
Other Inhibitors
This category encompasses a wide variety of inhibitors that do not fit into the standard classifications but are still critical for various biochemical and pharmacological research. These inhibitors may target unique or less-studied pathways, enzymes, and molecular interactions, providing valuable tools for specialized research areas. At CymitQuimica, we offer a diverse selection of high-quality inhibitors across multiple biological targets and research disciplines, enabling you to explore novel therapeutic avenues and deepen your understanding of complex biological processes.
Found 35802 products of "Other Inhibitors"
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Tyrosyl-alanyl-N-(1,3-dimethylbutyl)glycinamide
CAS:Tyrosyl-alanyl-N-(1,3-dimethylbutyl)glycinamide is a mu-opiate receptor agonist.Formula:C20H32N4O4Color and Shape:SolidMolecular weight:392.49MDK80908
CAS:MDK80908 (CAS# 1821380-90-8), a dual PPARα/γ agonist, improves insulin resistance and gluconeogenesis.Formula:C21H43NO2SColor and Shape:SolidMolecular weight:373.64CH 402
CAS:CH 402 inhibits lipid peroxidation.Formula:C12H15NNaO3SColor and Shape:SolidMolecular weight:276.31Ixazomib citrate EtOH
CAS:Ixazomib citrate (MLN9708), a prodrug of Ixazomib, is an oral, next-gen proteasome inhibitor with enhanced anti-cancer properties.Formula:C22H29BCl2N2O10Color and Shape:SolidMolecular weight:563.188SMTIN-P01
CAS:SMTIN-P01: Mitochondria-targeted Hsp90 inhibitor with triphenylphosphonium replacing PU-H71's isopropyl amine.Formula:C36H34BrIN5O2PSColor and Shape:SolidMolecular weight:838.5432ATM-1001
CAS:ATM-1001 is an inhibitor of the cancer-associated tropomyosin 3.1 (Tpm3.1), suppressing glucose-stimulated insulin secretion (GSIS) from the pancreatic islets.Formula:C30H36N4OColor and Shape:SolidMolecular weight:468.63Lck-IN-1
CAS:Lck-IN-1 is a potent inhibitor of lymphocyte protein tyrosine kinase (Lck) [1].Formula:C14H15N5Color and Shape:SolidMolecular weight:253.3UCB-6786
CAS:UCB-6786 inhibits TNF signaling by stabilizing asymmetric trimer form, showing selectivity and a dose-response.Formula:C16H16N2OColor and Shape:SolidMolecular weight:252.31FE-999024 free base
CAS:FE-999024 is a selective tissue kalkinase-like inhibitor that significantly inhibits plasma kalkinase-like activity in the pancreas.Formula:C26H31ClN6O2Color and Shape:SolidMolecular weight:495.02Pranolium
CAS:Pranolium is a quaternary dimethyl derivative of Propranolol, a well-known powerful betareceptor-blocking agent.Formula:C18H26NO2Color and Shape:SolidMolecular weight:288.41QD325
CAS:QD325 is a potent redox modulator treating Pancreatic Ductal Adenocarcinoma, inducing stress responses in cancer cells.Formula:C20H13N3O2Purity:98%Color and Shape:SolidMolecular weight:327.34BPyO-34
CAS:BPyO-34 is a novel apoptosis signal-regulating kinase 1 (ASK1) inhibitor with IC50 of 0.52μM in vitro in kinase assay.Formula:C32H29FN2O5SColor and Shape:SolidMolecular weight:572.65Kahweol palmitate
CAS:Kahweol palmitate, a semi-synthetic from coffee, blocks bone deterioration, cancer growth, DNA damage, and oxidative stress.Formula:C36H56O4Color and Shape:SolidMolecular weight:552.83CYP1A1 inhibitor 8a
CAS:CYP1A1 inhibitor 8a blocks B[a]P activation of AhR in yeast, shields human cells from B[a]P harm.Formula:C17H17NO4Color and Shape:SolidMolecular weight:299.32Ambenoxan
CAS:Ambenoxan is a centrally acting muscle relaxant.Formula:C14H21NO4Color and Shape:SolidMolecular weight:267.32Sulfonyl quinoxaline 1
CAS:Sulfonyl quinoxaline 1 is an inhibitor of RhoG-hepcidin uptake.Formula:C14H9ClN2O2SColor and Shape:SolidMolecular weight:304.75CV 6504
CAS:CV 6504 is a dual inhibitor of thromboxane A2 synthetase and 5-lipoxygenase. It also possesses oxygen scavenging activity.Formula:C15H15NO2Color and Shape:SolidMolecular weight:241.29N 0745
CAS:N 0745 inhibits 2-[125I]-iodomelatonin binding to median eminence/pars tuberalis membranes with an affinity similar to that of melatonin.Formula:C20H22N2O2Color and Shape:SolidMolecular weight:322.4Valyl-ochratoxin A
CAS:Valyl-ochratoxin A is a phenylalanyl moiety of ochratoxin A replaced by valine. It is a yeast valyl-tRNA synthetase inhibitor.Formula:C16H18ClNO6Purity:98%Color and Shape:SolidMolecular weight:355.77SAHA-BPyne
CAS:SAHA is an HDAC inhibitor; its derivative SAHA-BPyne labels proteins in cells/proteomes, used in click chemistry, with an IC50 of ~3 μM.Formula:C27H31N3O5Color and Shape:SolidMolecular weight:477.55
