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(2,625 products)
- Cytoskeletal Signaling(1,585 products)
- DNA Damage/DNA Repair(2,872 products)
- Endocrinology/Hormones(3,759 products)
- Enzyme(3,673 products)
- GPCR/G-Protein(9,051 products)
- Immunology and Inflammation(3,945 products)
- Influenza Virus(300 products)
- JAK/STAT signaling(417 products)
- MAPK Signaling(1,259 products)
- Membrane Transporter/Ion Channel(3,163 products)
- Metabolism(10,148 products)
- Microbiology/Virology(7,672 products)
- Neuroscience(10,549 products)
- Other Inhibitors(35,858 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(1,744 products)
Show 16 more subcategories
Found 66516 products of "Inhibitors"
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VU 0364739 hydrochloride
CAS:VU 0364739 hydrochloride (VU 0364739 HCl) is a phospholipase D2 (PLD2) inhibitor that induces apoptosis and can be used in cancer research.Formula:C26H28ClFN4O2Purity:99.36%Color and Shape:SolidMolecular weight:482.98Linopirdine dihydrochloride
CAS:KV7 (KCNQ) voltage-gated potassium channels blockerFormula:C26H22ClN3OPurity:98%Color and Shape:SolidMolecular weight:427.93LY5
CAS:LY5 is an inhibitor of STAT3 that acts by inhibiting cell viability, cell migration, and angiogenesis in medulloblastoma cells.Formula:C15H11N3O4SPurity:98%Color and Shape:SolidMolecular weight:329.33FTR-1335
CAS:FTR1335: CaNMT inhibitor with 0.49 nM IC50. Targets fungi, effective on fluconazole-resistant Candida. Blocks protein myristoylation, crucial for selectivity.Formula:C31H34N4O2SColor and Shape:SolidMolecular weight:526.69Edunol
CAS:Edunol is a pterocarpan isolated from Harpalyce brasiliana. It has shown antimyotoxic, antiproteolytic and PLA2 inhibitor properties.Formula:C21H20O5Color and Shape:SolidMolecular weight:352.38MAT2A-IN-1
CAS:MAT2A-IN-1 suppresses MAT2A, key for MTAP-deficient cancer cell growth; studied for gastric, colon, liver, pancreatic cancers.Formula:C29H28F2N6O4Color and Shape:SolidMolecular weight:562.57α-Synuclein inhibitor 5
CAS:α-Synuclein inhibitor 5 is a potent inhibitor of α-Synuclein (α-Syn) aggregation across the blood-brain barrier (IC50: 1.22 μM), with 94.3% inhibition at 30 μM.Formula:C20H18N2O6SColor and Shape:SolidMolecular weight:414.43EP009
CAS:EP009, a novel, selective, and orally active inhibitor of JAK3, induces therapeutic response in T-cell malignancies.Formula:C14H24O2Color and Shape:SolidMolecular weight:224.34APX2014
CAS:APX2014 is a novel potent and specific Ref-1 inhibitor, blocking in vitro cell proliferation and activating apoptosis via PARP cleavage.Formula:C18H19NO5Color and Shape:SolidMolecular weight:329.35WEN05-03
CAS:WEN05-03 is a novel inhibitor of type III secretion system ATPase EscN from enteropathogenic Eecherichia coli.Formula:C17H14N4O4SColor and Shape:SolidMolecular weight:370.38U-83836E
CAS:U-83836E (lazaroid ) Possesses neuroprotective activity and anti-tumor activity, inhibits tumor necrosis factor and reverses endotoxin-induced shock.Formula:C30H46Cl2N6O2Purity:99.33%Color and Shape:SolidMolecular weight:593.63BRAF inhibitor
CAS:BRAF inhibitor is an inhibitor of B-Raf.Formula:C22H18F2N4O3SPurity:98.2% - 98.41%Color and Shape:SolidMolecular weight:456.47Ref: TM-T10599
1mg44.00€5mg87.00€1mL*10mM (DMSO)99.00€10mg137.00€25mg236.00€50mg371.00€100mg530.00€200mg770.00€PARP-2-IN-3
CAS:PARP-2-IN-3 is used in the study of breast cancer as a PARP-2 inhibitor with antitumor activity that induces apoptosis (apoptosis) and necrosis in cancer cells.
Formula:C20H20ClN3O3Purity:99.33%Color and Shape:SolidMolecular weight:385.84Fadrozole HCl hydrate
CAS:Fadrozole is a selective inhibitor of aromatase. It also effective in the treatment of estrogen-dependent diseases including breast cancer.Formula:C14H13N3ClHH2OPurity:98%Color and Shape:SolidMolecular weight:268.74CS-722 Free base
CAS:CS-722 Free base: synthetic muscle relaxant; inhibits spinal reflex and sodium/calcium currents affecting synaptic activity.Formula:C16H19ClN2O4Purity:99.52%Color and Shape:SolidMolecular weight:338.79Ref: TM-T10893
1mg109.00€2mg163.00€5mg243.00€1mL*10mM (DMSO)244.00€10mg355.00€25mg532.00€50mg750.00€100mg1,009.00€PD1-PDL1-IN 1
CAS:PD1-PDL1-IN 1 is a potent inhibitor of programmed cell death 1 (PD-1),and used as immune modulator.Formula:C14H23N7O6Purity:98%Color and Shape:SolidMolecular weight:385.38JNJ-2408068
CAS:JNJ-2408068 inhibits RSV with EC50 of 2.1 nM; blocks fusion (EC50=0.9 nM) by targeting F protein.Formula:C22H30N6OPurity:98%Color and Shape:SolidMolecular weight:394.51UbcH5c-IN-1
CAS:UbcH5c-IN-1 is a selective small-molecule Ubiquitin-conjugating enzyme UbcH5c inhibitor (Kd: 283 nM for E2 UbcH5c-IN-1 by covalent binding with Cys85).Formula:C22H21BrO3Purity:98%Color and Shape:SolidMolecular weight:413.3Me6TREN 4HCl
CAS:Me6TREN 4HCl: potent hematopoietic mobilizer, outperforms G-CSF/AMD3100, activates MMP-9, disrupts SDF-1α/CXCR4.Formula:C12H34Cl4N4Color and Shape:SolidMolecular weight:376.24HBX28258
CAS:HBX28258, a human USP7 inhibitor, binds covalently and selectively deactivates USP7 in colon cancer and kidney cells.Formula:C26H30ClN3OPurity:98%Color and Shape:SolidMolecular weight:435.99
