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 36042 products of "Other Inhibitors"
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PD-1/PD-L1-IN-23
CAS:PD-1/PD-L1-IN-23: potent, oral PD-1/PD-L1 inhibitor; L7's ester prodrug; exhibits strong antitumor effects.Formula:C32H30BrCl2N3O6Color and Shape:SolidMolecular weight:703.41Plumbemycin B
CAS:Plumbemycin B is isolated from Streptomyces plumbeus; an L-threonine antagonist.Formula:C12H21N4O8PColor and Shape:SolidMolecular weight:380.29AFP-07
CAS:AFP-07 is a highly selective and potent agonist. It was used for the prostacyclin receptor.Formula:C22H29F2NaO5Purity:98%Color and Shape:SolidMolecular weight:434.45NAZ2329
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:501.56PBX-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:C24H21N3O6Molecular weight:447.44L 731735
CAS:L 731735 is a farnesyltransferase inhibitor.Formula:C19H40N4O4SPurity:98%Color and Shape:SolidMolecular weight:420.61CYP121A1-IN-1
CYP121A1-IN-1: Strong inhibitor for CYP121A1, hinders Mycobacterium tuberculosis growth (MIC 90 ~6.25 μM), reduces mycocyclosin synthesis.Formula:C22H20N4OColor and Shape:SolidMolecular weight:356.42Hoe 892
CAS:Hoe 892 is a stable thia-thimo-analogue of prostacyclin and acts as a platelet aggregation inhibitor.Formula:C20H33NO4SColor and Shape:SolidMolecular weight:383.55Pralatrexate, (R)-
CAS:Pralatrexate is a high-affinity DHFR inhibitor targeting RFC-1, used in cancer treatment and immunosuppression.Formula:C23H23N7O5Purity:98%Color and Shape:SolidMolecular weight:477.47ROPA
CAS:ROPA, a potent PKCalpha and PKCgamma activator, promotes tumor growth through PKC-activation.Formula:C28H32O6Purity:98%Color and Shape:SolidMolecular weight:464.55Squalestatin 2
CAS:Squalestatin 2 is an inhibitor of squalene synthase.Formula:C33H44O13Purity:98%Color and Shape:SolidMolecular weight:648.69PF1070A
CAS:PF1070A is a natural cyclic tetrapeptide HDAC Inhibitor through the inhibition of PfHDAC1 catalytic activity, potently inducing the synthesis of metallothioneinFormula:C31H44N4O6Color and Shape:SolidMolecular weight:568.7Neuraminidase-IN-7
Neuraminidase-IN-7, a thiophene, inhibits neuraminidase (IC50 0.03 μM), showing promise for flu research.Formula:C21H20N2O6SColor and Shape:SolidMolecular weight:428.46Cryptopleurine
CAS:Cryptopleurine is an inhibitor of gene products associated with cell proliferation, survival, invasion and angiogenesis. It acts by targeting the NF-κB pathway.Formula:C24H27NO3Purity:98%Color and Shape:SolidMolecular weight:377.48WS-898
<p>WS-898 boosts paclitaxel efficacy in resistant cells by inhibiting ABCB1; IC50: SW620/Ad300 - 5.0 nM, KB-C2 - 3.67 nM, HEK293/ABCB1 - 3.68 nM.</p>Formula:C33H25N7OSColor and Shape:SolidMolecular weight:567.66E-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:435.87UCN-02
CAS:UCN-02 (7-epi-Hydroxystaurosporine) is a PKC inhibitor produced by Streptomyces N-126 strain, which inhibits PKA.Formula:C28H26N4O4Purity:98%Color and Shape:SolidMolecular weight:482.53FR 901537
CAS:FR 901537 is a new aromatase inhibitor with antitumor effects.Formula:C23H29N3O6S2Purity:98%Color and Shape:SolidMolecular weight:507.62Deoxyfuconojirimycin hydrochloride
CAS:Deoxyfuconojirimycin hydrochloride acts as a specific competitive inhibitor targeting human liver α-L-fucosidase.Formula:C6H14ClNO3Color and Shape:SolidMolecular weight:183.63Lorajmine
CAS:Lorajmine, a monochloroacetyl derivative of ajmaline, is a class Ia antiarrhythmic agent that is rapidly hydrolyzed to ajmaline by plasma and tissue esterases.Formula:C22H27ClN2O3Purity:98%Color and Shape:SolidMolecular weight:402.91
