
OAT
Organic anion transporters are a family of membrane proteins that mediate the uptake and excretion of various endogenous and exogenous organic anions, including drugs, toxins, and metabolic byproducts. OATs are primarily expressed in the kidneys and liver, where they play a crucial role in detoxification and drug clearance. Dysregulation of OAT function can lead to drug toxicity and kidney disorders. At CymitQuimica, we provide a variety of OAT modulators to support your research in pharmacology, toxicology, and renal function.
Found 27 products of "OAT"
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URAT1 inhibitor 1
CAS:<p>URAT1 inhibitor 1 (1g) is an inhibitor of uric acid transporter 1 (URAT1) (IC50: 32 nM), has the potential to treat hyperuricemia associated with gout.</p>Formula:C19H15Br2N5O2S2Purity:98%Color and Shape:SolidMolecular weight:569.29KPH2f
CAS:<p>KPH2f: dual URAT1/GLUT9 inhibitor, orally active, IC50: 0.24μM (URAT1), 9.37μM (GLUT9), minimal OAT1/ABCG2 impact.</p>Formula:C24H16N3NaO2SColor and Shape:SolidMolecular weight:433.46Cyazofamid
CAS:<p>Cyazofamid functions as a fungicide by impairing the production of ATP. It inhibits Organic Cation Transporter 3 (OCT3) and OAT1 with IC50 values of 1.54 and 17.3 μM, respectively.</p>Formula:C13H13ClN4O2SColor and Shape:SolidMolecular weight:324.79hURAT1 inhibitor 2
CAS:<p>hURAT1 inhibitor 2 (Compound 5) is an inhibitor of hURAT1 (uric acid transporter 1, SLC22A12) with an IC50 of 18 nM. It also exhibits some inhibitory activity against OATP1B1, with an IC50 of 0.73 μM. hURAT1 inhibitor 2 can be used in research related to hyperuricemia, gout, and other diseases associated with abnormal uric acid metabolism.</p>Formula:C17H11Br2FO3Color and Shape:SolidMolecular weight:442.074URAT1 inhibitor 3
<p>URAT1 inhibitor 3: potent oral URAT1 blocker, IC50=0.8 nM, for gout/hyperuricemia study.</p>Formula:C14H8Cl2N2O2Color and Shape:SolidMolecular weight:307.13URAT1 inhibitor 2
<p>URAT1 inhibitor 2: oral URAT1/CYP blocker, IC50 of 1.36μM (URAT1), 16.97μM (CYP1A2), 5.22μM (CYP2C9); potential gout treatment.</p>Formula:C21H18BrN3O2SColor and Shape:SolidMolecular weight:456.36TRPV1 antagonist 10
CAS:<p>TRPV1 antagonist 10 is a potent, orally active TRPV1 antagonist with an IC50 of 33.06 nM and serves as a moderate to weak inhibitor of URAT1 (IC50 = 22.51 μM) and GLUT9 (inhibition of 60.25% at 50 μM). It exhibits analgesic and urate-lowering properties and is applicable for research in hyperuricemia and inflammatory pain.</p>Formula:C16H14N2O5Color and Shape:SolidMolecular weight:314.293

