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Proteasas / Proteasoma

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"

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Se han encontrado 1039 productos de "Proteasas / Proteasoma"

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  • TNK2-IN-1

    CAS:
    <p>TNK2-IN-1 is a TNK2 inhibitor (IC50: 224 nM) that can be used in cancer research.</p>
    Fórmula:C23H24N6O2
    Forma y color:Solid
    Peso molecular:416.48
  • Moxicoumone

    CAS:
    <p>Moxicoumone is an anticoagulant agent.</p>
    Fórmula:C22H30N2O6
    Pureza:98%
    Forma y color:Solid
    Peso molecular:418.48
  • K 579

    CAS:
    <p>K 579 is a dipeptidyl peptidase IV inhibitor.</p>
    Fórmula:C17H24N6O
    Pureza:98%
    Forma y color:Solid
    Peso molecular:328.41
  • PTIQ

    CAS:
    <p>MMP-3 expression inhibitor</p>
    Fórmula:C13H17NO3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:235.28
  • RO-9187

    CAS:
    <p>RO-9187 is an effective HCV virus replication inhibitor(IC50: 171 nM).</p>
    Fórmula:C9H12N6O5
    Pureza:98%
    Forma y color:Solid
    Peso molecular:284.23
  • Ro 09-1679

    CAS:
    <p>Ro 09-1679 is a thrombin inhibitor.</p>
    Fórmula:C22H39N9O6
    Pureza:98%
    Forma y color:Solid
    Peso molecular:525.6
  • N-Phenylthiourea

    CAS:
    <p>N-Phenylthiourea (Phenylthiocarbamide) is EC 1.14.18.1 (tyrosinase) inhibitor, a diphenolase inhibitor, and a non-competitive inhibitor of the PvdP tyrosinase.</p>
    Fórmula:C7H8N2S
    Pureza:99.71%
    Forma y color:Solid
    Peso molecular:152.22
  • Tyrphostin A46

    CAS:
    <p>Tyrphostin A46 is an antagonist of the epidermal growth factor-urogastrone receptor.</p>
    Fórmula:C10H8N2O3
    Pureza:98%
    Forma y color:Off-White Solid
    Peso molecular:204.18
  • JPM-OEt

    CAS:
    <p>JPM-OEt: broad-spectrum, covalent cysteine cathepsin inhibitor with antitumor effects.</p>
    Fórmula:C20H28N2O6
    Pureza:98%
    Forma y color:Solid
    Peso molecular:392.45
  • KIN1400

    CAS:
    <p>KIN1400 activates IRF3, boosts antiviral immunity, stimulates IFNbeta, and inhibits WNV, DV, and HCV.</p>
    Fórmula:C24H17F2N3O2S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:449.47
  • Grazoprevir sodium salt

    CAS:
    Grazoprevir sodium salt is a selective Hepatitis C virus NS3/4a protease inhibitor with broad activity across genotypes and resistant variants.
    Fórmula:C38H50N6NaO9S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:789.9
  • Prodipine hydrochloride

    CAS:
    <p>Prodipine hydrochloride for purified and plasma Dipeptidyl peptidase IV (DPP IV) from the rabbit (IC50 of 4.5 μM and 30 μM, respectively).</p>
    Fórmula:C20H26ClN
    Pureza:98%
    Forma y color:Solid
    Peso molecular:315.88
  • ZM223 hydrochloride (2031177-48-5 free base)


    <p>ZM223 hydrochloride is an orally active, potent non-covalent inhibitor of NEDD8 activating enzyme (NAE), and with excellent anticancer activity.</p>
    Fórmula:C23H18ClF3N4O2S2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:538.99
  • FK-448 Free base

    CAS:
    <p>FK-448 Free base is an effective and specific inhibitor of chymotrypsin, with an IC50 of 720 nM.</p>
    Fórmula:C25H30N2O3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:406.52
  • (S)-BI-1001

    CAS:
    <p>(S)-BI-1001 is an active S-enantiomer of BI-1001. (S)-BI-1001 has antiviral potency against HIV-1 integrase (IC50: 28 nM, and EC50: 450 nM and a Kd: 4.7 μM).</p>
    Fórmula:C19H15BrClNO3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:420.68
  • BMS-986094

    CAS:
    <p>INX 08189 is an RNA-directed RNA polymerase (NS5B) inhibitor.</p>
    Fórmula:C30H39N6O9P
    Forma y color:Solid
    Peso molecular:658.64
  • Navuridine

    CAS:
    <p>Navuridine (AZdU) is an oral active inhibitor of HIV reverse transcriptase with a relatively short half-life.</p>
    Fórmula:C9H11N5O4
    Pureza:99.83%
    Forma y color:Solid
    Peso molecular:253.22
  • p-Aminobenzamidine dihydrochloride

    CAS:
    <p>4-Aminobenzamidine dihydrochloride (p-Aminobenzamidine dihydrochloride) is a strong trypsin inhibitor and a relatively weak inhibitor of urokinase type</p>
    Fórmula:C7H11Cl2N3
    Pureza:99.00% - 99.56%
    Forma y color:Solid
    Peso molecular:208.088
  • LB-30057

    CAS:
    <p>LB-30057 is used as an oral thrombin inhibitor.</p>
    Fórmula:C26H31N5O3S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:493.62
  • U 27391

    CAS:
    <p>U 27391 is a metalloproteinase inhibitor. It acts by inhibits the action of human recombinant interleukin-1beta and glycosaminoglycan synthesis.</p>
    Fórmula:C23H36N4O5
    Pureza:98%
    Forma y color:Solid
    Peso molecular:448.56
  • MDK0734

    CAS:
    <p>MDK0734 is a selective inhibitor of cathepsin B endopeptidase and exopeptidase activities.</p>
    Fórmula:C15H17N3O2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:271.31
  • MDL-101146, (S)-

    CAS:
    <p>MDL-101146, (S)- is an effective orally active inhibitor of human neutrophil elastase.</p>
    Fórmula:C29H37F5N4O6
    Pureza:98%
    Forma y color:Solid
    Peso molecular:632.62
  • PMPA sodium

    CAS:
    <p>PMPA sodium is a potent and selective glutamate carboxypeptidase 2 (GCP II/N-acetylated a-linked dipeptidase/NAALADase) inhibitor.</p>
    Fórmula:C6H11Na4O7P
    Pureza:98%
    Forma y color:Solid
    Peso molecular:318.08
  • IMB-26

    CAS:
    <p>IMB-26 is an HCV inhibitor (EC50: 2.1 μM) and has shown potent anti-HCV effects.</p>
    Fórmula:C20H23BrN2O6
    Forma y color:Solid
    Peso molecular:467.31
  • Tyrosinase-IN-4

    CAS:
    <p>Tyrosinase-IN-4, a potent inhibitor, has uses in skin-whitening, food preservation, cosmetics, agriculture, and medicine.</p>
    Fórmula:C15H9ClO3
    Forma y color:Solid
    Peso molecular:272.68
  • Desethyl KBT-3022

    CAS:
    <p>Desethyl KBT-3022 is an active metabolite of the antiplatelet compound KBT-3022.</p>
    Fórmula:C23H20N2O4S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:420.48
  • PF-00356231 hydrochloride

    CAS:
    <p>PF-00356231 hydrochloride is an inhibitor of matrix metalloproteinase MMP-12 with IC50 of 1.4 μM.</p>
    Fórmula:C25H21ClN2O3S
    Pureza:98.39%
    Forma y color:Solid
    Peso molecular:464.96
  • DTS

    CAS:
    <p>DTS is a selective and isoform-specific RSK1 kinase inhibitor. It also has broad cancer therapeutic potential.</p>
    Fórmula:C14H14S3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:278.46
  • Calpain Inhibitor XII

    CAS:
    <p>Calpain Inhibitor XII (Z-L-Nva-CONH-CH2-2-Py) is a calpain I inhibitor that inhibits calpain II and cathepsin B.</p>
    Fórmula:C26H34N4O5
    Forma y color:Solid
    Peso molecular:482.57
  • STOCK2S-26016

    CAS:
    <p>WNK-IN-B, a cell-permeable diaminoacridine, selectively inhibits WNK signaling in mpkDCT/MOVAS by targeting SPAK/OSR1 CCT domain.</p>
    Fórmula:C20H19N3O2
    Forma y color:Solid
    Peso molecular:333.38
  • AL-9

    CAS:
    <p>AL-9 is a GT-1b and GT-2a replication inhibitor.</p>
    Fórmula:C23H22N4O3
    Pureza:98%
    Forma y color:Solid
    Peso molecular:402.45
  • NNGH

    CAS:
    <p>NNGH is a matrix metalloproteinase 3 (MMP-3) inhibitor with anticancer activity that counteracts the inhibitory effects of E2 and DHT on RANKL membrane-binding.</p>
    Fórmula:C13H20N2O5S
    Pureza:98.41%
    Forma y color:Solid
    Peso molecular:316.37
  • AA9 TG2 inhibitor

    CAS:
    <p>AA9 is a novel transglutaminase (TG2) inhibitor.</p>
    Fórmula:C32H36N4O5
    Forma y color:Solid
    Peso molecular:556.65
  • Desirudin

    CAS:
    <p>Desirudin (CGP 39393) inhibits thrombin, prevents thrombosis, and is used in thrombocytopenia research.</p>
    Forma y color:Solid
  • Cyclophilin inhibitor 3

    CAS:
    <p>Cyclophilin inhibitor 3 (compound 7c), a potent inhibitor of cyclophilin A (CypA), exhibited potent anti-HCV effects with an EC50 value of 4.2 μM.</p>
    Fórmula:C34H38N4O6
    Forma y color:Solid
    Peso molecular:598.69
  • Diprotin B

    CAS:
    <p>Diprotin B is a dipeptidyl peptidase IV inhibitor.</p>
    Fórmula:C16H29N3O4
    Pureza:98%
    Forma y color:White Lyophilized Powder
    Peso molecular:327.42
  • ZD-0892

    CAS:
    <p>ZD-0892: potent, selective neutrophil elastase inhibitor; Ki 6.7 nM (human), 200 nM (porcine).</p>
    Fórmula:C24H32F3N3O5
    Pureza:95% - 99.53%
    Forma y color:Solid
    Peso molecular:499.52
  • FQ

    CAS:
    <p>FQ is a novel reversible inhibitor of mixed-type tyrosinase.</p>
    Fórmula:C14H9FN2O
    Forma y color:Solid
    Peso molecular:240.23
  • SLK/STK10-IN-1

    CAS:
    <p>SLK/STK10-IN-1 is a selective and potent inhibitor of SLK and STK10 with potential antitumor activity.</p>
    Fórmula:C17H13ClN2O3
    Pureza:99.34%
    Forma y color:Solid
    Peso molecular:328.75
  • RID-F

    CAS:
    <p>RID-F is an inhibitor of the nonpeptidic proteasome.</p>
    Fórmula:C38H50N2O2
    Pureza:98%
    Forma y color:Solid
    Peso molecular:566.82
  • ADAMTS-5 Inhibitor

    CAS:
    <p>ADAMTS-5 Inhibitor is an inhibitor of ADAMTS-5 with an IC50 of 1.1 µM and can be used in studies about cartilage destruction in arthritis.</p>
    Fórmula:C16H11ClF3N3OS3
    Pureza:99.66%
    Forma y color:Solid
    Peso molecular:449.92
  • BC-05

    CAS:
    <p>BC-05, an orally active inhibitor targeting CD13 and the proteasome, displays potent inhibition with IC50 values of 0.13 μM against human CD13 and 1.39 μM for</p>
    Fórmula:C21H29BN2O9
    Pureza:98%
    Forma y color:Solid
    Peso molecular:464.27
  • TNIK-IN-1

    CAS:
    <p>TNIK-IN-1 is an inhibitor of Traf2- and Nck-interacting kinase (TNIK).</p>
    Fórmula:C19H17N5O3S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:395.43
  • Diethyl pyimDC

    CAS:
    <p>Diethyl pyimDC is an inhibitor of human collagen prolyl 4-hydroxylase 1 (CP4H1).</p>
    Fórmula:C14H15N3O4
    Forma y color:Solid
    Peso molecular:289.29
  • Aldumastat

    CAS:
    Aldumastat (GLPG1972) is a highly potent, specific and orally active inhibitor of ADAMTS-5.Aldumastat is used for the study of osteoarthritis of the knee.
    Fórmula:C20H24F2N4O3
    Pureza:99.87%
    Forma y color:Solid
    Peso molecular:406.43
  • Tyrosinase-IN-7

    CAS:
    <p>Tyrosinase-IN-7 is a small-molecule tyrosinase inhibitor (IC50 1.57 μM) that suppresses melanin activity and cell growth with low cytotoxicity.</p>
    Fórmula:C15H10O5
    Pureza:99%
    Forma y color:Solid
    Peso molecular:270.24
  • MK-4882

    CAS:
    <p>MK-4882 is an effective inhibitor of HCV NS5A.</p>
    Fórmula:C42H50N8O7
    Pureza:98%
    Forma y color:Solid
    Peso molecular:778.9
  • Efegatran sulfate

    CAS:
    <p>Efegatran sulfate (LY294468 sulfate) is a potent thrombin inhibitor used in the treatment of thrombotic disorders.</p>
    Fórmula:C21H34N6O7S
    Pureza:≥98% - ≥98%
    Forma y color:Solid
    Peso molecular:514.6
  • HCV-IN-34

    CAS:
    <p>HCV-IN-35, an oral HCV blocker, has an EC50 of 0.010 μM and a CC50 of 7.5 μM, indicating strong antiviral effects.</p>
    Fórmula:C31H36ClN5
    Forma y color:Solid
    Peso molecular:514.1
  • Tanomastat

    CAS:
    <p>Tanomastat is an orally bioavailable and non-peptidic biphenyl matrix metalloproteinases inhibitor.</p>
    Fórmula:C23H19ClO3S
    Pureza:98%
    Forma y color:Solid
    Peso molecular:410.91