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(2,942 products)
- Apoptosis(6,646 products)
- Cell Cycle/Checkpoint(4,922 products)
- Chromatin/Epigenetics(2,639 products)
- Cytoskeletal Signaling(1,594 products)
- DNA Damage/DNA Repair(2,863 products)
- Endocrinology/Hormones(3,765 products)
- Enzyme(3,675 products)
- GPCR/G-Protein(9,483 products)
- Immunology and Inflammation(3,959 products)
- Influenza Virus(301 products)
- JAK/STAT signaling(418 products)
- MAPK Signaling(1,271 products)
- Membrane Transporter/Ion Channel(3,406 products)
- Metabolism(10,173 products)
- Microbiology/Virology(7,955 products)
- Neuroscience(11,147 products)
- Other Inhibitors(35,860 products)
- Oxidation-Reduction(41 products)
- PI3K/Akt/mTOR Signaling(1,440 products)
- Proteases/Proteasome(1,693 products)
- Stem Cell and Derivatives(732 products)
- Tyrosine Kinase/Adaptors(1,989 products)
- Ubiquitination(1,746 products)
Show 16 more subcategories
Found 66507 products of "Inhibitors"
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Silvestrol
CAS:Silvestrol is a eukaryotic translation initiation factor 4A inhibitor. Silvestrol causes autophagy and caspase-mediated apoptosis.Formula:C34H38O13Purity:98%Color and Shape:SolidMolecular weight:654.66XY153
XY153 (8l) is a BD2 selective BET inhibitor targeting BRD4, 3 & 2 with IC50s: 0.79, 5.31 & 5.09 nM, useful in acute myeloid leukemia & cancer research.Formula:C33H34FN3O4Color and Shape:SolidMolecular weight:555.64MA242
CAS:MA242 is a nuclear factor of activated T cells 1 (NFAT1) for Pancreatic Cancer Therapy and dual inhibitor of murine double minute 2 (MDM2).Formula:C26H21ClF3N3O5SPurity:98%Color and Shape:SolidMolecular weight:579.98(2S,3R)-LP99
CAS:(2S,3R)-LP99 is a less active enantiomer of LP99.Formula:C26H30ClN3O4SPurity:98%Color and Shape:SolidMolecular weight:516.05Keap1-Nrf2-IN-1 TFA
Keap1-Nrf2-IN-1 TFA (compound35) is a potent inhibitor (IC50: 43 nM) protecting against acetaminophen liver damage.Formula:C26H25F3N2O9SColor and Shape:SolidMolecular weight:598.544-Bromo A23187
CAS:4-Bromo A23187 is a halogenated analog of the calcium ionophore A-23187. 4-Bromo A23187 is a calcium modulator and induces apoptosis in different cells.Formula:C29H36BrN3O6Purity:98%Color and Shape:SolidMolecular weight:602.52MsbA-IN-3
MsbA-IN-3 is a potent and highly selective MsbA inhibitor (IC50: 2 nM). MsbA-IN-3 inhibits Escherichia coli activity (MIC: 35 μM).Formula:C24H22Cl2N2O4SColor and Shape:SolidMolecular weight:505.41Daeatal
CAS:Dynorphin A ethylamide (1-9), the opioid activities were examined in the bioassays.Formula:C56H93N19O10Purity:98%Color and Shape:SolidMolecular weight:1192.46Urease-IN-2
Urease-IN-2 is a non-competitive inhibitor of urease (IC50: 0.94 μM, Ki: 1.6 μM) that non-competitively inhibits Jack bean urease (JBU).Formula:C26H25N5O5S3Color and Shape:SolidMolecular weight:583.7LIT-001 free base
CAS:LIT-001, a nonpeptide OT-R agonist, enhances mouse autism-like behavior, with EC50=55 nM and Ki=226 nM.Formula:C28H33N7O2SPurity:98%Color and Shape:SolidMolecular weight:531.67Prohibitin ligand 1
Compound 22i, a prohibitin ligand, protects the heart at nanomolar levels by inducing STAT3 phosphorylation.Formula:C20H22N2OColor and Shape:SolidMolecular weight:306.4Antibacterial agent 88
Antibacterial agent 88 is an effective antibacterial agent against B. subtilis (MIC: 4 μg/ml) with MIC values of ≤0.0156 μg/mL for MRSA, MRSE and S. aureus.Formula:C31H44N2O6SColor and Shape:SolidMolecular weight:572.76G-479
CAS:G-479, a potent MEK inhibitor and improved analogue of GDC-0623, has distributed polarity enhancing bioactivity.Formula:C16H15FIN5O4Color and Shape:SolidMolecular weight:487.22Icariside 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:402.39α-Amylase-IN-1
CAS:α-Amylase-IN-1 is an α-Amylase inhibitor (IC50: 0.5509 μM).Formula:C18H18N2O3Purity:99.92%Color and Shape:SoildMolecular weight:310.35JNJ-1250132
CAS:JNJ-1250132 is a steroidal progesterone receptor modulator that inhibits binding of the receptor to DNA in vitro.Formula:C33H41NO4Color and Shape:SolidMolecular weight:515.688(S),15(S)-DiHETE
CAS:8(S),15(S)-DiHETE, from 15(S)-HETE's oxidation by 15-LO, triggers eosinophil movement at 1.5 μM; it counteracts pain and LTB4 effects.Formula:C20H32O4Color and Shape:SolidMolecular weight:336.47LY210073
CAS:LY210073 is an antagonist of the Leukotriene B4 (LTB4) receptor (IC50: 6.2 nM).Formula:C30H28O8Purity:98%Color and Shape:SolidMolecular weight:516.54Aeroplysinin 1
CAS:Aeroplysinin I is an antibacterial compound from the sponge. It has cytotoxic activity against colon cancer cells by promoting β-catenin degradation.Formula:C9H9Br2NO3Color and Shape:SolidMolecular weight:338.98L 731735
CAS:L 731735 is a farnesyltransferase inhibitor.Formula:C19H40N4O4SPurity:98%Color and Shape:SolidMolecular weight:420.61
