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>3-hydroxy-4,4-dimethylpyrrolidin-2-one is a dienophile that reacts with cyclopentadiene to produce a cycloadduct. It is an efficient catalyst for the production of polymers and acrylates from dienophiles. This compound can be used in a solid phase synthesis. 3-hydroxy-4,4-dimethylpyrrolidin-2-one has been shown to react with benzoic acid to produce n-substituted isoprenes. These interactions are important for nature as they are part of the biosynthesis of natural products such as hormones and vitamins.</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>1-(2-Oxopropyl)-2,3-dihydro-1H-indole-2,3-dione is a neutral compound that belongs to the class of ketones. It has been found to be decarboxylated in alkaline conditions and is oxidized by halomethyl radicals. The compound is also recyclized from isatin and reacts with phenols. 1-(2-Oxopropyl)-2,3-dihydro-1H-indole-2,3-dione has been found to form heterocyclic compounds when mixed with benzaldehyde and nitromethane.</p>

<p>2-Nitrobenzene-1-carbothioamide is a hydroxylamine derivative that inhibits the activity of degraders, such as nitrosoperoxycarbonic acid, which breaks down clots. It also has an inhibitory effect on the activity of clotting enzymes and sirtuin. The compound has been shown to be useful in diagnosis of cancer and other diseases. 2-Nitrobenzene-1-carbothioamide is used in conjunction with a radioactive isotope for diagnosis. It can be conjugated to diagnostic agents for use in imaging studies or it can be used as a reagent for the identification of proteins or nucleic acids. 2-Nitrobenzene-1-carbothioamide is also used as an organic solvent in diagnostic chemistry, due to its relatively low toxicity and high stability in organic solvents.</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-furoate is a polycyclic compound that has been shown to have activity against deacetylases. It is believed to work by binding to the catalytic site of the enzyme, thereby inhibiting acetylation reactions. This results in increased levels of histone acetylation and an improvement in cognition. Methyl 5-(bromomethyl)-2-furoate also has been shown to inhibit phosphodiesterases, which are enzymes that break down cyclic nucleotides in cells.END&gt;</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,5R)-2,5-Dimethylpyrrolidine HCl ee is a chiral molecule that is the active form of 2,5-dimethypyrrolidine hydrochloride. It is a colorless solid with a melting point of 87 °C. The substance has the chemical formula C4H9NHCl and molecular weight of 206.75 g/mol. It can be classified as an asymmetric compound because it does not have an equal number of atoms on each side of its plane of symmetry. (2R,5R)-2,5-Dimethylpyrrolidine HCl ee has been shown to have antihypertensive properties in rats and rabbits. It also has been used for the treatment of essential tremor and Parkinson's disease. This drug is characterized by being flammable and soluble in ethanol and diethyl ether but insoluble in water. Recrystallized (2R,5R)-</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Furan-3-carbohydrazide is a gaseous molecule with an electron configuration of 5s2p3d1. This molecule has a molecular weight of 102.06 and refractivity of 1.5. Furan-3-carbohydrazide has two optical isomers, one with a dipole moment of 1.9 debye and the other with a dipole moment of 3.2 debye, as well as two different electronic structures: five-membered and six-membered. The five-membered electronic structure is more stable than the six-membered electronic structure because it has lower energy levels for the electrons in the orbitals. Furan-3-carbohydrazide is an exothermic molecule that can be synthesized by reacting pyrrole and thiourea in the presence of hydrazine hydrate.</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>6,8-dimethyl-3H,4H-imidazo[1,5-a][1,3,5]triazin-4-one is a cytotoxic compound that binds to chloride anions in the cell membrane and causes disruption of the ionic equilibrium. It also binds to human cells by coordinating with the anionic sites on the cell surface. This drug has been shown to inhibit growth and induce apoptosis in bladder cancer cells. 6,8-Dimethyl-3H,4H-imidazo[1,5-a][1,3,5]triazin-4-one also inhibits tumor growth in mice transplanted with human bladder cancer cells. The drug works by binding to DNA bases and causing crosslinking of DNA chains. This leads to inhibition of RNA synthesis and 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>2-[(Pyridin-3-ylmethyl)-amino]-ethanol is the methanol analogue of the coordination compound 2-[(pyridin-2-ylmethyl)-amino]-ethanol. The molecule has a chain structure, with two coordination bonds and a total of six atoms. It is a dimeric molecule that can be polymerized to form polymers. The structure is metallic with antiferromagnetic coupling between the two metal centers, which can be assembled into larger structures. This compound interacts with other molecules at the coordinated sites where it binds. Magnetism results from the unpaired electron spins on each metal center and from spin-spin interactions between these centers.</p>

<p>9-Ethyl-9H-carbazole-3,6-dicarbaldehyde (9ECDA) is a fluorescent molecule that has been shown to have anticholinesterase activity. This compound is being developed for the treatment of cervical cancer and other cancers. 9ECDA is synthesized by reacting 2,4,5,6-tetrafluorobenzaldehyde with excess ethyl acetoacetate in the presence of sodium methoxide. 9ECDA can be used as a fluorescent probe for the detection of anions in water. This compound also has optical properties that are dependent on its anion conjugation state. The fluorescence of 9ECDA is quenched when it binds to butyrylcholinesterase and other anionic binding sites.</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-Bromothiophen-2-yl)methanol is a reactive, hydrocarbon group that can be used in the synthesis of natural products. It is a synthetic product, and it has been shown to react with sulfur to form a molecule. (3-Bromothiophen-2-yl)methanol is an innovative, natural product that can be used in the synthesis of polymers. This product also reacts with ammonia to form a tetracyclic compound. The optical properties of (3-bromothiophen-2-yl)methanol are recording and hydrocarbon.</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>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 3-iodo-4-methylthiophene-2-carboxylate is an organic compound that is structurally related to the thiophene carboxylates. It has potent antagonist properties and selective actions in bioisosterism, as well as high yields of up to 94%. The compound also has a chemotype that is important when considering the synthesis of an organic molecule. Methyl 3-iodo-4-methylthiophene-2-carboxylate is used in organic chemistry as a reagent for the synthesis of functional groups and intramolecular reactions. This compound can be synthesized regioselectively by using anions, such as fluoride, to form the desired product.<br>Methyl 3-iodo-4-methylthiophene-2 carboxylate has shown antifungal activity against Candida albicans and antibacterial activity against Staphylococcus aureus. This natural product</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>