Composés apparentés aux enzymes, aux peptides et aux protéines

<p>Serotonin receptor 5-HT2C agonist</p>

<p>Proton pump inhibitor; anti-ulcer</p>

<p>5,6-Diamino-1,3-dimethyl uracil hydrate is a purine derivative that inhibits the growth of cancer cells by blocking the enzyme ribonucleotide reductase. This leads to a decrease in DNA synthesis, protein synthesis, and cell division. The anticancer activity of 5,6-Diamino-1,3-dimethyl uracil hydrate is due to its ability to inhibit the formation of ATP and the GTP cycle. It also has a potent inhibitory effect on the structural analysis of DNA and RNA. 5,6-Diamino-1,3-dimethyl uracil hydrate has been shown to produce apoptotic effects in many types of cancer cells. This drug also has specific agonist properties for G protein coupled receptors that are responsible for activating apoptosis.</p>

<p>Imipramine N-oxide hydrate is a polymer drug that belongs to the group of amines. It inhibits the activity of CYP450 enzymes and has been shown to be effective in treating inflammatory bowel disease (IBD). Imipramine N-oxide hydrate prevents adenosine A3 receptor activation and suppresses the production of dinucleotide phosphate, which may be responsible for its effectiveness in treating IBD. Imipramine N-oxide hydrate also has an effect on liver cells, which may lead to its effectiveness in treating infectious diseases. The drug is not active against autoimmune diseases, but it may have an effect on toll-like receptors.</p>

<p>Morantel citrate is a drug that belongs to the class of anthelmintics. It works by inhibiting the membrane system in nematodes, which leads to paralysis and death. Morantel citrate has been shown to be effective against Ostertagia ostertagi, Ancylostoma caninum, and Uncinaria stenocephala. Morantel citrate is not active against nematode species that are resistant to anthelmintics (e.g., Ascaris suum). The oral dose of morantel citrate for cattle is 0.5-1 mg/kg and for sheep 1-2 mg/kg body weight. This drug is poorly absorbed from the gastrointestinal tract and only about 10% of the dose reaches systemic circulation. Morantel citrate is metabolized in the liver by cytochrome P450 enzymes and excreted in urine as metabolites or unchanged drug.</p>

<p>Dopamine (D2 and D3) receptor agonist; has anti-parkinson effects</p>

<p>Zinc dihydrogen phosphate dihydrate is a white crystalline solid that is an inorganic acid. It is soluble in water and has a low solubility in organic solvents. The zinc salt of the compound reacts with magnesium to form a precipitate. Zinc dihydrogen phosphate dihydrate can be prepared by reacting ethylene diamine with sodium hydroxide solution, which forms zinc hydroxide and hydrogen phosphate ions. This reaction can also be done by adding potassium dichromate to copper chloride or metal hydroxides. The analytical method for this compound involves the use of sodium citrate, hydrochloric acid, and sodium carbonate.</p>

<p>Amfenac sodium salt hydrate is a nonsteroidal anti-inflammatory drug that inhibits prostaglandin synthesis. It has been shown to have minimal toxicity and inhibit the production of PGE2 in vitro. Amfenac sodium salt hydrate has also been shown to have anti-inflammatory properties in vivo, as it was able to inhibit bowel disease in rats. Amfenac sodium salt hydrate also has a protective effect against mitochondrial membrane depolarization in basic fibroblasts, which may be due to its ability to maintain levels of ATP.</p>

<p>L-Serine beta-lactone tetrafluoroborate salt is a fine chemical that is used as a reagent, complex compound and building block in the synthesis of other compounds. It is also an important intermediate for the production of pharmaceuticals and agrochemicals. L-Serine beta-lactone tetrafluoroborate salt has been shown to be a versatile building block in organic synthesis. This product may react with acids to produce hydrogen fluoride gas, which can cause injury or death through inhalation or contact with skin, eyes or clothing.</p>

<p>Hexadentate chelator</p>

<p>Dimethylglyoxime is a pesticide that has been used to control insects and nematodes. It has been found to be effective in controlling mosquitoes, flies, and other pests. This compound is also used as an extractor in microextraction. Dimethylglyoxime is not toxic to humans and does not cause any adverse effects on the environment or human health. It can be used with chlorine for wastewater treatment.</p>

<p>Estrogen receptor modulator</p>

<p>Glycocholic acid sodium salt monohydrate is a compound that is used in the production of pharmaceuticals, agrochemicals, and other organic chemicals. It is also used as an intermediate to produce carboxylic acids, amino acids, and other building blocks. Glycocholic acid sodium salt monohydrate is soluble in water and has a high boiling point. It can be used for reactions with alcohols and amines to form esters or amides respectively. This compound can be used as a reagent for the synthesis of peptides, proteins, carbohydrates, and nucleosides. Glycocholic acid sodium salt monohydrate has been shown to have anti-inflammatory properties by inhibiting prostaglandin biosynthesis.</p>

<p>Please enquire for more information about rec IL-2 (human) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Kisspeptin-10 is a peptide hormone that belongs to the family of kisspeptins. It is an intracellular regulator of calcium, which plays an important role in the regulation of cell growth and differentiation. The effect of kisspeptin-10 on cytosolic calcium levels can be used as a potential drug target for cancer treatment. It has been shown that kisspeptin-10 inhibits ovarian activity by reducing the production of luteinizing hormone (LH) and follicle stimulating hormone (FSH). Kisspeptin-10 also regulates bone metabolism by inhibiting osteoblasts and promoting osteoclasts, leading to increased bone resorption.</p>

<p>Ghrelin is a peptide hormone that regulates appetite and has been shown to have potent anti-cachectic effects in animal models. It is thought to be an important regulator of body weight, insulin resistance, and metabolism. Ghrelin is synthesized in the stomach and released into the bloodstream when the stomach is empty. Ghrelin binds to ghrelin receptors in the hypothalamus, which stimulate growth hormone release from the pituitary gland. This hormone also binds to other cells in the hypothalamus, such as neurons that produce orexin, which may account for its effects on sleep patterns. Ghrelin has been shown to inhibit tumor growth by suppressing angiogenesis and inducing apoptosis. The molecular weight of ghrelin is 3497 Da. The sequence of ghrelin consists of 28 amino acids: Gly-Ser-Ser(octanoyl)-Phe-Leu-Ser-Pro-Glu-His-Gln-Lys-Ala</p>

<p>Alkaloid with anti-tumoral activity</p>

<p>1,1'-Dioctadecyl-3,3,3',3'-tetramethylindodicarbocyanine perchlorate (DiI) is a useful scaffold for the synthesis of complex compounds. It is a high-quality research chemical that is used in the synthesis of speciality chemicals and fine chemicals. DiI reacts with diazonium salts to produce blue or red fluorescent compounds. This compound can be used as a reagent for the production of amino acids or amines. It also reacts with other organic compounds to form complexes. The CAS number for DiI is 127274-91-3.</p>

<p>o-Phenanthroline monohydrochloride monohydrate is a ligand that is used in crystallography to study the crystal structure of metal ions. It has been shown to be an efficient catalyst for the ring-opening of chloroformates, and can also be used as an analytical reagent that is capable of detecting chlorine in organic compounds. The hydrate form of o-phenanthroline monohydrochloride has a molecular formula of C12H14ClN3O4·2H2O and a molecular weight of 392.7 g/mol.</p>

<p>N-Ethyl-N-(2-hydroxy-3-sulfopropyl)-3-methylaniline sodium salt dihydrate (NMS) is a functional group with a side effect profile that is characterized by low incidence of adverse events. This drug has been shown to be well tolerated in clinical use, and there is evidence that it may be useful for the treatment of infectious diseases. Clinical studies have demonstrated that NMS can improve fatty acid and cholesterol levels, as well as reducing carnitine palmitoyltransferase activity. These effects are due to the inhibition of lipoprotein lipase, cholesterol esterase and carnitine palmitoyltransferase enzymes. In addition, NMS has been shown to be effective against dermatitis caused by atopic dermatitis or psoriasis.</p>