Building Blocks

<p>Trifluoroacetic acid is a nonsteroidal anti-inflammatory drug that belongs to the group of carboxylic acids. Benzene-1,3,5-tricarbaldehyde is used as an intermediate in the synthesis of trifluoroacetic acid and has been shown to be effective against microbial infections. It has been shown to inhibit the growth of bacteria such as Staphylococcus aureus and Bacillus cereus by disrupting their DNA replication. Benzene-1,3,5-tricarbaldehyde also inhibits the production of inflammatory cytokines and reduces inflammation. The compound has chemical stability and does not react with human serum or other biological fluids.</p>

<p>Versatile small molecule scaffold</p>

<p>PF-04965842 is an anti-inflammatory drug that belongs to the class of Jak1 inhibitors. It is used in the treatment of alopecia areata, dermatitis, and bowel disease. PF-04965842 is a selective inhibitor of JAK3 and blocks signaling through this pathway. PF-04965842 has been shown to have long-term efficacy in the treatment of inflammatory skin diseases such as atopic dermatitis and psoriasis. In addition, it has been demonstrated to be effective in reducing symptoms associated with inflammatory bowel disease (IBD) and ulcerative colitis. PF-04965842 also inhibits the production of proinflammatory cytokines by inhibiting the activation of inflammatory cells in the skin or gut.</p>

<p>Versatile small molecule scaffold</p>

<p>4-Azidophenylmethanol is a nucleophilic amine that can be synthesized from the reaction of an azide with a methoxide. 4-Azidophenylmethanol can be used to generate nitro groups in organic synthesis. It has also been shown to have cytotoxic activity against prostate cancer cells and malignant brain cancer. 4-Azidophenylmethanol also has the ability to react with squamous carcinoma cells, forming methides and causing cell death. This chemical is stable at low temperatures and does not react with water.</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>A building block research chemical</p>

<p>Precursor of melanine synthesis in bacteria</p>

<p>D,L-Homotryptophan is a fine chemical that is used as a building block in the synthesis of complex compounds. It has been used as a reagent, speciality chemical, and intermediate. D,L-Homotryptophan is also versatile in its use as a building block for the synthesis of various chemicals. This compound has been shown to react with other chemicals to form useful scaffolds.</p>

<p>Homovanillic acid is widely used as a fluorogenic substrate of peroxidase. The reaction is however not specific and has been shown to react also with soybean lipoxygenase in the presence of hydrogen peroxide. Excitation and emission wavelengths for homovanillic acid are 312 and 420 nm, respectively.</p>

<p>Potential antioxidant; pharmaceutical intermediate</p>

4-Hydroxyphenylacetic acid is a sesquiterpene lactone that is found in the essential oils of plants such as valerian, lemon balm and rosemary. It has been shown to have high antioxidant activity and can inhibit carcinoid syndrome. This compound has also been shown to have properties similar to p-hydroxybenzoic acid, which is an inhibitor of polyphenol oxidase. 4-Hydroxyphenylacetic acid inhibits some enzyme activities, such as polymerase chain reaction (PCR) and DNA synthesis. It also binds to dinucleotide phosphate and can be used for the treatment of diseases related to energy metabolism.

<p>2-Hydroxyphenylacetic acid is a hydroxylated phenolic acid that is structurally similar to other phenolic acids. It is present in many plants, including tea leaves and coffee beans, where it acts as an antioxidant. 2-Hydroxyphenylacetic acid has been found in the urine of humans and animals following ingestion of excessive amounts of these plants. It is also found in urine samples from patients with certain types of kidney disease. The synthesis of 2-hydroxyphenylacetic acid can be achieved by reacting ethylene diamine with sodium hydroxide solution or hydrochloric acid.</p>

<p>3-Hydroxyphenylacetic acid is an organic compound with the formula CH(OH)(CH)COOH. It is a quinoid, meaning that it contains a benzene ring with one of the hydrogens replaced by a hydroxyl group. 3-Hydroxybenzoic acid is an important intermediate in the synthesis of several pharmaceuticals, including antipyrine and salicylic acid. It can be synthesized from phenol or benzoic acid. 3-Hydroxybenzoic acid has been shown to have antimicrobial properties against various bacteria and fungi, as well as hypoglycemic effects in rats. This compound was also shown to inhibit 4-hydroxyphenylacetate (4-HPAA) reductase activity and dopamine oxidation, two key enzymes involved in energy metabolism.</p>

<p>7-Hydroxyquinoline-(1H)-2-one is a quinoline derivative that binds to epidermal growth factor (EGF) receptors. It has been shown to inhibit the chloride current in neurons, which may be due to its ability to bind to the dopamine receptors in these cells. 7-Hydroxyquinoline-(1H)-2-one also inhibits DNA and protein synthesis by binding to nucleophilic nitrogen atoms and protonated nitrogen atoms, respectively. It has been shown to have an inhibitory effect on cancer cell growth in control experiments. This drug is not active against normal cells because it does not bind well to them. 7-Hydroxyquinoline-(1H)-2-one binds with high affinity to piperazine and this interaction can be used as a fluorescent probe for the presence of quinoline derivatives.</p>

<p>Used for treatment of Alzheimer's disease and Friedreich's ataxia</p>

<p>4'-Hydroxy-2,2':6',2''-terpyridine is a molecule with the molecular formula C24H22N4O8. It is an organic compound that belongs to the group of heterocycles. It has been found to be a ligand for metal ions and has been shown to interact with particles at temperatures below 20°C. 4'-Hydroxy-2,2':6',2''-terpyridine crystallizes in two polymorphs: tetragonally (alpha) at room temperature and trigonally (beta) at temperatures below 20°C. The alpha form has been observed to undergo a photophysical reaction as it absorbs light and emits light in the ultraviolet region of the spectrum.</p>

<p>Please enquire for more information about trans-3-Hydroxy-L-proline including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Reduces brain amyloid plaques; induces neprilysin expression</p>