Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1-Methyl-2-(trichloroacetyl)imidazole is a small molecule that is synthesized for the treatment of cancer. It interacts with dna and inhibits its function by binding to the minor groove in DNA, which causes conformational changes. 1-Methyl-2-(trichloroacetyl)imidazole has been shown to be effective against cancer cells that are resistant to other anticancer compounds. The molecular target for this compound is not fully understood, but it may work by inhibiting DNA synthesis or by inducing apoptosis. 1-Methyl-2-(trichloroacetyl)imidazole has shown some activity against leukemia and colon cancer cell lines in vitro and in vivo.</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-2-oxocyclohexanecarboxylate is a diterpene alkaloid that has been prepared by the Friedel-Crafts reaction of ethyl bromoacetate and cyclohexane. The product is an intramolecular arylation, which means that the two carbons in the ring are bonded to each other. This type of reaction usually produces a group specific functional group, such as an acid chloride or ester, but in this case it produces an alcohol. 3-Bromo-2-oxocyclohexanecarboxylate is used as a precursor for silver salts which are used to make photographic film.</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>1,3-Dichloropentane is a molecule that consists of chlorine and hydrogen atoms. It has been studied extensively in kinetic isotope effect experiments for its transport properties. The kinetic isotope effect is the change in reaction rate due to the presence of an atom with an atomic mass different from the reactant or product. 1,3-Dichloropentane has also been studied for its role in cell membrane transport. This molecule is not reactive, but it does have a reactive isotope effect on cells when it reacts with chlorine atoms.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>7-Hydroxy-4-oxo-4H-chromene-2-carboxylic acid is a molecule that is found in the human body. It has been shown to have cationic polymer activity and to inhibit the growth of bacteria by binding to the hydroxyl group of DNA. 7-Hydroxy-4-oxo-4H-chromene-2-carboxylic acid has potent inhibitory activity against Gram positive and Gram negative bacteria, including Mycobacterium tuberculosis and Staphylococcus aureus. This compound can be used as an antibiotic for bacterial infections due to its ability to bind with high concentrations of the hydroxyl group on 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>2-(Prop-2-en-1-yl)cyclopentan-1-one (propargyl alcohol) is a heterocyclic compound that is the simplest member of the cyclopentanones. It has been shown to be an effective inhibitor of human viruses such as Hepatitis C virus, HIV, and influenza A virus. The antiviral activity of propargyl alcohol is attributed to its ability to inhibit viral DNA polymerase and RNA polymerase in the infected cells. Propargyl alcohol also inhibits glycol dimethyl ether, which is a cofactor for some cellular enzymes involved in lipid metabolism. This compound can also act as a substrate for allylation reactions with other compounds such as 1,3 butadiene or ethylene.</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>3,6-Dihydro-2H-thiopyran-5-carbaldehyde is an aldehyde that is used as an intermediate in the synthesis of crotonaldehyde. It reacts with hydrogen sulfide in the presence of an acidic catalyst to produce acrolein and water. The reaction product can be boiled off to generate a crude form of crotonaldehyde. 3,6-Dihydro-2H-thiopyran-5-carbaldehyde has been patented by BASF SE under patent number EP0992871.</p>

<p>1-(2-Oxopropyl)pyrrolidine-2,5-dione is a reactive molecule that can be used to conjugate biomolecules and synthetic polymers. It has been immobilized on the surface of polymer particles or in polymer matrices, which allows for the efficient separation of biomolecules and synthetic polymers. This molecule is also reactive with thiol groups and can be used to crosslink biomolecules and synthetic polymers. 1-(2-Oxopropyl)pyrrolidine-2,5-dione has been shown to react with immobilized proteins and 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>3-Phenyl-2-propyn-1-amine hydrochloride is a dopamine β-hydroxylase inhibitor that can be detected in urine. It is used to study the effects of various drugs and chemicals on the metabolism of dopamine, noradrenaline, and other catecholamines. 3PPPA has been shown to inhibit the activity of cytochrome P450 enzymes and blocks adrenergic receptors. This drug also inhibits the synthesis of epinephrine from norepinephrine by blocking its conversion to epinephrine. 3PPPA may also be used as a receptor blocker for diagnosis or treatment of asthma or allergic reactions by preventing the release of histamine, which is released from mast cells in response to an allergen, causing inflammation.</p>

<p>1-Bromo-2-fluoro-3-nitrobenzene is a synthetic chemical that is used as an intermediate in the synthesis of various dyes. It can be obtained by the diazotization of acetyl nitrite and acetonitrile, followed by acetylation with acetic anhydride and hydrolysis with sodium hydroxide. The bromoaniline formed after this reaction is then converted to 1-bromo-2-fluoro-3-nitrobenzene by refluxing it with nitric acid. This chemical can also be synthesized from bromines and chloride in the presence of a diazo salt. It reacts with fluoride or halogens to produce fluorobenzene derivatives, which are used as intermediates for other organic compounds.</p>

<p>Please enquire for more information about Boc-4-(4-fluorophenyl)-piperidine-4-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Bromo-1,3,5-triisopropylbenzene is an ethylene acetal that is prepared by the catalyzed reaction of aryl chlorides and anhydrous zinc bromide in the presence of triethylamine. The selectivities of this method are high because it can produce mainly a single isomer. The stereoselectivity is also high because the reaction proceeds with the formation of only one stereoisomer. The mechanism for this reaction involves a nucleophilic substitution of the halogenated aryl chloride with the trialkylborane, which generates two different products. This product has been used in the synthesis of biphenyls and nitro compounds.</p>

<p>8-Bromoisoquinoline is a bifunctional alkylating agent that is used to synthesize esters and amides. It is commonly used for the synthesis of amino acids, peptides, and other biologically active molecules. 8-Bromoisoquinoline has been shown to have a synergistic effect with hydroxyalkyl carbamates, which may be due to its ability to form an ionic bond with the carboxylic acid in these compounds. This chemical can also react with nitro groups and serve as a chlorinating agent, as well as react with anions such as phosphate and acetate. 8-Bromoisoquinoline can be synthesized by reacting ethyl bromoacetate with tetrahydroisoquinolinium chloride in hydrochloric acid or isopropyl alcohol.</p>

<p>N-Boc-ethanolamine is a naturally occurring antimicrobial peptide that has been shown to have an inhibitory effect on the growth of cancer cells in vitro. It also inhibits glucose production in the body and has been used in the treatment of diabetes mellitus. N-Boc-ethanolamine is synthesized by solid-phase synthesis with ferrocenecarboxylic acid, followed by reaction with aldehyde groups and subsequent hydrogenation. This compound has potent inhibition against cancer cells and can be used as a chemotherapeutic agent for cancer treatment. The hydrogen bond between this compound and β-unsaturated ketones leads to its photochemical properties. Cellular uptake of N-Boc-ethanolamine was observed when it was conjugated to polymers such as polyethylene glycol (PEG).</p>

<p>N-Boc-3-hydroxypyrrolidine is a synthetic, orally available, broad spectrum antibiotic that inhibits bacterial DNA gyrase and topoisomerase IV. It has been shown to be effective against methicillin-resistant Staphylococcus aureus (MRSA) and resistant strains of other bacteria such as Pseudomonas aeruginosa. N-Boc-3-hydroxypyrrolidine is an amide that binds to the active site of PI3Kδ and inhibits its activity. This inhibition prevents the phosphorylation of Akt, leading to decreased production of inflammatory cytokines and chemokines. N-Boc-3-hydroxypyrrolidine also has immunosuppressive effects on T cells in vitro.</p>

<p>Please enquire for more information about 5-Bromo-1-methyl-1H-1,2,3-triazole including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 5-Bromo-oxazole-2-carboxylic acid methyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Bromobenzene-d5 is a chemical compound that can be used as a chemical reagent for the production of other chemicals. It has a molecular weight of 188.21 and a melting point of -100°C. Bromobenzene-d5 has shown to be reactive with chloride and tert-butyl isocyanate, which are both strong bases. The molecule has an amorphous nature and exhibits vibrational properties at high frequencies. Bromobenzene-d5 also shows polarizability in the intramolecular hydrogen bond region, which is evident by an NMR spectrum of heterocycle bromobenzene-d5.</p>