitrite by reacting with HNO2, which may be due to its chemical formula and functionalities.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>