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(2,832 products)
- Apoptosis(6,315 products)
- Cell Cycle/Checkpoint(4,875 products)
- Chromatin/Epigenetics(2,611 products)
- Cytoskeletal Signaling(1,564 products)
- DNA Damage/DNA Repair(2,873 products)
- Endocrinology/Hormones(3,754 products)
- Enzyme(3,672 products)
- GPCR/G-Protein(9,014 products)
- Immunology and Inflammation(3,900 products)
- Influenza Virus(300 products)
- JAK/STAT signaling(415 products)
- MAPK Signaling(1,256 products)
- Membrane Transporter/Ion Channel(3,154 products)
- Metabolism(10,139 products)
- Microbiology/Virology(7,620 products)
- Neuroscience(10,369 products)
- Other Inhibitors(35,851 products)
- Oxidation-Reduction(40 products)
- PI3K/Akt/mTOR Signaling(1,429 products)
- Proteases/Proteasome(1,690 products)
- Stem Cell and Derivatives(734 products)
- Tyrosine Kinase/Adaptors(1,982 products)
- Ubiquitination(1,725 products)
Show 16 more subcategories
Found 66522 products of "Inhibitors"
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AM9405
AM9405: peripheral CB1/5-HT3 agonist, suppresses gut motility, relieves GI disorder symptoms in mice.Formula:C24H33BrN2O2Purity:98%Color and Shape:SolidMolecular weight:461.44ADU-S100 disodium salt
CAS:ADU-S100 (MIW815) disodium salt is an activator of stimulator of interferon genes (STING).Formula:C20H22N10Na2O10P2S2Purity:98%Color and Shape:SolidMolecular weight:734.51CU-2010
CAS:CU-2010 is a synthetic compound that reduces blood loss and aids recovery post-cardiac surgery.Formula:C37H42N6O6SColor and Shape:SolidMolecular weight:698.83DFBTA
DFBTA inhibits ANO1 with IC50 of 24 nM, effectively treating inflammatory pain orally.Formula:C18H10ClF2NO3SColor and Shape:SolidMolecular weight:393.79EGFR-IN-3
EGFR-IN-3 is an EGFR inhibitor with antitumor activity.EGFR-IN-3 inhibits EGFRwt-TK, induces apoptosis (cell death), and can block cells in the G2/M phase.Formula:C24H18F4N6O2SPurity:98.1%Color and Shape:SolidMolecular weight:530.5Fosmanogepix
CAS:Fosmanogepix (APX001) is a broad-spectrum oral antifungal that targets Gwt1 enzyme, transforming into active APX001A in the body.Formula:C22H21N4O6PPurity:98%Color and Shape:SolidMolecular weight:468.40Icariside F2
CAS:Icariside F2 modestly inhibits α-glucosidase (4.6-12%) and has antioxidant properties, plus strong NF-κB inhibition (IC50: 16.25±2.19 μM).Formula:C18H26O10Purity:98%Color and Shape:SolidMolecular weight:402.39CEP-14083
CAS:CEP-14083: potent ALK inhibitor, effective in NPM/ALK T-cell lymphoma, binds ATP site; IC50=11 nmol/L, also inhibits insulin receptor, preclinical efficacy.Formula:C31H30N6O2Color and Shape:SolidMolecular weight:518.61FTI-2628
CAS:FTI-2628 is a novel inhibitor of protein farnesyltransferase (FT), inhibiting the growth of P. falciparum in red blood cells and suppressing parasitemia.Formula:C31H34N4O3SColor and Shape:SolidMolecular weight:542.69Sapintoxin D
CAS:Sapintoxin D is a fluorescent phorbol ester and selective activator of protein kinase C.Formula:C30H37NO8Color and Shape:SolidMolecular weight:539.62TAK-637
CAS:TAK-637 is a tachykinin 1 (NK1) receptor antagonist.Formula:C30H25F6N3O2Purity:98%Color and Shape:SolidMolecular weight:573.53PARP7-IN-12
CAS:PARP7-IN-12, a potent inhibitor targeting PARP7, exhibits an IC50 of 7.836 nM. This compound is applicable in cancer research.Formula:C23H27ClF3N5O5Color and Shape:SolidMolecular weight:545.94M1069
M1069 is an oral A2A/A2B receptor antagonist, 100x more selective over A1/A3, with antitumor properties by blocking adenosine's immunosuppressive effects.Formula:C25H30N4O8SColor and Shape:SolidMolecular weight:546.59L 739749
CAS:L 739749 is a CAAX peptidomimetic. It is also an inhibitor of farnesyl-protein transferase.Formula:C24H41N3O6S2Purity:98%Color and Shape:SolidMolecular weight:531.73EGFR-IN-47
EGFR-IN-47: strong oral EGFRL858R/T790M/C797S blocker, induces cell death; promising for NSCLC research. IC50: 0.01 μM.Formula:C29H35N7Color and Shape:SolidMolecular weight:481.64PROTAC FKBP Degrader-3
CAS:PROTAC FKBP Degrader-3, with FKBP and VHL binding groups linked, is a potent FKBP degrader.Formula:C68H90N6O17SPurity:98%Color and Shape:SolidMolecular weight:1295.54SPR719
CAS:SPR719 is an inhibitor of gyrase B, has bactericidal activity.Formula:C21H25FN6O3Purity:98%Color and Shape:SolidMolecular weight:428.46Dinordrin I diacetate
CAS:Dinordrin I diacetate is an implantation inhibitor and hormone.Formula:C25H32O4Purity:98%Color and Shape:SolidMolecular weight:396.52MY-875
MY-875 inhibits microtubule formation, binds like colchicine (IC50: 0.92 μM), activates Hippo pathway, and induces apoptosis with anticancer properties.Formula:C21H25NO6Color and Shape:SolidMolecular weight:387.43IT-066 HCl
CAS:IT-066 HCl is a histamine H2 receptor antagonist.Formula:C19H25ClN4O3Color and Shape:SolidMolecular weight:392.88
