GLPBio

URAT1

URAT1, also known as SLC22A12, is an organic anion and urate transporter. It regulates urate levels of blood and is required for urate reabsorption of kidney.

Products Related to URAT1(14)

  • GC15440 structure
    GC15440Lesinurad
    CAS: 878672-00-5
    Purity: >98.00%

    A URAT1 inhibitor

  • GC19373 structure
    GC19373Verinurad
    CAS: 1352792-74-5
    Purity: >99.00%

    Verinurad is an urate transporter inhibitor with EC50 value of 0.05 uM.

  • GC36439 structure
    GC36439Lesinurad sodium
    CAS: 1151516-14-1
    Purity: >99.50%

    Lesinurad sodium is a URAT1 and OAT inhibitor, is determined to be a substrate for the kidney transporters OAT1 and OAT3 with Km values of 0.85 and 2 ?M, respectively.

  • GC63422 structure
    GC63422Ruzinurad
    CAS: 1638327-48-6
    Purity: >99.00%

    Ruzinurad is a highly selective URATl inhibitor (WO2020088641, compound I).

  • GC65362 structure
    GC65362URAT1 inhibitor 1
    CAS: 2268720-62-1
    Purity: >98%

    URAT1 inhibitor 1 (1g) is a uric acid transporter 1 (URAT1) inhibitor, with an IC50 of 32 nM.

  • GC69779 structure
    GC69779Puliginurad
    CAS: 2013582-27-7
    Purity: >99.00%

    Puliginurad (YL-90148) is an effective inhibitor of urate transporter protein (URAT). Puliginurad can be used in research on hyperuricemia and gout.

  • GC70152 structure
    GC70152Xininurad
    CAS: 2365178-28-3
    Purity: >99.00%

    Xininurad (XNW3009) is a urate transporter (URAT) inhibitor.

  • GC71155 structure
    GC71155URAT1 inhibitor 3
    CAS: 2850331-30-3
    Purity: >98.00%

    URAT1 inhibitor 3 is a potent, orally active, selective URAT1 inhibitor with an IC50 value of 0.8 nM.

  • GC71285 structure
    GC71285URAT1&XO inhibitor 1
    CAS: 2669726-78-5
    Purity: >99.00%

    URAT1&XO inhibitor 1 (compound 29) is a dual inhibitor of both URAT1 (IC50=~10 μM) and Xanthine Oxidase (IC50=1.01 μM).

  • GC71286 structure
    GC71286URAT1 inhibitor 6
    CAS: 2244807-49-4

    URAT1 inhibitor 6 (Compound 1h) is a potent URAT1 inhibitor (IC50: 35 nM for hURAT1).

  • GC71287 structure
    GC71287URAT1 inhibitor 8
    CAS: 1632005-33-4
    Purity: >98.00%

    URAT1 inhibitor 8 (example 247) is a potent URAT1 inhibitor, with an IC50 of 0.001 μM.

  • GC71288 structure
    GC71288URAT1&XO inhibitor 2
    CAS: 1239488-96-0
    Purity: >98.00%

    URAT1&XO inhibitor 2 (Compound BDEO) is a dual inhibitor of xanthine oxidase and URAT1, with IC50 of 3.3 μM for xanthine oxidase.

  • GC81725 structure
    GC81725TRPV1 antagonist 10
    CAS: 896584-55-7
    Purity: >98.50%

    TRPV1 antagonist 10 is an orally active and potent TRPV1 antagonist ( IC 50 = 33.06 nM), moderate to weak URAT1 ( IC 50 = 22.51 μM) and GLUT9 (60.25% at 50 μM) inhibitor.

  • GC81738 structure
    GC81738URAT1 inhibitor 7
    CAS: 1632002-28-8
    Purity: >98.00%

    URAT1 inhibitor 7 (compound 10f) is a potent URAT1 inhibitor, with an IC 50 of 12 nM.