Proteasi/Proteasoma
Gli inibitori delle proteasi e del proteasoma sono composti che bloccano l'attività delle proteasi e del proteasoma, che sono coinvolti nella degradazione e nel turnover delle proteine. Questi inibitori sono fondamentali per studiare la regolazione dell'omeostasi proteica, il controllo del ciclo cellulare e l'apoptosi. Gli inibitori delle proteasi e del proteasoma vengono anche utilizzati nel trattamento di malattie come il cancro, dove la degradazione anomala delle proteine svolge un ruolo nella progressione della malattia. Inibendo le proteasi o il proteasoma, questi composti possono indurre la morte cellulare nelle cellule tumorali e sono strumenti critici sia per la ricerca di base che per lo sviluppo terapeutico. Presso CymitQuimica, offriamo una vasta gamma di inibitori delle proteasi e del proteasoma di alta qualità per supportare la tua ricerca in biochimica, biologia cellulare e sviluppo di farmaci.
Sottocategorie di "Proteasi/Proteasoma"
- Acetil-CoA carbossilasi(35 prodotti)
- Cisteina proteasi(110 prodotti)
- DPP-4(20 prodotti)
- Glutaminasi(43 prodotti)
- Proteasi HIV(494 prodotti)
- PAI-1(25 prodotti)
- Inibitori della proteasi(50 prodotti)
- Ricettore attivato dalla proteasi(53 prodotti)
- Proteasoma(95 prodotti)
- Proteasi serina(56 prodotti)
- p97(15 prodotti)
Mostrare 3 più sottocategorie
Trovati 1092 prodotti di "Proteasi/Proteasoma"
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MG-132
CAS:Formula:C26H41N3O5Purezza:>95.0%(qNMR)Colore e forma:White to Light yellow powder to crystalPeso molecolare:475.63Nafamostat Mesylate
CAS:Formula:C19H17N5O2·2CH4O3SPurezza:>98.0%(HPLC)Colore e forma:White to Almost white powder to crystalPeso molecolare:539.58Gabexate Mesylate
CAS:Formula:C16H23N3O4·CH4O3SPurezza:>97.0%(N)Colore e forma:White to Almost white powder to crystalPeso molecolare:417.482-Iodoacetamide [for Biochemical Research]
CAS:Formula:C2H4INOPurezza:>98.0%(N)Colore e forma:White to Light yellow powder to crystalPeso molecolare:184.96Atazanavir Sulfate
CAS:Formula:C38H52N6O7·H2SO4Purezza:>98.0%(HPLC)Colore e forma:White to Almost white powder to crystalPeso molecolare:802.941,10-Phenanthroline Monohydrate [for Biochemical Research]
CAS:Formula:C12H8N2·H2OPurezza:>99.0%(T)Colore e forma:White powder to crystalPeso molecolare:198.23Atazanavir
CAS:Formula:C38H52N6O7Purezza:>95.0%(HPLC)Colore e forma:White to Light yellow powder to crystalPeso molecolare:704.87Ritonavir
CAS:Formula:C37H48N6O5S2Purezza:>98.0%(HPLC)(N)Colore e forma:White to Almost white powder to crystalinePeso molecolare:720.95Nelfinavir Mesylate
CAS:Formula:C32H45N3O4S·CH4O3SPurezza:>97.0%(HPLC)Colore e forma:White to Almost white powder to crystalPeso molecolare:663.89Disodium Dihydrogen Ethylenediaminetetraacetate Dihydrate [for Biochemical Research]
CAS:Formula:C10H14N2Na2O8·2H2OPurezza:>99.0%(T)Colore e forma:White powder to crystalinePeso molecolare:372.24Benzylsulfonyl Fluoride [for Biochemical Research]
CAS:Formula:C7H7FO2SPurezza:>98.0%(GC)Colore e forma:White to Almost white powder to crystalPeso molecolare:174.19Limonin
CAS:Formula:C26H30O8Purezza:>95.0%(HPLC)Colore e forma:White to Almost white powder to crystalPeso molecolare:470.524-(2-Aminoethyl)benzenesulfonyl Fluoride Hydrochloride [for Biochemical Research]
CAS:Formula:C8H10FNO2S·HClPurezza:>99.0%(HPLC)Colore e forma:White to Almost white powder to crystalPeso molecolare:239.69Ethylene Glycol Bis(2-aminoethyl Ether)-N,N,N',N'-tetraacetic Acid [for Biochemical Research]
CAS:Formula:C14H24N2O10Purezza:>95.0%(T)Colore e forma:White to Almost white powder to crystalPeso molecolare:380.35Camostat Mesylate
CAS:Formula:C20H22N4O5·CH4O3SPurezza:>98.0%(HPLC)Colore e forma:White to Almost white powder to crystalPeso molecolare:494.52Benzoic acid, 4-[(aminoiminomethyl)amino]-, 6-(aminoiminomethyl)-2-naphthalenyl ester, dimethanesulfonate
CAS:Formula:C20H21N5O5SPurezza:98%Colore e forma:SolidPeso molecolare:443.4762Elsulfavirine
CAS:Elsulfavirine (VM-1500) is an HIV-1 infection reverse transcriptase inhibitor. It is a new anti-HIV drug.Formula:C24H17BrCl2FN3O5SPurezza:99.66%Colore e forma:SolidPeso molecolare:629.28Ref: IN-DA0032JK
5g22,00€10g26,00€1kg229,00€25g30,00€50g40,00€100g59,00€10kgPrezzo su richiesta250g114,00€500g164,00€Q-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:C26H25F2N3O6Purezza:97.8% - 98.95%Colore e forma:SolidPeso molecolare:513.5LSP-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:C24H22ClN5OPurezza:99.51%Colore e forma:SolidPeso molecolare:431.92RA190
CAS:<p>RA190 inhibits proteasome function by covalently binding to cysteine 88 of ubiquitin receptor RPN13.</p>Formula:C28H23Cl5N2O2Purezza:97.7%Colore e forma:SolidPeso molecolare:596.76Retagliptin Phosphate
CAS:<p>Retagliptin Phosphate (SP 2086) is pharmaceutical composition of DPP-4 inhibitor, for treating type-2 diabetes.</p>Formula:C19H21F6N4O7PPurezza:98.70%Colore e forma:SolidPeso molecolare:562.36BJJF078
CAS:BJJF078, an aminopiperidine, inhibits human/mouse TG2 (IC50: 41/54 nM) and TG1 (IC50: 0.16 μM), may be used in MS studies.Formula:C27H29N3O6SPurezza:99.56%Colore e forma:SoildPeso molecolare:523.6Gly-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>Formula:C13H17ClN4O4Purezza:99.84%Colore e forma:SolidPeso molecolare:328.753-Deazaadenosine hydrochloride
CAS:3-Deazaadenosine HCl blocks SAH hydrolase (Ki: 3.9 μM), with anti-inflammatory, anti-proliferative, and anti-HIV effects.Formula:C11H15ClN4O4Purezza:98.48%Colore e forma:SolidPeso molecolare:302.71DBPR108
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:C16H25FN4O2Purezza:99.68%Colore e forma:SolidPeso molecolare:324.39DPP-IV-IN-2
CAS: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).Formula:C18H26N4O5Purezza:99.08%Colore e forma:SolidPeso molecolare:378.42Salicylanilide
CAS:<p>Salicylanilide (2-Hydroxybenzanilide)s are a group of compounds with antiviral potency, antibacterial and antifungal activities.</p>Formula:C13H11NO2Purezza:99.55%Colore e forma:White To Off-White Crystalline PowderPeso molecolare:213.23Ruzasvir
CAS:Ruzasvir (MK-8408) is a novel and potent pan-genotypic inhibitor of hepatitis C virus NS5A with antiviral activity.Formula:C49H55FN10O7SPurezza:96.87% - 99.93%Colore e forma:SolidPeso molecolare:947.093-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:C33H49N3O7S2Purezza:96%Colore e forma:SolidPeso molecolare:663.88814-(2-Aminoethyl)benzenesulfonyl fluoride, HCl
CAS:Formula:C8H11ClFNO2SPurezza:98%Colore e forma:SolidPeso molecolare:239.6948(2S)-2-[(2S,3R)-3-amino-2-hydroxy-4-phenylbutanamido]-4-methylpentanoic acid
CAS:Formula:C16H24N2O4Purezza:98%Colore e forma:SolidPeso molecolare:308.3728Ref: IN-DA00370Q
1g132,00€5g223,00€10g532,00€25gPrezzo su richiesta50gPrezzo su richiesta100gPrezzo su richiesta10mg29,00€250gPrezzo su richiesta50mg34,00€100mg44,00€250mg68,00€Sitagliptin
CAS:Sitagliptin (MK0431), an oral DPP-4 inhibitor, treats type 2 diabetes alone or with metformin/thiazolidinedione by increasing incretins and insulin.Formula:C16H15F6N5OPurezza:99.33% - 99.83%Colore e forma:Yellow GreasePeso molecolare:407.31RAMB4
CAS:RAMB4 (PTP1B-IN-9) is a ubiquitin-proteasome system (UPS)-stressor,with anticancer activity.Formula:C19H13Cl4NOPurezza:98.89% - 99.38%Colore e forma:SolidPeso molecolare:413.12BRD-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.Formula:C19H17N3O2SPurezza:98.01% - 99.05%Colore e forma:SolidPeso molecolare:351.42Mecarbinate
CAS:Mecarbinate (Dimecarbin) is arbidol hydrochloride's chemical intermediate.Formula:C13H15NO3Purezza:99.28%Colore e forma:Off-White Crystalline PowderPeso molecolare:233.263-Aminopropionitrile fumarate (2:1)
CAS:3-Aminopropionitrile fumarate (2:1) (β-Aminopropionitrile fumarate) is an organic compound and antirheumatic agent used in veterinary medicine.Formula:C4H4O4·2C3H6N2Purezza:99.76% - 99.79%Colore e forma:White Crystalline PowderPeso molecolare:256.26Probenecid
CAS:<p>Probenecid (Benemid) is a benzoic acid derivative with antihyperuricemic property.</p>Formula:C13H19NO4SPurezza:98.95% - 99.84%Colore e forma:Crystals From Dil Alcohol Pleasant Aftertaste (Ntp 1992)Peso molecolare:285.36Benzenemethanesulfonyl fluoride
CAS:Formula:C7H7FO2SPurezza:99%Colore e forma:SolidPeso molecolare:174.1927Ref: IN-DA00I6AP
1g25,00€5g39,00€10g55,00€25g90,00€50g127,00€100g166,00€250g505,00€500gPrezzo su richiestaARP-100
CAS:ARP-100 (MMP-2 Inhibitor III) is a potent and selective matrix metalloproteinase MMP-2 inhibitor (IC50=12 nM).Formula:C17H20N2O5SPurezza:97.18%Colore e forma:SolidPeso molecolare:364.42KW-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.Formula:C29H31N5O5SPurezza:99.28%Colore e forma:SolidPeso molecolare:561.65Bivalirudin acetate
Bivalirudin acetate is a thrombin inhibitor, a peptide-based anticoagulant, used for research on acute coronary syndrome.Formula:C100H142N24O35Purezza:99.84%Colore e forma:SolidPeso molecolare:2240.34Incyclinide
CAS:<p>Incyclinide (COL-3) is a matrix metalloproteinase (MMP) inhibitor.</p>Formula:C19H17NO7Purezza:97.99%Colore e forma:SolidPeso molecolare:371.34Saxagliptin hydrate
CAS:Saxagliptin hydrate (Onglyza hydrate) is a selective and reversible DPP4 inhibitor (IC50: 26 nM; Ki: 1.3 nM).Formula:C18H25N3O2·H2OPurezza:99.52%Colore e forma:SolidPeso molecolare:333.43Aprotinin
CAS:<p>Aprotinin (Traskolan) is a broad-spectrum serine protease (BPTI) inhibitor. Aprotinin is an antifibrinolytic agent. Cost-effective and quality-assured.</p>Formula:C284H432N84O79S7Purezza:98%Colore e forma:SolidPeso molecolare:6511.51Anisindione
CAS:Anisindione, a synthetic indanedione, inhibits vitamin K, blocking factors II, VII, IX, X, and proteins C, S.Formula:C16H12O3Purezza:98.25%Colore e forma:Pale Yellow Crystals From Acetic Acid Or Ethanol SolidPeso molecolare:252.26Dolutegravir intermediate-1
CAS:Dolutegravir intermediate-1 is a synthetic precursor for HIV-1 treatment from patent WO 2016125192 A2.Formula:C13H17NO8Purezza:99.52%Colore e forma:SolidPeso molecolare:315.282-Oxiranecarboxylic acid, 3-[[[(1S)-3-methyl-1-[[(3-methylbutyl)amino]carbonyl]butyl]amino]carbonyl]-, ethyl ester, (2S,3S)-
CAS:Formula:C17H30N2O5Purezza:98%Colore e forma:SolidPeso molecolare:342.4305Sofosbuvir impurity G
CAS:Sofosbuvir impurity G is both a diastereomer of Sofosbuvir and an impurity of Sofosbuvir which is an inhibitor of HCV RNA replication.Formula:C22H29FN3O9PPurezza:98.04%Colore e forma:SolidPeso molecolare:529.45Levovirin
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:C8H12N4O5Purezza:99.81% - >99.99%Colore e forma:SolidPeso molecolare:244.20Ethylenediaminetetraacetic acid disodium salt dihydrate
CAS:Formula:C10H18N2Na2O10Purezza:97%Colore e forma:SolidPeso molecolare:372.2369LDN-27219
CAS:LDN-27219 is a potent hTGase inhibitor with IC50 of 0.6 uM.Formula:C20H16N4O2S2Purezza:99.01% - 99.38%Colore e forma:SolidPeso molecolare:408.51,10-Phenanthroline hydrate
CAS:Formula:C12H10N2OPurezza:98%Colore e forma:SolidPeso molecolare:198.2206CL-82198
CAS:<p>CL-82198, a selective MMP-13 inhibitor, serves as a pharmacological intervention to halt the progression of osteoarthritis (OA).</p>Formula:C17H22N2O3Purezza:95.91%Colore e forma:SolidPeso molecolare:302.373-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:C32H45N3O4SPurezza:98%Colore e forma:SolidPeso molecolare:567.7824Ref: IN-DA00BBLC
1g57,00€5g128,00€25g262,00€5mg30,00€100gPrezzo su richiesta10mg30,00€50mg30,00€100mg37,00€250mg44,00€(Rac)-Telinavir
CAS:<p>N1 compound with anti-HIV activity; contains dimethyl, phenyl, quinoline groups.</p>Formula:C33H44N6O5Purezza:99.30%Colore e forma:SolidPeso molecolare:604.74Benzoic acid, 4-[[6-[(aminoiminomethyl)amino]-1-oxohexyl]oxy]-, ethylester, monomethanesulfonate
CAS:Formula:C17H27N3O7SPurezza:98%Colore e forma:SolidPeso molecolare:417.4772Bestatin hydrochloride
CAS:Formula:C16H25ClN2O4Purezza:98%Colore e forma:SolidPeso molecolare:344.8337Ref: IN-DA003O5U
1g542,00€5gPrezzo su richiesta10mg61,00€25mg94,00€50mg148,00€100mg191,00€250mg197,00€500mg333,00€PF-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:C27H27N3O2Purezza:99.92%Colore e forma:SolidPeso molecolare:425.52NBD-556
CAS: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.Formula:C17H24ClN3O2Purezza:99.79%Colore e forma:SolidPeso molecolare:337.84L-Leucinamide, N-[(phenylmethoxy)carbonyl]-L-leucyl-N-[(1S)-1-formyl-3-methylbutyl]-
CAS:Formula:C26H41N3O5Purezza:98%Colore e forma:SolidPeso molecolare:475.6208Ref: IN-DA0072SK
1gPrezzo su richiesta5mg68,00€10mg90,00€25mg124,00€50mg168,00€100mg229,00€250mg500,00€Dabigatran 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:C34H41N7O5Purezza:98.19% - 99.98%Colore e forma:White PowderPeso molecolare: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:C7H11NO4SPurezza:99.91%Colore e forma:SolidPeso molecolare:205.23BAY-85-8501
CAS:BAY-85-8501 is a selective, reversible and potent inhibitor of Human Neutrophil Elastase (HNE; IC50 of 65 pM)Formula:C22H17F3N4O3SPurezza:99.16%Colore e forma:SolidPeso molecolare:474.46HCV-IN-29
CAS:<p>HCV-IN-29 is a hepatitis C virus (HCV) inhibitor.</p>Formula:C26H32Cl4N6Purezza:99.89%Colore e forma:SolidPeso molecolare:570.38Dabigatran ethyl ester hydrochloride
CAS:Dabigatran prevents blood clots, inhibiting NQO2 and thrombin with IC50 0.8 μM.Formula:C27H30ClN7O3Purezza:99.65%Colore e forma:SolidPeso molecolare:536.03GSK2838232
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:C48H73ClN2O6Purezza:97.97%Colore e forma:SolidPeso molecolare:809.56Ethylene glycol bis(2-aminoethyl ether)-N,N,N',N'-tetraacetic acid
CAS:Formula:C14H24N2O10Purezza:97%Colore e forma:SolidPeso molecolare:380.3478Ref: IN-DA0034HK
5gPrezzo su richiesta10g21,00€1kg124,00€25g25,00€50g25,00€5kg563,00€100g34,00€250g60,00€500g75,00€50kgPrezzo su richiesta(ETHYLENEDINITRILO)TETRAACETIC ACID, TRISODIUM SALT HYDRATE
CAS:Formula:C10H18N2NaO9Purezza:97%Colore e forma:SolidPeso molecolare:333.2477N-Tosyl-L-phenylalanine chloromethyl ketone
CAS:Formula:C17H18ClNO3SPurezza:97%Colore e forma:SolidPeso molecolare:351.8477Flanvotumab
CAS:Flanvotumab (IMC-20D7S) is a humanized antibody targeting TYRP1 with strong antitumor effects via NK cells and ADCC.Purezza:> 95%Colore e forma:LiquidPeso molecolare:145.42 kDaIslatravir
CAS:Islatravir (MK-8591) is an effective anti-HIV-1 agent.Formula:C12H12FN5O3Purezza:98.77%Colore e forma:SolidPeso molecolare:293.25Begelomab
CAS:Begelomab (SAND-26) is a mouse-derived monoclonal antibody targeting DPP-4/CD26. Begelomab can be used to study severe refractory inflammatory myopathies.Purezza:97.8% (SDS-PAGE); 98.3% (SEC-HPLC) - 97.8% (SDS-PAGE); 98.3% (SEC-HPLC)Colore e forma:LiquidAvoralstat
CAS:Avoralstat (BCX4161) is an oral plasma kallikrein (PKK) inhibitor. Which is used for the treatment of hereditary angioedema.Formula:C28H27N5O5Purezza:99.77%Colore e forma:SolidPeso molecolare:513.544-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:C7H5ClO3Purezza:98.59%Colore e forma:Off-White To Light Beige PowderPeso molecolare:172.57ML604440
CAS:ML604440 is a cell permeable proteasome β1i (LMP2) subunit inhibitor.Formula:C17H24BF3N2O4Purezza:97.06%Colore e forma:SolidPeso molecolare:388.19BLT-1
CAS:<p>BLT-1 is a scavenger receptor BI (SR-BI)inhibitor.</p>Formula:C12H23N3SPurezza:97.97%Colore e forma:SolidPeso molecolare:241.4Sofosbuvir 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:C34H45FN4O13P2Purezza:98.05%Colore e forma:SolidPeso molecolare:798.69Trelagliptin
CAS:Trelagliptin (SYR-472) is a highly specific and long-acting DPP-4 inhibitor.Formula:C18H20FN5O2Purezza:98.88%Colore e forma:SolidPeso molecolare:357.38MK-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).Formula:C12H16N4O4Purezza:98.48%Colore e forma:SolidPeso molecolare:280.28Fostemsavir Tris
CAS:Fostemsavir Tris (BMS-663068 Tris) is the prodrug of BMS-626529,is a oral, safe and effective inhibitor of HIV-1 attachment.Formula:C29H37N8O11PPurezza:99.45%Colore e forma:SolidPeso molecolare:704.62PMSF
CAS:PMSF (Phenylmethylsulfonyl fluoride) is an irreversible inhibitor of serine/cysteine protease , preparation of cell lysates. High-Quality, Low-Cost!Formula:C7H7FO2SPurezza:97.75% - 99.88%Colore e forma:White To Cream SolidPeso molecolare:174.19Carboxypeptidase C
CAS:Carboxypeptidase C removes COOH-terminal amino acids and others in peptides for biochemical studies.Colore e forma:SolidAc-[Nle4,D-Phe7]-α-MSH (4-10)-NH2
CAS:Ac-[Nle4,D-Phe7]-α-MSH (4-10)-NH2, a melanotropin derivative and melanocyte-stimulating hormone, activates tyrosinase and demonstrates a thermoregulatory effectFormula:C47H64N14O10Colore e forma:SolidPeso molecolare:985.1Chymotrypsinogen
CAS:Chymotrypsinogen is an inactive precursor of Chymotrypsin . Chymotrypsin is a serine protease produced by the pancreas [1] [2] .Colore e forma:SolidZG36
ZG36, a human Caseinolytic protease P (ClpP) agonist, non-selectively degrades respiratory chain complexes and reduces mitochondrial DNA, causing mitochondrialColore e forma:Odour SolidHCV-IN-4
CAS:HCV-IN-4: Potent, oral HCV NS5A inhibitor; effective vs GT1a/b, GT2b, GT3a, Y93H, L31V; EC90s: 3 pM-0.02 nM.Formula:C52H58FN9O8Purezza:98%Colore e forma:SolidPeso molecolare:956.07Suc-AAP-Abu-pNA
CAS:Suc-AAP-Abu-pNA is a specific substrate for pancreatic elastase (Km = 100 μM; Kcat/Km = 35,300 s-1 M-1 for rat pancreatic elastase; Km = 30 μM; Kcat/Km = 351,Formula:C25H34N6O9Colore e forma:SolidPeso molecolare:562.57SFTI-1
CAS:SFTI-1, a cyclic peptide trypsin inhibitor comprising 14 amino acid residues, is a potent Bowman-Birk inhibitor.Formula:C67H104N18O18S2Colore e forma:SolidPeso molecolare:1513.78AR-H067637
CAS: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.Formula:C21H21ClF2N4O4Colore e forma:SolidPeso molecolare:466.87PROTAC CG167
PROTAC CG167 is a potent and selective PROTAC degrader of CypA. It degrades CypA in a dose-dependent manner in Jurkat cells, with a DC50 of 123 nM. Additionally, PROTAC CG167 exhibits antiviral activity by inhibiting HIV-1 and HCV. (Pink: CypA Ligand; Black: Linker; Blue: E3LigaseLigand)Formula:C65H79N13O11SColore e forma:SolidPeso molecolare:1250.47Zetomipzomib maleate
CAS:Zetomipzomib maleate (KZR-616) selectively targets LMP7/2 in immunoproteasomes, potential for autoimmune research.Formula:C34H46N4O12Colore e forma:SolidPeso molecolare:702.758TP0597850
CAS: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].Formula:C41H57N9O13SColore e forma:SolidPeso molecolare:916.01PF 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:C25H20N2O3SPurezza:99.35%Colore e forma:SolidPeso molecolare:428.5N-CBZ-Phe-Arg-AMC
CAS:Z-FR-AMC substrate for serine proteases; cathepsins, kallikrein, plasmin. Substrate: 330/390 nm; Product: 342/441 nm.Formula:C33H36N6O6Purezza:98%Colore e forma:White To Off-White PowderPeso molecolare:612.68Lonodelestat TFA
<p>Lonodelestat TFA, an oral peptide, selectively inhibits hNE, potentially aiding in CF research.</p>Formula:C73H112F3N15O21Colore e forma:SolidPeso molecolare:1592.75Dansyl-Glu-Gly-Arg-Chloromethylketone
CAS:Dansyl-Glu-Gly-Arg-Chloromethylketone is a protease inhibitor that specifically impedes serine/threonine proteases and has been shown to inhibit activatedFormula:C26H36ClN7O7SColore e forma:SolidPeso molecolare:626.12CRA-2059 TFA
CRA-2059 is a highly specific and selective tryptase inhibitor, with a Ki of 620 pM for recombinant human tryptase-β (rHTβ)[1][2].Colore e forma:SolidSofosbuvir impurity J
CAS:Sofosbuvir impurity J is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity.Formula:C22H30FN4O8PPurezza:98%Colore e forma:SolidPeso molecolare:528.47Chetoseminudin B
CAS:Chetoseminudin B exhibits inhibitory activity against mushroom tyrosinase, with an IC 50 value of 31.7 μM [1].Formula:C17H21N3O3S2Colore e forma:SolidPeso molecolare:379.5DPP8/9-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>Colore e forma:Odour SolidAc-PAL-AMC
CAS:Ac-PAL-AMC is a β1i/LMP2-specific substrate that fluoresces when cleaved; useful for measuring immunoproteasome activity.Formula:C26H34N4O6Colore e forma:SolidPeso molecolare:498.57Cathepsin D and E FRET Substrate
CAS:Mca-GKPILFFRL-Dpa-r-amide, FRET substrate for cathepsin D and E. Also cleaved by napsin A.Formula:C85H122N22O19Colore e forma:SolidPeso molecolare:1756.046Roseltide rT1
CAS:Roseltide rT1 is a neutrophil elastase inhibitor (IC50=0.47 μM) and is rich in cysteine, classified as one of the Roseltides (rT1-rT8). It has the potential to inhibit related diseases by improving neutrophil elastase-stimulated cAMP accumulation in vitro.Formula:C110H177N31O31S6Colore e forma:SolidPeso molecolare:2622.16Histatin 5
CAS:Histatin 5, a human saliva peptide, blocks MMP-2 and MMP-9 at IC50s of 0.57/0.25 μM and kills fungi.Formula:C133H195N51O33Purezza:98%Colore e forma:SolidPeso molecolare:3036.29HIV-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:C14H10N4O4SPurezza:99.33%Colore e forma:SolidPeso molecolare:330.32Neutrophil elastase inhibitor 4
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.Formula:C20H21N3O5Colore e forma:SolidPeso molecolare:383.4BPHA
CAS: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.Formula:C21H20N2O4SPurezza:99.44%Colore e forma:SolidPeso molecolare:396.46Dnp-P-Cha-G-Cys(Me)-HA-K(Nma)-NH2
CAS: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).Formula:C49H68N14O12SColore e forma:SolidPeso molecolare:1077.22Talabostat
CAS:<p>Talabostat (PT100, Val-boroPro) is a potent, nonselective and orally available dipeptidyl peptidase IV (DPP-IV) inhibitor with a Ki of 0.18 nM.</p>Formula:C9H19BN2O3Colore e forma:SolidPeso molecolare:214.07PR 39 (porcine) acetate
PR 39 (porcine) acetate is a noncompetitive, reversible and allosteric proteasome inhibitor.Purezza:98%Colore e forma:LiquidPeso molecolare:N/ACepeginterferon alfa-2b
CAS:<p>Cepeginterferon alfa-2b: pegylated interferon with 20 kDa PEG for HCV, PV, ET research.</p>Colore e forma:LiquidADAM8-IN-1
CAS:<p>ADAM8-IN-1 is a potent ADAM8 inhibitor with an IC 50 value of 73 nM.</p>Formula:C44H44Br4N6O12S2Colore e forma:SolidPeso molecolare:1232.6MMP-3 Inhibitor
CAS: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.Formula:C27H46N10O9SPurezza:98.87%Colore e forma:SolidPeso molecolare:686.78HCVP-IN-1
CAS:HCVP-IN-1 (compound 1) is a hepatitis C viral polymerase (HCVP) inhibitor.Formula:C30H34FN5O3Colore e forma:SolidPeso molecolare:531.632Acetyl-Calpastatin(184-210)(human) TFA
Acetyl-Calpastatin(184-210)(human) TFA inhibits μ-calpain (Ki 0.2 nM) and cathepsin L (Ki 6 μM) selectively and reversibly.Formula:C144H231F3N36O46SColore e forma:SolidPeso molecolare:3291.65Tyrosinase-IN-38
Tyrosinase-IN-38 (compound 6b) is a competitive inhibitor of tyrosinase, demonstrating an IC50 of 25.82 μM and exhibits antioxidant activity.Colore e forma:Odour SolidCys-TAT(47-57) acetate(583836-55-9 Free base)
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.Formula:C69H128N34O16SPurezza:95.1100%Colore e forma:SolidPeso molecolare:1722.04Talabostat isomer mesylate
Talabostat isomer mesylate, a PT100/Val-boroPro variant, is a potent oral DPP-IV inhibitor (Ki: 0.18 nM).Formula:C10H23BN2O6SPurezza:98%Colore e forma:SolidPeso molecolare:310.18Sofigatran
CAS:Sofigatran (MCC-977) is an oral anticoagulant targeting thrombin for cardiovascular research.Formula:C24H44N4O4SColore e forma:SolidPeso molecolare:484.7Cathepsin D and E FRET Substrate acetate(839730-93-7 Free base)
Fluorogenic substrate for cathepsins D & E; cleaves at Phe-Phe bond; not for B, H, L. Useful for assays and studies.Colore e forma:Odour SolidTAPI1 acetate
TAPI1 acetate (TNF-α processing inhibitor-1) is a TACE (ADAM17) inhibitor that inhibits shedding of TNF-α cytokine receptors; MMP inhibitor .Formula:C28H41N5O7Purezza:98.82% - 99.94%Colore e forma:SolidPeso molecolare:559.65Sofosbuvir impurity A
CAS:Sofosbuvir impurity A is an diastereoisomer of Sofosbuvir. Sofosbuvir is anHCV RNA replication inhibitor ,with potent anti-hepatitis C virus activity.Formula:C22H29FN3O9PPurezza:98%Colore e forma:SolidPeso molecolare:529.45Fotagliptin
CAS:Fotagliptin is a dipeptidyl peptidase IV inhibitor.Formula:C17H19FN6OColore e forma:SolidPeso molecolare:342.37N-CBZ-Phe-Arg-AMC TFA
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.Formula:C35H37F3N6O8Purezza:99.88%Colore e forma:SolidPeso molecolare:726.7CRA-2059 hydrochloride
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].Colore e forma:Solid7-Methoxy obtusifolin
CAS:7-Methoxy obtusifolin (Compound 4) is a chemical compound that acts as a competitive inhibitor of the enzyme tyrosinase, displaying an inhibitory concentrationFormula:C17H14O6Colore e forma:SolidPeso molecolare:314.29(-)-Taxifolin
CAS:(-)-Taxifolin, less active enantiomer with anti-tyrosinase, collagenase inhibition (IC50 = 193.3 μM), antifibrotic, antioxidant properties.Formula:C15H12O7Colore e forma:SolidPeso molecolare:304.25Ellipyrone A
Ellipyrone A: γ-pyrone macrocycle, inhibits DPP-4 (IC50=0.35mM), α-glucosidase (IC50=0.74mM), α-amylase (IC50=0.59mM).Formula:C25H34O8Colore e forma:SolidPeso molecolare:462.53Leptosin D
CAS:Leptosin D, a thiodiketopiperazine alkaloid derived from mushrooms, effectively inhibits tyrosinase activity, demonstrating an inhibition concentration (IC50)Formula:C25H24N4O3S2Colore e forma:SolidPeso molecolare:492.61Phaeosphaone D
CAS:Phaeosphaone D, a thiodiketopiperazine from Phaeosphaeria fuckelii fungus, inhibits mushroom tyrosinase (IC50 = 33.2 μM).Formula:C20H27N3O3S2Colore e forma:SolidPeso molecolare:421.58midesteine
CAS:Midesteine (MR-889) is a small molecule neutrophil elastase inhibitor used in the treatment of bronchitis, asthma and chronic lung disease.Formula:C12H13NO3S3Purezza:99.87% - 99.98%Colore e forma:SolidPeso molecolare:315.43Enzyme-IN-1
CAS: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。Formula:C36H50N4O7Colore e forma:SolidPeso molecolare:650.8Sadopeptins B
Sadopeptins B, a natural product isolated from Streptomyces sp., is a potent proteasome inhibitor [1].Formula:C48H69N9O13SColore e forma:SolidPeso molecolare:1012.18NS5A-IN-1
NS5A-IN-1 is a proagent of the HCV NS5A inhibitor Pibrentasvir (ABT-530).Formula:C72H86F5N10O14PColore e forma:SolidPeso molecolare:1441.48Sulodexide
CAS:Sulodexide is an orally administered combination of glycosaminoglycans, consisting of low molecular weight heparin (80%) and dermatan sulfate (20%). It demonstrates antithrombotic properties by interacting with antithrombin III (AT III) and heparin cofactor II (HC II), and by inhibiting thrombin formation. Additionally, sulodexide enhances profibrinolytic activity by releasing tissue plasminogen activator (tPA). It also offers endothelial protection, possesses anti-inflammatory effects, and alleviates chronic venous disease.Colore e forma:SolidTilpisertib fosmecarbil TFA
CAS:Tilpisertib fosmecarbil TFA, the TFA salt form of Tilpisertib, acts as an inhibitor of serine/threonine kinases. This compound also exhibits anti-inflammatory activity.Formula:C37H37ClF3N8O9PColore e forma:SolidPeso molecolare:861.16VPLSLYSG
CAS:<p>VPLSLYSG, an octapeptide, degraded by MMP-9, MMP-1, MMP-2; potential MMP substrate uses.</p>Formula:C39H62N8O12Colore e forma:SolidPeso molecolare:834.96Tyrosinase/elastase-IN-1
Tyrosinase/elastase-IN-1, a triterpenoid extracted from the leaves of Rubus fraxinifolius, exhibits inhibitory activities against both tyrosinase and elastaseFormula:C33H52O5Colore e forma:SolidPeso molecolare:528.76Leptosphaerodione
CAS:Leptosphaerodione from Remotididymella sp.: a potent UPS inhibitor with 3.2 μM IC50 in HeLa cells; anti-tumor.Formula:C21H22O5Colore e forma:SolidPeso molecolare:354.4Bictegravir Sodium
CAS:Bictegravir Sodium is an HIV-1 integrase inhibitor with 7.5 nM IC50, offering strong, selective anti-HIV effects and minimal toxicity.Formula:C21H17F3N3NaO5Purezza:99.97%Colore e forma:SolidPeso molecolare:471.36α 1(I) Collagen (614-639), human
CAS:This is a peptide inhibitor of collagen fibrillar matrix assembly.Formula:C134H189N37O39Purezza:98%Colore e forma:SolidPeso molecolare:2942.16Alisporivir
CAS:Alisporivir (Debio-025) is a cyclophilin A inhibitor that disrupts the interaction between CypA and NS5A. HCV activity in vivo and in vitro.Formula:C63H113N11O12Purezza:99.95%Colore e forma:SolidPeso molecolare:1216.64RJS308
<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:C63H75N13O11SColore e forma:SolidPeso molecolare:1222.42FFAGLDD TFA
<p>FFAGLDD TFA: MMP9 peptide for controlled DOX delivery to cytoplasm.</p>Formula:C39H50F3N7O14Purezza:98%Colore e forma:SolidPeso molecolare:897.85Cathepsin C-IN-6
Cathepsin C-IN-6 (compound 2), an E-64c-hydrazideas-derived inhibitor of cathepsin C, possesses anti-inflammatory properties and impedes neutrophil elastaseFormula:C24H35N5O4·xC2HF3O2Colore e forma:SolidNitidanin
<p>Nitidanin is a useful organic compound for research related to life sciences and the catalog number is T125599.</p>Formula:C21H24O8Colore e forma:SolidPeso molecolare:404.415NS5A-IN-4
CAS: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.Formula:C47H48N8O6Colore e forma:SolidPeso molecolare:820.93C-telopeptide
CAS:C-telopeptide from type I collagen is released during bone resorption; it correlates with bone mineral density.Formula:C34H56N14O13Purezza:98%Colore e forma:SolidPeso molecolare:868.9Ac-DEMEEC-OH
CAS:Ac-DEMEEC-OH is a competitive inhibitor of the HCV NS3 protease with a Ki of 0.6 µM.Formula:C29H44N6O16S2Colore e forma:SolidPeso molecolare:796.82Dutogliptin tartrate
CAS:Dutogliptin tartrate is an effective and selective oral dipeptide-peptide-4 (DPP4) inhibitor for the treatment of type 2 diabetes mellitus.Formula:C14H26BN3O9Purezza:98%Colore e forma:SolidPeso molecolare:391.18Sofosbuvir impurity M
CAS:Sofosbuvir impurity M is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity.Formula:C22H30N3O10PPurezza:98%Colore e forma:SolidPeso molecolare:527.467CL 82198 hydrochloride
CAS:CL 82198 hydrochloride selectively inhibits MMP-13, not MMP-1/9/TACE, and blocks HP75 invasion and neurotoxicity in zebrafish.Formula:C17H23ClN2O3Colore e forma:SolidPeso molecolare:338.83Histargin
CAS:<p>Histargin is an enzyme inhibitor separated from Streptomyces roseoviridis.</p>Formula:C14H25N7O4Colore e forma:SolidPeso molecolare:355.39Recombinant Proteinase K
Recombinant Proteinase K: serine protease, cleaves carboxy-terminus peptides, digests proteins, purifies nucleic acids.Colore e forma:SolidDutogliptin
CAS:Dutogliptin (PHX-1149 free base) is an oral, effective and selective dipeptide-peptide-4 (DPP4) inhibitor for the treatment of type 2 diabetes mellitus.Formula:C10H20BN3O3Purezza:98%Colore e forma:SolidPeso molecolare:241.10AL-611
CAS:<p>AL-611 is an HCV NS5B polymerase inhibitor ( EC 50 = 5 nM).</p>Formula:C25H33F2N6O8PColore e forma:SolidPeso molecolare:614.544GSK2336805
CAS:<p>GSK-2336805, an HCV NS5A inhibitor, is effective against genotypes 1, 4, 5, and some of 6.</p>Formula:C42H52N8O8Colore e forma:SolidPeso molecolare:796.91Peptide 74
CAS:Peptide 74 is a synthetic peptide. It also inhibits the activated form of this enzyme.Formula:C62H107N23O20S2Purezza:98%Colore e forma:SolidPeso molecolare:1558.79APC-6860
CAS:APC-6860, a serine protease inhibitor, targets multiple enzymes; most potent against human urokinase (Ki: 0.1 µM). Used in cancer research.Formula:C9H7IN2SColore e forma:SolidPeso molecolare:302.13Histatin 5 (TFA)(115966-68-2,free)
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 μMFormula:C135H196F3N51O35Purezza:98%Colore e forma:SolidPeso molecolare:3150.32Tyrosinase-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:C15H19NO3Colore e forma:SolidPeso molecolare:261.32Acetyl-Calpastatin(184-210)(human)
CAS:Calpain inhibitor, Ki 0.2 nM for calpain I/II, doesn't affect papain/trypsin/cat L. Raises Aβ42, Aβ40 secretion & Aβ42/Aβ40 ratio.Formula:C142H230N36O44SPurezza:98%Colore e forma:SolidPeso molecolare:3177.65AP-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:C18H16N4SPurezza:99.87%Colore e forma:SoildPeso molecolare:320.41Obtusifolin-2-O-glucoside
CAS:Obtusifolin-2-O-glucoside (compound 7), a tyrosinase inhibitor with an IC50 value of 9.2 μM, can be isolated from cassia seed [1].Formula:C22H22O10Colore e forma:SolidPeso molecolare:446.4PS 915
CAS:PS 915 is a substrate for colorimetric assay. It was used for plasma antithrombin.Formula:C27H36ClN7O6Purezza:98%Colore e forma:SolidPeso molecolare:590.08NVP-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:C15H20Cl2N6OColore e forma:SolidPeso molecolare:371.27Pseudostellarin G
CAS:<p>Pseudostellarin G, a naturally occurring cyclo-octapeptide, exhibits inhibitory activity against tyrosinase and suppresses melanin production.</p>Formula:C42H56N8O9Colore e forma:SolidPeso molecolare:816.94KKI-5
CAS:<p>KKI 5: Serine protease inhibitor, blocks kallikrein & plasmin, potential for cancer therapy & angioedema treatment.</p>Formula:C35H55N11O9Purezza:98%Colore e forma:SolidPeso molecolare:773.88Radalbuvir
CAS:Radalbuvir (GS-9669) is an investigational antiviral agent for the treatment of hepatitis C virus (HCV) infection as an NS5B inhibitor.Formula:C30H41NO6SColore e forma:SolidPeso molecolare:543.716-Acetylnimbandiol
CAS:6-Acetylnimbandiol, a non-toxic agent, inhibits tyrosinase (IC50=69.85 μM), melanin, and MITF; useful in melanoma studies.Formula:C28H34O8Colore e forma:SolidPeso molecolare:498.56Nostosin G
Nostosin G, a linear peptide with Hpla, Hty, and argininal, inhibits trypsin effectively (IC50 = 0.1 μM).Formula:C25H33N5O6Colore e forma:SolidPeso molecolare:499.56GCPII-IN-1
CAS:<p>GCPII-IN-1, a potent PSMA inhibitor, binds with 44.3 nM affinity.</p>Formula:C12H21N3O7Colore e forma:SolidPeso molecolare:319.314Stevia Powder
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.Colore e forma:Odour SolidBMS-767778
CAS:BMS-767778, a DPP-4 inhibitor, is used potentially for the treatment of type 2 diabetes.Formula:C19H20Cl2N4O2Colore e forma:SolidPeso molecolare:407.29Sofosbuvir impurity H
Sofosbuvir impurity H, an diastereoisomer of Sofosbuvir, is the impurity of Sofosbuvir.Formula:C29H33FN3O10PPurezza:98%Colore e forma:SolidPeso molecolare:633.56Plasma kallikrein-IN-1
CAS:Plasma kallikrein-IN-1 is a PKK inhibitor with an IC 50 value of 0.5 nM.Formula:C23H25F2N7OColore e forma:SolidPeso molecolare:453.498RXP470
CAS:RXP470 is a potent and selective MMP-12 inhibitor (Ki 0.24 nM).Formula:C35H35BrClN4O10PColore e forma:SolidPeso molecolare:818Rivulariapeptolides 1155
Rivulariapeptolides 1155 inhibits chymotrypsin (41.84 nM), elastase (4.94 nM), and proteinase K (56.54 nM).Formula:C59H81N9O15Colore e forma:SolidPeso molecolare:1156.33Befovacimab
CAS:<p>Befovacimab, a human IgG2 antibody, targets TFPI for hemophilia A/B research.</p>Colore e forma:LiquidTMC647055 Choline salt
TMC647055 choline salt is a selective and cell-permeating inhibitor of HCV NS5B (IC50: 34 nM).Formula:C37H53N5O8SPurezza:98%Colore e forma:SolidPeso molecolare:727.91MMP-9/MMP-13 Inhibitor I
CAS:MMP-9/MMP-13 Inhibitor I is a dual inhibitor of MMP-9 and MMP-13 with IC50 of both 0.9 nM.Formula:C25H25N3O6SColore e forma:SolidPeso molecolare:495.55Rivulariapeptolides 1121
Rivulariapeptolides 1121 inhibits serine proteases: chymotrypsin (IC50=35.52 nM), elastase (13.24 nM), proteinase K (48.05 nM).Formula:C56H83N9O15Colore e forma:SolidPeso molecolare:1122.31Linagliptin Methyldimer
CAS:<p>Linagliptin Methyldimer is a potent dipeptidyl peptidase IV inhibitor, IC50=6 pM.</p>Formula:C50H56N16O4Purezza:97.23%Colore e forma:SolidPeso molecolare:945.08BAY 1217224
CAS:<p>BAY 1217224 is a neutral, non-prodrug Thrombin inhibitor with good oral pharmacokinetics.</p>Formula:C24H27ClFN3O5Colore e forma:SolidPeso molecolare:491.94PSI-7409
CAS:<p>PSI-7409 is the active 5'-triphosphate metabolite of Sofosbuvir (PSI-7977).</p>Formula:C10H16FN2O14P3Purezza:98%Colore e forma:SolidPeso molecolare:500.16JC-10
CAS:JC-10 is a potent inhibitor of metalloproteinases and is often used as a probe.Formula:C25H29Cl2IN4Purezza:95%Colore e forma:SolidPeso molecolare:583.34α 1 Antichymotrypsin, Human Plasma
CAS: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.Colore e forma:SolidMK-6169
CAS:MK-6169 is an effective Pan-Genotype Hepatitis C Virus NS5A inhibitor. It also has Optimized Activity against Common Resistance-Associated Substitutions.Formula:C54H62FN9O8SPurezza:98%Colore e forma:SolidPeso molecolare:1016.2Cathepsin K inhibitor 7
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.Colore e forma:Odour SolidNIM811
CAS:NIM811 is an orally bioavailable dual inhibitor of mitochondrial permeability transition and cyclophilin.Formula:C62H111N11O12Purezza:98%Colore e forma:SolidPeso molecolare:1202.635
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