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-Phenyl-3H-imidazo[4,5-b]pyridine is a ligand that binds with high affinity to the GABA receptor. It has an aromatic ring and two phenyl groups. 3-Phenyl-3H-imidazo[4,5-b]pyridine is a member of the class of pyridine derivatives. This compound has been shown to have nervous system effects in animals and humans, including sedative and hypnotic effects.</p>

Merocyanine is a polymethine dye that has been shown to have antimicrobial activity. It binds to DNA by intercalating between the base pairs, and it has been reported to inhibit the growth of Gram-positive bacteria. Merocyanine may be used for the treatment of Gram-positive bacterial infections such as staphylococcus aureus, streptococcus pyogenes, and enterobacteriaceae. This molecule also exhibits quaternary salt properties and can be used as an antiseptic.

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-Butoxy-4-oxobutanoic acid (BABA) is an anti-inflammatory agent that belongs to the class of prodrugs. It is a monomer that is polymerized in vivo to form polycarboxylic acids which are then metabolized by hydrogenase. BABA has been shown to be useful for treating inflammatory bowel disease, as well as other autoimmune diseases. The chemical stability of BABA has also been demonstrated in microcapsules and it can be used for the treatment of bowel disease, such as ulcerative colitis and Crohn's disease.</p>

Versatile small molecule scaffold

<p>1-Iodo-3-methoxypropane is a ligand that belongs to the polyhedron class. The crystal structure of this compound has been determined by x-ray and thermal analysis. It is stable at room temperature, but decomposes at higher temperatures. 1-Iodo-3-methoxypropane can be used as a ligand in coordination chemistry, or as an intermediate in organic synthesis. It has been shown to form stable complexes with metal ions such as copper(II) and silver(I). The 1-iodo-3-methoxypropane molecule contains two oxygen atoms that are bonded to each other through a triple bond. These atoms are part of the ligand’s backbone and allow it to coordinate well with metal ions.</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>N'-Hydroxy-5,7-dimethylpyrazolo[1,5-a]pyrimidine-3-carboximidamide is a potent and selective inhibitor of the ion channel TRPM8. It has been shown to inhibit TRPM8 by binding to the extracellular domain of the receptor. This inhibition leads to an increase in intracellular calcium levels and activation of downstream signaling pathways that are responsible for pain perception. N'-Hydroxy-5,7-dimethylpyrazolo[1,5-a]pyrimidine-3-carboximidamide is a potent and selective inhibitor of the ion channel TRPM8. It has been shown to inhibit TRPM8 by binding to the extracellular domain of the receptor. This inhibition leads to an increase in intracellular calcium levels and activation of downstream signaling pathways that are responsible for pain perception.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>7,8-Dichloro-1,2,3,4-tetrahydroisoquinoline (7,8-DCT) is a natural compound that can be found in the leaves of the plant "Erythroxylum coca". It has been studied for its potential use as an anticancer drug. 7,8-DCT inhibits the growth of prostate cancer cells and has shown inhibitory properties on α2-adrenergic receptors. This compound also inhibits bacterial growth by disrupting fatty acid biosynthesis and reducing its uptake by mitochondria. 7,8-DCT has also been shown to have antimicrobial resistance. 7,8-DCT is a structural analog of cocaine and acts as a competitive inhibitor to inhibit the enzyme fatty acid amide hydrolase (FAAH). The inhibition of FAAH leads to increased levels of anandamide which is known to modulate pain perception.<br>!-- <br>--&gt;</p>

<p>Versatile small molecule scaffold</p>

<p>2-Chloro-3-methylbenzaldehyde is a reagent that is used in organic synthesis. It is an isomeric form of 2-chlorobenzaldehyde. 2-Chloro-3-methylbenzaldehyde can be prepared by the reaction of benzaldehyde with magnesium, which produces chloral and methyl alcohol. The chloride ion then reacts with the methyl alcohol to produce 2-chloro-3-methylbenzaldehyde. It has been shown that it can be used as a grignard reagent to make substituted ketones or esters. This compound also exhibits dihedral symmetry and has two planar forms, one of which is more stable than the other in solution.</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-Bromo-N-phenylaniline is a carbonylative synthetic that yields acridone and triarylamines. The abundances of electron ionization reactions for this compound are in the range of 1.5 to 3.0%. Dehalogenation reactions have been observed with arylation and amination reactions, but not with carbolines or diarylamines. 2-Bromo-N-phenylaniline has been shown to act as a ligand for metal ions and catalyze amination reactions involving diarylamines.</p>

<p>2-(Aminomethyl)phenol hydrochloride is a transition metal-containing compound that has an oxidation potential of 1.5 volts. It is used as a catalyst in the oxidation of organic compounds and as a molybdenum cofactor in the enzyme sulfite oxidase, which catalyzes the conversion of sulfite to sulfate. This substance also functions as a colorant and an oxidant in dyeing and printing processes. 2-Aminophenol hydrochloride has been used for the treatment of respiratory diseases, such as asthma, bronchitis and emphysema, due to its ability to inhibit inflammation.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

3-(2-Amino-thiazol-4-yl)-chromen-2-one is a synthetic compound that exhibits cytotoxic activity in vitro. It has been shown to have antibacterial, antiviral, and antifungal activities. 3-(2-Amino-thiazol-4-yl)-chromen-2-one inhibits the growth of bacteria by binding to DNA. The mechanism of action of this compound is similar to cisplatin, a widely used anticancer drug. 3-(2-Amino-thiazol-4-yl)-chromen-2-one binds to the minor groove of DNA, forming an interstrand crosslink between two adjacent base pairs that prevents DNA replication and transcription. This compound also has potential as a cancer therapeutic due to its ability to inhibit the growth of tumour cells without affecting noncancerous cells.

<p>N-Benzylmorpholin-3-one is a chiral, exocyclic amine oxidation agent that is used in organic synthesis. The compound has been shown to be effective in the chemoselective oxidation of imines and lactams, which are important reaction intermediates. It has been shown to be effective in controlling the regioselectivity of the reaction, with a high degree of chemoselectivity. N-Benzylmorpholin-3-one is also capable of oxidising cations such as quaternary ammonium salts and tertiary amines.</p>

<p>Versatile small molecule scaffold</p>

<p>1-Ethynyl-4-methoxynaphthalene is a synthetic estrogen that can be used as an analogue of estrone. It is also a formylation product of anisole, which is synthesized from formaldehyde and phenol. This compound has been shown to act as an agonist for the estrogen receptor, in addition to having the ability to induce bromination. The Corey-Fuchs reaction yields 1-ethynyl-4-methoxynaphthalene by reacting 4-methoxybenzaldehyde with ethyne.</p>

<p>1-tert-Butyl-1H-imidazole-2-thiol is a halogenated aromatic compound that is used as a solvent, a ligand in organometallic chemistry, and as an intermediate in the synthesis of other organic compounds. This chemical has been shown to undergo halide exchange reactions with metal ions such as magnesium chloride, aluminum chloride, and zinc chloride. It also has been shown to react with carboxylates to form 1-tert-butyl-1H-imidazole-2-carboxylate. The bond cleavage of the thiol group can be induced by reaction with iodosobenzene diacetate or hydrochloric acid. 1-tert-Butyl-1H-imidazole-2-thiol is soluble in ethers and benzene. The molecule has two thiol groups that can undergo disulfide bond formation, which may be catalyzed by copper(</p>

<p>2-Hydrazinoquinoxaline is a potent cytotoxic agent that inhibits methionine aminopeptidase, an enzyme that regulates the synthesis of proteins. 2-Hydrazinoquinoxaline has been shown to be active against cancer cells in culture and to produce cytostatic effects in vivo. The IC50 value for 2-hydrazinoquinoxaline was found to be less than 1 μM with an ED50 of approximately 10 μM, which indicates that this drug is more potent than some other quinoxalines. 2-Hydrazinoquinoxaline is not active against bacteria, but it has been shown to inhibit the growth of P. aeruginosa in vitro.</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-(Benzyloxy)-3,5-dibromobenzaldehyde (2BDBA) is a carbonyl group with synthons. It is also known as a potential drug candidate for the treatment of cancer and other diseases. The interaction between 2BDBA and the carbonyl group has been investigated with advances in nature, analyses, energies, crystallographic, supramolecular and isomorphous studies. The fingerprint of the compound was found to be different from those of the other similar compounds. The interactions between 2BDBA and other molecules have been studied with advanced analytical techniques such as FTIR spectroscopy, which has given an insight into how these interactions take place.</p>

3,5-Dibromo-2-methoxybenzaldehyde (3,5-DMB) is a x-ray crystal structure of a molecule. It is an organic compound that has the chemical formula of C10H8O4Br. 3,5-DMB is an intermediate in the synthesis of 6-methoxy-2-naphthol and has been crystallized from ethanolic solutions. 3,5-DMB can be efficiently synthesized by reacting malononitrile with piperidine in microwave irradiation. A reaction mechanism for this synthesis was proposed which involves the formation of a nitrile oxide intermediate followed by a one electron oxidation to form 3,5-DMB. This method can be used to generate high yields of 3,5-DMB in minutes and hours with good purity.

<p>Versatile small molecule scaffold</p>

<p>3-Hydroxy-N,N,3-trimethylbutanamide is a liquid at room temperature. It is an additive that can be used in the production of nitrocellulose and as a preservative for nitrate film. 3-Hydroxy-N,N,3-trimethylbutanamide decomposes on exposure to UV light to form nitric oxide. It is also used as a photoinitiator in the synthesis of polymers by free radical polymerization reactions. The liquid composition can be thermally treated to produce stable silver nanoparticles.</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>