Proteases/Proteassoma
Os inibidores de proteases e proteassomas são compostos que bloqueiam a atividade das proteases e do proteassoma, que estão envolvidos na degradação e renovação de proteínas. Esses inibidores são vitais para estudar a regulação da homeostase de proteínas, controle do ciclo celular e apoptose. Inibidores de proteases e proteassomas também são utilizados no tratamento de doenças como o câncer, onde a degradação anormal de proteínas desempenha um papel na progressão da doença. Ao inibir proteases ou o proteassoma, esses compostos podem induzir a morte celular em células cancerígenas e são ferramentas essenciais tanto na pesquisa básica quanto no desenvolvimento terapêutico. Na CymitQuimica, oferecemos uma ampla gama de inibidores de proteases e proteassomas de alta qualidade para apoiar sua pesquisa em bioquímica, biologia celular e desenvolvimento de medicamentos.
Subcategorias de "Proteases/Proteassoma"
- Acetil- CoA Carboxilase(34 produtos)
- Cisteína Protease(96 produtos)
- DPP-4(20 produtos)
- Glutaminase(40 produtos)
- HIV Protease(449 produtos)
- PAI-1(25 produtos)
- Inibidores de Protease(50 produtos)
- Receptor activado por protease(53 produtos)
- Proteassoma(94 produtos)
- Protease serina(50 produtos)
- p97(14 produtos)
Exibir 3 mais subcategorias
Foram encontrados 1044 produtos de "Proteases/Proteassoma"
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H-Pro-Lys-OH TFA
<p>H-Pro-Lys-OH TFA is a dipeptide composed of proline and lysine, serving as a substrate for imino dipeptidase (prolinase). Additionally, it can be utilized in peptide synthesis.</p>Fórmula:C13H22F3N3O5Cor e Forma:SolidPeso molecular:357.332'-β-C-Ethynyladenosine
CAS:<p>2'-β-C-Ethynyladenosine is a nucleoside analog that potently inhibits hepatitis C virus (HCV) replication by targeting the viral NS5B polymerase.</p>Fórmula:C12H13N5O4Cor e Forma:SolidPeso molecular:291.26Teneligliptin hydrobromide hydrate
CAS:<p>Teneligliptin hydrobromide hydrate: potent, long-lasting DPP-4 inhibitor with ~1 nM IC50.</p>Fórmula:C22H33BrN6O2SCor e Forma:SolidPeso molecular:525.51Sivelestat Sodium Tetrahydrate
CAS:Fórmula:C20H21N2NaO7S·4H2OPureza:>95.0%(T)(HPLC)Cor e Forma:White to Light yellow powder to crystalPeso molecular:528.50MMP-8 Inhibitor I
CAS:<p>MMP-8 Inhibitor I is a selective inhibitor of the neutrophil collagenase matrix metalloproteinase-8 (MMP-8) with an IC50 value of 4 nM.</p>Fórmula:C17H18N2O5SCor e Forma:SolidPeso molecular:362.4PKSI-527
CAS:<p>PKSI-527 inhibits plasma kallikrein (Ki=0.81μM), selective vs. glandular kallikrein/thrombin/urokinase/Xa, reduces bradykinin, affects clotting times.</p>Fórmula:C25H32ClN3O4Cor e Forma:SolidPeso molecular:473.99PSI-6206 13C,d3
CAS:<p>PSI-6206 13CD3 is the deuterium labeled PSI-6206. PSI-6206 is a potent and selective HCV NS5B polymerase inhibitor.</p>Fórmula:C10H13FN2O5Pureza:98%Cor e Forma:SolidPeso molecular:264.23NQ301
CAS:<p>NQ301, an antithrombotic agent, inhibits collagen-challenged rabbit platelet aggregation (IC50: 10 mg/mL).</p>Fórmula:C18H12ClNO3Pureza:99.74% - 99.76%Cor e Forma:SolidPeso molecular:325.754-Phenoxybenzylamine
CAS:<p>4-Phenoxybenzylamine inhibits the function of the NS3 protein by stabilizing an inactive conformation with an IC50 of about 500 μM against HCV NS3/4a .</p>Fórmula:C13H13NOPureza:97.26%Cor e Forma:SolidPeso molecular:199.25MMP-9-IN-1
CAS:<p>MMP-9-IN-1 is an inhibitor of specific matrix metalloproteinase-9 (MMP-9).</p>Fórmula:C16H17F2N3O3SPureza:99.21% - 99.86%Cor e Forma:SolidPeso molecular:369.39Coblopasvir dihydrochloride
CAS:<p>Coblopasvir dihydrochloride can be used to study chronic HCV infection and is a pan-genotypic nonstructural protein 5A (NS5A) inhibitor.</p>Fórmula:C41H52Cl2N8O8Pureza:99.33%Cor e Forma:SolidPeso molecular:855.81Dolutegravir
CAS:<p>Dolutegravir (GSK1349572), HIV integrase inhibitor with IC50 of 2.7 nM, partly effective against some raltegravir-resistant HIV strains.</p>Fórmula:C20H19F2N3O5Pureza:98.97% - 99.75%Cor e Forma:White To Pale Yellow SolidPeso molecular:419.38Raltegravir potassium
CAS:<p>Raltegravir potassium (MK 0518 potassium salt) salt(MK0518 potassium salt) is a potent integrase (IN) inhibitor, used to treat HIV infection.</p>Fórmula:C20H20FN6O5·KPureza:98% - 99.55%Cor e Forma:Off-White SolidPeso molecular:482.51MUN57694
CAS:<p>MUN57694 is an inhibitor of 26S proteasome.</p>Fórmula:C23H25N3O4Pureza:99%Cor e Forma:SolidPeso molecular:407.46Balicatib
CAS:<p>Balicatib (AAE581) is a potent and selective inhibitor of cathepsin K, used in trials studying the treatment of osteoporosis.</p>Fórmula:C23H33N5O2Pureza:97.78% - 98.17%Cor e Forma:White To Off-White Solid PowderPeso molecular:411.54Temsavir
CAS:<p>Temsavir (BMS626529) is a novel attachment inhibitor that targets HIV-1 gp120 and prevents its binding to CD4+ T cells.</p>Fórmula:C24H23N7O4Pureza:99.14%Cor e Forma:SolidPeso molecular:473.48PSI-6206
CAS:<p>PSI-6206 (RO 2433) (RO2433) is a selective HCV RNA polymerase inhibitor.</p>Fórmula:C10H13FN2O5Pureza:98% - 99.79%Cor e Forma:SolidPeso molecular:260.22Marimastat
CAS:<p>Marimastat (BB2516) (BB-2516) is a potent, broad spectrum matrix metalloprotease (MMP) inhibitor.</p>Fórmula:C15H29N3O5Pureza:97.46% - 98.11%Cor e Forma:SolidPeso molecular:331.41HZ-1157
CAS:<p>HZ-1157 (DHFR-inhibitor) is a hepatitis C virus (HCV) inhibitor with inhibitory activities toward HCV NS3/4A protease.</p>Fórmula:C12H16N4OPureza:98.23%Cor e Forma:SolidPeso molecular:232.28Dabigatran Etexilate Mesylate
CAS:<p>Dabigatran Etexilate Mesylate (BIBR 1048MS) is the orally active prodrug of dabigatran. Dabigatran is a reversible and selective, direct thrombin inhibitor.</p>Fórmula:C34H41N7O5·CH4O3SPureza:99.91%Cor e Forma:SolidPeso molecular:723.84Fostemsavir
CAS:<p>Fostemsavir (BMS-663068) is an HIV-1 attachment inhibitor in development for the treatment of HIV-1 infection.</p>Fórmula:C25H26N7O8PPureza:98.95%Cor e Forma:SolidPeso molecular:583.49Saxagliptin
CAS:<p>Saxagliptin (BMS-477118) is a selective and reversible DPP4 inhibitor with IC50 of 26 nM.</p>Fórmula:C18H25N3O2Pureza:99.17% - 99.95%Cor e Forma:SolidPeso molecular:315.41Alloxan monohydrate
CAS:<p>Alloxan Monohydrate is a glucose analog used to induce diabetes by destroying beta-cells.</p>Fórmula:C4H4N2O5Pureza:99.01% - 99.42%Cor e Forma:Off-White To Beige-Yellowish Crystalline PowderPeso molecular:160.09Z-IETD-FMK
CAS:<p>Z-IETD-FMK (Z-IE(OMe)TD(OMe)-FMK) is a selective caspase 8 inhibitor, which has cell permeable.</p>Fórmula:C30H43FN4O11Pureza:95% - 99.81%Cor e Forma:SolidPeso molecular:654.68lavendustin B
CAS:<p>Lavendustin B inhibits Tyrosine Kinase and HIV-1 integrase-LEDGF/p75 interaction.</p>Fórmula:C21H19NO5Pureza:95.72%Cor e Forma:Off-White SolidPeso molecular:365.38E-64
CAS:<p>E-64 (Proteinase inhibitor E 64) is an irreversible and specific cysteine protease inhibitor. The IC50 of E-64 for papain is 9 nM.</p>Fórmula:C15H27N5O5Pureza:98% - 99.95%Cor e Forma:White SolidPeso molecular:357.41T-26c
CAS:<p>T-26c is highly potent and selective matrix metalloproteinase-13 (MMP-13) inhibitor (IC50: 6.75 pM).</p>Fórmula:C24H21N3O6SPureza:>99.99%Cor e Forma:SolidPeso molecular:479.51NM107
CAS:<p>NM107, a ribonucleoside, inhibits HCV NS5B polymerase. It has broad antiviral properties with EC50 of 1.85 μM in wild-type cells.</p>Fórmula:C10H15N3O5Pureza:97.85%Cor e Forma:White To Off-White PowderPeso molecular:257.24L-006235
CAS:L-006235 is a potent and reversible inhibitor of cathepsin K with IC50 of 0.25 nM.Fórmula:C24H30N6O2SPureza:99.37%Cor e Forma:SolidPeso molecular:466.6Tegobuvir
CAS:<p>Tegobuvir (GS 333126) is a specific and covalent HCV NS5B polymerase inhibitor.</p>Fórmula:C25H14F7N5Pureza:99.21%Cor e Forma:SolidPeso molecular:517.47-Amino-4-methylcoumarin-3-acetic acid
CAS:<p>7-Amino-4-methylcoumarin-3-acetic acid (7-Amino-4-methylcoumarin) is more suitable as a substrate for enteropeptidase than GD(4)K-NA.</p>Fórmula:C12H11NO4Pureza:98.38%Cor e Forma:SolidPeso molecular:233.22Ivachtin
CAS:<p>Ivachtin (Caspase-3 Inhibitor VII) is a nonpeptide, noncompetitive and reversibl caspase-3 inhibitor(IC50 = 23 nM) and is a modest inhibitor of the remaining</p>Fórmula:C20H21N3O7SPureza:99.74%Cor e Forma:SolidPeso molecular:447.46Delavirdine mesylate
CAS:<p>Delavirdine mesylate (BHAP-U 90152 (mesylate)) is a non-nucleoside reverse transcriptase inhibitor (NNRTI).</p>Fórmula:C23H32N6O6S2Pureza:99.99%Cor e Forma:Light Brown SolidPeso molecular:552.67Coblopasvir
CAS:<p>Coblopasvir is a pan-genotypic non-structural protein 5A (NS5A) inhibitor. It can be used to study chronic hepatitis C virus infection.</p>Fórmula:C41H50N8O8Pureza:99.33%Cor e Forma:SolidPeso molecular:782.88Rolipram
CAS:<p>Rolipram (SB 95952) is a phosphodiesterase 4 inhibitor with antidepressant properties.</p>Fórmula:C16H21NO3Pureza:99.22% - >99.99%Cor e Forma:SolidPeso molecular:275.342-(2-bromophenyl)-5-chloro-4H-3,1-benzoxazin-4-one
CAS:<p>2-(2-bromophenyl)-5-chloro-4H-3,1-benzoxazin-4-one is an human neutrophil elastase inhibitor.</p>Fórmula:C14H7BrClNO2Pureza:97.36%Cor e Forma:SolidPeso molecular:336.57Ombitasvir
CAS:<p>Ombitasvir (ABT-267) inhibits HCV protein NS5A, effective orally, EC50: 0.82-19.3 pM (genotypes 1-5), 366 pM (genotype 6a).</p>Fórmula:C50H67N7O8Pureza:97.27% - 99.56%Cor e Forma:SolidPeso molecular:894.11RO8191
CAS:<p>RO8191 (CDM-3008) (CDM-3008) is an agonist of interferon (IFN) receptor.</p>Fórmula:C14H5F6N5OPureza:98% - 98.85%Cor e Forma:SolidPeso molecular:373.21Clemizole
CAS:<p>Clemizole is an H1 histamine receptor antagonist, can inhibit NS4B's RNA binding and hepatitis C virus (HCV) replication.</p>Fórmula:C19H20ClN3Pureza:98% - 99.65%Cor e Forma:SolidPeso molecular:325.84ONX-0914
CAS:<p>ONX-0914 (PR-957) is an effective and specific immunoproteasome inhibitor, which has minimal cross-reactivity for the constitutive proteasome.</p>Fórmula:C31H40N4O7Pureza:98.24% - 99.31%Cor e Forma:SolidPeso molecular:580.67Elbasvir
CAS:<p>Elbasvir (MK-8742) is an NS5A inhibitor developed for chronic HCV treatment.</p>Fórmula:C49H55N9O7Pureza:98.95% - 99.85%Cor e Forma:SolidPeso molecular:882.02Odanacatib
CAS:<p>Odanacatib is an inhibitor of cathepsin K with potential anti-osteoporotic activity.</p>Fórmula:C25H27F4N3O3SPureza:98.53% - 99.53%Cor e Forma:SolidPeso molecular:525.56XMD16-5
CAS:<p>XMD16-5 blocks TNK2, linked to advanced lung/prostate cancers and breast cancer metastasis in mice; disrupts signaling in several tumors.</p>Fórmula:C23H24N6O2Pureza:98.89% - 99.98%Cor e Forma:SolidPeso molecular:416.48BMS-707035
CAS:<p>BMS-707035 is a specific HIV-I integrase (IN) inhibitor with IC50 of 15 nM. Phase 2.</p>Fórmula:C17H19FN4O5SPureza:99.78%Cor e Forma:SolidPeso molecular:410.42XMD8-87
CAS:<p>XMD8-87 (ACK1-B19), a TNK2 inhibitor, strongly blocks TNK2 phosphorylation and mutations in tumors.</p>Fórmula:C24H27N7O2Pureza:98.05% - 99.89%Cor e Forma:SolidPeso molecular:445.52Darunavir
CAS:<p>Darunavir (TMC114) is an HIV PROTEASE INHIBITOR that is used in the treatment of AIDS and HIV INFECTIONS.</p>Fórmula:C27H37N3O7SPureza:99.67% - 99.76%Cor e Forma:White Amorphous SolidPeso molecular:547.66Etravirine
CAS:<p>Etravirine (R165335) is a diarylpyrimidine non-nucleoside reverse transcriptase inhibitor.</p>Fórmula:C20H15BrN6OPureza:97.61% - 99.74%Cor e Forma:White To Off-White SolidPeso molecular:435.28Lusutrombopag
CAS:<p>Lusutrombopag (Mulpleta) is an orally bioavailable, small molecule thrombopoietin (TPO) receptor agonist for chronic liver disease (CLD) patients with</p>Fórmula:C29H32Cl2N2O5SPureza:99.96%Cor e Forma:SolidPeso molecular:591.55Bemnifosbuvir hemisulfate
CAS:<p>Bemnifosbuvir hemisulfate (AT-527) is a potent inhibitor of HCV virus replication.</p>Fórmula:C48H68F2N14O18P2SPureza:99.98%Cor e Forma:SolidPeso molecular:1261.15Ximelagatran
CAS:<p>Ximelagatran, oral direct thrombin inhibitor, transforms to active melagatran in body.</p>Fórmula:C24H35N5O5Pureza:95.48% - 99.60%Cor e Forma:SolidPeso molecular:473.572-CHLOROMETHYL-1,1-DIOXO-1,2-DIHYDRO-1λ*6*-BENZO[D]ISOTHIAZOL-3-ONE
CAS:<p>2-CHLOROMETHYL-1,1-DIOXO-1,2-DIHYDRO-1LAMBDA*6*-BENZO[D]ISOTHIAZOL-3-ONE targets the Neutrophil elastase (human).</p>Fórmula:C8H6ClNO3SPureza:97.28%Cor e Forma:SolidPeso molecular:231.66Raltegravir
CAS:<p>Raltegravir (MK-0518) is a pyrrolidinone derivative and HIV INTEGRASE INHIBITOR that is used in combination with other ANTI-HIV AGENTS for the treatment of HIV</p>Fórmula:C20H21FN6O5Pureza:99.86% - >99.99%Cor e Forma:SolidPeso molecular:444.42SB-734117
CAS:<p>SB-734117 inhibits productive replication of several HCMV strains.</p>Fórmula:C14H16N6OPureza:99.72%Cor e Forma:SolidPeso molecular:284.32MDL-28170
CAS:<p>MDL-28170 (Calpain Inhibitor III) is a Cysteine protease.</p>Fórmula:C22H26N2O4Pureza:95.06%Cor e Forma:SolidPeso molecular:382.45Ledipasvir hydrochloride
CAS:<p>Ledipasvir hydrochloride, a hepatitis C NS5A inhibitor, has EC50 of 34 pM (1a) and 4 pM (1b), also inhibits SARS-CoV 3CL pro (IC50 1.62 µM).</p>Fórmula:C49H55ClF2N8O6Cor e Forma:SolidPeso molecular:925.46UAMC00039 dihydrochloride
CAS:<p>UAMC00039 dihydrochloride is a potent, reversible and competitive dipeptidyl peptidase II inhibitor with an IC50 of 0.48 nM.</p>Fórmula:C16H26Cl3N3OPureza:>99.99%Cor e Forma:SolidPeso molecular:382.76AF 399
CAS:<p>AF 399 is a CCR4 antagonist. It reverses the tumor-promoting environment.</p>Fórmula:C12H17N3O3SPureza:99.83%Cor e Forma:SolidPeso molecular:283.35(S,S)-TAPI-1
CAS:<p>"(S,S)-TAPI-1, an isomer of TAPI-1, inhibits MMPs and TACE (ADAM17), reducing cell surface protein shedding."</p>Fórmula:C26H37N5O5Cor e Forma:SolidPeso molecular:499.6Efegatran
CAS:<p>Efegatran is a hematologic agent and platelet aggregation inhibitor.</p>Fórmula:C21H32N6O3Cor e Forma:SolidPeso molecular:416.522-Cyanopyrimidine
CAS:<p>2-Cyanopyrimidine (m-Hydroxyphenylpropionic acid) is inhibitor of cathepsin K(IC50 : 170 nM)</p>Fórmula:C5H3N3Pureza:99.27%Cor e Forma:Crystalline SolidPeso molecular:105.1GW280264X
CAS:<p>GW280264X (Carbamic acid) is an inhibitor of ADAM17 .</p>Fórmula:C28H41N5O6SPureza:99.51%Cor e Forma:SolidPeso molecular:575.72Proteasome inhibitor IX
CAS:<p>Proteasome inhibitor IX (PS-IX) is an inhibitor of chymotrypsin-like activity of the 20S proteasome (IC50 ~1 μM).</p>Fórmula:C20H21B2NO5Pureza:99.77%Cor e Forma:SolidPeso molecular:377.01Grazoprevir hydrate
CAS:<p>Grazoprevir: Hepatitis C protease inhibitor effective against various genotypes, including drug-resistant strains.</p>Fórmula:C38H52N6O10SPureza:98%Cor e Forma:SolidPeso molecular:784.92FT011
CAS:<p>FT011, a direct anti-fibrotic agent,attenuates cardiac remodelling and dysfunction in experimental diabetic cardiomyopathy.</p>Fórmula:C20H17NO5Pureza:98.98%Cor e Forma:SolidPeso molecular:351.35PythiDC
CAS:<p>PythiDC is a selective collagen prolyl 4-hydroxylase inhibitor, neither causing general toxicity nor disrupting iron homeostasis.</p>Fórmula:C10H6N2O4SPureza:98.13%Cor e Forma:SolidPeso molecular:250.23VCH-916 free acid(1200133-34-1 free base)
CAS:<p>VCH-916 is a novel nonnucleoside HCV NS5B polymerase inhibitor.</p>Fórmula:C26H37NO4SPureza:98.45%Cor e Forma:SolidPeso molecular:459.64Histatin 5 acetate
<p>Histatin 5 acetate inhibits the activity of the host matrix metalloproteinases MMP-2 and MMP-9 with IC50s of 0.57 and 0.25 μM, respectively.</p>Fórmula:C135H199N51O35Pureza:98.72%Cor e Forma:SolidPeso molecular:3096.35Proteinase K
CAS:<p>Proteinase K (Protease K) is a non-specific serine protease. Proteinase K hydrolyzes peptide bonds and is used for protein digestion. Cost-effective and quality-assured.</p>Fórmula:C29H27N2O12PPureza:98%Cor e Forma:SolidPeso molecular:626.511Ac-DEVD-AMC
CAS:<p>Ac-DEVD-AMC (AC-ASP-MET-GLN-ASP-7-AMINO-4-METHYLCOUMARIN) is the substrate of Caspase-3 .</p>Fórmula:C30H37N5O13Pureza:98.20%Cor e Forma:White PowderPeso molecular:675.64NSC 405020
CAS:<p>NSC 405020 is a noncatalytic inhibitor of MT1-MMP.</p>Fórmula:C12H15Cl2NOPureza:96.93% - 99.07%Cor e Forma:SolidPeso molecular:260.16Belnacasan
CAS:<p>Belnacasan (VX-765) is an orally active IL-converting enzyme/caspase-1 inhibitor.</p>Fórmula:C24H33ClN4O6Pureza:96.53% - 99.5%Cor e Forma:SolidPeso molecular:508.99Anagliptin hydrochloride
CAS:<p>Anagliptin (SK-0403) hydrochloride: potent, selective oral DPP-4 inhibitor; IC50: DPP-4 3.8 nM, DPP-8 68 nM, DPP-9 60 nM.</p>Fórmula:C19H26ClN7O2Cor e Forma:SolidPeso molecular:419.91Simeprevir
CAS:<p>Simeprevir (TMC435) is a potent HCV NS3/4A protease inhibitor, and inhibits HCV replication with EC50 of 8 nM.</p>Fórmula:C38H47N5O7S2Pureza:99.45% - 99.92%Cor e Forma:SolidPeso molecular:749.94HIV-1 Nef-IN-1
CAS:<p>HIV-1 Nef-IN-1 is an inhibitor of HIV-1 Nef protein. It efficiently competes for Nef-SH3Hck interactions(Kd : 6.7 μM).</p>Fórmula:C18H16O2Pureza:99.90%Cor e Forma:SolidPeso molecular:264.32Dolutegravir sodium
CAS:<p>Dolutegravir sodium (GSK-1349572A) salt(DTG; GSK1349572) is an HIV integrase inhibitor(IC50: 2.7 nM), modest activity against raltegravir-resistant signature</p>Fórmula:C20H18F2N3NaO5Pureza:98% - 99.46%Cor e Forma:SolidPeso molecular:441.36Patamostat
CAS:<p>Patamostat (E-3123) inhibits trypsin, plasmin, and thrombin; may reduce acute pancreatitis progression. IC50: trypsin 39 nM, plasmin 950 nM, thrombin 1.9 μM.</p>Fórmula:C20H20N4O4SCor e Forma:SolidPeso molecular:412.46TCH-165
CAS:<p>TCH-165 boosts 20S proteasome levels, enhancing IDP breakdown.</p>Fórmula:C39H37N3O3Pureza:98.2% - 98.75%Cor e Forma:SolidPeso molecular:595.73TAPI-1 trifluoroacetate (163847-77-6(free base))
<p>TAPI-1 is an ADAM17/TACE inhibitor, which blocks shedding of cytokine receptors.</p>Fórmula:C28H38F3N5O7Pureza:98.06%Cor e Forma:SolidPeso molecular:613.62Grazoprevir
CAS:<p>Grazoprevir (MK-5172) is a protease inhibitor targeting hepatitis C virus NS3/4A used for treating chronic HCV genotypes 1 or 4 infections. Cost-effective and quality-assured.</p>Fórmula:C38H50N6O9SPureza:99.36% - >99.99%Cor e Forma:SolidPeso molecular:766.9Ditiocarb sodium
CAS:<p>Ditiocarb sodium (Sodium diethyldithiocarbamate) (sodium diethiocarbamate) is a copper reagent, which reacts with Cu2 + solution to form a complex and improves</p>Fórmula:C5H10NNaS2Pureza:98.04%Cor e Forma:White Solid CrystallinePeso molecular:171.26RN-18
CAS:<p>RN-18 is an inhibitor of HIV-1 viral infectivity factor (IC50: 6 μM in nonpermissive H9 cells).</p>Fórmula:C20H16N2O4SPureza:97.21% - 98.39%Cor e Forma:SolidPeso molecular:380.42Chlorcyclizine
CAS:<p>CHLORCYCLIZINE is a histamine H1 antagonist and a potent hepatitis C virus (HCV) entry inhibitor.</p>Fórmula:C18H21ClN2Pureza:98.75%Cor e Forma:SolidPeso molecular:300.83KGP94
CAS:<p>KGP94 is a potent, selective, and competitive inhibitor of the lysosomal endopeptidase enzyme.</p>Fórmula:C14H12BrN3OSPureza:99.6%Cor e Forma:SolidPeso molecular:350.23ML281
CAS:<p>ML281 is a potent and selective STK33 inhibitor with IC50 of 14 nM.</p>Fórmula:C22H19N3O2SPureza:99.12% - 99.87%Cor e Forma:SolidPeso molecular:389.47Bortezomib-pinanediol
CAS:<p>Bortezomib-pinanediol is a proteasome inhibitor. is a prodrug of Bortezomib.</p>Fórmula:C29H39BN4O4Pureza:97.5%Cor e Forma:Yellow SolidPeso molecular:518.46Tenofovir alafenamide
CAS:<p>Tenofovir alafenamide (GS-7340) is a nucleotide reverse transcriptase inhibitor (NRTI) and a novel ester prodrug of the antiretroviral tenofovir.</p>Fórmula:C21H29N6O5PPureza:99.68% - 99.81%Cor e Forma:SolidPeso molecular:476.47SU 4942
CAS:<p>SU-4942 is a modulator of tyrosine kinase signaling.</p>Fórmula:C15H10BrNOPureza:99% - 99.32%Cor e Forma:SolidPeso molecular:300.15Alvelestat
CAS:<p>Alvelestat (AZD9668) is an orally bioavailable, selective and reversible inhibitor of human neutrophil elastase (NE), with potential anti-inflammatory activity.</p>Fórmula:C25H22F3N5O4SPureza:98% - >99.99%Cor e Forma:SolidPeso molecular:545.53Voxilaprevir
CAS:<p>Voxilaprevir is an inhibitor of hepatitis C virus (HCV) nonstructural (NS) protein 3/4A protease.</p>Fórmula:C40H52F4N6O9SPureza:99.83% - 99.93%Cor e Forma:SolidPeso molecular:868.93Mericitabine
CAS:<p>Mericitabine (R-7128) is an HCV inhibitor that terminates RNA chains, halting replication.</p>Fórmula:C18H26FN3O6Pureza:97.77% - 98.54%Cor e Forma:SolidPeso molecular:399.41Darunavir Ethanolate
CAS:<p>Darunavir Ethanolate (UIC 94017) is an HIV PROTEASE INHIBITOR that is used in the treatment of AIDS and HIV INFECTIONS.</p>Fórmula:C29H43N3O8SPureza:99.84% - 99.86%Cor e Forma:SolidPeso molecular:593.74Cilastatin
CAS:<p>Cilastatin (MK0791): protects imipenem from renal breakdown; inhibits leukotriene D4 metabolism.</p>Fórmula:C16H26N2O5SPureza:97.76% - 99.71%Cor e Forma:SolidPeso molecular:358.45Talabostat mesylate
CAS:<p>Talabostat mesylate (PT100): Oral DPP4 inhibitor, IC50 0.18 nM, targets tumor-linked proteins, boosts hematopoiesis.</p>Fórmula:C10H23BN2O6SPureza:98% - 99.91%Cor e Forma:SolidPeso molecular:310.18Clemizole hydrochloride
CAS:<p>Clemizole hydrochloride blocks H1 histamine receptors and inhibits HCV replication and NS4B RNA binding.</p>Fórmula:C19H21Cl2N3Pureza:>99.99%Cor e Forma:SolidPeso molecular:362.3Nelfinavir Mesylate
CAS:<p>Nelfinavir Mesylate (Viracept) is an effective HIV protease inhibitor (Ki: 2 nM).</p>Fórmula:C33H49N3O7S2Pureza:95.81% - 98.51%Cor e Forma:A White Or Almost White PowderPeso molecular:663.897-benzyl-5,6-dimethyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine
CAS:<p>7-benzyl-5,6-dimethyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine is a inhibitor of Hepatitis C Virus(HCV).</p>Fórmula:C15H16N4Pureza:99.22%Cor e Forma:SolidPeso molecular:252.31Glecaprevir
CAS:<p>Glecaprevir (ABT-493) is an HCV NS3/4A protease inhibitor, (IC50s: 3.5-11.3 nM).</p>Fórmula:C38H46F4N6O9SPureza:99.16% - 99.69%Cor e Forma:SolidPeso molecular:838.87STK16-IN-1
CAS:<p>STK16-IN-1 is an inhibitor of STK16 kinase (IC50: 295 nM).</p>Fórmula:C17H12FN3OPureza:99.52%Cor e Forma:SolidPeso molecular:293.3LDC4297 hydrochloride
CAS:<p>LDC4297 hydrochloride is a selective and potent CDK7 inhibitor with broad-spectrum antiviral activity, useful for research on viral infections.</p>Fórmula:C23H29ClN8OCor e Forma:SolidPeso molecular:468.98GSK-A1
CAS:<p>GSK-A1 is a specific inhibitor of PI4KA, also inhibited calcium-driven PRL secretion without affecting calcium signaling and Prl expression.</p>Fórmula:C29H27FN6O4SPureza:98.03% - 98.97%Cor e Forma:SolidPeso molecular:574.63Carbobenzoxyproline
CAS:<p>Carbobenzoxyproline (Carbobenzoxy-S-proline) is a prolidase inhibitor.</p>Fórmula:C13H15NO4Pureza:99.79%Cor e Forma:White To Light Yellow Crystal PowderPeso molecular:249.26PF-00835231
CAS:<p>PF-00835231 is a CoV-2 cysteine 3C-like protease (3CLpro) inhibitor, with IC50s of 0.27 nM and 4 nM for SARS CoV-2 and SARS CoV-1 3CLpro, respectively.PF-</p>Fórmula:C24H32N4O6Pureza:97.83%Cor e Forma:SolidPeso molecular:472.53CH 5450
CAS:<p>CH 5450 (Z-Ile-Glu-Pro-Phe-Ome) (Z-Ile-Glu-Pro-Phe-Ome) is a short peptide inhibitor of chymase in the human heart</p>Fórmula:C34H44N4O9Pureza:95.93%Cor e Forma:SolidPeso molecular:652.73Rusalatide acetate (497221-38-2 free base)
CAS:<p>Rusalatide acetate (TP508 amide acetate), a regenerated peptide, alleviates radiation-induced gastrointestinal injury by activating stem cells.</p>Fórmula:C99H151N29O37SPureza:>99.99%Cor e Forma:SolidPeso molecular:2371.5Hepln-13
CAS:<p>Hepln-13 is a hepsin inhibitor that acts by hindering prostate cancer bone metastasis.</p>Fórmula:C17H13BrN2Pureza:97.67%Cor e Forma:SolidPeso molecular:325.2(Arg)9 TFA (143413-47-2 free base)
CAS:<p>(Arg)9 TFA (Peptide R9 TFA) is a cell-penetrating peptide. (Arg)9 TFA exhibits neuroprotective activity with an IC50 of 0.78 μM in the glutamic acid model.</p>Fórmula:C56H111F3N36O12Pureza:>99.99%Cor e Forma:SolidPeso molecular:1537.714-Isopropylcatechol
CAS:<p>4-Isopropylcatechol is a potent depigmenting agent and is of use in the topical therapy of selected patients with hypermelanosis.</p>Fórmula:C9H12O2Pureza:97.93%Cor e Forma:SolidPeso molecular:152.19Azvudine
CAS:<p>Azvudine (FNC) is a powerful NRTI effective against HIV, HBV, HCV, and resistant strains.</p>Fórmula:C9H11FN6O4Pureza:99.76% - >99.99%Cor e Forma:SolidPeso molecular:286.22Z-YVAD-FMK
CAS:<p>AA-Z-YVAD-FMK is a Irreversible caspase-1 inhibitor,with anti-inflammatory and anti-tumor activities.</p>Fórmula:C31H39FN4O9Pureza:98.00%Cor e Forma:SolidPeso molecular:630.66Enfuvirtide acetate
CAS:<p>Enfuvirtide acetate salt is a linear synthetic peptide made of 36 amino acids. It has an acetylated N-terminus and a carboxamide C-terminus.</p>Fórmula:C206H305N51O66Pureza:99.34%Cor e Forma:SolidPeso molecular:4552Diprotin A
CAS:<p>Diprotin A (Ile-Pro-Ile) (Ile-Pro-Ile) is a dipeptidyl peptidase IV (DPP-IV) inhibitor.</p>Fórmula:C17H31N3O4Pureza:99.29%Cor e Forma:White PowderPeso molecular:341.45GI254023X
CAS:<p>GI254023X is a MMP9 and ADAM10 inhibitor with IC50 values of 2.5 and 5.3 nM.Cost-effective and quality-assured.</p>Fórmula:C21H33N3O4Pureza:98.21% - 98.56%Cor e Forma:SolidPeso molecular:391.5Paritaprevir free base
CAS:<p>Paritaprevir (ABT-450) is an oral HCV NS3/NS4A protease inhibitor with potential against genotype 1, disrupting viral replication.</p>Fórmula:C40H43N7O7SPureza:95% - 99.26%Cor e Forma:SolidPeso molecular:765.89Bictegravir
CAS:<p>Bictegravir (GS-9883) is a potent inhibitor of HIV-1 integrase (IC50: 7.5 nM).</p>Fórmula:C21H18F3N3O5Pureza:97.6% - 99.51%Cor e Forma:SolidPeso molecular:449.38ABT530
CAS:<p>ABT530 (Pibrentasvir) is an HCV NS5A inhibitor with EC50s ranging from 1.4-5.0 pM against HCV replicons containing NS5A from genotypes 1-6.</p>Fórmula:C57H65F5N10O8Pureza:99.15% - 99.93%Cor e Forma:SolidPeso molecular:1113.18TMC647055 Choline Hydroxide Salt
<p>TMC647055 is a potent HCV NS5B inhibitor with low toxicity and good pharmacokinetics, under clinical evaluation.</p>Fórmula:C37H53N5O8SPureza:99.44%Cor e Forma:SolidPeso molecular:727.91Brensocatib
CAS:<p>Brensocatib (AZD7986) is a Dipeptidyl peptidase 1 (DPP1) inhibitor (pIC50s: 6.85, 7.7, 7.6, 7.8, and 7.8 in human, rat, mouse, rabbit, and dog, respectively).</p>Fórmula:C23H24N4O4Pureza:97.55%Cor e Forma:SolidPeso molecular:420.46Apelin-17 (human, bovine) acetate
<p>Apelin-17 (human, bovine) acetate is an endogenous apelin receptor agonist. Potently inhibits forskolin-stimulated cAMP accumulation (pIC50 = 9.94).</p>Fórmula:C98H160N34O22SPureza:99.36%Cor e Forma:SolidPeso molecular:2198.63Rilpivirine
CAS:<p>Rilpivirine (R278474) is a diarylpyrimidine derivative and reverse transcriptase inhibitor with antiviral activity against HIV-1 that is used in the treatment</p>Fórmula:C22H18N6Pureza:97.22% - 98.83%Cor e Forma:SolidPeso molecular:366.42CASP3 Activator 1541
CAS:<p>CASP3 Activator 1541 is an activator of the proenzyme forms of caspase-3, and induces cell death.</p>Fórmula:C24H17N3O4Pureza:98.84%Cor e Forma:SolidPeso molecular:411.41EIDD-1931
CAS:<p>EIDD-1931 (Beta-d-N4-hydroxycytidine) is a ribonucleoside analog with antiviral activity. It inhibits replication of SARS-CoV, MERS-CoV, and SARS-CoV-2.</p>Fórmula:C9H13N3O6Pureza:99.14% - 99.73%Cor e Forma:SolidPeso molecular:259.22GSK-690693
CAS:<p>GSK-690693 is a pan-Akt inhibitor targeting Akt1/2/3 with IC50 of 2 nM/13 nM/9 nM, also sensitive to the AGC kinase family: PKA, PrkX and PKC isozymes. Phase 1.</p>Fórmula:C21H27N7O3Pureza:98.07% - 99.77%Cor e Forma:SolidPeso molecular:425.483-O-Ethyl-L-ascorbic acid
CAS:3-O-Ethyl-L-ascorbic acid is a cosmetic tyrosinase inhibitor with whitening ability and is a stabilized vitamin C derivative.Fórmula:C8H12O6Pureza:97.35% - 99.99%Cor e Forma:White To Very Pale Yellow Crystalline Powder Solid PowderPeso molecular:204.18PSI-6130
CAS:<p>PSI-6130 (R 1656) is a potent and selective HCV NS5B polymerase inhibitor. PSI-6130 inhibits HCV replication with a mean IC50 of 0.6 μM.</p>Fórmula:C10H14FN3O4Pureza:98.63% - 99.79%Cor e Forma:SolidPeso molecular:259.23Asunaprevir
CAS:<p>Asunaprevir (BMS-650032) is an effective hepatitis C virus (HCV) NS3 protease inhibitor.</p>Fórmula:C35H46ClN5O9SPureza:99.34% - 99.8%Cor e Forma:SolidPeso molecular:748.29PTACH
CAS:<p>PTACH (Cpd 51) (NCH-51) is a SAHA-based inhibitor of human HDAC. It can potently inhibit the growth of various human Y cells (EC50: 1 to 10 μM).</p>Fórmula:C20H26N2O2S2Pureza:87.44% - 99.74%Cor e Forma:SolidPeso molecular:390.56Daclatasvir
CAS:<p>Daclatasvir (EBP 883/BMS-790052) is a potent HCV NS5A inhibitor with EC50 9-50 pM across various genotypes. Phase 3.</p>Fórmula:C40H50N8O6Pureza:99.81%Cor e Forma:SolidPeso molecular:738.88CA-074 methyl ester
CAS:<p>CA-074 methyl ester (Cathepsin B Inhibitor IV) is a selective inhibitor of Cathepsin B (IC50=36.3 nM). neuroprotective effect. High-Quality, Low-Cost!</p>Fórmula:C19H31N3O6Pureza:97.26% - 99.58%Cor e Forma:SolidPeso molecular:397.47Peptide T acetate(106362-32-7 free base)
<p>Peptide T acetate is an octapeptide from the V2 region of HIV-1 gp120.</p>Fórmula:C37H59N9O18Pureza:99.47%Cor e Forma:SolidPeso molecular:917.91Letermovir
CAS:<p>Letermovir (AIC246) (AIC246) is a novel anti-CMV compound (EC50: about 5 nM in fibroblast cells). It targets the pUL56 subunit of the viral terminase complex.</p>Fórmula:C29H28F4N4O4Pureza:99.85% - 99.87%Cor e Forma:SolidPeso molecular:572.55Bemnifosbuvir
CAS:<p>Bemnifosbuvir (AT-511) is a novel phosphoramidate prodrug of 2'-fluoro-2'-C-methylguanosine-5'-monophosphate that has potent in vitro activity against HCV.</p>Fórmula:C24H33FN7O7PPureza:99.35% - 99.54%Cor e Forma:SolidPeso molecular:581.53LY 3000328
CAS:<p>LY 3000328 (Cathepsin S inhibitor) is a selective inhibitor of cathepsin S.Cost-effective and quality-assured.</p>Fórmula:C25H29FN4O5Pureza:97.83% - 99.54%Cor e Forma:SolidPeso molecular:484.524-Butylresorcinol
CAS:<p>4-Butylresorcinol (Butylresorcinol) is a potent inhibitor of tyrosinase(IC50 : 11.27 μM), and is used in cosmetics as a depigmenting agent.</p>Fórmula:C10H14O2Pureza:98.64% - ≥95%Cor e Forma:Light Beige Solid PowderPeso molecular:166.22Daclatasvir dihydrochloride
CAS:<p>Daclatasvir dihydrochloride is an oral antiviral that treats chronic hepatitis C by inhibiting HCV's NS5A; rare liver enzyme elevation, seldom causes jaundice.</p>Fórmula:C40H52Cl2N8O6Pureza:99.67%Cor e Forma:SolidPeso molecular:811.8Ixazomib citrate
CAS:<p>Ixazomib citrate (MLN9708), a prodrug of Ixazomib (MMLN-2238), is an oral 2nd-gen proteasome inhibitor with anti-cancer potential (IC50: 3.4 nM).</p>Fórmula:C20H23BCl2N2O9Pureza:98.37% - >99.99%Cor e Forma:SolidPeso molecular:517.12Paritaprevir
CAS:<p>Paritaprevir (ABT450) 是一种非结构蛋白 3/4A 蛋白酶抑制剂，对 HCV 1a 和 HCV 1b 的 EC50 值分别为 1 和 0.21 nM。它也是SARS-CoV 3CLpro 的抑制剂，IC50为 1.31 μM。</p>Fórmula:C40H43N7O7SPureza:99.72%Cor e Forma:SolidPeso molecular:765.88Avatrombopag
CAS:<p>Avatrombopag (YM477) is a new oral thrombopoietin (TPO) receptor agonist, activating TPO receptor and increasing megakaryocytic proliferation/differentiation</p>Fórmula:C29H34Cl2N6O3S2Pureza:99.01% - 99.63%Cor e Forma:SolidPeso molecular:649.65S 3304
CAS:<p>S 3304 is a novel matrix metalloproteinases inhibitor which is specific for MMP-2 and MMP-9.</p>Fórmula:C24H20N2O4S2Pureza:98.09%Cor e Forma:SolidPeso molecular:464.56Velpatasvir
CAS:<p>Velpatasvir (GS-5816), also known as GS-5816, is a potent and selective Hepatitis C virus NS5A inhibitor.</p>Fórmula:C49H54N8O8Pureza:99.17% - 99.83%Cor e Forma:SolidPeso molecular:883Boc-Asp(OMe)-fluoromethyl ketone
CAS:<p>Boc-Asp(OMe)-FMK is a broad-spectrum caspase inhibitor that blocks Fas-mediated processes without affecting IL-8 chemotaxis.</p>Fórmula:C11H18FNO5Pureza:≥98%Cor e Forma:SolidPeso molecular:263.26Obefazimod
CAS:<p>Obefazimod (ABX-464) is a potent anti-HIV agent. ABX464 inhibits HIV-1 replication in stimulated peripheral blood mononuclear cells (PBMCs).</p>Fórmula:C16H10ClF3N2OPureza:99.86%Cor e Forma:SolidPeso molecular:338.71KKI-5 acetate(97145-43-2 free base)
<p>KKI-5 acetate: Serine protease inhibitor, targets kallikrein/plasmin, potential anticancer and angioedema therapy.</p>Fórmula:C37H59N11O11Pureza:99.44%Cor e Forma:SolidPeso molecular:833.95Tris(4-aminophenyl)methane
CAS:<p>Tris(4-aminophenyl)methane (Leucopararosaniline), a triphenylmethane dye, is a weak HCV helicase inhibitor.</p>Fórmula:C19H19N3Pureza:95.73%Cor e Forma:Beige Solid CrystallinePeso molecular:289.37JNJ0966
CAS:<p>JNJ0966 is a highly selective MMP-9 zymogen inhibitor (IC50: 440 nM).</p>Fórmula:C16H16N4O2S2Pureza:99.46% - 99.62%Cor e Forma:SolidPeso molecular:360.45Omarigliptin
CAS:<p>Omarigliptin is a potent and selective oral dipeptidyl peptidase 4 (DPP4) inhibitor with IC50 value of 1.6 nM. Cost-effective and quality-assured.</p>Fórmula:C17H20F2N4O3SPureza:99.68% - 99.77%Cor e Forma:SolidPeso molecular:398.43Thiamine disulfide
CAS:<p>Thiamine disulfide (Algoneurina) , also known as thiamin or vitamin B1, is a vitamin found in food and manufactured as a dietary supplement and medication.</p>Fórmula:C24H34N8O4S2Pureza:99.81%Cor e Forma:CoaPeso molecular:562.71Y-29794 Tosylate
CAS:<p>Y-29794 Tosylate (Y-29794) is an orally active, effective, and specific non-peptide-prolyl endopeptidase (PPCE) inhibitor.</p>Fórmula:C30H42N2O4S3Pureza:99.86%Cor e Forma:SolidPeso molecular:590.86GK921
CAS:<p>GK921 is a transglutaminase 2 (TGase) inhibitor.</p>Fórmula:C21H20N4OPureza:97.44% - 99.49%Cor e Forma:SolidPeso molecular:344.41HIV-1 Inhibitor 18A
CAS:<p>HIV-1 Inhibitor 18A (HIV-1 Inhibitor-18A) specifically inhibits the entry of multiple HIV-1 isolates.</p>Fórmula:C14H11N5O2SPureza:99.79%Cor e Forma:SolidPeso molecular:313.33CTTHWGFTLC, CYCLIC acetate(244082-19-7 free base)
<p>CTTHWGFTLC, CYCLIC acetate is an inhibitor for matrix metalloproteinases (MMP)-2 and MMP-9.</p>Fórmula:C54H75N13O16S2Pureza:99.71%Cor e Forma:SolidPeso molecular:1226.39Dabigatran
CAS:<p>Dabigatran (BIBR 953ZW), a thrombin inhibitor, prevents thrombus formation, reducing stroke and embolism risk in nonvalvular atrial fibrillation patients.</p>Fórmula:C25H25N7O3Pureza:97.44% - 98.7%Cor e Forma:Tan SolidPeso molecular:471.51CeMMEC13
CAS:<p>CeMMEC13 is an isoquinolinone that selectively inhibits the second bromodomain of TAF1 (IC50 = 2.1 μM).</p>Fórmula:C19H16N2O4Pureza:98.52%Cor e Forma:SolidPeso molecular:336.34Doravirine
CAS:<p>Doravirine (MK-1439) is a non-nucleoside reverse transcriptase inhibitor, used in the treatment of HIV/AIDS.</p>Fórmula:C17H11ClF3N5O3Pureza:99.65% - 99.79%Cor e Forma:SolidPeso molecular:425.75L-Albizziin
CAS:<p>L-Albizziin (L-beta-Ureidoalanine) is a glutamase inhibitor and is a glutaminyl-tRNA synthetase inhibitor.</p>Fórmula:C4H9N3O3Pureza:99.98%Cor e Forma:White PowderPeso molecular:147.13Anagliptin
CAS:<p>Anagliptin (SK-0403) is a potent Inhibitor of DPP-4(IC50 of 3.8 nM), for the treatment of type 2 diabetes mellitus.</p>Fórmula:C19H25N7O2Pureza:97.59% - 99.98%Cor e Forma:SolidPeso molecular:383.45P-113 acetate
<p>P-113 acetate: AMP from histatin 5, treats gingivitis and HIV-related oral candidiasis safely and effectively.</p>Fórmula:C73H114N28O15Pureza:97.4%Cor e Forma:SolidPeso molecular:1623.86Samatasvir
CAS:<p>Samatasvir (ATOLIHZIXHZSBA-BTSKBWHGSA-N) is a pan-genotypic inhibitor of the HCV non-structural protein 5A.</p>Fórmula:C47H48N8O6S2Pureza:98.03%Cor e Forma:SolidPeso molecular:885.06Glutaminase C-IN-1
CAS:<p>Glutaminase C-IN-1 (Compound 968) is a Glutaminase C allosteric inhibitor.</p>Fórmula:C27H27BrN2OPureza:99.68% - >99.99%Cor e Forma:SolidPeso molecular:475.422,4-Dioxaspiro(5.5)undec-8-ene, 3-(2-furanyl)-
CAS:<p>2,4-Dioxaspiro(5.5)undec-8-ene, 3-(2-furanyl)- (Ulinastatin) ,as an urinary trypsin inhibitor (UTI), is a glycoprotein that is isolated from healthy human urine</p>Fórmula:C13H16O3Pureza:99.53% - 99.81%Cor e Forma:SolidPeso molecular:220.26Ixazomib
CAS:<p>Ixazomib (MLN2238) is a boron-based peptide proteasome inhibitor targeting β5 site (IC50: 3.4 nM), also affecting β1 and β2 sites.</p>Fórmula:C14H19BCl2N2O4Pureza:98% - 98.92%Cor e Forma:SolidPeso molecular:361.03Batimastat
CAS:<p>Batimastat (BB94) (BB-94) is an effective, broad-spectrum matrix metalloprotease (MMP) inhibitor.</p>Fórmula:C23H31N3O4S2Pureza:98.15% - 99.5%Cor e Forma:SolidPeso molecular:477.64Elvitegravir
CAS:<p>Elvitegravir (JTK-303) is an HIV integrase inhibitor and CYP2C9 inducer.</p>Fórmula:C23H23ClFNO5Pureza:98.43% - 99.57%Cor e Forma:SolidPeso molecular:447.88Telaprevir
CAS:<p>Telaprevir (Incivek) (VX-950) is an effective inhibitor of HCV NS3-4A serine protease (IC50: 0.35 μM).</p>Fórmula:C36H53N7O6Pureza:96.9% - 98.89%Cor e Forma:SolidPeso molecular:679.854-Chloro-2-(trifluoroacetyl)aniline hydrochloride
CAS:<p>4-Chloro-2-(trifluoroacetyl)aniline hydrochloride is an inhibitor of HIV-1 RT (HIV reverse transcriptase) .</p>Fórmula:C8H6Cl2F3NOPureza:97.15%Cor e Forma:SolidPeso molecular:260.04Ceritinib
CAS:<p>Ceritinib (LDK378) is an ALK inhibitor with selective, ATP-competitive, and oral activity. Ceritinib has antitumor activity. Cost-effective and quality-assured.</p>Fórmula:C28H36ClN5O3SPureza:98.52% - 99.77%Cor e Forma:SolidPeso molecular:558.14CGS 27023A
CAS:<p>CGS 27023A is a non-peptidic, potent, and orally active stromelysin inhibitor.</p>Fórmula:C18H24ClN3O5SPureza:99.08%Cor e Forma:SolidPeso molecular:429.92Picolamine
CAS:<p>Picolamine acts as a potential inhibitor of DPP-4.</p>Fórmula:C6H8N2Pureza:98.3%Cor e Forma:Light Yellow LiquidPeso molecular:108.14SB-3CT
CAS:<p>SB-3CT is a potent and specific gelatinase inhibitor for MMP-2(Ki=13.9 nM) and MMP-9(Ki=600 nM).</p>Fórmula:C15H14O3S2Pureza:98% - 99.38%Cor e Forma:SolidPeso molecular:306.4S-methyl-KE-298
CAS:S-methyl-KE-298 is the second main metabolite in plasma,is a methyl conjugate of deacetyl-KE-298.KE-298 inhibits matrix metalloproteinase (MMP-1) productionFórmula:C13H16O3SPureza:97.33%Cor e Forma:SolidPeso molecular:252.33Tenofovir alafenamide hemifumarate
CAS:<p>Tenofovir alafenamide hemifumarate (GS-7340 hemifumarate) is an oral phosphonoamidate prodrug of the HIV reverse transcriptase nucleotide inhibitor tenofovir.</p>Fórmula:C21H29N6O5PC4H4O4Pureza:99.33% - 99.96%Cor e Forma:SolidPeso molecular:534.51Trelagliptin succinate
CAS:<p>Trelagliptin succinate (SYR-472 succinate) is a long-acting inhibitor of dipeptidyl peptidase-4 (DPP-4), being developed for the treatment of type 2 diabetes (</p>Fórmula:C22H26FN5O6Pureza:99.27% - 99.92%Cor e Forma:SolidPeso molecular:475.47Ilomastat
CAS:<p>Ilomastat (GM6001) (GM6001, Galardin) is a broad spectrum matrix metalloprotease (MMP) inhibitor.</p>Fórmula:C20H28N4O4Pureza:97.04% - 99.51%Cor e Forma:SolidPeso molecular:388.462-Benzylsuccinic acid
CAS:<p>2-Benzylsuccinic acid (DL-Benzylsuccinic acid) is a bacterial xenobiotic metabolite.</p>Fórmula:C11H12O4Pureza:99.01% - ≥95%Cor e Forma:SolidPeso molecular:208.21(R)-MG-132
CAS:<p>(R)-MG-132 (Z-Leu-D-leu-leu-al) is the enantiomer of MG-132. (R)-MG-132 stereoisomer is a more potent proteasome inhibitor than MG-132.</p>Fórmula:C26H41N3O5Pureza:98.45%Cor e Forma:SolidPeso molecular:475.62NBD-557
CAS:<p>NBD-557 is a potentially HIV-1 inhibitor.</p>Fórmula:C17H24BrN3O2Pureza:99.52%Cor e Forma:SolidPeso molecular:382.3Sofosbuvir
CAS:<p>Sofosbuvir (GS 7977) is a uridine monophosphate analog inhibitor of hepatitis C virus (HCV) polymerase NS5B that is used as an antiviral agent in the treatment</p>Fórmula:C22H29FN3O9PPureza:99.77% - 99.82%Cor e Forma:SolidPeso molecular:529.45Vesnarinone
CAS:<p>Vesnarinone (Arkin) (INN) is a mixed phosphodiesterase 3 inhibitor and ion-channel modifier that has modest, dose-dependent, positive inotropic activity, but</p>Fórmula:C22H25N3O4Pureza:96.69% - 98.13%Cor e Forma:SolidPeso molecular:395.45Lersivirine
CAS:<p>Lersivirine (UK-453061)(UK 453061) is a second-generation non-nucleoside reverse transcriptase inhibitor (NNRTI) under development for HIV infection therapy.</p>Fórmula:C17H18N4O2Pureza:98.01%Cor e Forma:SolidPeso molecular:310.35Boceprevir
CAS:<p>Boceprevir (SCH 503034), an oral HCV NS3 protease inhibitor, has a Ki of 14 nM and EC90 of 350 nM.</p>Fórmula:C27H45N5O5Pureza:95% - 99.16%Cor e Forma:SolidPeso molecular:519.68Trovirdine
CAS:<p>Trovirdine (LY300046) is a thiourea non-nucleoside reverse transcriptase inhibitor.</p>Fórmula:C13H13BrN4SPureza:98.12% - 98.50%Cor e Forma:SolidPeso molecular:337.24HCV-IN-31
CAS:<p>HCV-IN-31 is a HCV inhibitor with an EC50/EC95 of 15.7 μM.</p>Fórmula:C12H17FN6O3Pureza:99.83%Cor e Forma:SolidPeso molecular:312.3VCH-916
CAS:<p>VCH-916 is a new nonnucleoside inhibitor of HCV NS5B polymerase.</p>Fórmula:C26H36KNO4SPureza:98%Cor e Forma:SolidPeso molecular:497.732-PMPA
CAS:<p>2-PMPA (2-(Phosphonomethyl)pentanedioic acid) is a potent and selective inhibitor of glutamate carboxypeptidase II (GCPII) (IC50=300 pM).</p>Fórmula:C6H11O7PPureza:97.4% - 99.5%Cor e Forma:SolidPeso molecular:226.12Bz-RS-ISer(3-Ph)-Ome
CAS:<p>Bz-RS-ISer(3-Ph)-Ome (Methyl (2R,3S)-3-(benzoylamino)-2-hydroxy-3-phenylpropanoate) is a paclitaxel derivative that inhibits the HSV replication cycle.</p>Fórmula:C17H17NO4Pureza:99.36% - 99.89%Cor e Forma:White CrystalPeso molecular:299.32Ledipasvir (acetone)
CAS:<p>Ledipasvir (acetone) (GS-5885 acetone) is an HCV NS5A polymerase inhibitor, used for the treatment of hepatitis C virus infection.</p>Fórmula:C52H60F2N8O7Pureza:99.72%Cor e Forma:SolidPeso molecular:947.08Methylchloroisothiazolinone/Methylisothiazolinone Mixture
CAS:<p>Methylchloroisothiazolinone/Methylisothiazolinone Mixture (Kathon 886MW),a preservative, activates MMPs in human bronchial epithelial cells.</p>Fórmula:C8H9ClN2O2S2Cor e Forma:SolidPeso molecular:264.75KP-457
CAS:<p>KP-457 is a ADAM17 and a TNFα converting enzyme TACE inhibitor that blocks the production of soluble TNF (sTNF).</p>Fórmula:C21H24N2O7S2Pureza:98.33%Cor e Forma:SolidPeso molecular:480.56Sitagliptin phosphate monohydrate
CAS:<p>Sitagliptin phosphate monohydrate (MK-0431 phosphate monohydrate) is a potent inhibitor of DPP-IV with IC50 of 19 nM in Caco-2 cell extracts.</p>Fórmula:C16H15F6N5O·H3PO4·H2OPureza:99.85% - 99.98%Cor e Forma:White Or Almost White Crystalline PowderPeso molecular:523.33(1S,2R)-Alicapistat
CAS:<p>(1S,2R)-Alicapistat inhibits calpains 1 and 2, shows promise for Alzheimer's, and has an IC50 of 395 nM.</p>Fórmula:C25H27N3O4Pureza:99.60%Cor e Forma:SoildPeso molecular:433.5Ledipasvir
CAS:<p>Ledipasvir (GS-5885) is a Hepatitis C Virus NS5A Inhibitor.</p>Fórmula:C49H54F2N8O6Pureza:99.96%Cor e Forma:SolidPeso molecular:889Rilpivirine HCl
CAS:<p>Rilpivirine HCl (Rilpivirine hydrochloride) is an NNRTI inhibitor with antiviral activity that inhibits the HIV virus.</p>Fórmula:C22H19ClN6Pureza:99.48%Cor e Forma:SolidPeso molecular:402.88(R)-Trolox
CAS:<p>(R)-Trolox is a selective tyrosinase inhibitor used in food, cosmetics, and pharmaceutical products.</p>Fórmula:C14H18O4Pureza:99.88%Cor e Forma:SolidPeso molecular:250.29Teneligliptin
CAS:<p>Teneligliptin (MP-513), potent DPP-4 inhibitor, IC50 ~1 nM, blocks DPP-4 in human/rat plasma and recombinant forms.</p>Fórmula:C22H30N6OSPureza:99.73%Cor e Forma:SolidPeso molecular:426.58Nelfinavir
CAS:<p>Nelfinavir (AG1341), with Ki=2 nM, is an HIV treatment and broad-spectrum anticancer drug.</p>Fórmula:C32H45N3O4SPureza:98.16% - 99.5%Cor e Forma:White To Off-White Crystalline PowderPeso molecular:567.78Danoprevir
CAS:<p>Danoprevir (RG7227) is a peptidomimetic inhibitor of the NS3/4A protease(IC50=0.2-3.5 nM) of hepatitis C virus (HCV).</p>Fórmula:C35H46FN5O9SPureza:98% - 99.35%Cor e Forma:SolidPeso molecular:731.83PSI
CAS:<p>PSI is a proteasome inhibitor.</p>Fórmula:C32H50N4O8Pureza:97% - 98.33%Cor e Forma:SolidPeso molecular:618.76Lanadelumab
CAS:<p>Lanadelumab (SHP643), a humanized IgG1 antibody, inhibits plasma kallikrein and its interaction with HMWK, supporting hereditary angioedema research.</p>Pureza:95% - 95%Cor e Forma:LiquidGalegenimab
CAS:<p>Galegenimab (FHTR 2163; RG 6147; RO 7171009) is an HTRA1 antibody fragment for AMD research.</p>Pureza:95% - 95%Cor e Forma:LiquidKZR-504
CAS:KZR-504 is a selective inhibitor of immunoproteasome low molecular mass polypeptide 2 (LMP2) (IC50s: 51 nM, 4.274 μM for LMP2 and LMP7, respectively).Fórmula:C21H23N3O6Cor e Forma:SolidPeso molecular:413.42Triton X-45(n=4)
CAS:<p>Triton X-45: nonionic, low HLB surfactant, dispersible in water, high Krafft point, relevant for HCV research.</p>Fórmula:C22H38O5Cor e Forma:SolidPeso molecular:382.53
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