Proteasas / Proteasoma
Los inhibidores de proteasas y proteasomas son compuestos que bloquean la actividad de las proteasas y del proteasoma, que están involucrados en la degradación y renovación de proteínas. Estos inhibidores son vitales para estudiar la regulación de la homeostasis proteica, el control del ciclo celular y la apoptosis. Los inhibidores de proteasas y proteasomas también se utilizan en el tratamiento de enfermedades como el cáncer, donde la degradación anormal de proteínas desempeña un papel en la progresión de la enfermedad. Al inhibir las proteasas o el proteasoma, estos compuestos pueden inducir la muerte celular en células cancerosas y son herramientas esenciales tanto en la investigación básica como en el desarrollo terapéutico. En CymitQuimica, ofrecemos una amplia gama de inhibidores de proteasas y proteasomas de alta calidad para apoyar su investigación en bioquímica, biología celular y desarrollo de fármacos.
Subcategorías de "Proteasas / Proteasoma"
- Acetil-CoA Carboxilasa(35 productos)
- Cisteína proteasa(110 productos)
- DPP-4(20 productos)
- Glutaminasa(43 productos)
- Proteasa del VIH(497 productos)
- PAI-1(25 productos)
- Inhibidores de la proteasa(50 productos)
- Receptor activado por proteasa(54 productos)
- Proteasoma(95 productos)
- Serina proteasa(56 productos)
- p97(15 productos)
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Se han encontrado 1094 productos de "Proteasas / Proteasoma"
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Benzoic acid, 4-[[6-[(aminoiminomethyl)amino]-1-oxohexyl]oxy]-, ethylester, monomethanesulfonate
CAS:Fórmula:C17H27N3O7SPureza:98%Forma y color:SolidPeso molecular:417.4772KW-2450 Formate
KW-2450 Formate is an IGF-1R/IR tyrosine kinase inhibitor with antitumor effects that acts through inhibition of Aurora A and B kinases.KW-2450 Formate inhibits the growth of TNBC xenografts and induces tetraploid accumulation.Fórmula:C29H31N5O5SPureza:99.28%Forma y color:SolidPeso molecular:561.65Avoralstat
CAS:Avoralstat (BCX4161) is an oral plasma kallikrein (PKK) inhibitor. Which is used for the treatment of hereditary angioedema.Fórmula:C28H27N5O5Pureza:99.77%Forma y color:SolidPeso molecular:513.54Sitagliptin
CAS:Sitagliptin (MK0431), an oral DPP-4 inhibitor, treats type 2 diabetes alone or with metformin/thiazolidinedione by increasing incretins and insulin.Fórmula:C16H15F6N5OPureza:99.33% - 99.83%Forma y color:Yellow GreasePeso molecular:407.31LSP-249
CAS:<p>LSP-249 is a plasma kallikrein inhibitor under the study for angioedema, with an EC50 less than 100 nM in cell.</p>Fórmula:C24H22ClN5OPureza:99.51%Forma y color:SolidPeso molecular:431.92ARP-100
CAS:ARP-100 (MMP-2 Inhibitor III) is a potent and selective matrix metalloproteinase MMP-2 inhibitor (IC50=12 nM).Fórmula:C17H20N2O5SPureza:97.18%Forma y color:SolidPeso molecular:364.42Sofosbuvir impurity F
CAS:<p>Sofosbuvir impurity F (Sofosbuvir 3',5'-Bis-(S)-phosphate) is both a diastereomer of Sofosbuvir and an impurity of Sofosbuvir which is an inhibitor of HCV RNA</p>Fórmula:C34H45FN4O13P2Pureza:98.05%Forma y color:SolidPeso molecular:798.69L-Leucinamide, N-[(phenylmethoxy)carbonyl]-L-leucyl-N-[(1S)-1-formyl-3-methylbutyl]-
CAS:Fórmula:C26H41N3O5Pureza:98%Forma y color:SolidPeso molecular:475.6208Ref: IN-DA0072SK
1gA consultar5mg68,00€10mg90,00€25mg124,00€50mg168,00€100mg229,00€250mg500,00€500mgA consultarBJJF078
CAS:BJJF078, an aminopiperidine, inhibits human/mouse TG2 (IC50: 41/54 nM) and TG1 (IC50: 0.16 μM), may be used in MS studies.Fórmula:C27H29N3O6SPureza:99.56%Forma y color:SoildPeso molecular:523.6Ruzasvir
CAS:Ruzasvir (MK-8408) is a novel and potent pan-genotypic inhibitor of hepatitis C virus NS5A with antiviral activity.Fórmula:C49H55FN10O7SPureza:96.87% - 99.93%Forma y color:SolidPeso molecular:947.09Probenecid
CAS:<p>Probenecid (Benemid) is a benzoic acid derivative with antihyperuricemic property.</p>Fórmula:C13H19NO4SPureza:98.95% - 99.84%Forma y color:Crystals From Dil Alcohol Pleasant Aftertaste (Ntp 1992)Peso molecular:285.36Fostemsavir Tris
CAS:Fostemsavir Tris (BMS-663068 Tris) is the prodrug of BMS-626529,is a oral, safe and effective inhibitor of HIV-1 attachment.Fórmula:C29H37N8O11PPureza:99.45%Forma y color:SolidPeso molecular:704.62BAY-85-8501
CAS:BAY-85-8501 is a selective, reversible and potent inhibitor of Human Neutrophil Elastase (HNE; IC50 of 65 pM)Fórmula:C22H17F3N4O3SPureza:99.16%Forma y color:SolidPeso molecular:474.46Gly-Pro-pNA hydrochloride
CAS:<p>Gly-Pro-pNA hydrochloride (Gly-Pro p-nitroanilide hydrochloride) is a dipeptidyl peptidase inhibitor that inhibits dipeptidyl peptidase II, dipeptidyl peptidase</p>Fórmula:C13H17ClN4O4Pureza:99.84%Forma y color:SolidPeso molecular:328.75BLT-1
CAS:<p>BLT-1 is a scavenger receptor BI (SR-BI)inhibitor.</p>Fórmula:C12H23N3SPureza:97.97%Forma y color:SolidPeso molecular:241.4MK-0608
CAS:MK-0608 is an orally bioavailable HCV replication inhibitor in vitro(EC50 = 0.3 μM and EC90=1.3 μM in the subgenomic-replicon assay).Fórmula:C12H16N4O4Pureza:98.48%Forma y color:SolidPeso molecular:280.28Anisindione
CAS:Anisindione, a synthetic indanedione, inhibits vitamin K, blocking factors II, VII, IX, X, and proteins C, S.Fórmula:C16H12O3Pureza:98.25%Forma y color:Pale Yellow Crystals From Acetic Acid Or Ethanol SolidPeso molecular:252.26Begelomab
CAS:Begelomab (SAND-26) is a mouse-derived monoclonal antibody targeting DPP-4/CD26. Begelomab can be used to study severe refractory inflammatory myopathies.Pureza:97.8% (SDS-PAGE); 98.3% (SEC-HPLC) - 97.8% (SDS-PAGE); 98.3% (SEC-HPLC)Forma y color:LiquidBRD-6929
CAS:BRD-6929, a brain-targeted HDAC1/2 inhibitor (IC50 1/8 nM), enhances gnidimacrin's anti-HIV effect, useful in mood behavior studies.Fórmula:C19H17N3O2SPureza:98.01% - 99.05%Forma y color:SolidPeso molecular:351.421,10-Phenanthroline hydrate
CAS:Fórmula:C12H10N2OPureza:98%Forma y color:SolidPeso molecular:198.2206
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