
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 37921 products of "Other Inhibitors"
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Deldeprevir Na
CAS:<p>Deldeprevir Na is an Antiviral Polyprotein cleavage inhibitor. HCV NS3/4A inhibitor.</p>Formula:C45H55F2N6NaO8S2Color and Shape:SolidMolecular weight:933.08Phyllosinol
CAS:<p>Phyllosinol is an antifungal antibiotic.</p>Formula:C7H8O4Color and Shape:SolidMolecular weight:156.136Echinocandin B nucleus
CAS:<p>Echinocandin B nucleus (A-30912 A nucleus) is the reaction product catalyzed by Echinocandin B decarboxylase. It serves as an intermediate in the semisynthetic production of antifungal agents.</p>Formula:C34H51N7O15Color and Shape:SolidMolecular weight:797.807NVP-CFC218
CAS:<p>NVP-CFC218 is a novel potent and selective p53-HDM2 inhibitor.</p>Formula:C37H45ClN4O4Color and Shape:SolidMolecular weight:645.23Pinselin
CAS:<p>Pinselin is a nitrogen-containing heterocyclic antibiotic with yeast-inhibiting properties.</p>Formula:C16H12O6Color and Shape:SolidMolecular weight:300.263Cedarmycin B
CAS:<p>Cedarmycin B exhibits activity against Candida, Cryptococcus neoformans, and Aspergillus fumigatus, with a minimum inhibitory concentration (MIC) ranging from 12.5 to 50 μg/mL.</p>Formula:C12H18O4Color and Shape:SolidMolecular weight:226.269Anticancer agent 78
<p>Anticancer agent 78: anti-aromatase (IC50=0.9 μM), cytotoxic, potential in breast cancer research.</p>Formula:C19H14BrNO4Color and Shape:SolidMolecular weight:400.22E-3030 free acid
CAS:<p>E-3030 free acid, a PPAR agonist, lowers blood glucose, triglycerides, and insulin; boosts adiponectin; reduces apo C-III; and raises lipoprotein lipase.</p>Formula:C22H23ClFNO5Purity:98%Color and Shape:SolidMolecular weight:435.87Glucosylquestiomycin
CAS:<p>Glucosylquestiomycin exhibits activity against Gram-positive bacteria, Gram-negative bacteria, and yeast.</p>Formula:C18H18N2O7Color and Shape:SolidMolecular weight:374.345GSK065
CAS:<p>GSK065 is a potent inhibitor of kynurenine-3-monooxygenase (KMO).</p>Formula:C17H15ClN2O4Color and Shape:SolidMolecular weight:346.77Deoxyfrenolicin
CAS:<p>Deoxyfrenolicin is a quinone antibiotic that can be isolated from the fermentation broth of the Streptomyces roseofulvus strain AM-3867 and belongs to the frenolicin class of antibiotics. This compound exhibits in vitro antibacterial activity and is effective in inhibiting the activity of Mycoplasma gallisepticum.</p>Formula:C18H18O6Color and Shape:SolidMolecular weight:330.332DGY-08-097
CAS:<p>DGY-08-097: potent HCV NS3 degrader, low resistance risk, strong inhibition in cells, DC50 of 50nM at 4h.</p>Formula:C60H76N10O14Color and Shape:SolidMolecular weight:1161.3T-3861174
CAS:<p>T-3861174 is a prolyl tRNA synthetase (PRS) inhibitor, exhibiting significant in vitro anti-tumor activity with GCN2-ATF4 pathway activation.</p>Formula:C26H25FN6O2Color and Shape:SolidMolecular weight:472.51L 668750
CAS:<p>L 668750 is an inhibitor of platelet-activating factor.</p>Formula:C25H34O9SPurity:98%Color and Shape:SolidMolecular weight:510.6Efrapeptin F
CAS:<p>Efrapeptin F, from Tolypocladium fungi, inhibits mitochondrial complex V and targets nutrient-deprived tumor cells.</p>Formula:C82H141N18O16Color and Shape:SolidMolecular weight:1635.11Glucoallosamidin A
CAS:<p>Glucoallosamidin A is a glycoside antibiotic that inhibits chitinase activity. It effectively suppresses the chitinase enzyme in Candida albicans [ATCC 10231], exhibiting an IC50 of 3.4 μg/mL.</p>Formula:C26H44N4O14Color and Shape:SolidMolecular weight:636.646Henagliflozin
CAS:<p>Henagliflozin (SHR3824): an oral, selective SGLT2 inhibitor, weak on SGLT1.</p>Formula:C22H24ClFO7Color and Shape:SolidMolecular weight:454.87Resorcinomycin A
CAS:<p>Resorcinomycin A is an antibiotic with potent antimycobacterial activity and relatively weaker activity against mycoplasma.</p>Formula:C14H20N4O5Color and Shape:SolidMolecular weight:324.332DWN-12088 HCl
CAS:<p>DWN-12088 HCl is the salt form of DWN-12088 Free Base, an orally administered small molecule prolyl-tRNA synthetase (PRS) inhibitor</p>Formula:C15H21Cl4N3OColor and Shape:SolidMolecular weight:401.15Feigrisolide C
CAS:<p>Feigrisolide C is a lactone produced by the bacterium Streptomyces griseus.</p>Formula:C21H36O7Color and Shape:SolidMolecular weight:400.506Aeruginosin 98-B
CAS:<p>Aeruginosin 98-B, a protease inhibitor, effectively inhibits trypsin, plasmin, and thrombin with IC50 values of 0.6, 7.0, and 10.0 μg/mL, respectively.</p>Formula:C29H46N6O9SColor and Shape:SolidMolecular weight:654.78Megovalicin A
CAS:<p>Megovalicin A is effective against Bacillus subtilis and Escherichia coli.</p>Formula:C35H63NO8Color and Shape:SolidMolecular weight:625.88KT5926
CAS:<p>KT5926 selectively inhibits myosin light chain kinase and NGF-dependent neurite growth; it's a K-252a analogue.</p>Formula:C30H27N3O6Purity:98%Color and Shape:SolidMolecular weight:525.5517β-HSD1-IN-1
<p>17β-HSD1-IN-1 (Compound 1) can be used in the non-small cell lung cancer (NSCLC) research.</p>Formula:C21H21NO3Color and Shape:SolidMolecular weight:335.411-Demethyltomaymycin
CAS:<p>11-Demethyltomaymycin is an antibiotic that exhibits antiviral activity against Escherichia coli T1 and T3 bacteriophages, along with antibacterial properties against Gram-positive bacteria. Furthermore, it shows cytotoxic effects on leukemia L1210 cells.</p>Formula:C15H18N2O4Color and Shape:SolidMolecular weight:290.314PKG1α activator 3
<p>PKG1α activator 3 is a PKG1α activator (EC50basal/partial=13/0.52 μM).</p>Formula:C27H26Cl2N2O6Color and Shape:SolidMolecular weight:545.41CYP1B1-IN-2
<p>CYP1B1-IN-2 (compound 9j) is a highly potent and selective inhibitor of CYP1B1, a cytochrome P450 enzyme. It exhibits an IC50 value of 0.52 nM [1].</p>Formula:C20H11F3O2Color and Shape:SolidMolecular weight:340.3Bulgecin A
CAS:<p>Bulgecin A is an inhibitor of binuclear metallo-beta-lactamases and Lytic transglycosolase.</p>Formula:C16H29N3O14S2Color and Shape:SolidMolecular weight:551.54Retelliptine
CAS:<p>Retelliptine, a DNA topoisomerase II inhibitor, is used potentially for the treatment of cancer.</p>Formula:C25H32N4OPurity:98%Color and Shape:SolidMolecular weight:404.55Polyoxin J
CAS:<p>Polyoxin J is a nucleoside antifungal antibiotic, notably effective against sheath blight in rice.</p>Formula:C17H25N5O12Molecular weight:491.41L 739749
CAS:<p>L 739749 is a CAAX peptidomimetic. It is also an inhibitor of farnesyl-protein transferase.</p>Formula:C24H41N3O6S2Purity:98%Color and Shape:SolidMolecular weight:531.73Flavomycoin
CAS:<p>Flavomycoin is an antibiotic known for its antifungal properties.</p>Formula:C40H66O12Color and Shape:SolidMolecular weight:738.945Antiviral agent 7
<p>Antiviral agent 7 is a peptide-based coating that kills viruses.</p>Formula:C29H31F2N3O6Color and Shape:SolidMolecular weight:555.57Glaucarubin
CAS:<p>Glaucarubin is a bitter lactone naturally found in the fruits of Simaruba glauca. It is employed as an anti-amebic agent in research focused on amebiasis. The compound exhibits good tolerability, with a median lethal dose (LD50) of 1,600 mg/kg in mice and 6,400 mg/kg in rats.</p>Formula:C25H36O10Molecular weight:496.55Ambelline
CAS:<p>Ambelline has antitumor activity.</p>Formula:C18H21NO5Purity:98%Color and Shape:SolidMolecular weight:331.36Carbacyclin
CAS:<p>Carbacyclin, a PGI2 analog, is a prostacyclin (PGI2) receptor agonist and vasodilator with potent inhibitory platelet aggregation.</p>Formula:C21H34O4Purity:98%Color and Shape:SolidMolecular weight:350.49DN-F01
<p>DN-F01 exhibits a potent calcium-dependent inhibitory effect on cardiac myofibrillar ATPase activity, with an IC50 of 11 ± 4 nmol/L.</p>Formula:C22H16N2O2Color and Shape:SolidMolecular weight:340.37GR-112000
CAS:<p>GR-112000 is a peptide-based tachykinin NK2 receptor antagonist.</p>Formula:C30H36N6O3Color and Shape:SolidMolecular weight:528.652-n-Heptyl-4-quinolinol
CAS:<p>2-n-Heptyl-4-quinolinol exhibits activity against Candida albicans, Staphylococcus aureus, Vibrio anguillarum, and Vibrio harveyi.</p>Formula:C16H21NOColor and Shape:SolidMolecular weight:243.34β-Prumycin hydrochloride
CAS:<p>β-Prumycin hydrochloride is a carbohydrate antibiotic that exhibits antifungal properties and possesses mild antibacterial activity.</p>Formula:C8H19Cl2N3O4Color and Shape:SolidMolecular weight:292.16Haliangicin A
CAS:<p>Haliangicin A exhibits antifungal activity against filamentous fungi and also affects oomycetes, though it does not possess antibacterial properties.</p>Formula:C22H32O5Color and Shape:SolidMolecular weight:376.49METTL3-IN-2
CAS:<p>METTL3-IN-2, a potent METTL3 inhibitor, exhibits an IC50 value of 6.1 nM, effectively impairing the proliferation of Caov3 cancer cells.</p>Formula:C25H26N8OColor and Shape:SolidMolecular weight:454.53Methylenomycin A
CAS:<p>Methylenomycin A is a cyclopentanone-derived antibiotic effective against both Gram-negative and Gram-positive bacteria.</p>Formula:C9H10O4Color and Shape:SolidMolecular weight:182.173Cytochalasin G
CAS:<p>Cytochalasin G exhibits reversible inhibition of cytokinesis and also inhibits macrophage phagocytosis and exocytosis, among other biological activities.</p>Formula:C29H34N2O4Color and Shape:SolidMolecular weight:474.591Acetoxycycloheximide
CAS:<p>Acetoxycycloheximide triggers TNF receptor 1, prompts apoptosis, and cytochrome c release by activating c-Jun N-terminal kinase.</p>Formula:C17H25NO6Color and Shape:SolidMolecular weight:339.38Dehydroindapamide
CAS:<p>Dehydroindapamide, an indole form of Indapamide, is utilized to quantify the turnover rate of Indapamide in CYP3A4, which is approximately 10 times higher than that of Indoline, with slightly enhanced affinity for CYP3A4.</p>Formula:C16H14ClN3O3SColor and Shape:SolidMolecular weight:363.82Pacidamycin D
CAS:<p>Pacidamycin D is an antibiotic of the Pacidamycin class, demonstrating activity against Pseudomonas aeruginosa with a minimum inhibitory concentration (MIC) of 4-16 μg/mL. It shows no efficacy against other Gram-negative or Gram-positive bacteria, nor does it affect drug-resistant strains of Pseudomonas aeruginosa.</p>Formula:C32H41N9O10Color and Shape:SolidMolecular weight:711.722(R)-NVS-ZP7-4
CAS:<p>(R)-NVS-ZP7-4, an R-isomer, inhibits ZIP7 to study ER zinc impact & Notch pathway.</p>Formula:C28H28FN5OSPurity:98%Color and Shape:SolidMolecular weight:501.62(±)-ANAP hydrochloride (1185251-08-4 free base)
<p>(±)-ANAP hydrochloride is the amino acid analog of prodan. It can be used as a fluorescent probes and enhance environmental sensitivity.</p>Formula:C15H17ClN2O3Purity:98%Color and Shape:SolidMolecular weight:308.76AZ-PFKFB3-67 quarterhydrate
<p>AZ-PFKFB3-67 quarterhydrate inhibits PFKFB3 (IC50: 11 nM), PFKFB2 (159 nM), and PFKFB1 (1130 nM).</p>Formula:C26H27N5O4Color and Shape:SolidMolecular weight:460.01

