
Modulatori enzimatici
I modulatori enzimatici sono composti che possono aumentare o inibire l'attività degli enzimi, regolando così la velocità delle reazioni biochimiche. Questi modulatori svolgono un ruolo cruciale nel controllo delle vie metaboliche, della segnalazione cellulare e di vari processi fisiologici. I modulatori enzimatici sono ampiamente utilizzati nella ricerca e nello sviluppo di farmaci per studiare le funzioni enzimatiche e sviluppare agenti terapeutici. Presso CymitQuimica, offriamo una gamma completa di modulatori enzimatici di alta qualità per supportare la vostra ricerca nella regolazione enzimatica e nella scoperta di farmaci.
Sottocategorie di "Modulatori enzimatici"
Trovati 693 prodotti di "Modulatori enzimatici"
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Tranexamic acid
CAS:<p>Ligand of plasminogen; used for bleeding control</p>Formula:C8H15NO2Purezza:Min. 95%Colore e forma:White PowderPeso molecolare:157.21 g/molA 196
CAS:<p>Selective inhibitor histone methyltransferases SUV420H1 and SUV420H2 (IC50 values = 25 nM and 144 nM, respectively). Reduces histone H4K20me2 and H4K20me3 expression whilst increasing H4K20me1 global expression. Inhibits formation of p53-binding protein 1 (53BP1) foci upon ionizing radiation and reduces NHEJ-mediated DNA-break repair.</p>Formula:C18H16Cl2N4Purezza:Min. 95%Colore e forma:SolidPeso molecolare:359.25 g/molSB 271046 hydrochloride
CAS:<p>5-HT6 serotonin receptor antagonist; anti-convulsant</p>Formula:C20H22CIN3O3S2·HClPurezza:Min. 95%Peso molecolare:591.91 g/molNVP-TAE684
CAS:Inhibitor of NPM-ALK kinaseFormula:C30H40ClN7O3SPurezza:Min. 95%Peso molecolare:614.2 g/molBML 257
CAS:Inhibits Akt translocation by targeting the pleckstrin homology (PH) domain. Inhibits hepatitis C virus NS5B RNA-dependent RNA polymerase (IC50 = 79 µM). Attenuates cannabinoid agonist-mediated proliferation of neural stem/precursor cells.Formula:C21H14N2O2Purezza:Min. 95%Colore e forma:PowderPeso molecolare:326.35 g/molZofenopril calcium
CAS:Angiotensin-converting enzyme inhibitor; antioxidantFormula:C44H46N2O8S4•CaPurezza:Min. 95%Colore e forma:PowderPeso molecolare:899.17 g/molMG 132
CAS:MG 132 is a modified tripeptide that acts as proteasomal inhibitor. In 2006, MG 132 has been experimentally tested in in vitro cell-based and in vivo models for to assess its use in the medical treatment of Parkinson's disease.Formula:C26H41N3O5Purezza:Min. 95%Colore e forma:PowderPeso molecolare:475.30462SU 3327
CAS:<p>SU 3327, originally introduced as a thiadiazole JNK inhibitor (De et al. 2009) has recently been identified as having antibiotic activity against a broad range of bacteria including drug-resistant gram positive and negative strains (Strokes et al. 2020). This molecule has been given the fictional name ‘Halicin’ inspired by the AI approach used to discover its novel biological activity.</p>Formula:C5H3N5O2S3Purezza:Min. 95%Colore e forma:PowderPeso molecolare:261.31 g/molGinkgolic acid (C13:0)
CAS:Sumoylation inhibitor; reported to inhibit histone acetylation transferaseFormula:C20H32O3Purezza:Min. 95%Colore e forma:White PowderPeso molecolare:320.47 g/mol1-NM-PP1
CAS:<p>1-NM-PP1, also known as 1NM-PP1, is an inhibitor of the Src kinase. Studies have shown that 1-NM-PP1 inhibits analog-sensitive kinases (as-kinases) characterised by a small amino acid as gatekeeper of the ATP binding site. Tested to prevent parasitic infections, 1-NM-PP1 inhibited the Toxoplasma gondii life cycle when used at a higher concentration than 500 nM.</p>Formula:C20H21N5Purezza:Min. 95%Colore e forma:PowderPeso molecolare:331.1797Rapamycin-13C,d3 (contains d0) - Technical Grade
CAS:Prodotto controllato<p>Binds to FK506 binding proteins (FKBPs) to form a complex that inhibits mammalian targets of rapamycin (mTOR). Blocks p70 S6 kinase activation by interleukin-2 and thereby inhibits proliferation of T cells. Induces differentiation of human pluripotent stem cells (hPSCs) to mesendoderm and blood progenitor cells.</p>Formula:C50CH76D3NO13Purezza:Min. 95%Peso molecolare:918.18 g/molSurfen
CAS:Small molecule antagonist of heparan sulfate that binds to glycosaminoglycans electrostatically. Surfen neutralised anti-coagulant activity of unfractionated and low molecular weight heparins, inhibited enzymatic sulfation and degradation reactions. Surfen also blocked signalling and cell adhesion to fibronectin that was triggered by heparan sulphate.Formula:C21H22Cl2N6OPurezza:Min. 95%Peso molecolare:445.34 g/molCCT 241533 hydrochloride
CAS:<p>Potent and specific inhibitor of checkpoint kinase CHK2 with IC50 of 3 nM. CCT 241533 binds to the ATP pocket of CHK2 and shows minimal cross-reactivity against related kinases. CCT 241533 blocked the activity of CHK2 and impaired DNA repair in response to DNA damage in human tumoral cell lines. The compound did not potentiate genotoxicity of several genotoxic compounds but it did potentiate the cytotoxicity of a PARP inhibitor olaparib.</p>Formula:C23H27FN4O4•HClPurezza:Min. 95%Peso molecolare:478.94 g/molErlotinib base
CAS:Tyrosine kinase inhibitor; affects EGFR receptor; pancreatic cancer treatmentFormula:C22H23N3O4Purezza:Min. 99 Area-%Colore e forma:PowderPeso molecolare:393.44 g/molSimvastatin Na
CAS:Simvastatin Na is the salt form of Simvastatin. It acts as HMG-CoA reductase inhibitor and suppresses TNF-mediated NF-kappaB activation.Formula:C25H39O6NaPurezza:Min. 95%Colore e forma:Beige To Brown SolidPeso molecolare:458.56 g/mol(3R,5R)-Rosuvastatin sodium salt
CAS:<p>Inhibitor of HMG-CoA reductase</p>Formula:C22H27FN3O6S·NaPurezza:Min. 95%Peso molecolare:503.52 g/molSU11652
CAS:<p>Inhibitor of FLT3 kinase and acid sphingomyelinase</p>Formula:C22H27ClN4O2Purezza:Min. 95%Peso molecolare:414.93 g/molTolcapone - Bio-X ™
CAS:Prodotto controllato<p>Tolcapone is a catechol-O-methyltransferase (COMT) inhibitor that is used as adjunct therapy to manage symptoms of Parkinson’s disease. Although its precise mechanism is unknown, it is thought to be an inhibitor of COMT and allows for a greater reduction in the symptoms of Parkinson’s.</p>Formula:C14H11NO5Purezza:Min. 95%Colore e forma:PowderPeso molecolare:273.24 g/molGI 254023X
CAS:<p>Inhibitor of ADAM10 metalloprotease</p>Formula:C21H33N3O4Purezza:Min. 95%Peso molecolare:391.5 g/molTegafur - Bio-X ™
CAS:<p>Tegafur is an antineoplastic agent that is used for the treatment of gastric and colorectal cancers in combination with other medications. This drug is a prodrug of 5-fluorouracil and has anticancer properties by inhibiting thymidylate synthase during DNA synthesis. Additionally, Tegafur causes disruptions of RNA functions.<br><br>Tegafur 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>Formula:C8H9FN2O3Purezza:Min. 95%Colore e forma:PowderPeso molecolare:200.17 g/mol
