7 Results for "

urate-lowering

" in MedChemExpress (MCE) Product Catalog:
Products (7)

7 Results for "urate-lowering" in MCE Product Catalog:

Cat. No.: HY-172774
CAS No.: 896584-55-7
TRPV1 antagonist 10 is an orally active and potent TRPV1 antagonist (IC50 = 33.06 nM), moderate to weak URAT1 (IC50 = 22.51 μM) and GLUT9 (60.25% at 50 μM) inhibitor. TRPV1 antagonist 10 has analgesic and urate-lowering effect. TRPV1 antagonist 10 can be studied for research in hyperuricemia and inflammatory pain .
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Cat. No.: HY-151432
CAS No.: 2850331-30-3
Purity:  98.02%
Target:  

URAT1

Research Areas:  

Inflammation/Immunology

URAT1 inhibitor 3 is a potent, orally active, selective URAT1 inhibitor with an IC50 value of 0.8 nM. URAT1 inhibitor 3 has urate-lowering efficacy. URAT1 inhibitor 3 can be used in research of gout and hyperuricemi .
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Cat. No.: HY-123383
CAS No.: 16795-96-3
Target:  

Xanthine Oxidase

Research Areas:  

Metabolic Disease

Renierol is an orally active xanthine oxidase (XO) inhibitor. Renierol has urate-lowering activity .
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Cat. No.: HY-152033
CAS No.: 2700292-02-8
Target:  

URAT1 GLUT

Research Areas:  

Metabolic Disease

URAT1 inhibitor 4, a Lesinurad derivative, is a potent and orally active URAT1 inhibitor with an IC50 of 7.56 μM. URAT1 inhibitor 4 has higher in vivo urate-lowering efficacy than Lesinurad (HY-15258) .
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Cat. No.: HY-175309
CAS No.: 2516232-89-4
Target:  

URAT1

Research Areas:  

Metabolic Disease

URAT1-IN-14 is a potent and orally active Urate transporter 1 (URAT1) inhibitor. URAT1-IN-14 inhibits the human URAT1 in HEK293 cells with an IC50 of 0.72 μM. URAT1-IN-14 exhibits low cytotoxic in Hep-G2 cells. URAT1-IN-14 shows urate-lowering effect in hyperuricemia mouse models. URAT1-IN-14 can be used for the study of hyperuricemia and gout .
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Cat. No.: HY-182294
Target:  

URAT1

HYJ-2 is a URAT1 inhibitor and urate-lowering agent. HYJ-2 inhibits URAT1-mediated urate transport and interacts with key residues within the URAT1 binding pocket. HYJ-2 reduces serum urate levels in hyperuricemic mice without inducing liver or kidney injury. HYJ-2 shows low cytotoxicity to hepatocytes and renal cells. HYJ-2 does not significantly induce hepatocyte apoptosis or mitochondrial dysfunction. HYJ-2 can be used in studies related to hyperuricemia and gout .
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Cat. No.: HY-131321
CAS No.: 887945-96-2
Research Areas:  

Metabolic Disease

Febuxostat 67M-1 is an active metabolite of Febuxostat (HY-14268). Febuxostat 67M-1 retains inhibitory activity against Xanthine Oxidase, but its plasma concentration is much lower than that of Febuxostat. Febuxostat 67M-1 can be used in the research of hyperuricemia .
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