Building Blocks

<p>2-Acetoxybenzonitrile is an atypical, acidic organic compound with a molecular weight of 136.06 g/mol. It has a melting point of -5.5 °C and decomposes spontaneously at high temperatures to form benzonitrile, carbon dioxide, and water. 2-Acetoxybenzonitrile is able to act as a competitive inhibitor of acetylsalicylic acid (ASA) in the kinetic determination of ASA using acetylation as the rate-determining step. In this experiment, 2-acetoxybenzonitrile was found to be an effective inhibitor of acetylation with a KI value of 1.8 x 10 M. The spectrometer can be used to determine the molecular weight and purity of 2-acetoxybenzonitrile by measuring its absorbance in the ultraviolet region.<br>2-Acetoxybenzonitrile binds metal cations such as Cu(II), Fe(</p>

<p>L-Proline methyl ester hydrochloride is an organic compound that is classified as a trifluoroacetic acid ester. It has significant antiproliferative activity and induces apoptotic cell death in colorectal carcinoma cells. L-Proline methyl ester hydrochloride also inhibits the proliferation of lymphocytes by inhibiting protein synthesis, which may be due to its conformational properties. L-Proline methyl ester hydrochloride is synthesized by reacting L-proline with trifluoroacetic acid and subsequently hydrolyzing the resulting ester with hydrochloric acid. The synthesis can be carried out in two steps: first, a chloride ion is added to the protonated form of the amine; second, the protonated form of the amine reacts with hydrophobic compounds such as dodecyl amines or ethyl acetate to form an alkyl group. This reaction can also be carried out using</p>

<p>Styrene-divinylbenzene sulfonated copolymer also called Dowex 50W 8X hydrogen form, strongly acidic resin, is a fine mesh spherical ion exchange resin made from a microporous styrene / divinylbenzene (DVB) co-polymer with a sulfonic acid group. Styrene-divinylbenzene sulfonated copolymers are used in fine chemical and pharmaceutical column separations.</p>

<p>1-Cyano-2-hydroxy-3-butene is a mitochondrial toxin that causes apoptosis in liver cells. It has been shown to cause liver lesions in CD1 mice. 1-Cyano-2-hydroxy-3-butene reduces the mitochondrial membrane potential, which leads to a decrease in ATP production and an increase in reactive oxygen species (ROS) production. This toxin also inhibits the transcriptional activity of nuclear receptors and induces the expression of cytochrome P450 2E1, leading to increased detoxification enzyme activity. 1-Cyano-2-hydroxy-3-butene is activated by mitochondria, which leads to its ability to cause apoptosis of liver cells.</p>

<p>2-Chloro-1,1,1-trimethoxyethane is a reagent that is used in the synthesis of recombinant proteins. It is also used to produce monoclonal antibodies. Fatty acids can be analyzed by using these reagents as they are soluble in this solvent. The structural analysis of fatty acids has been shown to have anticancer activity. 2-Chloro-1,1,1-trimethoxyethane reacts with glycosyl residues on lysine residues in proteins and produces an acid that causes the protein to unfold and denature. This reaction has been shown to have anticancer activity against cervical cancer cells in human liver cells.</p>

<p>Versatile small molecule scaffold</p>

<p>1-(4-Ethoxycarbonylphenyl)piperazine is an enantiopure phosphatase inhibitor. It is used in the treatment of cancer and other life-threatening diseases. 1-(4-Ethoxycarbonylphenyl)piperazine inhibits phosphatases, which are enzymes that catalyze hydrolysis of phosphate groups from substrates. This inhibition leads to a decrease in the production of fatty acids and cholesterol, resulting in a reduction in body mass index. The drug has been shown to be effective against animal models for cancer, with an effective dose of 100 mg/kg intraperitoneally. In addition, 1-(4-ethoxycarbonylphenyl)piperazine has been shown to inhibit cardiac phosphatases and increase cardiac uptake by inhibiting acylation reactions.</p>

<p>8-Anilino-1-naphthalenesulfonic acid is a potent and selective inhibitor of the proteasome. It inhibits the activity of the proteasome and leads to neuronal death. 8-Anilino-1-naphthalenesulfonic acid has been shown to have antioxidative properties in a Langmuir adsorption isotherm study. This compound also has fluorescence, which makes it useful as a fluorescent probe for protein identification in human serum. 8-Anilino-1-naphthalenesulfonic acid binds to proteins with hydrophobic regions, such as lipids and phospholipids, due to its hydrophobic effect. It can be used as an analytical method for determining the protein content in water samples.</p>

4-Ethoxybenzaldehyde is a chemical compound with antioxidant properties. It has been found to inhibit the proliferation of cervical cancer cells and melanoma cells, as well as to protect against radiation-induced oxidative damage in human skin. 4-Ethoxybenzaldehyde also inhibits the influenza virus by interfering with its ability to replicate. This compound is used in many different products, including cosmetics and pharmaceuticals. The most common use of 4-ethoxybenzaldehyde is as an excipient in tablet formulations. In this application, it can be used to maintain drug stability and improve disintegration time. In addition, it may have some anti-inflammatory effects that are related to its ability to inhibit the production of prostaglandins and leukotrienes. 4-Ethoxybenzaldehyde has been shown to have antioxidant properties for diabetics as well as for patients with autoimmune diseases such as multiple sclerosis and systemic lupus erythematosus (SLE). The

3-Amino-4-methylbenzonitrile is an organic compound that is produced by the oxidative dehydrogenation of 3,4-dimethylaniline. It has been shown to undergo a number of reactions, including hydrochloric acid transfer hydrogenation and diazotization. This reaction yields 3-amino-4-methylbenzonitrile, dimethylamine and anilines. The transfer hydrogenation of nitroarenes with 3-amino-4-methylbenzonitrile gives 3-(3,4)-diaminobenzonitrile and 2,6-dinitrotoluene. The optimization of this reaction has led to the discovery of new nitrite derivatives as a result of the addition of nitrite in the presence of 3-amino-4-methylbenzonitrile.

<p>3,4-Difluoro-5-nitrobenzonitrile is a hepatotoxic compound that is found in the environment. It has been shown to cause cirrhosis and overgrowth of the liver. 3,4-Difluoro-5-nitrobenzonitrile also inhibits hepatic encephalopathy and may be used to treat liver disease. This toxicant has been detected in the bowel and duodenum of humans with nonalcoholic steatohepatitis, as well as in the jejunum and duodenum of mice with spontaneous steatohepatitis. It also causes nonalcoholic steatohepatitis when given orally to rats.</p>

<p>4-Cyclopentylbenzaldehyde is a homologous compound that is used in the synthesis of other compounds. It is an organic compound with a monoxide group and a cyclohexenyl group. 4-Cyclopentylbenzaldehyde can be prepared by the oxidation of benzene or by the formylation of cyclohexene. This compound can be used in acylation reactions. The yields of this chemical are high, which makes it useful for laboratory purposes. 4-Cyclopentylbenzaldehyde has been shown to undergo carbonylation reactions and catalysis at higher temperatures and pressures. It also reacts with mesitylene, although not toluene, under these conditions.</p>

2-Fluoro-4-(hydroxymethyl)phenol is a versatile building block, which can be used as a reagent to synthesize complex compounds. 2-Fluoro-4-(hydroxymethyl)phenol is also a useful building block for the synthesis of various pharmaceuticals, such as selective androgen receptor modulators (SARMs). It has been reported that 2-fluoro-4-(hydroxymethyl)phenol inhibits the activity of human liver cytochrome P450 enzymes. In addition, this compound has been used as an intermediate in the synthesis of some research chemicals. 2-Fluoro-4-(hydroxymethyl)phenol has CAS number 96740-93-1 and is a high quality chemical with many uses.

<p>1,1'-(Azodicarbonyl)dipiperidine is an organic compound that has been shown to be a radiosensitizing agent. It is used in the treatment of ovarian cancer and inhibits cell growth by inducing apoptosis. 1,1'-(Azodicarbonyl)dipiperidine modifies the cellular response to ionizing radiation by sensitizing cells to radiation and increasing the amount of DNA damage caused by radiation. This compound was found to increase the radiosensitivity of cells in vitro; however, it does not induce apoptosis in non-malignant cells. The effects are observed at low doses and are more pronounced when combined with other agents such as 3-aminobenzamide (3AB).</p>

Acetylcysteine is a drug that inhibits the growth of bacteria and viruses. Acetylcysteine is a precursor to the amino acid cysteine and has been shown to have antiviral properties against herpes simplex virus. It also has protective effects on human liver cells by preventing lipid peroxidation, which may be due to its antioxidant activity. Acetylcysteine can be used as an analytical method for particle size, thermal expansion, and hydrogen chloride content in industrial processes. Its use in metabolic disorders and cancer therapy is limited because it does not cross the blood-brain barrier easily. Acetylcysteine has been shown to inhibit HIV infection by blocking reverse transcriptase activity, but it cannot cure HIV infection.

<p>Pyrene is a chemical compound that has been found to bind to DNA and inhibit the transcription of genetic information. It has been used as a fluorescence probe in biochemical research, wastewater treatment, and surface methodology. As a redox probe, pyrene can be used to measure the redox potential of reaction solutions. Pyrene has also been used as an analytical method for measuring transfer reactions in biological studies.</p>

<p>Orcinol monohydrate is a high quality chemical that can be used as a reagent, complex compound, or useful intermediate in the synthesis of fine chemicals. It is also an important building block in the synthesis of other compounds. This product has CAS No. 6153-39-5 and is classified as a speciality chemical. It is also a versatile building block that can be used as a reaction component in organic syntheses.</p>

<p>3-Hydroxy-2,3-dihydro-1H-indol-2-one (3HID) is a heterocyclic compound that contains a trifluoroacetate group. It is an intermediate in the synthesis of histamine, serotonin, and melatonin. 3HID is an inhibitor of the growth factor receptor, which inhibits the proliferation of human liver cells. 3HID also has a strong affinity for basic proteins such as albumin and hemoglobin. These interactions are thought to be important for its cytotoxic activity in cancer cells. 3HID can be synthesized by reacting acetyl chloride with 2-aminobutyric acid in the presence of potassium hydroxide or sodium hydroxide at room temperature, followed by hydrolysis with water. The reaction produces 3HID and acetic acid, which can be removed by distillation. The product can then be purified by recrystallization from methanol or</p>

5-Benzyloxyindole-3-glyoxylamide is a versatile building block that can be used in the synthesis of complex compounds. It has been shown to have a high quality and is useful as a reagent for research purposes. 5-Benzyloxyindole-3-glyoxylamide can be used as a reaction component and is useful as an intermediate in organic synthesis. 5BIGA has CAS number 22424-62-0 and is also known as 3-(benzyloxy)-5-(2,2,2-trifluoroethoxy)indole glyoxamide.

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

2-Methyl-6-(phenylethynyl)pyridine (MPEP) is a drug that is used in the treatment of Parkinson's disease. This drug inhibits the synthesis of proteins, including glutamate and dopamine, which are involved in Parkinson's disease. MPEP has been shown to be effective against Parkinson's disease by blocking protein synthesis in the caudate putamen and other brain regions. It also lowers locomotor activity and improves motor skills in rats. MPEP binds to response element-binding protein (RBP), which is involved in the regulation of gene expression. The binding of MPEP to RBP leads to an increase in levels of endogenous adenosine, which blocks the effects of dopamine and serotonin on postsynaptic neurons.

5-Chloro-2-methylaniline is an organic compound that is a member of the amines class. It has been shown to be genotoxic and carcinogenic in vivo. 5-Chloro-2-methylaniline binds to DNA and inhibits the synthesis of RNA, leading to cell death. It is also toxic to aquatic organisms by inhibiting cellular respiration and causing mutations. 5-Chloro-2-methylaniline has been shown to be genotoxic in vitro and in vivo, with chronic oral toxicity observed at dietary concentrations of 0.1% (10 ppm) in animals. The toxicity of this compound may be due to its ability to form hydrogen chloride when mixed with water or other acids.

4-Amino-5-chloro-2-methoxybenzoic acid is a compound that has been shown to be a potent 5-HT4 receptor agonist. It is used in the treatment of obesity and diabetes. The molecular structure of 4-Amino-5-chloro-2-methoxybenzoic acid consists of a carbonyl group and an amine group, which are bound to each other by a covalent bond. This molecule is found to bind to the 5HT4 receptor with high affinity, which leads to its efficacy as an antiobesity agent.

<p>2-Ionone is a carotenoid that is an intermediate in the biosynthesis of vitamin A. It is also used as a flavoring and fragrance additive and has been shown to have cancer-preventing properties. 2-Ionone inhibits the NADP-cytochrome P450 reductase, which prevents formation of NADPH, an essential cofactor in cellular respiration and biosynthesis of fatty acids. 2-Ionone also inhibits cell growth in vitro by interacting with the polymerase chain reaction (PCR) process. The physiological function of 2-Ionone is not well understood, but it has been shown to inhibit steric interactions between DNA molecules. 2-Ionone can be prepared industrially by photolysis or by thermal decomposition of acetophenone.</p>

<p>2-Methyl-2-phenylsuccinimide is a synthetic cannabinoid that has been found in urine samples. It is not known whether 2-methyl-2-phenylsuccinimide has any psychoactive effects. Phensuximide, a drug that is used to treat epilepsy, has been shown to interact with 2-methyl-2-phenylsuccinimide and other drugs. 5HT7 receptor agonists are thought to be involved in the treatment of depression and anxiety. The terminal half-life of 2-methyl-2-phenylsuccinimide is unknown at this time, but it may be shorter than that of phensuximide. Clinical studies have shown that carbamazepine and enzyme inducing antiepileptic drugs can decrease the concentration of 2-methyl-2-phenylsuccinimide in the blood. Chromatography techniques have been used to detect 2 methyl -2 phenyl</p>

<p>Tert-Butoxycarbonyl-L-leucine (tBOC-LL) is a tetrapeptide that is used as a drug substance in the synthesis of buserelin, a synthetic peptide hormone. It has been shown to have high reactivity in organic solvents and can be used in cationic polymerization reactions. tBOC-LL has been used to synthesize helical structures with high purity and yield. As it is not an amino acid, tBOC-LL does not occur naturally and must be synthesized.<br>Tert-Butoxycarbonyl-L-leucine (tBOC-LL) is available from Sigma Aldrich Chemie GmbH &amp; Co KG as:</p>

<p>Versatile small molecule scaffold</p>

<p>2-Amino-5-methylbenzoic acid is an anthranilic acid derivative that has been shown to have potent antitumor activity. It inhibits the growth of cancer cells and is effective against light emission. 2-Amino-5-methylbenzoic acid blocks the production of porphyrins, which are necessary for the production of heme, a cofactor in many enzymes. The compound also inhibits serine protease, which is involved in tumor cell proliferation and metastasis.<br>2-Amino-5-methylbenzoic acid has been shown to inhibit the growth of human liver cancer cells in vitro. This compound can be synthesized by a Suzuki coupling reaction with phenylacetic acid and 3-(2'-aminoethyl)aminobenzene.</p>

<p>Trifluoroacetic acid is a hydrophobic molecule that has been used in the synthesis of 1-anilinonaphthalene-8-sulphonic acid magnesium. The magnesium salt of this compound is soluble in water and can be obtained as a white solid. Trifluoroacetic acid has been shown to have anti-inflammatory effects by binding to chloride ions, which are present in high concentrations on the surface of inflamed cells. Trifluoroacetic acid also has a surfactant property, which may be due to its ability to form micelles with fatty acids. This property is important for drug absorption because it helps solubilize lipophilic drugs and improve their bioavailability.</p>

Penicillin V is an antibiotic that belongs to the class of penicillins. It is used in the treatment of bacterial infections, such as streptococcal pharyngitis and infectious diseases. Penicillin V binds to the penicillin-binding proteins, which are located on the outer surface of the bacterial membrane and prevent cell wall synthesis. This binding inhibits cell wall biosynthesis by preventing transpeptidation and transglycosylation reactions and leads to cell death. Penicillin V also inhibits the production of certain cytokines, including interleukin-1β (IL-1β) and tumor necrosis factor α (TNFα), which may be a result of its ability to inhibit Toll-like receptor 4 (TLR4). The solubility data for penicillin V was obtained from experiments conducted with experimental animals. The oral cephalosporins were shown to have a greater affinity for penicillin-binding proteins than pen

<p>Violuric acid is a chemical compound that is used in biological treatment. It has a hydroxyl group and UV absorption, which makes it reactive. Violuric acid undergoes protonation and deprotonation to form an acid complex with water. The nitrogen atoms in violuric acid can react with the oxygen atoms of water molecules to form nitrous acid, which then reacts with hydrogen peroxide to form an oxidizing agent. Violuric acid is synthesized by chain reactions between organic acids and inorganic acids. Violuric acid has a redox potential of −0.35 volts, making it an excellent reducing agent for organic compounds. In organic chemistry, violuric acid is used as a reducing agent for esters or amides.</p>

3-Amino-5-nitrobenzoic acid is a cyclic analog of diazepam. It has been shown to be an acceptor in the reduction of picric acid and nitro groups. 3-Amino-5-nitrobenzoic acid is a molecule which interacts with dopamine to produce pharmaceutical preparations.

<p>Fmoc-D-glu-OtBu is an amide that can be used as a screening reagent for the detection of carbohydrate and periplasmic compounds. It has been shown to inhibit hepatitis in humans, which may be due to its ability to bind with muramyl dipeptide. Fmoc-D-glu-OtBu has also been shown to synergize with other vaccines, such as tetanus and escherichia coli surface antigen.</p>

4-Chlorophenylacetic acid is a fatty acid that reacts with hydroxyl groups to form reaction intermediates. It has been used in antiestrogen therapy as it is able to inhibit the activity of estrogen. It has also been used in polymeric matrices to control the release of silver ions for the treatment of cancer. 4-Chlorophenylacetic acid is synthesized by acylation of phenylacetic acid with chloroacetyl chloride in the presence of hydrochloric acid and sephadex g-100. 4-Chlorophenylacetic acid has been shown to inhibit tumor growth in animal models, which may be due to its ability to induce apoptosis.

<p>3-Hydroxy-4-iodobenzaldehyde is a fluorophore that is used in the synthesis of amide compounds, as well as in the production of other synthetic molecules. 3-Hydroxy-4-iodobenzaldehyde has been shown to have pharmacokinetic properties that are similar to those of fluorescein, and can be used to study the distribution and metabolism of this compound. This compound also has an oxidation potential that is higher than that of fluorescein, which makes it more useful for studying drug metabolism. The labile nature of 3-hydroxy-4-iodobenzaldehyde means it will not remain intact for long periods of time.</p>

4-Methyl-7-(methylamino)-2H-chromen-2-one is a fine chemical that is used as a building block in the synthesis of other compounds. It has been used in research as a reagent and in the production of pharmaceuticals. 4-Methyl-7-(methylamino)-2H-chromen-2-one can be used to produce a variety of complex compounds, including those with versatile scaffolds. This compound has been shown to react with many different groups, such as alcohols, amines and thiols, which makes it an excellent intermediate for organic synthesis.

<p>Please enquire for more information about Ethyl 5-acetoxyindole-2-carboxylate 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>Piperitone is a natural product that is isolated from the roots of Piper aduncum L. It has shown antimicrobial activity against Gram-positive and Gram-negative bacteria, fungi, and protozoa. The compound has been used as a broad-spectrum antimicrobial agent to treat infectious diseases such as malaria, leishmaniasis, and trypanosomiasis. Piperitone's mechanism of action is not well understood but it may be due to its ability to inhibit fatty acid synthesis or by inhibiting the biosynthesis of hepg2 in human erythrocytes.</p>

<p>4-Ethoxy-3-hydroxybenzaldehyde (4EHB) is a thioacetal that has been shown to be an effective precursor for the synthesis of many other molecules, such as combretastatin a-4. It is prepared by reaction of ethylmagnesium bromide and acetone. 4EHB has been shown to have antifungal properties in vitro, and can be used in the treatment of cancer cells. This compound is volatile and can be easily detected with headspace techniques. The functional group of this molecule is an alcohol group, which is found on the ring structure. Spectroscopic analysis shows that it has a carbonyl group with an OH group attached to it.</p>

<p>Methanethiol is a compound that occurs naturally in the environment. It is used as a fungicide, insecticide and herbicide. Methanethiol inhibits the growth of microorganisms by binding to metal ions on the surface of cells. This prevents DNA replication and protein synthesis, leading to cell death. Methanethiol also has anti-inflammatory properties which may be due to its ability to inhibit adenosine A1 receptor activity in humans.</p>

<p>5-Hydroxyoxindole (5HO) is a naturally occurring molecule that is found in oxindole and other indoles. It has been shown to have regulatory effects on inflammatory diseases, notably in the treatment of colitis. 5HO possesses significant cytotoxicity against carcinoma cells and also has radical scavenging activity. This compound can be synthesized using a solid-phase synthesis method. The presence of 5HO in skin cells has been correlated with the production of skin pigment called melanin. In addition, this molecule has been shown to bind to picolinic acid, which may contribute to its anti-inflammatory properties. 5HO is also present in neurologic disorders such as Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis.</p>

Cyclopentylmethanol is a chemical compound with the molecular formula CH3OH. It is a colorless liquid that is soluble in water and has a distinctive, sweet odor. Cyclopentylmethanol is used as an intermediate in organic synthesis and as a solvent for nitrocellulose, cellulose acetate, cellulose nitrate, and similar materials. It reacts with chlorine at high temperatures to form chlorinated cyclopentylmethanols. This reaction can be used to synthesize hydroxyapatite (a mineral) from calcium phosphate (a mineral). Cyclopentylmethanol also reacts with nicotinic acetylcholine receptors in the brain, causing them to desensitize. Hydroxyapatite can also be synthesized by reacting cyclopentylmethanol with dinucleotide phosphate and hydroxyl group containing compounds such as esters or soluble guanylate cyclase enzymes. The reactions produce hydrogen

Versatile small molecule scaffold

N-Succinimidyl myristate is a long-chain fatty acid that contains a sulfur atom at its head. It is used in the production of diagnostic products and insulin analogs, as well as in the industrial production of organic solvents. N-Succinimidyl myristate reacts with serum albumin, forming an activated product that can be used in diagnostic tests. This reaction product is also used to bind proteins to fluorine atoms for use in industrial processes.

<p>Guanine is a purine base that is found in the DNA and RNA of all living cells. It plays an important role as a component of the nucleic acid molecule, where it is paired with cytosine. Guanine is involved in many chemical reactions and biological processes, including protein synthesis and cell division. The lack of guanine can lead to deficiency symptoms such as hemolytic anemia or erythrocyte cytoplasmic inclusion bodies. Guanine has been shown to have chemiluminescent properties, which can be used to detect its presence in samples containing DNA or RNA. This reaction occurs when guanine reacts with hydrogen peroxide (H2O2) to form guanidine (HN=C(NH2)NH2). The reaction produces excited states that emit light at a wavelength of 395 nm when they return to their ground state. Guanidine also has electrochemical impedance spectroscopy properties, which can be used for analytical purposes</p>

<p>Please enquire for more information about (2R)-4-Methyl-2-[2-oxo-2-[(phenylmethoxy)amino]ethyl]pentanoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

Versatile small molecule scaffold

1,8-Diazido-3,6-dioxaoctane is a synthetic molecule that is used in the synthesis of macrolactones, polymers, and biomolecules. It can be used as a bioconjugate to attach other functional groups to biomaterials and polymers, such as azido groups. This compound has high sensitivity and thermal stability with good solubility in organic solvents. 1,8-Diazido-3,6-dioxaoctane has been shown to be compatible with many functional groups and is an important monomer for use in cross-linked polymers.