hDHODH-IN-7
CAS No. 1644156-41-1
hDHODH-IN-7( —— )
Catalog No. M26162 CAS No. 1644156-41-1
DHODH-IN-9 (Compound 10k) is a nitrogen-containing analog and is a human dihydrorotatory dehydrogenase inhibitor.
Purity : >98% (HPLC)
Size | Price / USD | Stock | Quantity |
2MG | 264 | Get Quote |
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5MG | 404 | Get Quote |
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10MG | 593 | Get Quote |
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25MG | 888 | Get Quote |
|
50MG | 1251 | Get Quote |
|
100MG | 1692 | Get Quote |
|
500MG | 3402 | Get Quote |
|
1G | Get Quote | Get Quote |
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Biological Information
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Product NamehDHODH-IN-7
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NoteResearch use only, not for human use.
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Brief DescriptionDHODH-IN-9 (Compound 10k) is a nitrogen-containing analog and is a human dihydrorotatory dehydrogenase inhibitor.
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DescriptionDHODH-IN-9 (Compound 10k) is a nitrogen-containing analog and is a human dihydrorotatory dehydrogenase inhibitor. DHODH-IN-9 and pMIC50 of 7.4 have antiviral effects.(In Vitro):hDHODH-IN-7 is the corresponding pyridazine homologue from 3-chloro-6-cyclopropylpyridazine. There is almost no change, and the antiviral mode of action of the analogs with 5-cyclopyridine reflects the antiviral effect of homologues with 5-ethylpyrimidinyl groups to some extent. hDHODH-IN-7 is a good antiviral agent for such analogs.
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Synonyms——
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PathwayMetabolic Enzyme/Protease
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TargetDehydrogenase
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RecptorApoptosis
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Research Area——
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Indication——
Chemical Information
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CAS Number1644156-41-1
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Formula Weight366.4
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Molecular FormulaC21H23FN4O
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Purity>98% (HPLC)
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Solubility——
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SMILESCC(C)Oc1nn(c(C)c1Cc1ccccc1F)-c1ncc(cn1)C1CC1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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DHODH-IN-11
DHODH-IN-11 is a leflunomide derivative and weak dihydroorotate dehydrogenase (DHODH) inhibitor with a pKa of 5.03.A compound structurally related to leflunomide was designed, which contained furan ring (compound 14a).
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CAY10566
CAY10566 shows excellent cellular activity in blocking the conversion of saturated long-chain fatty acid-CoAs (LCFA-CoAs) to monounsaturated LCFA-CoAs in HepG2 cells (IC50=7.9 nM or 6.8 nM). CAY10566 is a potent, orally bioavailable and selective stearoyl-CoA desaturase1 (SCD1) inhibitor with IC50s of 4.5 and 26 nM in mouse and human enzymatic assays, respectively.
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Kakkalide
Kakkalide is a potent lactate dehydrogenase (LDH) inhibitor, it has anti-inflammatory effects.