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(2,523 products)
- Apoptosis(5,792 products)
- Cell Cycle/Checkpoint(4,449 products)
- Chromatin/Epigenetics(2,238 products)
- Cytoskeletal Signaling(1,383 products)
- DNA Damage/DNA Repair(2,825 products)
- Endocrinology/Hormones(3,507 products)
- Enzyme(3,640 products)
- GPCR/G-Protein(8,333 products)
- Immunology and Inflammation(3,526 products)
- Influenza Virus(296 products)
- JAK/STAT signaling(404 products)
- MAPK Signaling(1,202 products)
- Membrane Transporter/Ion Channel(2,790 products)
- Metabolism(9,448 products)
- Microbiology/Virology(6,981 products)
- Neuroscience(9,926 products)
- Other Inhibitors(37,926 products)
- Oxidation-Reduction(41 products)
- PI3K/Akt/mTOR Signaling(1,400 products)
- Proteases/Proteasome(1,597 products)
- Stem Cell and Derivatives(831 products)
- Tyrosine Kinase/Adaptors(2,016 products)
- Ubiquitination(1,650 products)
Show 16 more subcategories
Found 66641 products of "Inhibitors"
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LY 344864
CAS:<p>LY 344864, a specifc receptor agonist, is an affinity of 6 nM (Ki) at the recently cloned 5-HT1F receptor.</p>Formula:C21H22FN3OPurity:98%Color and Shape:SolidMolecular weight:351.42Naratuximab
CAS:<p>Naratuximab emtansine [1] is a humanized monoclonal antibody (Anti-TSPAN26/CD37 Reference Antibody (naratuximab)) that specifically targets CD37 (TSPAN26) and</p>Purity:98.3% (SDS-PAGE); 98.4% (SEC-HPLC) - 98.3% (SDS-PAGE); 98.4% (SEC-HPLC)Color and Shape:LiquidFlurochloridone
CAS:<p>Flurochloridone (R 40244) is a selective herbicide. Flurochloridone induces apoptosis and is regulated by mitochondrial dysfunction and oxidative stresses.</p>Formula:C12H10Cl2F3NOPurity:99.86%Color and Shape:SolidMolecular weight:312.12IEM 1754 2HBr
CAS:<p>IEM 1754 2HBr (IEM 1754 dihydrobromide) is a selective AMPA/kainate receptor blockers for GluR1 and GluR3 with IC50 of 6 μM.</p>Formula:C16H30N2·2HBrPurity:99.71% - 99.72%Color and Shape:SolidMolecular weight:412.25CNX-1351
CAS:<p>CNX-1351 is a potent and isoform-selective targeted covalent PI3Kα inhibitor.</p>Formula:C30H35N7O3SPurity:99.66% - 99.83%Color and Shape:SolidMolecular weight:573.71Vincristine
CAS:<p>Vincristine, a microtubule disruptor, inhibits mitosis in cancer cells, useful in leukemia research.</p>Formula:C46H56N4O10Purity:98.46% - >99.99%Color and Shape:SolidMolecular weight:824.96Pelubiprofen
CAS:<p>Pelubiprofen is a non-steroidal anti-inflammatory agent and a COX-2 inhibitor, which effectively reduces PGE(2) production by inhibiting COX activity.</p>Formula:C16H18O3Purity:99.69%Color and Shape:SolidMolecular weight:258.31Carboxypeptidase G2 (CPG2) Inhibitor
CAS:<p>Carboxypeptidase G2 (CPG2) Inhibitor (CPG2 Inhibitor) is a new CPG2 Inhibitor with antitumor activity.</p>Formula:C13H15NO6SPurity:99.96%Color and Shape:SolidMolecular weight:313.33SU11274
CAS:<p>SU11274 (Met Kinase Inhibitor)(IC50=10 nM) is a specific Met inhibitor. It shows no significant effects on PGDFRβ, EGFR or Tie2.</p>Formula:C28H30ClN5O4SPurity:98.62% - 99.53%Color and Shape:Orange PowderMolecular weight:568.09(S)-Tenofovir
CAS:<p>(S)-Tenofovir ((S)-PMPA) is the less active S-enantiomer of Tenofovir which is a nucleotide reverse transcriptase inhibitor.</p>Formula:C9H14N5O4PPurity:99.9%Color and Shape:SolidMolecular weight:287.21Calcipotriol monohydrate
CAS:<p>Calcipotriol monohydrate, a Vitamin D3 analog, binds well to the vitamin D receptor, used in psoriasis research.</p>Formula:C27H42O4Purity:99.95%Color and Shape:SolidMolecular weight:430.627-Methyladenine
CAS:<p>7-Methyladenine (NSC-7857) can be used as a marker of exposure to exogenous and carcinogenic methylating agents.</p>Formula:C6H7N5Purity:99.90%Color and Shape:SolidMolecular weight:149.15UNC0224
CAS:<p>UNC0224 is a selective inhibitor of G9a with a Ki of 2.6 nM and IC50 of 15 nM. UNC0224 also potently inhibits GLP with assay-dependent IC50 values of 20-58 nM.</p>Formula:C26H43N7O2Purity:99.80%Color and Shape:SolidMolecular weight:485.671-Tetralol, (S)-
CAS:<p>1-Tetralol, (S)- ((S)-1-Hydroxytetralin) can be used as a substrate of AKR1C1 in cell assays.</p>Formula:C10H12OPurity:≥98%Color and Shape:SolidMolecular weight:148.2Paroxetine hydrochloride hemihydrate
CAS:<p>Paroxetine hydrochloride hemihydrate (Paxil) is an effective and selective serotonin reuptake inhibitor (SSRI).</p>Formula:C38H44Cl2F2N2O7Purity:99.949%Color and Shape:SolidMolecular weight:749.67L-Cystathionine
CAS:<p>L-Cystathionine: nonprotein amino acid; important for sulfur amino acid metabolism; used in cardiovascular research.</p>Formula:C7H14N2O4SPurity:96.43% - >99.99%Color and Shape:SolidMolecular weight:222.26Ibandronic acid
CAS:<p>Ibandronic acid (Bonviva) is a third-generation amino-bisphosphonate with anti-resorptive and anti-hypercalcemic activities.</p>Formula:C9H23NO7P2Purity:94.84%Color and Shape:White Semi-SolidMolecular weight:319.23Polyquaternium-1
CAS:<p>Polyquaternium-1: a mild eye-safe preservative that inhibits microbes in multi-dose ophthalmic meds.</p>Formula:C22H48Cl3N3O6Purity:95%Color and Shape:SolidMolecular weight:556.99Bucillamine
CAS:<p>Bucillamine (DE019) protects against Ischemia/reperfusion injury in high-risk organ transplants and inhibits the production of VEGF.</p>Formula:C7H13NO3S2Purity:99.47%Color and Shape:SolidMolecular weight:223.31PF-05175157
CAS:<p>PF 05175157 is an inhibitor of acetyl-CoA carboxylase 1 (ACC1) and ACC2 (IC50s = 27, 33, 23.5, and 50.4 nM for human ACC1, human ACC2, rat ACC1, and rat ACC2,</p>Formula:C23H27N5O2Purity:98% - 99.92%Color and Shape:SolidMolecular weight:405.49XL413
CAS:<p>XL-413 is an oral CDC7 kinase inhibitor, potentially blocking DNA replication, mitosis, and cancer cell growth.</p>Formula:C14H12ClN3O2Purity:98.40% - >99.99%Color and Shape:SolidMolecular weight:289.72Perfluamine
CAS:<p>Perfluamine (FTPA) is a hydrophobic carrier fluid and can be used as a blood substitute.</p>Formula:C9F21NPurity:≥98%Color and Shape:Colorless Odorless Clear LiquidMolecular weight:521.07CP-547632
CAS:<p>CP-547632 is an oral ATP-competitive inhibitor of VEGFR-2/FGF kinase with IC50s of 11/9 nM, highly selective, has antitumor activity.</p>Formula:C20H24BrF2N5O3SPurity:99.39%Color and Shape:SolidMolecular weight:532.4PLX7904
CAS:<p>PLX7904 (PB04), a selective RAF inhibitor, blocks ERK1/2 in mutant BRAF melanoma without activating it in RAS mutants.</p>Formula:C24H22F2N6O3SPurity:99.51% - 99.66%Color and Shape:SolidMolecular weight:512.53E3330
CAS:<p>E3330 is a potent and selective APE1(Ref-1) inhibitor, which suppressed NF-kappa B DNA-binding activity.</p>Formula:C21H30O6Purity:99.52%Color and Shape:SolidMolecular weight:378.46Auristatin F
CAS:<p>Auristatin F is an effective inhibitor of microtubule and vascular damaging agent. Auristatin F can be used in antibody-drug conjugates.</p>Formula:C40H67N5O8Purity:98.41% - 99.25%Color and Shape:SolidMolecular weight:745.99Riviciclib hydrochloride
CAS:<p>Riviciclib hydrochloride (P276-00) is a novel CDK1, CDK4 and CDK9 inhibitor with IC50 of 79 nM, 63 nM and 20 nM, respectively. Phase 2/3.</p>Formula:C21H20ClNO5·HClPurity:99.51%Color and Shape:SolidMolecular weight:438.3Fluticasone furoate
CAS:<p>Fluticasone furoate (Avamys), a potent, trifluorinated steroid with anti-inflammatory effects, treats allergic rhinitis.</p>Formula:C27H29F3O6SPurity:99.82%Color and Shape:SolidMolecular weight:538.58Palosuran
CAS:Palosuran (ACT-058362) (ACT-058362) is a new potent and specific antagonist of the human UT receptor.Formula:C25H30N4O2Purity:99.65%Color and Shape:SolidMolecular weight:418.53Ellipticine
CAS:<p>Ellipticine is a powerful cancer drug with different actions, IC50: 0.27-1.48 μM for leukemia, breast cancer, neuroblastoma, glioblastoma.</p>Formula:C17H14N2Purity:97.26% - 99.88%Color and Shape:SolidMolecular weight:246.313,4-Dihydroxybenzylamine hydrobromide
CAS:<p>3,4-Dihydroxybenzylamine hydrobromide inhibits DNA polymerase and melanoma growth, varying with tyrosinase activity.</p>Formula:C7H10BrNO2Purity:98.49%Color and Shape:Light Beige Crystalline PowderMolecular weight:220.06IPA-3
CAS:<p>IPA-3 is a selective non-ATP competitive Pak1 inhibitor with IC50 of 2.5 μM, no inhibition to group II PAKs (PAKs 4-6).</p>Formula:C20H14O2S2Purity:97.40%Color and Shape:SolidMolecular weight:350.45Clopamide
CAS:<p>Clopamide (Brinaldix) is a piperidine and sulfamoylbenzamide-based diuretic with thiazide-like diuretic activity.</p>Formula:C14H20ClN3O3SPurity:99.71%Color and Shape:White To Yellowish Crystalline PowderMolecular weight:345.84Phorbol 12,13-dibutyrate
CAS:<p>Phorbol 12,13-dibutyrate (Phorbol dibutyrate) is a PKC activator that induces contraction of isolated rabbit vascular smooth muscle.</p>Formula:C28H40O8Purity:99.32% - 99.37%Color and Shape:SolidMolecular weight:504.61Dibenz[a,h]anthracene
CAS:<p>Dibenz[a,h]anthracene (CCRIS 208) has induced DNA damage and gene mutations in bacteria and gene mutations and transformation in several types of mammalian cell</p>Formula:C22H14Purity:99.97%Color and Shape:Colorless Plates Or Leaflets /Recrystallized/ From Acetic Acid Physical Description White Crystals Or Pale Yellow Solid Sublimes (Ntp 1992)Molecular weight:278.35Cot inhibitor-2
CAS:<p>Cot inhibitor-2: Potent, selective Tpl2/MAP3K8 blocker. IC50: 1.6 nM; hampers LPS-induced TNF-α, IC50: 0.3 μM. Orally active.</p>Formula:C26H25Cl2FN8Purity:98.87%Color and Shape:SolidMolecular weight:539.43Thiamethoxam
CAS:<p>Thiamethoxam ((E)-thiamethoxam) is an insecticide of broad-spectrum neonicotinoids.</p>Formula:C8H10ClN5O3SPurity:>99.99%Color and Shape:SolidMolecular weight:291.71TMPA
CAS:<p>TMPA is a nuclear receptor Nur77 and LKB1 interaction antagonist.</p>Formula:C21H32O6Purity:99.21%Color and Shape:SolidMolecular weight:380.48GSK-1268997
CAS:<p>GSK-1268997 is a bio-active chemical.</p>Formula:C21H23N7O3SPurity:99.33% - 99.81%Color and Shape:SolidMolecular weight:453.52Flumethasone pivalate
CAS:<p>Flumethasone pivalate: antipruritic, anti-inflammatory, and vasoconstrictor; for adrenocortical suppression, skin atrophy, and telangiectasia studies.</p>Formula:C27H36F2O6Purity:99.57% - 99.95%Color and Shape:SolidMolecular weight:494.57BAY1217389
CAS:<p>BAY 1217389 is an effective and selective inhibitor of the monopolar spindle 1 (MPS1) kinase (IC50<10 nM).</p>Formula:C27H24F5N5O3Purity:98.14% - 99.42%Color and Shape:SolidMolecular weight:561.5GW843682X
CAS:<p>GW843682X (GW843682) is a selective and ATP-competitive inhibitor of PLK1 and PLK3 (IC50s = 2.2 nM and 9.1 nM).</p>Formula:C22H18F3N3O4SPurity:99.92%Color and Shape:SolidMolecular weight:477.46NGB-2849
CAS:<p>NGB-2849 is a selective dopamine D3 receptor antagonist.</p>Formula:C29H29Cl2N3OColor and Shape:SolidMolecular weight:506.47c-Fms-IN-10
CAS:<p>c-Fms-IN-10 is a thieno[3,2-d]pyrimidine derivative, an FMS kinase inhibitor with IC50 of 2 nM, exhibiting anti-tumor properties.</p>Formula:C22H19N7OSPurity:98%Color and Shape:SolidMolecular weight:429.5Soporidine
CAS:<p>Soporidine, a strigolactone antagonist, blocks AtHTL, hindering SL signaling and seed germination.</p>Formula:C27H30F3NO3Purity:98%Color and Shape:SolidMolecular weight:473.53Inarigivir
CAS:<p>Inarigivir (ORI-9020) is a dinucleotide that can significantly reduce liver HBV DNA.</p>Formula:C20H26N7O10PSPurity:98%Color and Shape:SolidMolecular weight:587.5ZLD1039
CAS:<p>ZLD1039, an oral EZH2 inhibitor, shows strong PRC2 inhibition at low nanomolar IC50s, and halts breast cancer growth and spread.</p>Formula:C36H48N6O3Purity:99.5%Color and Shape:SolidMolecular weight:612.8GSK1829820A
CAS:<p>GSK1829820A is a Mycobacterium tuberculosis H37Rv non-cytotoxic inhibitor.</p>Formula:C15H15N3OSPurity:98%Color and Shape:SolidMolecular weight:285.36Vif-A3G Inhibitor N.41
CAS:<p>Vif-A3G Inhibitor N.41 is a HIV-1 inhibitor-targeting drug. It causes Vif-dependent degradation of human APOBEC3G, thereby inhibiting the Vif-A3G interaction.</p>Formula:C15H14N2O2Purity:98%Color and Shape:SolidMolecular weight:254.28Tuberine, (+)-
CAS:<p>Tuberine, (+)-: an alkaloid from Haplophyllum tuberculatum, fights Staphylococcus, Bacillus, Saccharomyces, and mildly inhibits E. coli.</p>Formula:C27H35NO6Color and Shape:SolidMolecular weight:469.57
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