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(2,762 products)
- Apoptosis(6,206 products)
- Cell Cycle/Checkpoint(4,811 products)
- Chromatin/Epigenetics(2,553 products)
- Cytoskeletal Signaling(1,519 products)
- DNA Damage/DNA Repair(2,906 products)
- Endocrinology/Hormones(3,703 products)
- Enzyme(3,671 products)
- GPCR/G-Protein(9,002 products)
- Immunology and Inflammation(3,748 products)
- Influenza Virus(297 products)
- JAK/STAT signaling(414 products)
- MAPK Signaling(1,244 products)
- Membrane Transporter/Ion Channel(3,106 products)
- Metabolism(10,125 products)
- Microbiology/Virology(7,567 products)
- Neuroscience(10,343 products)
- Other Inhibitors(35,806 products)
- Oxidation-Reduction(40 products)
- PI3K/Akt/mTOR Signaling(1,411 products)
- Proteases/Proteasome(1,681 products)
- Stem Cell and Derivatives(752 products)
- Tyrosine Kinase/Adaptors(1,949 products)
- Ubiquitination(1,716 products)
Show 16 more subcategories
Found 66605 products of "Inhibitors"
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Topoisomerase IV inhibitor 2
CAS:Compound 5d, a potent TOPO IV inhibitor (IC50: 0.35 μM), also inhibits DNA gyrase (IC50: 0.55 μM) and has antibacterial activity.Formula:C33H30FN7O6SPurity:98%Color and Shape:SolidMolecular weight:671.7Thi-DPPY
CAS:Thi-DPPY: Potent JAK3/BTK inhibitor (IC50: 1.38/62.4 nM), anti-proliferative, anti-inflammatory, potential in IPF research.Formula:C28H28ClN5O4SColor and Shape:SolidMolecular weight:566.07G3335
CAS:H-Trp-Glu-OH: Selective, reversible PPARγ modulator; cell-permeable; Kd ~8μM; potential diabetes lead.Formula:C16H19N3O5Color and Shape:SolidMolecular weight:333.34Boditrectinib
CAS:Boditrectinib: potent TKI, anti-cancer, researches cancer, inflammation, neurodegeneration, infections.Formula:C23H24F2N6OColor and Shape:SolidMolecular weight:438.47TriN2755
CAS:TriN2755, a synthetic triazene, induces apoptosis by alkylating DNA after N-demethylation; it's hydrophilic, photostable with low toxicity.Formula:C20H22N4O5Color and Shape:SolidMolecular weight:398.41Atelocantel
CAS:Atelocantel is an anthelmintic agent (veterinary drug).Formula:C13H17F2N3O2Color and Shape:SolidMolecular weight:285.29J-31
CAS:J-31 is an inactive conformation inhibitor of ITK.Formula:C21H19N3O4Color and Shape:SolidMolecular weight:377.39Lamotrigine isethionate
CAS:Water-soluble salt of lamotrigine . Displays anticonvulsant effects and inhibits glutamate release, possibly through inhibition of Na+, K+ and Ca2+ currents.Formula:C11H13Cl2N5O4SColor and Shape:SolidMolecular weight:382.22Zonisamide sodium
CAS:Zonisamide sodium is a 1,2 benzisoxazole derivative. It is the first agent of this chemical class to be developed as an antiepileptic drug.Formula:C8H8N2NaO3SPurity:98%Color and Shape:Off-White SolidMolecular weight:235.22JM6
CAS:JM6 is a weak kynurenine 3-monooxygenase (KMO) inhibitor that acts on mouse KMO (IC50: 19.85 μM). JM6 can be used to study Alzheimer's disease.Formula:C23H26N4O6S2Color and Shape:SolidMolecular weight:518.61Dyrk1A-IN-3
CAS:Dyrk1A-IN-3 is a selective DYRK1A inhibitor with an IC50 of 76 nM, useful for neurodegenerative disease research.Formula:C18H16N6Color and Shape:SolidMolecular weight:316.36VRX-0466617
CAS:VRX-0466617 is a novel selective Chk2 inhibitor.Formula:C19H20BrN5O2SColor and Shape:SolidMolecular weight:462.36(Z)-α-Cyanostilbene
CAS:(Z)-α-Cyanostilbene (compound 8), a dicyano-substituted acrylonitrile, exhibits selective antiproliferative effects on HeLa and HepG2 cells, with IC50 values ofFormula:C15H11NColor and Shape:SolidMolecular weight:205.25TRK-IN-14
CAS:TRK-IN-14 is a potent inhibitor of TRK. TRK-IN-13 has shown potential for TRK-related diseases.Formula:C24H21F2N5OColor and Shape:SolidMolecular weight:433.45(4E)-SUN9221
CAS:(4E)-SUN9221 is a potent dual α1-adrenergic receptor and 5-HT2 receptor antagonist that shows antihypertensive and antiplatelet aggregation activity inFormula:C25H31FN4O3Purity:97.79%Color and Shape:SolidMolecular weight:454.54Pyrithione Zinc
CAS:Pyrithione Zinc is a novel KMD5A inhibitor.Formula:C5H5NOSColor and Shape:SolidMolecular weight:127.16TAB29
CAS:TAB29 is a potent peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 (Pin1) inhibitor (IC50 of 874 nM), with therapeutic potential for human cancers.Formula:C28H22O3Purity:98%Color and Shape:SolidMolecular weight:406.47ML202
CAS:ML202 activates human pyruvate kinase M2, affecting PEP cooperativity with minimal impact on ADP binding.Formula:C18H17N3O3S2Color and Shape:SolidMolecular weight:387.48SB-332235
CAS:SB-332235 is an effective specific CXCR2 antagonist. And it is effectively inhibited CS-induced neutrophilia in a dose-dependent manner.Formula:C13H10Cl3N3O4SColor and Shape:SolidMolecular weight:410.66SLP120701 HCl
CAS:SLP120701 is a potent, selective inhibitor of sphingosine kinase 2, targeting S1P signaling linked to cancer, fibrosis, and sickle cell disease.
Formula:C20H30ClN5OColor and Shape:SolidMolecular weight:391.94
