Haletos orgânicos

<p>3,5-Dichlorobenzenesulphonyl chloride (3,5-DCBS) is a halogenated aromatic compound that can be synthesized by the debromination of 3,5-dichlorobenzene with hydrobromic acid. This compound has been shown to have anticancer activity against cell lines derived from human breast cancer, prostate cancer, and other cancers. It also has potent anticancer activity against tumor cells in animals. The anticancer activity of 3,5-DCBS is due to its ability to inhibit DNA synthesis and to induce apoptosis. 3,5-DCBS may act as an anti-inflammatory agent through inhibition of prostaglandin synthesis.</p>

<p>Please enquire for more information about pTH (1-84) (rat) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>PAR-2 (6-1) amide is a proteolytic enzyme that is activated by inflammatory stimuli. It has been shown to be a major contributor to the pathogenesis of inflammatory bowel disease, and is found in neurons, the bowel, and pancreatic acinar cells. PAR-2 (6-1) amide activates proteases such as trypsin and chymotrypsin and also functions as an antimicrobial peptide. Activation of PAR-2 (6-1) amide leads to the cleavage of proteins at specific sites on their amino acid chains. This cleavage can lead to changes in protein conformation or function. PAR-2 (6-1) amide has been shown to increase endothelial cell proliferation and inhibit bacterial growth, but does not have any effect on cultured normal human skin fibroblasts.</p>

<p>Please enquire for more information about Anti-Kentsin trifluoroacetate salt 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 Fmoc-L-Lys[Oct-(otBu)-Glu-(otBu)-AEEA-AEEA]-OH 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 4-Chlorophenyl-2-pyridinylmethanol 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 Intermedin-53 (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Glu(Glu(Glu-OH)-OH)-OH trifluoroacetate salt is a casein that is used as a model system for pancreatic β-cells. It has been shown to induce cell apoptosis in malignant cells and sequences that are associated with the development of pancreatic cancer. H-Glu(Glu(Glu-OH)-OH)-OH trifluoroacetate salt also induces endothelial cell proliferation and decreases cell function, which may be due to its ability to promote uptake of this compound.</p>

<p>H-Ser-Ile-Gly-Ser-Leu-Ala-Lys-OH trifluoroacetate salt is a recombinant, fluorescent, hydrazide, labile protein that has been synthesized with a murine amino acid sequence. This protein has been shown to be reactive with the cytokine IL2 and can be used for labeling of cells or proteins in cytometric analysis. The N-terminal end of this protein is acidic, allowing for it to react with periodate or hydroxylamine for tagging purposes.</p>

<p>Please enquire for more information about 6-Fluoro-3,4-Pyridinediamine 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 trans-4-Hydroxy-D-proline hydrochloride 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 Z-Leu-Glu(OMe)-Thr-DL-Asp(OMe)-fluoromethylketone including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Tribromomethyl phenyl sulfone is an alkylthio compound that has a cyclohexane ring and a hydroxy group. Tribromomethyl phenyl sulfone has high resistance to thermal expansion, hydrolysis, and radiation. It reacts with silver ions to form bromophenyl silver ion. This molecule can be formed through the reaction of diphenyl ether with hydrogen sulfide in the presence of light, or by the reaction of benzene with sodium hydroxide in the presence of light. Tribromomethyl phenyl sulfone is used as a stabilizer for plastics and other organic materials, as well as an antioxidant for rubber products.</p>

<p>3-Chloro-4-(3-fluorobenzyloxy)aniline is a potent inhibitor of the epidermal growth factor receptor (EGFR), which is a tyrosine kinase that plays an important role in the initiation and progression of cancer. The compound has been shown to inhibit the proliferation of human cancer cell lines, such as breast cancer and prostate cancer, by blocking EGFR signaling. 3-Chloro-4-(3-fluorobenzyloxy)aniline also inhibits the activity of other kinases, such as lapatinib and 2-amino-4-fluorobenzoic acid. This inhibition may be due to its ability to bind to the ATP binding site on these enzymes.</p>

<p>Please enquire for more information about Acetyl-(D-Phe2)-GRF (1-29) amide (human) trifluoroacetate salt 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 Z-Val-Asp(OMe)-Val-Ala-DL-Asp(OMe)-fluoromethylketone including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-D-Ser-OBzl hydrochloride salt is a monoclonal antibody that inhibits the activity of an enzyme called fatty acid synthase (FAS). It also binds to glycoconjugates, which are molecules that are involved in the inflammatory response. H-D-Ser-OBzl hydrochloride salt is used to treat various types of inflammatory diseases, such as arthritis and Crohn's disease. H-D-Ser-OBzl hydrochloride salt has been shown to inhibit tumor cell growth by binding to an enzyme called fatty acid synthase. H-D-Ser-OBzl hydrochloride salt also inhibits the production of inflammatory mediators, such as prostaglandins, leukotrienes and thromboxanes. The antiinflammatory effect of this drug may be due to its ability to inhibit prostaglandin synthesis.</p>

<p>N-[4-(2-Bromoacetyl)phenyl]methanesulfonamide is a chiral biocatalytic agent, which is synthesized by chemoenzymatic or enzymatic reactions. It has been used in enantioselective synthesis of 4-aminoacetophenone and as an antiarrhythmic agent. This compound is not active against bacterial infections.</p>

<p>Please enquire for more information about (D-Trp8)-Somatostatin-14 trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Bromo-6-chlorophenol is a reactive, thiourea-containing compound that undergoes catalytic reactions. 2-Bromo-6-chlorophenol reacts with sulfate in water to form chlorine radicals, which react with other organic compounds to produce chlorinated organic compounds. This reaction can be used for the oxidation of phenols and alcohols to yield chlorinated products. The yields of this process depend on the concentration of acetonitrile used in the reaction. Acetonitrile is also required for the conversion of dichlorinated benzenes to brominated products.</p>

<p>2-Chloro-5-iodopyridine is a synthetic compound that binds to nicotinic acetylcholine receptors, and is an agonist of these receptors. It has been shown to bind selectively to the alpha4beta2 subtype of these receptors. 2-Chloro-5-iodopyridine binds to the receptor by means of hydrogen bonding and chelation, which results in the activation of the receptor. This process leads to increased levels of catecholamines and other neurotransmitters, which causes changes in the heart rate and blood pressure. 2-Chloro-5-iodopyridine is a halogenated organic molecule that can be synthesized from sodium trifluoroacetate in two steps: first with chlorination followed by iodination. The synthesis can be carried out using copper (II) chloride as a catalyst or copper (I) iodide as an oxidant, followed by reduction with sodium borohydride.</p>

<p>Please enquire for more information about Mca-Pro-Leu-Ala-Nva-Dap (Dnp)-Ala-Arg-NH2 trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Bromopyridazine is a dechlorinated derivative of pyridazine that has been used as an agrochemical. 3-Bromopyridazine can be synthesized by aminocarbonylation at the 3-position, which is a nucleophilic substitution reaction. It has been shown to yield high yields and to react with nucleophiles such as chlorine or heterocycles such as cinnoline. 3-Bromopyridazine can also be obtained by cross coupling of 2-bromoacetophenone with benzaldehyde and pyridine in the presence of copper. The resulting product is then reacted with sodium nitrite in hydrochloric acid to produce 3-bromopyridazine. This compound may have potential use as a chemical intermediate for other compounds, due to its chemical stability and its ability to undergo cross coupling reactions.</p>

<p>Please enquire for more information about (D-Arg6,Asn10)-MCH (6-16) amide (human, mouse, rat) trifluoroacetate salt 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 3-Methylpentyl chloroformate 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 AQEE-30 (human) trifluoroacetate salt 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 Preptin (human) trifluoroacetate salt 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 Acetyl-(D-Phe2,Lys15,Arg16,Leu27)-VIP (1-7)-GRF (8-27) trifluoroacetate salt 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 Neuromedin U-25 (porcine) trifluoroacetate salt 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 TIMP-2 (145-168) (human, bovine) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>c4-Ethyl-2,3-dioxo-piperazine carbonyl chloride is a chloroformate that is used in the synthesis of carbamates. It is used in the production of triphosgene, which is an intermediate for the production of herbicides and pesticides. The impurities found in this substance are n-hexane, flow rate, chloride, chloroformate and solvents. This product can be synthesized by reacting c4-ethyl-2,3-dioxopiperazine with carbon tetrachloride. The reaction time required to produce this product is 2 hours at a temperature between 100°C and 150°C. The optimum pH range for the reaction is 8 - 10.</p>

<p>Amyloid beta-Protein (1-16) trifluoroacetate salt is a modified form of amyloid beta protein. It is synthesized by the modification of amino acids with trifluoroacetic acid and can be used to study the pathogenesis of Alzheimer's disease. Amyloid beta-Protein (1-16) trifluoroacetate salt has been shown to bind to β-amyloid, which is thought to be the main component of plaques in Alzheimer's disease. This binding inhibits the formation of β-amyloid aggregates, which are associated with neurotoxicity and neuronal cell death.</p>

<p>Chlorimuron-ethyl is a herbicide belonging to the class of pyrazole compounds. It inhibits plant growth by interfering with photosynthesis and chlorophyll synthesis. Chlorimuron-ethyl can be used in wastewater treatment, as well as applications to grow crops such as soybeans. The compound has been shown to have a sublethal effect on myeloma cells in vitro and has been shown to be an effective antimetastatic agent in vivo.</p>

<p>Nortropinone hydrochloride is a molecule with a pyridinium moiety. It is an antifertility agent that blocks the synthesis of serotonin, a neurotransmitter involved in mood, appetite, and sleep. Nortropinone hydrochloride has been shown to be very effective in the treatment of depression and cancer. Nortropinone hydrochloride also inhibits protein inhibitors such as monoamine reuptake and glutamate receptor subtypes.</p>

<p>Please enquire for more information about M65 trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Luteinizing Hormone-Releasing Hormone Antagonist trifluoroacetate salt is a potent antagonist of the luteinizing hormone-releasing hormone (LHRH) receptor. It is used specifically to treat platinum-resistant ovarian cancer, where it has been shown to be effective in reducing tumor size and volume. This drug has minimal toxicity and can be administered by injection or as a microcapsule. LHRH Antagonist trifluoroacetate salt is an analog of LHRH that has been modified so that it cannot cross the blood-brain barrier. It also binds to epidermal growth factor receptors, which are involved in cell proliferation, differentiation, and survival. Symptoms of overdose may include nausea, vomiting, headache, dizziness, seizures, and coma.</p>

<p>Please enquire for more information about H-Glu-Leu-Asp-[(2R,4S,5S)-5-amino-4-hydroxy-2,7-dimethyl-octanoyl]-Val-Glu-Phe-Gly-Gly-D-Arg-D-Arg-D-Arg-D-Arg-D-Arg-D-Arg-D-Arg-D-A rg-D-Arg-OH trifluoroacetate salt 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 BNP-45 (mouse) trifluoroacetate salt 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 Prion Protein (118-135) (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Trifluoromethyl phenylhydrazine HCl is a fine chemical that can be used as a versatile building block in the synthesis of complex compounds. It has been shown to be a useful intermediate for the preparation of research chemicals, reaction components and speciality chemicals. 3-Trifluoromethyl phenylhydrazine HCl belongs to CAS No. 3107-33-3 and can be used as a reagent in organic synthesis. The compound is high quality with a purity of over 99%.</p>

<p>3-Bromo-4-chloroaniline is a chloroaniline compound. It is synthesized by reacting hexamethylenetetramine with chlorine gas in the presence of formaldehyde and paraformaldehyde. 3-Bromo-4-chloroaniline has been used to produce other compounds, such as trimethylchlorosilane, which is used in the production of silicone rubber. Chloroanilines are toxic chemicals that can be found in the environment and react with formaldehyde to produce carcinogenic substances called halofuginones.</p>

<p>Please enquire for more information about (1S,4S)-2-Oxa-5-azabicyclo[2.2.1]heptane hydrochloride 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 Neuronostatin-13 (human, canine, porcine) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>H-Leu-Met-NH2 is a catecholamine that is found in the central nervous system and functions as a neurotransmitter. It has been shown to induce contractile response when injected into the carotid artery, with a maximal effect at doses of 0.5-5 mg/kg. The effect of H-Leu-Met-NH2 on cardiovascular function has not been studied. Catecholamines are also involved in other physiological processes, including regulation of blood pressure and respiration. This compound was originally isolated from adrenal glands and is found in plants such as beans and peas. The structure of this compound can be described as an h-leu-[met]-amide with a hydrochloride salt at the c-terminus.</p>

<p>Please enquire for more information about 3-Bromo-6-methylpicolinic acid 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 4-bromo-5-chloro-2-fluorobenzoic Acid 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 Ac-Arg-Cys-Met-5-aminopentanoyl-Arg-Val-Tyr-5-aminopentanoyl-Cys-NH2 trifluoroacetate salt (Disulfide bond) 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 Galacto-RGD trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>O-Ethoxybenzoyl chloride is a pesticide that belongs to the group of sildenafil. It inhibits the activity of prolyl endopeptidase, an enzyme that degrades the peptide hormone vasoactive intestinal polypeptide (VIP). This inhibition prevents degradation of VIP, which is important for the regulation of blood vessel tone. The compound has been shown to be effective against Sclerotinia sclerotiorum and Claviceps purpurea. O-Ethoxybenzoyl chloride has been shown to have a high level of tolerance in plants and animals. It also has been found to be safe for humans with its low toxicity levels and low acute toxicity. It is not classified as hazardous by the World Health Organization (WHO).</p>

<p>Please enquire for more information about Somatostatin-14 (7-14) trifluoroacetate salt 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 H-Arg(Pbf)-2-chlorotrityl resin (100-200 mesh) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Chloro-4-iodopyridine is an antibacterial agent that inhibits bacterial growth by interfering with the synthesis of folic acid. It has been shown to be effective against Escherichia coli, Staphylococcus aureus, and Pseudomonas aeruginosa. 2-Chloro-4-iodopyridine is a ligand that binds to metal ions such as copper and silver. The transfer of electrons from the metal ion to the ligand facilitates the cross-coupling reaction in organic synthesis. Cross-coupling reactions are also used in devices such as solar cells and hydrogen fuel cells.<br>2-Chloro-4-iodopyridine can also be used for photophysical experiments with single crystal x-ray diffraction studies.</p>

<p>Please enquire for more information about Met-RANTES (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>MeOSuc-Ala-Ala-Pro-Val-chloromethylketone is a serine protease inhibitor that has been shown to be effective against influenza virus and HIV. It was found to be active against a number of serine proteases, such as trypsin, chymotrypsin, and elastase. MeOSuc-Ala-Ala-Pro-Val-chloromethylketone also has chemotactic activity in thp1 cells and lung fibroblasts. It is activated by the addition of water and has been shown to inhibit the growth of soybean trypsin. However, it does not have any effect on human trypsin.</p>

<p>Trimeperidine hydrochloride is a postoperative analgesic that is used in the treatment of nerve pain and other conditions. Trimeperidine hydrochloride belongs to the group of active substances. It has been shown to be effective as an epidural anesthesia for patients undergoing surgery and has a clinical effect on the nervous system, including pain, nausea, vomiting, and muscle spasms. Trimeperidine hydrochloride works by inhibiting the central nervous system (CNS) enzyme coagulation factor XIIa. It also prevents excessive release of neurotransmitters from nerve cells.br&gt;br&gt;</p>

<p>1-Dodecylpyridinium Chloride is a quaternary ammonium salt that is used as an antimicrobial agent in a variety of products, such as pharmaceuticals, cosmetics, and household products. It has been shown to be toxic to humans at doses above 0.5 mg/kg. At sublethal doses, 1-dodecylpyridinium chloride inhibits the growth of bacteria by binding to the cationic sites on their cell surfaces and preventing them from attaching to other cells or molecules in their environment. 1-Dodecylpyridinium chloride also binds to the enzyme p-nitrophenyl phosphate reductase, which is required for bacterial growth. This inhibition leads to cell death by preventing ATP production and protein synthesis.</p>

<p>Please enquire for more information about 4-Bromo-3-methoxypyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Poly(tetrafluoroethylene-co-perfluoro(propylvinyl ether)) is a multilayer, unsaturated, vinylidene polymer. It has an impermeability that is similar to polytetrafluoroethylene (PTFE), but with improved mechanical properties. Poly(tetrafluoroethylene-co-perfluoro(propylvinyl ether)) can be used as a coating on surfaces that are exposed to chemical substances or in food packaging. This material is also used in the production of laminated products and copolymers.</p>

<p>Please enquire for more information about PAR-2 (6-1) amide (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>VIP is a potent vasoactive neuropeptide that is found in the heart, brain, and gut. It has been shown to be a potent inhibitor of guanethidine-induced contractions in the femoral vein, as well as atrial contractions. VIP also inhibits spontaneous contractions in the fundic region of the stomach and intestinal motility. VIP has been shown to inhibit vasoactive intestinal polypeptide-induced contractions in isolated rat ileum. VIP is expressed primarily in the enteric nervous system and throughout the gastrointestinal tract.</p>

<p>Please enquire for more information about Ac-Val-Glu-His-Asp-AFC trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Bromo-2-methoxyphenyl)acetic acid (BMPEA) is a hydroxylated derivative of aspartic acid. It has been shown to induce apoptotic cell death in various cell lines, including human lung cells and rat hippocampal cells. BMPEA is synthesized by the solid-phase method and is characterized by a constant structure. It can be used to treat degenerative diseases and other conditions where apoptosis is desirable, such as Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, retinitis pigmentosa, and Duchenne muscular dystrophy.</p>

<p>4-Bromo-2-methylthiophene is a linker that is used in the synthesis of metal carbonyls. It has been shown to be an efficient cross-linking agent for the preparation of polymers. 4-Bromo-2-methylthiophene can be isomerized to 2,5-dimethylthiophene by heating it with hydroxylamine. 4-Bromo-2-methylthiophene can also catalyze the alkylation of nucleophiles such as ammonia and dimethyl sulfate, as well as nucleophilic attack on carboxylic acid derivatives. This compound is acidic, due to its chloride substituent, which can react with basic groups such as hydroxyl groups or amines.</p>

<p>Please enquire for more information about H-Ile-2-chlorotrityl resin (200-400 mesh) 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 Thymosin alpha1 trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Osteostatin is a recombinant human protein that inhibits bone growth by binding to and neutralizing the effect of forskolin. Osteostatin also has an inhibitory effect on cancer cells, as it inhibits mitochondrial pathways and prevents the activation of factor receptors. Osteostatin blocks the synthesis of cAMP, which is necessary for cell proliferation in cancer cells. The inhibition of cAMP levels leads to a decrease in the production of proteins that stimulate bone growth, such as runx2.</p>

<p>Please enquire for more information about Biotinyl-5-aminopentanoyl-Antennapedia Homeobox (43-58) amide trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Fibrinopeptide A is a peptide that is released from the fibrinolysis of fibrinogen. It can be used as a blood marker for the diagnosis of bowel disease and primary pulmonary hypertension, but not for other diseases such as infectious diseases. Fibrinopeptide A has been shown to be an effective model system for studying thrombin-mediated fibrin polymerization in vitro. This drug also can be used as a tool for investigating the disulfide bond in fibrinogen.</p>

<p>4-Fluoropyrazole is a synthetic chemical that can be prepared by the transfer of fluorine from chloroformate to an isoxazole. It has been shown that 4-fluoropyrazole can be synthesized in high yields and with good functional groups, as well as being stable to air and moisture. The reaction takes place spontaneously at low temperatures, which makes it an attractive candidate for industrial production. The chemical crystallizes in the form of a trimerization product. The proton functioned group was not observed due to its instability. This compound has a chlorine atom attached to a pyrazole ring.</p>

<p>Please enquire for more information about Amyloid b-Protein (6-20) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(1,3-Benzodioxol-5-yl)-4,6-bis(trichloromethyl)-1,3,5-triazine is a triazine compound that contains a hydroxyl group and a carboxylic acid. It is used as a polymerization initiator for cationic polymerization. 2-(1,3-Benzodioxol-5-yl)-4,6-bis(trichloromethyl)-1,3,5-triazine is also used as a chemical treatment for water supplies and wastewater. This compound can absorb many organic compounds that are harmful to the environment such as pesticides and herbicides. 2-(1,3-Benzodioxol-5-yl)-4,6-bis(trichloromethyl)-1,3,5-triazine has been shown to function as an antiinflammatory agent through its hydrogen bonding properties.</p>

<p>H-D-Ala-Leu-Lys-AMC hydrochloride salt is a zymogen that is the substrate for tissue plasminogen activator (tPA). It has been shown to inhibit the activity of fibrinogen and thrombin, two proteins involved in coagulation. H-D-Ala-Leu-Lys-AMC hydrochloride salt also inhibits the hydrolysis of fibrin clots by serine proteases and prevents the formation of new clots by inhibiting the activation of annexin. This drug has been shown to be effective in animal models with established atherosclerosis.</p>

<p>Please enquire for more information about (Gln11)-Amyloid b-Protein (1-28) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Amino-5-chloro-N,3-dimethylbenzamide is a synthetic compound. It has been shown to induce necrotic cell death in mammalian cells. This compound was synthesized by the reaction of 2-aminoquinoline with a Grignard reagent, followed by nitration of the resultant amine. The synthesis of this compound was thermodynamically favorable and exhibited good solubility in water. The chlorantraniliprole and anthranilic acid moieties are activated with an acylation reaction, which allows them to bind to the ryanodine receptor and inhibit calcium release from the sarcoplasmic reticulum (SR) with ammonolysis. This inhibition leads to ferroptosis, a type of programmed necrosis.</p>

<p>3-Bromobenzonitrile is an organic compound that has a hydroxyl group and a bromine atom. It is an organic chemical compound that can be synthesized by the reaction of benzene with nitric acid and azide. 3-Bromobenzonitrile has been studied for its biological properties. It also reacts with amines, quinoline derivatives, and other reactive molecules to form new compounds. 3-Bromobenzonitrile has been shown to have transport properties, which can be determined using FT-IR spectroscopy techniques.</p>

<p>2-Chlorophenyl)diphenylmethanol is an antifungal drug that blocks the function of a calcium ionophore in fungal cells. It has been shown to be effective against a variety of filamentous fungi, including Aspergillus fumigatus, Candida albicans, and Trichosporon cutaneum. This drug is used as a topical antifungal agent for treatment of skin infections caused by these fungi. 2-Chlorophenyl)diphenylmethanol has been shown to have anti-inflammatory properties in animal models of kidney fibrosis and cell binding. Clinical data suggests that it can be used for the prevention or treatment of stem cell transplantation complications such as graft versus host disease and leukemia.</p>

<p>Please enquire for more information about (His(3-Me)2)-LHRH trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Cyclobutanesulfonyl chloride is a reagent that is used for the synthesis of 1-6-alkylcyclobutanes. It can be used to synthesize heterocyclic compounds, including those with high optical purity. Cyclobutanesulfonyl chloride has been shown to have antiviral and antiproliferative properties. It has also been shown to exhibit anticancer activity in vitro and in vivo. The mechanism of action for this compound is unclear, but it may inhibit protein synthesis by attacking the amino acid methionine in proteins or by inhibiting DNA replication.</p>

<p>Please enquire for more information about (Pen 5)-Urotensin II (4-11) (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Apelin-13 is a peptide hormone that is involved in the regulation of cardiovascular, respiratory and gastrointestinal functions. It has been shown to stimulate receptor activity and pain sensitivity in animal models. Apelin-13 has been shown to act as an opioid receptor agonist, meaning that it binds to the opioid receptors and activates them. This activation leads to an increase in the production of growth factors and matrix metalloproteinases, which are proteins that break down collagen and other substances in the body. The increased production of these substances can lead to inflammation and tissue destruction. Apelin-13 also interacts with several other receptors including CB2 (a cannabinoid receptor), GPCR (a G protein-coupled receptor), CRHR1 (a corticotropin releasing hormone receptor 1) and Naloxone (an opioid antagonist).</p>

<p>Please enquire for more information about H-Val-Tyr-Ser-betaNA hydrochloride salt 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 2-[Chloro(4-chlorophenyl)methyl]-pyridine 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 Suc-Ala-Ala-Pro-Phe-2,4-difluoroanilide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Neuromedin B is a peptide hormone that is produced by the hypothalamus and regulates many physiological processes such as energy metabolism, appetite, and sleep. Neuromedin B is a member of the family of guanine nucleotide-binding proteins (G proteins) that bind to G protein-coupled receptors on the surface of cells. It has been shown to stimulate calcium release from intracellular stores in response to an increase in cytosolic Ca2+. Neuromedin B has been shown to have anti-inflammatory effects on infectious diseases such as meningitis, sepsis, and tuberculosis, which may be due to its ability to inhibit neutrophil migration. Neuromedin B also stimulates hippocampal formation activity in rats during the rotarod test, which may be due to its effects on dopamine release.</p>

<p>Please enquire for more information about LIP2 (human) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>A component of Conus venom; antagonist of nicotinic acetylcholine receptors</p>

<p>3,4-Dichloroisocoumarin is an organic compound that has been shown to be a potent inhibitor of nuclear DNA polymerase. It has been shown to be a potential drug target for cancer treatment due to its ability to inhibit the polymerase chain reaction (PCR) and interfere with DNA replication. 3,4-Dichloroisocoumarin has also been shown to have reactive properties, which may lead to cell death by damaging cellular components such as proteins and lipids. The enzyme activity of 3,4-Dichloroisocoumarin is unknown. However, it is thought that the inhibition of DNA synthesis by this compound may be due to its ability to bind DNA in a manner that prevents transcription or replication.</p>

<p>Please enquire for more information about Fluorescein-6-carbonyl-Val-Glu(OMe)-Ile-DL-Asp(OMe)-fluoromethylketone 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 pTH-Related Protein (1-40) (human, mouse, rat) trifluoroacetate salt 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 VIP sulfoxide (human, mouse, rat) trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Benzyltributylammonium chloride is a quaternary ammonium salt that is used as a surfactant. It is commercially available in the form of its sodium salt, which is prepared by the reaction of benzyltriethylamine with trifluoroacetic acid and sodium carbonate. The surface methodology used to characterize the adsorption properties of this compound was Langmuir adsorption isotherms. The optimum concentration for this compound was found to be 0.05 M at 25°C, where it exhibits surface adsorption kinetics at a rate of 1.1 x 10-4 mol/cm2/s. Benzyltributylammonium chloride has strong hydroxyl groups, which gives it an affinity for water molecules and makes it an excellent surfactant for use in detergent formulations. It also chelates metal ions such as chloride and metal ions (e.g., zinc) that are present in hard</p>

<p>Histidine is a non-essential amino acid that has been shown to be involved in the regulation of cell growth and differentiation. It is also involved in the biosynthesis of nucleotides, collagen, and carnitine. Kinetic studies on histidine have been done by acetylation of histidine with acetic anhydride and pyridine. The kinetic method used was based on the reaction between histidine and p-nitrophenyl phosphate. The transfer reactions were performed with a strain containing lysine residues which were then adsorbed onto a surface-enhanced Raman spectroscopy (SERS) substrate. These experiments were performed using techniques such as resonance mass spectrometry (RMS), surface-enhanced Raman spectroscopy (SERS), and protonation selective mass spectrometry (PSMS).</p>

<p>The trifluorophenylboronic acid is a boronic acid that has been used in the synthesis of vitamin B12. This compound is often used as a catalyst for the Suzuki coupling reaction. It can also be used to synthesize amides and synthons. The trifluorophenylboronic acid is soluble in water, ethanol, and acetone. The pH of the solution depends on the type of base added. For example, when an amine is added to the solution, it increases to approximately 8-9. When a p-hydroxybenzoic acid is added to the solution, it decreases to approximately 2-3.</p>

<p>3,5-Bis(trifluoromethyl)phenylacetonitrile (3,5-BTFAPN) is a compound that has anticancer activity. It can be used to treat cancer by inhibiting the growth of cancer cells. 3,5-BTFAPN has been shown to be effective against some human cancer cell lines in vitro and in vivo. The drug was found to have cytotoxic effects by inducing apoptosis through changes in mitochondrial membrane potential and cytochrome c release. 3,5-BTFAPN also binds to DNA and forms adducts with guanine residues, which may explain its anticancer activity.</p>