Modulateurs d'enzymes
Les modulateurs d'enzymes sont des composés qui peuvent augmenter ou inhiber l'activité des enzymes, régulant ainsi la vitesse des réactions biochimiques. Ces modulateurs jouent un rôle essentiel dans le contrôle des voies métaboliques, de la signalisation cellulaire et de divers processus physiologiques. Les modulateurs d'enzymes sont largement utilisés dans la recherche et le développement de médicaments pour étudier les fonctions enzymatiques et développer des agents thérapeutiques. Chez CymitQuimica, nous proposons une gamme complète de modulateurs d'enzymes de haute qualité pour soutenir vos recherches sur la régulation enzymatique et la découverte de médicaments.
Sous-catégories appartenant à la catégorie "Modulateurs d'enzymes"
693 produits trouvés pour "Modulateurs d'enzymes"
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Lumiracoxib - Bio-X ™
CAS :Produit contrôlé<p>Lumiracoxib is a COX-2 selective non-steroidal anti-inflammatory drug that is used for the treatment of osteoarthritis. This drug inhibits prostaglandin synthesis via inhibition of COX-2.</p>Formule :C15H13ClFNO2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :293.72 g/molDovitinib base
CAS :<p>Receptor tyrosine kinase inhibitor; anti-angiogenesis; anti-oncogenesis</p>Formule :C21H21FN6ODegré de pureté :Min. 98 Area-%Couleur et forme :PowderMasse moléculaire :392.43 g/molAfatinib - Bio-X ™
CAS :<p>Afatinib is a small molecule that inhibits the activity of cellular kinases that are involved in the progression of cancer. It is an Irreversible inhibitor of three members of the ErbB family. This molecule binds covalently to cysteine 797 residue in HER2 and blocks downstream cellular signalling which inhibits cellular growth and promotes apoptosis. It has been researched for the treatment of non-small cell lung cancer (NSCLC), breast cancer, pancreatic cancer and colorectal cancer.</p>Formule :C24H25ClFN5O3Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :485.94 g/molCamostat mesylate - Bio-X ™
CAS :<p>Camostat is a serine protease inhibitor that is used for the treatment of chronic pancreatitis. This drug has shown to reduce inflammation and pain. Studies have shown that Camostat has also inhibited the entry of SARS-CoV-2 in lung cells by inhibiting the priming process of S-protein, necessary for the viral entry into host cells.</p>Formule :C20H22N4O5•CH4O3SDegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :494.52 g/molLOXO-305
CAS :<p>LOXO-305 is a small molecule inhibitor, which is a synthesized chemical compound designed to selectively target specific enzymes or pathways. Its source is rooted in medicinal chemistry and pharmacological research aimed at elucidating pathways involved in oncogenesis.</p>Formule :C22H21F4N5O3Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :479.43 g/molR-(-)-Arundic acid
CAS :<p>R-(-)-Arundic acid is a chiral compound, which is a derivative of arundic acid specifically designed for enantiomeric purity. It is sourced through synthetic organic chemistry processes, allowing for precise control over its stereochemistry. The mode of action of R-(-)-Arundic acid involves the inhibition of astrocyte activation by modulating the synthesis of certain cytokines and inflammatory mediators. This mechanism provides a neuroprotective effect, making it a valuable tool in the study of neurodegenerative diseases and brain injuries.</p>Formule :C11H22O2Degré de pureté :Min. 98 Area-%Couleur et forme :Clear Viscous LiquidMasse moléculaire :186.29 g/molAnastrozole - Bio-X ™
CAS :Produit contrôlé<p>Anastrozole is a non-steroidal drug that belongs to the class of aromatase inhibitors. It inhibits the production of estrogen by blocking the conversion of androgens to estrogens in peripheral tissues. The drug has been shown to be effective in treating breast cancer in postmenopausal women. In vitro assays have shown that Anastrozole can inhibit tumor growth as well as induce apoptosis in human serum cells, which suggests that it may be effective against a variety of cancers.</p>Formule :C17H19N5Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :293.37 g/molBrivanib alaninate
CAS :<p>VEGFR2 a tyrosine kinase receptor inhibitor; antineoplastic</p>Formule :C22H24FN5O4Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :441.18123Ulixertinib
CAS :<p>Inhibitor of ERK1 and ERK2 kinases</p>Formule :C21H22Cl2N4O2Degré de pureté :Min. 95%Couleur et forme :White PowderMasse moléculaire :433.33 g/molGefitinib hydrochloride
CAS :<p>RIPK2 protein kinase inhibitor; EGFR inhibitor</p>Formule :C22H24ClFN4O3·HClDegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :483.36 g/molCrenolanib
CAS :<p>Inhibits type III tyrosine kinases (PDGFRα, PDGFRβ, FLT3)</p>Formule :C26H29N5O2Degré de pureté :Min. 95%Couleur et forme :White To Yellow SolidMasse moléculaire :443.54 g/molBMS 754807
CAS :<p>A reversible inhibitor of IGF-1R kinase and insulin receptor. Has anti-growth effects in mesenchymal, epithelial and hematopoietic tumor types. Synergistic with other cytotoxic, hormonal and targeted anti-cancer therapy.</p>Formule :C23H24FN9ODegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :461.49 g/molAceclofenac - Bio-X ™
CAS :<p>Acecelofenac is a non-steroidal anti-inflammatory drug that is used in the treatment of osteoarthritis, arthritis, and ankylosing spondylitis. This drug is also a cyclooxygenase inhibitor and works by inhibiting this enzyme so that pain and inflammation is reduced.</p>Formule :C16H13Cl2NO4Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :354.18 g/molSivelestat
CAS :<p>Inhibitor of human neutrophil elastase</p>Formule :C20H22N2O7SDegré de pureté :Min. 95%Masse moléculaire :434.46 g/molMGCD 265
CAS :<p>Inhibits MET, VEGFR1-3, Tie and Ron tyrosine kinases; antineoplastic</p>Formule :C26H20FN5O2S2Degré de pureté :Min. 95%Masse moléculaire :517.60 g/molThioglycosyl Naphthalimide
CAS :<p>Thioglycosyl Naphthalimide is a highly potent human O-GlcNAcase (hOGA) inhibitor with good selectivity against human β-N-acetylhexosaminidase B (HsHexB).</p>Formule :C30H40N4O7SDegré de pureté :Min. 95%Masse moléculaire :600.73 g/molXMU MP 2
CAS :<p>BRK tyrosine kinase (PTK6) inhibitor; anti-proliferative in breast cancer cells</p>Formule :C32H33F3N8O2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :618.65 g/molCZC 25146
CAS :<p>Inhibitor of leucine-rich repeat kinase LRRK2Â</p>Formule :C22H25FN6O4SDegré de pureté :Min. 98 Area-%Couleur et forme :PowderMasse moléculaire :488.54 g/molMRK 560
CAS :<p>γ-secretase inhibitor; reduces amyloid-β in brainÂ</p>Formule :C19H17ClF5NO4S2Degré de pureté :Min. 95%Masse moléculaire :517.92 g/molGNE 6776
CAS :<p>Specific inhibitor of the ubiquitin specific protease-7 (USP7), which is a validated deubiquitinase of the E3 ubiquitin-protein ligase MDM2. The compound inhibits the USP7 deubiquitinase activity by binding to acidic amino acid residues important for the interaction with ubiquitin. Induces tumor cell death and enhances cytotoxicity of chemotherapeutic agents.</p>Formule :C20H20N4O2Degré de pureté :Min. 95%Masse moléculaire :348.4 g/molIdelalisib
CAS :<p>Idelalisib is a pharmaceutical drug that functions as a PI3Kδ inhibitor, developed through synthetic chemical processes. Its mode of action involves selectively targeting and inhibiting phosphatidylinositol 3-kinase delta (PI3Kδ), a lipid kinase that plays a crucial role in the signaling pathways responsible for cell proliferation, survival, and differentiation. By inhibiting this enzyme, Idelalisib effectively impedes pathways that are often hyperactivated in certain hematologic malignancies, thereby exerting antitumor effects.</p>Formule :C22H18FN7ODegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :415.42 g/molSRT1720 hydrochloride
CAS :<p>SIRT1 activator</p>Formule :C25H23N7OS·xHClDegré de pureté :Min. 98 Area-%Couleur et forme :PowderMasse moléculaire :469.56 g/molAG 221
CAS :<p>Inhibitor of isocitrate dehydrogenase 2</p>Formule :C19H17F6N7ODegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :473.38 g/molDCC 2036
CAS :<p>Inhibits multiple tyrosine kinases (Abl1, Src family kinases, Tie-2 and VEGFR-2)</p>Formule :C30H28FN7O3Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :553.59 g/molPeiminine
CAS :<p>Inhibitor of TGF-α, CTGF, ERK1/2, NF-κB and FasL; anti-inflammatory</p>Formule :C27H43NO3Degré de pureté :Min. 98 Area-%Masse moléculaire :429.64 g/molSGC AAK1 1
CAS :<p>Dual inhibitor of the adaptor protein 2-associated kinase 1 (AAK1) and BMP2-inducible kinase (BMP2K) with IC50 values of 270 nM and 1 μM, respectively. In a recent study, SGC AAK1 1 stabilised β-catenin, inhibited phosphorylation of the AP2 complex subunit mu protein (AP2M1) and activated Wnt signalling in in vitro experiments._x000D_</p>Formule :C21H25N5O3SDegré de pureté :Min. 95%Couleur et forme :SolidMasse moléculaire :427.52 g/molEbselen
CAS :<p>Ebselen is a non-toxic organoselenium compound with antioxidant, anti-inflammatory and cytoprotective properties. Ebselen is an inhibitor of lipoxygenases, nitric oxide (NO) synthases, protein kinase C, H+/K+-ATPase, thioredoxin reductase and NADPH oxidase. Recently, ebselen has been identified by several studies as a covalent inhibitor of the main protease Mpro from coronaviruses. For the SARS-CoV-2 main protease Mpro, the IC50 value is 0.67 μM and EC50 is 4.57 μM.</p>Formule :C13H9NOSeDegré de pureté :Min. 98 Area-%Couleur et forme :PowderMasse moléculaire :274.18 g/molMinaprine dihydrochloride
CAS :Produit contrôlé<p>Short acting monoamine oxidase inhibitor</p>Formule :C17H22N4O•(HCl)2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :371.3 g/molLY 2886721
CAS :<p>Inhibitor of BACE1 protease</p>Formule :C18H16F2N4O2SDegré de pureté :Min. 98 Area-%Couleur et forme :PowderMasse moléculaire :390.41 g/molZileuton- Bio-X ™
CAS :<p>Zileuton is an inhibitor of the 5-lipoxygenase enzyme, thus preventing the leukotrienes LTE4, LDT4, LTB4 and LTC4 from being formed. This in turn reduces inflammation, bronchoconstriction and mucus secretion in the airways. As a result, Zileuton can be used in the treatment and management of asthma and allergic rhinitis. Studies have shown that Zileuton has the potential to reverse dementia-related brain damage.</p>Formule :C11H12N2O2SDegré de pureté :(%) Min. 95%Couleur et forme :PowderMasse moléculaire :236.29 g/molMalotilate - Bio-X ™
CAS :<p>Malotilate is a pharmacological agent that is used to treat symptoms of hepatitis, bowel disease, and collagen diseases. This drug reduces collagen synthesis and cell migration activity of fibroblasts in vitro. It also has been shown to facilitate liver regeneration in rats.</p>Formule :C12H16O4S2Degré de pureté :(%) Min. 95%Couleur et forme :PowderMasse moléculaire :288.39 g/molKenpaullone
CAS :<p>Inhibitor of glycogen synthase 3 (GSK-3) and cyclin-dependent kinases CDK1, CDK2 and CDK5. Kenpaullone can substitute transcription factor Klf4 in reprogramming of fibroblast to induced pluripotent stem cells when using the method of ectopic expression of transcriptional factors. In an in vitro model for Alzheimer’s disease, kenpaullone decreased production of amyloid beta peptides Aβ40 and Aβ42.</p>Formule :C16H11BrN2ODegré de pureté :Min. 95%Couleur et forme :Yellow To Dark Yellow SolidMasse moléculaire :326.00548GSK 2606414
CAS :<p>Inhibitor of EIF2AK3/PERK kinases</p>Formule :C24H20F3N5ODegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :451.44 g/mol(S)-Mephenytoin - Bio-X ™
CAS :<p>(S)-Mephenytoin is a substrate of cytochrome P450 enzyme CYP2C19 (a hydroxylase). It is an effective anticonvulsant that improves control of seizures in patients. According to studies, the drug exhibits a genetic polymorphism in CYP2C19 that results in reduced metabolism in some individuals.</p>Formule :C12H14N2O2Degré de pureté :Min. 97 Area-%Couleur et forme :White PowderMasse moléculaire :218.25 g/molCA3
CAS :<p>Inhibits YAP/Tead transcriptional activity. Has anti-tumour effects on oesophageal adenocarcinoma with therapeutic potential in combination with 5-FU. Involved in ferroptosis, mediated by iron-dependent ROS.</p>Formule :C23H27N3O5S2Degré de pureté :Min. 95%Couleur et forme :White Off-White PowderMasse moléculaire :489.61 g/molEtimizol
CAS :<p>Analeptic</p>Formule :C9H14N4O2Degré de pureté :Min. 95%Masse moléculaire :210.23 g/molEtodolac - Bio-X ™
CAS :<p>Etodolac is a non-steroidal anti-inflammatory drug (NSAID) used to treat osteoarthritis and rheumatoid arthritis. It is also used to treat acute pain. This drug works by inhibiting prostaglandin synthesis from the inhibition of the enzyme cyclooxygenase.</p>Formule :C17H21NO3Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :287.35 g/molDMAT
CAS :<p>Inhibitor of protein kinase CK2</p>Formule :C9H7Br4N3Degré de pureté :Min. 95%Couleur et forme :White PowderMasse moléculaire :476.79 g/mol6-Thioguanine - Bio-X ™
CAS :<p>6-Thioguanine is a purine analog used in the therapy for leukemia and for remission consolidation in patients with acute nonlymphocytic anemia. This drug also has antimetabolite action. It replaces guanine during DNA replication. This substitution disrupts the accurate pairing of DNA bases, leading to errors in DNA replication and hinders cell division.</p>Formule :C5H5N5SDegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :167.19 g/molML 210
CAS :<p>Inhibitor of glutathione peroxidase GPX4</p>Formule :C22H20Cl2N4O4Degré de pureté :Min. 95%Couleur et forme :SolidMasse moléculaire :475.32 g/molTriptolide
CAS :<p>Inhibits RNAPII-mediated trasncription; immunosuppressant; anti-inflammatory</p>Formule :C20H24O6Degré de pureté :Min. 97 Area-%Couleur et forme :PowderMasse moléculaire :360.4 g/molBRD 6989
CAS :<p>A small molecule inhibitor with high selectivity for CDK8 over CDK19. Increases IL-10 production in stimulated human and murine macrophages and dendritic cells. Modulatory action on inflammatory responses has therapeutic potential.</p>Formule :C16H16N4Degré de pureté :Min. 95%Couleur et forme :SolidMasse moléculaire :264.33 g/molA 769662
CAS :<p>Allosteric activator of AMP-activated protein kinase (AMPK) acting on the AMPK-β subunit with therapeutic potential in metabolic disorders such as diabetes, obesity, etc. A769662 also blocks the differentiation of mouse embryonic stem cells (mESCs) and maintains the mESCs in naïve state even in the absence of leukemia inhibitory factor (2i/L).</p>Formule :C20H12N2O3SDegré de pureté :Min. 95%Couleur et forme :SolidMasse moléculaire :360.39 g/molTacrolimus - Bio-X ™
CAS :<p>Tacrolimus is a calcineurin inhibitor drug that is used for the prevention of rejection after an organ transplant. This drug can also be used in the treatment of severe atopic dermatitis. Tacrolimus’ mechanism of action is not well known however it is understood that this drug inhibits T-lymphocyte activation by binding to an intracellular protein called FKBP-12. This drug also has anti-inflammatory properties.</p>Formule :C44H69NO12Degré de pureté :Min. 95%Couleur et forme :White Off-White PowderMasse moléculaire :804.02 g/molAZD 9291
CAS :<p>A potent inhibitor of EGFR with sensitizing and T790M resistance mutations, selective over the wild-type form of the receptor. Causes tumour regression in EGFR mutant T790M transgenic and xenograft models in vivo.</p>Formule :C28H33N7O2Degré de pureté :Min. 97%Couleur et forme :SolidMasse moléculaire :499.61 g/molRamipril - Bio-X ™
CAS :<p>Ramipril is an angiotensin-converting enzyme (ACE) inhibitor. It is used in the treatment of high blood pressure, congestive heart failure and other cardiovascular diseases. Ramipril inhibits the conversion of angiotensin I to angiotensin II by blocking ACE, which lowers blood pressure and reduces fluid retention.This product is part of our Bio-X ™ Range. These products are aimed at life science researchers who need high quality ready-to-use products for assay development, screening or other R&D work. With a solubility datasheet and convenient vials, all of our Bio-X ™ products are in stock across our global warehouses for rapid delivery and ease of use.</p>Formule :C23H32N2O5Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :416.51 g/molR-Rolipram
CAS :<p>Inhibitor of PDE4 enzyme; anti-inflammatory</p>Formule :C16H21NO3Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :275.34 g/molAcalabrutinib
CAS :<p>Inhibitor of the Bruton tyrosine kinase</p>Formule :C26H23N7O2Degré de pureté :Min. 98 Area-%Couleur et forme :SolidMasse moléculaire :465.51 g/molFeprazone
CAS :<p>Anti-inflammatory; inducer of P450 II B family</p>Formule :C20H20N2O2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :320.39 g/molDiacerein - Bio-X ™
CAS :<p>Diacerein is a slow-onset anthraquinone IL-1 inhibitor that is used in the treatment of joint diseases such as osteoarthritis. This drug is also being studied for the treatment of insulin resistance and diabetes mellitus. Diacerein works to decrease inflammation and cartilage destruction by reducing the level of interleukin-1.</p>Formule :C19H12O8Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :368.29 g/mol
