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)
- GC39632LaflunimusCAS: 147076-36-6Purity: >99.00%
Laflunimus (HR325) is an immunosuppressive agent and an analogue of the Leflunomide-active metabolite A77 1726.
- GC60763DHODH-IN-11CAS: 1263303-95-2Purity: >99.50%
DHODH-IN-11 (Compound 14b) is a Leflunomide derivative and a weak dihydroorotate dehydrogenase (DHODH) inhibitor with a pKa of 5.03.
- GC62336CHIKV-IN-2CAS: 2361289-44-1Purity: >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.
- GC63418DHODH-IN-17CAS: 16344-26-6Purity: >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).
- GC63547DHODH-IN-16CAS: 2511248-11-4Purity: >99.50%
DHODH-IN-16 is a potent dihydroorotate dehydrogenase (DHODH) inhibitor with an IC50 of 0.396 nM for human DHODH.
- GC64074DSM705 hydrochlorideCAS: 2989908-08-7Purity: >99.00%
DSM705 hydrochloride, an orally active antimalarial compound, is a pyrrole-based Dihydroorotate Dehydrogenase (DHODH) inhibitor.
- GC65335PTC299CAS: 1256565-36-2Purity: >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.
- GC68972DHODH-IN-23CAS: 1346705-53-0Purity: >99.00%
DHODH-IN-23 (Compound A) is an orally active DHODH inhibitor that can be used for cancer research.
- GC71093hDHODH-IN-13CAS: 3032611-13-2Purity: >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.
- GC79566DHODH-IN-31Purity: >99.50%
DHODH-IN-31 is a human dihydroorotate dehydrogenase ( DHODH ) inhibitor with an IC 50 of 0.59 μM.
- GC79592(S)-DSM1465CAS: 3109381-05-4Purity: >99.50%
(S)-DSM1465 is a Plasmodium dihydroorotate dehydrogenase ( DHODH ) inhibitor.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC39234 | DHODH-IN-2 | 1644156-80-8 | >99.50% | |
| GC39374 | DHODH-IN-5 | 1644156-56-8 | >99.50% | |
| GC39632 | Laflunimus | 147076-36-6 | >99.00% | |
Laflunimus (HR325) is an immunosuppressive agent and an analogue of the Leflunomide-active metabolite A77 1726. | ||||
| GC60763 | DHODH-IN-11 | 1263303-95-2 | >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 | CHIKV-IN-2 | 2361289-44-1 | >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 | AG-636 | 1623416-31-8 | >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 | DHODH-IN-17 | 16344-26-6 | >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 | DSM502 | 2426616-55-7 | >99.50% | |
DSM502 is a pyrrole-based Dihydroorotate Dehydrogenase (DHODH) inhibitor. | ||||
| GC63547 | DHODH-IN-16 | 2511248-11-4 | >99.50% | |
DHODH-IN-16 is a potent dihydroorotate dehydrogenase (DHODH) inhibitor with an IC50 of 0.396 nM for human DHODH. | ||||
| GC64074 | DSM705 hydrochloride | 2989908-08-7 | >99.00% | |
DSM705 hydrochloride, an orally active antimalarial compound, is a pyrrole-based Dihydroorotate Dehydrogenase (DHODH) inhibitor. | ||||
| GC65335 | PTC299 | 1256565-36-2 | >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 | DHODH-IN-23 | 1346705-53-0 | >99.00% | |
DHODH-IN-23 (Compound A) is an orally active DHODH inhibitor that can be used for cancer research. | ||||
| GC71093 | hDHODH-IN-13 | 3032611-13-2 | >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 | DHODH-IN-31 | - | >99.50% | |
DHODH-IN-31 is a human dihydroorotate dehydrogenase ( DHODH ) inhibitor with an IC 50 of 0.59 μM. | ||||
| GC79592 | (S)-DSM1465 | 3109381-05-4 | >99.50% | |
(S)-DSM1465 is a Plasmodium dihydroorotate dehydrogenase ( DHODH ) inhibitor. | ||||
