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(2,622 products)
- Cytoskeletal Signaling(1,585 products)
- DNA Damage/DNA Repair(2,873 products)
- Endocrinology/Hormones(3,758 products)
- Enzyme(3,673 products)
- GPCR/G-Protein(9,049 products)
- Immunology and Inflammation(3,943 products)
- Influenza Virus(300 products)
- JAK/STAT signaling(417 products)
- MAPK Signaling(1,259 products)
- Membrane Transporter/Ion Channel(3,164 products)
- Metabolism(10,149 products)
- Microbiology/Virology(7,673 products)
- Neuroscience(10,547 products)
- Other Inhibitors(35,859 products)
- Oxidation-Reduction(41 products)
- PI3K/Akt/mTOR Signaling(1,435 products)
- Proteases/Proteasome(1,692 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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BTK inhibitor 20
CAS:BTK inhibitor 20 is a potent BTK inhibitor with an IC 50 of 8 nM .Formula:C37H42N8O4Color and Shape:SolidMolecular weight:662.78Mocravimod hydrochloride
CAS:Mocravimod hydrochloride (KRP-203) is an effecitive and orally active agonist of sphingosine 1-phosphate receptor type 1(S1PR1).Formula:C24H27Cl2NO3SPurity:90%Color and Shape:SolidMolecular weight:480.45Ref: TM-T12086
1mg66.00€5mg160.00€1mL*10mM (DMSO)169.00€10mg250.00€25mg507.00€50mg785.00€100mg1,054.00€RK-0133114
RK-0133114, R-enantiomer of RK-701, is a G9a inhibitor (IC50 = 3.7 μM) for SCD research.Formula:C26H30N4O3Color and Shape:SolidMolecular weight:446.54I-A09
CAS:I-A09 is a noncompetitive mPTPB inhibitor.Formula:C29H25N5O6Purity:98%Color and Shape:SolidMolecular weight:539.54(R)-3,4-DCPG
CAS:AMPA receptor antagonist with weak activity at NMDA receptors and little activity at kainate receptorsFormula:C10H9NO6Purity:98%Color and Shape:SolidMolecular weight:239.18Anticancer 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:354.42Kelatorphan
CAS:Kelatorphan is an enkephalin degrading enzyme full inhibitor.Formula:C14H18N2O5Purity:98%Color and Shape:SolidMolecular weight:294.3GW-813893
CAS:GW-813893: potent, selective oral factor Xa inhibitor; Ki 4.0 nM (FXa), 9.7 nM (prothrombinase).Formula:C17H22ClN3O5S2Purity:98%Color and Shape:SolidMolecular weight:447.96A-371191
CAS:A-371191 is an antagonist of Bcl-XL.Formula:C36H47N5O5S2Purity:98%Color and Shape:SolidMolecular weight:693.92Sapacitabine
CAS:Sapacitabine (CS682) is a nucleoside analog precursor with anticancer activity used in the study of leukemia.Formula:C26H42N4O5Purity:98.82%Color and Shape:SolidMolecular weight:490.64hCAIX-IN-16
CAS:hCAIX-IN-16 (Compound 12d), an inhibitor of hCA IX, exhibits inhibition constants (K i) of 190.0 nM for hCA IX and 187.9 nM for hCA XII.Formula:C20H20N8O2SPurity:98%Color and Shape:SolidMolecular weight:436.49RPC425 free base
CAS:RPC425 is a noncompetitive inhibitors of the Betaine-γ-Aminobutyric Acid Transporter 1 (BGT1).Formula:C22H27NO2S2Purity:98%Color and Shape:SolidMolecular weight:401.59IM-491
CAS:IM-491 is a TNF-alpha converting enzyme inhibitor.Formula:C25H28N4O4Color and Shape:SolidMolecular weight:448.51Levocabastine
CAS:Levocarbastine: 2nd-gen H1 antagonist, treats allergic conjunctivitis, selective NTS2 neurotensin inhibitor.Formula:C26H29FN2O2Color and Shape:SolidMolecular weight:420.52ARS-1323
CAS:ARS-1323 is the racemate of ARS-1620 and a mutant K-ras G12C inhibitor.Formula:C21H17ClF2N4O2Purity:99.53%Color and Shape:SolidMolecular weight:430.84Ref: TM-T10375
2mg38.00€5mg56.00€1mL*10mM (DMSO)63.00€10mg94.00€25mg129.00€50mg168.00€100mg235.00€200mg350.00€MDK-5432
CAS:MDK-5432, also known as AMPA stabilizer (R,R)-2a, is the most potent AMPA stabilizer.Formula:C20H28N2O4S2Color and Shape:SolidMolecular weight:424.58FLT3-IN-14
CAS:FLT3-IN-14: FLT3 inhibitor; FLT3-WT IC50=5.6nM, FLT3-ITD IC50=1.4nM; blocks Y591 phosphorylation; G1 arrest; pro-apoptotic.Formula:C25H24N6O2SColor and Shape:SolidMolecular weight:472.56Antibacterial agent 93
Antibacterial agent 93: potent aaRS inhibitor; effective against certain gram-positive and negative bacteria.Formula:C29H28Cl3N5O4Color and Shape:SolidMolecular weight:616.92Anti-inflammatory agent 63
CAS:Anti-inflammatory agent 63 exhibits potent inhibitory activity (EC50 = 5.33±0.57 μM) against lipopolysaccharide (LPS)-induced nitric oxide (NO) production inFormula:C18H15NO4Color and Shape:SolidMolecular weight:309.32Activated T Subunit
CAS:Activated T Subunit is employed in synthesizing exon-jumping oligomer conjugates that target specific sites within the human anti-muscular atrophy protein geneFormula:C31H34ClN4O5PColor and Shape:SolidMolecular weight:609.05Zika virus-IN-1
CAS:Zika virus-IN-1 is an inhibitor of Zika virus (EC50: 1.56 μM).Formula:C30H37N3O3SiColor and Shape:SolidMolecular weight:515.72Cmpd-A
CAS:Cmpd-A: Time-dependent CENP-E inhibitor, ATPase-blocking, induces mitotic arrest, halts cancer cell proliferation.Formula:C30H27F4N5O4SColor and Shape:SolidMolecular weight:629.63WAY-312084
CAS:WAY-312084 is an active compound.Formula:C12H11N3OS2Color and Shape:SolidMolecular weight:277.37JA-ACC
CAS:Jasmonyl-ACC (JA-ACC), a derivative of 1-aminocyclopropane-1-carboxylic acid (ACC)—the direct precursor to ethylene—impedes root growth in Arabidopsis, withFormula:C16H23NO4Color and Shape:SolidMolecular weight:293.36δ-Tocotrienol
CAS:δ-Tocotrienol (Delta-Tocotrienol) is a potential angiogenic inhibitor.Formula:C27H40O2Purity:99.86%Color and Shape:SolidMolecular weight:396.61Ref: TM-TMA2474
1mg46.00€5mg92.00€1mL*10mM (DMSO)101.00€10mg145.00€25mg281.00€50mg423.00€100mg625.00€SH-BC-893
CAS:SH-BC-893: Oral anti-cancer sphingolipid analog, prevents ceramide-related mitochondrial issues, and tackles diet-related obesity.Formula:C19H32ClNOColor and Shape:SolidMolecular weight:325.92SDH-IN-3
CAS:SDH-IN-3 is a succinate dehydrogenase (SDH) inhibitor, demonstrating potent antifungal activity with an inhibition concentration (IC50) of 7.2 μg/mL and anFormula:C15H11F2N3OSPurity:98%Color and Shape:SolidMolecular weight:319.33T-00127_HEV1
CAS:T-00127_HEV1 is an inhibitor of phosphatidylinositol 4-kinase III beta(PI4KIIIβ, IC50 = 60 nM).Formula:C22H29N5O3Purity:99.89%Color and Shape:SolidMolecular weight:411.5Ref: TM-T16967
1mg52.00€5mg113.00€10mg177.00€1mL*10mM (DMSO)234.00€25mg355.00€50mg530.00€100mg758.00€500mg1,558.00€TGR5 agonist 3
CAS:Compound 8, a cholic acid derivative, functions as a selective TGR5 agonist and exhibits an EC50 value of 5 μM [1].Formula:C28H48O5Color and Shape:SolidMolecular weight:464.68HA-29
CAS:HA-29 is an inhibitor of thromboxane A2 and prostaglandin endoperoxide receptors.Formula:C16H16N2O3Color and Shape:SolidMolecular weight:284.318(S)-HETE
CAS:8(S)-HETE activates mouse keratinocyte PKC (IC50: 100 μM) and PPARα (>0.3 μM); identified by chiral HPLC in murine skin.Formula:C20H32O3Color and Shape:SolidMolecular weight:320.47CCPG
CAS:CCPG is an agonist of excitatory Amino Acid.Formula:C6H9NO4Purity:98%Color and Shape:SolidMolecular weight:159.14Me-Indoxam
CAS:Me-Indoxam is an inhibitor of sPLA2. It has no effect on arachidonic acid release and platelet activating factor synthesis.Formula:C26H22N2O5Purity:98%Color and Shape:SolidMolecular weight:442.46Ras inhibitor 134
CAS:Ras inhibitor 134 can be used in studies about Ras.Formula:C23H21ClFN5O3Color and Shape:SoildMolecular weight:469.9Z-DEVD-CMK
CAS:Z-DEVD-CMK irreversibly inhibits various cathepsins in vitro [1].Formula:C27H35ClN4O12Color and Shape:SolidMolecular weight:643.04TCS 2510
CAS:TCS 2510 (CAY10598) 是一种选择性 PGE2 和 EP4 受体激动剂，可增强细胞内 cAMP 浓度和活性 β-caten 的丰度。TCS 2510 抑制TNF-α 产生，可用于研究代谢紊乱带来的疾病。Formula:C21H29N5O2Purity:98%Color and Shape:SolidMolecular weight:383.49Metabutoxycaine
CAS:Metabutoxycaine, a local anesthetic [1], serves to numb specific areas of the body.Formula:C17H28N2O3Color and Shape:SolidMolecular weight:308.42mGAT3/4-IN-2
CAS:mGAT3/4-IN-2 are potent inhibitors of mGAT3/mGAT4 with their pIC50 values of 5.44 and 5.25, respectively.Formula:C26H32ClN3OS2Color and Shape:SolidMolecular weight:502.13VU0364739
CAS:VU0364739, a selective phospholipase D2 (PLD2) inhibitor with an IC50 of 22 nM, effectively reduces cancer cell proliferation [1].Formula:C26H27FN4O2Purity:98%Color and Shape:SolidMolecular weight:446.52Amelparib
CAS:Amelparib (JPI-289) is an inhibitor of the poly-ADP-ribose polymerase.Formula:C19H25N3O3Purity:98%Color and Shape:SolidMolecular weight:343.42Autotaxin-IN-5
CAS:Autotaxin-IN-5 is an Autotaxin inhibitor. It has the potential to treat idiopathic pulmonary fibrosis.Formula:C30H29N9O2Purity:98%Color and Shape:SolidMolecular weight:547.61BM152054
CAS:BM152054 is a potent PPARγ ligand that induces glucose utilization in peripheral tissues by enhancing insulin action.Formula:C22H18N2O4S3Purity:99.56%Color and Shape:SolidMolecular weight:470.58LY 106737
CAS:LY 106737 is opioid antagonist in the class of phenylpiperidine.Formula:C21H27NOPurity:98%Color and Shape:SolidMolecular weight:309.45Biotin-PEG3-amide-C2-CO-Halofuginone
CAS:Biotin-PEG3-amide-C2-CO-Halofuginone is a derivative of halofuginone applicable in cancer research [1].Formula:C40H57BrClN7O10SColor and Shape:SolidMolecular weight:943.34Flurofamide
CAS:Flurofamide is an effective bacterial urease inhibitor and has potential in the treatment of infected urinary calculi.Formula:C7H9FN3O2PPurity:96.01% - 98%Color and Shape:SolidMolecular weight:217.14PLK1/p38γ-IN-1
CAS:PLK1/p38γ-IN-1 (compound 14) serves as a dual inhibitor targeting both PLK1 and p38γ kinases, effectively suppressing the proliferation of human hepatocellularFormula:C21H26ClN3O2Purity:98%Color and Shape:SolidMolecular weight:387.9OUP-16
CAS:OUP-16 is a potent and selective histamine H4 receptor agonist.Formula:C11H16N6OColor and Shape:SolidMolecular weight:248.28HP210
CAS:HP210, a selective glucocorticoid receptor modulator (SGRM), can suppress IL-1β and IL-6 mRNA expression, suggesting its utility in investigating inflammation-Formula:C22H19N3O2S2Purity:98%Color and Shape:SolidMolecular weight:421.54JAK-IN-17
"JAK-IN-17: Potent JAK inhibitor for studying ocular, skin, and respiratory diseases."Formula:C33H38F2N6O8Color and Shape:SolidMolecular weight:684.69SCH 206272
CAS:SCH 206272 is a potent, orally active antagonist of tachykinin NK(1), NK(2), and NK(3) receptor.Formula:C33H41Cl4N5O4Color and Shape:SolidMolecular weight:713.52
