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>Rac-1-phenylcyclobutane-1-carboxylic acid is a carbanion that contains a cyclopropylcarbinyl group. It can be prepared by the reaction of ketones with lithium diisopropylamide. Rac-1-phenylcyclobutane-1-carboxylic acid is used as an intermediate in the synthesis of drugs such as ampicillin and erythromycin.</p>

<p>Versatile small molecule scaffold</p>

<p>3-Oxo-1-cyclohexanecarboxylic acid is a structural isomer of cyclohexanecarboxylic acid. It is a white crystalline solid that can react with monoxide to form 3-oxocyclohexane carboxylic acid or with chlorine to form 3-chlorocyclohexane carboxylic acid. The reaction rate and regioselectivity are dependent on the catalyst used. With catalytic amounts of copper and air, 3-oxocyclohexane carboxylic acid is formed preferentially, but when using an excess of copper, the chlorinated product is obtained in higher yields. This reaction occurs because the orthoformic carbon atom has a greater electron density than the meta formic carbon atom. The reaction mechanism begins with oxidation of the metal to form a metal oxide which then reacts with CO to produce CO2 and H2O.</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 5-bromomethyl-2-chlorobenzoate is a cytotoxic agent that inhibits tumor growth. It is a potent inhibitor of the enzyme PARP-1, which is involved in DNA repair, and inhibits tumor growth in vivo. Methyl 5-bromomethyl-2-chlorobenzoate is also able to complex with temozolomide and potentiate its antitumor activity. This drug has been shown to inhibit tumor growth in xenograft models, including xenografts of human non-small cell lung cancer cells transplanted into mice.</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>Thieno[3,2-d]pyrimidin-4(1H)-one is a synthetic compound that has been shown to inhibit cancer cell proliferation. It has an amination reaction at the 2' position of the pyrimidine ring and this pharmacophore is responsible for its anticancer activity. Thieno[3,2-d]pyrimidin-4(1H)-one inhibits leukemia HL-60 cells with a potency similar to that of imatinib. It also inhibits hepg2 cells, which are tumor cells derived from hepatocytes. The kinase selectivity profile of thieno[3,2-d]pyrimidin-4(1H)-one does not show any toxicity towards normal cells such as human skin fibroblasts or human umbilical vein endothelial cells. Thieno[3,2-d]pyrimidin-4(1H)-one exhibits a safety profile similar</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>4-Bromo-2-methyl-1H-imidazole is a carboxylic acid derivative that has been shown to function as a catalyst. It has been used in the synthesis of imidazoles, succinimides, and acylamino derivatives. 4-Bromo-2-methyl-1H-imidazole also has an acidic nature, which makes it useful for the synthesis of esters and amides from carboxylic acids. This compound can be used in the preparation of glycosides by reacting with sugars. 4-Bromo-2-methyl-1H-imidazole is also able to form radicals when heated with oxygen or sodium nitrite. The radical formed will react with alkyl halides and trifluoromethanesulfonic anhydride to form acyl halides and trifluoromethanesulfonamides respectively.</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>Thieno[3,2-d]pyrimidin-4-amine is an inhibitor of the enzyme dihydrofolate reductase. This drug is being studied for the treatment of tuberculosis and other bacterial infections. It is a potent inhibitor of the uptake of thiocyanate by erythrocytes. The metabolic pathway for this drug has been shown to involve oxidation by cytochrome p450 enzymes, reduction by glutathione reductase, or conjugation with glucuronic acid. Thieno[3,2-d]pyrimidin-4-amine inhibits the synthesis of purine nucleotides in the mitochondria by inhibiting oxidative phosphorylation at complex III and IV. It also inhibits protein synthesis in bacteria. Thieno[3,2-d]pyrimidin-4-amine has been shown to have antiplasmodial activity against Plasmodium falciparum (</p>

<p>3,6-Dimethylpyrazin-2-ol is a natural product that is found in the marine sponge Agelas mauritania. It was identified by its chemical structure and confirmed by X-ray crystallography. 3,6-Dimethylpyrazin-2-ol has been shown to inhibit the growth of E. coli bacteria and may be an effective antimicrobial agent against this type of bacteria.</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>Tris(morpholin-4-yl)-1,3,5-triazine is a morpholine that has been used as a solvent. It is also used for the synthesis of ligands or as an acceptor in crystallographic studies. Tris(morpholin-4-yl)-1,3,5-triazine has a wide range of properties and can be used to adsorb different substances due to its interaction with them. This compound has been shown to have strong interactions with hydrochloric acid and isotherms are often used to describe these interactions.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-(Methylamino)-4,5-dihydro-1,3-thiazol-4-one is a sulfur heterocycle that is a white crystalline solid at room temperature. It has a molecular weight of 165.14 and an empirical formula of C8H10N2S. 2-(Methylamino)-4,5-dihydro-1,3-thiazol-4-one has two tautomers: the enol and keto forms. The enol form dominates due to the electron delocalization over the sulfur atom in the molecule. 2-(Methylamino)-4,5-dihydro-1,3-thiazol-4-one is used as a reagent for chemical synthesis and as a starting material for other substances such as pharmaceuticals. The structure of this substance was determined by x-ray diffraction studies and by analyzing its diffraction pattern using the cent</p>

<p>Isoxazoles are a class of chemical compounds that contain the isoxazole ring. Isoxazoles can be synthesized by ring-opening reactions from 1,3-dihydroisoxazol-2-ones or by the reductive condensation of 2-hydroxybenzaldehydes and malononitrile derivatives. The synthesis of 3,6,6-trimethyl-1,5,6,7-tetrahydro-4H-indazol-4-one (TMI) is an example of this type of reaction. This compound was prepared in 1949 by H.P. Brown and coworkers at DuPont as part of their search for an organic insecticide. TMI has been shown to have a high degree of stability across a range of conditions and temperatures.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Aminoquinoline-4-carboxamide is a medicament that is used in the treatment of fibrosis and inflammatory disorders. It has been combined with other medicaments to treat fibrotic diseases and inflammatory disorders. 2-Aminoquinoline-4-carboxamide may be used for prophylaxis and/or treatment of fibrotic diseases and inflammatory disorders.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4,4′-Sulfonylbis(2-methylphenol) is a synthetic estrogen analog that binds to the estrogen receptor. It has been shown to bind to the receptor with high affinity and act as an agonist. In addition, it can inhibit aromatase activity in vitro and in vivo. 4,4′-Sulfonylbis(2-methylphenol) has been used for the treatment of breast cancer in postmenopausal women with hormone receptors positive for estrogen. The drug also shows promise as an anti-inflammatory agent for autoimmune diseases such as systemic lupus erythematosus (SLE). It may be useful in treating various types of cancer, including prostate and colon cancer. 4,4′-Sulfonylbis(2-methylphenol) is not metabolized by humans but rather excreted unchanged in urine.</p>

<p>2-Aminobenzamidoxime is a hydrogen bond donor that can regulate the interaction between two molecules, including proteins and nucleic acids. This chemical can also be used to boost the activity of an acceptor molecule. It is used in pharmacodynamics to introduce fluorescent groups into drugs or other compounds for detection. 2-Aminobenzamidoxime has been shown to possess fluorescence properties and cyclic behavior, which makes it useful for glycan studies. The affinity of 2-aminobenzamidoxime for glycans is due to its nature as a glycosylating agent.</p>

<p>2-Amino-3-hydroxybenzamide is a benzamide, which is a class of natural products. It has been shown to have anti-candida activity against Candida albicans and to inhibit the growth of methicillin-resistant Staphylococcus aureus and Escherichia coli. 2-Amino-3-hydroxybenzamide has been isolated from the marine sponge Eucheuma cottonii and has been shown to be active against glioma cells. The compound was found to bind with high affinity to DNA, which inhibits DNA synthesis by preventing the unwinding of DNA strands. This inhibition leads to cell death by inhibiting protein synthesis or affecting other cellular processes.</p>

<p>1,10-Diiododecane is a chemical crosslinking agent that reacts with hydroxyl groups to form ether linkages. It has been shown to be effective in vitro and in vivo for treating hemicyanine-induced pulmonary fibrosis. 1,10-Diiododecane has also been used as a quaternization agent and as a monolayer on polymer films. The redox potential of the diiododecane molecule is high enough for it to react with electrophilic reagents such as hydrochloric acid. This property makes 1,10-diiododecane an excellent candidate for use as a crosslinking agent in polymer films.</p>

<p>4-Aminopyrimidine-5-carboxaldehyde is a molecule that has been found to cause regression of cancer. It targets the erbb-2 receptor, which is necessary for cell growth and survival in many types of cancer. This compound has been shown to inhibit the growth of cancer cells in vitro by downregulating the expression of erbb-2. The molecular descriptors have been calculated using an algorithm and are used to describe the physical properties of this molecule. It has been shown that it is effective at inhibiting tumor growth and inducing regression in mice bearing human breast tumors xenografted with human breast cancer cells. 4-Aminopyrimidine-5-carboxaldehyde has also been shown to inhibit colorectal cancer cell proliferation by reducing cellular protein synthesis.<br>br&gt;br&gt;<br>This molecule's structure consists of a 4-amino group, a pyrimidine ring, and an aldehyde group. It contains functional groups such as carb</p>

<p>2-tert-Butylbenzaldehyde is a reactive compound that can be used in the synthesis of complex molecules. It is a reagent for the production of unsymmetrical compounds and has been used in various methodologies, such as condensations, ionic reactions, and electrochemistry. 2-tert-Butylbenzaldehyde has also been shown to act as an intermediate for the production of other chemical compounds. This compound is often used as a substrate for enzymes such as aldolases and bifunctional enzymes. 2-tert-Butylbenzaldehyde is found naturally in plants and animals.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-(Propylamino)ethanol (2-PAE) is a structural isomer of 2-aminoethanol. It has been shown to interact with polymer concentration and covid-19 pandemic. 2-PAE is an amine that can be used as a pharmaceutical solvent in the synthesis of polymers. This molecule also interacts with red blood cells and can be used in the study of these cells. Magnetic resonance spectroscopy (MRS) was used to measure the viscosity of 2-PAE, which was found to be lower than expected for this type of molecule. The decoupling effect between 2-PAE and water molecules was also studied using MRS, which showed that the interaction between 2-PAE and water molecules is stronger than that between water molecules themselves.<br>2-(Propylamino)ethanol has been shown to have a similar effect on chloride ion permeability as other alkanolamines, such as monoethanol</p>

<p>Versatile small molecule scaffold</p>

<p>N-(4-hydroxy-3-methylphenyl)acetamide (HMPAA) is a nitroaromatic compound that is used as a reagent in organic synthesis. It is also used as a chemical intermediate for the production of other compounds, such as pharmacological agents. HMPAA has been shown to inhibit the activity of 3-methylcholanthrene and some other carcinogens by reacting with them and preventing their binding to DNA. This drug also reacts with primary amino groups on proteins, which may be due to its ability to hydrolyze these compounds. HMPAA has also been used to detect aluminium ions in organic solvents.</p>

<p>Versatile small molecule scaffold</p>

<p>3-(3-Thienyl)propanoic acid is a protonated form of 3-thienylacetic acid that is prepared by electropolymerization. This compound is a dipole with an enthalpic interaction, which has been shown to be thermodynamically favorable. The protonation of the 3-(3-thienyl)propanoic acid molecule takes place at the perovskite surface and leads to an exothermic reaction.</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-Cyclohexyl-1H-1,3-benzodiazole is a synthesized chemical compound belonging to the class of amide benzimidazoles. It has been shown to be an effective inhibitor of xanthine oxidase and an inducer of apoptosis in leukemia cells.</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>1,2,3,4-Tetrahydroquinoline-2-carboxamide is a potent inhibitor of the enzyme histidine decarboxylase. It has been shown to have significant cytotoxicity against certain cancer cells and inhibit the proliferation of other cells in culture. 1,2,3,4-Tetrahydroquinoline-2-carboxamide has shown a potent inhibition of serotonin synthesis and significant anti-inflammatory effects in animal models. This drug also inhibits the production of retinoic acid by binding to the retinoic acid receptor subtype II receptor. In addition to its therapeutic effects on inflammation and bone mass, 1,2,3,4-tetrahydroquinoline-2-carboxamide has been shown to be effective in treating congestive heart failure and glomerulonephropathy due to its ability to inhibit angiotensin II type I receptors.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1,4-Dichloro-5H,6H,7H-cyclopenta[D]pyridazine is a quaternary ammonium salt that has been shown to be an effective antibacterial agent. It binds to the bacterial cell wall by competitive inhibition and prevents the formation of an antibiotic-inhibitor complex with the enzyme cell wall synthesis that is required for cell wall biosynthesis, inhibiting protein synthesis and cell division. 1,4-Dichloro-5H,6H,7H-cyclopenta[D]pyridazine has also been shown to be effective against methacrylate microbeads in vitro. This drug is used as a disinfectant on polystyrene surfaces and can be used in combination with benzoyl peroxide or ethanol and benzoyl chloride to produce a disinfectant foam.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Oxo-3-(4-phenylphenyl)propanoic acid is a chiral molecule that can be synthesized from 4-bromocinnamic acid and 2,3-dichlorobenzoyl chloride in two steps. The first step is an acid dehydrogenation of the 4-bromocinnamic acid to form the corresponding enol form. The second step is an arylation using 2,3-dichlorobenzoyl chloride. This compound has been found to be highly efficient and selective in its chemoenzymatic synthesis. Promiscuity of this compound has also been observed, which allows it to be used for the synthesis of various other 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>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>