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(6,257 products)
- Cell Cycle/Checkpoint(4,835 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(8,978 products)
- Immunology and Inflammation(3,782 products)
- Influenza Virus(299 products)
- JAK/STAT signaling(415 products)
- MAPK Signaling(1,249 products)
- Membrane Transporter/Ion Channel(3,148 products)
- Metabolism(10,142 products)
- Microbiology/Virology(7,590 products)
- Neuroscience(10,343 products)
- Other Inhibitors(35,823 products)
- Oxidation-Reduction(40 products)
- PI3K/Akt/mTOR Signaling(1,414 products)
- Proteases/Proteasome(1,680 products)
- Stem Cell and Derivatives(746 products)
- Tyrosine Kinase/Adaptors(1,950 products)
- Ubiquitination(1,719 products)
Show 16 more subcategories
Found 66564 products of "Inhibitors"
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Kahweol Acetate
CAS:Kahweol Acetate, a semi-synthetic coffee bean derivative, inhibits osteoclasts, cancer cells, DNA damage, and oxidative stress.Formula:C22H28O4Color and Shape:SolidMolecular weight:356.46LP 12 hydrochloride hydrate
LP 12 hydrochloride hydrate: potent, selective 5-HT7 agonist (Ki: 0.13 nM); less affinity for D2, 5-HT1A/2A receptors.Formula:C32H39N3O·HCl·xH2OColor and Shape:SolidTHR-β agonist 5
CAS:THR-β agonist 5 (compound 54) is a potent THR-β agonist, with an EC 50 of <50 nM [1].Formula:C22H23N5O2Color and Shape:SolidMolecular weight:389.45PD 135158
CAS:PD 135158 is a CCK2 receptor antagonist.Formula:C42H61N5O11Purity:98%Color and Shape:SolidMolecular weight:811.96KRAS G12D inhibitor 12
KRAS G12D inhibitor 12 targets Ras protein for cancer research. (Patent WO2021108683A1, Compound 134)Formula:C23H21ClFN5O3Color and Shape:SolidMolecular weight:469.9NS2B/NS3-IN-5
Compound 25b inhibits DENV2/ZIKV NS2B/NS3 proteases; IC50: ZIKV 0.67μM, DENV2 4.38μM.Formula:C14H9IN2O3SColor and Shape:SolidMolecular weight:412.2Imolamine hydrochloride
CAS:Imolamine hydrochloride is a blood platelet aggregation antagonist.Formula:C14H21ClN4OColor and Shape:SolidMolecular weight:296.80Hsp90-IN-16
Hsp90-IN-16, a selective HSP90 inhibitor, targets HER2+ cancers with 6 μM IC50 in HCC1954 cells, blocking client proteins and inducing apoptosis.Formula:C30H26FN3O6Color and Shape:SolidMolecular weight:543.54GLS1 Inhibitor-5
GLS1 Inhibitor-5 (24y): Selective, oral glutaminase 1 inhibitor; IC50 68 nM; induces apoptosis; anti-tumor.Color and Shape:Solid8-Deazafolic acid
CAS:8-Deazafolic acid inhibits folate-dependent bacteria S. faecium & L. casei, and fights lymphoid leukemia L1210 in mice.Formula:C20H20N6O6Purity:98%Color and Shape:SolidMolecular weight:440.41XIAP/cIAP1 antagonist-1
Potent oral XIAP/cIAP1 inhibitor with EC50s: XIAP 5.1 nM, cIAP1 0.32 nM; curbs tumor growth in vivo.
Color and Shape:SolidArtemisiane E
CAS:Artemisiane E is a potent PI3K/AKT pathway inhibitor with an IC 50 of 8.9 μM .Formula:C20H22O5Color and Shape:SolidMolecular weight:342.39Antifungal agent 28
Antifungal 28 disrupts Candida, hits fluconazole-resistant strains, and inhibits biofilms.Formula:C22H29N5OSColor and Shape:SolidMolecular weight:411.56Terguride
CAS:Terguride: treats hyperprolactinemia, blocks 5-HT2A/B, activates dopamine receptors, studied for PAH.Formula:C20H28N4OColor and Shape:SolidMolecular weight:340.46GABAA receptor agonist 1
Compound 3e, a potent GABAA agonist, targets GABA sites and has potential anti-depressive effects in mice.Formula:C20H30O3Color and Shape:SolidMolecular weight:318.45ATM Inhibitor-2
ATM Inhibitor -2 is a potent and selective inhibitor of ATM (IC50<1 nM).Formula:C26H31N7O3Color and Shape:SolidMolecular weight:489.57CYP11B1-IN-2
CYP11B1-IN-2 selectively inhibits human and rat CYP11B1 (IC50: 9/25 nM) orally to research cortisol-related diseases.Color and Shape:SolidAM-3189
CAS:AM-3189: potent, selective GPR40 agonist with low CNS penetration, good pharmacokinetics, and efficacy mirroring AMG 837.Formula:C27H25ClN2O3Color and Shape:SolidMolecular weight:460.95sEH inhibitor-1
TCPU (sEH inhibitor-1) is a potent oral human sEH blocker with IC50s of 0.4 nM (human) and 5.3 nM (mouse).
Color and Shape:SolidD-Cl-amidine hydrochloride
D-Cl-amidine hydrochloride is a potent and highly selective inhibitor of PAD1. It exhibits excellent tolerance and does not induce significant toxicity [1].Formula:C14H20Cl2N4O2Color and Shape:SolidMolecular weight:347.24
