8 Results for "

DHODH-IN-1

" in MedChemExpress (MCE) Product Catalog:
Products (8)

8 Results for "DHODH-IN-1" in MCE Product Catalog:

Cat. No.: HY-135282
CAS No.: 1800296-63-2
Purity:  98.65%
Research Areas:  

Infection

DHODH-IN-1 (compound 18d) is a potent Dihydroorotate Dehydrogenase (DHODH) inhibitor with an IC50 of 25 nM. DHODH-IN-1 is an inhibitor of pyrimidine biosynthesis pathway [1].
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5
5 Cited Publications
Cat. No.: HY-13423
CAS No.: 380315-80-0
Purity:  99.88%
Tenovin-1, a p53 activator, protects p53 from MDM2-mediated degradation. Tenovin-1 acts through inhibition of the protein-deacetylating activities of SirT1 and SirT2. Tenovin-1 is also a dihydroorotate dehydrogenase (DHODH) inhibitor .
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Cat. No.: HY-N7961
CAS No.: 102811-39-2
(E/Z)-Ginkgolic acid C17:2, isolated from Ginkgo biloba, can bind with human dihydroorotate dehydrogenase (DHODH) tightly .
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Cat. No.: HY-Y0244
CAS No.: 6298-19-7
2-Chloropyridin-3-amine is a heterocyclic amine that serves as a pharmaceutical intermediate for the synthesis of dihydroorotate dehydrogenase (DHODH) inhibitors .
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Cat. No.: HY-142843
CAS No.: 2764662-15-7
Research Areas:  

Inflammation/Immunology

RORγt/DHODH-IN-1 (compound (R)-14d) is a potent and orally active dual RORγt/DHODH inhibitor, with IC50s of 0.083 μM and 0.172 μM, respectively. RORγt/DHODH-IN-1 exhibits remarkable in vivo anti-inflammatory activity [1].
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Cat. No.: HY-169220S
CAS No.: 3000567-76-7
RORγ/DHODH-IN-1 (compound 1404), a deuterium labeled compound, is a dual RORγ and DHODH inhibitor with IC50 values of 9.7 nM and 100 nM, repaectively. RORγ/DHODH-IN-1 blocks the replication of SARS-CoV-2, HCMV, and non-enveloped DNA virus (HAdV5) [1].
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Cat. No.: HY-176728
Research Areas:  

Infection

DHODH-IN-27 (WF-8) is a dihydroacetate dehydrogenase (DHODH) inhibitor with an IC50 of 64.97 μM. DHODH-IN-27 can be used as an anti-DHODH herbicide .
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Cat. No.: HY-117908
CAS No.: 1281861-06-0
Research Areas:  

Infection

DSM267 is a triazolopyrimidine inhibitor of Plasmodium falciparum dihydroorotate dehydrogenase (PfDHODH), with an IC50 of 38 nM, while its IC50 against human DHODH exceeds 100000 nM. DSM267 is used for the in vitro systematic screening and characterization of the resistance evolution pathways of Plasmodium falciparum to DHODH inhibitors .
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