
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 37926 products of "Other Inhibitors"
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BMS-748730
CAS:<p>BMS-748730, also known as 4′-Hydroxy Dasatinib, is a Dasatinib metabolite.</p>Formula:C22H26ClN7O3SColor and Shape:SolidMolecular weight:504.01GSK065
CAS:<p>GSK065 is a potent inhibitor of kynurenine-3-monooxygenase (KMO).</p>Formula:C17H15ClN2O4Color and Shape:SolidMolecular weight:346.77ONO-8809
CAS:<p>ONO-8809: Thromboxane A2 antagonist, reduces airway hyperresponse, macrophage accumulation, and MMP-9 in SHRSP brains.</p>Formula:C30H46BrNO4SPurity:98%Color and Shape:SolidMolecular weight:596.66Antibiotic MA 144M2
CAS:<p>Antibiotic MA 144M2, an anthracycline glycoside, targets gram-positive bacteria and tumors, derived from Streptomyces and aclacinomycin A conversion.</p>Formula:C42H55NO16Color and Shape:SolidMolecular weight:829.88Symplostatin 1
CAS:<p>Symplostatin 1 is a dolastatin 10 analog from the marine cyanobacterium Symploca hydnoides.</p>Formula:C43H70N6O6SColor and Shape:SolidMolecular weight:799.12Zurletrectinib
CAS:<p>Zurletrectinib is a tyrosine kinase inhibitor with potential as an antineoplastic agent.</p>Formula:C19H19F2N7O2Color and Shape:SolidMolecular weight:415.4Anti-ToCV agent 1
<p>Anti-ToCV agent 1 can be used as a potential anti-ToCV drug.</p>Formula:C22H19FN2O5SColor and Shape:SolidMolecular weight:442.46NA 0362
CAS:<p>NA 0362 is a derivative of SF 2370 that inhibits smooth muscle contraction.</p>Formula:C28H26N4O4Color and Shape:SolidMolecular weight:482.53Methyl Streptonigrin
CAS:<p>Methyl Streptonigrin is an ABCG2 transporter function inhibitor.</p>Formula:C26H24N4O8Purity:98%Color and Shape:SolidMolecular weight:520.49PZ-3022
CAS:<p>PZ-3022 is an orally active, conformational PanK activator that counteracts C3-CoA inhibition. In a mouse model of propionic acidemia, it elevates hepatic CoASH and C2-CoA levels while reducing C3-CoA, making it useful for studying mitochondrial defects in propionic acidemia.</p>Formula:C20H21N5OColor and Shape:SolidMolecular weight:347.41DAD dichloride
<p>DAD dichloride is a 3rd-gen photoelectric switch, blocks K+ channels, and helps in visual function research.</p>Formula:C26H42Cl2N6OColor and Shape:SolidMolecular weight:525.56GSK579289A
CAS:<p>GSK579289A is an inhibitor of benzimidazole thiophene.</p>Formula:C26H27ClN4O3SPurity:98%Color and Shape:SolidMolecular weight:511.04Peridinin
CAS:<p>Peridinin is an exceptionally potent and membrane-embedded inhibitor of bilayer lipid peroxidation.</p>Formula:C39H50O7Color and Shape:SolidMolecular weight:630.81RK-582
CAS:<p>RK-582: oral spiroindolinone tankyrase inhibitor, halts colon cancer growth in COLO-320DM mouse model.</p>Formula:C27H35FN6O3Color and Shape:SolidMolecular weight:510.6AKR1C3-IN-8
<p>AKR1C3-IN-8 (Compound 5) is an effective and selective AKR1C3 inhibitor (IC50=0.069 μM). AKR1C3-IN-8 has antitumor activity.</p>Formula:C23H20N4O3Color and Shape:SolidMolecular weight:400.43ALK5-IN-7
CAS:<p>ALK5-IN-7 inhibits ALK5, useful in TGF-β disease research like cancer, fibrosis, and autoimmune disorders. See WO2021129621A1.</p>Formula:C26H28N4O3SColor and Shape:SolidMolecular weight:476.59Medermycin
CAS:<p>Lactoquinomycin A is a quinone antibiotic displaying activity against Gram-positive bacteria and some Gram-negative bacteria, though its efficacy is weaker against the latter and it is ineffective against fungi. It inhibits various cell lines, including lymphoma L5178Y progenitor cells, doxorubicin-resistant cells, bleomycin-resistant cells, human leukemia K562 cells, murine leukemia L-1210 cells, and murine leukemia P388 cells, with ID50 values (μg/mL) of 0.02, 0.006, 0.008, 0.033, 0.013, and 0.03, respectively.</p>Formula:C24H27NO8Color and Shape:SolidMolecular weight:457.473G-9791
CAS:<p>G-9791 is an effective and selective inhibitor of group-I PAK.</p>Formula:C26H26ClFN6O2Purity:98%Color and Shape:SolidMolecular weight:508.98BMS-554417
CAS:<p>BMS-554417 inhibits IGF-IR/insulin receptors, curbing cell proliferation and tumor growth, with IC50 values of 120 nm–>8.5 μmol/L.</p>Formula:C28H30ClN7O2Color and Shape:SolidMolecular weight:532.04PI3K-IN-27
CAS:<p>PI3K-IN-27 is a potent PI3K inhibitor, relevant for cancer and immune disease research. See patent WO2021233227A1.</p>Formula:C30H26F2N6O2SColor and Shape:SolidMolecular weight:572.63L-Tyrosyl-L-glutamic acid
CAS:<p>L-Tyrosyl-L-glutamic acid acts as an inhibitor of the amino acid permease GAP1.</p>Formula:C14H18N2O6Color and Shape:SolidMolecular weight:310.3Tzc 5665
CAS:<p>Tzc 5665 is a pyridazinone derivative with vasodilatory and beta-adrenergic blocking activities and type III phosphodiesterase inhibitory action.</p>Formula:C31H38ClN5O7Color and Shape:SolidMolecular weight:628.12PI4KIIIbeta-IN-11
CAS:<p>PI4KIIIbeta-IN-11 is a PI4KIIIβ inhibitor (mean pIC50=9.1) that can be used to study diseases caused by RNA viruses and Plasmodium falciparum.</p>Formula:C33H39N7O3Color and Shape:SolidMolecular weight:581.71Pyrisulfoxin A
CAS:<p>Pyrisulfoxin A is an antibiotic that can be found in Streptomyces callfornicus [BS-75].</p>Formula:C13H13N3O3SColor and Shape:SolidMolecular weight:291.326Megovalicin A
CAS:<p>Megovalicin A is effective against Bacillus subtilis and Escherichia coli.</p>Formula:C35H63NO8Color and Shape:SolidMolecular weight:625.88NSC 357754
CAS:<p>NSC 357754 is an inhibitor of Claudin. It can enhance transepithelial electrical resistance and reduce specific cation permeability. NSC 357754 is useful for research involving Claudin-2 and/or Claudin-15 mediated intestinal disorders.</p>Formula:C26H20N4O2Color and Shape:SolidMolecular weight:420.463Z57346765
CAS:<p>Z57346765 is a specific PGK1 inhibitor that inhibits PGK1-dependent cell proliferation by decreasing the metabolic enzyme activity of PGK1 during glycolysis.</p>Formula:C17H18N4OPurity:99.85%Color and Shape:SolidMolecular weight:294.35PRN694
CAS:<p>PRN694 is a potent, irreversible ITK/RLK inhibitor with IC50s: 0.3/1.4 nM; offers lasting effector cell suppression.</p>Formula:C28H35F2N5O2SPurity:98%Color and Shape:SolidMolecular weight:543.67LX2761
CAS:<p>LX2761 is a stable inhibitor for SGLT1/2 with IC50s of 2.2/2.7 nM; it targets SGLT1 in the GI tract.</p>Formula:C32H47N3O6SPurity:98%Color and Shape:SolidMolecular weight:601.80Gentamicin C1
CAS:<p>Gentamicin C1 is a broad-spectrum aminoglycoside antibiotic with antibacterial activity.</p>Formula:C21H43N5O7Color and Shape:SolidMolecular weight:477.595Hymenidin
CAS:<p>Hymenidin, isolated from the Okinawan sponge Hymeniacidon sp., is a 5-hydroxytryptaminergic receptor antagonist and voltage-gated potassium channel inhibitor.</p>Formula:C11H12BrN5OPurity:96.85% - 99.52%Color and Shape:SolidMolecular weight:310.15Oiligodendrocyte differentiation promoter 1
CAS:<p>Oiligodendrocyte differentiation promoter 1 is a promoter of oiligodendrocyte differentiation .</p>Formula:C25H25Cl2NO5Purity:98%Color and Shape:SolidMolecular weight:490.38Zetomipzomib
CAS:<p>KZR-616: Immunoproteasome inhibitor targeting LMP7 (IC50: 39/57 nM) & LMP2 (IC50: 131/179 nM), potential in autoimmune disease research.</p>Formula:C30H42N4O8Color and Shape:SolidMolecular weight:586.68SID 125240931
CAS:<p>SID 125240931 is a regulator of fluorine-activated proteins (FAPs). This compound disrupts the binding between fluoride and FAPs.</p>Formula:C19H24N4O3SColor and Shape:SolidMolecular weight:388.48UCN-02
CAS:<p>UCN-02 (7-epi-Hydroxystaurosporine) is a PKC inhibitor produced by Streptomyces N-126 strain, which inhibits PKA.</p>Formula:C28H26N4O4Purity:98%Color and Shape:SolidMolecular weight:482.53Epithienamycin F
CAS:<p>Epithienamycin F is a carbapenem antibiotic with activity against both Gram-positive and Gram-negative bacteria.</p>Formula:C13H18N2O8S2Color and Shape:SolidMolecular weight:394.421ZL-Pin13
CAS:<p>ZL-Pin13: potent Pin1 inhibitor (IC50: 67 nM), halts MDA-MB-231 cell growth, reduces Pin1 substrates.</p>Formula:C24H23ClN2O3SColor and Shape:SoildMolecular weight:454.97Leucomycin A7
CAS:<p>Leucomycin A7 is a component of the leucomycin complex, isolated from *Streptomyces kitasatoensis*. It possesses antibacterial activity, effectively inhibiting the growth of gram-positive bacteria, while its inhibitory effect on gram-negative bacteria is comparatively weaker.</p>Formula:C38H63NO14Color and Shape:SolidMolecular weight:757.905Melanocin A
CAS:<p>Melanocin A is an inhibitor of melanin biosynthesis. It suppresses the synthesis of melanin and tyrosinase with an IC50 of 9.0 nM and MIC of 0.9 μM. Additionally, Melanocin A exhibits antioxidant properties.</p>Formula:C18H14N2O5Color and Shape:SolidMolecular weight:338.31Salfredin C1
CAS:<p>Salfredin C1 is an inhibitor of aldose reductase.</p>Formula:C13H11NO6Color and Shape:SolidMolecular weight:277.229Fleephilone
CAS:<p>Fleephilone is a fungal metabolite isolated from Trichoderma harzianum. It acts as an HIV REV/RRE binding inhibitor, hindering the interaction between REV protein and RRE RNA with an IC50 of 7.6 μM.</p>Formula:C24H27NO7Color and Shape:SolidMolecular weight:441.474Fusarielin A
CAS:<p>Fusarielin A is a natural product found in the genus Fusarium.</p>Formula:C25H38O4Color and Shape:SolidMolecular weight:402.57GNE-203
CAS:<p>GNE-203 is a Met inhibitor.</p>Formula:C30H29Cl2F3N8O3Color and Shape:SolidMolecular weight:677.50MSK-195
CAS:<p>MSK-195 is an effective TRPV1 agonist.</p>Formula:C28H40N2O5Purity:98%Color and Shape:SolidMolecular weight:484.63PEN-866
CAS:<p>PEN-866, a conjugate of HSP90i and SN-38, may control early NSCLC tumor growth.</p>Formula:C49H49N7O9Color and Shape:SolidMolecular weight:879.95Pyridoxatin
CAS:<p>Pyridoxatin: fungal metabolite; blocks TBARS production, prevents AAPH-induced hemolysis, and acts against C. albicans.</p>Formula:C15H21NO3Color and Shape:SolidMolecular weight:263.33PF1070A
CAS:<p>PF1070A is a natural cyclic tetrapeptide HDAC Inhibitor through the inhibition of PfHDAC1 catalytic activity, potently inducing the synthesis of metallothionein</p>Formula:C31H44N4O6Color and Shape:SolidMolecular weight:568.7SX 3202
CAS:<p>SX 3202 is an aldose reductase inhibitor being developed for the treatment of diabetic neuropathy.</p>Formula:C17H11BrFN3O4Color and Shape:SolidMolecular weight:420.19P-gp inhibitor 2
CAS:<p>Potent P-gp inhibitor 2 reverses Doxorubicin resistance in colorectal carcinoma cells with IC50 of 0.22 µM.</p>Formula:C29H26N2O6Color and Shape:SolidMolecular weight:498.53JBIR-22
CAS:<p>JBIR-22 is a natural inhibitor for protein−protein interaction of the homodimer of proteasome assembly factor 3.</p>Formula:C23H33NO6Color and Shape:SolidMolecular weight:419.51

