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>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>5-Ethyl-2-hydrazinyl-6-methyl-3,4-dihydropyrimidin-4-one is a hydrazine compound that has been shown to have antiinflammatory and analgesic properties. It binds to the pyrimidine ring of nucleosides and inhibits their incorporation into DNA and RNA. The compound also has a role in the metabolism of aromatic amino acids, such as tyrosine. 5EHTP is an inhibitor of acetylacetone synthase, which converts acetoacetate into acetylacetone. This inhibition prevents the conversion of acetoacetate into other products, such as 4-hydroxybutanal. 5EHTP also inhibits isatin dehydrogenase, which catalyzes the oxidation of isatin to 2,5-diketopiperazine (ketopiperazine).</p>

<p>2-(3,5-Dimethyl-1H-pyrazol-1-yl)-6-methylpyrimidin-4-ol is a tautomeric form of 2-(3,5-dimethylpyrazol-1-yl)-6-[(2R,3S)-3,5-dimethoxyphenyl]pyrimidin-4-ol. It is a potent inhibitor of lipases and has been shown to have antiinflammatory properties. The drug has also been found to decrease the number of inflammatory cells in the bowel and can be used for the treatment of inflammatory bowel disease. The drug may also be effective for treating other autoimmune diseases such as thyroiditis and scleroderma. This drug also has cancer prevention effects because it inhibits cell division and tumor growth by binding to DNA.</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-Bromo-1-methyl-2,5-dihydro-1H-pyrrole-2,5-dione is a fluorescent molecule that can be used as a phosphine. It has been shown to be a useful tool for investigating the nature of phosphines and their reactions with other molecules. This compound has also been used in the kinetic modification of drugs to optimise their therapeutic properties. 3-Bromo-1-methyl-2,5-dihydro-1H-pyrrole-2,5-dione has been conjugated with biotin to create a reactive disulfide bond that can be visualised using fluorescent microscopy. The unmodified form of 3BMPD is used in molecular modelling studies as a model system for reactive disulfide bonds. 3BMPD can also be modified by reacting it with thiols or maleimides to produce reactive disulfides that are useful in conjug</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-(Benzo[d][1,3]dioxol-5-yl)thiourea is a molecule that belongs to the class of heterocycles. The molecular geometry of this compound has been calculated at the density functional theory level using the B3LYP hybrid functional. The hyperpolarizability of 1-(benzo[d][1,3]dioxol-5-yl)thiourea has been calculated by using the polarizability and frequency parameters in conjunction with the frequency spectrum. The optimum values for these parameters have been determined from an analysis of the electronic structure and density theory.</p>

<p>Versatile small molecule scaffold</p>

<p>2,3-Dichloro-6-nitroaniline is a nitro compound that is used as an antibacterial agent. It has been shown to inhibit the growth of Staphylococcus bacteria, with a selectivity for gram-positive organisms. 2,3-Dichloro-6-nitroaniline has also been shown to have catalytic effects on the reaction of nitroarenes with morpholine in the presence of alginic acid. This chemical can be synthesized by reacting sodium nitrite with morpholine and dichloroacetamide in boiling water and then adding zinc chloride. The reaction time varies depending on the concentration of reactants. 2,3-Dichloro-6-nitroaniline has anti HIV activity due to its ability to block electron transfer in viral DNA polymerases.</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-Chloro-4-nitroisoquinoline is an antagonist of the alpha2-adrenergic receptor. It binds to the receptor and blocks the binding of agonists such as clonidine, causing a decrease in lipolysis and vasoconstriction. This agent has been shown to have a low affinity for other receptors, such as dopamine, histamine, serotonin, acetylcholine, and opioid receptors. 1-Chloro-4-nitroisoquinoline has been used to treat hypertension, Raynaud's phenomenon (a disorder that causes reduced blood flow to the fingers or toes), and benign prostatic hypertrophy (enlargement of the prostate).</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>2-(4-Methoxyphenyl)malondialdehyde is a synthetic chemical that is used as a reagent for the synthesis of piperidine derivatives. It can be readily prepared using hydrogen chloride and a hydrocarbon solvent in the presence of an acid catalyst. 2-(4-Methoxyphenyl)malondialdehyde has been used in the synthesis of bone morphogenetic proteins and other molecules, such as dorsomorphin and ldn-193189.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Iodopyridazine is a trifunctional molecule that has been used as a luminophor. It can be synthesized by palladium-catalyzed cross-coupling of 3-bromopyridazine with diethyl ester, yielding the desired product. This product is an organic solvent that contains nitrogen atoms and exhibits enhanced fluorescent properties. The supramolecular chemistry of this compound has been studied extensively, and it has been shown to have nucleophilic functionalities, which make it useful in cross-coupling reactions.</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-Chloro-5,6,7,8-tetrahydroquinoline-3-carbonitrile is an anhydrous organic compound that is used as a starting material for the synthesis of pharmaceuticals. It is prepared by the reaction of anhydrous ethanol with benzoyl chloride and hydrogen chloride in the presence of a catalyst. The product has been shown to be stable at room temperature.</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>Tert-butyl pyridine-3-carboxylate is a synthetic precursor to the anti-HIV drug, 3,4-dihydro-2(1H)-quinolinone. It is an activated molecule that can be used in organic synthesis as an amide or ester activator for the formation of amides and esters from carboxylic acids. Tert-butyl pyridine-3-carboxylate binds to the e3 ubiquitin ligase, which prevents its ability to interact with other proteins such as HIV protease. This drug also has a proton at the methyl nicotinate nitrogen atom, which may contribute to its activity against HIV.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>8-Bromo-4-chloroquinoline is a chemotherapeutic that inhibits the growth of cells in the human fibroblast cell line. It also has cytotoxic properties and can be used to treat breast cancer, colon cancer, and leukemia. Cytotoxicity is seen at concentrations of 8-bromo-4-chloroquinoline that are below the concentration required for DNA synthesis inhibition. The mechanism of action of 8-bromo-4-chloroquinoline is not well understood, but it may involve interaction with cytochrome P450 1A1 (CYP1A1) or other cellular proteins.</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>