APIs para pesquisa e impurezas

Please enquire for more information about Mezlocillin impurity III including the price, delivery time and more detailed product information at the technical inquiry form on this page

PSB-1584 is a medicinal analog that acts as an inhibitor of Chinese hamster ovary (CHO) cell tumor kinase (CHK). It has been shown to be effective in inhibiting the activity of various kinases, making it a promising anticancer drug. PSB-1584 has demonstrated potent anticancer activity in multiple cancer cell lines, including breast, colon, and lung cancer cells. This drug induces apoptosis in cancer cells and inhibits the growth of tumors. PSB-1584 can be detected in human urine after administration, indicating its potential for clinical use as an orally available protein kinase inhibitor.

Please enquire for more information about PDdEC-NB including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Benzyl (4-(4-(4-hydroxyphenyl)piperazin-1-yl)phenyl)carbamate including the price, delivery time and more detailed product information at the technical inquiry form on this page

N-Methyl-4-phenylpiperidine is a synthetic drug that acts as a stimulant. It is a structural analog of the neurotransmitter acetylcholine and has been shown to have similar effects in knockout mice. N-Methyl-4-phenylpiperidine is metabolized by hydrolysis of the amide group, leading to the formation of alphaprodine and hydroxyphenylacetic acid. This drug has been shown to inhibit dopamine and serotonin uptake in rats, which may be related to its psychostimulant effects. Clinical pharmacology studies have shown that this drug can increase blood pressure, heart rate, and respiration rates in humans.

Please enquire for more information about 7-Hydroxydibenz[b,f][1,4]oxazepin-11(10H)-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

MK-0249 is a potent inhibitor of hyaluronan-mediated tumor cell proliferation and migration. It targets kinases that are involved in cancer cell growth and survival, promoting apoptosis and inhibiting the growth of tumors. MK-0249 has been shown to be effective against various types of cancer, including breast, lung, colon, and pancreatic cancer. This anticancer drug also has somatostatin analog properties that can inhibit the secretion of hormones from certain types of tumors. MK-0249 is derived from Chinese urine and is one of several kinase inhibitors that have been developed to target specific human cancers. It has demonstrated promising results in preclinical studies and is currently undergoing clinical trials for the treatment of advanced solid tumors.

Unc-926 is a pluripotent stem cell (PSC) that can differentiate into cells from all three germ layers. Unc-926 cells have been shown to be glucose-dependent and utilize the mitochondrial respiratory chain for respiration. These cells are capable of differentiating into insulin-producing beta cells and pancreatic islet cells, which can be used in the treatment of diabetes.

4-Amino-1-[3,5-di-O-(4-chlorobenzoyl)-2-deoxy-α-D-ribofuranosyl]-1,3,5-triazin-2(1H)-one (4AAT) is an analytical chemical that is used for research and development purposes. 4AAT is a metabolite of the antibiotic ampicillin and has been identified as an impurity in the drug product. It can be synthesized from 2-(4'-chlorophenyl)benzaldehyde, 3,5'-di-O-(4'-chlorobenzoyl)-2',3'-dideoxyribose and sodium azide in a two step process with 98% purity. 4AATs are also found to be present in natural products such as honey or sugar cane juice.

Please enquire for more information about 16α-Methyl clobetasone butyrate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Gemcitabine diphosphate triethylamine salt is an inhibitor that has been shown to be effective in the treatment of various forms of cancer. It works by inhibiting the activity of kinases, which are enzymes involved in the regulation of cell growth and division. Gemcitabine diphosphate triethylamine salt is a prodrug that is converted to its active form, gemcitabine, in vivo. This drug has been shown to inhibit the uptake of xylose by cancer cells, leading to decreased protein synthesis and induction of apoptosis. In addition, it has been found to be effective against human and Chinese medicinal tumor cells. Gemcitabine diphosphate triethylamine salt is a promising treatment option for patients with cancer who have not responded well to traditional chemotherapy or radiation therapy.

Please enquire for more information about 5-Hydroxydeferasirox including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about (S)-Cy-BINAP including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-(Hydrazinecarbonyl)pyridin-1-ium-1-olate is a medicinal compound that has been shown to have potent anticancer properties. It is an analog of a kinase inhibitor and has been found to inhibit the activity of several kinases in human cancer cells, leading to apoptosis or programmed cell death. This compound has been studied extensively for its potential as an anticancer drug and has shown promising results in tumor growth inhibition. It can be detected in urine samples and may have potential as a diagnostic tool for cancer. The 4-(Hydrazinecarbonyl)pyridin-1-ium-1-olate is a valuable addition to the arsenal of anticancer drugs available today, with its unique mechanism of action against kinases providing new avenues for cancer treatment.

Paritaprevir is a medicinal compound that acts as an inhibitor of protein kinases. It has been shown to be effective against various types of cancer cells, including those found in the urine and tumors. Paritaprevir is an analog of a Chinese anticancer compound and has been shown to induce apoptosis in human cancer cells. This potent kinase inhibitor selectively targets specific kinases involved in cancer cell proliferation, making it a promising candidate for the treatment of cancer. Its ability to inhibit kinases also makes it an attractive therapeutic option for other diseases that involve aberrant kinase activity.

Isoquinine is a potent compound with promising anticancer activity. It has been shown to have inhibitory activity against protein kinases, which are enzymes involved in the regulation of cell cycle and proliferation. Isoquinine can act as an inhibitor of kinase inhibitors, leading to a decrease in tumor growth and inducing apoptosis in tumor cells. In addition to its potential as an anticancer agent, Isoquinine has also shown antitumor activity against Alzheimer's disease. This compound is a carboxylic acid that can bind to specific targets within cells and inhibit their function, making it a promising candidate for future drug development. Its unique mechanism of action makes it an attractive target for further study and exploration.

Lactiflorin is a natural compound that has been found to have potent inhibitory effects on cancer cells. This medicinal plant extract is commonly used in Chinese traditional medicine as an anticancer agent. Lactiflorin has been shown to induce cell cycle arrest and promote apoptosis in human cancer cells by inhibiting the activity of protein kinases, which are essential for tumor growth and survival. Additionally, lactiflorin analogs have been developed with even greater potency against cancer cells. In preclinical studies, lactiflorin and its derivatives have demonstrated promising results as potential therapeutic inhibitors for various types of cancers. Furthermore, lactiflorin has also shown potential as a non-invasive biomarker for early detection of certain cancers through analysis of urine samples.