
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 35851 products of "Other Inhibitors"
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MRS2279
CAS:Selective, high affinity competitive antagonist of the P2Y1 receptorFormula:C13H18ClN5O8P2Purity:98%Color and Shape:SolidMolecular weight:469.71GR-71251
CAS:GR-71251 is a Tachykinin receptor antagonist.
Formula:C74H105N19O13Color and Shape:SolidMolecular weight:1468.74STA 2
CAS:STA 2 is an analogue of TXA2, a thromboxane receptor in the colonic epithelium.Formula:C21H34O3SColor and Shape:SolidMolecular weight:366.56LAF-153
CAS:LAF-153 is a reversible Methionine Aminopeptidase‑2 (MetAP-2) Inhibitor.Formula:C18H32N2O7Color and Shape:SolidMolecular weight:388.46MK-1220
CAS:MK-1220 is a novel Macrocyclic Inhibitor of Hepatitis C Virus NS3/4A Protease with Improved Preclinical Plasma Exposure.Formula:C40H53N5O9SColor and Shape:SolidMolecular weight:779.94Kaitocephalin
CAS:Kaitocephalin: naturally occurring, non-selective antagonist blocking glutamate receptors, made by Eupenicillium shearii fungus.Formula:C18H21Cl2N3O9Color and Shape:SolidMolecular weight:494.28AZ0108
CAS:AZ0108, an oral PARP1,2,6 inhibitor, selectively blocks centrosome clustering, is viable for in vivo studies, and doesn't inhibit PARP3/TNKS1.Formula:C24H20F4N6O2Color and Shape:SolidMolecular weight:500.45MDL-27210
CAS:MDL-27210 is the ethyl ester prodrug of a potent angiotensin-converting enzyme inhibitor, MDL-27088.Formula:C27H32N2O5Color and Shape:SolidMolecular weight:464.55SID 125240931
CAS:SID 125240931 is a regulator of fluorine-activated proteins (FAPs). This compound disrupts the binding between fluoride and FAPs.Formula:C19H24N4O3SColor and Shape:SolidMolecular weight:388.48SphK1-IN-1
SphK1-IN-1: SphK1 ATPase inhibitor, IC50=2.48 μM, potential for cancer research.Formula:C22H22N6O2Color and Shape:SolidMolecular weight:402.45PDE-I2
CAS:PDE-I2 is a parasite schizogony inhibitor.Formula:C25H23N5O8Color and Shape:SolidMolecular weight:521.48PIKfyve-IN-1
PIKfyve-IN-1: potent, cell-active inhibitor for PIKfyve research, IC50=6.9 nM.Formula:C20H21N5Color and Shape:SolidMolecular weight:331.41AY 17,605
CAS:AY 17,605 is an inhibitor of bovine heart and rat brain nucleoside-3',5'- monophosphate phosphodiesterase.Formula:C25H36O5Color and Shape:SolidMolecular weight:416.55LY 178210
CAS:LY 178210 is a 5-hydroxytryptamine receptor agonist.Formula:C18H25N3OColor and Shape:SolidMolecular weight:299.41LMD-A
CAS:LMD-A, also known as CCR8 antagonist LMD-A, is a CCR8 antagonist.Formula:C27H32N4O4SColor and Shape:SolidMolecular weight:508.63WS-898
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.Formula:C33H25N7OSColor and Shape:SolidMolecular weight:567.66FTO-IN-1 TFA
FTO-IN-1 TFA: FTO enzyme inhibitor, anti-obesity, IC50 < 1μM, potential cancer research tool.Formula:C20H17Cl2F3N4O4Color and Shape:SolidMolecular weight:505.27Tilpisertib fosmecarbil
CAS:Tilpisertib fosmecarbil is a potent inhibitor of serine/threonine kinases with anti-inflammatory properties.Formula:C35H36ClN8O7PColor and Shape:SolidMolecular weight:747.14ETP-47037
CAS:ETP-47037: strong PI3Kα inhibitor (IC50: 0.99 nM), also targets PI3Kβ, δ, γ; may protect telomeres.Formula:C20H27N9O3SColor and Shape:SolidMolecular weight:473.55Steroid sulfatase/17β-HSD1-IN-1
Steroid sulfatase/17β-HSD1-IN-1 is a highly effective inhibitor of both steroid sulfatase and 17β-hydroxysteroid dehydrogenase type 1 (17β-HSD1) activities,Formula:C19H18N2O5SColor and Shape:SolidMolecular weight:386.42

