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(2,746 products)
- Apoptosis(6,181 products)
- Cell Cycle/Checkpoint(4,806 products)
- Chromatin/Epigenetics(2,567 products)
- Cytoskeletal Signaling(1,498 products)
- DNA Damage/DNA Repair(2,897 products)
- Endocrinology/Hormones(3,701 products)
- Enzyme(3,671 products)
- GPCR/G-Protein(8,960 products)
- Immunology and Inflammation(3,692 products)
- Influenza Virus(296 products)
- JAK/STAT signaling(414 products)
- MAPK Signaling(1,244 products)
- Membrane Transporter/Ion Channel(3,135 products)
- Metabolism(10,101 products)
- Microbiology/Virology(7,550 products)
- Neuroscience(10,300 products)
- Other Inhibitors(35,772 products)
- Oxidation-Reduction(40 products)
- PI3K/Akt/mTOR Signaling(1,400 products)
- Proteases/Proteasome(1,670 products)
- Stem Cell and Derivatives(742 products)
- Tyrosine Kinase/Adaptors(1,922 products)
- Ubiquitination(1,715 products)
Show 16 more subcategories
Found 66578 products of "Inhibitors"
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Cav 3.2 inhibitor 3
Cav 3.2 inhibitor 3 is a potent inhibitor of the Cav3.2 T-type Ca2+channel (IC50: 0.1534 μM) and has a low binding affinity for D2 receptors.Formula:C32H37N3O2Color and Shape:SolidMolecular weight:495.66Chitin synthase inhibitor 11
Potent CHS inhibitor with an IC50 of 0.10 mM; exhibits broad-spectrum antifungal properties.Formula:C24H24N4O8Color and Shape:SolidMolecular weight:496.47Leukotriene B4 dimethyl amide
CAS:LTB4 dimethyl amide: inhibits human neutrophil degranulation and rat lysozyme release; antagonizes LTB4 receptor on guinea pig lung membranes (Ki = 130 nM).Formula:C22H37NO3Color and Shape:SolidMolecular weight:363.53Gepotidacin mesylate dihydrate
CAS:Gepotidacin mesylate dihydrate (GSK2140944 mesylate dihydrate) is an antibiotic and an inhibitor of bacterial type II topoisomerase.Formula:C25H36N6O8SPurity:99.85%Color and Shape:SolidMolecular weight:580.65ELOVL1-IN-2
CAS:ELOVL1-IN-2 weakly inhibits ELOVL1 enzyme (IC50: 21 μM) and shows moderate potency in HEK293 cells (IC50: 6.7 μM).Formula:C18H15FN2OPurity:99.94%Color and Shape:SolidMolecular weight:294.32Emprumapimod
CAS:Emprumapimod, an oral p38α MAPK inhibitor, targets RPMI-8226 cells, curbs LPS-induced IL-6; IC50: 100 pM; for cardiomyopathy, acute pain.Formula:C24H29F2N5O3Purity:99.21% - >99.99%Color and Shape:SolidMolecular weight:473.52Vofopitant
CAS:Vofopitant (GR 205171) is a potent NK1 receptor antagonist with anxiolytic and antiemetic activity for the study of post-traumatic stress disorder (PTSD).Formula:C21H23F3N6OPurity:97.86%Color and Shape:SolidMolecular weight:432.44ZD 7155 hydrochloride
CAS:ZD 7155 hydrochloride is an angiotensin II receptor type 1 (AT1 receptor) antagonist.Formula:C26H27ClN6OPurity:99.8%Color and Shape:SolidMolecular weight:474.98Ref: TM-T13390
1mg42.00€5mg88.00€10mg135.00€25mg235.00€50mg396.00€100mg635.00€200mg887.00€1mL*10mM (DMSO)90.00€Etamicastat hydrochloride
CAS:Etamicastat hydrochloride (BIA 5-453 hydrochloride) is a peripherally selective dopamine beta-hydroxylase inhibitor that reduces hypertension.Formula:C14H16ClF2N3OSPurity:98.54%Color and Shape:SolidMolecular weight:347.81Ref: TM-T11238L
1mg80.00€5mg173.00€10mg259.00€25mg423.00€50mg577.00€100mg827.00€1mL*10mM (DMSO)190.00€Odevixibat
CAS:Odevixibat (A4250) is a selective oral inhibitor for ileal bile acid transport, potentially treating primary biliary cirrhosis.Formula:C37H48N4O8S2Purity:99.53% - 99.83%Color and Shape:SolidMolecular weight:740.93SJ6986
CAS:SJ6986 is a potent, selective and orally active GSPT1/2 degrader. SJ6986 degrades GSPT1 with a DC 50 of 2.1 nM (D max 99%) [1].Formula:C20H14F3N3O7SPurity:99.73%Color and Shape:SolidMolecular weight:497.4Ref: TM-T41257
5mg52.00€10mg86.00€25mg140.00€50mg245.00€100mg378.00€500mg898.00€1mL*10mM (DMSO)59.00€JNJ-6204
CAS:JNJ-6204 is a deuterated compound that efficiently inhibits CSNK1D and CSNK1E.Formula:C19H11D6FN6OPurity:97.42% - 99.87%Color and Shape:SolidMolecular weight:370.41Vecabrutinib
CAS:Vecabrutinib (SNS-062) is a potent and noncovalent BTK and ITK inhibitor (Kd: 0.3 nM and 2.2 nM, respectively). Vecabrutinib displays an IC50 of 24 nM for ITK.
Formula:C22H24ClF4N7O2Purity:99.74%Color and Shape:SolidMolecular weight:529.92NRX-1532
NRX-1532 is a small molecule β-catenin:β-TrCP interaction enhancer.Formula:C16H11F3N4O2Purity:98.95% - 99.94%Color and Shape:SolidMolecular weight:348.28Ref: TM-T61172
1mg147.00€5mg358.00€10mg597.00€25mg1,153.00€50mg1,549.00€100mg2,088.00€500mg4,185.00€1mL*10mM (DMSO)394.00€Elacytarabine
CAS:Elacytarabine (M7594 0037), a lipid-conjugated derivative of the nucleoside analog cytarabine, is an antineoplastic drug. It has cytotoxicity in solid tumors.Formula:C27H45N3O6Purity:97.69%Color and Shape:SolidMolecular weight:507.66LLY-283
CAS:LLY-283, PRMT5 inhibitor, IC50 22 nM, Kd 6 nM, oral, selective, with antitumor effects.Formula:C17H18N4O4Purity:99.49%Color and Shape:SolidMolecular weight:342.35SY-5609
CAS:SY-5609 (CDK7-IN-3) is a selective non-covalent CDK7 inhibitor, with weak inhibitory activity against CDK2, CDK9 and CDK12.Cost-effective and quality-assured.Formula:C23H26F3N6OPPurity:99.34% - >99.99%Color and Shape:SolidMolecular weight:490.46Ref: TM-T36038
1mg139.00€2mg200.00€5mg343.00€10mg553.00€25mgTo inquire50mgTo inquire1mL*10mM (DMSO)373.00€Umibecestat
CAS:Umibecestat inhibits human and mouse BACE-1 (IC50: 11 nM & 10 nM), potentially for Alzheimer's research.Formula:C19H15ClF7N5O2Purity:99.88%Color and Shape:SolidMolecular weight:513.8Ref: TM-T13253
1mg163.00€5mg334.00€10mg485.00€25mg807.00€50mg1,099.00€100mg1,485.00€1mL*10mM (DMSO)376.00€GSK3368715 dihydrochloride
CAS:GSK3368715 dihydrochloride (EPZ019997 dihydrochloride) is a PRMTs inhibitor , with anticancer activity, for the study of advanced solid tumors.Formula:C20H40Cl2N4O2Purity:99.66% - 99.66%Color and Shape:SolidMolecular weight:439.46AZD-5672
CAS:AZD-5672 is an antagonist of CCR5 with an IC50 of 0.32 nM.Formula:C32H38F2N2O5S2Purity:98.1%Color and Shape:SolidMolecular weight:632.78Ref: TM-T30260
1mg192.00€5mg434.00€10mg610.00€25mg888.00€50mg1,243.00€100mg1,693.00€1mL*10mM (DMSO)530.00€
