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 35861 products of "Other Inhibitors"
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Polyoxin E
CAS:Polyoxin E is a nucleoside antifungal antibiotic that demonstrates significant effectiveness against rice sheath blight.Formula:C17H23N5O13Color and Shape:SolidMolecular weight:505.39TSWV-IN-1
TSWV-IN-1 is an anti-TSWV drug with potential TSWV N.Formula:C26H31FO4S2Color and Shape:SolidMolecular weight:490.65FCE-24379
CAS:FCE-24379 is a selective antagonist of vascular serotonin receptors that has been shown to lowers blood pressure in hypertensive rats.Formula:C20H22N4O2Color and Shape:SolidMolecular weight:350.41AB 5046A
CAS:AB 5046A is a chlorosis inducing substance isolated from Nodulisporium SP.Formula:C10H14O4Color and Shape:SolidMolecular weight:198.22P-gp modulator 1
CAS:P-gp modulator 1 is a high affinity and orally available P-glycoprotein (Pgp) modulatorFormula:C41H72N2O6Purity:98%Color and Shape:SolidMolecular weight:689.02Lipohexin
CAS:Lipohexin is a peptide antibiotic that exhibits activity against Gram-positive bacteria. It competitively inhibits human placental proline endopeptidase (proline endopeptidase) with an IC50 of 3.5 μM. Additionally, Lipohexin inhibits proline endopeptidase from Flavobacterium meningosepticum, with an IC50 of 25 μM.Formula:C39H68N6O9Color and Shape:SolidMolecular weight:764.992AZD-4121 tert-butylammonium
CAS:AZD-4121 tert-butylammonium is an oral cholesterol absorption inhibitor targeting NPC1L1 for the treatment of dyslipidaemia.Formula:C40H50F2N4O7SColor and Shape:SolidMolecular weight:768.91Griseolic acid C
CAS:Griseolic acid C (Dihydrodeoxygriseolic acid) is an antibiotic found in the Streptomyces griseoaurantiacus SANK43894 strain. This compound is a potent inhibitor of cyclic adenosine monophosphate (cAMP) phosphodiesterase [EC 3.1.4.17], with an IC50 of 0.12 μM (enzyme sourced from rat brain tissue).Formula:C14H15N5O7Color and Shape:SolidMolecular weight:365.298PPARα agonist 1
PPARα agonist 1 is a complete and potent PPARα agonist.Formula:C27H34O4Color and Shape:SolidMolecular weight:422.56PTP1B-IN-18
PTP1B-IN-18 is an orally active, fully mixed protein tyrosine phosphatase 1B (PTP1B) inhibitor (Ki: 35.2 μM).PTP1B-IN-18 can be used to study type 2 diabetes.Formula:C26H19N3O4SColor and Shape:SolidMolecular weight:469.51Mifepristone methochloride
CAS:Mifepristone methochloride is a glucocorticoid antagonist. This product will be sold for research use only.Formula:C30H38ClNO2Color and Shape:SolidMolecular weight:480.08LGB-321 HCl
CAS:LGB-321: potent, selective PIM kinase inhibitor, active against PIM2, halts diverse blood cancers' growth, orally effective in mice.Formula:C23H23ClF3N5O2Color and Shape:SolidMolecular weight:493.9122-HDHA
CAS:22-HDHA is an oxidation product of docosahexaenoic acid .Formula:C22H32O3Color and Shape:SolidMolecular weight:344.49Enpp-1-IN-12
ENPP1-IN-12 is a potent, oral ENPP1 inhibitor with a Ki of 41 nM and anti-tumor properties.Formula:C17H19N5O3SColor and Shape:SolidMolecular weight:373.43Fosfocytocin
CAS:Fosfocytocin can be found in the Pseudomonas fluorescens strain PK-52 and exhibits very weak antibacterial activity.Formula:C12H20N4O13P2Color and Shape:SolidMolecular weight:490.254Azicemicin A
CAS:Azicemicin A exhibits mild antibacterial activity and shows no acute toxicity when administered via intraperitoneal injection to mice at a dosage of 150 mg/kg.Formula:C23H25NO9Color and Shape:SolidMolecular weight:459.446Chandrananimycin C
CAS:Chandrananimycin C exhibits activity against Mucor fungi and demonstrates anti-tumor properties against cancer cell lines such as CCL HT29, MFXF 529L, and MACL McF-7.Formula:C17H16N2O3Color and Shape:SolidMolecular weight:296.32SPR7
SPR7 is a potent and selective rhodesain inhibitor (Ki: 0.51 nM). SPR7 exhibited antiparasitic effects against T. b. brucei (EC50: 1.65 μM).Formula:C30H32ClN3O3Color and Shape:SolidMolecular weight:518.05Leucomycin A9
CAS:Leucomycin A9 is a macrolide antibiotic known for its potent activity against Gram-positive bacteria. It is also effective against spirochetes, rickettsiae, and chlamydiae.Formula:C37H61NO14Color and Shape:SolidMolecular weight:743.878Salfredin C1
CAS:Salfredin C1 is an inhibitor of aldose reductase.Formula:C13H11NO6Color and Shape:SolidMolecular weight:277.229
