Building Blocks

<p>4-Imidazoleacetic acid HCl is a fluorescent probe that binds to the α1 subunit of the dinucleotide phosphate (NADH) oxidoreductase. It has been shown to inhibit mitochondrial functions, which may be due to its ability to inhibit the pentose phosphate pathway and reduce reactive oxygen species levels. 4-Imidazoleacetic acid HCl has also shown inhibitory properties against congestive heart failure by acting on the mitochondria and inhibiting energy metabolism. It can also be used as a chemical biology tool for studying protein interactions with NADH dehydrogenase. The x-ray crystal structures have revealed that 4-imidazoleacetic acid HCl binds to the active site of NADH oxidoreductase with an orientation that mimics a substrate molecule. This allows it to bind tightly and disrupt enzyme activity.</p>

<p>D-amino acid</p>

<p>Versatile small molecule scaffold</p>

<p>Tyrosinase inhibitor; skin whitener</p>

<p>2',4',6'-Trihydroxyacetophenone monohydrate is a monosodium salt of 2,4,6-trihydroxyacetophenone. It has been shown to inhibit the production of leukemia inhibitory factor (LIF) in vitro. LIF is a cytokine that regulates cell differentiation and proliferation. The matrix effect of 2',4',6'-trihydroxyacetophenone monohydrate on polymerase chain reaction was also studied with the use of a matrix-assisted laser desorption ionization time-of-flight mass spectrometer. This study revealed that the matrix effect is due to the inhibition of cyclase activity by ptelefolia and structural analysis revealed that this inhibition may be due to an interaction with nitrite ion. Preparative high performance liquid chromatography (HPLC) was used for the separation and purification of coumarin derivatives from 2',4',6'-trihydroxyacetophenone monohydrate. The toxicological studies</p>

<p>2,6,8-Trichloropurine ammonium salt is a reaction product of 2,6,8-trichloropurine and ammonium hydroxide. It has been shown to inhibit the synthesis of protein in tissue cultures and to be cytotoxic.</p>

<p>Tris(phenylthio)methane is a formylating reagent that reacts with ethyl formate to produce the nitro compound. It is used in the preparation of β-amino acids and as an asymmetric synthesis catalyst. Tris(phenylthio)methane can be used as a polymerization initiator for metathesis reactions, such as the Suzuki reaction. It has been shown to be a good nucleophile and polymerizing agent when combined with hydrochloric acid or silver trifluoromethanesulfonate. Tris(phenylthio)methane may also react with chloride in the presence of base to produce phosphoric acid esters.</p>

<p>2-Iodo-5-nitrobenzoic acid is a reactive molecule that reacts with terminal alkynes to form a fluorescent compound. It was immobilized on an electrode and used as a probe in voltammetry studies. 2-Iodo-5-nitrobenzoic acid is also used as a reagent in the synthesis of amides, which are important in many biochemical reactions. The use of this compound may be limited by the toxicity to cells, which can be increased through the presence of cisplatin or 3-aminobenzoic acid. The microenvironment around cancer cells may also alter the reactivity of 2-iodo-5-nitrobenzoic acid.</p>

<p>Please enquire for more information about Kisspeptin-234 trifluoroacetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1,2,3,6-Tetrahydropyridine is an experimental drug that acts as a dopamine receptor antagonist. It has been shown to induce neuronal death in the presence of excess dopamine by inhibiting the uptake of dopamine by neurons. The nitrogen atom in position 6 may be involved in binding to the receptor and initiating the conformational change needed for activation. Tetrahydropyridine binds to the D1 and D2 receptors with high affinity, but it does not bind to D4 receptors. Tetrahydropyridine can also inhibit locomotor activity in mice and rats.</p>

<p>Pyrimidine nucleobase; component of nucleic acids</p>

<p>Versatile small molecule scaffold</p>

<p>Fmoc-L-m-Tyrosine is a reagent that is used in organic synthesis. It is a complex compound that can be synthesized from m-tyrosine and t-butyl bromoacetate. Fmoc-L-m-Tyrosine is also a useful intermediate for the preparation of other compounds, such as pharmaceuticals and agrochemicals. It has been shown to be a fine chemical that has a wide range of applications in the field of biotechnology and pharmaceuticals. Fmoc-L-m Tyrosine is also a versatile building block with many possible reactions, making it an excellent candidate for research chemicals, including speciality chemicals. The CAS number for this compound is 204384-71-4 and it's molecular weight is 262.3 g/mol.br&gt;</p>

<p>4-Chlorophenyl[3-(trifluoromethyl)phenyl]methanone is a chemical compound that can be used as a reaction component or a reagent. It is often used as a building block in organic synthesis, due to its high quality and versatility. 4-Chlorophenyl[3-(trifluoromethyl)phenyl]methanone is soluble in organic solvents and has been shown to have no significant toxicity. This chemical is also useful for the production of complex compounds with various applications, such as pharmaceuticals, agrochemicals, and dyes.</p>

<p>Tert-butyl 3-formyl-5H,6H,7H,8H-[1,2,4]triazolo[4,3-α]pyrazine-7-carboxylate is a research chemical that is used as a building block in the synthesis of complex compounds. It is also used as a reagent and a speciality chemical. Tert-butyl 3-formyl-5H,6H,7H,8H-[1,2,4]triazolo[4,3-α]pyrazine-7-carboxylate is an intermediate in the synthesis of other chemicals with high quality and versatile building blocks. It has been used in reactions to produce various heterocycles including 1-(2'-aminophenoxy)propane hydrochloride.</p>

<p>1,2-Phenylenedimethanamine dihydrochloride is a colorless to white crystalline solid that is soluble in diethyl ether, ethyl acetate and methanol. It is insoluble in water and most organic solvents. 1,2-Phenylenedimethanamine dihydrochloride is used as a reagent for the preparation of primary amines from alkyl halides. This chemical has been shown to be stable in air and remains unchanged when heated at 100°C. Synonyms include: 2-Amino-1,2-phenylene dichloride; 2-Amino-1,2-diphenylethane dichloride; 2-[(1,2)-Phenylenebis(amino)]dichloroethene; 2-[(1,2)-Phenylenebis(amino)]dichloroethene; and Phen</p>

2-Thiohydantoin is an organic compound that has been structurally characterized. The molecule is planar with a shape that can be described as a chair with both arms. It has been shown to have some interesting biological properties, including the ability to inhibit bowel disease and cancerous growths. 2-Thiohydantoin was also found to be an effective inhibitor of the mitochondrial membrane potential in rats and mice, suggesting it may work by inhibiting mitochondria. 2-Thiohydantoin has also been shown to increase the formation of hydrogen fluoride and other reactive oxygen species, which may contribute to its anti-bacterial activity.

3,3,3-Trifluoropropane-1,2-diamine dihydrochloride is a high quality chemical that belongs to the group of useful building blocks. It is a versatile and complex compound that can be used in research or as a reagent. 3,3,3-Trifluoropropane-1,2-diamine dihydrochloride is also a reaction component for the synthesis of other compounds. This compound has been used as an intermediate for the production of pharmaceuticals and pesticides. It has been studied for its ability to inhibit protein kinase C (PKC) and calcium ion channels.

<p>3-(Trifluoromethyl)phenylacetone is a chiral iminium-type organocatalyst that is used in asymmetric organic reactions. This compound has been shown to be effective for the synthesis of chiral amines and hydroxyl groups, as well as biotransformations. 3-(Trifluoromethyl)phenylacetone binds to substrates through hydrogen bonding, steric interactions, and electrostatic interactions. It also has a high affinity for hydroxides and isosteres. 3-(Trifluoromethyl)phenylacetone can be used as an alternative to L-proline in certain biotransformations because it binds more tightly to the enzyme than L-proline does.</p>

4-Aminobutan-2-one hydrochloride is a β-unsaturated compound that can be synthesized by the condensation of methyl ketone and sulfide. This reaction converts the carbonyl group to an aminoketone group. The isomers of 4-aminobutan-2-one hydrochloride include 3,4-dimethylketone and 2,3,5,6-tetramethylketone. 4-Aminobutan-2-one hydrochloride can be used as a precursor for nitriles and sulfur compounds. It also selectively reacts with sodium sulfide in water to produce cyanoacetate or with sodium hydroxide to produce hydrogen cyanide and sulfides.