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Dihydroorotate Dehydrogenase

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Dihydroorotate dehydrogenase (DHODH) is the fourth enzyme in the de novo pyrimidine biosynthesis pathway, serving as the catalyst to oxidize the dihydroorotate to orotic acid in the biosynthesis of uridine monophosphate (UMP). DHODH is a known target for autoimmune diseases as well as an important target for malaria.

Based on localization and electron acceptor, DHODHs have classified into two families: Family 1 members are soluble proteins localized to the cytosol, while family 2 members are membrane proteins localized to the inner mitochondrial membrane. Family 1 is further subdivided into family 1A and family 1B, which use fumarate and NAD+ (respectively) as electron acceptors. Family 2 DHODH enzymes use respiratory quinones as electron acceptors.

Products Related to Dihydroorotate Dehydrogenase(15)

  • GC39234 structure
    GC39234DHODH-IN-2
    CAS: 1644156-80-8
    Purity: >99.50%
  • GC39374 structure
    GC39374DHODH-IN-5
    CAS: 1644156-56-8
    Purity: >99.50%
  • GC39632 structure
    GC39632Laflunimus
    CAS: 147076-36-6
    Purity: >99.00%

    Laflunimus (HR325) is an immunosuppressive agent and an analogue of the Leflunomide-active metabolite A77 1726.

  • GC60763 structure
    GC60763DHODH-IN-11
    CAS: 1263303-95-2
    Purity: >99.50%

    DHODH-IN-11 (Compound 14b) is a Leflunomide derivative and a weak dihydroorotate dehydrogenase (DHODH) inhibitor with a pKa of 5.03.

  • GC62336 structure
    GC62336CHIKV-IN-2
    CAS: 2361289-44-1
    Purity: >98.00%

    CHIKV-IN-2 is a potent inhibitor against Chikungunya virus (CHIKV), with excellent cellular antiviral activity (EC90=270 nM) and improved liver microsomal stability.

  • GC62470 structure
    GC62470AG-636
    CAS: 1623416-31-8
    Purity: >98.00%

    AG-636 is a potent, reversible, selective and orally active dihydroorotate dehydrogenase (DHODH) inhibitor with an IC50 of 17 nM. AG-636 has strong anticancer effects.

  • GC63418 structure
    GC63418DHODH-IN-17
    CAS: 16344-26-6
    Purity: >99.50%

    DHODH-IN-17, a 2-anilino nicotinic acid, is a human DHODH inhibitor (IC50=0.40 μM). DHODH-IN-17 can be used for theresearch of acute myeloid leukemia (AML).

  • GC63533 structure
    GC63533DSM502
    CAS: 2426616-55-7
    Purity: >99.50%

    DSM502 is a pyrrole-based Dihydroorotate Dehydrogenase (DHODH) inhibitor.

  • GC63547 structure
    GC63547DHODH-IN-16
    CAS: 2511248-11-4
    Purity: >99.50%

    DHODH-IN-16 is a potent dihydroorotate dehydrogenase (DHODH) inhibitor with an IC50 of 0.396 nM for human DHODH.

  • GC64074 structure
    GC64074DSM705 hydrochloride
    CAS: 2989908-08-7
    Purity: >99.00%

    DSM705 hydrochloride, an orally active antimalarial compound, is a pyrrole-based Dihydroorotate Dehydrogenase (DHODH) inhibitor.

  • GC65335 structure
    GC65335PTC299
    CAS: 1256565-36-2
    Purity: >99.00%

    PTC299 is an orally active inhibitor of VEGFA mRNA translation that selectively inhibits VEGF protein synthesis at the post-transcriptional level. PTC299 is also a potent inhibitor of dihydroorotate dehydrogenase (DHODH). PTC299 shows good oral bioavailability and lack of off-target kinase inhibition and myelosuppression. PTC299 can be useful for the research of hematologic malignancies.

  • GC68972 structure
    GC68972DHODH-IN-23
    CAS: 1346705-53-0
    Purity: >99.00%

    DHODH-IN-23 (Compound A) is an orally active DHODH inhibitor that can be used for cancer research.

  • GC71093 structure
    GC71093hDHODH-IN-13
    CAS: 3032611-13-2
    Purity: >99.00%

    hDHODH-IN-13 (compound w2) is an inhibitor of human dihydroorotate dehydrogenase (hDHODH) with an IC50 value of 173.4 nM. hDHODH-IN-13 can be used in the research of IBD.

  • GC79566 structure
    GC79566DHODH-IN-31
    Purity: >99.50%

    DHODH-IN-31 is a human dihydroorotate dehydrogenase ( DHODH ) inhibitor with an IC 50 of 0.59 μM.

  • GC79592 structure
    GC79592(S)-DSM1465
    CAS: 3109381-05-4
    Purity: >99.50%

    (S)-DSM1465 is a Plasmodium dihydroorotate dehydrogenase ( DHODH ) inhibitor.