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(2,855 products)
- Apoptosis(6,375 products)
- Cell Cycle/Checkpoint(4,911 products)
- Chromatin/Epigenetics(2,633 products)
- Cytoskeletal Signaling(1,588 products)
- DNA Damage/DNA Repair(2,868 products)
- Endocrinology/Hormones(3,765 products)
- Enzyme(3,673 products)
- GPCR/G-Protein(9,054 products)
- Immunology and Inflammation(3,954 products)
- Influenza Virus(300 products)
- JAK/STAT signaling(417 products)
- MAPK Signaling(1,259 products)
- Membrane Transporter/Ion Channel(3,163 products)
- Metabolism(10,157 products)
- Microbiology/Virology(7,674 products)
- Neuroscience(10,550 products)
- Other Inhibitors(35,862 products)
- Oxidation-Reduction(41 products)
- PI3K/Akt/mTOR Signaling(1,438 products)
- Proteases/Proteasome(1,692 products)
- Stem Cell and Derivatives(733 products)
- Tyrosine Kinase/Adaptors(1,992 products)
- Ubiquitination(1,744 products)
Show 16 more subcategories
Found 66512 products of "Inhibitors"
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Shegansu B
CAS:Shegansu B exhibits significant in vitro anti-influenza viral activity in MDCK cells.Formula:C30H26O8Purity:98%Color and Shape:SolidMolecular weight:514.52N-(Azido-PEG3)-N-(PEG2-NH-Boc)-PEG3-acid
CAS:N-(Azido-PEG3)-N-(PEG2-NH-Boc)-PEG3-acid is a polyethylene glycol (PEG)-based linker for the development of proteolysis targeting chimeras (PROTACs)[1].Formula:C29H55N5O13Purity:98%Color and Shape:SolidMolecular weight:681.77BAM(8-22)
CAS:Potent MRGPRX1 agonist peptide; first found in bovine adrenal glands. Non-opioid, lacking met-enkephalin motif. EC50: 8-150 nM.Formula:C91H127N25O23SPurity:98%Color and Shape:SolidMolecular weight:1971.22Acein
ACE ligand with Kd of 2.79 nM; doesn't affect ACE activity ≤500 nM; boosts dopamine release in striatum via NMDA + D-serine.Formula:C43H68N10O13Purity:98%Color and Shape:SolidMolecular weight:932.5VEGFR-2-IN-31
VEGFR-2-IN-31 (compound 3i), a robust VEGFR-2 inhibitor (IC50=8.93 nM), serves as an anti-prostate cancer agent by arresting the cell cycle at the S-phase andFormula:C15H10F2N4OPurity:98%Color and Shape:SolidMolecular weight:300.26Influenza A NP(366-374) Strain A/PR/8/35
CAS:This peptide is an H2-Db-restricted epitope from the Influenza A/PR/8/34 nucleoprotein.Formula:C38H63N11O18S2Purity:98%Color and Shape:SolidMolecular weight:1026.1BODIPY FL thalidomide
CAS:BODIPY FL thalidomide is a fluorescent probe that binds human cereblon protein with high affinity, exhibiting a dissociation constant (Kd) of 3.6 nM [1].Formula:C37H43BF2N6O7Color and Shape:SolidMolecular weight:732.58β-Amyloid (1-15)
CAS:β-Amyloid (1-15) (Amyloid β-Protein (1-15)) is a fragment of β-amyloid protein used in the study of Alzheimer's disease.Formula:C78H107N25O27Purity:99.88%Color and Shape:SolidMolecular weight:1826.84Hydroquinone diacetate
CAS:Hydroquinone diacetate (NSC-9277) is an OH• inibitor with IC50 of 7.59 μM.Formula:C10H10O4Purity:99.75%Color and Shape:White Crystalline PowderMolecular weight:194.1824,25-Dihydroxycycloartan-3-one
CAS:(24xi)-24,25-Dihydroxycycloartan-3-one exhibits inhibitory effects on both EBV-EA and NOR 1 activation.Formula:C30H50O3Purity:98%Color and Shape:SolidMolecular weight:458.727RTI-13951-33 hydrochloride
RTI-13951-33 HCl: potent, selective GPR88 agonist; brain-penetrant; EC50 = 25nM; curbs rat alcohol behaviors.Formula:C28H35Cl2N3O3Purity:98%Color and Shape:SolidMolecular weight:532.5Traxillaside
CAS:Traxillaside has significant neuroprotective activities against glutamate-induced toxicity in primary cultures of rat cortical cells .Formula:C28H36O12Purity:98%Color and Shape:SolidMolecular weight:564.584EMD527040
CAS:EMD527040 is a potent αvβ6 antagonist with antifibrotic effects, used in carcinoma and liver fibrosis research.Formula:C29H32Cl2N4O5Color and Shape:SolidMolecular weight:587.5Anticancer agent 157
Anticancer Agent 157 (compound 15) is a nitric oxide (NO) inhibitor with IC50 values of 0.62 μg/mL, exhibiting both anti-inflammatory and anticancer effects.Formula:C14H20O2Purity:98%Color and Shape:SolidMolecular weight:220.31(S)-BAY-293
CAS:(S)-BAY-293 is a potent pan-KRAS inhibitor for the study of primary non-small lung and pancreatic cancers.
Formula:C25H28N4O2SPurity:98%Color and Shape:SolidMolecular weight:448.58tetrathiomolybdate
CAS:Tetrathiomolybdate (TM) promotes the dimerization of the metal-binding domain (WLN4) of the cellular copper efflux protein ATP7B through its characteristicFormula:MoS4Color and Shape:SolidMolecular weight:224.2Paraherquamide E
CAS:Fungal-derived paraherquamide E kills C. elegans and O. fasciatus, reduces T. colubriformis eggs in gerbils.Formula:C28H35N3O4Color and Shape:SolidMolecular weight:477.60514,15 β-Dihydroxyklaineanone
CAS:14,15beta-Dihydroxyklaineanone (14,15beta-Dihydroxyklaineanone) is a bittersweet compound isolated from Eurycoma longifolia with antischistosomal activity.Formula:C20H28O8Purity:99.04%Color and Shape:SolidMolecular weight:396.43[D-Pro2] Spantide I TFA
[D-Pro2] Spantide I TFA is an analog of Spantide I, a selective antagonist of the NK1 receptor [1].Formula:C75H108N20O13·xC2HF3O2Purity:98%Color and Shape:SolidMal-C2-cyclohexylcarboxyl-hydrazide TFA
CAS:Mal-C2-cyclohexylcarboxyl-hydrazide TFA is a alkyl chain-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules.Formula:C14H18F3N3O5Purity:98%Color and Shape:SolidMolecular weight:365.31
