
Proteases/Proteasome
Protease and proteasome inhibitors are compounds that block the activity of proteases and the proteasome, which are involved in protein degradation and turnover. These inhibitors are vital for studying the regulation of protein homeostasis, cell cycle control, and apoptosis. Protease and proteasome inhibitors are also used in the treatment of diseases such as cancer, where abnormal protein degradation plays a role in disease progression. By inhibiting proteases or the proteasome, these compounds can induce cell death in cancer cells and are critical tools in both basic research and therapeutic development. At CymitQuimica, we provide a wide range of high-quality protease and proteasome inhibitors to support your research in biochemistry, cell biology, and drug development.
Subcategories of "Proteases/Proteasome"
- Acetyl-CoA Carboxylase(36 products)
- Cysteine Protease(111 products)
- DPP-4(24 products)
- Glutaminase(44 products)
- HIV Protease(501 products)
- PAI-1(26 products)
- Protease Inhibitors(50 products)
- Protease-activated Receptor(54 products)
- Proteasome(89 products)
- Serine Protease(54 products)
- p97(15 products)
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Found 993 products of "Proteases/Proteasome"
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ADAMTS-5-IN-2
CAS:ADAMTS-5-IN-2 is a potent inhibitor of ADAMTS-5, exhibiting an IC50 of 0.71 µM, and holds potential for osteoarthritis research.Formula:C17H15N3OSColor and Shape:SolidMolecular weight:309.39HCV-IN-35
CAS:HCV-IN-35 is a potent inhibitor of HCV and shows potential for infectious disease research.Formula:C30H36ClN5Color and Shape:SolidMolecular weight:502.09Calpain-2-IN-1
CAS:Calpain-2-IN-1 is a selective calpain-2 inhibitor with Ki values of 181 nM for calpain-1 and 7.8 nM for calpain-2, applicable for neurodegenerative diseases a.Formula:C28H37N3O7Color and Shape:SolidMolecular weight:527.61Tyrosinase-IN-10
CAS:Tyrosinase-IN-10 serves as a partially competitive inhibitor of tyrosinase, demonstrating an inhibition concentration (IC50) value of 1.6 μM against the enzyme'Formula:C16H12O4Color and Shape:SolidMolecular weight:268.26TPO agonist 1
CAS:TPO agonist 1, Thrombopoietin (TPO) mimetic, promotes platelet/megakaryocyte production, for thrombocytopenia research.Formula:C25H22N8O2Purity:98%Color and Shape:SolidMolecular weight:466.49TAPI-0
CAS:TAPI-0 is a matrix metalloprotease (MMP) and TACE inhibitor.Formula:C24H32N4O5Color and Shape:SolidMolecular weight:456.53NAAA-IN-2
CAS:NAAA-IN-2, a selective inhibitor with 50 nM IC50, targets NAAA, an enzyme hydrolyzing PEA/OEA, and may aid inflammation and pain studies.Formula:C11H13N3O2SColor and Shape:SolidMolecular weight:251.3Safironil
CAS:Safironil, a novel antifibrotic, competitively inhibits collagen synthesis and modulates fibrosis, impacting type I/III collagen levels.Formula:C15H23N3O4Purity:99.83%Color and Shape:SolidMolecular weight:309.36Ref: TM-T67961
1mg64.00€5mg136.00€10mg192.00€25mg334.00€50mg477.00€100mg662.00€200mg892.00€1mL*10mM (DMSO)137.00€MMP-1-IN-1
MMP-1-IN-1 is a highly potent MMP-1 inhibitor with an IC 50 of 0.034 μM .Formula:C14H17ClN2O3Color and Shape:SolidMolecular weight:296.75AZD-1236
CAS:AZD1236 is a selective inhibitor for human MMP-9/MMP-12, less effective in rodents, and reduces lung injury and inflammation.Formula:C15H19ClN4O5SColor and Shape:SolidMolecular weight:402.85(3S,4S)-A2-32-01
(3S,4S)-A2-32-01, a less active (S,S)-enantiomer of A2-32-01. A2-32-01 is a potent caseinolytic protein proteases (ClpP) inhibitor .Formula:C19H27NO2Color and Shape:SolidMolecular weight:301.42Azo-Resveratrol
CAS:Azo-Resveratrol is an analog of Resveratrol used as a potent tyrosinase inhibitor.Formula:C12H10N2O3Color and Shape:SolidMolecular weight:230.22HCV-IN-34
CAS: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.Formula:C31H36ClN5Color and Shape:SolidMolecular weight:514.1Butabindide
CAS:Butabindide (UCL-1397) selectively inhibits TPP II, protecting CCK-8, with Ki of 10 μM (TPP I) and 7 nM (TPP II).Formula:C17H25N3O2Color and Shape:SolidMolecular weight:303.4Tyrosinase-IN-7
CAS:Tyrosinase-IN-7 is a small-molecule tyrosinase inhibitor (IC50 1.57 μM) that suppresses melanin activity and cell growth with low cytotoxicity.Formula:C15H10O5Purity:99%Color and Shape:SolidMolecular weight:270.24BC-05
CAS: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 forFormula:C21H29BN2O9Purity:98%Color and Shape:SolidMolecular weight:464.27RID-F
CAS:RID-F is an inhibitor of the nonpeptidic proteasome.Formula:C38H50N2O2Purity:98%Color and Shape:SolidMolecular weight:566.82AL-9
CAS:AL-9 is a GT-1b and GT-2a replication inhibitor.Formula:C23H22N4O3Purity:98%Color and Shape:SolidMolecular weight:402.45PMPA sodium
CAS:PMPA sodium is a potent and selective glutamate carboxypeptidase 2 (GCP II/N-acetylated a-linked dipeptidase/NAALADase) inhibitor.Formula:C6H11Na4O7PPurity:98%Color and Shape:SolidMolecular weight:318.08Ono 3307 Free Base
CAS:Ono 3307 Free Base is a new synthetic protease inhibitorFormula:C14H14N4O4SColor and Shape:SolidMolecular weight:334.35Tyrosinase-IN-11
CAS:Tyrosinase-IN-11: potent inhibitor, IC50 - 50nM/64nM (L-tyrosinase/L-dopa), antioxidant, low toxicity, for hyperpigmentation study.Formula:C15H14O5Color and Shape:SolidMolecular weight:274.27Kallikrein 5-IN-2
CAS:Kallikrein 5-IN-2 inhibits KLK5 (pIC50=7.1); may normalize skin shedding, lessen inflammation & itching.Formula:C23H22N6OColor and Shape:SolidMolecular weight:398.46VA4 TG2 inhibitor
CAS:VA4 is a novel irreversible TG2 transamidase site-specific inhibitor.Formula:C33H41N5O6SColor and Shape:SolidMolecular weight:635.77AZD5248
CAS:AZD-5248 is a potent, selective, first generation, oral inhibitor of dipeptidyl peptidase 1 (DPP1).Formula:C22H22N4O2Color and Shape:SolidMolecular weight:374.44Cysteine protease inhibitor-2
CAS:Cysteine protease inhibitor from US20070032499A1; halts DCT116 at 6.5μM, PC3 at 4.4μM.Formula:C13H5N5OPurity:98%Color and Shape:SolidMolecular weight:247.21Calpain Inhibitor XII
CAS:Calpain Inhibitor XII (Z-L-Nva-CONH-CH2-2-Py) is a calpain I inhibitor that inhibits calpain II and cathepsin B.
Formula:C26H34N4O5Color and Shape:SolidMolecular weight:482.57RWJ-58643 HCl
CAS:RWJ 58643 inhibits beta-tryptase & trypsin; at 100µg with budesonide 200µg, reduces symptoms & IL-5; high doses cause late eosinophilia.Formula:C20H27ClN6O4SColor and Shape:SolidMolecular weight:482.984CA 074
CAS:CA 074 is a potent inhibitor of cathepsin B with a Ki value of 2 to 5 nM.CA 074 inhibits ischemic hippocampal neuronal death in primates and attenuates
Formula:C18H29N3O6Purity:97.80%Color and Shape:SolidMolecular weight:383.44BMS-363131
CAS:BMS-363131 (BMS363131) is a potent and selective trypsin inhibitor with an IC50 value of <1.7 nM.Formula:C28H40N6O5Purity:97.99%Color and Shape:SolidMolecular weight:540.65XMU-MP-2
CAS:XMU-MP-2 is a potent and selective protease inhibitor with anticancer activity that inhibits the growth of oncogenic BRK-driven tumors in a mouse xenograft
Formula:C32H33F3N8O2Purity:99.29%Color and Shape:SolidMolecular weight:618.65α-Glucosidase-IN-5
CAS:α-Glucosidase-IN-5 (compound 8) is isolated from a twig extract of Polyalthia cinnamomea which is a potent α-glucosidase inhibitor with an IC50 of 57.9 µM.Formula:C15H13NO3Color and Shape:SolidMolecular weight:255.27SAP2-IN-1
CAS:SAP2-IN-1 inhibits secreted aspartate protease 2 (IC50: 0.92 μM), doesn't work in vitro, and helps research infections.Formula:C34H29NO7Color and Shape:SolidMolecular weight:563.6Odalasvir
CAS:Odalasvir is a novel NS5A inhibitor for the treatment of hepatitis C.Formula:C60H72N8O6Color and Shape:SolidMolecular weight:1001.26Glutaminase-IN-4
CAS:Glutaminase-IN-4 (compound 2a) is a glutaminase (GLS) inhibitor (IC50: 2.3 μM).Formula:C23H22N6O2S2Color and Shape:SolidMolecular weight:478.59L 658758
CAS:L 658758 is an inhibitor of serine proteinase.Formula:C16H20N2O9SColor and Shape:SolidMolecular weight:416.4ND-322 HCl
CAS:ND-322 HCl (ND 322 Hydrochloride) is a selective inhibitor of MT1-MMP and MMP2 and reduces in vitro melanoma cell growth, migration and invasion.Formula:C15H16ClNO3S2Purity:99.49%Color and Shape:SolidMolecular weight:357.88Ref: TM-T28145
1mg152.00€5mg334.00€10mg492.00€25mg780.00€50mg1,044.00€100mg1,414.00€1mL*10mM (DMSO)349.00€2',5-Difluoro-2'-deoxycytidine
CAS:2',5-Difluoro-2'-deoxycytidine has potent anti-HCV activity and toxicity to rRNA.Formula:C9H11F2N3O4Purity:98%Color and Shape:SolidMolecular weight:263.2OM-189
CAS:OM-189 is a selective inhibitor of synthetic thrombin.Formula:C24H36N6O3SPurity:98%Color and Shape:SolidMolecular weight:488.65Tyrosinase-IN-1
CAS:Tyrosinase-IN-1: potent inhibitor for skin-whitening & food preservation with uses in cosmetics & medicine.Formula:C10H9N3O2S2Color and Shape:SolidMolecular weight:267.33Adafosbuvir PM
CAS:Adafosbuvir PM (AL-335 PM) is a small molecule NS5B inhibitor that can be used to study chronic hepatitis C.Formula:C10H13FN2O6Purity:98.39%Color and Shape:SolidMolecular weight:276.22ZD-0892
CAS:ZD-0892: potent, selective neutrophil elastase inhibitor; Ki 6.7 nM (human), 200 nM (porcine).Formula:C24H32F3N3O5Purity:95% - 99.53%Color and Shape:SolidMolecular weight:499.52Pyrithione cadmium
CAS:Pyrithione cadmium suppresses tumor growth in vitro and in vivo through inhibition of proteasomal deubiquitinaseFormula:C10H8CdN2O2S2Color and Shape:SolidMolecular weight:364.73GM 1489
CAS:GM 1489 is an MMP inhibitor, effective against MMP-1, -2, -3, -8, -9, reduces cancer cell invasion, and prevents ear thickening in mice.Formula:C27H33N3O4Color and Shape:SolidMolecular weight:463.57I 432
CAS:I 432 is a TMPRSS2 (transmembrane serine proteinase 2) inhibitor (Ki =0.9 nM).Formula:C33H35Cl2F6N5O7SColor and Shape:SolidMolecular weight:830.62BR351
CAS:BR351 is a brain penetrant MMP inhibitor (IC50s: 4, 2, 11, 50 nM for MMP2, MMP8, MMP9 and MMP13).Formula:C20H25FN2O5SPurity:98%Color and Shape:SolidMolecular weight:424.49EI-1
CAS:EI-1 is an inhibitor of Hepatitis C virus entry.Formula:C16H19F3N6O3Color and Shape:SolidMolecular weight:400.36Gü1303
CAS:Gü1303 is a highly potent and reversible inhibitor of Cathepsin K (CatK), with a Ki value of 0.91 nM for mature CatK (mCatK).Formula:C20H22N4O3Color and Shape:SolidMolecular weight:366.41ABT-770
CAS:ABT-770: an orally potent and selective MMP inhibitor, shown to reduce tumor growth in animal models.Formula:C22H22F3N3O6Color and Shape:SolidMolecular weight:481.42Antiviral agent 30
CAS:Antiviral Agent 30 (Example 118) is an active compound against HCV and RSV with an inhibitory concentration (IC 50) of greater than 25μM [1].Formula:C21H32N2O3SColor and Shape:SolidMolecular weight:392.56A-933548
CAS:A-933548: potent calpain inhibitor, selective vs. cathepsins, stable, effective in cell assays.Formula:C25H21N5O3Purity:98%Color and Shape:SolidMolecular weight:439.47SP-Chymostatin B
CAS:SP-Chymostatin B inhibits proteases like chymotrypsin and papain; less effective on human elastase; works at 100-200 μg/ml.Formula:C30H41N7O6Purity:98%Color and Shape:SolidMolecular weight:595.69Efegatran sulfate
CAS:Efegatran sulfate (LY294468 sulfate) is a potent thrombin inhibitor used in the treatment of thrombotic disorders.Formula:C21H34N6O7SPurity:≥98% - ≥98%Color and Shape:SolidMolecular weight:514.6TNIK-IN-4
CAS:TNIK-IN-4: strong TNIK inhibitor, IC50 of 0.61 μM, suppresses HCT116 colorectal cancer cells.Formula:C20H16FN3O3Color and Shape:SolidMolecular weight:365.36DPP-IV-IN-1
CAS:DPP-IV-IN-1 is an effective inhibitor of dipeptidyl peptidase IV (DPP-IV), a serine protease (IC50: 4.6 nM).Formula:C11H18FN3O2Purity:98%Color and Shape:SolidMolecular weight:243.28Gemigliptin Tartrate(911637-19-9 free base)
CAS:Gemigliptin Tartrate (LC15-0444 tartrate) is a highly selective, reversible and competitive inhibitor of dipeptidyl peptidase-4 (DPP-4).Formula:C22H25F8N5O8Purity:>99.99%Color and Shape:SolidMolecular weight:639.45MMP2-IN-2
CAS:MMP2-IN-2 is an MMP-2 inhibitor that inhibits MMP-13, MMP-9, and MMP-8, and can be used in the study of cancer and immune diseases.Formula:C13H8N4O4Purity:98.09%Color and Shape:SolidMolecular weight:284.23Lodelaben
CAS:Lodelaben (Declaben, SC-39026) is a reversible, non-competitive,specific inhibitor of human neutrophil elastase (HNE) with high potency (IC50=0.5 μM).Formula:C25H41ClO3Purity:99.62% - >99.99%Color and Shape:SolidMolecular weight:425.04(Rac)-Tanomastat
CAS:Tanomastat (BAY 12-9566) is an oral biphenyl MMP inhibitor; blocks MMP-2, -3, -9, -13, with anti-invasive and anti-metastatic properties.Formula:C23H19ClO3SColor and Shape:SolidMolecular weight:410.91BC-23
CAS:BC-23 (NSC 45382) is a proteasome inhibitor with antitumor and antimicrobial activity for the study of leukemia and small cell lung cancer.Formula:C21H14ClN3O4SPurity:98%Color and Shape:SolidMolecular weight:439.87GSK2793660 HCl
CAS:GSK2793660 is a irreversible covalent α,β-unsaturated amide based DPP1 inhibitor.Formula:C22H32ClN3O3Color and Shape:SolidMolecular weight:421.96Cysteine Protease inhibitor
CAS:Cysteine protease inhibitors are inhibitors of cysteine proteases. Target: Cysteine ProteaseFormula:C18H14N4OPurity:98%Color and Shape:SolidMolecular weight:302.33GSK2793660 free base
CAS:GSK-2793660, a cathepsin C inhibitor, may treat cystic fibrosis and related lung conditions.Formula:C22H31N3O3Color and Shape:SolidMolecular weight:385.5Elastase-IN-1
CAS:Elastase-IN-1 (Compound Q11) is a non-toxic elastase inhibitor with an IC 50 of 0.897 μM [1].Formula:C17H12N4O3Color and Shape:SolidMolecular weight:320.3Plasma kallikrein-IN-3
CAS:Plasma kallikrein-IN-3 is a potent inhibitor (IC50: 0.15 μM) used in hereditary angioedema and diabetic eye disease research.Formula:C20H23N5O2Color and Shape:SolidMolecular weight:365.43HCV-IN-3
CAS:HCV-IN-3 is a hepatitis C virus (HCV) NS3/4a protein inhibitor (IC50: 20 μM; Kd: 29 μM).Formula:C13H11F2NOPurity:98%Color and Shape:SolidMolecular weight:235.23Tanomastat
CAS:Tanomastat is an orally bioavailable and non-peptidic biphenyl matrix metalloproteinases inhibitor.Formula:C23H19ClO3SPurity:98%Color and Shape:SolidMolecular weight:410.91Diprotin B
CAS:Diprotin B is a dipeptidyl peptidase IV inhibitor.Formula:C16H29N3O4Purity:98%Color and Shape:White Lyophilized PowderMolecular weight:327.42AGG-523
CAS:AGG-523, an aggrecanase inhibitor, may slow cartilage wear after joint injury by reducing ARG-aggrecan in rats.Formula:C28H29FN2O4Color and Shape:SolidMolecular weight:476.54Cathepsin L/S-IN-1
Cathepsin L/S-IN-1 inhibits Cathepsin L & S (IC50: 4.10 & 1.79 μM) and reduces metastasis in pancreatic cancer cells.Formula:C29H33BrN4O4SColor and Shape:SolidMolecular weight:613.57Ro 09-1679
CAS:Ro 09-1679 is a thrombin inhibitor.Formula:C22H39N9O6Purity:98%Color and Shape:SolidMolecular weight:525.6THDP-17
CAS:THDP-17 is a inhibitor of glutaminase. THDP-17 shows a partial uncompetitive inhibition in vitro.Formula:C12H16N2SPurity:98%Color and Shape:SolidMolecular weight:220.33p-APMSF (hydrochloride)
CAS:p-APMSF irreversibly inhibits several serine proteases; Ki: 1.02-1.54 μM; selective over chymotrypsin and acetylcholinesterase.Formula:C8H10ClFN2O2SColor and Shape:SolidMolecular weight:252.69ABT-518
CAS:ABT-518 is an inhibitor of matrix metalloproteinases, which are associated with tumor growth and development of metastasis.Formula:C21H22F3NO8SColor and Shape:SolidMolecular weight:505.46PF-06279794
CAS:PF-06279794 is a potent, selective and ATP-competitive TNIK inhibitor.Formula:C22H20N4OColor and Shape:SolidMolecular weight:356.42MMP13-IN-4
CAS:MMP13-IN-4 (compound 13) is a potent, selective MMP-13 inhibitor with an IC50 of 14.6 μM, implicated in the pathology of osteoarthritis (OA) [1].Formula:C21H17BrN4O5Purity:98%Color and Shape:SolidMolecular weight:485.29JPM-OEt
CAS:JPM-OEt: broad-spectrum, covalent cysteine cathepsin inhibitor with antitumor effects.Formula:C20H28N2O6Purity:98%Color and Shape:SolidMolecular weight:392.45ACH-806
CAS:ACH-806 is an NS4A antagonist. It can inhibit Hepatitis C Virus (HCV) replication with an EC50 of 14 nM.Formula:C19H20F3N3O2SPurity:98%Color and Shape:SolidMolecular weight:411.44Grazoprevir sodium salt
CAS:Grazoprevir sodium salt is a selective Hepatitis C virus NS3/4a protease inhibitor with broad activity across genotypes and resistant variants.Formula:C38H50N6NaO9SPurity:98%Color and Shape:SolidMolecular weight:789.9Prodipine hydrochloride
CAS:Prodipine hydrochloride for purified and plasma Dipeptidyl peptidase IV (DPP IV) from the rabbit (IC50 of 4.5 μM and 30 μM, respectively).Formula:C20H26ClNPurity:98%Color and Shape:SolidMolecular weight:315.88DTS
CAS:DTS is a selective and isoform-specific RSK1 kinase inhibitor. It also has broad cancer therapeutic potential.Formula:C14H14S3Purity:98%Color and Shape:SolidMolecular weight:278.46AGLME
CAS:AGLME is used in a direct enzymatic assay for activated Hageman factor measuring the ability of Hageman factor to hydrolyze the cpd.Formula:C11H21N3O4Color and Shape:SolidMolecular weight:259.3Z-LLF-CHO
CAS:Z-LLF-CHO (Z-Leu-Leu-Phe-CHO) effectively inhibits the chymotrypsin-like activity of the pituitary multicatalytic proteinase complex with a Ki value of 460 nM.Formula:C29H39N3O5Purity:98%Color and Shape:SolidMolecular weight:509.64Cyclophilin inhibitor 3
CAS: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.Formula:C34H38N4O6Color and Shape:SolidMolecular weight:598.69Desirudin
CAS:Desirudin (CGP 39393) inhibits thrombin, prevents thrombosis, and is used in thrombocytopenia research.Color and Shape:SolidAA9 TG2 inhibitor
CAS:AA9 is a novel transglutaminase (TG2) inhibitor.Formula:C32H36N4O5Color and Shape:SolidMolecular weight:556.65Gosogliptin
CAS:Gosogliptin is a potent, orally active, highly selective, reversible and competitive inhibitor of DPP-4, increasing the level of intestinal GLP-1 and GIP.Formula:C17H24F2N6OPurity:99.74%Color and Shape:SolidMolecular weight:366.41STOCK2S-26016
CAS:WNK-IN-B, a cell-permeable diaminoacridine, selectively inhibits WNK signaling in mpkDCT/MOVAS by targeting SPAK/OSR1 CCT domain.Formula:C20H19N3O2Color and Shape:SolidMolecular weight:333.38Desethyl KBT-3022
CAS:Desethyl KBT-3022 is an active metabolite of the antiplatelet compound KBT-3022.Formula:C23H20N2O4SPurity:98%Color and Shape:SolidMolecular weight:420.48IMB-26
CAS:IMB-26 is an HCV inhibitor (EC50: 2.1 μM) and has shown potent anti-HCV effects.Formula:C20H23BrN2O6Color and Shape:SolidMolecular weight:467.31MDL-101146, (S)-
CAS:MDL-101146, (S)- is an effective orally active inhibitor of human neutrophil elastase.Formula:C29H37F5N4O6Purity:98%Color and Shape:SolidMolecular weight:632.62U 27391
CAS:U 27391 is a metalloproteinase inhibitor. It acts by inhibits the action of human recombinant interleukin-1beta and glycosaminoglycan synthesis.Formula:C23H36N4O5Purity:98%Color and Shape:SolidMolecular weight:448.56LB-30057
CAS:LB-30057 is used as an oral thrombin inhibitor.Formula:C26H31N5O3SPurity:98%Color and Shape:SolidMolecular weight:493.62BMS-986094
CAS:INX 08189 is an RNA-directed RNA polymerase (NS5B) inhibitor.Formula:C30H39N6O9PColor and Shape:SolidMolecular weight:658.64CP4d inhibitor
CAS:CP4d is a novel reversible tg2 transamidase site-specific inhibitorFormula:C18H13N5O5Color and Shape:SolidMolecular weight:379.33FK-448 Free base
CAS:FK-448 Free base is an effective and specific inhibitor of chymotrypsin, with an IC50 of 720 nM.Formula:C25H30N2O3Purity:98%Color and Shape:SolidMolecular weight:406.52KIN1400
CAS:KIN1400 activates IRF3, boosts antiviral immunity, stimulates IFNbeta, and inhibits WNV, DV, and HCV.Formula:C24H17F2N3O2SPurity:98%Color and Shape:SolidMolecular weight:449.47AZD6564
CAS:AZD6564 is a fibrinolysis inhibitor which acts via interference of a protein-protein interaction.Formula:C13H22N2O2Color and Shape:SolidMolecular weight:238.33Proteasome-IN-1
CAS:Proteasome-IN-1 is an inhibitor of proteasome.Formula:C42H35N5O3Purity:98%Color and Shape:SolidMolecular weight:657.76BI-L 45XX
CAS:BI-L 45XX, an anti-inflammatory benzimidazole derivative, has inhibitory effects on neutrophil function.Formula:C10H9F3N2O2SColor and Shape:SolidMolecular weight:278.25Tyrphostin 47
CAS:Tyrphostin 47 inhibits the protein-tyrosine kinase activity of EGF-R.Formula:C10H8N2O2SColor and Shape:SolidMolecular weight:220.25
