
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 35858 products of "Other Inhibitors"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
PBX-7011
CAS:PBX-7011, an active camptothecin derivative, binds to the DDX5 protein in cells and induces cell death through DDX5 protein degradation [1].Formula:C24H21N3O6Color and Shape:SolidMolecular weight:447.44MPro N3
CAS:Mpro inhibitor blocks MHV-A29, HCoV-229E, FOPV (IC50: 2.7–8.8 μM), and SARS-CoV-2 (IC50: 16.8 μM) in plaque assays.Formula:C35H48N6O8Color and Shape:SolidMolecular weight:680.79ND-654
CAS:ND-654 is an acetyl CoA carboxylase inhibitor.Formula:C29H33N3O8SColor and Shape:SolidMolecular weight:583.65Steroid sulfatase/17β-HSD1-IN-4
Steroid sulfatase/17β-HSD1-IN-4 (compound 37) is a potent dual inhibitor of steroid sulfatase ( STS ) and 17β-hydroxysteroid dehydrogenase type 1 ( 17β HSD1 ).Formula:C18H17N3O4S2Color and Shape:SolidMolecular weight:403.489-O-Demethyltrigonostemone
CAS:9-O-Demethyltrigonostemone is a natural IDO1 inhibitor, cytotoxic and antiplasmodial agent from the Roots of Strophioblachia fimbricalyx.Formula:C19H20O4Color and Shape:SolidMolecular weight:312.36Metocurine chloride
CAS:Metocurine: a muscle relaxant, not for kidney failure patients as it's kidney-excreted.Formula:C40H48Cl2N2O6Color and Shape:SolidMolecular weight:723.72LH secretion antagonist 1
CAS:LH secretion antagonist 1 is an antagonist of luteinizing hormone secretion with analgesic activity.Formula:C18H24ClNO2Purity:98%Color and Shape:SolidMolecular weight:321.84Methyl 5-thia-6,8,11,14-eicosatetraenoate
CAS:Methyl 5-thia-6,8,11,14-eicosatetraenoate is a bioactive chemical.Formula:C20H32O2SColor and Shape:SolidMolecular weight:336.53Luminacin G2
CAS:Luminacin G2 exhibits potent inhibitory effects on capillary formation (IC50 < 0.1 μg/mL).Formula:C25H36O8Color and Shape:SolidMolecular weight:464.55Oxamicetin
CAS:Oxamicetin is a nucleoside antibiotic with antibacterial and antimycobacterial properties.Formula:C29H42N6O10Color and Shape:SolidMolecular weight:634.678Cyclophellitol
CAS:Cyclophellitol is an inhibitor of β-glycosidase, with an IC50 of 0.8 μg/mL.Formula:C7H12O5Color and Shape:SolidMolecular weight:176.167Panclicin B
CAS:Panclicin B is an effective inhibitor of pancreatic lipase (pancreaticlipase).Formula:C26H47NO5Molecular weight:453.65511β-Hydroxy-17α-methyltestosterone
CAS:11β-Hydroxy-17α-methyltestosterone is a metabolite of 17α-methyltestosterone.Formula:C20H30O3Color and Shape:SolidMolecular weight:318.45PF-06305591 dihydrate
PF-06305591 dihydrate is a potent and highly selective voltage gated sodium channel NaV1.8 blocker (IC 50 = 15 nM) with an excellent preclinical in vitro ADMEFormula:C15H26N4O3Color and Shape:SolidMolecular weight:310.39Anti-ToCV agent 1
Anti-ToCV agent 1 can be used as a potential anti-ToCV drug.Formula:C22H19FN2O5SColor and Shape:SolidMolecular weight:442.46Plumbemycin B
CAS:Plumbemycin B is isolated from Streptomyces plumbeus; an L-threonine antagonist.Formula:C12H21N4O8PColor and Shape:SolidMolecular weight:380.29Sannamycin G
CAS:Sannamycin G (Istamycin X0) is an aminoglycoside antibiotic that exhibits only weak antibacterial activity against a limited range of bacteria.Formula:C14H30N4O4Color and Shape:SolidMolecular weight:318.412RSV-IN-5
CAS:RSV-IN-5: Dual inhibitor for RSV fusion proteins, effective on wild-type A2 and D486N mutant with EC50s of 2.0 nM & 8.1 nM. Potent anti-RSV.Formula:C28H37N7O2Color and Shape:SolidMolecular weight:503.64NAZ2329
CAS:NAZ2329: Cell-permeable, targets R5 RPTPs, inhibits hPTPRZ1 (IC50=7.5 μM) & hPTPRG (IC50=4.8 μM), hampers glioblastoma growth, affects stem cell traits.Formula:C21H18F3NO4S3Color and Shape:SoildMolecular weight:501.56Calphostin A
CAS:Calphostins, from Cladosporium fungus, inhibit PKC; calphostin C is most potent, used as a biochemical tool.Formula:C44H38O12Color and Shape:SolidMolecular weight:758.77

