Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>alpha-Cyano-3-hydroxycinnamic acid is a mitochondrial matrix analog that has been shown to inhibit the uptake of carnitine, glutamate, and branched-chain amino acids. This compound also inhibits the activity of glyceraldehyde-3-phosphate dehydrogenase and dodecyl CoA dehydrogenase, which are enzymes involved in the production of cellular energy. alpha-Cyano-3-hydroxycinnamic acid also inhibits the synthesis of mitochondrial DNA and RNA. The compound binds to the enzyme succinate dehydrogenase, inhibiting its function. This inhibition leads to a decrease in cellular energy production and an increase in oxidative stress.</p>

<p>Versatile small molecule scaffold</p>

<p>Inhibitor of SIRT1 deacetylase</p>

<p>Versatile small molecule scaffold</p>

<p>4-Chloro-1H-imidazo[4,5-c]pyridine (4CI) is a nucleoside analog that inhibits the replication of RNA and DNA. It has significant inhibitory activity against herpes simplex virus type 1 and human immunodeficiency virus type 1 (HIV-1). 4CI inhibits the synthesis of adenosine, an important component in the synthesis of RNA and DNA. This drug also has antiviral properties against influenza A and B viruses. 4CI's effect on plasma cholesterol levels is thought to be due to inhibition of 3-hydroxy-3-methylglutaryl coenzyme A reductase.</p>

<p>Versatile small molecule scaffold</p>

<p>2-Cyanobenzaldehyde is an aldehyde that reacts with nucleophiles such as trifluoromethanesulfonic acid to form a molecule. 2-Cyanobenzaldehyde has potent inhibitory activity against the kinase glycogen synthase kinase 3 (GSK3) and can be used to treat autoimmune diseases. It also reacts with hydrochloric acid in solution to form an intermediate, which is then reacted with glycine and ATP to produce a chiral compound. The product of this reaction has been shown to be active methylene, which was synthesized by asymmetric synthesis.</p>

<p>4-Chlorophenylacetylene is a compound that is created by the reaction of chloroform and acetylene. The reaction yield can be increased by using a catalytic amount of silicon, which increases the rate of hydration. Terminal alkynes react with 4-chlorophenylacetylene to form polymers, which are insoluble in most solvents. 4-Chlorophenylacetylene has been shown to have inhibitory activity against the growth of bacteria and fungi when tested in model species such as Escherichia coli and Saccharomyces cerevisiae.</p>

<p>1-[(4-Chlorophenyl)phenylmethyl]piperazine is an analytical reagent that is used in the determination of meclozine, a drug used for the treatment of nausea and vomiting. 1-[(4-Chlorophenyl)phenylmethyl]piperazine is a nucleophile, which means that it can donate electrons to other molecules. It can be used as a catalyst to increase the rate of chemical reactions. 1-[(4-Chlorophenyl)phenylmethyl]piperazine may also be used in wastewater treatment because it has been shown to have phospholipidosis inhibiting properties. The levorotatory form (1R-enantiomer) of this compound has been shown to inhibit protein synthesis in vitro and is an amine oxidase inhibitor that binds to proteins with nitrogen atoms. This nucleophilic compound may also be converted into an n-oxide or dinucleotide phosphate by hydrochloric acid and</p>

<p>Versatile small molecule scaffold</p>

<p>Creatine phosphate di(tris) salt is a cyclase and rectifier of potassium ion channels. It is a potent activator of calcium ion channels, expressed in the cells of the ng108-15 mouse neuroblastoma line. Creatine phosphate di(tris) salt also potently activates guanylate cyclase and l-type calcium ion channels. This drug has been shown to stimulate prostaglandin synthesis and inhibit the production of prostaglandin E1 in biological chemistry studies. Creatine phosphate di(tris) salt is a cyclase and rectifier of potassium ion channels. It is a potent activator of calcium ion channels, expressed in the cells of the ng108-15 mouse neuroblastoma line. Creatine phosphate di(tris) salt also potently activates guanylate cyclase and l-type calcium ion channels. This drug has been shown to stimulate prostaglandin synthesis and inhibit the production of prostaglandin E1 in</p>

<p>Please enquire for more information about 2-Chloro-4-fluoropyridine-5-boronic acid, pinacol ester including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Versatile small molecule scaffold</p>

<p>Chlorinating agents are used in the production of pharmaceutical preparations and other chemical products. They react with amines to form diazonium salts, which can then be reduced to azo compounds. N-Chlorosuccinimide is a chlorinating agent that reacts with amines to form diazonium salts. It is used primarily as an injection solution for the treatment of trichomoniasis and other sexually transmitted diseases, but it also has been used in the preparation of pharmaceutical preparations. The reaction mechanism for N-chlorosuccinimide is not well understood, but it may involve a free radical intermediate or electron transfer from the chlorine atom to the carbon atom. Diazonium salts are formed by the reaction between an amine and an acid chloride. The addition of sodium hydroxide produces the corresponding azo compound. The reaction mechanism for N-chlorosuccinimide is not well understood, but it may involve a free radical intermediate or</p>

<p>Versatile small molecule scaffold</p>

<p>Please enquire for more information about 5-Chloropyridine-2-boronicacid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Cinnoline is a chemical compound that is structurally similar to phenol, containing a hydroxyl group, two nitrogen atoms and a cyclic structure. Cinnoline has been shown to have anti-inflammatory activity in rats with adjuvant-induced arthritis. The mechanism of the anti-inflammatory effect of cinnoline is not fully understood, but it may be due to its stability and ability to bind to biological molecules or its conformational properties. Cinnoline does not react with nitric acid, making it a good candidate for use in infectious diseases such as tuberculosis. It has also been shown to be stable in human serum and has low pharmacokinetic properties. The fluorescence intensity of cinnoline was found to increase when exposed to an electrochemical potential and can be used as a probe molecule for pharmacokinetics studies.</p>

<p>3-(Chlorosulfonyl)benzoic acid is a synthetic compound that inhibits histone lysine methylation. It has been shown to protect against neuronal injury and cognitive impairment. 3-(Chlorosulfonyl)benzoic acid also has an inhibitory effect on the activation of Sirt2, which is an enzyme involved in cellular processes such as cancer, diabetes, inflammation, and aging. 3-(Chlorosulfonyl)benzoic acid has low potency and is not very soluble in water. It can be used to treat metabolic disorders by increasing the amount of insulin released from the pancreas and lowering blood glucose levels.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Bis[2-(perfluorohexyl)ethyl] Phosphate is a perfluorinated, fluorinated chemical that is used in wastewater treatment. It is also found in human serum and organisms, as well as in the drinking water of some communities. Bis[2-(perfluorohexyl)ethyl] Phosphate has been detected in the maternal serum and urine of women who are pregnant or breast-feeding. It may be associated with adverse effects on neurodevelopmental outcomes in children. Bis[2-(perfluorohexyl)ethyl] Phosphate can be removed from drinking water by using an ultrasonic extraction system. This method uses sound waves to extract the chemical from water and other liquids and is effective at removing small amounts (less than 10 parts per billion). The analytical method for this compound is low detection, which means that it can only detect concentrations of up to 0.1 part per billion (ppb). However, this method</p>

<p>Versatile small molecule scaffold</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>Versatile small molecule scaffold</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>Please enquire for more information about tert-Butyl 7-formyl-3,4-dihydro-2H-1,4-benzoxazine-4-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

Versatile small molecule scaffold

<p>3-Methyl-2-phenylbutanenitrile is a synthetic, nucleophilic blocker that binds to the active site of the enzyme and inhibits its function. 3-Methyl-2-phenylbutanenitrile is able to bind to calcium antagonist sites on the enzyme and inhibit their function. This product has been shown to be efficient in multigram amounts. The synthesis of this product has been optimized by using a cavitation reaction rate efficient method that is not limited by the solubility of reactants or products. Crystallography revealed that this product contains an amine group, which can act as a nucleophile in reactions with alkylthio groups, such as those found in proteins. 3-Methyl-2-phenylbutanenitrile is immobilized through dioxolane chemistry, which prevents it from interacting with other chemical species.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2,3,5-Trimethoxybenzaldehyde is the hydrolysis product of coumarin. It can be synthesized from 2,3-dimethoxybenzaldehyde and acetyl chloride. 2,3,5-Trimethoxybenzaldehyde can also be obtained by hydrolysis of coumarin with aqueous sodium hydroxide or potassium hydroxide. This compound is used as a natural flavoring agent in food products.</p>

<p>Versatile small molecule scaffold</p>

<p>1-(3-Hydroxythiophen-2-yl)ethan-1-one is a hydrolyzable compound that has been shown to have microbicidal activity against food spoilage bacteria such as Bacillus cereus and Clostridium perfringens. It inhibits the growth of these bacteria by inhibiting the synthesis of bacterial cell walls, which leads to cell death.</p>

<p>Versatile small molecule scaffold</p>

<p>3-Dimethylamino-1-phenyl-1-propanol is a chiral phenoxy propylamine optical isomer with a residue of carbonyl. It is a racemic mixture of two optical isomers and has the ability to form diastereoisomeric salts. 3-Dimethylamino-1-phenyl-1-propanol is an intermediate in the synthesis of fluoxetine, which is used to treat depression. This substance also has antihistamine and sedative properties, as well as other pharmacological effects that have not been studied extensively.</p>

<p>Versatile small molecule scaffold</p>

<p>1,3-Thiazinane-2-thione is an allylamine that can be used in the synthesis of a variety of compounds. 1,3-Thiazinane-2-thione is also an activator for carbon-carbon bond formation. This compound can be synthesized from an alkyl halide and an aldehyde by reaction with sulfur and heat. The stereoselectivity of this reaction has been shown using x-ray crystallography.</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-Chloropropanoyl)urea is a urea derivative. It has been used as an intermediate in the synthesis of tranquilizers and reaction products. 3-Chloropropanoyl)urea has been shown to react with aliphatic hydrocarbons, cycloaliphatic compounds, piperidine, or acylurea. The resulting products are chlorinated or carboxylic acid derivatives.</p>

Versatile small molecule scaffold

<p>Methanesulfonyl acetate is a chemical that is used in the chemical industry as a solvent and as a conditioner for polymers. Methanesulfonyl acetate has been shown to have effects on blood pressure and cancer cells, where it inhibits the growth of cancer cells by inhibiting DNA synthesis. Methanesulfonyl acetate also binds strongly to chlorine atoms and is soluble in nonpolar solvents. The molecular weight of methanesulfonyl acetate is 164.19 g/mol and its melting point is -13°C. <br>Methanesulfonyl Acetate Chemical Formula: CH3SO2COCH3<br>Molecular Weight: 164.19 g/mol<br>Melting Point: -13°C<br>Boiling Point: 210°C<br>Density: 1.07 g/cm3 <br>Solubility in Water: Insoluble <br>Appearance: Pale yellow liquid</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>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>1-(Ethenesulfonyl)-4-nitrobenzene (1ESNB) is a pyrazoline that has been used as an oxidant in cyclic aliphatic and heterocyclic syntheses. 1ESNB is also used to form phosphate derivatives, which are important in the pharmaceutical industry. 1ESNB can be prepared by the organocatalytic coupling of ethyl sulfone with nitrobenzene. The azomethine ylide can be generated from 1ESNB through oxidation with potassium permanganate or ozone, followed by addition of an aliphatic amine. This reaction gives a quinolinium salt that can be converted to a sulfone using thionyl chloride or oxalyl chloride. A cycloaddition reaction can then convert the sulfone into a biologically active molecule such as methotrexate or daunorubicin.</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>Benzyl Cyanoformate is a diagnostic agent that is used in the synthesis of amide compounds. It has a structure that includes an active methylene and nitrogen atoms. Benzyl Cyanoformate is synthesized through asymmetric synthesis, which encompasses the use of amines, inhibitors, and solid-phase synthesis. This compound has been shown to inhibit the activity of some receptor proteins by binding to them and preventing their activation, thus acting as an antagonist. Benzyl Cyanoformate binds to the enzyme carboxy with hydrochloric acid as a catalyst. The v600e mutation in K-ras can lead to increased sensitivity to this inhibitor; however, it is not known if this mutation confers sensitivity or resistance to other inhibitors of K-ras.</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>

(2R,5R)-2-Methyl-5-(prop-1-en-2-yl)cyclohexan-1-one is an enantiomer of (2S,5S)-2-methyl-5-(prop-1-en-2-yl)cyclohexan -1 -one. It belongs to the class of saponins and has been shown to have a synergistic effect with glutamic acid in the synthesis of deionized water. It can be used as a test drug for the detection of staphylococcus bacteria.

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

5-Methyl-2-pyrazinecarboxamide is a synthetic sulfa drug that inhibits the growth of mycobacterium avium, which is a bacterium found in the environment that can cause tuberculosis. 5-Methyl-2-pyrazinecarboxamide has been shown to have potent antitumor activity in tumor cell lines and has been shown to be effective against tuberculosis in mice. This molecule is synthesised from pyrazinoic acid, an organometallic compound, and sulfamethazine. The molecular descriptors obtained from this molecule are used to validate its anticancer activity in other tumor cells. The photophysical properties of this molecule have also been studied extensively.

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

Versatile small molecule scaffold

<p>tert-Butyl 6-aminohexanoate is a benzene derivative that is used as a spacer in organic synthesis. It reacts with potassium carbonate to form tert-butyl 6-aminocaproate and tert-butyl 2,6-dinitrophenolate. The tert-butyl group has an amino group at one end and a carboxylic acid group at the other end. This tertiary amine is made by reacting benzene with potassium hydroxide and adding 1-4c alkyl chloride. The tertiary amine functional group is reactive towards electrophilic aromatic substitution reactions, such as nitration or halogenation.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>2-(Chloromethyl)-1,4-dioxaspiro[4.5]decane is a catalytic agent that is used in the synthesis of acetates and cyclohexanone. It can be used to produce a variety of organic compounds by using different starting materials, such as acetates and cyclohexanone. 2-(Chloromethyl)-1,4-dioxaspiro[4.5]decane has been shown to react with epichlorohydrin to form a chloromethylated product at room temperature. The reaction proceeds via an addition-elimination mechanism and produces two products: 1,4-dioxaspiro[4.5]decane and chloroacetate.</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

Versatile small molecule scaffold

<p>4-Isopropylcyclohexylmethanol is a synthetic chemical that is used as a fragrance. It is found in plants such as Paeonia suffruticosa and is used in the synthesis of linalool oxide. 4-Isopropylcyclohexylmethanol has been shown to bind to histone proteins, which may have an effect on gene expression. This chemical also has a vapor pressure of 0.0013 mmHg at 25°C and can be detected by electrochemical method at a concentration of 10 ppm. 4-Isopropylcyclohexylmethanol has been shown to react with eugenol in benzene, forming methyl cinnamate and methyl ethyl alkanal.</p>

<p>2-[4-(Hydroxymethyl)cyclohex-3-en-1-yl]propan-2-ol is an isomer of alpha-terpineol. It is the major component of the essential oil from Litsea cubeba, an evergreen tree native to China, Taiwan and Thailand. Alpha-terpineol has been shown to have a broad spectrum of antimicrobial activity against various strains of intestinal bacteria. The methyl group in alpha-terpineol interacts with bacterial 16S ribosomal RNA, inhibiting protein synthesis. Alpha-terpineol also has hydroxylase activity that binds preferentially to hydroxylases in the intestines, which may be responsible for its antimicrobial effects.</p>

<p>3-Methyl-1-phenyl-5-(piperidin-1-yl)-1H-pyrazole-4-carbaldehyde (MPPC) is a crosslinked polymer that spontaneously forms nanoparticles. The Langmuir isotherm was used to characterize the parameters of this polymer. A chitosan gel, magnetic nanoparticle and thermodynamic techniques were used to study the characteristics of MPPC. The kinetic and endothermic studies were carried out using magnetic nanoparticles. This polymer has been shown to desorb from chitosan gels and magnetic nanoparticles, which can be useful for drug delivery applications.</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>

9H-Xanthene-9-methanol is an orthogonal protecting group for amines, carbanions, and other nucleophiles. It is a multistep process that yields a cationic intermediate, which can be used for the synthesis of amine-containing compounds. 9H-Xanthene-9-methanol is also used in the deprotection of photolabile groups such as sulfonyl chlorides and tosylates. The reactivity of this reagent is optimized when it is combined with acidic solvents, such as dichloromethane or chloroform.

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>