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Search Results for " dhodh "

Targets

61

Compounds

3

Natural Products

4

Recombinant Proteins

Cat No. Product Name Synonyms Targets
T11027 DHODH-IN-4 Dehydrogenase
DHODH-IN-4 is a human and Plasmodium falciparum dihydroorotate dehydrogenase (DHODH) inhibitor. The IC50 values of PfDHODH and HsDHODH are 4 μM and 0.18 μM, respectively. DHODH-IN-4 has antimalarial activity.
T11019 DHODH-IN-1 Dehydrogenase
DHODH-IN-1 is a potent dihydroorotate dehydrogenase (DHODH) inhibitor with IC50 of 25 nM. DHODH-IN-1 is an inhibitor of the pyrimidine biosynthetic pathway.
T11023 DHODH-IN-14 Dehydrogenase
DHODH-IN-14 is an analog of hydroxyfuran pyrimidine A771726. DHODH-IN-14 is a dihydroorotate dehydrogenase (DHODH) inhibitor IC50 0.49 μM mouse liver DHODH. DHODH-IN-14 can be used for rheumatoid arthritis.
T11022 DHODH-IN-13 Dehydrogenase
DHODH-IN-13 is an inhibitor of DHODH with IC50 of 4.3 μM for rat liver. DHODH-IN-13 can be used in studies about rheumatoid arthritis.
T40168 DHODH-IN-16 Dehydrogenase
DHODH-IN-16 is an effective inhibitor of dihydroorotate dehydrogenase (DHODH, IC50 = 0.396 nM for human).
T11030 DHODH-IN-8 Dehydrogenase
DHODH-IN-8 has antimalarial activity. DHODH-IN-8 is an inhibitor of human and Plasmodium falciparum dihydroorotate dehydrogenase (DHODH) with IC50 of 0.13 μM and 47.4 μM, and Kis of 0.016 μM and 5.6 μM, respectively.
T11024 DHODH-IN-15 Dehydrogenase
DHODH-IN-15 is the hydroxyfuran analogue of A771726. DHODH-IN-15 is a dihydroorotate dehydrogenase (DHODH) inhibitor with an IC50 of 11 μM for rat liver DHODH. DHODH-IN-15 can be used for rheumatoid arthritis.
T11021 DHODH-IN-12 Dehydrogenase
DHODH-IN-12 is a leflunomide derivative and a weak dihydrorotate dehydrogenase (DHODH) inhibitor with a pKa of 5.07.
T11020 DHODH-IN-11 Dehydrogenase , DNA/RNA Synthesis
DHODH-IN-11 is a leflunomide derivative and weak dihydroorotate dehydrogenase (DHODH) inhibitor with a pKa of 5.03.
T67875 DHODH-IN-23 Dehydrogenase
DHODH-IN-23 is a DHODH inhibitor with oral activity. DHODH-IN-23 is often used in cancer research.
T60364 DHODH-IN-17 Dehydrogenase
DHODH-IN-17 is a human DHODH inhibitor with an IC50 of 0.40 μM. DHODH-IN-17 is a 2- anilino nicotinic acid that can be used in the study of acute myeloid leukemia (AML).
T11031 HDHODH-IN-7 DHODH-IN-9 Dehydrogenase
hDHODH-IN-7 (DHODH-IN-9) is a nitrogen-containing analog and is a human dihydrorotatory dehydrogenase inhibitor. hDHODH-IN-7 and pMIC50 of 7.4 have antiviral effects.
T11028 HDHODH-IN-4 DHODH-IN-5 Dehydrogenase
hDHODH-IN-4 (DHODH-IN-5) is a potent inhibitor of human dihydrogen dehydrogenase (DHODH). For human recombinant DHODH, its pIC50 is 7.8. hDHODH-IN-4 inhibits measles virus replication with a pMIC50 of 8.8.
T11025 HDHODH-IN-3 DHODH-IN-2 Dehydrogenase
hDHODH-IN-3 is an inhibitor of human dihydroorotate dehydrogenase with a pMIC50 value of 8.6. hDHODH-IN-3 can inhibit measles virus replication.
T11029 HDHODH-IN-5 DHODH-IN-7 Dehydrogenase
hDHODH-IN-5 is an inhibitor of human dihydroorotate dehydrogenase (hDHODH, IC50 = 0.91 μM).
T40309 DHODH-IN-18
DHODH-IN-18 is a human DHODH inhibitor ( IC 50 = 0.2 nM).
T11026 DHODH-IN-3 Others
DHODH-IN-3 is an effective inhibitor of human dihydroorotate dehydrogenase (HsDHODH) with IC50 value of 261 nM. DHODH-IN-3 binds to the ubiquinone binding cavity in DHODH with a Kiapp of 32 nM. DHODH-IN-3 has the potenti...
T63148 DHODH-IN-20
Dhodh-in-20 (Compound 133) is a potent inhibitor of DHODH. Among them, DHODH is an iron-containing flavin-dependent enzyme that is present in the inner membrane of human mitochondria. DHODH-IN-20 showed an inhibitory eff...
T63617 DHODH-IN-21
DHODH-IN-21 is an orally active, selective dihydrolactate dehydrogenase (DHODH) inhibitor (IC50: 1.1 nM). DHODH-IN-21 exhibits anticancer effects and can be used to study acute myeloid leukemia (AML).
T63880 DHODH-IN-22
DHODH-IN-22 is a potent, selective, orally active inhibitor of dihydroorotic dehydrogenase (DHODH) (IC50: 0.3 nM) and can be used in acute myeloid leukaemia (AML) studies.
T63652 DHODH-IN-19
DHODH-IN-19 is a potent inhibitor of DHODH. DHODH-IN-19 has shown research potential for cancer and inflammatory diseases.
T62462 RORγt/DHODH-IN-2
RORγt/DHODH-IN-2 (compound 1) is a potent dual RORγt/DHODH inhibitor that can be used in the study of inflammatory bowel disease (IBD).
T64146 RORγt/DHODH-IN-3
RORγt/DHODH-IN-3 (compound (S)-14d) is a potent, orally active dual inhibitor of RORγt (IC50: 0.098 μM) and DHODH (IC50: 0.432 μM).RORγt/DHODH-IN-1 has significant in vivo anti-inflammatory effects.
T64145 RORγt/DHODH-IN-1
RORγt/DHODH-IN-1 (compound (R)-14d) is a potent, orally active dual inhibitor of RORγt (IC50: 0.083 μM) and DHODH (IC50: 0.172 μM), which exhibits significant in vivo anti-inflammatory effects.
T9394 CHIKV-IN-2 Dehydrogenase
CHIKV-IN-2, a chemical compound, exhibits potent inhibitory activity against the enzyme Dihydroorotate Dehydrogenase (DHODH), crucial for pyrimidine synthesis affecting various viruses' replication. It serves as an effec...
T9121 AG-636 Dehydrogenase , DNA/RNA Synthesis
AG-636 is a potent, reversible, selective and orally active DHODH inhibitor(IC50 of 17 nM). It has strong anticancer effects.
T8767 PfDHODH-IN-2 Dehydrogenase , Parasite
PfDHODH-IN-2 is a dihydrothiophenone derivative, is a potent Plasmodium falciparum dihydroorotate dehydrogenase (PfDHODH, IC50 : 1.11 μM) inhibitor . It is used an antimalarial agent and can be used for the research of m...
T14501 BAY-2402234 Dehydrogenase , DNA/RNA Synthesis
BAY-2402234 is an inhibitor of dihydroorotate dehydrogenase (DHODH) for the treatment of myeloid malignancies.BAY 2402234 is a selective low-nanomolar inhibitor of human DHODH enzymatic activity.
T2601 Vidofludimus SC12267,4sc-101 Dehydrogenase , DNA/RNA Synthesis , Interleukin
Vidofludimus (SC12267) (4SC-101, SC12267) is a novel small molecule inhibitor of dihydroorotate dehydrogenase (DHODH).
T13774 ML390 Others , Dehydrogenase
ML390 exerts its potent differentiation effect on multiple leukemia models.
T1818 Tenovin-6 Tenovin 6 Dehydrogenase , Sirtuin , Autophagy
Tenovin-6 is a p53 transcriptional activity agonist.
T1919 Tenovin-1 Tenovin 1 Mdm2 , Dehydrogenase , Sirtuin , p53 , Autophagy
Tenovin-1 inhibits protein-deacetylating activities of SirT1 and SirT2 and protects against MDM2-mediated p53 degradation, which involves ubiquitination.
T8480 Tenovin-6 Hydrochloride Dehydrogenase , Sirtuin , HDAC , p53 , Autophagy
Tenovin-6 Hydrochloride is an SIRT1, SIRT2 and HDAC8 inhibitor(IC50s of 21 μM, 10 μM, and 67 μM for SirT1, SirT2, and SirT3, respectively), and is also a potent p53 activator .
T10384 Farudodstat ASLAN003 Apoptosis , Dehydrogenase , DNA/RNA Synthesis
Farudodstat (ASLAN003) is an orally active and potent inhibitor of DHODH (Human Dihydroorotate Dehydrogenase) with antitumor activity. It has the potential to be a first-in-class candidate in AML.
T5013 Brequinar Bipenquinate,NSC 368390,DUP785 Virus Protease , Dehydrogenase , DNA/RNA Synthesis
Brequinar (NSC-368390) is a potent inhibitor of dihydroorotate dehydrogenase, with potent activities against a broad spectrum of viruses.
T1159 Leflunomide SU101,RS-34821,HWA486 Others , Dehydrogenase , AhR
Leflunomide (HWA486) is an immunomodulatory agent used in the therapy of rheumatoid arthritis and psoriatic arthritis.
T12574 PTC299 Emvododstat,(4-chlorophenyl) (1S)-6-chloro-1-(4-methoxyphenyl)-1,3,4,9-tetrahydropyrido[3,4-b]indole-2-carboxylate VEGFR , Dehydrogenase
PTC299 ((4-chlorophenyl) (1S)-6-chloro-1-(4-methoxyphenyl)-1,3,4,9-tetrahydropyrido[3,4-b]indole-2-carboxylate) is an orally active inhibitor of VEGFA mRNA translation and selectively inhibits VEGF protein synthesis at t...
T11546 HDHODH-IN-1 Dehydrogenase
hDHODH-IN-1 is a human dihydroorotate dehydrogenase (hDHODH) inhibitor with an anti-inflammatory effect.
T12438 PfDHODH-IN-1 Dehydrogenase , Parasite
PfDHODH-IN-1 is an analogue of the active Leflunomide metabolite, has antimalarial activity.
T78932 HDHODH-IN-12 DNA/RNA Synthesis
hDHODH-IN-12 is a potent inhibitor of dihydroorotate dehydrogenase (DHODH), exhibiting an inhibitory concentration (IC50) of 0.421 μM. As the rate-limiting enzyme in the de novo synthesis of pyrimidines, critical for DNA...
T72948 HDHODH-IN-11
hDHODH-IN-11, a potent inhibitor of human dihydroorotate dehydrogenase (hDHODH), exhibits an IC50 value of 7.2 nM and has low cytotoxicity. It is applicable in acute myeloid leukemia (AML) research.
T61226 HDHODH-IN-9
hDHODH-IN-9 (Compound 3k) is a highly potent inhibitor of hDHODH, exhibiting an IC50 of 0.34 μM. It displays significant cytotoxic activity against MCF-7 and A375 cells, while maintaining good selectivity. With its chara...
T64360 HDHODH-IN-8 Dehydrogenase
hDHODH-IN-8 is a potent inhibitor of human dihydroorotate dehydrogenase (hDHODH) with an IC50 of 16 nM. hDHODH-IN-8 has potent antiproliferative activity and excellent aqueous solubility. hDHODH-IN-8 has the potential fo...
T63037 HDHODH-IN-10
hDHODH-IN-10 is a selective, orally active, potent hDHODH inhibitor (IC50: 10.9 nM) that forms hydrogen bonds with key residues Arg136 and Gln47. hDHODH-IN-10 inhibits the proliferation of cancer cells and can be used to...
T11547 HDHODH-IN-2 Others
hDHODH-IN-2 is an analogue of the active metabolite of Leflunomide. hDHODH-IN-2 is a human dihydroorotate dehydrogenase (hDHODH) inhibitor with anti-inflammatory activity.
T82223 HDHODH-IN-13
hDHODH-IN-13 (compound w2), an inhibitor of human dihydroorotate dehydrogenase (hDHODH), exhibits an IC50 of 173.4 nM and has potential research applications in studying inflammatory bowel disease (IBD) [1].
T27300 Olorofim Olorofim,F901318,F-901318
Olorofim is a novel selective antifungal compound with inhibitory effect on Aspergillus fumigatus DHODH (IC50: 44 nM) and almost no inhibitory effect on human DHODH (>100 uM).Olorofim has good efficacy against various pa...
T8332 Bipenquinate Dehydrogenase
Bipenquinate is a potent and selective inhibitor of dihydroorotate dehydrogenase (DHODH) with IC50 of 20 nM, blocking de novo pyrimidine biosynthesis.
T27214 DSM421 DSM 421,DSM-421 Dehydrogenase
DSM421 (DSM-421) is a dihydrodehydrogenase inhibitor (DHODH) that is in preclinical development as a potential treatment option for malaria and has shown activity against field isolates of both P. falciparum and P. vivax...
T40087 DSM502
DSM502, a pyrrole-based Dihydroorotate Dehydrogenase (DHODH) inhibitor, demonstrates potent nanomolar activity against Plasmodium DHODH and Plasmodium parasites, while not inhibiting mammalian DHODHs.

Compounds

DHODH-IN-4
T11027
Synonym:
Target: Dehydrogenase
DHODH-IN-1
T11019
Synonym:
Target: Dehydrogenase
DHODH-IN-14
T11023
Synonym:
Target: Dehydrogenase
DHODH-IN-13
T11022
Synonym:
Target: Dehydrogenase
DHODH-IN-16
T40168
Synonym:
Target: Dehydrogenase
DHODH-IN-8
T11030
Synonym:
Target: Dehydrogenase
DHODH-IN-15
T11024
Synonym:
Target: Dehydrogenase
DHODH-IN-12
T11021
Synonym:
Target: Dehydrogenase
DHODH-IN-11
T11020
Synonym:
Target: Dehydrogenase, DNA/RNA Synthesis
DHODH-IN-23
T67875
Synonym:
Target: Dehydrogenase
DHODH-IN-17
T60364
Synonym:
Target: Dehydrogenase
hDHODH-IN-7
T11031
Synonym: DHODH-IN-9
Target: Dehydrogenase
hDHODH-IN-4
T11028
Synonym: DHODH-IN-5
Target: Dehydrogenase
hDHODH-IN-3
T11025
Synonym: DHODH-IN-2
Target: Dehydrogenase
hDHODH-IN-5
T11029
Synonym: DHODH-IN-7
Target: Dehydrogenase
DHODH-IN-18
T40309
Synonym:
Target:
DHODH-IN-3
T11026
Synonym:
Target: Others
DHODH-IN-20
T63148
Synonym:
Target:
DHODH-IN-21
T63617
Synonym:
Target:
DHODH-IN-22
T63880
Synonym:
Target:
DHODH-IN-19
T63652
Synonym:
Target:
RORγt/DHODH-IN-2
T62462
Synonym:
Target:
RORγt/DHODH-IN-3
T64146
Synonym:
Target:
RORγt/DHODH-IN-1
T64145
Synonym:
Target:
CHIKV-IN-2
T9394
Synonym:
Target: Dehydrogenase
AG-636
T9121
Synonym:
Target: Dehydrogenase, DNA/RNA Synthesis
PfDHODH-IN-2
T8767
Synonym:
Target: Dehydrogenase, Parasite
BAY-2402234
T14501
Synonym:
Target: Dehydrogenase, DNA/RNA Synthesis
Vidofludimus
T2601
Synonym: SC12267,4sc-101
Target: Dehydrogenase, DNA/RNA Synthesis, Interleukin
ML390
T13774
Synonym:
Target: Others, Dehydrogenase
Tenovin-6
T1818
Synonym: Tenovin 6
Target: Dehydrogenase, Sirtuin, Autophagy
Tenovin-1
T1919
Synonym: Tenovin 1
Target: Mdm2, Dehydrogenase, Sirtuin, p53, Autophagy
Tenovin-6 Hydrochloride
T8480
Synonym:
Target: Dehydrogenase, Sirtuin, HDAC, p53, Autophagy
Farudodstat
T10384
Synonym: ASLAN003
Target: Apoptosis, Dehydrogenase, DNA/RNA Synthesis
Brequinar
T5013
Synonym: Bipenquinate,NSC 368390,DUP785
Target: Virus Protease, Dehydrogenase, DNA/RNA Synthesis
Leflunomide
T1159
Synonym: SU101,RS-34821,HWA486
Target: Others, Dehydrogenase, AhR
PTC299
T12574
Synonym: Emvododstat,(4-chlorophenyl) (1S)-6-chloro-1-(4-methoxyphenyl)-1,3,4,9-tetrahydropyrido[3,4-b]indole-2-carboxylate
Target: VEGFR, Dehydrogenase
hDHODH-IN-1
T11546
Synonym:
Target: Dehydrogenase
PfDHODH-IN-1
T12438
Synonym:
Target: Dehydrogenase, Parasite
hDHODH-IN-12
T78932
Synonym:
Target: DNA/RNA Synthesis
hDHODH-IN-11
T72948
Synonym:
Target:
hDHODH-IN-9
T61226
Synonym:
Target:
hDHODH-IN-8
T64360
Synonym:
Target: Dehydrogenase
hDHODH-IN-10
T63037
Synonym:
Target:
hDHODH-IN-2
T11547
Synonym:
Target: Others
hDHODH-IN-13
T82223
Synonym:
Target:
Olorofim
T27300
Synonym: Olorofim,F901318,F-901318
Target:
Bipenquinate
T8332
Synonym:
Target: Dehydrogenase
DSM421
T27214
Synonym: DSM 421,DSM-421
Target: Dehydrogenase
DSM502
T40087
Synonym:
Target:
1 2
Cat No. Product Name Synonyms Targets
TN2373 (E/Z)-Ginkgolic acid C17:2 Ginkgolic Acid C17:2 Dehydrogenase
(E/Z)-Ginkgolic acid C17:2 (Ginkgolic Acid C17:2) is a natural product that can be extracted from Ginkgo biloba and targets human dihydroorotic acid dehydrogenase (DHODH).
T0746 Orotic acid Vitamin B13,6-Carboxyuracil Nucleoside Antimetabolite/Analog , Dehydrogenase , Endogenous Metabolite
Orotic acid (Vitamin B13) is an intermediate product in pyrimidine metabolism.
T3271 Orotic acid zinc Orotic acid zinc salt dihydrate,Zinc Orotate Nucleoside Antimetabolite/Analog , Others , Endogenous Metabolite
Orotic acid zinc (Zinc Orotate) salt dihydrate is an intermediate product in pyrimidine synthesis.

Recombinant Proteins

Cat No. Product Name Species Expression System
TMPH-01225 DHODH Protein, Human, Recombinant (His) Human E. coli
Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor.
TMPH-02850 DHODH Protein, Mouse, Recombinant (His) Mouse E. coli
Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor.
TMPH-03278 DHODH Protein, Rat, Recombinant (His) Rat E. coli
Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor.
TMPH-02627 DHODH Protein, Mouse, Recombinant (E. coli, His) Mouse E. coli
Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor.
TargetMol