
Proteases/Proteassoma
Os inibidores de proteases e proteassomas são compostos que bloqueiam a atividade das proteases e do proteassoma, que estão envolvidos na degradação e renovação de proteínas. Esses inibidores são vitais para estudar a regulação da homeostase de proteínas, controle do ciclo celular e apoptose. Inibidores de proteases e proteassomas também são utilizados no tratamento de doenças como o câncer, onde a degradação anormal de proteínas desempenha um papel na progressão da doença. Ao inibir proteases ou o proteassoma, esses compostos podem induzir a morte celular em células cancerígenas e são ferramentas essenciais tanto na pesquisa básica quanto no desenvolvimento terapêutico. Na CymitQuimica, oferecemos uma ampla gama de inibidores de proteases e proteassomas de alta qualidade para apoiar sua pesquisa em bioquímica, biologia celular e desenvolvimento de medicamentos.
Subcategorias de "Proteases/Proteassoma"
- Acetil- CoA Carboxilase(34 produtos)
- Cisteína Protease(96 produtos)
- DPP-4(20 produtos)
- Glutaminase(40 produtos)
- HIV Protease(449 produtos)
- PAI-1(25 produtos)
- Inibidores de Protease(50 produtos)
- Receptor activado por protease(53 produtos)
- Proteassoma(94 produtos)
- Protease serina(50 produtos)
- p97(14 produtos)
Exibir 3 mais subcategorias
Foram encontrados 1044 produtos de "Proteases/Proteassoma"
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Atazanavir Sulfate
CAS:Fórmula:C38H52N6O7·H2SO4Pureza:>98.0%(HPLC)Cor e Forma:White to Almost white powder to crystalPeso molecular:802.94Gabexate Mesylate
CAS:Fórmula:C16H23N3O4·CH4O3SPureza:>97.0%(N)Cor e Forma:White to Almost white powder to crystalPeso molecular:417.48Disodium Dihydrogen Ethylenediaminetetraacetate Dihydrate [for Biochemical Research]
CAS:Fórmula:C10H14N2Na2O8·2H2OPureza:>99.0%(T)Cor e Forma:White powder to crystalinePeso molecular:372.24Nelfinavir Mesylate
CAS:Fórmula:C32H45N3O4S·CH4O3SPureza:>97.0%(HPLC)Cor e Forma:White to Almost white powder to crystalPeso molecular:663.89Ethylene Glycol Bis(2-aminoethyl Ether)-N,N,N',N'-tetraacetic Acid [for Biochemical Research]
CAS:Fórmula:C14H24N2O10Pureza:>95.0%(T)Cor e Forma:White to Almost white powder to crystalPeso molecular:380.35Nafamostat Mesylate
CAS:Fórmula:C19H17N5O2·2CH4O3SPureza:>98.0%(HPLC)Cor e Forma:White to Almost white powder to crystalPeso molecular:539.58Atazanavir
CAS:Fórmula:C38H52N6O7Pureza:>95.0%(HPLC)Cor e Forma:White to Light yellow powder to crystalPeso molecular:704.87Limonin
CAS:Fórmula:C26H30O8Pureza:>95.0%(HPLC)Cor e Forma:White to Almost white powder to crystalPeso molecular:470.52Ritonavir
CAS:Fórmula:C37H48N6O5S2Pureza:>98.0%(HPLC)(N)Cor e Forma:White to Almost white powder to crystalinePeso molecular:720.951,10-Phenanthroline Monohydrate [for Biochemical Research]
CAS:Fórmula:C12H8N2·H2OPureza:>99.0%(T)Cor e Forma:White powder to crystalPeso molecular:198.23Camostat Mesylate
CAS:Fórmula:C20H22N4O5·CH4O3SPureza:>98.0%(HPLC)Cor e Forma:White to Almost white powder to crystalPeso molecular:494.52Benzylsulfonyl Fluoride [for Biochemical Research]
CAS:Fórmula:C7H7FO2SPureza:>98.0%(GC)Cor e Forma:White to Almost white powder to crystalPeso molecular:174.192-Iodoacetamide [for Biochemical Research]
CAS:Fórmula:C2H4INOPureza:>98.0%(N)Cor e Forma:White to Light yellow powder to crystalPeso molecular:184.964-(2-Aminoethyl)benzenesulfonyl Fluoride Hydrochloride [for Biochemical Research]
CAS:Fórmula:C8H10FNO2S·HClPureza:>99.0%(HPLC)Cor e Forma:White to Almost white powder to crystalPeso molecular:239.69MG-132
CAS:Fórmula:C26H41N3O5Pureza:>95.0%(qNMR)Cor e Forma:White to Light yellow powder to crystalPeso molecular:475.634-Chlorosalicylic acid
CAS:<p>4-Chlorosalicylic acid (4-Chloro-2-hydroxybenzoic acid, 4-chloro salicylic acid) is antimicrobial compositions comprising a metal salt and a benzoic acid analog</p>Fórmula:C7H5ClO3Pureza:98.59%Cor e Forma:Off-White To Light Beige PowderPeso molecular:172.57Salicylanilide
CAS:<p>Salicylanilide (2-Hydroxybenzanilide)s are a group of compounds with antiviral potency, antibacterial and antifungal activities.</p>Fórmula:C13H11NO2Pureza:99.55%Cor e Forma:White To Off-White Crystalline PowderPeso molecular:213.23Fostemsavir Tris
CAS:<p>Fostemsavir Tris (BMS-663068 Tris) is the prodrug of BMS-626529,is a oral, safe and effective inhibitor of HIV-1 attachment.</p>Fórmula:C29H37N8O11PPureza:99.45%Cor e Forma:SolidPeso molecular:704.62Anisindione
CAS:<p>Anisindione, a synthetic indanedione, inhibits vitamin K, blocking factors II, VII, IX, X, and proteins C, S.</p>Fórmula:C16H12O3Pureza:98.25%Cor e Forma:Pale Yellow Crystals From Acetic Acid Or Ethanol SolidPeso molecular:252.26Retagliptin Phosphate
CAS:<p>Retagliptin Phosphate (SP 2086) is pharmaceutical composition of DPP-4 inhibitor, for treating type-2 diabetes.</p>Fórmula:C19H21F6N4O7PPureza:98.70%Cor e Forma:SolidPeso molecular:562.36Elsulfavirine
CAS:<p>Elsulfavirine (VM-1500) is an HIV-1 infection reverse transcriptase inhibitor. It is a new anti-HIV drug.</p>Fórmula:C24H17BrCl2FN3O5SPureza:99.66%Cor e Forma:SolidPeso molecular:629.28MK-0608
CAS:<p>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).</p>Fórmula:C12H16N4O4Pureza:98.48%Cor e Forma:SolidPeso molecular:280.28LDN-27219
CAS:<p>LDN-27219 is a potent hTGase inhibitor with IC50 of 0.6 uM.</p>Fórmula:C20H16N4O2S2Pureza:99.01% - 99.38%Cor e Forma:SolidPeso molecular:408.5Sofosbuvir impurity G
CAS:<p>Sofosbuvir impurity G is both a diastereomer of Sofosbuvir and an impurity of Sofosbuvir which is an inhibitor of HCV RNA replication.</p>Fórmula:C22H29FN3O9PPureza:98.04%Cor e Forma:SolidPeso molecular:529.45Gly-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%Cor e Forma:SolidPeso molecular:328.75Denagliptin
CAS:<p>Denagliptin is a small molecule dipeptidyl peptidase IV (DPP-4) inhibitor for the treatment of endocrine Ü metabolic diseases and can be used in the study of</p>Fórmula:C20H18F3N3OPureza:99.12%Cor e Forma:SolidPeso molecular:373.37Flanvotumab
CAS:<p>Flanvotumab (IMC-20D7S) is a humanized antibody targeting TYRP1 with strong antitumor effects via NK cells and ADCC.</p>Pureza:> 95%Cor e Forma:LiquidPeso molecular:145.42 kDaBLT-1
CAS:<p>BLT-1 is a scavenger receptor BI (SR-BI)inhibitor.</p>Fórmula:C12H23N3SPureza:97.97%Cor e Forma:SolidPeso molecular:241.4Begelomab
CAS:<p>Begelomab (SAND-26) is a mouse-derived monoclonal antibody targeting DPP-4/CD26. Begelomab can be used to study severe refractory inflammatory myopathies.</p>Pureza:97.8% (SDS-PAGE); 98.3% (SEC-HPLC) - 97.8% (SDS-PAGE); 98.3% (SEC-HPLC)Cor e Forma:LiquidAprotinin
CAS:<p>Aprotinin (Traskolan) is a broad-spectrum serine protease (BPTI) inhibitor. Aprotinin is an antifibrinolytic agent. Cost-effective and quality-assured.</p>Fórmula:C284H432N84O79S7Pureza:98%Cor e Forma:SolidPeso molecular:6511.51ML604440
CAS:ML604440 is a cell permeable proteasome β1i (LMP2) subunit inhibitor.Fórmula:C17H24BF3N2O4Pureza:97.06%Cor e Forma:SolidPeso molecular:388.19Islatravir
CAS:<p>Islatravir (MK-8591) is an effective anti-HIV-1 agent.</p>Fórmula:C12H12FN5O3Pureza:98.77%Cor e Forma:SolidPeso molecular:293.25RAMB4
CAS:<p>RAMB4 (PTP1B-IN-9) is a ubiquitin-proteasome system (UPS)-stressor,with anticancer activity.</p>Fórmula:C19H13Cl4NOPureza:98.89% - 99.38%Cor e Forma:SolidPeso molecular:413.12Sitagliptin
CAS:<p>Sitagliptin (MK0431), an oral DPP-4 inhibitor, treats type 2 diabetes alone or with metformin/thiazolidinedione by increasing incretins and insulin.</p>Fórmula:C16H15F6N5OPureza:99.33% - 99.83%Cor e Forma:Yellow GreasePeso molecular:407.31BJJF078
CAS:<p>BJJF078, an aminopiperidine, inhibits human/mouse TG2 (IC50: 41/54 nM) and TG1 (IC50: 0.16 μM), may be used in MS studies.</p>Fórmula:C27H29N3O6SPureza:98.19%Cor e Forma:SoildPeso molecular:523.6Ruzasvir
CAS:<p>Ruzasvir (MK-8408) is a novel and potent pan-genotypic inhibitor of hepatitis C virus NS5A with antiviral activity.</p>Fórmula:C49H55FN10O7SPureza:96.87% - 96.88%Cor e Forma:SolidPeso molecular:947.09Fenofibric acid
CAS:<p>Fenofibric acid (FNF acid) is the active form of fenofibrate, a synthetic phenoxy-isobutyric acid derivate with antihyperlipidemic activity.</p>Fórmula:C17H15ClO4Pureza:99.36%Cor e Forma:White Or Almost White Crystalline PowderPeso molecular:318.75BRD-6929
CAS:<p>BRD-6929, a brain-targeted HDAC1/2 inhibitor (IC50 1/8 nM), enhances gnidimacrin's anti-HIV effect, useful in mood behavior studies.</p>Fórmula:C19H17N3O2SPureza:98.01% - 99.05%Cor e Forma:SolidPeso molecular:351.42Dolutegravir intermediate-1
CAS:<p>Dolutegravir intermediate-1 is a synthetic precursor for HIV-1 treatment from patent WO 2016125192 A2.</p>Fórmula:C13H17NO8Pureza:99.52%Cor e Forma:SolidPeso molecular:315.28LSP-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%Cor e Forma:SolidPeso molecular:431.92Avoralstat
CAS:<p>Avoralstat (BCX4161) is an oral plasma kallikrein (PKK) inhibitor. Which is used for the treatment of hereditary angioedema.</p>Fórmula:C28H27N5O5Pureza:99.77%Cor e Forma:SolidPeso molecular:513.54ARP-100
CAS:<p>ARP-100 (MMP-2 Inhibitor III) is a potent and selective matrix metalloproteinase MMP-2 inhibitor (IC50=12 nM).</p>Fórmula:C17H20N2O5SPureza:97.18%Cor e Forma:SolidPeso molecular:364.42L-Leucinamide, N-[(phenylmethoxy)carbonyl]-L-leucyl-N-[(1S)-1-formyl-3-methylbutyl]-
CAS:Fórmula:C26H41N3O5Pureza:98%Cor e Forma:SolidPeso molecular:475.6208Ref: IN-DA0072SK
1gA consultar5mg68,00€10mg90,00€25mg124,00€50mg168,00€100mg229,00€250mg500,00€500mgA consultarMecarbinate
CAS:<p>Mecarbinate (Dimecarbin) is arbidol hydrochloride's chemical intermediate.</p>Fórmula:C13H15NO3Pureza:99.28%Cor e Forma:Off-White Crystalline PowderPeso molecular:233.26Q-VD-OPH
CAS:<p>Q-VD-OPh is an irreversible caspase inhibitor with an IC50 value of 48 nM against caspase-7 and between 25 and 400 nM against caspase-1, 3, 8, 9, 10, 12.</p>Fórmula:C26H25F2N3O6Pureza:97.8% - 98.95%Cor e Forma:SolidPeso molecular:513.5Hck-IN-1
CAS:<p>Hck-IN-1 selectively inhibits Nef:Hck, IC50: 2.8 μM; >20 μM for Hck alone. Potent HIV-1 Nef antagonist, IC50: 100-300 nM for HIV-1 replication.</p>Fórmula:C16H11ClN6O3SPureza:99.07%Cor e Forma:SolidPeso molecular:402.812-Oxiranecarboxylic acid, 3-[[[(1S)-3-methyl-1-[[(3-methylbutyl)amino]carbonyl]butyl]amino]carbonyl]-, ethyl ester, (2S,3S)-
CAS:Fórmula:C17H30N2O5Pureza:98%Cor e Forma:SolidPeso molecular:342.4305



