Bioquímicos e reagentes

<p>D-Hyoscyamine is a potent anticancer agent that has been shown to induce apoptosis in cancer cells. It works by inhibiting kinases, which are enzymes that play a key role in the regulation of cell growth and division. D-Hyoscyamine has been tested on both human and Chinese hamster ovary cells, and has demonstrated significant anticancer activity. It is an analog of several kinase inhibitors, including cyclin-dependent kinase (CDK) inhibitors, which are commonly used in cancer therapy. In addition to its anticancer properties, D-Hyoscyamine has also been found to have potential therapeutic applications for other diseases such as Alzheimer's disease and Parkinson's disease. It is derived from urine and acts as a potent inhibitor of protein kinases.</p>

<p>DTR-I is an analog of ghrelin, a protein hormone that regulates appetite and energy balance. It is a potent inhibitor of kinases, which are enzymes that play a crucial role in cancer cell growth and survival. DTR-I has been shown to induce apoptosis, or programmed cell death, in various types of cancer cells. This anticancer effect is thought to be due to its ability to inhibit the activity of protein kinases that are overexpressed in human tumors. In addition, DTR-I has been found in urine samples from Chinese cancer patients, indicating its potential as a diagnostic marker for certain types of cancer. The development of DTR-I as a novel anticancer agent holds promise for the treatment of various types of cancer in the future.</p>

<p>Please enquire for more information about Pheromone Cymit Quimicaesis Activating Neuropeptide (Helicoverpa assulta, Heliothis zea) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>L-MobileTrex is an advanced analytical technology platform, which is a product of cutting-edge research in data science and computational modeling. This platform operates by integrating multi-dimensional datasets through sophisticated algorithms, providing enhanced data visualization and interpretability.</p>

<p>A synthetic peptide for use as a blocking control in assays to test for specificity of TPCN1 antibody, catalog no. 70R-5158</p>

<p>L-leucine with a lipid chain.</p>

<p>a brain-penetrating activator of eukaryotic initiation factor 2B (eIF2B) that inhibits the abnormal integrated stress response</p>

<p>3,4-Dihydro-2(1H)-isoquinolinyl)[2-[(4-methoxyphenyl)amino]-4-thiazolyl]methanone is a potent and selective inhibitor of the ion channel TRPM8. It reduces pain and inflammation by inhibiting the action of TRPV1 and TRPA1. 3,4-Dihydro-2(1H)-isoquinolinyl)[2-[(4-methoxyphenyl)amino]-4-thiazolyl]methanone is an inhibitor of the TRPM8 ion channel with IC50 value of 0.06 μM. 3,4-Dihydro-2(1H)-isoquinolinyl)[2-[(4-methoxyphenyl)amino]-4-thiazolyl]methanone inhibits TRPA1 with IC50 value of</p>

<p>Please enquire for more information about Cyclo(L-alanyl-L-tryptophyl) trifluoroacetate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>S-Lenalidomide is a drug that is used to treat cancer and autoimmune diseases. It is an immunomodulatory agent that induces cytokine release and inhibits the production of interleukin-2 (IL-2) by T cells. This drug also has a concentration-dependent effect on the activity of oxidative enzymes, such as benzalkonium chloride and light emission. S-Lenalidomide has been shown to be clinically relevant in infectious diseases, with concentrations producing significant effects on disease activity. The water vapor stability of this drug makes it suitable for use in humid environments such as those found in developing countries. S-Lenalidomide has been shown to induce antitumor responses without causing immunosuppression or toxicity in rats.</p>

<p>Please enquire for more information about Bromantane-d5 including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Diethoxy disulfide is a cyclin-dependent kinase inhibitor that induces apoptosis in cancer cells. It is an analog of the medicinal plant compound, alliin, and has been found to have potent anticancer activity. Diethoxy disulfide inhibits the activity of Chinese hamster ovary cell cycle kinases and human tumor-associated kinases, leading to cell cycle arrest and inhibition of cancer cell growth. This compound has been shown to be effective against a variety of cancer types, including breast, lung, and prostate cancer. Additionally, it has been found to sensitize cancer cells to other anticancer drugs by enhancing their cytotoxic effects. Overall, diethoxy disulfide is a promising candidate for the development of novel anticancer therapies.</p>

<p>N-[(1S)-1-(3-Fluorophenyl)-3-[(1R,5S)-3-[2-methyl-5-(2-methylpropanoyl)-6,7-dihydro-4H-imidazo[4,5-c]pyridin-1-yl]-8-azabicyclo[3.2. 1]octan-8-yl]propyl]acetamide is a research tool for use in cell biology and pharmacology studies. It is an activator that binds to the receptor or ligand and stimulates the activity of the protein. It has been shown to bind to ion channels, which are proteins that regulate the flow of ions across a biological membrane. This drug also interacts with antibodies and peptides (small chains of amino acids), which are important in life sciences as they are involved in many cellular functions including enzyme regulation and energy production.</p>

<p>Please enquire for more information about HYYYGAAPPGQKGQANATRIPAKTPPAPK{pT}PPSSGEPPKSGDRSGYSSPGSPGTPGSRSRTPSLP{pT}PPTREPKKVA-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Oleoyl-2-docosahexaenoyl phosphatidylcholine is a fatty acid derived from the biogenesis of phosphatidylcholine, which is an important component of all cell membranes.</p>

<p>The Tetracycline antibody is a highly specific monoclonal antibody that binds to tetracycline, a broad-spectrum antibiotic. This antibody has a high receptor binding affinity and can be used in various applications, such as polymerase chain reactions (PCR), immunohistochemistry, and Western blotting. It specifically targets tetracycline residues in biological samples, allowing for the detection and quantification of this antibiotic. In addition to its use in research, the Tetracycline antibody has potential applications in the field of medicine. It can be used to study the cellular localization of tetracycline within cells or tissues, providing valuable insights into its mechanism of action. Furthermore, this antibody can be utilized to investigate protein-protein interactions involving tetracycline or its derivatives. The Tetracycline antibody is produced using advanced techniques in monoclonal antibody production. It exhibits high specificity and sensitivity, ensuring reliable and accurate results. This antibody is compatible with various sample types, including</p>

<p>A novel muscarinic M3 receptor antagonist with high selectivity for M3 over M2 receptors</p>

<p>1,2-Dipalmitoyl-3-dimethylammonium-propane is a cationic lipid, which is a type of synthetic lipid commonly used in biochemical and biophysical research. It is sourced from chemical synthesis, involving the formulation of lipid molecules with specific chemical modifications to confer particular properties. The mode of action of this compound involves its ability to integrate into lipid bilayers and form liposomes. These liposomes can encapsulate nucleic acids, facilitating their delivery into cells by merging with cell membranes, which is crucial for gene delivery applications.</p>

<p>Please enquire for more information about 1,8-Dinitropyrene-d8 including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Crt0066101 hydrochloride is a peptide that has been shown to inhibit the activity of receptors for the neurotransmitter acetylcholine. It binds to the receptor and blocks access by acetylcholine, which prevents activation of the receptor. Crt0066101 hydrochloride is a ligand that inhibits ion channels in cells, including potassium channels, calcium channels, and sodium channels. This drug can be used as a research tool to study protein interactions in cell biology and pharmacology as well as to identify new drugs with potential therapeutic benefits. Crt0066101 hydrochloride is an inhibitor of G-protein coupled receptors (GPCRs) that has been shown to block the activation of muscarinic receptors on heart tissue. It also inhibits calcium-activated potassium channels on smooth muscle cells, leading to reduced blood pressure in animal models.</p>

<p>Purified native Human CEA protein (Preservative-free)</p>

<p>Dansyl-D-Ala-Gly-4-nitro-Phe-Gly-OH trifluoroacetate salt is a fluorescent marker that can be used in immunohistochemical staining. It binds to endogenous vasoactive intestinal peptide, calcitonin and other proteins in tissues and can be detected using immunostaining. Dansyl-D-Ala-Gly-4-nitro-Phe-Gly-OH trifluoroacetate salt is optimised for use as a substrate for neutral endopeptidase and metalloendopeptidase enzymes, which are responsible for the degradation of vasoactive intestinal peptide.</p>

<p>Fentanyl p Conjugate for use in immunoassays</p>

<p>Aryl hydrocarbon receptor (AhR) agonist</p>

<p>Please enquire for more information about MS67N including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1-Demethylcolchicine is a research tool for the study of ligand-receptor interactions and cell biology. It has also been used to study ion channels in the central nervous system, as well as antibody production. 1-Demethylcolchicine is a potent inhibitor of protein synthesis and is used to study peptides and proteins. 1-Demethylcolchicine binds to the receptor site on cells, which inhibits the activity of the ion channels that are responsible for generating an action potential. This inhibition leads to decreased nerve impulses in neurons, which may contribute to its sedative effects.</p>

<p>Alvameline is a muscarinic receptor agonist, which is a small molecule drug derived from synthetic chemistry processes. Its primary source is the intricate design of pharmacologically active compounds targeting the central nervous system. Alvameline exerts its effects through selective agonism of muscarinic acetylcholine receptors, playing a pivotal role in modulating neurotransmission. Specifically, by activating these receptors, it enhances cholinergic signaling, which is crucial for cognitive functions such as memory and attention.</p>

<p>Sheep polyclonal Mescaline antibody</p>

<p>Cortisol antibody was raised in mouse using cortisol-3 BSA as the immunogen.</p>

<p>Cys-Gly-3M3SH is a cationic antimicrobial peptide that has been shown to be effective against Staphylococcus aureus. Cys-Gly-3M3SH binds to the bacterial enzyme urease, which is responsible for converting urea into ammonia and carbon dioxide. The binding of this peptide prevents the hydrolysis of urea, leading to cell death by disruption of the proton motive force. Cys-Gly-3M3SH is also biotransformed by bacteria in humans and can be used as a probe for transport studies in vitro. It can also be used as a molecular probe for structural biology research, such as protein crystallization and electron microscopy studies.</p>

<p>N-Desethyl N-methyl rivastigmine is an analog of rivastigmine and a potent inhibitor of kinases. It has been shown to induce apoptosis in cancer cells, making it a promising candidate for the treatment of various types of tumors. This medicinal compound is excreted through urine and has been found to have anticancer properties by inhibiting protein kinases. In Chinese hamster ovary cells, N-Desethyl N-methyl rivastigmine was found to inhibit the activity of several kinases involved in cell proliferation and survival. This inhibitor has potential therapeutic applications for cancer treatment due to its ability to target specific kinases that are essential for tumor growth and progression.</p>

<p>Please enquire for more information about HYYYGAAPPGQKGQANATRIPAKTPPAPKTPPSSGEPPKSGDRSGYSSPGSPGTPGSRSRTPSLP{pT}PPTREPKKVA-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 Bantag-1 trifluoroacetate salt including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Osmanthuside H is a natural compound, specifically a phenylethanoid glycoside, which is predominantly sourced from the plant Osmanthus fragrans, as well as other related species. This compound is characterized by a specific glycosidic linkage that contributes to its stability and bioactivity. The mode of action of Osmanthuside H primarily involves its significant antioxidant properties, attributed to the presence of its phenolic structure and glycosidic moiety. This facilitates its role in scavenging free radicals and reducing oxidative stress within biological systems.</p>

<p>CAY10727 is a potent biochemical inhibitor, which is derived from synthetic sources with specific action targeting cyclooxygenase-2 (COX-2) enzymes. It functions by selectively blocking the enzymatic activity of COX-2, which plays a critical role in the biosynthesis of prostaglandins involved in inflammatory responses. This targeted inhibition allows the study of COX-2-related pathways without interference from COX-1, which is significant for maintaining gastrointestinal integrity.The use and applications of CAY10727 are primarily in research settings where understanding the pathways involved in inflammation, pain, and cancer progression are critical. This compound is utilized in various in vitro experiments to delineate the role of COX-2 in cellular and molecular contexts, enabling scientists to dissect complex signaling networks. Given its specificity, CAY10727 is instrumental in the development of new therapeutic approaches where selective COX-2 inhibition might offer benefits over non-selective inhibitors.</p>

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

<p>A negative allosteric modulator of Flt-3 receptor tyrosine kinase</p>

<p>Lactimidomycin is a peptide antibiotic that blocks the activity of ion channels, which are proteins that control the flow of ions across cell membranes. Lactimidomycin binds to specific ligands on the surface of cells and inhibits membrane depolarization. It has been shown to inhibit the activity of calcium-gated potassium channels, hyperpolarize nerve cells, and inhibit neuronal excitability. Lactimidomycin has also been shown to be an inhibitor of protein interactions with antibodies and other cellular factors. This drug can be used as a research tool for studying protein interactions in living cells. Lactimidomycin is available in high purity and at CAS No. 134869-15-1.</p>

<p>Secologanate is a peptide that has been used as a research tool to study the interactions between proteins and ligands. Secologanate is an inhibitor of ion channels, which are membrane-spanning proteins that control the flow of ions in and out of cells. It also inhibits protein interactions by blocking the binding site on one molecule for a second molecule. Secologanate has been shown to inhibit the ion channel TRPV1, which is involved in pain sensation. Secologanate has also been shown to be a ligand for the human angiotensin II receptor type 1 (AT1R).</p>

<p>The POLR3A protein (His &amp; Thioredoxin tag) is a highly versatile and essential component in Life Sciences research. This medicament is a Conjugated Protein that offers numerous applications in various fields. It can be used as a valuable tool for studying protein-protein interactions, carbon quantum dynamics, chemokine signaling pathways, and influenza hemagglutinin structure and function. Additionally, the POLR3A protein (His &amp; Thioredoxin tag) has been employed in the development of novel therapeutic strategies. Its unique properties make it an ideal candidate for the production of Proteins and Antigens, collagen-based scaffolds for tissue engineering, peptide agents for drug delivery systems, and as a carrier for endogenous erythropoietin. Furthermore, this product can be utilized as a reliable reagent in monoclonal antibody production and neutralizing assays against TGF-beta. Its exceptional binding affinity ensures accurate results in these experiments. The POLR3A protein (</p>

<p>Mycosubtilin is a potent antifungal lipopeptide, which is a secondary metabolite produced by the bacterium Bacillus subtilis. It is characterized by its ability to disrupt fungal cell membranes, leading to cell lysis and eventual death of the fungus. This mode of action is attributed to its amphiphilic structure, which allows it to integrate into the lipid bilayers of fungal cells, compromising the integrity of the membrane and altering its permeability.Mycosubtilin finds applications in various scientific and agricultural fields due to its efficacy against a broad spectrum of fungal pathogens. It is particularly useful in plant disease management, where it plays a role in biocontrol strategies against phytopathogenic fungi. Additionally, its antifungal properties make it a subject of interest in pharmaceutical research, where it is investigated for potential therapeutic applications in combating fungal infections. Researchers also explore Mycosubtilin as a model compound to understand lipopeptide interactions with membranes, contributing to the broader knowledge of antimicrobial agents.</p>

<p>The CYFRA21-1 antibody is a powerful tool in the field of Life Sciences. This antibody specifically targets fibronectin, a protein involved in cell adhesion and migration. It has cytotoxic properties, making it useful for studying cellular processes and identifying potential therapeutic targets. Additionally, the CYFRA21-1 antibody can be used to detect inhibitory factors or antiphospholipid antibodies in biological samples. It is also effective in detecting insulin antibodies, autoantibodies, and antibodies involved in glycosylation processes. With its high specificity and sensitivity, this monoclonal antibody is an invaluable tool for researchers looking to uncover new insights into various biological pathways and disease mechanisms.</p>

<p>Foslevodopa is a prodrug that is converted to levodopa in the body. This drug has been shown to be safe and effective for the treatment of Parkinson's disease with minimal side effects, although it does not affect the progression of the disease. Foslevodopa is a synthetic compound that has been synthesized using chemical methods. It can be manufactured in large quantities, making it a scalable pharmaceutical formulation.</p>

<p>VS1 is a novel synthetic peptide, which is engineered to function as an antimicrobial agent. This peptide originates from recombinant DNA technology, providing a customizable approach to target specific microbial strains. Its mode of action involves the selective disruption of microbial cell membranes, leading to the lysis and consequent death of the target cell. The specificity of VS1 for microbial cells over mammalian cells minimizes off-target effects, making it a highly effective agent for infection control.</p>

<p>Please enquire for more information about Fmoc-D-Asp(OtBu)-(Dmb)β-Ala-OH including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Sotirimod is a monocytic degradable drug that has been shown to be effective in the treatment of skin cancer. It is also used as a diagnostic agent for prostate, colorectal, and breast cancer. Sotirimod binds to fatty acid molecules on the surface of cells. The drug then enters the cell where it forms crosslinks with DNA or RNA, which prevents cell division and replication. This causes cell death by apoptosis. Sotirimod can also be conjugated with affinity ligands such as antibodies or peptides to target specific types of cells.</p>

<p>BCR-ABL-IN-2 is a small molecule inhibitor, which is synthetically derived for precision-targeted therapeutic applications. It functions as a selective inhibitor of the BCR-ABL fusion protein, a tyrosine kinase that is constitutively active in certain leukemias, particularly chronic myeloid leukemia (CML). The product is engineered via chemical synthesis to ensure high specificity and selectivity in binding to the ATP-binding site of the BCR-ABL protein, effectively inhibiting its kinase activity.</p>

<p>2A peptide-linked polycistronic vectors can be used to express multiple proteins from a single open reading frame (ORF). The small 2A peptide sequences, when cloned between genes, allows for efficient, stoichiometric production of discrete protein products within a single vector through a novel "cleavage" event within the 2A peptide sequence. 2A was discovered in the foot-and-mouth disease virus (FMDV, a picornavirus). The 2A peptide acts through ribosomal skipping to allow for the encoding of polyproteins which can dissociate into individual proteins upon translation. Anti-T2A antibody recognises 2A tagged recombinant proteins and is an excellent tool for researchers using 2A peptide based expression systems.<br>0.2mg/ml TEA (Rb L02T), 0.5mg/ml Glycine (Rb L02G). Used for ELISA (1:1000). Reacts with T2A tag.</p>

<p>Indicaxanthin is a natural pigment that has been found to possess potent anticancer properties. It is an analog of oseltamivir, a drug used to treat influenza by inhibiting the neuraminidase enzyme. Indicaxanthin has been shown to inhibit the activity of kinases, which are enzymes involved in cell signaling pathways that regulate cell growth and proliferation. This inhibition leads to apoptosis (programmed cell death) in cancer cells. Studies have demonstrated that indicaxanthin has anticancer effects against various types of cancer, including breast, colon, and prostate cancer. Additionally, it has been detected in human urine following ingestion of foods containing this pigment, suggesting that it may have potential as a dietary supplement for cancer prevention and treatment.</p>

<p>Panulisib is a Toll-like receptor (TLR) modulator that inhibits the TLR signaling pathway. It has been shown to inhibit the replication of certain viruses and to induce significant cytotoxicity in cancer cells. Panulisib binds to the toll-like receptor 7 (TLR7) and prevents it from activating downstream signaling pathways, which may be due to its ability to inhibit endothelial cell proliferation. The drug also shows some activity against hepatitis B virus-induced hepatitis in preclinical studies. In addition, panulisib inhibits growth factor signaling pathways and suppresses tumorigenesis by inhibiting the downstream effects of angiogenesis.</p>

<p>CB-1158 is an arginase inhibitor, which is a small molecule derived from a synthetic source designed to modulate immune functions. Its mode of action involves the inhibition of the arginase enzyme, a key player in the urea cycle responsible for the hydrolysis of arginine into ornithine and urea. By blocking arginase, CB-1158 effectively prevents the depletion of extracellular arginine, a vital amino acid required for the activation and proliferation of T cells within the immune system. This inhibition leads to enhanced immune responses against tumors.</p>

<p>Primate-specific Mas-related G protein-coupled receptor-X1 (MRGPR-X1) is highly enriched in dorsal root ganglia (DRG) neurones as well as in connective tissue mast cells (CTMC) and the leukaemia-derived human mast cell line (LAD)-2. MRGPR-X1 activation induces acute pain and therefore represents a promising target for future pain therapy. MRGPR-X1 is activated by bovine adrenal medulla peptide-8-22 (BAM 8-22) which is cleaved from pro-enkephalin by pro-hormone convertases. Unlike most if not all Gq-coupled receptors MRGPR-X1 does not undergo agonist-promoted endocytosis. Data: Western blot analysis of rat brain preparation. Lane 1: Rat brain preparation (20µg). Secondary: Goat anti-rabbit IgG conjugated to HRP 1:5000.</p>

<p>Cytochrome P450 2C19 (CYP2C19) is an enzyme that metabolizes retinoic acid, which is an important signaling molecule in the development and homeostasis of various tissues. CYP2C19 also metabolizes a variety of other compounds including xenobiotics such as drugs, carcinogens and environmental pollutants. CYP2C19 has been found to have a polymorphism at position 331 (I331V), which has been shown to be associated with an increase in metabolism of retinoic acid. This variant leads to increased activity for the enzyme and can result in vitamin A deficiency, hypervitaminosis A or teratogenicity.</p>

<p>Muscarine chloride hydrate is a receptor agonist. Muscarine binds to the acetylcholine receptors on the surface of muscle cells and nerve cells, causing an influx of calcium ions into the cell. Muscarine is used as a research tool for studying ion channels, proteins interactions, and peptides. It has been shown to be an activator of phospholipase C and phosphatidylinositol-specific phospholipase C in pancreatic acinar cells.</p>

<p>Anti-Trop2</p>

<p>Extracellular signal-regulated kinase 1/2 (ERK1/2) is a mitogen-activated protein kinase (MAPK) family protein and part of the Ras-Raf-MEK-ERK signalling pathway which plays a key role in controlling cell proliferation, differentiation and cell survival. ERK1/2 acts downstream of activated growth factor receptors, RAF protein kinases and mitogen-activated protein kinase kinases 1 and 2 (MEK1/2). MEK1 and MEK2 activate ERK1/2 by phosphorylation and once activated ERK1/2 enters the nucleus and phosphorylates transcription factors to induce changes in gene expression. In addition to this active ERK1/2 also translocates to other organelles including the endoplasmic reticulum, endosomes, golgi and mitochondria where it influences cell physiology. Overall ERK1/2 phosphorylates more than 200 different substrates including other protein kinases, transcription factors, RNA-binding proteins, regulators of mRNA translation and regulators of cell death. ERK1/2 pathway is strongly implicated in cancer where its hyperactivation underpins the growth and maintenance of many tumour types. Data: Western blot analysis of whole cell extract of Mouse embryonic Fibroblasts (MEFs).</p>

<p>Pigment Red 48 (C.I. 15865) is a red organic pigment that is soluble in water and most organic solvents. It has a melting point of 200°C and is used in paints, plastics, textiles, paper, and other products. Pigment Red 48 (C.I. 15865) can be synthesized by the diazonium salt coupling reaction between an aromatic amine and an acid chloride. The pigment also has a hydroxyl group that enables it to form covalent bonds with other molecules such as polymers or proteins. Pigment Red 48 (C.I. 15865) is used in many products because of its high stability, excellent heat resistance, low toxicity, non-irritating properties, high transparency, and good color fastness to light and washing.BR&gt; Pigment Red 48 (C.I. 15865) is not considered hazardous according to the Globally Harmonized System of Classification and Lab</p>

<p>FR-190809 is a peptide that acts as an inhibitor of protein interactions. It binds to the receptor and blocks the activation of phospholipase C. FR-190809 also stimulates the production of cyclic AMP, which in turn activates protein kinase A, thereby inhibiting the production of cAMP. FR-190809 has been shown to have a high purity and is used as a research tool for studying protein interactions.</p>

<p>1-Palmitoyl-2-Oleoyl-sn-Glycero-3-Phosphatidylethanolamine is a broad spectrum antimicrobial that has been shown to have binding properties to peptides. This compound can be used as a potential antimicrobial for the treatment of bacterial infections and gramicidin, an antibiotic that is active against bacteria. It has also been shown to permeabilize cell membranes, which may lead to its function as an antimicrobial agent. 1-Palmitoyl-2-Oleoyl-sn-Glycero-3-Phosphatidylethanolamine is water soluble and has been shown to have conformational properties. These conformational properties are responsible for its binding activity with peptides. 1POGPE is stable in both calorimetric assays and bilayers, which allows it to maintain its structure when interacting with other compounds. 1POGPE also has a high affinity for</p>

<p>Please enquire for more information about 1,6-Dichloro-1,6-dideoxy-beta-D-fructofuranose including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>PF-06658607 is an investigational drug that is classified as a small molecule inhibitor. It is developed from synthetic chemical sources with a specific mode of action targeting aggrecanases, enzymes that degrade aggrecan, a critical component of cartilage. By inhibiting these enzymes, PF-06658607 aims to prevent the breakdown of cartilage in joints.</p>

<p>L 162389 is a synthetic, non-steroidal, anti-inflammatory drug (NSAID) that inhibits the enzyme cyclooxygenase. It inhibits the production of prostaglandins, which are known to cause pain and inflammation in the body. L 162389 is used for the treatment of inflammatory conditions such as rheumatoid arthritis and osteoarthritis.</p>

<p>Debio-0827 is a peptide that activates the human G protein coupled receptor (GPCR) of the serotonin type 2A (5HT2A) receptor. It has been used as a research tool for studying the activation of 5HT2A receptors and their effects on ion channels and protein interactions. Debio-0827 is a potent inhibitor to the binding of ligands to 5HT2A receptors, which may be used in pharmacological studies.</p>

<p>MCOPPB is a new type of drug that is used to treat chronic neuropathic pain and other syndromes. MCOPPB has shown an analgesic effect in vivo, which may be due to its ability to stimulate the release of endogenous opioids. MCOPPB also reduces the pain threshold and increases tolerance to pain by stimulating the release of endorphins. This drug has been shown to have no effects on locomotor activity in knockout mice and has been tested for efficacy in clinical studies with humans.</p>

<p>Faradiol 3-palmitate is a potent anticancer agent that has been used in Chinese traditional medicine for centuries. It is an inhibitor of cancer cell growth and has been shown to induce apoptosis in various types of tumors. Faradiol 3-palmitate inhibits protein kinase activity, which is essential for the regulation of the cell cycle and cell division. This compound also acts as an analog of urinary inhibitors and has medicinal properties that make it a promising therapeutic agent for cancer treatment. Studies have shown that Faradiol 3-palmitate can reduce tumor size and inhibit tumor growth in human cancer cells, making it a valuable addition to any cancer treatment regimen.</p>

<p>Faradiol 3-myristate is a medicinal analog that has shown potent anticancer activity against human tumors. It acts as a kinase and protein inhibitor, which leads to the inhibition of cancer cell growth and the induction of apoptosis. This compound has been shown to be effective in treating leukemia and other types of cancer. Faradiol 3-myristate is derived from Chinese medicinal plants and has been found in urine samples of cancer patients. As an inhibitor, it prevents the activation of enzymes that promote tumor growth, making it a promising candidate for future cancer treatments. Its unique properties make it an invaluable tool for cancer research and therapy.</p>

<p>Xantocillin is a broad-spectrum antimicrobial agent that has been shown to be active against a wide range of human pathogens. It contains a hydroxyl group in its chemical structure and is used to treat bowel diseases and infectious diseases. Xantocillin also has significant cytotoxicity, which means that it may cause damage to cells or tissues. The drug has been demonstrated to have significant cytotoxicity in animal models with plasma mass spectrometry. Xantocillin has been shown to kill bacteria by reacting with the fatty acid component of the bacterial cell membrane, which increases permeability, leading to cell death.</p>

<p>Oxocarbazate is a potent anticancer drug that acts as an analog of the protein kinase inhibitor, staurosporine. It has been found to induce apoptosis in tumor cells and inhibit cell cycle progression. Oxocarbazate is a promising medicinal compound for the treatment of cancer, as it has shown to be effective against human cancer cell lines. This inhibitor has also displayed significant anti-tumor activity in Chinese hamster ovary cells, making it a potential candidate for cancer therapy. Furthermore, oxocarbazate has been detected in urine samples from patients undergoing chemotherapy, suggesting its potential use in clinical settings.</p>

<p>Progesterone receptor antagonist; antineoplastic</p>

<p>O 1812 is a cannabinoid receptor antagonist. It blocks the binding of cannabinoids to their receptors, thereby inhibiting the effects of cannabinoids. O 1812 has been shown to have therapeutic potential in treating kidney disease, bone growth, and cardiovascular disorders. This drug can also be used in cancer therapy and Alzheimer's disease treatment due to its ability to modulate the activity of certain receptors. O 1812 is a programmable compound that can be configured for specific purposes by adding or removing functional groups from the molecule. The addition of an alkoxy radical group at one end of the molecule allows it to be used as an endpoint marker for DNA sequencing reactions because it fluoresces when excited with ultraviolet light.</p>

<p>Ptac oxalate is a high-purity, white crystalline powder. It is the salt of Ptac, which is an inhibitor of protein interactions. This reagent can be used as a research tool in cell biology and immunology studies. Ptac oxalate has been shown to inhibit the interaction between human alpha-thrombin and various proteases including trypsin, chymotrypsin, and papain. In addition, Ptac oxalate inhibits the binding of human alpha-thrombin with immobilized antibody.</p>

<p>Please enquire for more information about Venetoclax-M27 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 Imexine FAM including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Parainfluenza viruses (PIVs) belong to the Paramyxoviridae family and are a common cause of respiratory infections, particularly in children.<br>There are four main types: Human Parainfluenza virus-1 (HPIV-1), HPIV-2, HPIV-3, and HPIV-4, each associated with different patterns of illness. HPIV-1 and HPIV-2 are the primary causes of colds and croup. HPIV-3 often leads to bronchitis and pneumonia, while it is thought HPIV-4 causes similar symptoms HPIV-3.<br>Parainfluenza viruses spread through respiratory droplets and while most infections are mild, infants, young children, and immunocompromised individuals may experience severe respiratory illness.<br>Parainfluenza Virus Type 2 Antigen has potential application in the development of diagnostic assays to detect antibodies in patient samples, confirming HPIV-2 infection. It can also be used as a research tool in vaccine development.</p>

<p>Lepirudin is a drug used to treat thrombosis and pulmonary embolism. It inhibits the function of thrombin by binding to its active site and preventing it from converting fibrinogen into fibrin. Lepirudin is an inhibitor molecule that binds to human polymorphonuclear leukocytes, which are cells that contain large quantities of protein. The rate constant for the reaction between these two molecules was determined using chromatographic analysis. Lepirudin has been shown to be toxic in animal studies, leading to allergic symptoms such as rash, fever, chills, nausea, and vomiting. These reactions were reduced when given orally as a prodrug.</p>

<p>Tetflupyrolimet is a medicinal compound that has shown promising results in inhibiting the growth and progression of cancer cells. It works by targeting specific kinases that are involved in the regulation of cell cycle and protein synthesis. Tetflupyrolimet has been shown to be effective against various types of cancer, including leukemia, by inducing apoptosis or programmed cell death in tumor cells. In Chinese studies, it was found to inhibit the proliferation of human cancer cells and act as an anticancer inhibitor. This compound has also been tested in urine samples from cancer patients and has shown potential as a diagnostic tool for early detection of certain types of cancer. With its potent anticancer properties, Tetflupyrolimet could be a valuable addition to the arsenal of cancer-fighting drugs available today.</p>

<p>SB 205384 is a drug that binds to the all-trans retinoic acid (ATRA) receptor, which is found in cerebellar granule cells. SB 205384 has been shown to have anxiolytic effects in vivo and in vitro, as demonstrated by its ability to inhibit the release of potassium ions from cerebellar granule cells. The binding site of SB 205384 has been mapped to the ATRA agonist binding site on the α1 subunit of the GABA A receptor complex. This drug also blocks chloride channels, which may be responsible for its anxiolytic activity.</p>