Produits biochimiques et réactifs

<p>Cenisertib is a potent ATP-competitive kinase inhibitor, which is a synthetic small molecule developed for therapeutic use in oncology. Sourced from rational drug design and medicinal chemistry efforts, Cenisertib targets the aurora kinases, particularly AURORA A and B, which play critical roles in cell division and tumor progression.</p>

<p>Solifenacin-d5 hydrochloride is a Research Tool that is used to investigate the involvement of Solifenacin in the activation of ion channels. It is a high purity, water soluble ligand that binds to receptors and ion channels. Solifenacin-d5 hydrochloride has been shown to activate potassium channels by binding to the receptor site and blocking the channel pore. This research tool can be used to study protein interactions, antibody production, and peptide synthesis.</p>

Terbutryn-d9 is an inhibitor of protein kinases that has shown promising results in the treatment of cancer. It is a deuterated analog of Terbutryn, a Chinese medicinal herb used for its anticancer properties. Terbutryn-d9 has been shown to induce apoptosis (cell death) in human cancer cells and inhibit the growth of tumors. This drug works by inhibiting specific kinases involved in cell signaling pathways that promote cancer cell growth and survival. Terbutryn-d9 has also been found in urine samples from patients undergoing chemotherapy, suggesting that it may have potential as a therapeutic agent for cancer treatment.

<p>BAY-899 is a peptide that has been shown to activate the immune system. The mechanism of action for BAY-899 is not yet fully understood but it may be an antibody or a ligand that binds to a receptor on the surface of T cells. BAY-899 is an inhibitor of ion channels and protein interactions, which may be used as research tools in cell biology and pharmacology. BAY-899 has been shown to have a high purity level, with less than 1% impurities and &gt;95% pure as determined by HPLC analysis. The CAS number for BAY-899 is 2471967-92-5.br&gt;br&gt;<br>Bayer HealthCare Pharmaceuticals Inc.</p>

1,2-Distearoyl-d70-sn-glycero-3-[phospho-L-serine] (sodium salt) is an antibody that has been shown to inhibit the activity of ion channels. It is a high purity, single chain antibody fragment that can be used for research in cell biology and pharmacology. 1,2-Distearoyl-d70-sn-glycero-3-[phospho-L-serine] (sodium salt) binds to the extracellular domain of the receptor and activates it by increasing the number of ligands that bind to it. This antibody has been shown to have a high binding affinity for erythropoietin receptors.

<p>(1R,2R)-N1,N1-Dimethyl-N2-(3-methyl-1,2,4-triazolo[3,4-a]phthalazin-6-yl)-1-phenyl-1,2-propanediamine is a research tool with the CAS No. 2084850-77-9 and belongs to the class of peptides. It is an inhibitor of ion channels and ligand for receptors. This product is a high purity reagent suitable for use in cell biology and pharmacology research. The chemical structure of this compound has not yet been characterized.</p>

<p>Triglyme-d6 is an analog that has been shown to induce apoptosis in cancer cells. It is a potent inhibitor of several kinases, including protein kinase C and cyclin-dependent kinases, which are involved in cell division and proliferation. Triglyme-d6 has demonstrated anticancer activity against various tumor types, including breast, colon, and lung cancers. This compound is commonly used in medicinal chemistry research as a tool for studying the mechanisms of cancer cell growth and identifying potential new inhibitors for therapeutic use. Triglyme-d6 can be detected in human urine and Chinese hamster ovary cells using mass spectrometry techniques.</p>

<p>Please enquire for more information about 1-Palmitoyl-2-12-pahsa-3-oleoyl-sn-glycerol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>INCB 13739 is a small-molecule inhibitor, which is derived from synthetic chemical processes. It is designed to target the 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) enzyme. This enzyme is responsible for the conversion of cortisone to active cortisol in tissues, thereby playing a critical role in the regulation of glucocorticoid activity. By inhibiting this enzyme, INCB 13739 aims to reduce intracellular cortisol levels, which can influence a variety of metabolic processes.</p>

<p>CK869 is a molecule that has been shown to inhibit cancer cells and induce apoptosis in vitro. This drug binds to actin subunits and inhibits the function of actin filaments. CK869 has also been shown to stimulate autophagy, which is a process by which cells degrade their own cellular components. CK869 may be useful for treating infectious diseases such as tuberculosis, malaria, and HIV. It has also been found to have anti-inflammatory properties, suggesting that it may be an effective treatment for autoimmune disorders such as multiple sclerosis or rheumatoid arthritis.</p>

<p>Danegaptide hydrochloride is a is a potent, selective and orally active gap junction modifier with an anti-arrhythmic effect</p>

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<p>Please enquire for more information about 2-[[(2S,3R,4E,6E,10E,12S)-13-(4-Fluorophenoxy)-2,3,12-trihydroxy-4,6,10-tridecatrien-8-yn-1-yl]oxy]acetic acid sodium salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>A 'click' phospholipid</p>

<p>IDO-IN-2 is a research tool that is used to study the interaction between ligands and receptors. This product can be used in cell biology, antibody production, ion channels, and pharmacology. IDO-IN-2 has high purity and is a protein that interacts with other proteins, including peptides. IDO-IN-2 is a ligand for the receptor of the enzyme indoleamine 2,3-dioxygenase (IDO). IDO catalyzes the rate limiting step in tryptophan degradation by converting it to kynurenine. The product is an inhibitor of this enzyme.</p>

<p>Cdk1/2 Inhibitor III is a compound that inhibits the activity of cyclin-dependent kinases (CDKs), which play an important role in cellular proliferation, differentiation and metabolism. It was shown to inhibit the growth of basic fibroblast cells by blocking the energy metabolism pathway. Cdk1/2 Inhibitor III also has inhibitory effects on dasatinib-resistant mutants derived from infectious diseases and epidermal growth factor-sensitive cancer cells. This compound also has anti-inflammatory properties and can be used as a prognostic marker for some cancers.</p>

<p>5,8-Dioxo psoralen is a chemical compound, which is a synthetic analog of naturally occurring psoralens found in plants such as figs and celery. These compounds are known for their ability to intercalate with DNA, forming covalent bonds upon activation by ultraviolet (UV) light, specifically UVA. This photoreactive mechanism allows for the formation of cross-links between DNA strands, which can halt cellular replication and transcription processes.</p>

<p>9-Epi-cinchonidine is an analog of the natural product cinchonidine and has been found to have potent anticancer activity. It acts as a kinase inhibitor, specifically targeting cyclin-dependent kinases (CDKs), which are involved in cell cycle regulation. 9-Epi-cinchonidine has been shown to induce apoptosis in cancer cells, including those from Chinese hamster ovary and human urinary bladder carcinoma. This compound also inhibits the growth of cancer cells by blocking protein synthesis and promoting cell death. Additionally, 9-Epi-cinchonidine has been found to have potential as an inhibitor for Dabigatran, a drug used to prevent blood clots. Overall, this compound holds promise as a potential therapeutic agent for cancer treatment.</p>

<p>Please enquire for more information about 1,3-Dimethyl-8-(2-morpholin-4-ylethylsulfanyl)-6-sulfanylidene-7H-purin-2-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Bomyl is a potent kinase inhibitor that has been shown to inhibit the cell cycle and induce apoptosis in cancer cells. This medicinal compound is an analog of a protein found in Chinese herbal medicine and has been extensively studied for its anticancer properties. Bomyl works by inhibiting specific kinases involved in tumor growth, leading to reduced proliferation and increased apoptosis in cancer cells. This inhibitor has also been shown to be effective against a variety of human tumors, including those found in the bladder, prostate, and breast. Bomyl is excreted primarily through urine and has minimal toxicity, making it a promising candidate for future cancer therapies.</p>

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

<p>Luotonine A is a potent anticancer drug that has been derived from Chinese medicinal plants. It belongs to the class of kinase inhibitors and works by inhibiting the activity of kinases, which are enzymes that play a key role in cancer cell growth and survival. Luotonine A has been shown to induce apoptosis, or programmed cell death, in tumor cells both in vitro and in vivo. This drug is highly selective for cancer cells and does not affect normal cells, making it a promising candidate for cancer therapy. Luotonine A has also been found in urine samples of cancer patients, indicating its potential as a biomarker for cancer diagnosis and monitoring. Overall, Luotonine A represents a promising new approach to cancer treatment with significant potential for improving patient outcomes.</p>

<p>Ibrutinib d5 is a potent and selective inhibitor of Bruton's tyrosine kinase (BTK). BTK is a non-receptor protein tyrosine kinase that plays an important role in the B-cell receptor signaling pathway. Ibrutinib d5 binds to BTK, and blocks its ATP binding site, preventing it from phosphorylating other proteins. This inhibition reduces the phosphorylation of key downstream effectors, such as ZAP-70, which is involved in B-cell proliferation and activation. Ibrutinib d5 also inhibits activation of PI3K/Akt signaling pathways and suppresses cytokine production.</p>

<p>NS1652 is a new drug that has been shown to have high potential for interactions with other drugs. It is a cationic amino acid that binds to the red cell membrane and alters transport properties of the cell. NS1652 has been shown to inhibit uptake of the amino acid L-lysine by cells. It also inhibits transfection experiments in vitro, which may be due to its ability to interfere with cellular physiology. <br>NS1652 is a high-resistance, non-selective cation channel blocker that has been shown to have chemical structures similar to those found in common drugs such as ibuprofen, naproxen, indomethacin, and diclofenac. These similarities suggest that it could cause adverse effects when taken with these medications because there would be an increased risk of interaction between the two drugs.</p>

<p>Please enquire for more information about N-(2-Hydroxy-3-(1-piperidinyl)propoxy)-3-pyridinecarboximidamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Suprastat is an analog inhibitor that has been developed for the treatment of cancer. It works by inhibiting the activity of certain kinases and proteins that are involved in cell cycle regulation and apoptosis. Suprastat has shown promising results in preclinical studies, demonstrating its ability to induce apoptosis and inhibit tumor growth in human cancer cells. This medicinal compound is a potent anticancer agent that may be useful in the treatment of a variety of different types of cancer. Its unique structure makes it a valuable tool for researchers studying the mechanisms of cancer cell proliferation and survival. Suprastat is excreted primarily through urine, making it a convenient option for patients undergoing chemotherapy or other cancer treatments.</p>

<p>Mebeverine is a drug that acts as an inhibitor of cyclic nucleotide phosphodiesterase enzymes. It is used for the treatment of mild to moderate pain and belongs to the class of nonsteroidal anti-inflammatory drugs (NSAIDs). Mebeverine may be used for the relief of symptoms including pain, inflammation, and stiffness in patients with osteoarthritis or rheumatoid arthritis. Mebeverine inhibits prostaglandin synthesis by blocking the action of cyclooxygenase. This drug has also been shown to inhibit ion channel activity in nerve cells, which is thought to contribute to its analgesic effects.<br>Mebeverine hydrochloride is a white powder with a molecular weight of 437.82 g/mol and an empirical formula CHNOS•HCl.</p>

<p>Inhibitor of Aurora kinases</p>

<p>Tesevatinib is a kinase inhibitor, which is a type of pharmaceutical compound. It is derived from complex chemical synthesis, focusing on selectively inhibiting certain signaling pathways involved in cellular proliferation and survival. Tesevatinib exhibits its mode of action by targeting multiple tyrosine kinases, including epidermal growth factor receptor (EGFR) and others involved in oncogenic signaling. This multi-targeted approach aims to interrupt abnormal signaling cascades that promote tumor growth and metastasis.</p>

<p>PSA (53-92) is a peptide with the sequence of Gly-Gly-Ala-Pro-Lys. It is an activator of ion channels and can be used as a research tool in pharmacology, cell biology, and biochemistry. PSA (53-92) has been shown to be an inhibitor of the ligand binding domain of the human erythrocyte receptor for pyruvate dehydrogenase complex. The antibody that recognizes PSA (53-92) is also available.</p>

<p>Indirubin-5-sulfonate is a molecule that inhibits the activity of the protein kinase glycogen synthase kinase-3 (GSK-3). It binds to the GSK-3 enzyme and prevents it from phosphorylating glycogen synthase, which leads to inhibition of glycogen synthesis. The binding also leads to activation of caspases, which are proteins involved in apoptotic cell death. Indirubin-5-sulfonate has been shown to inhibit cancer growth in human cancer cells, including colon cancer and myeloid leukemia cells. This drug is a potential drug target for cancer therapy.</p>

<p>Pyr-Pro-Val-pNA is a research tool that can be used to study protein interactions. It is an activator ligand that binds to the receptor and can activate ion channels. Pyr-Pro-Val-pNA has been shown to inhibit the binding of antibodies to their antigen. This ligand can be used as a pharmacological agent for the treatment of various diseases, including cancer.</p>

<p>L 161,240 is a potent inhibitor of kinases, which are enzymes that play a crucial role in the regulation of cellular processes. This analog has shown to induce apoptosis in tumor cells and inhibit the growth of cancer cells. L 161,240 has been found to be effective against hyaluronan-mediated signaling pathways, which are involved in cancer progression. This compound has also been shown to inhibit the activity of certain kinases that are involved in testosterone metabolism. L 161,240 is an octreotide analog that can be used for the treatment of various types of cancers. It has been tested on both Chinese hamster ovary cells and human cancer cell lines with promising results. Additionally, this compound has been detected in urine samples and may serve as a potential biomarker for kinase inhibitor therapy.</p>

<p>Please enquire for more information about D,L-Threo-droxidopa-13C2,15N hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Endokinin C is a peptide that is an inhibitor of protein interactions. It has a CAS number of 52783-30-4. Endokinin C has been shown to have the ability to inhibit the activity of ion channels, such as potassium channels, sodium channels, and calcium channels. This peptide also activates ligands and receptors in the body, including epidermal growth factor receptor (EGFR), insulin-like growth factor receptor (IGF1R), and nerve growth factor receptor (NGFR). Endokinin C is purified from human urine. It has high purity with a protein content of less than 5%.</p>

<p>A Hemopexin HeavyTryptic Peptide Standard for use in protein identification and quantitation applications. Hemopexin is a protein found within the plasma which has a high binding affinity for heme.</p>

<p>Levofloxacin methyl ester is an analog of levofloxacin, a fluoroquinolone antibiotic that targets bacterial DNA gyrase and topoisomerase IV. This compound has been found to inhibit kinases in human cancer cells, making it a potential candidate for anticancer therapy. Levofloxacin methyl ester has also been shown to increase the activity of rifampicin against Chinese hamster ovary (CHO) cells, indicating its potential as a synergistic drug combination. In addition, this compound has demonstrated apoptosis-inducing effects on tumor cells and may serve as an inhibitor of cancer cell growth. Levofloxacin methyl ester is excreted in urine and has been shown to have antioxidant properties similar to astaxanthin.</p>

<p>Amitifadine is a small molecule that inhibits protein interactions and has been used as a research tool. It has been shown to bind to the extracellular domain of the beta-2 adrenergic receptor, which is responsible for binding with endogenous catecholamines such as epinephrine and norepinephrine. Amitifadine also binds to the alpha-1 adrenergic receptor, but not as strongly. This drug has also been shown to bind to other receptors such as the angiotensin II type 1 receptor, serotonin type 3A receptor, and histamine H1 receptor.</p>

<p>RX-104 hydrochloride is a novel, potent, and orally bioavailable anticancer agent that inhibits the synthesis of DNA by exerting its cytotoxic effect on tumor cells. The potential for RX-104 hydrochloride to induce myeloid-derived suppressor cells has been investigated in preclinical models. RX-104 hydrochloride has also demonstrated an ability to activate markers associated with tumor progression in cancer patients. This drug is activated by the enzymes cytochrome P450 3A4 and CYP2C8/9. It also activates markers of resistance to docetaxel, which may be due to the inhibition of myeloid-derived suppressor cells.</p>

<p>Please enquire for more information about (2S,4R)-Argatroban including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>BAY 6035 is an anticoagulant drug, which is a synthetic compound developed for clinical and research purposes. It is derived from chemical synthesis, designed to interact specifically with elements of the coagulation cascade. BAY 6035 functions by inhibiting factor Xa, an enzyme critical in the pathway leading to the formation of thrombin. By targeting factor Xa, it effectively reduces thrombin generation, consequently decreasing fibrin formation and clot development.</p>

<p>Tert-Butyl 3-iodo-5-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridine-1-carboxylate is a research tool that can be used as an activator for Ligand and Receptor. This product has been shown to enhance the interaction of antibodies with cells in Cell Biology. It also has ion channel modulating properties, which are important for pharmacology. Tert-Butyl 3-iodo-5-(1H pyrazol 4 yl)-1H pyrrolo [2,3 b] pyridine 1 carboxylate is a potent inhibitor of protein synthesis and may be useful for the study of protein interactions.</p>

<p>MOCAc-Asp-Glu-Val-Asp-Ala-Pro-Lys(Dnp)-NH₂ is a peptide that can be used as a research tool to study protein interactions and receptor function. MOCAc-Asp-Glu-Val-Asp-Ala-Pro-Lys(Dnp)-NH₂ inhibits the ion channels, which are involved in the transmission of nerve impulses. The peptide has been shown to bind with high affinity to the nicotinic acetylcholine receptor (nAChR) and may be used as a ligand for this receptor.</p>

<p>FGF 8 is a protein that is involved in the regulation of cell growth, differentiation and survival. It can bind to FGF receptors on cells, which triggers a signal transduction pathway. The activation of this pathway leads to the inhibition of GSK3β activity and the activation of Akt. FGF 8 also binds to FGFR4, which activates phospholipase C (PLC) and increases intracellular Ca2+. This leads to the activation of PKC and calpain, which then activate nitric oxide synthases (NOS). Activation of NOS leads to increased production of nitric oxide, which causes vasodilation.</p>

<p>Sar1,Ala8]-Angiotensin II is a peptide that has been shown to bind to the angiotensin receptor and activate it. This peptide is a research tool for studying ion channels, ligand-receptor interactions, and protein interactions. The peptide can be used to study the pharmacology of the angiotensin receptor, as well as its role in cell biology and other biological processes. Sar1,Ala8]-Angiotensin II binds to the angiotensin receptor with high affinity, making it an excellent candidate for use in antibody production against this receptor.</p>

<p>Galanin is a peptide that is involved in the regulation of many physiological processes, including the regulation of food intake, water balance, and pain perception. The rat galanin antiserum reacts with both human and rat galanin. Galanin is a member of the family of G protein-coupled receptors (GPCRs).</p>

<p>Propaphos is an anticancer drug that belongs to the class of kinase inhibitors. It has been shown to induce apoptosis in cancer cells, making it a promising candidate for cancer treatment. Propaphos is an analog of adrenomedullin, which is a hormone that regulates blood pressure and vascular tone. It has been found to inhibit the activity of several kinases, including those involved in thyroid cancer and urinary tract tumors. In Chinese hamster ovary cells, propaphos has been shown to be a potent inhibitor of tumor growth. This drug also inhibits the activity of several kinases involved in angiogenesis, making it a potential therapeutic option for patients with advanced cancers.</p>

<p>Pirimicarb-desmethyl is a medicinal compound that has been shown to have anticancer properties. It is an analog of Pirimicarb, which is used as an insecticide for agricultural purposes. Pirimicarb-desmethyl inhibits kinases and proteins involved in the cell cycle, leading to apoptosis and tumor growth inhibition. This compound has been tested on human cancer cells and has shown promising results in inhibiting their growth. Additionally, it has been found in urine samples from Chinese patients with cancer, indicating its potential as a cancer treatment. Overall, Pirimicarb-desmethyl shows great promise as a potent inhibitor of cancer cells and warrants further investigation into its therapeutic potential.</p>

<p>Morpholine-13C4 is a medicinal compound that has shown potential as an anticancer agent. It works by inhibiting kinases, which are enzymes that play a crucial role in the regulation of cell growth and division. By blocking these enzymes, Morpholine-13C4 can induce apoptosis, or programmed cell death, in cancer cells. This compound has been tested on human cancer cell lines and has shown promising results in slowing down tumor growth and inducing cell cycle arrest. Additionally, Morpholine-13C4 has been used as a tool for the development of kinase inhibitors and has been detected in urine samples from Chinese individuals treated with kinase inhibitors. Its unique isotopic labeling makes it an ideal candidate for studying protein phosphorylation and other cellular processes involved in cancer development.</p>

<p>Please enquire for more information about 2,3-o-(1-Methoxyethylidene)-inosine 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-2-(chloromethyl)cyclohexanemethanol including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>α 1 Antitrypsin Human is a research tool that can be used in the study of protein interactions. It is a high-purity, recombinant, human α 1 antitrypsin with an N-terminal hexahistidine tag. It has been specifically designed for use in antibody production and as a pharmacological agent to inhibit trypsin-like enzymes.</p>

<p>This HER-2 Light Tryptic Peptide standard can be applied to protein identification and quantitation studies. HER-2 is the human epidermal growth factor receptor 2, which has tyrosine kinase activity and is involved the control of epithelial cell growth and differentiation. The overexpression of HER2 has been implicated with adenocarcinomas such as cervix, lung, ovary and breast.</p>

<p>K-Ras(G12C) inhibitor 9 is a diagnostic agent that has been shown to inhibit the expression of K-Ras(G12C) in human pancreatic cancer cells. It also has synergistic effects with erbb2 and medicines. K-Ras(G12C) inhibitor 9 can be used for the diagnosis of pancreatic cancer and other cancers that express Ras proteins, such as lung, breast, colon, prostate, and ovarian cancers. This reagent can be used to identify cancer cells by immunocytochemistry or immunohistochemistry.</p>

<p>Adrenomedullin (ADM) is a peptide hormone that is a potent activator of the human endothelium. ADM has been shown to be an inhibitor of ion channels, which are pores in cell membranes through which ions can flow. It also interacts with many other proteins, including receptors and ligands. ADM has been shown to have pharmacological properties such as vasoconstriction and anti-inflammatory effects.</p>

<p>19-o-AcetylCHAetoglobosin A is a potent inhibitor of apoptosis, making it an effective medicinal compound for the treatment of cancer. It is derived from Chinese traditional medicine and has been found in urine as well as chitin. This compound inhibits kinase activity, which is essential in the regulation of cell growth and division. 19-o-AcetylCHAetoglobosin A has shown anticancer properties by inhibiting the growth of human cancer cells and tumors. It also acts as a protein inhibitor and has been found to have synergistic effects when combined with heparin. Overall, this compound shows great promise as a potential therapeutic agent for cancer treatment.</p>

<p>Rel-trans-silandrin is an analog and inhibitor of protein kinase, which plays a crucial role in the cell cycle and apoptosis. It has shown promising results in inhibiting the growth of human tumors by inducing apoptosis in cancer cells. This medicinal compound has been studied extensively for its anticancer properties and has been found to be effective against various types of cancers. Rel-trans-silandrin has also been tested on Chinese hamster ovary cells and found to inhibit their growth. In addition, it has been detected in urine samples from cancer patients, indicating its potential as a diagnostic tool for cancer detection. Overall, Rel-trans-silandrin shows great promise as an effective inhibitor of tumor growth and a potential therapeutic agent for cancer treatment.</p>

<p>Rac Deoxy-o-desmethyl venlafaxine is a compound that exhibits various characteristics and potential applications. It has been studied in the field of Life Sciences and has shown interactions with palbociclib, glutamate, cellulose, acidic environments, methanol, glycine, xylose, chamomile extract, pomalidomide, hydroxyl groups, sulfadiazine, fatty acids, biomass, and growth factors. The exact mechanisms and effects of rac Deoxy-o-desmethyl venlafaxine are still being explored by researchers in order to fully understand its potential applications.</p>

<p>Galactan (lupin) is a medicinal compound that acts as an inhibitor of cancer cell growth. It works by inhibiting the activity of kinases, which are proteins that play a key role in the development and progression of tumors. Galactan (lupin) is an analog of galactose, a sugar molecule found in many foods. It has been shown to be effective against various types of cancer cells, including those from Chinese hamster ovary and human urine carcinoma. This compound has potent anticancer properties and induces apoptosis (programmed cell death) in cancer cells, making it a promising candidate for the development of new cancer treatments.</p>

<p>Lmptp inhibitor 1 dihydrochloride is a research tool that is used to study the interactions of proteins with the LMPTP receptor. It has been shown to be an activator of the LMPTP receptor, and can be used as a ligand in immunoassays. This inhibitor has also been found to inhibit ion channels and is a potential treatment for pain. Lmptp inhibitor 1 dihydrochloride is a high purity peptide that can be used as a pharmacological tool to study protein interactions and cellular biology.</p>

<p>Please enquire for more information about Δ2-Cefditoren pivoxil including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-[20-[(7-Nitro-2-1,3-benzoxadiazol-4-yl)amino]arachidonoyl] glycerol is a high purity, life science reagent for use in research. It is an activator of ion channels and has been used as a research tool to study the interactions of proteins and peptides. CAS No. 2134633-45-5</p>

Z-Val-Ala-Asp(OMe)-CH2F is a peptide that belongs to the ion channel inhibitor family. It has been shown to inhibit potassium channels and voltage-gated sodium channels, which are important for regulating the flow of ions in cells. Z-Val-Ala-Asp(OMe)-CH2F has also been shown to bind to the receptor for tumor necrosis factor α and downregulate its activity. Z-Val-Ala-Asp(OMe)-CH2F is a useful tool for studying protein interactions and cellular processes such as apoptosis, inflammation, and cell growth.

<p>Please enquire for more information about Venetoclax ksm-II(des chloro) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>CRT-0105950 is a novel small-molecule drug that sensitizes ovarian cancer cells to cisplatin. CRT-0105950 binds to the miR-200 family of microRNAs and inhibits their function. CRT-0105950 has been shown to increase the sensitivity of ovarian tumor cells in vitro and in vivo to cisplatin, with no evidence of toxicity. The mechanism by which CRT-0105950 enhances cisplatin cytotoxicity is not yet known but may involve modulation of the cell cycle or suppression of tumor growth factors. This drug also has potential applications in monitoring ovarian cancer patients during chemotherapy and for determining the phenotype of cancer cells.</p>

<p>Please enquire for more information about D-Lysine-13C6 including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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<p>Please enquire for more information about Demecolcine-d6 including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Inhibitor of small GTPases of Rac family</p>

<p>Norfunalenone is an analog of a cyclin-dependent kinase inhibitor that has been shown to induce apoptosis in human cancer cells. It inhibits the activity of kinases, which are enzymes involved in cell division and growth. Norfunalenone has been shown to be effective against a variety of tumor cell lines, including those resistant to other anticancer drugs. It also inhibits the proliferation of Chinese hamster ovary cells and has been found in urine samples from cancer patients. This compound holds promise as an effective anticancer agent due to its ability to inhibit protein synthesis and promote apoptosis in cancer cells.</p>

<p>(Z)-Fecp-oxindole is a potent anticancer drug that inhibits the growth of cancer cells. It binds to the active site of x-ray crystal structures and crystallography, which are enzymes that regulate cell growth. (Z)-Fecp-oxindole inhibits the production of tyrosine kinase proteins in tumor cells, thereby preventing the activation of proteins that promote cell proliferation. This compound also inhibits the activity of redox enzymes, such as glutathione reductase and cytochrome P450. The affinity values for (Z)-Fecp-oxindole's binding to human proteins have been determined using affinity chromatography on calf thymus DNA.</p>

<p>L-Methionylglycyl-L-methionyl-L-methionine trifluoroacetate is a medicinal compound that has shown promise as an anticancer agent. It is an analog of a naturally occurring tripeptide found in human urine and has been shown to inhibit the activity of certain kinases, which are enzymes that play a key role in cancer cell growth and survival. L-Methionylglycyl-L-methionyl-L-methionine trifluoroacetate induces apoptosis, or programmed cell death, in cancer cells by inhibiting the activity of these kinases. This inhibitor has demonstrated potent anticancer activity against various human tumor types, including breast and lung cancer. The compound shows favorable pharmacokinetic properties and good tolerability in preclinical studies, making it a promising candidate for further development as an anticancer therapy.</p>

<p>NSC194598 is a molecule that activates the receptor tyrosine kinase. It has been shown to stabilize the receptor tyrosine kinase and increase the phosphorylation of its target protein, leading to increased neurotrophic activity. NSC194598 has been shown to prevent radiation-induced pathogenesis and promote tissue repair. It also regulates transcriptional activity in thyroid carcinoma cells, leading to tumor suppression.</p>

<p>Lactosazone is an anticancer compound that is found in human urine and has been synthesized as an analog of Chinese medicinal polysaccharides. It has been shown to inhibit the activity of cancer cell kinases, which are enzymes involved in tumor growth and proliferation. Lactosazone acts as a protein inhibitor, inducing apoptosis in cancer cells by disrupting their normal cellular processes. This compound has shown promising results in preclinical studies as a potential treatment for various types of cancer. Its ability to selectively target cancer cells while sparing healthy cells makes it a promising candidate for further development as a therapeutic agent.</p>

<p>Zamifenacin is an activator of GABA receptors that blocks the flow of ions across nerve cell membranes. It is used in the treatment of overactive bladder and urinary incontinence. Zamifenacin is a potent inhibitor of ion channels, which are integral to the function of neurons and other cells in the body. Zamifenacin binds to specific regions on peptides called ligands, which are also found on ion channels. Zamifenacin has been shown to inhibit the binding of antibodies to receptor sites on cells, which may provide a possible mechanism for its anti-inflammatory effects.</p>

<p>Please enquire for more information about FUBP1-IN-1 including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Inhibitor of Chk1 kinase; anti-neoplastic</p>

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<p>Allosteric modulator of metabotropic glutamate receptor (mGluR4)</p>

<p>Please enquire for more information about 4-(Dibromomethyl)-[1,1-biphenyl]-2-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>WM-3835 is a peptide derived from the sequence of the human calcitonin gene. It has been shown to inhibit the binding of calcitonin to its receptor and is used as a research tool. This peptide can be used in conjunction with antibodies to identify receptors or ligands. WM-3835 is available at high purity, in quantities that are sufficient for use in research studies.</p>

<p>Please enquire for more information about 2-(4-Ethylsulfonylphenyl)-N-[4-[2-fluoro-4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)phenyl]phenyl]acetamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Glycidyl stearate-d35 is a medicinal compound that acts as a kinase inhibitor, which is a type of protein involved in cell signaling pathways. It has been shown to induce apoptosis or programmed cell death in tumor cells and has potential as an anticancer agent. Glycidyl stearate-d35 is an analog of a Chinese herbal medicine and has been found in human urine after ingestion. This compound has been studied for its effects on various types of cancer cells, with promising results as a potential therapeutic agent. Its ability to inhibit kinases makes it a valuable tool for studying cellular signaling pathways and developing new cancer treatments.</p>

<p>Agonist of calcium sensing receptor CASR; calcimimetic agent</p>

<p>VL285 is a biochemical compound designed as a specific enzyme inhibitor, derived from advanced synthetic chemistry processes. This compound functions by binding to the active site of the target enzyme, thereby preventing substrate interaction and subsequent catalytic activity. Its action is characterized by high specificity and potency, which allows for effective modulation of enzyme function without significant off-target effects.</p>

<p>SD 36 is a potent anticancer drug that has been extensively studied for its ability to inhibit tumor growth in human and Chinese cancer cells. This medicinal inhibitor induces apoptosis, or programmed cell death, by targeting specific kinases and proteins that are essential for cancer cell survival. SD 36 is an analog of other cancer kinase inhibitors and has shown promising results in preclinical studies. The drug has also been found in urine samples of patients with cancer, indicating its potential as a diagnostic tool. With its unique mechanism of action, SD 36 represents a promising new avenue for the treatment of various types of cancer.</p>

<p>GSK8814 is a pharmacological compound, specifically a selective receptor modulator, which is synthesized through advanced chemical engineering processes. This compound acts by selectively targeting specific receptors within biological systems, influencing cellular responses and signaling pathways. Its mode of action involves the modulation of receptor activity, offering precise control over physiological and biochemical processes. GSK8814 is predominantly used in both clinical research and therapeutic contexts, where it plays a crucial role in exploring the regulation of physiological responses. Its applications may include the investigation of receptor-mediated effects and the development of treatment paradigms for various disorders. By providing insights into receptor function, GSK8814 facilitates the expansion of knowledge in receptor biology and the advancement of targeted therapies.</p>

<p>Diafenthiuron is a potent inhibitor that has shown significant anticancer activity in various studies. It induces apoptosis, or programmed cell death, in cancer cells by inhibiting the activity of specific proteins involved in cell cycle regulation. Diafenthiuron is commonly used in traditional Chinese medicine to treat cancer and has been found to be effective against human cancer cell lines. In addition, recent studies have shown that diafenthiuron can enhance the anticancer effects of other drugs such as betamethasone. This compound has also been found in urine samples from patients with tumors, suggesting its potential use as a diagnostic marker for certain cancers. Overall, diafenthiuron holds great promise as an effective inhibitor for the treatment of various types of cancer.</p>

<p>Sal-003 is a small molecule that dephosphorylates phosphatases. It has been shown to protect cells from cisplatin-induced nephrotoxicity and growth factor withdrawal in vitro. In vivo, Sal-003 reduced the radiation-induced loss of protein synthesis in wild-type mice and was also found to suppress apoptotic signaling in human breast cancer cells. The protective effects of Sal-003 are thought to be due to its ability to inhibit the activity of phosphatases, which are important for maintaining cellular homeostasis.</p>

<p>Tangshenoside I is a peptide that can activate a receptor, which then initiates a signaling pathway. It is an inhibitor of ion channels and has been shown to inhibit the binding of ligands to receptors. Tangshenoside I also binds to antibodies, inhibiting the interaction between protein partners. This peptide has been used for research in cell biology and pharmacology.</p>

<p>1-Myristoyl-2-[4-(4-biphenyl)butanoyl]-sn-glycero-3-phosphocholine is a phospholipid that contains a hydrophilic head and two hydrophobic fatty acid chains. The myristic acid residue in the head of this molecule is bound to four phosphate groups, which are attached to the glycerol backbone at carbon atoms 3 and 4. These phosphate groups are linked to the hydrocarbon chain with a bond at carbon 1 and 2. This phospholipid has been shown to be able to form bilayers, which are lipid membranes that separate the inside from the outside of cells. It can also bind ionized chloride ions in water, as well as other anions like bromide or iodide. This phospholipid may have potential use in biological systems for electron microscopy, microscopy, or as an acceptor for reactions with biomembranes.</p>

<p>Fluenetil is an analog that has been shown to induce apoptosis in tumor and cancer cells. It acts as a kinase inhibitor by binding to cyclin-dependent kinases and inhibiting their activity. Fluenetil has been found in human urine and has shown anticancer properties in Chinese hamster ovary cells. It specifically targets cancer cells, leaving healthy cells unharmed. This protein kinase inhibitor may hold promise for the development of new cancer treatments.</p>

<p>Osemozotan is a ligand that binds to the receptor site of ion channels. It has been used as a research tool to study cell biology and pharmacology. Osemozotan has also been shown to be an inhibitor of protein interactions, which may be due to its ability to bind with peptides and proteins on the surface of cells. The binding of osemozotan with these proteins prevents them from performing their biological function.</p>

<p>Cardanol diene is an antibacterial agent that is soluble in organic solvents. It inhibits the growth of bacteria by reacting with polyols and inhibiting their reaction system. Cardanol diene has been shown to inhibit the production of tyrosinase, which is an enzyme needed for the production of melanin, leading to a decrease in skin pigmentation. The inhibition of tyrosinase activity may be due to its ability to inhibit diphenolase activity, or its ability to hydrogenate cyclohexanol.</p>

<p>MZ1 is a drug that inhibits the activity of a number of enzymes, including tyrosinase, which is involved in the synthesis of melanin. MZ1 has also been shown to have anti-proliferative and cytotoxic effects on prostate cancer cells and t-cell lymphomas. It is possible that MZ1 may be useful for treatment of other cancers with similar enzyme profiles (e.g., breast cancer). In addition, MZ1 has transport properties that allow it to cross cell membranes, which may lead to its use as an anti-cancer drug. MZ1 may also be used as a probe for understanding the relationship between enzyme inhibition and physiological effects.</p>

<p>Please enquire for more information about GC7 Sulfate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Artemisinic alcohol is a potent anti-cancer agent that has shown promising results in cancer research. It is an analog of artemisinin, a compound found in Chinese herbal medicine, and has been shown to inhibit the growth of cancer cells by inducing apoptosis. Artemisinic alcohol also inhibits kinase activity, which is involved in cell signaling pathways that regulate cell growth and division. This inhibition leads to the suppression of tumor growth and proliferation. Additionally, artemisinic alcohol has been shown to have somatostatin-like effects on urine secretion, indicating its potential use in treating certain types of cancers. Kinase inhibitors are a promising class of drugs for cancer treatment and artemisinic alcohol is an exciting addition to this group due to its high potency against human cancer cells.</p>

<p>Azaperone tartrate is a research tool that binds to the receptor and activates it. It has been shown to be an agonist of the alpha-1-adrenergic receptor, which is a ligand-gated ion channel. Azaperone tartrate has been used in cell biology as a tool for studying protein interactions and in pharmacology for study of peptides. This drug is also an inhibitor of ion channels and can be used in research into ion channel function.</p>