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(34 products)
- Cysteine Protease(96 products)
- DPP-4(20 products)
- Glutaminase(40 products)
- HIV Protease(447 products)
- PAI-1(25 products)
- Protease Inhibitors(50 products)
- Protease-activated Receptor(54 products)
- Proteasome(94 products)
- Serine Protease(50 products)
- p97(14 products)
Show 3 more subcategories
Found 1045 products of "Proteases/Proteasome"
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Nafamostat Mesylate
CAS:Formula:C19H17N5O2·2CH4O3SPurity:>98.0%(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:539.58Disodium Dihydrogen Ethylenediaminetetraacetate Dihydrate [for Biochemical Research]
CAS:Formula:C10H14N2Na2O8·2H2OPurity:>99.0%(T)Color and Shape:White powder to crystalineMolecular weight:372.24Ritonavir
CAS:Formula:C37H48N6O5S2Purity:>98.0%(HPLC)(N)Color and Shape:White to Almost white powder to crystalineMolecular weight:720.954-(2-Aminoethyl)benzenesulfonyl Fluoride Hydrochloride [for Biochemical Research]
CAS:Formula:C8H10FNO2S·HClPurity:>99.0%(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:239.69Camostat Mesylate
CAS:Formula:C20H22N4O5·CH4O3SPurity:>98.0%(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:494.52Atazanavir Sulfate
CAS:Formula:C38H52N6O7·H2SO4Purity:>98.0%(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:802.94Ethylene Glycol Bis(2-aminoethyl Ether)-N,N,N',N'-tetraacetic Acid [for Biochemical Research]
CAS:Formula:C14H24N2O10Purity:>95.0%(T)Color and Shape:White to Almost white powder to crystalMolecular weight:380.35MG-132
CAS:Formula:C26H41N3O5Purity:>95.0%(qNMR)Color and Shape:White to Light yellow powder to crystalMolecular weight:475.632-Iodoacetamide [for Biochemical Research]
CAS:Formula:C2H4INOPurity:>98.0%(N)Color and Shape:White to Light yellow powder to crystalMolecular weight:184.96Benzylsulfonyl Fluoride [for Biochemical Research]
CAS:Formula:C7H7FO2SPurity:>98.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:174.19Limonin
CAS:Formula:C26H30O8Purity:>95.0%(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:470.521,10-Phenanthroline Monohydrate [for Biochemical Research]
CAS:Formula:C12H8N2·H2OPurity:>99.0%(T)Color and Shape:White powder to crystalMolecular weight:198.23Nelfinavir Mesylate
CAS:Formula:C32H45N3O4S·CH4O3SPurity:>97.0%(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:663.89Atazanavir
CAS:Formula:C38H52N6O7Purity:>95.0%(HPLC)Color and Shape:White to Light yellow powder to crystalMolecular weight:704.87Gabexate Mesylate
CAS:Formula:C16H23N3O4·CH4O3SPurity:>97.0%(N)Color and Shape:White to Almost white powder to crystalMolecular weight:417.48MK-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>Formula:C12H16N4O4Purity:98.48%Color and Shape:SolidMolecular weight:280.28Elsulfavirine
CAS:<p>Elsulfavirine (VM-1500) is an HIV-1 infection reverse transcriptase inhibitor. It is a new anti-HIV drug.</p>Formula:C24H17BrCl2FN3O5SPurity:99.66%Color and Shape:SolidMolecular weight:629.28PF-3450074
CAS:<p>PF-3450074 (PF-74) is a specific HIV-1 inhibitor, blocking viral replication and uncoating at submicromolar EC50=8-640 nM.</p>Formula:C27H27N3O2Purity:99.92%Color and Shape:SolidMolecular weight:425.52LDN-27219
CAS:<p>LDN-27219 is a potent hTGase inhibitor with IC50 of 0.6 uM.</p>Formula:C20H16N4O2S2Purity:99.01% - 99.38%Color and Shape:SolidMolecular weight:408.5Salicylanilide
CAS:<p>Salicylanilide (2-Hydroxybenzanilide)s are a group of compounds with antiviral potency, antibacterial and antifungal activities.</p>Formula:C13H11NO2Purity:99.55%Color and Shape:White To Off-White Crystalline PowderMolecular weight:213.23PMSF
CAS:<p>PMSF (Phenylmethylsulfonyl fluoride) is an irreversible inhibitor of serine/cysteine protease , preparation of cell lysates. High-Quality, Low-Cost!</p>Formula:C7H7FO2SPurity:97.75% - 99.88%Color and Shape:White To Cream SolidMolecular weight:174.19Islatravir
CAS:<p>Islatravir (MK-8591) is an effective anti-HIV-1 agent.</p>Formula:C12H12FN5O3Purity:98.77%Color and Shape:SolidMolecular weight:293.25Q-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>Formula:C26H25F2N3O6Purity:97.8% - 98.95%Color and Shape:SolidMolecular weight:513.5Ruzasvir
CAS:<p>Ruzasvir (MK-8408) is a novel and potent pan-genotypic inhibitor of hepatitis C virus NS5A with antiviral activity.</p>Formula:C49H55FN10O7SPurity:96.87% - 96.88%Color and Shape:SolidMolecular weight:947.09Denagliptin
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>Formula:C20H18F3N3OPurity:99.12%Color and Shape:SolidMolecular weight:373.37Begelomab
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>Purity:97.8% (SDS-PAGE); 98.3% (SEC-HPLC) - 97.8% (SDS-PAGE); 98.3% (SEC-HPLC)Color and Shape:LiquidCL-82198
CAS:<p>CL-82198, a selective MMP-13 inhibitor, serves as a pharmacological intervention to halt the progression of osteoarthritis (OA).</p>Formula:C17H22N2O3Purity:95.91%Color and Shape:SolidMolecular weight:302.37Probenecid
CAS:<p>Probenecid (Benemid) is a benzoic acid derivative with antihyperuricemic property.</p>Formula:C13H19NO4SPurity:98.95% - 99.84%Color and Shape:Crystals From Dil Alcohol Pleasant Aftertaste (Ntp 1992)Molecular weight:285.36GSK2838232
CAS:<p>GSK2838232 inhibit HIV reverse transcriptase activity across a broad panel of HIV-1 isolates,GSK2838232 is novel human immune virus (HIV) maturation inhibitor.</p>Formula:C48H73ClN2O6Purity:97.97%Color and Shape:SolidMolecular weight:809.56Tenofovir diphosphate TEA
CAS:<p>Tenofovir diphosphate TEA (TFV-DP TEA) is an ATP-competitive DNA polymerase inhibitor that inhibits HIV-1 reverse transcriptase that\has anti-HIV/HBV potential.</p>Formula:C9H16N5O10P3·C6H15NPurity:93.45% - 98.51%Color and Shape:SolidMolecular weight:548.36Sitagliptin
CAS:<p>Sitagliptin (MK0431), an oral DPP-4 inhibitor, treats type 2 diabetes alone or with metformin/thiazolidinedione by increasing incretins and insulin.</p>Formula:C16H15F6N5OPurity:99.33% - 99.83%Color and Shape:Yellow GreaseMolecular weight:407.314-(2-Aminoethyl)benzenesulfonyl fluoride, HCl
CAS:Formula:C8H11ClFNO2SPurity:98%Color and Shape:SolidMolecular weight:239.6948ML604440
CAS:<p>ML604440 is a cell permeable proteasome β1i (LMP2) subunit inhibitor.</p>Formula:C17H24BF3N2O4Purity:97.06%Color and Shape:SolidMolecular weight:388.19Dolutegravir intermediate-1
CAS:<p>Dolutegravir intermediate-1 is a synthetic precursor for HIV-1 treatment from patent WO 2016125192 A2.</p>Formula:C13H17NO8Purity:99.52%Color and Shape:SolidMolecular weight:315.28Fenofibric acid
CAS:<p>Fenofibric acid (FNF acid) is the active form of fenofibrate, a synthetic phenoxy-isobutyric acid derivate with antihyperlipidemic activity.</p>Formula:C17H15ClO4Purity:99.36%Color and Shape:White Or Almost White Crystalline PowderMolecular weight:318.75Bestatin hydrochloride
CAS:Formula:C16H25ClN2O4Purity:98%Color and Shape:SolidMolecular weight:344.8337Ref: IN-DA003O5U
1g542.00€5gTo inquire10mg61.00€25mg94.00€50mg148.00€100mg191.00€250mg197.00€500mg333.00€Mecarbinate
CAS:<p>Mecarbinate (Dimecarbin) is arbidol hydrochloride's chemical intermediate.</p>Formula:C13H15NO3Purity:99.28%Color and Shape:Off-White Crystalline PowderMolecular weight:233.26BRD-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>Formula:C19H17N3O2SPurity:98.01% - 99.05%Color and Shape:SolidMolecular weight:351.42Ethylenediaminetetraacetic acid disodium salt dihydrate
CAS:Formula:C10H18N2Na2O10Purity:97%Color and Shape:SolidMolecular weight:372.23693-Isoquinolinecarboxamide, N-(1,1-dimethylethyl)decahydro-2-[(2R,3R)-2-hydroxy-3-[(3-hydroxy-2-methylbenzoyl)amino]-4-(phenylthio)butyl]-, (3S,4aS,8aS)-, methanesulfonate (1:1)
CAS:Formula:C33H49N3O7S2Purity:96%Color and Shape:SolidMolecular weight:663.8881KW-2450 Formate
<p>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.</p>Formula:C29H31N5O5SPurity:99.28%Color and Shape:SolidMolecular weight:561.65HCV-IN-29
CAS:<p>HCV-IN-29 is a hepatitis C virus (HCV) inhibitor.</p>Formula:C26H32Cl4N6Purity:99.89%Color and Shape:SolidMolecular weight:570.38Avoralstat
CAS:<p>Avoralstat (BCX4161) is an oral plasma kallikrein (PKK) inhibitor. Which is used for the treatment of hereditary angioedema.</p>Formula:C28H27N5O5Purity:99.77%Color and Shape:SolidMolecular weight: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>Formula:C17H20N2O5SPurity:97.18%Color and Shape:SolidMolecular weight:364.42Aprotinin
CAS:<p>Aprotinin (Traskolan) is a broad-spectrum serine protease (BPTI) inhibitor. Aprotinin is an antifibrinolytic agent. Cost-effective and quality-assured.</p>Formula:C284H432N84O79S7Purity:98%Color and Shape:SolidMolecular weight:6511.51PTBP1-RNA-binding inhibitor P6 TFA
<p>PTBP1-RNA-binding inhibitor P6 TFA is a stapled peptide inhibitor of PTBP1, used to inhibit RNA alternative splicing events regulated by PTBP1.</p>Color and Shape:Odour Solid2-Oxiranecarboxylic acid, 3-[[[(1S)-3-methyl-1-[[(3-methylbutyl)amino]carbonyl]butyl]amino]carbonyl]-, ethyl ester, (2S,3S)-
CAS:Formula:C17H30N2O5Purity:98%Color and Shape:SolidMolecular weight:342.4305(2S)-2-[(2S,3R)-3-amino-2-hydroxy-4-phenylbutanamido]-4-methylpentanoic acid
CAS:Formula:C16H24N2O4Purity:98%Color and Shape:SolidMolecular weight:308.3728Ref: IN-DA00370Q
1g132.00€5g223.00€10g532.00€25gTo inquire50gTo inquire100gTo inquire10mg29.00€250gTo inquire100mg44.00€250mg68.00€BJJF078
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>Formula:C27H29N3O6SPurity:98.19%Color and Shape:SoildMolecular weight:523.6Trelagliptin
CAS:<p>Trelagliptin (SYR-472) is a highly specific and long-acting DPP-4 inhibitor.</p>Formula:C18H20FN5O2Purity:98.88%Color and Shape:SolidMolecular weight:357.38Sofosbuvir 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>Formula:C22H29FN3O9PPurity:98.04%Color and Shape:SolidMolecular weight:529.45Benzoic acid, 4-[(aminoiminomethyl)amino]-, 6-(aminoiminomethyl)-2-naphthalenyl ester, dimethanesulfonate
CAS:Formula:C20H21N5O5SPurity:98%Color and Shape:SolidMolecular weight:443.4762Benzenemethanesulfonyl fluoride
CAS:Formula:C7H7FO2SPurity:99%Color and Shape:SolidMolecular weight:174.1927Ref: IN-DA00I6AP
1g25.00€5g39.00€10g55.00€1kgTo inquire25g93.00€2kgTo inquire50g137.00€5kgTo inquire100g181.00€250g572.00€(Rac)-Telinavir
CAS:<p>N1 compound with anti-HIV activity; contains dimethyl, phenyl, quinoline groups.</p>Formula:C33H44N6O5Purity:99.30%Color and Shape:SolidMolecular weight:604.74Bivalirudin acetate
<p>Bivalirudin acetate is a thrombin inhibitor, a peptide-based anticoagulant, used for research on acute coronary syndrome.</p>Formula:C100H142N24O35Purity:99.84%Color and Shape:SolidMolecular weight:2240.343-Deazaadenosine hydrochloride
CAS:<p>3-Deazaadenosine HCl blocks SAH hydrolase (Ki: 3.9 μM), with anti-inflammatory, anti-proliferative, and anti-HIV effects.</p>Formula:C11H15ClN4O4Purity:98.48%Color and Shape:SolidMolecular weight:302.71Levovirin
CAS:<p>Levovirin (L-Ribavirin) is a guanosine nucleoside analog that has immunomodulatory activity and is used in the study of hepatitis C virus infection.</p>Formula:C8H12N4O5Purity:99.81% - >99.99%Color and Shape:SolidMolecular weight:244.20TERT-IN-1
CAS:<p>TERT-IN-1 has anti-HIV activity and can be used to study HIV infection.</p>Formula:C16H20ClN3SPurity:99.31%Color and Shape:SoildMolecular weight:321.87Incyclinide
CAS:<p>Incyclinide (COL-3) is a matrix metalloproteinase (MMP) inhibitor.</p>Formula:C19H17NO7Purity:97.99%Color and Shape:SolidMolecular weight:371.34LSP-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>Formula:C24H22ClN5OPurity:99.51%Color and Shape:SolidMolecular weight:431.92Dabigatran etexilate
CAS:<p>Dabigatran etexilate (BIBR 1048) is a thrombin inhibitor, which acts by binding and blocking thrombogenic activity and the prevention of thrombus formation.</p>Formula:C34H41N7O5Purity:98.19% - 99.98%Color and Shape:White PowderMolecular weight:627.73(Rac)-Telmesteine
CAS:<p>(Rac)-Telmesteine (3,4-Thiazolidinedicarboxylic Acid 3-Ethyl Ester) is an inhibitor of protease and is thus a suitable enzyme stabilizer.</p>Formula:C7H11NO4SPurity:99.91%Color and Shape:SolidMolecular weight:205.23BAY-85-8501
CAS:<p>BAY-85-8501 is a selective, reversible and potent inhibitor of Human Neutrophil Elastase (HNE; IC50 of 65 pM)</p>Formula:C22H17F3N4O3SPurity:99.16%Color and Shape:SolidMolecular weight:474.46Saxagliptin hydrate
CAS:<p>Saxagliptin hydrate (Onglyza hydrate) is a selective and reversible DPP4 inhibitor (IC50: 26 nM; Ki: 1.3 nM).</p>Formula:C18H25N3O2·H2OPurity:99.52%Color and Shape:SolidMolecular weight:333.43RA190
CAS:<p>RA190 inhibits proteasome function by covalently binding to cysteine 88 of ubiquitin receptor RPN13.</p>Formula:C28H23Cl5N2O2Purity:97.7%Color and Shape:SolidMolecular weight:596.76DBPR108
CAS:<p>DBPR108 is an orally bioavailable dipeptide-derived DPP4 inhibitor (IC50: 15 nM) and it has no inhibition on DDP8 and DPP9.</p>Formula:C16H25FN4O2Purity:99.68%Color and Shape:SolidMolecular weight:324.39DPP-IV-IN-2
CAS:<p>DPP-IV-IN-2 (H-Lys(4-nitro-Z)-pyrrolidide) is an inhibitor of both DP8/9 and dipeptidyl peptidase IV (IC50s: 0.1 and 0.95 μM).</p>Formula:C18H26N4O5Purity:99.08%Color and Shape:SolidMolecular weight:378.42Dabigatran ethyl ester hydrochloride
CAS:<p>Dabigatran prevents blood clots, inhibiting NQO2 and thrombin with IC50 0.8 μM.</p>Formula:C27H30ClN7O3Purity:99.65%Color and Shape:SolidMolecular weight:536.03L-Leucinamide, N-[(phenylmethoxy)carbonyl]-L-leucyl-N-[(1S)-1-formyl-3-methylbutyl]-
CAS:Formula:C26H41N3O5Purity:98%Color and Shape:SolidMolecular weight:475.6208Ref: IN-DA00BBLC
1g57.00€5g128.00€25g262.00€5mg30.00€100gTo inquire10mg30.00€50mg30.00€100mg37.00€250mg44.00€Ref: IN-DA0034HK
5gTo inquire10g21.00€1kg124.00€25g25.00€50g25.00€5kg563.00€100g34.00€250g60.00€500g75.00€50kgTo inquire1,10-Phenanthroline hydrate
CAS:Formula:C12H10N2OPurity:98%Color and Shape:SolidMolecular weight:198.2206(ETHYLENEDINITRILO)TETRAACETIC ACID, TRISODIUM SALT HYDRATE
CAS:Formula:C10H18N2NaO9Purity:97%Color and Shape:SolidMolecular weight:333.2477Flanvotumab
CAS:<p>Flanvotumab (IMC-20D7S) is a humanized antibody targeting TYRP1 with strong antitumor effects via NK cells and ADCC.</p>Purity:> 95%Color and Shape:LiquidMolecular weight:145.42 kDa3-Isoquinolinecarboxamide, N-(1,1-dimethylethyl)decahydro-2-[(2R,3R)-2-hydroxy-3-[(3-hydroxy-2-methylbenzoyl)amino]-4-(phenylthio)butyl]-, (3S,4aS,8aS)-
CAS:Formula:C32H45N3O4SPurity:98%Color and Shape:SolidMolecular weight:567.7824Hck-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>Formula:C16H11ClN6O3SPurity:99.07%Color and Shape:SolidMolecular weight:402.81Anisindione
CAS:<p>Anisindione, a synthetic indanedione, inhibits vitamin K, blocking factors II, VII, IX, X, and proteins C, S.</p>Formula:C16H12O3Purity:98.25%Color and Shape:Pale Yellow Crystals From Acetic Acid Or Ethanol SolidMolecular weight:252.26RAMB4
CAS:<p>RAMB4 (PTP1B-IN-9) is a ubiquitin-proteasome system (UPS)-stressor,with anticancer activity.</p>Formula:C19H13Cl4NOPurity:98.89% - 99.38%Color and Shape:SolidMolecular weight:413.124-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>Formula:C7H5ClO3Purity:98.59%Color and Shape:Off-White To Light Beige PowderMolecular weight:172.57Retagliptin Phosphate
CAS:<p>Retagliptin Phosphate (SP 2086) is pharmaceutical composition of DPP-4 inhibitor, for treating type-2 diabetes.</p>Formula:C19H21F6N4O7PPurity:98.70%Color and Shape:SolidMolecular weight:562.363-Aminopropionitrile fumarate (2:1)
CAS:<p>3-Aminopropionitrile fumarate (2:1) (β-Aminopropionitrile fumarate) is an organic compound and antirheumatic agent used in veterinary medicine.</p>Formula:C4H4O4·2C3H6N2Purity:99.76% - >99.99%Color and Shape:White Crystalline PowderMolecular weight:256.26Sofosbuvir 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>Formula:C34H45FN4O13P2Purity:98.05%Color and Shape:SolidMolecular weight:798.69BLT-1
CAS:<p>BLT-1 is a scavenger receptor BI (SR-BI)inhibitor.</p>Formula:C12H23N3SPurity:97.97%Color and Shape:SolidMolecular weight:241.4Fostemsavir 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>Formula:C29H37N8O11PPurity:99.45%Color and Shape:SolidMolecular weight:704.62Ref: IN-DA0032JK
5g22.00€10g26.00€1kg229.00€25g30.00€50g40.00€100g59.00€10kgTo inquire250g114.00€500g164.00€Benzoic acid, 4-[[6-[(aminoiminomethyl)amino]-1-oxohexyl]oxy]-, ethylester, monomethanesulfonate
CAS:Formula:C17H27N3O7SPurity:98%Color and Shape:SolidMolecular weight:417.4772Ethylene glycol bis(2-aminoethyl ether)-N,N,N',N'-tetraacetic acid
CAS:Formula:C14H24N2O10Purity:97%Color and Shape:SolidMolecular weight:380.3478NBD-556
CAS:<p>NBD-556 is a small molecule mimetic of CD4. NBD-556 recognizes the HIV-1 envelope protein gp120 and induces restructuring of gp120 analogous to CD4 binding.</p>Formula:C17H24ClN3O2Purity:99.79%Color and Shape:SolidMolecular weight:337.84N-Tosyl-L-phenylalanine chloromethyl ketone
CAS:Formula:C17H18ClNO3SPurity:97%Color and Shape:SolidMolecular weight:351.8477BPHA
CAS:<p>BPHA is a selective oral inhibitor of MMP-2/9/14 (IC50: 12/16/17 nM), not affecting MMP-1/3/7, with anti-angiogenic and anti-tumor properties.</p>Formula:C21H20N2O4SPurity:99.44%Color and Shape:SolidMolecular weight:396.46Cathepsin C-IN-6
<p>Cathepsin C-IN-6 (compound 2), an E-64c-hydrazideas-derived inhibitor of cathepsin C, possesses anti-inflammatory properties and impedes neutrophil elastase</p>Formula:C24H35N5O4·xC2HF3O2Color and Shape:SolidZG36
<p>ZG36, a human Caseinolytic protease P (ClpP) agonist, non-selectively degrades respiratory chain complexes and reduces mitochondrial DNA, causing mitochondrial</p>Color and Shape:Odour SolidAR-H067637
CAS:<p>AR-H067637 is a fast-acting, reversible thrombin inhibitor with K(i) 2-4 nM; it also reduces clot-bound thrombin and platelet activation/aggregation.</p>Formula:C21H21ClF2N4O4Color and Shape:SolidMolecular weight:466.87N-CBZ-Phe-Arg-AMC
CAS:<p>Z-FR-AMC substrate for serine proteases; cathepsins, kallikrein, plasmin. Substrate: 330/390 nm; Product: 342/441 nm.</p>Formula:C33H36N6O6Purity:98%Color and Shape:White To Off-White PowderMolecular weight:612.68Zetomipzomib maleate
CAS:<p>Zetomipzomib maleate (KZR-616) selectively targets LMP7/2 in immunoproteasomes, potential for autoimmune research.</p>Formula:C34H46N4O12Color and Shape:SolidMolecular weight:702.758CRA-2059
CAS:<p>CRA-2059 is a potent and selective inhibitor of tryptase, particularly targeting recombinant human tryptase-β (rHTβ), with a K i of 620 pM.</p>Formula:C34H46N12O8Purity:97.68%Color and Shape:SolidMolecular weight:750.818ADAM8-IN-1
CAS:<p>ADAM8-IN-1 is a potent ADAM8 inhibitor with an IC 50 value of 73 nM.</p>Formula:C44H44Br4N6O12S2Color and Shape:SolidMolecular weight:1232.6MMP-3 Inhibitor
CAS:<p>MMP-3 Inhibitor is a peptide matrix metalloproteinase-3 (MMP-3) inhibitor with a Ki value of 95 nM.MMP-3 inhibitor has anticancer and antitumor activity.</p>Formula:C27H46N10O9SPurity:98.87%Color and Shape:SolidMolecular weight:686.78(-)-Taxifolin
CAS:<p>(-)-Taxifolin, less active enantiomer with anti-tyrosinase, collagenase inhibition (IC50 = 193.3 μM), antifibrotic, antioxidant properties.</p>Formula:C15H12O7Color and Shape:SolidMolecular weight:304.25TP0597850
CAS:<p>TP0597850, a selective MMP2 inhibitor with an IC50 value of 0.22 nM, demonstrates a prolonged dissociation half-life from MMP2 (t1/2 = 265 minutes) [1].</p>Formula:C41H57N9O13SColor and Shape:SolidMolecular weight:916.01TAPI1 acetate
<p>TAPI1 acetate (TNF-α processing inhibitor-1) is a TACE (ADAM17) inhibitor that inhibits shedding of TNF-α cytokine receptors; MMP inhibitor .</p>Formula:C28H41N5O7Purity:98.82% - 99.94%Color and Shape:SolidMolecular weight:559.65Leptosin D
CAS:<p>Leptosin D, a thiodiketopiperazine alkaloid derived from mushrooms, effectively inhibits tyrosinase activity, demonstrating an inhibition concentration (IC50)</p>Formula:C25H24N4O3S2Color and Shape:SolidMolecular weight:492.61HCVP-IN-1
CAS:<p>HCVP-IN-1 (compound 1) is a hepatitis C viral polymerase (HCVP) inhibitor.</p>Formula:C30H34FN5O3Color and Shape:SolidMolecular weight:531.632Cathepsin K inhibitor 7
<p>Cathepsin K Inhibitor7 (compound 7) is an inhibitor of Cathepsin K, exhibiting a pKi value of 7.3. It is utilized in research on osteoporosis.</p>Color and Shape:Odour SolidSofosbuvir impurity A
CAS:<p>Sofosbuvir impurity A is an diastereoisomer of Sofosbuvir. Sofosbuvir is anHCV RNA replication inhibitor ,with potent anti-hepatitis C virus activity.</p>Formula:C22H29FN3O9PPurity:98%Color and Shape:SolidMolecular weight:529.45Imitrodast
CAS:<p>Imitrodast is a small molecule thromboxane A2 synthase (TXA2 synthase) inhibitor for the treatment of immune system disorders, respiratory disorders, and</p>Formula:C13H12N2O2SPurity:98.39%Color and Shape:SolidMolecular weight:260.31Ellipyrone A
<p>Ellipyrone A: γ-pyrone macrocycle, inhibits DPP-4 (IC50=0.35mM), α-glucosidase (IC50=0.74mM), α-amylase (IC50=0.59mM).</p>Formula:C25H34O8Color and Shape:SolidMolecular weight:462.53Neutrophil elastase inhibitor 4
<p>Neutrophil elastase inhibitor 4 (compound 4f) is a competitive inhibitor of human neutrophil elastase (HNE) with IC50 of 42.30 nM and Ki of 8.04 nM.</p>Formula:C20H21N3O5Color and Shape:SolidMolecular weight:383.4HCV-IN-4
CAS:<p>HCV-IN-4: Potent, oral HCV NS5A inhibitor; effective vs GT1a/b, GT2b, GT3a, Y93H, L31V; EC90s: 3 pM-0.02 nM.</p>Formula:C52H58FN9O8Purity:98%Color and Shape:SolidMolecular weight:956.07Chetoseminudin B
CAS:<p>Chetoseminudin B exhibits inhibitory activity against mushroom tyrosinase, with an IC 50 value of 31.7 μM [1].</p>Formula:C17H21N3O3S2Color and Shape:SolidMolecular weight:379.5Sofosbuvir impurity J
CAS:<p>Sofosbuvir impurity J is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity.</p>Formula:C22H30FN4O8PPurity:98%Color and Shape:SolidMolecular weight:528.476-Acetylnimbandiol
CAS:<p>6-Acetylnimbandiol, a non-toxic agent, inhibits tyrosinase (IC50=69.85 μM), melanin, and MITF; useful in melanoma studies.</p>Formula:C28H34O8Color and Shape:SolidMolecular weight:498.56α 1(I) Collagen (614-639), human
CAS:<p>This is a peptide inhibitor of collagen fibrillar matrix assembly.</p>Formula:C134H189N37O39Purity:98%Color and Shape:SolidMolecular weight:2942.16PF 00356231
CAS:<p>PF 00356231 is a selectivity inhibitor MMP-12 and can be used in studies about the treatment of emphysema and chronic obstructive pulmonary disease (COPD).</p>Formula:C25H20N2O3SPurity:99.35%Color and Shape:SolidMolecular weight:428.5Dnp-P-Cha-G-Cys(Me)-HA-K(Nma)-NH2
CAS:<p>Dnp-P-Cha-G-Cys(Me)-HA-K(Nma)-NH2 is a fluorogenic probe for MMP-1 and MMP-9 detection, releasing fluorescent Nma upon cleavage (Ex/Em: 340/440 nm).</p>Formula:C49H68N14O12SColor and Shape:SolidMolecular weight:1077.22Bictegravir Sodium
CAS:<p>Bictegravir Sodium is an HIV-1 integrase inhibitor with 7.5 nM IC50, offering strong, selective anti-HIV effects and minimal toxicity.</p>Formula:C21H17F3N3NaO5Purity:99.97%Color and Shape:SolidMolecular weight:471.36HIV-1 inhibitor-6
CAS:<p>HIV-1 inhibitor-6 (3-Pyridinecarboxamide, 1,4-dihydro-1-methyl-N-(5-nitro-1,2-benzisothiazol-3-yl)-4-oxo-) is a potent HIV-1 pre-mRNA selective splicing</p>Formula:C14H10N4O4SPurity:99.33%Color and Shape:SolidMolecular weight:330.32JC-10
CAS:<p>JC-10 is a potent inhibitor of metalloproteinases and is often used as a probe.</p>Formula:C25H29Cl2IN4Purity:95%Color and Shape:SolidMolecular weight:583.34Enzyme-IN-1
CAS:<p>Enzyme-IN-1（compound 1）为基于肽的N端亲核试剂（Ntn）水解酶抑制剂，特别针对20S蛋白酶体的糜胰蛋白酶样活性（CT-L）进行抑制，可能展现出抗炎特性。</p>Formula:C36H50N4O7Color and Shape:SolidMolecular weight:650.8Cepeginterferon alfa-2b
CAS:<p>Cepeginterferon alfa-2b: pegylated interferon with 20 kDa PEG for HCV, PV, ET research.</p>Color and Shape:LiquidCys-TAT(47-57) acetate(583836-55-9 Free base)
<p>Cys-TAT(47-57) acetate is derived from the HIV-1 transactivating protein. Cys-TAT(47-57) acetate is an arginine rich peptide that can penetrate cells.</p>Formula:C69H128N34O16SPurity:95.1100%Color and Shape:SolidMolecular weight:1722.04RJS308
<p>RJS308 is a PROTAC degrader of cyclosporin A (cyclosporin A) with a DC50 of 284 nM. It exhibits antiviral activity by inhibiting the replication of HIV-1 and HCV. (Pink: ligand for target protein CypA ligand-2; Black: linker; Blue: ligand for E3 ligase VHL (S,R,S)-AHPC-Me)</p>Formula:C63H75N13O11SColor and Shape:SolidMolecular weight:1222.42Talabostat isomer mesylate
<p>Talabostat isomer mesylate, a PT100/Val-boroPro variant, is a potent oral DPP-IV inhibitor (Ki: 0.18 nM).</p>Formula:C10H23BN2O6SPurity:98%Color and Shape:SolidMolecular weight:310.18PPACK II
CAS:<p>PPACK II is an irreversible and specific glandular and plasma kallikreins inhibitor [1] .</p>Formula:C25H33ClN6O3Color and Shape:SolidMolecular weight:501.02Rivulariapeptolides 1121
<p>Rivulariapeptolides 1121 inhibits serine proteases: chymotrypsin (IC50=35.52 nM), elastase (13.24 nM), proteinase K (48.05 nM).</p>Formula:C56H83N9O15Color and Shape:SolidMolecular weight:1122.31Fotagliptin
CAS:<p>Fotagliptin is a dipeptidyl peptidase IV inhibitor.</p>Formula:C17H19FN6OColor and Shape:SolidMolecular weight:342.37N-CBZ-Phe-Arg-AMC TFA
<p>N-CBZ-Phe-Arg-AMC TFA (Z-FR-AMC TFA) is a fluorescent substrate for serine proteases. assess the activity of trypsin, plasmin, and cathepsin.</p>Formula:C35H37F3N6O8Purity:99.88%Color and Shape:SolidMolecular weight:726.7CRA-2059 hydrochloride
<p>CRA-2059 hydrochloride is a highly specific and selective tryptase inhibitor, with a Ki of 620 pM for recombinant human tryptase-β (rHTβ)[1][2].</p>Color and Shape:Solid7-Methoxy obtusifolin
CAS:<p>7-Methoxy obtusifolin (Compound 4) is a chemical compound that acts as a competitive inhibitor of the enzyme tyrosinase, displaying an inhibitory concentration</p>Formula:C17H14O6Color and Shape:SolidMolecular weight:314.29Tyrosinase/elastase-IN-1
<p>Tyrosinase/elastase-IN-1, a triterpenoid extracted from the leaves of Rubus fraxinifolius, exhibits inhibitory activities against both tyrosinase and elastase</p>Formula:C33H52O5Color and Shape:SolidMolecular weight:528.76DPP8/9-IN-1
<p>DPP8/9-IN-1 (Compound 16) is a selective covalent inhibitor of dipeptidyl peptidase 8 and 9 (DPP8/9), with IC50 values of 14 nM and 298 nM, respectively. It irreversibly binds to the active site serine (such as S730 in DPP9) through a phosphate ester warhead, blocking substrate binding and inhibiting DPP8/9-mediated protein processing. DPP8/9-IN-1 holds potential for research in cancer and inflammatory diseases.</p>Color and Shape:Odour SolidSofigatran
CAS:<p>Sofigatran (MCC-977) is an oral anticoagulant targeting thrombin for cardiovascular research.</p>Formula:C24H44N4O4SColor and Shape:SolidMolecular weight:484.7L 659286
CAS:<p>L 659286 is one kind of cephalosporin derivative.</p>Formula:C17H21N5O7S2Color and Shape:SolidMolecular weight:471.51Nitidanin
<p>Nitidanin is a useful organic compound for research related to life sciences and the catalog number is T125599.</p>Formula:C21H24O8Color and Shape:SolidMolecular weight:404.415Dutogliptin tartrate
CAS:<p>Dutogliptin tartrate is an effective and selective oral dipeptide-peptide-4 (DPP4) inhibitor for the treatment of type 2 diabetes mellitus.</p>Formula:C14H26BN3O9Purity:98%Color and Shape:SolidMolecular weight:391.18NS5A-IN-1
<p>NS5A-IN-1 is a proagent of the HCV NS5A inhibitor Pibrentasvir (ABT-530).</p>Formula:C72H86F5N10O14PColor and Shape:SolidMolecular weight:1441.48Ac-[Nle4,D-Phe7]-α-MSH (4-10)-NH2
CAS:<p>Ac-[Nle4,D-Phe7]-α-MSH (4-10)-NH2, a melanotropin derivative and melanocyte-stimulating hormone, activates tyrosinase and demonstrates a thermoregulatory effect</p>Formula:C47H64N14O10Color and Shape:SolidMolecular weight:985.1Sofosbuvir impurity M
CAS:<p>Sofosbuvir impurity M is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity.</p>Formula:C22H30N3O10PPurity:98%Color and Shape:SolidMolecular weight:527.467Cathepsin D and E FRET Substrate
CAS:<p>Mca-GKPILFFRL-Dpa-r-amide, FRET substrate for cathepsin D and E. Also cleaved by napsin A.</p>Formula:C85H122N22O19Color and Shape:SolidMolecular weight:1756.046FFAGLDD TFA
<p>FFAGLDD TFA: MMP9 peptide for controlled DOX delivery to cytoplasm.</p>Formula:C39H50F3N7O14Purity:98%Color and Shape:SolidMolecular weight:897.85L-Methionine-DL-sulfoximine
CAS:<p>MSO blocks glutamine synthetase, impacts astroglia, and is used in convulsant research.</p>Formula:C5H12N2O3SPurity:99.56% - ≥98%Color and Shape:White Crystalline PowderMolecular weight:180.23NS5A-IN-4
CAS:<p>NS5A-IN-4 (Compound 1.12) is a hepatitis C inhibitor effective against multiple genotypes, with IC50 values ranging from 1.2 to 2296 pM.</p>Formula:C47H48N8O6Color and Shape:SolidMolecular weight:820.93GCPII-IN-1
CAS:<p>GCPII-IN-1, a potent PSMA inhibitor, binds with 44.3 nM affinity.</p>Formula:C12H21N3O7Color and Shape:SolidMolecular weight:319.314AL-611
CAS:<p>AL-611 is an HCV NS5B polymerase inhibitor ( EC 50 = 5 nM).</p>Formula:C25H33F2N6O8PColor and Shape:SolidMolecular weight:614.544Radalbuvir
CAS:<p>Radalbuvir (GS-9669) is an investigational antiviral agent for the treatment of hepatitis C virus (HCV) infection as an NS5B inhibitor.</p>Formula:C30H41NO6SColor and Shape:SolidMolecular weight:543.71Rivulariapeptolides 1155
<p>Rivulariapeptolides 1155 inhibits chymotrypsin (41.84 nM), elastase (4.94 nM), and proteinase K (56.54 nM).</p>Formula:C59H81N9O15Color and Shape:SolidMolecular weight:1156.33Recombinant Proteinase K
<p>Recombinant Proteinase K: serine protease, cleaves carboxy-terminus peptides, digests proteins, purifies nucleic acids.</p>Color and Shape:SolidGSK2336805
CAS:<p>GSK-2336805, an HCV NS5A inhibitor, is effective against genotypes 1, 4, 5, and some of 6.</p>Formula:C42H52N8O8Color and Shape:SolidMolecular weight:796.91Leptosphaerodione
CAS:<p>Leptosphaerodione from Remotididymella sp.: a potent UPS inhibitor with 3.2 μM IC50 in HeLa cells; anti-tumor.</p>Formula:C21H22O5Color and Shape:SolidMolecular weight:354.4Histargin
CAS:<p>Histargin is an enzyme inhibitor separated from Streptomyces roseoviridis.</p>Formula:C14H25N7O4Color and Shape:SolidMolecular weight:355.39Proteasome-IN-7
<p>Proteasome-IN-7 (Compound 6f) is a macrolactam-based epoxyketone proteasome inhibitor with an IC50 value of 37.92 nM against the 20S proteasome ChT-L subunit. It exhibits potent antiproliferative effects on multiple myeloma, acute lymphoblastic leukemia, and non-small cell lung cancer.</p>Formula:C48H56N6O10SColor and Shape:SolidMolecular weight:909.06Peptide 74
CAS:<p>Peptide 74 is a synthetic peptide. It also inhibits the activated form of this enzyme.</p>Formula:C62H107N23O20S2Purity:98%Color and Shape:SolidMolecular weight:1558.79α 1 Antichymotrypsin, Human Plasma
CAS:<p>Alpha 1 Antichymotrypsin, Human Plasma is an inhibitor of serine proteases. This compound is present in amyloid lesions associated with Alzheimer's disease and can be utilized in Alzheimer's research.</p>Color and Shape:SolidAPC-6860
CAS:<p>APC-6860, a serine protease inhibitor, targets multiple enzymes; most potent against human urokinase (Ki: 0.1 µM). Used in cancer research.</p>Formula:C9H7IN2SColor and Shape:SolidMolecular weight:302.13PSI-7409
CAS:<p>PSI-7409 is the active 5'-triphosphate metabolite of Sofosbuvir (PSI-7977).</p>Formula:C10H16FN2O14P3Purity:98%Color and Shape:SolidMolecular weight:500.16AMG-222
CAS:<p>AMG-222 (ALS-2-0426, ALS-20426) is a DPP-4 inhibitor and may be used in the treatment of type 2 diabetes.</p>Formula:C32H39N9O3Color and Shape:SolidMolecular weight:597.71Ac-VDQQD-pNA
CAS:<p>Ac-VDQQD-pNA serves as a substrate for Caspase 2, which cleaves it to yield the yellow compound pNA (p-nitroaniline).</p>Formula:C31H43N9O14Color and Shape:SolidMolecular weight:765.73Sitagliptin fenilalanil hydrochloride
CAS:<p>Sitagliptin phenylalanine hydrochloride, a dipeptidyl peptidase-4 (DPP-4) inhibitor [1], is a chemical compound utilized in medical applications.</p>Formula:C25H25ClF6N6O2Color and Shape:SolidMolecular weight:590.95PS 915
CAS:<p>PS 915 is a substrate for colorimetric assay. It was used for plasma antithrombin.</p>Formula:C27H36ClN7O6Purity:98%Color and Shape:SolidMolecular weight:590.08Fotagliptin benzoate
CAS:<p>Fotagliptin benzoate, a DPP-4 inhibitor (IC50=2.27 nM), is safe in rats/dogs, useful for Type 2 diabetes research.</p>Formula:C24H25FN6O3Color and Shape:SolidMolecular weight:464.49HCV-IN-41
CAS:<p>HCV-IN-41: potent HCV inhibitor; EC50 - 0.006762 nM (1b), 5.183 nM (2a), 1.365 nM (3a), 142.2 nM (4a); hinders RNA replication.</p>Formula:C48H56N6O8Color and Shape:SolidMolecular weight:844.99Befovacimab
CAS:<p>Befovacimab, a human IgG2 antibody, targets TFPI for hemophilia A/B research.</p>Color and Shape:LiquidBerotralstat
CAS:<p>Berotralstat (BCX7353) is an oral, low-toxicity, specific kallikrein inhibitor for hereditary angioedema research, blocking bradykinin release.</p>Formula:C30H26F4N6OColor and Shape:SolidMolecular weight:562.56Tyrosinase-IN-34
<p>Tyrosinase-IN-34 (compound 5a), a human tyrosinase inhibitor (IC 50: 3.5 μM), shows promise in regulating melanogenesis and pigmentation.</p>Formula:C19H14BrClN4OColor and Shape:SolidMolecular weight:429.7Histatin 5 (TFA)(115966-68-2,free)
<p>Histatin 5 (TFA)(115966-68-2,free) (Histatin 5 (TFA)) inhibits the activity of the host matrix metalloproteinases MMP-2 and MMP-9 with IC50s of 0.57 and 0.25 μM</p>Formula:C135H196F3N51O35Purity:98%Color and Shape:SolidMolecular weight:3150.32NVP-DPP728 dihydrochloride
CAS:<p>NVP-DPP728 dihydrochloride is a potent, selective DPP-IV inhibitor with a Ki of 11 nM, useful in diabetes research.</p>Formula:C15H20Cl2N6OColor and Shape:SolidMolecular weight:371.27Stevia Powder
<p>Stevia Powder, a natural sweetener, possesses antioxidant properties. It regulates antifibrotic pathways in cirrhotic rats, demonstrated by a reduction in hepatic stellate cells and decreased expression of matrix metalloproteinases MMP2 and MMP13. Furthermore, it increases the antifibrotic molecule Smad7, which helps prevent the elevation of serum necrosis and bile retention markers, thereby inhibiting the progression of liver fibrosis.</p>Color and Shape:Odour SolidCP-346086 dihydrate
CAS:<p>CP-346086 dihydrate is a strong oral MTP inhibitor with 2.0 nM IC50, reducing cholesterol and triglycerides in vivo.</p>Formula:C26H26F3N5O3Color and Shape:SolidMolecular weight:513.521Ecallantide TFA
<p>Ecallantide (DX-88) TFA, a specific recombinant plasma kallikrein inhibitor, directly inhibits bradykinin production and is indicated for the prevention of</p>Color and Shape:Odour SolidPseudostellarin G
CAS:<p>Pseudostellarin G, a naturally occurring cyclo-octapeptide, exhibits inhibitory activity against tyrosinase and suppresses melanin production.</p>Formula:C42H56N8O9Color and Shape:SolidMolecular weight:816.94MK-6169
CAS:<p>MK-6169 is an effective Pan-Genotype Hepatitis C Virus NS5A inhibitor. It also has Optimized Activity against Common Resistance-Associated Substitutions.</p>Formula:C54H62FN9O8SPurity:98%Color and Shape:SolidMolecular weight:1016.2KKI-5
CAS:<p>KKI 5: Serine protease inhibitor, blocks kallikrein & plasmin, potential for cancer therapy & angioedema treatment.</p>Formula:C35H55N11O9Purity:98%Color and Shape:SolidMolecular weight:773.88Dutogliptin
CAS:<p>Dutogliptin (PHX-1149 free base) is an oral, effective and selective dipeptide-peptide-4 (DPP4) inhibitor for the treatment of type 2 diabetes mellitus.</p>Formula:C10H20BN3O3Purity:98%Color and Shape:SolidMolecular weight:241.10CL 82198 hydrochloride
CAS:<p>CL 82198 hydrochloride selectively inhibits MMP-13, not MMP-1/9/TACE, and blocks HP75 invasion and neurotoxicity in zebrafish.</p>Formula:C17H23ClN2O3Color and Shape:SolidMolecular weight:338.83Acetyl-Calpastatin(184-210)(human)
CAS:<p>Calpain inhibitor, Ki 0.2 nM for calpain I/II, doesn't affect papain/trypsin/cat L. Raises Aβ42, Aβ40 secretion & Aβ42/Aβ40 ratio.</p>Formula:C142H230N36O44SPurity:98%Color and Shape:SolidMolecular weight:3177.65Anticancer agent 114
<p>Anticancer agent 114: oral dipeptide boronic acid, proteasome inhibitor, IC 50 = 2.2 nM, halts RPMI-8226 cell growth, for multiple myeloma research.</p>Formula:C28H33BF6N2O7Color and Shape:SolidMolecular weight:634.37AP-C2
CAS:<p>AP-C2 is a potent small molecule guanosine 3',5'-cyclic monophosphate (cGMP)-dependent protein kinase II (cGKII) inhibitor with a pIC50 of 5.2 for cGKII.</p>Formula:C18H16N4SPurity:99.87%Color and Shape:SoildMolecular weight:320.41C-telopeptide
CAS:<p>C-telopeptide from type I collagen is released during bone resorption; it correlates with bone mineral density.</p>Formula:C34H56N14O13Purity:98%Color and Shape:SolidMolecular weight:868.9Tyrosinase-IN-32
<p>Tyrosinase-IN-32 (compound 11), a hydroxamate-based alkaloid extracted from black pepper (Piper nigrum L.), functions as an inhibitor of mushroom tyrosinase. In addition to its inhibitory properties, it exhibits antioxidant activity.</p>Formula:C15H19NO3Color and Shape:SolidMolecular weight:261.32EP 171
CAS:<p>EP 171 is a potent agonist of TP-receptors.</p>Formula:C23H29FO5Color and Shape:SolidMolecular weight:404.47Elastatinal
CAS:<p>Elastatinal is an elastase inhibitor. It is found in culture filtrates of various species of actinomyces.</p>Formula:C21H36N8O7Color and Shape:Yellowish SolidMolecular weight:512.56Ac-DEMEEC-OH
CAS:<p>Ac-DEMEEC-OH is a competitive inhibitor of the HCV NS3 protease with a Ki of 0.6 µM.</p>Formula:C29H44N6O16S2Color and Shape:SolidMolecular weight:796.82HIV-1 TAT (48-60) Acetate
<p>Lilotomab (HH1) is a murine anti-CD37 antibody that can be used to synthesize anti-CD37 antibody-radionuclide couplings.</p>Formula:C72H135N35O18Purity:99.93%Color and Shape:SoildMolecular weight:1779.07STK33-IN-1
CAS:<p>STK33-IN-1 (compound 1) is a STK33 inhibitor, with an IC 50 of 7 nM.</p>Formula:C24H27N7O2Color and Shape:SolidMolecular weight:445.527GSK2818713
CAS:<p>GSK2818713 is a novel Hepatitis C NS5A replication complex inhibitor.</p>Formula:C46H56N8O8Color and Shape:SolidMolecular weight:849.002FiVe1
CAS:<p>FiVe1 is a vimentin-binding compound that disrupts mitosis in cancer cells, causing cell death, with an IC50 of 234 nM in FOXC2-HMLER.</p>Formula:C18H16Cl2N4Purity:99.67%Color and Shape:SolidMolecular weight:359.25BMS-767778
CAS:<p>BMS-767778, a DPP-4 inhibitor, is used potentially for the treatment of type 2 diabetes.</p>Formula:C19H20Cl2N4O2Color and Shape:SolidMolecular weight:407.29Linagliptin Methyldimer
CAS:<p>Linagliptin Methyldimer is a potent dipeptidyl peptidase IV inhibitor, IC50=6 pM.</p>Formula:C50H56N16O4Purity:97.23%Color and Shape:SolidMolecular weight:945.08RXP470
CAS:<p>RXP470 is a potent and selective MMP-12 inhibitor (Ki 0.24 nM).</p>Formula:C35H35BrClN4O10PColor and Shape:SolidMolecular weight:818Plasma kallikrein-IN-1
CAS:<p>Plasma kallikrein-IN-1 is a PKK inhibitor with an IC 50 value of 0.5 nM.</p>Formula:C23H25F2N7OColor and Shape:SolidMolecular weight:453.498Paritaprevir dihydrate
CAS:<p>Paritaprevir dihydrate: potent oral HCV NS3/4A inhibitor (EC50: 0.21-1 nM), SARS-CoV-3CL blocker (IC50: 1.31 μM), metabolized by CYP3A, boosted by Ritonavir.</p>Formula:C40H47N7O9SColor and Shape:SolidMolecular weight:801.91CTTHWGFTLC, CYCLIC
CAS:<p>CTT Gelatinase Inhibitor peptide blocks MMP-2/9, hindering cancer by stopping tumor growth.</p>Formula:C52H71N13O14S2Purity:98%Color and Shape:SolidMolecular weight:1166.33midesteine
CAS:<p>Midesteine (MR-889) is a small molecule neutrophil elastase inhibitor used in the treatment of bronchitis, asthma and chronic lung disease.</p>Formula:C12H13NO3S3Purity:99.52% - 99.98%Color and Shape:SolidMolecular weight:315.43
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