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(2,849 products)
- Apoptosis(6,366 products)
- Cell Cycle/Checkpoint(4,907 products)
- Chromatin/Epigenetics(2,623 products)
- Cytoskeletal Signaling(1,585 products)
- DNA Damage/DNA Repair(2,872 products)
- Endocrinology/Hormones(3,759 products)
- Enzyme(3,673 products)
- GPCR/G-Protein(9,051 products)
- Immunology and Inflammation(3,945 products)
- Influenza Virus(300 products)
- JAK/STAT signaling(417 products)
- MAPK Signaling(1,259 products)
- Membrane Transporter/Ion Channel(3,162 products)
- Metabolism(10,149 products)
- Microbiology/Virology(7,672 products)
- Neuroscience(10,549 products)
- Other Inhibitors(35,857 products)
- Oxidation-Reduction(41 products)
- PI3K/Akt/mTOR Signaling(1,435 products)
- Proteases/Proteasome(1,693 products)
- Stem Cell and Derivatives(734 products)
- Tyrosine Kinase/Adaptors(1,991 products)
- Ubiquitination(1,743 products)
Show 16 more subcategories
Found 66517 products of "Inhibitors"
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CL2E-SN38
CAS:CL2E-SN-38 is a structurally stable and highly releasable antibody-drug conjugate (ADC) incorporating SN-38, the active metabolite of Irinotecan and a potentFormula:C87H116N14O24Color and Shape:SolidMolecular weight:1741.93DYRKs-IN-2
CAS:DYRKs-IN-2 has antitumor activity. DYRKs-IN-2 is a potent DYRKs inhibitor with IC50s of 30.6 nM and 12.8 nM for DYRK1B and DYRK1A, respectively.Formula:C32H38ClN9O3Purity:98%Color and Shape:SolidMolecular weight:632.16TZP-102
CAS:TZP-102 is a potent, oral, ghrelin receptor agonist that has been shown to improve diabetic gastroparesis symptoms.Formula:C28H44N4O4Color and Shape:SolidMolecular weight:500.67Palmitic acid sodium
CAS:Palmitic acid sodium (Sodium palmitate), a saturated fatty acid, promotes adipogenesis and cellular lipoatrophy in a variety of cell lines.Formula:C16H31NaO2Purity:99.57% - 99.87%Color and Shape:SolidMolecular weight:278.41Senexin C
CAS:Senexin C is a CDK8/19 inhibitor with anticancer activity.Senexin C inhibits the growth of MV4-11 leukemia cells.Formula:C28H27N5OPurity:98.06%Color and Shape:SolidMolecular weight:449.55OSBP-IN-1
CAS:OSBP-IN-1 (compound 12), an analogue of Schweinfurthins, selectively targets oxysterol-binding protein (OSBP) and exhibits antitumor activity [1].Formula:C30H36O6Color and Shape:SolidMolecular weight:492.6Levuglandin E2
CAS:Levuglandin E2 is a secoprostanoid from prostaglandin endoperoxide.Formula:C20H32O5Color and Shape:SolidMolecular weight:352.47PRMT5-IN-16
CAS:PRMT5-IN-16 (Compound 20) is an antitumor PRMT5 inhibitor linked to epigenetic changes.Formula:C25H34N8O2Color and Shape:SolidMolecular weight:478.592-Furoyl-LIGRLO-amide TFA
CAS:2-Furoyl-LIGRLO-amide TFA is a potent and selective agonist of the proteinase-activated receptor 2 (PAR2), exhibiting a pD2 value of 7.0 [1] [2].Formula:C38H64F3N11O10Color and Shape:SolidMolecular weight:891.98Nurr1 agonist 7
CAS:Nurr1 agonist 7 is an agonist of Nurr1 (EC50: 0.12 μM), which can be used to study neurological disorders such as Parkinson's disease.Formula:C18H20O3Purity:99.79%Color and Shape:SolidMolecular weight:284.35NNMT-IN-4
CAS:NNMT-IN-4 (compound 38) is a selective, uncompetitive inhibitor of nicotinamide N-methyltransferase (NNMT) with in vitro biochemical and cell-based assay IC50Formula:C9H11N3OColor and Shape:SolidMolecular weight:177.2Magmas-IN-1
CAS:Magmas-IN-1 (compound 9), a small molecule Magmas inhibitor (SMMI), targets the mitochondria-associated granulocyte-macrophage colony-stimulating factor (GM-CSFFormula:C20H27N3OPurity:98%Color and Shape:SolidMolecular weight:325.45Terevalefim
CAS:Terevalefim (ANG-3777) is an hepatocyte growth factor (HGF) mimetic. Terevalefim selectively activates the c-Met receptor.Formula:C9H8N2SPurity:99.8%Color and Shape:SolidMolecular weight:176.24Ref: TM-T37596
1mg52.00€5mg113.00€1mL*10mM (DMSO)113.00€10mg200.00€25mg349.00€50mg510.00€100mg712.00€500mg1,459.00€AMOR
CAS:AMOR is unique to plant cell walls and enhances plant fertilization efficiency and capacityFormula:C13H22O12Color and Shape:SolidMolecular weight:370.31SID 26681509
CAS:SID 26681509 is a selective, reversible and competitive human cathepsin L inhibitor (IC50 of 56 nM).Formula:C27H33N5O5SPurity:99.18%Color and Shape:SolidMolecular weight:539.65Ref: TM-T12909
1mg63.00€5mg137.00€1mL*10mM (DMSO)163.00€10mg205.00€25mg414.00€50mg618.00€100mg882.00€Glucocorticoid receptor agonist-2 Ala-Ala-Mal
CAS:Glucocorticoid receptor agonist-2 Ala-Ala-Mal (compound 79) serves as a precursor for synthesizing anti-inflammatory antibody-drug conjugate (ADC) molecules andFormula:C47H50F2N4O12Color and Shape:SolidMolecular weight:900.92DGKα-IN-3
CAS:DGKα-IN-3 (example 25), with an IC50 of 283 nM, is a selective DGKα inhibitor that augments anti-PD-1's anti-tumor activity by promoting T cell proliferationFormula:C26H27F3N4O3Color and Shape:SolidMolecular weight:500.51BU-E 75
CAS:BU-E 75 is an agonist of the histamine H2.Formula:C21H24F2N6Color and Shape:SolidMolecular weight:398.45rac-CCT-250863
CAS:Rac-CCT-250863, a potent Nek2 inhibitor, exhibits selectivity for Nek2 over PLK1, MPS1, Cdk2 and Aurora A.Formula:C24H25F3N4O2SColor and Shape:SolidMolecular weight:490.54Arrhythmic-Targeting Compound 1
CAS:Arrhythmic-Targeting Compound 1 is used for arrhythmic disease, with nitrogen-containing spirocycles.Formula:C25H29N3O4SPurity:98%Color and Shape:SolidMolecular weight:467.58AC-4
CAS:AC-4 is a blocker of photoswitchable TRPV1 channel.Formula:C26H25F3N4O2SColor and Shape:SolidMolecular weight:514.56ENT-C225
CAS:ENT-C225 is a potent TrkB neurotrophin receptor (TrkBR) activator with neuroprotective activity for the study of Alzheimer's disease and Parkinson's disease.Formula:C26H40N4O5Purity:99.36% - 99.36%Color and Shape:SolidMolecular weight:488.62JND3229
CAS:JND3229 inhibits EGFRC797S; IC50: 5.8-30.5 nM; halts cell growth; effective in non-small cell lung cancer study.Formula:C33H41ClN8O2Purity:98.75%Color and Shape:SolidMolecular weight:617.18Pomaglumetad methionil hydrochloride
CAS:LY2140023 hydrochloride: oral methionine prodrug of LY404039, a selective mGlu2/3 agonist, studied for schizophrenia.Formula:C12H19ClN2O7S2Purity:98.57%Color and Shape:SolidMolecular weight:402.87c-Fms-IN-14
CAS:c-Fms-IN-14 (Example 76) is a potent inhibitor of the c-Fms kinase with an IC50 of 4 nM, utilized in cancer and autoimmune disease research [1].Formula:C26H24N6OPurity:98%Color and Shape:SolidMolecular weight:436.51Myrrhterpenoid O
CAS:Unfortunately, you did not provide the description of the chemical compound that needs to be rewritten.Formula:C16H20O3Purity:98%Color and Shape:SolidMolecular weight:260.33Ac-VAD-CHO
CAS:Ac-Val-Ala-Asp-CHO (Ac-VAD-CHO) serves as a pan-caspase inhibitor and preserves mitochondrial membrane potential (MMP) while preventing the release ofFormula:C14H23N3O6Purity:98%Color and Shape:SolidMolecular weight:329.35Cgp 57813
CAS:CGP 57813 is a lipophilic compound, which can be used as an inhibitor of HIV-1 protease.Formula:C43H58N4O8Color and Shape:SolidMolecular weight:758.94Gly-Gly-Phe-Gly-NH-CH2-O-CH2COOH
CAS:Gly-Gly-Phe-Gly-NH-CH2-O-CH2COOH is an ADC linker utilized in the synthesis of drug-linker conjugates specific to ADCs, notably for creating Deruxtecan, aFormula:C18H25N5O7Color and Shape:SolidMolecular weight:423.42SSR 69071
CAS:SSR69071: selective neutrophil elastase inhibitor, stronger for humans (Ki=0.0168 nM), may treat COPD, asthma, and reduce heart injury.Formula:C27H32N4O7SColor and Shape:SolidMolecular weight:556.63PARPYnD
CAS:PARPYnD: Photoaffinity PARP probe; inhibits PARP2, PARP1, PARP6 (IC50: 6, 38, 230 nM); tags PARP1/2 with N3 fluorescent probe.Formula:C34H31N9O3Color and Shape:SolidMolecular weight:613.67GNE-3476
CAS:GNE-3476 is an NMDA PAM with low GluN2A efficacy, AMPAR activity, and weak at GluN2B receptors.Formula:C18H22N4OSColor and Shape:SolidMolecular weight:342.46Murabutide
CAS:Murabutide, a safe synthetic immunomodulator, diminishes the expression of CD4 and CCR5 receptors and promotes the secretion of high levels of beta-chemokines,Formula:C23H40N4O11Color and Shape:SolidMolecular weight:548.58VPC 32183 (S)
CAS:VPC 32183 (S) is an LPA1/LPA3 antagonist with no agonist effect on human/mammal LPA receptors.Formula:C33H54N3O6PColor and Shape:SolidMolecular weight:619.78Ac-Lys-Val-Cit-PABC-MMAE
CAS:Ac-Lys-Val-Cit-PABC-MMAE is a conjugate comprising an antibody-drug conjugate (ADC) linker (peptide Ac-Lys-Val-Cit-PABC) and the cytotoxic agent monomethylFormula:C66H108N12O14Color and Shape:SolidMolecular weight:1293.64Deoxynybomycin
CAS:Deoxynybomycin, a selective anti-tumor agent, inhibits topoisomerase I and induces apoptosis.Formula:C16H14N2O3Purity:98%Color and Shape:SolidMolecular weight:282.29Mitemcinal
CAS:Mitemcinal is a motilin agonist.Formula:C40H69NO12Color and Shape:SolidMolecular weight:755.98LX-1031
CAS:LX-1031 is an effective inhibitor of tryptophan 5-hydroxylase. LX-1031 decreases serotonin (5-HT) synthesis peripherally.Formula:C28H25F3N4O4Purity:97.123% - 98.97%Color and Shape:SolidMolecular weight:538.52Ref: TM-T15796
1mg55.00€5mg120.00€1mL*10mM (DMSO)143.00€10mg187.00€25mg376.00€50mg597.00€100mg938.00€200mg1,264.00€B-Raf IN 5
CAS:B-Raf IN 5 is a potent inhibitor of the protein kinase B-Raf (IC50: 2.0 nM). B-Raf IN 5 resists rapid metabolism and does not bind to the secondary target PXR.Formula:C23H18ClF3N6O3S2Color and Shape:SolidMolecular weight:583.01Nicotinoyl azide
CAS:Nicotinoyl azide (N-Az) is a probe of light-activated chemical. It has been used to measure the solvent accessibility of purine nucleobases.Formula:C6H4N4OPurity:96.1%Color and Shape:SolidMolecular weight:148.12WAY-612453
CAS:WAY-612453 is an active compound utilized in researching amyloid diseases and synucleinopathies.Formula:C9H8Cl2N4SColor and Shape:SolidMolecular weight:275.16Antitumor agent-93
CAS:Antitumor agent-93 (compound 7D) effectively inhibits the proliferation of multiple tumor cell lines, including MDA-MB-231 and HCT-116 [1].Formula:C22H20O8Color and Shape:SolidMolecular weight:412.394-Hydroperoxyifosfamide
CAS:4-Hydroperoxyifosfamide is an anticancer agent capable of penetrating the blood-brain barrier (BBB) [1].Formula:C7H15Cl2N2O4PColor and Shape:SolidMolecular weight:293.09β-Catenin modulator-4
CAS:β-Catenin modulator-4 (compound IIa-92), encompassing oxazole and thiazole moieties, acts as a potent and selective modulator of β-Catenin [1].Formula:C21H21ClN2O2SColor and Shape:SolidMolecular weight:400.92cGAS-IN-1
CAS:cGAS-IN-1 (compound C20), a flavonoid that acts as a Cyclic GMP-AMP Synthase (cGAS) inhibitor, demonstrates IC50 values of 2.28 μM for human cGAS and 1.44 μMFormula:C18H19NO8Color and Shape:SolidMolecular weight:377.35Z-PDLDA-NHOH
CAS:Z-PDLDA-NHOH is a potent, specific vertebrate collagenase inhibitor [1].Formula:C22H32N4O6Color and Shape:SolidMolecular weight:448.512′,3′-cGMP triethylamine
CAS:Guanosine 2',3'-cyclic phosphate triethylamine, commonly known as 2′,3′-cGMP triethylamine, is an active compound utilizable in numerous research investigationsFormula:C16H27N6O7PColor and Shape:SolidMolecular weight:446.4Anticancer agent 121
CAS:Anticancer agent 121, a human lactate dehydrogenase A (hLDHA) inhibitor, exhibits potent anticancer activities, suitable for use in anticancer research [1].Formula:C19H18N2O3SColor and Shape:SolidMolecular weight:354.42MAO-B-IN-26
CAS:MAO-B-IN-26 (Compound IC9) serves as both a MAO-B and acetylcholinesterase inhibitor.Formula:C17H12BrNOPurity:98%Color and Shape:SolidMolecular weight:326.19Q-VD(OMe)-OPh
CAS:Q-VD-OPh: broad-spectrum, non-toxic caspase inhibitor; cost-effective, specific for apoptotic inhibition.Formula:C27H27F2N3O6Purity:98%Color and Shape:SolidMolecular weight:527.52
