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 35804 products of "Other Inhibitors"
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FTI-2153 TFA
FTI-2153 TFA inhibits farnesyltransferase with high selectivity (IC50: 1.4 nM), over 3000x more than Rap1A processing.Formula:C27H31F3N4O5SColor and Shape:SolidMolecular weight:580.62Resorcinomycin A
CAS:Resorcinomycin A is an antibiotic with potent antimycobacterial activity and relatively weaker activity against mycoplasma.Formula:C14H20N4O5Color and Shape:SolidMolecular weight:324.332Glucoallosamidin B
CAS:Glucoallosamidin B is a glycoside antibiotic identifiable in the Streptomyces species strain (Streptomycessp. SA-684). It functions as an inhibitor of chitinase activity. Experiments demonstrate that Glucoallosamidin B significantly inhibits the chitinase of Candida albicans (ATCC 10231), with an IC50 value of 0.8 μg/mL.
Formula:C25H42N4O14Color and Shape:SolidMolecular weight:622.619Oxamicetin
CAS:Oxamicetin is a nucleoside antibiotic with antibacterial and antimycobacterial properties.Formula:C29H42N6O10Color and Shape:SolidMolecular weight:634.678Cytochalasin F
CAS:Cytochalasin F reversibly inhibits cytokinesis and possesses various biological activities including the inhibition of macrophage endocytosis and exocytosis.Formula:C29H37NO5Color and Shape:SolidMolecular weight:479.608Unoprostone isopropyl
CAS:Unoprostone isopropyl, a prostanoid and synthetic docosanoid, is approved for the treatment of ocular hypertension and open-angle glaucoma.Formula:C25H44O5Purity:98%Color and Shape:SolidMolecular weight:424.61Furaquinocin A
CAS:Furaquinocin A has the ability to kill HeLa S3 and B16 melanoma cells, yet it lacks antibacterial activity.Formula:C22H26O7Color and Shape:SolidMolecular weight:402.438iMDK quarterhydrate
iMDK quarterhydrate, PI3K inhibitor, blocks MDK growth; suppresses NSCLC safely with MEK inhibitor.Formula:C21H15FN2O3SColor and Shape:SolidMolecular weight:380.91S-2,3-Dicarboxyaziridine
CAS:S-2,3-Dicarboxyaziridine is a metabolite that can be isolated from Streptomyces species and exhibits antibacterial activity.Formula:C4H5NO4Color and Shape:SolidMolecular weight:131.087Plumbemycin B
CAS:Plumbemycin B is isolated from Streptomyces plumbeus; an L-threonine antagonist.Formula:C12H21N4O8PColor and Shape:SolidMolecular weight:380.29NAZ2329
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:501.56VU6028418
VU6028418 is a highly selective, potent, orally active M4mAChR antagonist that acts on hM4 (IC50: 4.1 nM).
Color and Shape:LiquidCYP121A1-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:356.42HYL001
CAS:HYL001 (compound 338) is a potent inhibitor of the TGFβ receptor 1 (ALK5), exhibiting approximately nine times the efficacy of its structurally related counterpart, galunisertib, in eliminating liver metastasis tumors generated in mice.Formula:C21H18N4OColor and Shape:SolidMolecular weight:342.39ONO-DI-004
CAS:ONO-DI-004 is a selective EP1 Prostanoid receptor agonist.Formula:C24H38O6Color and Shape:SolidMolecular weight:422.55XR8-89
CAS:XR8-89, a potent PLpro inhibitor (IC50=0.1μM), blocks SARS-CoV-2 replication; useful for research.Formula:C29H36N4O2SColor and Shape:SolidMolecular weight:504.69PF1070A
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:568.7Trk-IN-8
Trk-IN-8: TRK inhibitor with IC50 of 0.42 nM (TRKA), 0.89 nM (TRKA-G595R), 1.5 nM (TRKC-G623R).Formula:C18H16F2N6O2Color and Shape:SolidMolecular weight:386.36Ciprokiren
CAS:Ciprokiren, a renin inhibitor by Roche, halts human renin; IC50: 0.07/0.65 nmol/L. Lowers blood pressure in animals. Preclinical development ceased.Formula:C37H55N5O8SColor and Shape:SolidMolecular weight:729.93ATR-IN-7
CAS:ATR-IN-7 is a potent inhibitor of ATR.Formula:C21H22FN7OColor and Shape:SolidMolecular weight:407.44
