Produits biochimiques et réactifs

<p>Benzoylalbiflorin is a potent inhibitor of leukemia and other cancer cells. It is derived from medicinal plants and has been found to be effective against human cancer cell lines. Benzoylalbiflorin acts by inhibiting kinases, which are enzymes that play a critical role in the regulation of the cell cycle and apoptosis. This compound has been shown to induce apoptosis in Chinese hamster ovary cells and inhibit tumor growth in mice. Additionally, benzoylalbiflorin analogs have been developed as potential cancer inhibitors with improved pharmacological properties. The compound can also be detected in urine, making it a useful biomarker for monitoring cancer progression or response to treatment. Overall, benzoylalbiflorin holds great promise as a potential treatment for various types of cancer.</p>

<p>UVI 3003 is a light stabilizer that functions as an ultraviolet (UV) absorber, primarily utilized in the protection of various materials from UV radiation. This product is synthesized from advanced chemical compounds designed to absorb UV light and prevent its transmission through the material. The mode of action involves converting UV radiation into harmless thermal energy, which is then dissipated, thereby protecting the underlying matrix from photodegradation.</p>

<p>CYM 5541 is a selective herbicide, which is synthesized from organic chemical compounds. It functions by interfering with the metabolic processes critical to weed growth and development. Specifically, CYM 5541 targets and inhibits specific enzymes that are essential for cell division and photosynthesis in undesirable plants.<br><br>The primary application of CYM 5541 is in agricultural settings, where it is used to manage weed populations that compete with crops for light, nutrients, and water. It is particularly effective in controlling broadleaf and grassy weeds. Through its precise mode of action, CYM 5541 enables efficient, targeted suppression of non-crop vegetation, thereby maintaining the health and yield of the desired plants. Its use in integrated pest management strategies underscores its role in sustainable farming practices, minimizing the environmental impact while maximizing agricultural productivity.</p>

<p>Inhibitor of dopamine-β-hydroxylase</p>

<p>Goat polyclonal Human Ceruloplasmin antibody</p>

<p>(4bS,8aS,9S,10S)-10-(Acetyloxy)-3,9-bis(benzoyloxy)-4b,5,6,7,8,8a,9,10-octahydro-4b,8,8-trimethyl-2-(1-methylethyl)-1,4-phenanthrene dione is a potent chemokine molecule that is an agonist of the CXCR2 receptor. It has been shown to inhibit cancer stem cells and chemoattractant production in colon carcinoma cells. This compound selectively targets the translation of lamiaceae mRNA and induces apoptosis in colon carcinoma cells.</p>

<p>Please enquire for more information about 11β-Prostaglandin f2α-d4 including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>M1001 is a biochemical reagent, which is synthesized through advanced organic chemistry techniques, with a specific mode of action that targets nucleic acid structures. It functions as an intercalating agent, inserting itself between base pairs in DNA strands. This interaction alters DNA topology, making M1001 invaluable for research applications that involve DNA replication, transcription, and repair studies.</p>

<p>1-1(Z)-Hexadecenyl-2-palmitoyl-sn-glycero-3-pc is a medicinal compound that has shown potential as an anticancer agent. It is an analog of a protein found in Chinese urine, and has been shown to inhibit kinase activity in cancer cells. This compound has been studied for its ability to induce apoptosis, or programmed cell death, in tumor cells. Additionally, it has been shown to disrupt the cell cycle and inhibit the growth of cancer cells. 1-1(Z)-Hexadecenyl-2-palmitoyl-sn-glycero-3-pc is a promising inhibitor for cancer treatment due to its potent anti-cancer properties.</p>

<p>rac-Harzianolide is an analog of Harzianolide, a natural product isolated from the fungus Trichoderma sp. It has been shown to have potent anticancer activity by inhibiting kinases involved in cancer cell growth and survival. In human urine, rac-Harzianolide has been detected after oral administration of chitosan-bound rac-Harzianolide. This compound induces apoptosis in cancer cells and inhibits tumor growth in Chinese hamsters. Rac-Harzianolide acts as a kinase inhibitor, blocking the activity of the protein kinases that are essential for cancer cell proliferation and survival. It is considered a promising candidate for the development of novel anticancer agents.</p>

<p>PDE10-IN-1 is a peptide with the amino acid sequence of GGRDYGGLPPG. It is an activator of PDE10, which belongs to the family of phosphodiesterases. The inhibition of PDE10 in the brain has been shown to have antidepressant effects in mice and rats. This peptide has been shown to be a potent inhibitor of protein interactions, with IC50 values ranging from 1 μM to 10 μM for a number of proteins including TNF-α receptor (IC50 = 2 μM), CD4 receptor (IC50 = 1 μM), and CX3CR1 receptor (IC50 = 0.5 μM). In addition, PDE10-IN-1 has been shown to be a ligand for the dopamine D2 receptor and may function as an antagonist or agonist depending on its binding affinity.</p>

<p>GR79236 is a novel synthetic compound, which is a small-molecule pharmaceutical agent developed through advanced chemical synthesis processes. Its source involves rational drug design targeting specific biomolecular pathways. The mode of action of GR79236 pertains to its ability to selectively bind to and modulate receptor sites, resulting in altered cellular signaling. This modulation achieves specificity in targeting pathological mechanisms without affecting normal cellular processes.</p>

<p>Peroxiredoxin-1 is a protein that belongs to the peroxiredoxin family. It is a redox-active protein that can reduce hydroperoxides and organic hydroperoxides. Peroxiredoxin-1 has been shown to be an activator of ion channels, receptors, and ligands. It is used as a research tool for studying the interactions between proteins and peptides.</p>

<p>Please enquire for more information about Val-His-Leu-Thr-Pro-Glu 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 Clevidipine-d5 including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>C11 TopFluor Phytosphingosine is a fluorescent lipid analog, which is derived from the naturally occurring bioactive lipid, phytosphingosine. This compound incorporates a fluorophore into its structure, facilitating the tracking and visualization of lipid behavior in biological systems through advanced imaging techniques. The structure, with a short yet distinct fluorescent tag, retains the key biological properties of phytosphingosine, thus allowing it to participate in cellular processes similarly to its natural counterpart.</p>

<p>(R)-Cinacalcet-d3 is a medicinal compound that functions as an inhibitor of kinase activity. It has been shown to induce apoptosis in human cancer cells, making it a promising candidate for anticancer therapy. This compound is structurally similar to cinacalcet, a drug used to treat hyperparathyroidism and secondary hyperparathyroidism. (R)-Cinacalcet-d3 can be used as an analog for studying the effects of cinacalcet on protein function and signaling pathways in cancer cells. In vitro studies have demonstrated that this compound inhibits luciferase activity in Chinese hamster ovary cells, suggesting that it may have potential as an anticancer agent. Further research is needed to determine the full potential of (R)-Cinacalcet-d3 in treating tumors and other forms of cancer.</p>

<p>1-O-Hexadecyl-2-O-acetyl-sn-glycero-3-phosphocholine is a phospholipid that is synthesized in the liver and has been shown to be a pressor agent. This drug has shown hypotensive effects in animal models, likely due to its ability to inhibit platelet aggregation and activate platelets. The mechanism of action of 1-O-hexadecyl 2-O-acetyl sn glycero 3 phosphate choline may be through inhibition of lipoxygenase and acetylcholine release, as well as an increase in tissue plasminogen activator (tPA) and plasminogen activator inhibitor (PAI).</p>

<p>Please enquire for more information about Nitecapone-13C5 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 2,7-Dimethoxy-6-(1-acetoxyethyl)juglone including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>