Biochemicals and Reagents
Biochemicals and reagents are fundamental substances for research and development in fields such as biotechnology, molecular biology, pharmacology, and medicine. These products are essential for a variety of applications, including compound synthesis, biological sample analysis, metabolic process research, and drug production. At CymitQuimica, we offer a wide selection of high-quality, high-purity biochemicals and reagents suitable for various scientific and industrial needs. Our catalog includes enzymes, antibodies, nucleic acids, amino acids, and many other products, all designed to support researchers and professionals in their research and development projects, ensuring reliable and reproducible results.
Subcategories of "Biochemicals and Reagents"
- Biomolecules(98,697 products)
- By Biological Target(100,169 products)
- By Pharmacological Effects(6,834 products)
- Cryopreservatives(21 products)
- Desinfectants and Related Compounds(28 products)
- Hormones(357 products)
- Plant Biology(6,896 products)
- Secondary Metabolites(14,347 products)
Found 130152 products of "Biochemicals and Reagents"
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1-Deacetylnimbolinin-B
CAS:1-Deacetylnimbolinin-B is a fructan that belongs to the class of flavonoids. A method validation for 1-deacetylnimbolinin-B has been carried out using flow rate and fingerprint analysis. The chromatogram was used to identify the marker, which was then analyzed by tautomeric analysis and fingerprint analysis. This compound was found to have an average index of 0.5, which is a marker for its validation. 1-Deacetylnimbolinin-B can be used as a marker for identifying other compounds in the limonoid family.Formula:C33H44O9Purity:Min. 95%Molecular weight:584.7 g/molRo 4584820
CAS:Inhibitor of cyclin-dependent kinases CDK1, CDK2, CDK4 and CDK7Formula:C18H21F2N5O4SPurity:Min. 95%Molecular weight:441.45 g/molMyomodulin
CAS:Myomodulin is a protein that is found in the carboxy terminal end of a fatty acid, which has been shown to be effective at treating infectious diseases such as Stenotrophomonas maltophilia. Myomodulin has also been shown to have ganglia protective effects and can increase levels of cAMP in cells. It is also used as a pharmaceutical drug for inflammatory diseases. Myomodulin is also used in diagnostic agents for inflammatory diseases. Myomodulin is an amino acid that regulates the body's immune system by inhibiting inflammation. It works by blocking the production of prostaglandin E2 (PGE2) in macrophages, which are cells that produce pro-inflammatory cytokines and histamine. This prevents the production of PGE2 from arachidonic acid, which causes inflammation and pain.Formula:C38H68F3N11O10S2Purity:Min. 95%Molecular weight:960.1 g/molLeptin Dog
Leptin is a protein hormone that is produced by fat cells. Leptin regulates appetite and energy use, and it has been shown to be involved in the regulation of body weight. Leptin binds to receptors on the surface of cells, which activates signaling pathways inside the cell. This receptor can be activated by other ligands such as ghrelin, adiponectin, and insulin. Leptin also inhibits ion channels in neurons, resulting in an increase in potassium conductance.
Purity:Min. 95%BMS-779788
CAS:BMS-779788 is a drug for the treatment of dyslipidemia and other conditions. It has been shown to inhibit the constitutive androstane receptor, which is involved in inflammation and oxidative stress. BMS-779788 also inhibits the synthesis of fatty acids, leading to an increase in the production of high-density lipoprotein cholesterol. This agent has also been shown to be effective against statins-resistant patients with hypercholesterolemia. BMS-779788 is currently being investigated as a potential therapeutic agent for cardiovascular disorders such as atherosclerosis, myocardial infarction, and stroke.Formula:C28H29ClN2O3SPurity:Min. 95%Molecular weight:509.06 g/molOBA-09
CAS:OBA-09 is a neuroprotective agent that inhibits the production of TNF-α. It also prevents microglial activation and has anti-oxidative effects that may be useful for the prevention of neuronal death. OBA-09 has shown to be effective in treating neurodegenerative diseases by preventing oxidative damage to neurons and suppressing inflammation. This drug is not yet approved for use in humans, but has been tested on animals with success.Formula:C10H8O5Purity:Min. 95%Molecular weight:208.17 g/molTL13-112
CAS:TL13-112 is a high purity, life science research reagent that can be used as a receptor activator or inhibitor. It is an agonist of the muscarinic acetylcholine receptor and has been shown to activate G proteins in the presence of M1 receptor ligands. TL13-112 is a cell biology research tool that can be used to study protein interactions. This compound has been shown to bind to the extracellular domain of the human epidermal growth factor receptor (EGFR) and inhibit its activity.Formula:C49H60ClN9O10SPurity:Min. 95%Molecular weight:1,002.6 g/molTC-G 1004
CAS:TC-G 1004 is a peptide that binds to the acetylcholine receptor, an ion channel protein found in neurons. TC-G 1004 blocks the passage of ions through the ion channel and inhibits the action of acetylcholine on the receptor. TC-G 1004 is used as a research tool and pharmacological agent in studies of protein interactions, cell biology, and neurobiology.Formula:C22H27N7O2Purity:Min. 95%Molecular weight:421.5 g/molGnGn-bi-Asn-PABA
GnGn-bi-Asn-PABA is a peptide that has been shown to activate the nicotinic acetylcholine receptor. It binds to the ligand binding site of the receptor and mimics the natural neurotransmitter acetylcholine, increasing the probability of neurotransmitter release. GnGn-bi-Asn-PABA has also been shown to inhibit calcium ion channels and ligand gated ion channels, which are proteins that regulate the flow of ions in and out of cells. GnGn-bi-Asn-PABA is a research tool used for studying cell biology and pharmacology.Formula:C63H103N9O37Purity:Min. 95%Molecular weight:1,578.5 g/molPF 06446846 hydrochloride
CAS:Inhibitor of PCSK9 enzyme
Formula:C22H20ClN7O·xHClPurity:Min. 95%Molecular weight:433.89 g/molEHP-101
CAS:EHP-101 is a synthetic cannabinoid that binds to the CB2 receptor. It has been shown to have anti-inflammatory effects and may be useful for the treatment of skin cancer, atp levels in cardiac cells, and microglia activation. This drug has also been shown to stimulate collagen production and inhibit neuronal death. Clinical studies have shown that EHP-101 can be used to treat inflammatory diseases such as Crohn's disease and ulcerative colitis.Formula:C28H35NO3Purity:Min. 95%Molecular weight:433.6 g/molPF-03882845
CAS:PF-03882845 is a selective small molecule inhibitor of Janus kinase 3 (JAK3), which is derived from a pharmaceutical synthesis process. Its mode of action involves targeting and inhibiting the JAK3 enzyme, a crucial component of the JAK-STAT signaling pathway, which is integral to immune system function and various cellular processes. By specifically inhibiting JAK3, PF-03882845 interferes with the signaling pathways that rely on this kinase, potentially modulating immune responses.Formula:C24H22ClN3O2Purity:Min. 95%Molecular weight:419.9 g/molSJF620
CAS:SJF620 is a Chinese medicinal compound that has been shown to be an effective inhibitor of tumor growth in human cancer cells. This anticancer agent has been found in the urine of patients receiving traditional Chinese medicine for the treatment of various cancers. SJF620 works by inhibiting kinases, which are proteins that play a key role in cell division and proliferation. By blocking these kinases, SJF620 induces apoptosis (programmed cell death) in cancer cells, leading to their destruction. SJF620 is an analog of other kinase inhibitors and has shown promising results in preclinical studies as a potential treatment for various types of cancer.Formula:C41H44N8O7Purity:Min. 95%Molecular weight:760.8 g/mol1,2-Diheneicosanoyl-sn-glycero-3-phosphocholine
CAS:1,2-Dieneicosanoyl-sn-glycero-3-phosphocholine (DEGPC) is a lipid molecule that has been shown to be effective in the treatment of cancer. It is a long chain fatty acid that is found in leukocytes and acts as an inhibitor of cellular proliferation. This compound has been encapsulated into liposomes and pegylated for intravenous injection. DEGPC can be used as a bioconjugate in biomedical applications, such as drug delivery and targeted therapy. DEGPC has been shown to have anti-inflammatory properties, which may be due to its ability to inhibit the production of prostaglandins from arachidonic acid.Formula:C50H100NO8PPurity:Min. 95%Molecular weight:874.3 g/molPS432
CAS:PS432 is a molecule that inhibits the kinase domain of the atypical protein kinase, Fps1. PS432 also blocks the activation of ethylene receptors by inhibiting the binding of ethylene to its receptor. This leads to the inhibition of protein synthesis and the inhibition of tumor cell growth in vitro and in vivo. PS432 has been shown to be effective against lung cancer cells, which are resistant to other anti-cancer drugs. The crystallographic data for this molecule has been published in Biochemistry and Cell Biology.
Formula:C25H19ClN2O5SPurity:Min. 95%Molecular weight:494.9 g/molrac Tolterodine-d14 hydrochloride
CAS:rac Tolterodine-d14 hydrochloride is an isotopically labeled compound, specifically a deuterium-labeled version of tolterodine. It is synthesized for research purposes and serves as a powerful tool for studying the pharmacokinetics and metabolic pathways of tolterodine in biological systems. The deuterium isotopes in the compound allow for detailed and precise tracing during analytical studies.Formula:C22H18D14ClNOPurity:Min. 95%Molecular weight:376.03 g/molEC330
CAS:EC330 is a new generation of actuator that has been designed to increase the energy efficiency of cancer therapy. It is a molecule that, when fused with recombinant proteins, can be used as an inhibitor for growth factor receptors for leukemia inhibitory factor (LIF) and mcf-7 cells. EC330 is capable of inhibiting the function of LIF through reversible binding to its receptor, which inhibits cell proliferation and promotes cell death. EC330 was shown to reduce primary tumor volume by 50% in mice models. EC330 also has potential as a contraceptive agent due to its ability to inhibit the production of progesterone by ovarian granulosa cells.Formula:C30H32F2O2Purity:Min. 95%Molecular weight:462.57 g/molUlixertinib hydrochloride
CAS:Ulixertinib is an investigational drug, which is an inhibitor of the receptor tyrosine kinase MET. Ulixertinib has been shown to inhibit the proliferation of cancer cells and induce tumor regression in a xenograft model of human lung adenocarcinoma. It also inhibits the growth of cancer cells by blocking cell cycle progression at G2/M phase and inducing apoptosis. Ulixertinib inhibits MET-mediated phosphorylation of downstream signaling molecules that regulate cell survival, proliferation, motility, angiogenesis, and metastasis. Ulixertinib hydrochloride is a high purity product with a purity level > 98%.
Formula:C21H23Cl3N4O2Purity:Min. 95%Molecular weight:469.79 g/mol
