Inhibitors
Inhibitors are molecules that bind to enzymes, receptors, or other proteins to reduce or block their biological activity. These compounds are widely used in research to study biological pathways, understand disease mechanisms, and develop therapeutic drugs. Inhibitors play a crucial role in the treatment of various diseases, including cancer, cardiovascular diseases, and infections. At CymitQuimica, we provide a diverse range of high-quality inhibitors to support your research in biochemistry, cell biology, and pharmaceutical development.
Subcategories of "Inhibitors"
- Angiogenesis(2,758 products)
- Apoptosis(6,191 products)
- Cell Cycle/Checkpoint(4,808 products)
- Chromatin/Epigenetics(2,580 products)
- Cytoskeletal Signaling(1,503 products)
- DNA Damage/DNA Repair(2,887 products)
- Endocrinology/Hormones(3,702 products)
- Enzyme(3,671 products)
- GPCR/G-Protein(8,965 products)
- Immunology and Inflammation(3,700 products)
- Influenza Virus(296 products)
- JAK/STAT signaling(414 products)
- MAPK Signaling(1,248 products)
- Membrane Transporter/Ion Channel(3,136 products)
- Metabolism(10,096 products)
- Microbiology/Virology(7,554 products)
- Neuroscience(10,304 products)
- Other Inhibitors(35,764 products)
- Oxidation-Reduction(39 products)
- PI3K/Akt/mTOR Signaling(1,402 products)
- Proteases/Proteasome(1,672 products)
- Stem Cell and Derivatives(741 products)
- Tyrosine Kinase/Adaptors(1,922 products)
- Ubiquitination(1,716 products)
Show 16 more subcategories
Found 66571 products of "Inhibitors"
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CP-64434 hydrate
CAS:CP-64434 hydrate is an antibiotic; anti-proliferative HDAC inhibitor.Formula:C37H70N2O12Color and Shape:SolidMolecular weight:734.96M1002
CAS:M1002, a HIF-2 agonist, boosts HIF-2alpha/ARNT activation and alters HIF-281alpha PAS-B, working with PHD inhibitors.Formula:C15H8F6N2O2SPurity:99.98%Color and Shape:SolidMolecular weight:394.29Ref: TM-T61822
1mg49.00€5mg92.00€10mg144.00€25mg235.00€50mg350.00€100mg515.00€500mg1,071.00€1mL*10mM (DMSO)108.00€BChE-IN-7
CAS:BChE-IN-7 inhibits AChE/BChE selectively and reversibly; IC50 for BChE: 0.06 μM; crosses blood-brain barrier, protects neurons from Aβ toxicity.Formula:C21H24N2O2Color and Shape:SolidMolecular weight:336.43PI4KIII β inhibitor 3
CAS:PI4KIII beta inhibitor 3 is a novel and high effective inhibitor of PI4KIIIβ (IC50 of 5.7 nM).Formula:C22H22N8OSPurity:98%Color and Shape:SolidMolecular weight:446.53Infliximab
CAS:Infliximab is a chimeric monoclonal antibody that inhibits TNF-α. Infliximab can be used to treat Crohn's disease and rheumatoid arthritis. Cost-effective and quality-assured.Purity:98% - 99.70%Color and Shape:LiquidMolecular weight:145.98 kDa(R)-CPP
CAS:(R)-CPP is a NMDA antagonist.Formula:C8H17N2O5PPurity:98%Color and Shape:SolidMolecular weight:252.2Tubulin/MMP-IN-2
CAS:Tubulin/MMP-IN-2 blocks tubulin polymerization, MMP-2/-3/-9, induces apoptosis, aids cancer research, IC50: 24.95, 31.60, 22.37 µM.Formula:C40H48NO11PColor and Shape:SolidMolecular weight:749.78(+/-)-Marmesin
CAS:Marmesin is a novel angiogenesis inhibitor.Formula:C14H14O4Purity:98.00% - 98.00%Color and Shape:SolidMolecular weight:246.26RS 14203
CAS:RS 14203 is a selective type 4 phosphodiesterase (PDE4) inhibitor.Formula:C19H13N5O3Purity:98%Color and Shape:SolidMolecular weight:359.34CSV0C018875
CAS:CSV0C018875 is a quinoline-based EHMT2/G9a inhibitor with lower cytotoxicity than BIX-01294 [1].Formula:C18H17ClN2OColor and Shape:SolidMolecular weight:312.79ML179
CAS:ML179 is a potent and selective inverse agonist of liver receptor homolog-1 (LRH1, NR5A2) with IC50 of 320 nM.Formula:C21H25F3N4O2Purity:99.77%Color and Shape:SolidMolecular weight:422.44Ref: TM-T8954
1mg34.00€5mg75.00€10mg110.00€25mg220.00€50mg321.00€100mg469.00€200mg645.00€1mL*10mM (DMSO)92.00€SU-13197
CAS:SU-13197 is an antiarrhythmic drug with oral activity.Formula:C20H23Cl2N3Purity:98%Color and Shape:SolidMolecular weight:376.33AR 12456
CAS:AR-12456 is a Trapidil derivative that prevents serum hyperlipidemia in guinea pigs.Formula:C17H30N6OColor and Shape:SolidMolecular weight:334.46AMG8163
CAS:AMG8163 is an antagonist of vanilloid receptor TRPV1.Formula:C25H22F3N5O4SColor and Shape:SolidMolecular weight:545.53Alimadol
CAS:Alimadol is an opioid analgesic.Formula:C19H23NOColor and Shape:SolidMolecular weight:281.39EVT-101 HCl
CAS:EVT-101, a unique GluN2B antagonist, binds differently at GluN1/GluN2B interface with its own subcavity.Formula:C16H15Cl2F3N4Color and Shape:SolidMolecular weight:391.22Aldose reductase-IN-6
CAS:AR inhibitor Aldose reductase-IN-6: IC50 3.164 μM, Ki 0.018 μM, non-toxic to normal cells.Formula:C20H16N4O2SColor and Shape:SolidMolecular weight:376.43Sodium 3-nitrobenzenesulfonate
CAS:Sodium 3-nitrobenzenesulfonate is a mild oxidant that stabilizes fabric color during printing and pad dyeing.Formula:C6H4NNaO5SPurity:99.8%Color and Shape:Colourless Solid AmorphousMolecular weight:225.15F-050
CAS:F-050 inhibits platelet aggregation, potentially treating thrombosis in guinea pigs, rabbits, and rats.Formula:C21H20OColor and Shape:SolidMolecular weight:288.38MBC-11
CAS:MBC-11: First bone-targeting bisphosphonate-etidronate conjugate with araC, may treat TIBD.Formula:C11H20N3O14P3Purity:>99.99% - >99.99%Color and Shape:SolidMolecular weight:511.21L-Ornithine lactam hydrochloride
CAS:L-Ornithine lactam is a synthetic intermediate. It has been used in the synthesis of dipeptidyl peptidase 4 (DPP-4) inhibitors, as well as signaling peptides.Formula:C5H11ClN2OColor and Shape:SolidMolecular weight:150.606Apoptosis inducer 5d
CAS:Apoptosis inducer 5D is a new type of inducer that induces cell death by activating the apoptosis of cancer cells.Formula:C20H14BrN3Color and Shape:SolidMolecular weight:376.25Gadoleic Acid
CAS:Gadoleic acid, a monounsaturated fat, inhibits p53 at 1.2 nM, varies in liver with rat diet.Formula:C20H38O2Color and Shape:SolidMolecular weight:310.51Scaff10-8
CAS:Scaff10-8 blocks AKAP-Lbc-RhoA, aiding aquaporin-2 movement in kidney cells.Formula:C22H18O6Purity:98%Color and Shape:SolidMolecular weight:378.37S 312
CAS:S 312 is a calcium antagonist.Formula:C20H22N2O4SColor and Shape:SolidMolecular weight:386.46Eg5 Inhibitor V, trans-24
CAS:Eg5 Inhibitor V, trans-24 is a specific and potent Eg5 inhibitor that can be used in cancer research with an IC50 value of 0.65 uM.Formula:C26H21N3O3Purity:99.75%Color and Shape:SolidMolecular weight:423.46Ref: TM-T11155
1mg96.00€5mg193.00€10mg289.00€25mg469.00€50mg642.00€100mg858.00€200mg1,153.00€1mL*10mM (DMSO)215.00€BI-L 45XX
CAS:BI-L 45XX, an anti-inflammatory benzimidazole derivative, has inhibitory effects on neutrophil function.Formula:C10H9F3N2O2SColor and Shape:SolidMolecular weight:278.25Nafenopin
CAS:Nafenopin is a peroxisome proliferator, it is used to promote liver tumors and has been used as an antihyperlipoproteinemic agent.Formula:C20H22O3Purity:98%Color and Shape:SolidMolecular weight:310.39PCS1055 dihydrochloride
CAS:PCS1055 is a selective M4 antagonist (IC50: 18.1 nM, Ki: 6.5 nM) and potent AChE inhibitor with >100-fold M1/M3/M5 selectivity.Formula:C27H34Cl2N4Purity:98%Color and Shape:SolidMolecular weight:485.49AKT-IN-8
CAS:AKT-IN-8 is a potent inhibitor of AKT, acting on AKT1 (IC50: 4.46 nM), AKT2 (IC50: 2.44 nM) and AKT3 (IC50: 9.47 nM).Formula:C22H25ClN6O3Color and Shape:SolidMolecular weight:456.93CR4056
CAS:CR4056 (6-(1H-imidazol-1-yl)-2-phenylquinazoline) is a selective inhibitor of MAO-A with IC50 of 202.7 nM and a ligand of I2-imidazoline receptor with IC50 ofFormula:C17H12N4Purity:98.73%Color and Shape:SolidMolecular weight:272.3c-Met-IN-14
CAS:c-Met-IN-14: selective c-Met kinase inhibitor, IC50 2.89 nM, anticancer, stops G2/M phase, induces A549 cell apoptosis.Formula:C34H38ClFN4O7SColor and Shape:SolidMolecular weight:701.2Cercosporamide
CAS:Cercosporamide is a ATP-competitive Pkc1 kinase inhibitor (IC50 <50 nM; Ki <7 nM). It also is a unique Mnk inhibitor.Formula:C16H13NO7Purity:98%Color and Shape:SolidMolecular weight:331.28K 579
CAS:K 579 is a dipeptidyl peptidase IV inhibitor.Formula:C17H24N6OPurity:98%Color and Shape:SolidMolecular weight:328.41Glutaminyl Cyclase Inhibitor 5
Glutaminyl Cyclase Inhibitor 5 is a potent, selective inhibitor of human glutaminyl cyclase (hQC), demonstrating an inhibition concentration half-max (IC 50) ofFormula:C22H30N6OColor and Shape:SolidMolecular weight:394.51CBP501
CAS:CBP501 peptide inhibits kinases like MAPKAP-K2/C-Tak1/CHK1, preventing Cdc25C function and blocking the entry into mitosis.Formula:C86H122F5N29O17Color and Shape:SolidMolecular weight:1929.062'-Ethyl Simvastatin
CAS:2'-Ethyl Simvastatin is a Mevinolin analog with HMG-CoA reductase inhibition.Formula:C23H34O5Purity:98%Color and Shape:SolidMolecular weight:390.51SCH 50911 hydrochloride
CAS:SCH 50911 hydrochloride is a selective, orally-active and competitive antagonist of γ-Aminobutyric acid B GABA(B) receptor(IC50 : 1.1 μM).Formula:C8H16ClNO3Purity:98%Color and Shape:SolidMolecular weight:209.67Dibutyl maleate
CAS:Dibutyl maleate (DBM (VAN)) is a diester of the Maleic Acid and can be used as an intermediate of the synthesis of antibacterial compounds.Formula:C12H20O4Purity:97.08%Color and Shape:Colourless LiquidMolecular weight:228.28HBV-IN-10
CAS:HBV-IN-10, an isomer of compound 6, inhibits HBsAg with EC50 between 0.1-1 μM (Patent WO2021204258A1).Formula:C23H24FN7OColor and Shape:SolidMolecular weight:433.48Hoechst 33342 analog 2
CAS:Hoechst 33342 analog 2 is an analog of Hoechst 33342 which is a DNA minor groove binder.Formula:C25H23IN6OPurity:98%Color and Shape:SolidMolecular weight:550.39PF-4950834
CAS:PF-4950834, a ATP-competitive, selective Rho kinase inhibitor, provides therapeutic benefits in chronic inflammatory diseases.Formula:C21H19N3O2Purity:98%Color and Shape:SolidMolecular weight:345.39Hisphen
CAS:Hisphen shows antileukemic activity.Formula:C19H24Cl2N4O3Color and Shape:SolidMolecular weight:427.32Paliroden
CAS:Paliroden: an oral, non-peptide neuro-nutrient stimulant used in Alzheimer's and Parkinson's research.Formula:C26H24F3NPurity:96.21% - 99.83%Color and Shape:SolidMolecular weight:407.47CD2019
CAS:CD2019: RARbeta agonist, promotes axonal growth, targets PI3K in adult spinal cord repair.Formula:C25H26O3Color and Shape:SolidMolecular weight:374.47ML218
CAS:ML218 is an inhibitor of T-type Ca2+ channels (Cav3.1, Cav3.2, Cav3.3).ML218 inhibits the synaptic activity of subthalamic nucleus (STN) neurons.Formula:C19H26Cl2N2OPurity:99.2% - 99.45%Color and Shape:SolidMolecular weight:369.33(S)-p38 MAPK Inhibitor III
CAS:(S)-p38 MAPK inhibitor III: a cell-permeable, methylsulfanylimidazole; IC50s: 0.90 µM for p38 MAPK, 0.37 µM TNF-α, 0.044 µM IL-1β.Formula:C23H21FN4SColor and Shape:SolidMolecular weight:404.5FR 62765
CAS:FR 62765 is a derivative of WF-3681, an aldose reductase inhibitor.Formula:C16H18O5Color and Shape:SolidMolecular weight:290.31EGFR/C797S-IN-1
CAS:EGFR/C797S-IN-1: Potent EGFR-C797S inhibitor, IC50 of 0.128 µM, dose-dependent p-EGFR suppression, anti-tumor properties.Formula:C28H30N4O3Color and Shape:SolidMolecular weight:470.56DDD100097
CAS:DDD100097 is a N-myristoyltransferase inhibitor with potential inhibitory effects on Trypanosoma brucei, which can be used to study neurological disorders.Formula:C22H30Cl2F2N4O2SPurity:98.89%Color and Shape:SolidMolecular weight:523.47
