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(2,795 products)
- Apoptosis(6,256 products)
- Cell Cycle/Checkpoint(4,836 products)
- Chromatin/Epigenetics(2,591 products)
- Cytoskeletal Signaling(1,534 products)
- DNA Damage/DNA Repair(2,880 products)
- Endocrinology/Hormones(3,748 products)
- Enzyme(3,670 products)
- GPCR/G-Protein(8,981 products)
- Immunology and Inflammation(3,789 products)
- Influenza Virus(299 products)
- JAK/STAT signaling(415 products)
- MAPK Signaling(1,250 products)
- Membrane Transporter/Ion Channel(3,148 products)
- Metabolism(10,143 products)
- Microbiology/Virology(7,591 products)
- Neuroscience(10,343 products)
- Other Inhibitors(35,823 products)
- Oxidation-Reduction(40 products)
- PI3K/Akt/mTOR Signaling(1,420 products)
- Proteases/Proteasome(1,680 products)
- Stem Cell and Derivatives(748 products)
- Tyrosine Kinase/Adaptors(1,958 products)
- Ubiquitination(1,720 products)
Show 16 more subcategories
Found 66564 products of "Inhibitors"
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3'-Hydroxy Repaglinide
CAS:'3'-Hydroxy Repaglinide, a CYP2C8 metabolite of Repaglinide, treats type II diabetes.Formula:C27H36N2O5Purity:98%Color and Shape:SolidMolecular weight:468.59AVE 0991
CAS:AVE 0991 is a nonpeptide analog of angiotensin-(1-7), a Mas agonist with inhibitory effects on [125I]-Ang-(1-7) and on neuroinflammation in Alzheimer's disease.Formula:C29H32N4O5S2Purity:99.73%Color and Shape:SolidMolecular weight:580.72SOS1-IN-6
CAS:SOS1-IN-6 (compound 33-P1) is a potent inhibitor of SOS1, acting on SOS1-G12D (IC50: 14.9 nM) and SOS1-G12V (IC50: 73.3 nM).Formula:C26H28F3N3O2Color and Shape:SolidMolecular weight:471.51NCI-006
CAS:NCI-006, an LDH inhibitor, slows tumor growth and enhances pyruvate's role in mitochondrial metabolism.Formula:C31H24F2N4O4S3Color and Shape:SolidMolecular weight:650.74TIY-7
TIY-7 is a selective, orally active inhibitor of the promyosin receptor kinase (TRK) enzyme. TIY-7 exhibited anti-tumour effects in a mouse xenograft model.Color and Shape:SolidGNE-616
CAS:GNE-616: a potent, stable, oral Nav1.7 inhibitor; Ki: 0.79 nM, Kd: 0.38 nM; for chronic pain.Formula:C24H23F4N5O3SPurity:98%Color and Shape:SolidMolecular weight:537.53KT2-962
CAS:KT2-962 is a TXA2/prostaglandin endoperoxide receptor antagonist.Formula:C23H27ClNNaO5S2Color and Shape:SolidMolecular weight:520.04HS-731
CAS:HS-731 is a μ-Opioid Receptor Agonist.Formula:C20H26N2O5Color and Shape:SolidMolecular weight:374.43GPBAR1-IN-3
CAS:GPBAR1-IN-3 (Compound 14) is both a selective agonist for GPBAR1, with an EC50 value of 0.17 μM, and an antagonist for CysLT1R [1].Formula:C21H23NO2Color and Shape:SolidMolecular weight:321.41TD-0212 TFA
CAS:TD-0212 TFA is an oral AT1 receptor antagonist & NEP inhibitor with pKi 8.9 & pIC50 9.2.Formula:C30H35F4N3O6SPurity:98%Color and Shape:SolidMolecular weight:641.67hA3AR agonist 1
hA3AR agonist 1 is a potent human A 3 adenosine receptor (hA 3 AR) agonist (Ki = 2.40 nM) .Formula:C10H14N6OSColor and Shape:SolidMolecular weight:266.32hCAII-IN-5
CAS:hCAII-IN-5 (compound 12h) is a potent, selective inhibitor of human carbonic anhydrase II (hCA II) with an inhibition constant (IC50) of 4.55 µM [1].Formula:C29H18N2O7Color and Shape:SolidMolecular weight:506.46SLC4101431
SLC4101431 is a potent SphK2 inhibitor with Ki value of 90 nM.Formula:C29H28ClN7OSColor and Shape:SolidMolecular weight:558.1RMS-07
CAS:RMS-07, a covalent MPS1/TTK inhibitor, has an IC50 of 13.1 nM, targeting a kinase hinge cysteine.Formula:C35H40N8O2Color and Shape:SolidMolecular weight:604.74IDO1-IN-13
IDO1-IN-13 is a potent IDO1 inhibitor (IC50: 61.6 nM, EC50: 30 nM in HeLa) that reduces kyn/trp ratio by 51% in SK-OV-3 tumors.Formula:C20H16BrN5O2SColor and Shape:SolidMolecular weight:470.34NF-κB-IN-4
NF-κB-IN-4 (compound 17) is a potent inhibitor of NF-κB pathway which can cross blood brain barrier (BBB).Formula:C18H15FN4OColor and Shape:SolidMolecular weight:322.34rel-MDM2/4-p53-IN-2
Potent dual MDM2/MDM4 inhibitor & p53 activator; IC50: 70.7 nM (MDM2), 81.4 nM (MDM4); regulates cell cycle, triggers apoptosis, anti-cancer.Formula:C25H17Cl3FN3O3Color and Shape:SolidMolecular weight:532.78DH376
CAS:DH376 inhibits DAGLα in a time and dose dependent manner in mouse brain. DH376 shows picomolar activity.Formula:C31H28F2N4O3Color and Shape:SolidMolecular weight:542.58Heme Oxygenase-1-IN-2
Heme Oxygenase-1-IN-2 is a novel inhibitor of heme oxygenase-1 (HO-1), displaying potent antiproliferative activity in vitro, with an IC50 value of 0.95 μM.Formula:C19H18ClN3OColor and Shape:SolidMolecular weight:339.82Azaphilone-9
CAS:AZA-9 inhibits cancer growth by blocking HuR-ARE RNA binding; IC50=1.2μM.Formula:C21H23BrO5Color and Shape:SolidMolecular weight:435.31
