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>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Cyclopropylthiazole is a thiazole derivative that has immunosuppressive properties. It binds to the receptor subtype for glutamate, which is responsible for pain transmission, and inhibits the production of proinflammatory cytokines. Cyclopropylthiazole has been shown to be effective in the treatment of cancer, as well as other diseases such as choroidal neovascularization and metabolic disorders. This drug can be present in two geometric isomers due to its chiral nature: cis- and trans-. The cis-isomer is more potent than the trans-isomer.</p>

Versatile small molecule scaffold

<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>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>

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>

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>2-Ethoxy-3,4-dihydro-2H-1-benzopyran is a reagent that can be used for the preparation of various compounds. It is often used as a source of hydride transfer in enzymatic assays. 2-Ethoxy-3,4-dihydro-2H-1-benzopyran reacts with alkyl halides and acetonitrile to form quaternary ammonium salts and vinyl ethers respectively. The reaction proceeds by hydration, amine addition, or irradiation. This compound can also be used to prepare reactive naphthalenes and amines through an alkylation reaction. The reaction can be carried out at temperatures ranging from -78°C to 100°C.</p>

<p>Dimethyl Acetylsuccinate is a chemical compound that is used as an antiretroviral agent. It has been shown to be effective in the treatment of HIV-infected individuals with significant cytotoxicity and long-term efficacy. Dimethyl Acetylsuccinate is also used for the treatment of bowel diseases, such as ulcerative colitis and Crohn's disease, by reducing inflammation in the gut. This drug was found to be effective at removing reactive oxygen species from wastewater during its use as a coagulant in water treatment plants. Dimethyl Acetylsuccinate is not active against infectious diseases such as tuberculosis or malaria, but it does have some activity against influenza virus.</p>

<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>

<p>Mesulfamoyl chloride is a sulphamic acid derivative that acts as an inhibitor of the enzyme sulphotransferase, which is involved in the conversion of sulphamates to sulphones. It has been used in clinical studies for the treatment of cancer and infectious diseases such as hepatitis. Mesulfamoyl chloride has been shown to be effective against oestrone sulphatase and serine proteases, which are enzymes that can lead to cell proliferation.</p>

<p>Versatile small molecule scaffold</p>

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

<p>2-(1-Chloro-ethyl)-pyridine is a triazole that is used as a chlorination catalyst. It has been shown to be an effective catalyst for the chlorination of ketones and acetylpyridine. 2-(1-Chloro-ethyl)-pyridine also catalyzes the transfer hydrogenation of pyridines, which can be useful in the synthesis of pharmaceuticals. Mechanistically, 2-(1-Chloro-ethyl)-pyridine is mononuclear with two active chlorine atoms and exhibits both nucleophilic and electrophilic properties.</p>

<p>Versatile small molecule scaffold</p>

<p>Octahydro-1H-quinolizin-1-one is a drug that has been shown to be an effective treatment for inflammatory diseases, including inflammatory bowel disease and mucopolysaccharidosis. It binds to the M1 receptors in tissues, which leads to the inhibition of proinflammatory cytokines such as interleukin-1 (IL-1) and tumor necrosis factor (TNF). Octahydro-1H-quinolizin-1-one also has been shown to be an allosteric modulator for the IL-4 receptor. The drug also inhibits etoposide induced apoptosis in cancer cells, suggesting it may have therapeutic potential against cancer.</p>

<p>Menthone is a terpene with a carbonyl group. It has been shown to have in vitro antifungal activity against some strains of bacteria and fungi. Menthone has been found to inhibit the enzyme DPP-IV, which is involved in the production of proinflammatory cytokines, such as IL-8. Menthone can be synthesized by reacting menthol with acetyl chloride. The structure of menthone can be confirmed using nuclear magnetic resonance spectroscopy (NMR). Isomenthone is another name for menthone that refers to one of its stereoisomers, or two molecules that are mirror images of each other. Isomenthone has also been shown to inhibit DPP-IV.</p>

<p>4-[(2,4-Dinitrophenyl)amino]butanoic acid (4DNPA) is an acceptor for elongating ribosomes and is involved in the covalent binding of peptidyl tRNA to aminoacyl tRNA synthetase. 4DNPA has been shown to be reactive with the subunit of bacterial ribosomes and form covalent complexes. It also reacts with peptidyl-tRNA, forming a covalent adduct. This adduct blocks the peptidyl site on the ribosome and prevents protein synthesis.</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>2-Ethenyl-9H-fluorene (2EF) is a monomer that can be polymerized to form poly(2EF). The chemical properties of 2EF are similar to those of vinyl chloride, but the processability of 2EF is better. This monomer can be reacted with acrylates or methacrylates to produce polymers with good mechanical strength and water resistance. The polymerization reaction is catalyzed by an acrylate or methacrylate co-monomer and a cocatalyst such as ammonium peroxydisulfate. 2EF can also be used as a precursor for other compounds such as 9H-fluorenone, peroxides, ozonides, unsaturated alkyls, and chlorinated solvents.</p>

<p>N-(2-Propynyl)succinimide is a conjugate that inhibits the growth of bacteria by binding to the cell wall. It binds to the β-unsaturated ketones found in bacterial cell walls, which are normally involved in the synthesis of carbohydrates. N-(2-Propynyl)succinimide may also bind to nucleophiles such as cysteine residues and reversibly bind to cellular components. This drug has been shown to have antimycobacterial activity against Mycobacterium tuberculosis and Mycobacterium avium complex, but not against Mycobacterium leprae.</p>

2-(4-Pyridyl)indane-1,3-dione is a cytotoxic agent that inhibits the growth of cancer cells. It has been shown to be selective against colon and breast cancers in laboratory testing. 2-(4-Pyridyl)indane-1,3-dione blocks the progression of cancer by inhibiting the synthesis of DNA. This drug also has anti-inflammatory properties that may be due to its ability to inhibit prostaglandin synthesis. The cytotoxicity of 2-(4-pyridyl)indane-1,3-dione was tested on HT29 colon cancer cells and MDA-MB231 breast cancer cells in vitro. The drug showed an IC50 value of 0.21±0.03 μM for HT29 cells and 0.22±0.02 μM for MDA-MB231 cells, which is indicative of its potency as a cytotoxic agent against these cell lines

<p>Dibenzylaminemonoacetate is a hydroxy fatty acid that can be found in adipose tissue. It is an acylation reaction product of a fatty acid and aminoacetaldehyde, which is derived from the hydrolysis of the amino acid L-phenylalanine. Dibenzylaminemonoacetate has been shown to have anti-inflammatory effects in vitro and in vivo by activating PPARγ. When tested in mice, this compound was found to decrease levels of pro-inflammatory cytokines such as IL-1β, IL-6, and TNFα, while increasing levels of anti-inflammatory cytokines such as IL-10 and TGFβ. The mechanism behind these effects is not yet known but may be due to dibenzylaminemonoacetate’s ability to bind to amine groups on proteins or its ability to act as an antagonist for the α2A adrenergic receptor.</p>

<p>Racemic octahydro-1H-isoindol-1-one is a compound that has been shown to have both inhibitory and stimulatory effects on the adrenergic receptors. It blocks the ATP-sensitive K+ channel, which causes an increase in intracellular calcium levels. This leads to the activation of phospholipase A2 and protein kinase C. Racemic octahydro-1H-isoindol-1-one also inhibits 5HT3 receptor antagonists, which are implicated in nausea and vomiting. Racemic octahydro-1H-isoindol-1-one also has been found to be a selective inhibitor of tyrosine kinases. The racemic mixture of octahydro isoindole 1, one isomer being more potent than the other. Racemic octahydro isoindole 1, one is a competitive inhibitor at serotonin transporter (SERT) and norepinephrine transporter (NET).</p>

<p>2-Bromocyclopent-2-en-1-one is a synthetic bidentate ligand with the formula CHClBr. It has been used in organic synthesis as a nucleophilic reagent. 2-Bromocyclopent-2-en-1-one is also an active methylene group, which can undergo substitution reactions to form cationic intermediates. The chloride and hydroxy groups on the molecule are stereoselective, allowing for two different orientation of the substituents on the same carbon atom. This class of compounds encompasses many antimicrobial agents, such as chlorhexidine, hexachlorophene, and trichlorocarbanilide.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Crotonyl chloride is a chemical compound that contains a hydroxyl group (-OH) and an amide (-CONH). It can be used in the synthesis of epidermal growth factor. Crotonyl chloride also has the ability to inhibit the growth of cancer cells by binding to surface receptors on the cell membrane, which leads to apoptosis. It is used as a polymerase chain reaction (PCR) substrate film for sodium carbonate and chloride yields. This chemical can be synthesized using an asymmetric synthesis with nitrogen atoms, amines, and sodium carbonate.</p>

<p>1-Phenylcyclopentan-1-ol is an estrogenic compound that has been shown to be a potent contraceptive. It inhibits the production of estrogens, which are responsible for the development and maintenance of female reproductive tissues. 1-Phenylcyclopentan-1-ol also has anti-cancer activity, as it can inhibit the growth of cancer cells by inhibiting protein synthesis or cell division. This compound has been shown to have no effect on fertility in rats and rabbits. 1-Phenylcyclopentan-1-ol is also an alkoxy radical scavenger and can be used as a treatment for fatty acid peroxidation.</p>

<p>Ethyl 3-oxooctanoate is a chiral, reactive, and stereoselective compound that is produced by the ring-opening of trifluoroacetic acid with octanal. It can be used in the synthesis of epoxides, propiolic acid, and agrichemicals. Ethyl 3-oxooctanoate has also been found to be a pheromone for male grasshoppers. This compound has been shown to react with acetaldehyde and form a carbonyl group, which is necessary for its reactivity. Ethyl 3-oxooctanoate has two different reactive groups: an electrophilic carbonyl group and a nucleophilic carboxylic acid group. These two reactive groups make it multidimensional in terms of reactivity.</p>

2,2-Dimethyl-1-indanone is a carbonyl group with an aromatic hydrocarbon that has been shown to have anti-inflammatory properties. It has been found in the blood of patients with inflammatory bowel disease and also in Alzheimer's disease patients. This active methylene is a pyrimidine compound that has been shown to be useful in the synthesis of polymers used in copolymerization and condensation reactions. The compound can also be used as an intermediate for drugs against bowel diseases or Alzheimer's disease.

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>3-(2-methoxy-phenyl)-propan-1-ol is a phenylpropanoid glycoside that has been shown to have diagnostic potential for the detection of a number of diseases. The reaction rate of 3-(2-methoxy-phenyl)-propan-1-ol can be determined by integrating the intensity of the signal from an electron spectrometer. This compound can also be used as a marker in the diagnosis of diseases such as melanogenesis, where it is found in higher concentrations than normal in the skin and other tissues. It is insoluble in water and emits fluorescence when exposed to ultraviolet light, which makes it useful for diagnostic purposes.</p>

<p>Ethyl 4,4-diethoxy-3-oxobutanoate is a horticultural chemical that is used as a diagnostic agent for the detection of azides in human serum. It has been proposed to be used as an analog for ethyl 3,4,4-trimethoxybutanoate or methyl 3,4,4-trimethoxybutanoate. This chemical is reactive and can be damaging to cells and tissues. Studies have shown that it can also react with DNA bases such as thymine and cytosine to form crosslinks in the nucleic acid chain. Ethyl 4,4-diethoxy-3-oxobutanoate has been shown to be efficient in inducing positron emission from biomolecules like glucose and fatty acids.</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>

Benzyl N,N-dimethylcarbamate is an organic compound that is synthesized from benzyl chloride and dimethylcarbamic chloride. It has two stereoisomers: the S-isomer and the R-isomer. The S-isomer is more stable than the R-isomer and has a higher melting point. Benzyl N,N-dimethylcarbamate can be synthesized in the lab by reacting benzyl chloride with dimethylcarbamic chloride. This compound is also known as a transient molecule that decomposes rapidly when heated or exposed to light. Benzyl N,N-dimethylcarbamate has been shown to act as a modulator of calothrixin, which is a protein that regulates plant growth.

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>2,2-Dimethyl-3,4-dihydro-2H-1,4-benzoxazin-3-one is a potential cancer drug that belongs to the family of bromodomain inhibitors. It inhibits the transcriptional activity of the androgen receptor by binding to its DNA binding domain. This binding prevents the formation of a transcriptionally active complex with other proteins that are required for gene expression. Bromodomain inhibition has been shown to be effective in vivo and in vitro against castration resistant prostate cancer cells. 2,2-Dimethyl-3,4-dihydro-2H-1,4-benzoxazin-3-one also has an oral bioavailability profile that is suitable for oral administration as a therapeutic agent. This drug also binds to the terminal domain of family members, which may lead to increased potency against these enzymes.</p>

<p>Versatile small molecule scaffold</p>

<p>1-(2-Aminophenyl)ethanol is a benzyl amine that is used in the production of nitrosobenzene, which can be used as an oxidant. It has been patented for use in ion-exchange reactions and it interacts with primary alcohols to form catalytic hydrogen peroxide. 1-(2-Aminophenyl)ethanol has an oxidizing effect on organic compounds, which is due to its ability to release hydrogen peroxide when heated. The reaction is more efficient at higher temperatures and pH levels.</p>

<p>Versatile small molecule scaffold</p>

<p>Oxocane-2,8-dione is a cytosolic protein that has been shown to be diagnostic for cancer. It may also be used as a radiation sensitizer and an anticancer agent. Oxocane-2,8-dione is reactive with polycarboxylic acids, fatty acids, inorganic acids, and reactive functional groups. These reactions produce a variety of products including hydroxyl groups and molecules containing carboxyl or alcohol functional groups. Oxocane-2,8-dione has been shown to function as a growth factor for cells in culture.</p>

3-Methyldodecanal is a volatile compound that has an aliphatic odor and can be found in globally sourced food. It is part of the furan family of compounds, which are chemically similar to aliphatic alcohols. 3-Methyldodecanal can be found in many types of food, including fish, but also coffee and dairy products. This compound has been shown to have organoleptic properties.

<p>2-(Naphthalen-2-yl)propanal is an organic compound with the formula C12H10O. It is a colorless liquid that reacts as an electrophile, forming nitriles and cyclic ethers. 2-(Naphthalen-2-yl)propanal can be prepared by reacting naphthalene with nitric acid at room temperature, followed by hydrolysis of the resulting diazonium salt with water. This compound can also be prepared from malonodinitrile and sulfuric acid in ethanol.</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>1-Bromo-2-nitroethane is an organic solvent that has been found to be a useful chiral reagent for the synthesis of a variety of organic compounds. It can be used as a catalyst in asymmetric syntheses, and its high stereoselectivity makes it very useful in the construction of complex molecules. 1-Bromo-2-nitroethane is also used in the oxidation of cycloalkanes and carbonyls, which are oxidized by nitroalkanes to form nitro compounds. The catalytic efficiency of 1-bromo-2-nitroethane provides chemists with an excellent tool for synthesizing nitriles.</p>

<p>Versatile small molecule scaffold</p>

<p>Cyclohexane-1,4-dicarbonitrile is a solute that has been shown to have a dipole. It is an aromatic hydrocarbon with dichroic properties and can be oriented in the gas phase. The molecule is metastable and has an optimum pH of 6 or less. Cyclohexane-1,4-dicarbonitrile can be expressed as hydrogen chloride or chloride gas, depending on the acid catalyst used. The low energy of this compound makes it useful for hydrogenation reactions.</p>

<p>2-Chloro-9H-carbazole (2CzC) is a heterocyclic compound that belongs to the group of carbazoles. It can be used as medicine and has been shown to be a good control experiment for other carbazoles. The nucleophilicity of 2CzC is affected by the functional groups present in the molecule, and it has been shown to react with anions such as Cl-, Br-, or I-. This heterocycle also has two resonance forms, which are generated by the electron delocalization in the ring system. The gas phase kinetics of 2CzC have been found to follow an Arrhenius relationship, with k = 3.6x10^3 M^-1 s^-1 at 298 K. Yields for this compound have been found to be high, with 90% yield when synthesized from chloroacetone and phenylmagnesium bromide.</p>

<p>4-Hydroxy-3,5-bis(isopropyl)benzaldehyde is a synthetic chemical that is insoluble in water. It has been used as a starting material for the synthesis of other compounds and it can be synthesized from chloroform, acetone and ethanolamine. This compound has been shown to inhibit tyrosine kinase activity and may be useful in the treatment of diseases associated with this enzyme, such as cancer. 4-Hydroxy-3,5-bis(isopropyl)benzaldehyde has also been used as an intermediate for the synthesis of morpholino oligomers.</p>

<p>LY 345899 is a methyltransferase inhibitor that blocks the synthesis of fatty acid in cells. LY 345899 is used as an experimental drug for cancer treatment and other diseases. The mechanism of action of LY 345899 is not well understood, but it may involve regulating transcriptional regulation and protein synthesis in the mitochondria. Clinical trials have shown that LY 345899 has a clinical relevance in the treatment of cancer and autoimmune diseases.</p>