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(2,787 products)
- Apoptosis(6,265 products)
- Cell Cycle/Checkpoint(4,800 products)
- Chromatin/Epigenetics(2,446 products)
- Cytoskeletal Signaling(1,530 products)
- DNA Damage/DNA Repair(2,964 products)
- Endocrinology/Hormones(3,708 products)
- Enzyme(3,669 products)
- GPCR/G-Protein(9,019 products)
- Immunology and Inflammation(3,883 products)
- Influenza Virus(301 products)
- JAK/STAT signaling(414 products)
- MAPK Signaling(1,248 products)
- Membrane Transporter/Ion Channel(3,038 products)
- Metabolism(10,216 products)
- Microbiology/Virology(7,607 products)
- Neuroscience(10,383 products)
- Other Inhibitors(36,019 products)
- Oxidation-Reduction(42 products)
- PI3K/Akt/mTOR Signaling(1,442 products)
- Proteases/Proteasome(1,726 products)
- Stem Cell and Derivatives(823 products)
- Tyrosine Kinase/Adaptors(2,039 products)
- Ubiquitination(1,718 products)
Show 16 more subcategories
Found 66684 products of "Inhibitors"
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MCHR1 antagonist 3
CAS:MCHR1 antagonist 3, a potent antagonist of the melanin-concentrating hormone receptor-1 (MCHR1), is employed for the regulation of energy metabolism.Formula:C29H36N4O2Purity:98%Color and Shape:SolidMolecular weight:472.62LAS191954
CAS:LAS191954 is a selective, potent and orally active PI3Kδ inhibitor for inflammatory diseases treatment(IC50 : 2.6 nM).Formula:C20H15N9OPurity:98%Color and Shape:SolidMolecular weight:397.39SLIGRL-NH2 TFA
CAS:SLIGRL-NH2 TFA, also known as Protease-Activated Receptor-2 Activating Peptide TFA, is a Protease-Activated Receptor-2 (PAR-2) agonist [1].Formula:C31H57F3N10O9Color and Shape:SolidMolecular weight:770.84CYT-1010
CAS:CYT-1010, a mu-opioid receptor agonist; EC50: β-arrestin, 13.1 nM; cAMP, 0.0053 nM. Extracted from patent WO2013173730A2.Formula:C35H40N6O5Purity:98%Color and Shape:SolidMolecular weight:624.73CCT-271850
CAS:CCT-271850 is an inhibitor of the spindle checkpoint function of Monospindle 1.Formula:C24H29N7OPurity:98%Color and Shape:SolidMolecular weight:431.53CDK7-IN-14
CAS:CDK7-IN-14, a potent CDK7 inhibitor from pyrimidines, may treat transcriptionally dysregulated cancers (CN114249712A).Formula:C22H24F3N6OPPurity:99.48%Color and Shape:SolidMolecular weight:476.43Antileishmanial agent-23
CAS:Antileishmanial agent-23 (compound G1/9), a potent and selective trypanothione reductase (TR) inhibitor, exhibits an IC50 of 2.24 ± 0.52 μM.Formula:C20H17N3O4S2Purity:98%Color and Shape:SolidMolecular weight:427.5Ac-Val-Gln-aIle-Val-aTyr-Lys-NH2
CAS:Ac-Val-Gln-aIle-Val-aTyr-Lys-NH2 demonstrates serum stability and non-toxicity to neuronal cells, while selectively inhibiting the fibrilization of tau inFormula:C38H65N11O9Color and Shape:SolidMolecular weight:819.99Bisthianostat
CAS:Bisthianostat (CF367) is an oral HDAC inhibitor that blocks histone deacetylation, potentially disrupting cancer cell growth and inducing apoptosis.Formula:C15H18N4O3S2Color and Shape:SolidMolecular weight:366.46Oxamniquine
CAS:Oxamniquine is an effective compound for the treatment of schistosomiasis.Formula:C14H21N3O3Purity:98%Color and Shape:Pale Yellow Crystals From Isopropanol SolidMolecular weight:279.33RP-001 hydrochloride
CAS:RP-001 hydrochloride: S1P1 agonist, EC50 9 pM; low activity on S1P2-4, moderate S1P5 affinity.Formula:C24H25ClN4O4Purity:98%Color and Shape:SolidMolecular weight:468.93PIM1-IN-4
CAS:PIM1-IN-4: strong PIM1 inhibitor, also blocks SGK-1, PKA, CaMK-1, GSK3β, MSK1; promising for cancer studies.Formula:C27H25BrCl2CuN6OPurity:98%Color and Shape:SolidMolecular weight:663.88PARP1-IN-7
CAS:PARP1-IN-7 functions as an anticancer agent by inhibiting poly(ADP-ribose) polymerase-1 (PARP1).Formula:C24H23N5OColor and Shape:SolidMolecular weight:397.47ATAC21
CAS:ATAC21 is a linker-immune-stimulatory compound created by conjugating a noncleavable maleimide-PEG4 linker, which includes a succinimide group, with an immune-Formula:C38H50N12O21P2Color and Shape:SolidMolecular weight:1072.82IIIM-290
CAS:IIIM-290 is an oral CDK inhibitor (IC50s: 90 and 94 nM for CDK2/A and CDK9/T1).Formula:C23H21Cl2NO5Purity:98%Color and Shape:SolidMolecular weight:462.32Iganidipine
CAS:Iganidipine（NKY 722） is a new water-soluble Ca2+ antagonist with antihypertensive activity for research and neurological related diseases.Formula:C28H38N4O6Purity:96.3%Color and Shape:SolidMolecular weight:526.62SPM-242 racemate
CAS:SPM-242 racemate is an antagonist of S1P(3)-selective.Formula:C17H21ClNO6PSPurity:98%Color and Shape:SolidMolecular weight:433.844-Chloro-L-phenylalanine
CAS:<p>4-Chloro-L-phenalanine (L-PCPA) is an inhibitor of 5-HT biosynthesis and a non-specific antagonist of tryptophan hydroxylases (TPH1 and TPH2).</p>Formula:C9H10ClNO2Purity:99.76% - 99.96%Color and Shape:SolidMolecular weight:199.63TRK-IN-17
CAS:TRK-IN-17 is a potent TRK inhibitor with potential for cancer research, targeting neurotrophic factor-activated kinases. See WO2021148807A1 for details.Formula:C21H21F2N7SColor and Shape:SolidMolecular weight:441.5Benzyl alcohol, α-(4-(4-amino-2-methoxyphenoxy)butyl)-, acetate (ester)
CAS:Benzyl alcohol, alpha-(4-(4-amino-2-methoxyphenoxy)butyl)-, acetate (ester) is a bioactive chemical.Formula:C20H25NO4Color and Shape:SolidMolecular weight:343.42
