AZD9898
CAS No. 2042347-69-1
AZD9898( —— )
Catalog No. M26621 CAS No. 2042347-69-1
AZD9898 is an orally active leukotriene-C4 synthetase (LTC4S, glutathione S-transferase II) inhibitor, with an IC50 of 0.28 nM. AZD9898 has the potential to treat asthma. AZD9898 mitigates the GABA binding and hepatic toxicity signal.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 528 | Get Quote |
|
10MG | 755 | Get Quote |
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25MG | 1152 | Get Quote |
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50MG | 1548 | Get Quote |
|
100MG | Get Quote | Get Quote |
|
200MG | Get Quote | Get Quote |
|
500MG | Get Quote | Get Quote |
|
1G | Get Quote | Get Quote |
|
Biological Information
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Product NameAZD9898
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NoteResearch use only, not for human use.
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Brief DescriptionAZD9898 is an orally active leukotriene-C4 synthetase (LTC4S, glutathione S-transferase II) inhibitor, with an IC50 of 0.28 nM. AZD9898 has the potential to treat asthma. AZD9898 mitigates the GABA binding and hepatic toxicity signal.
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DescriptionAZD9898 is an orally active leukotriene-C4 synthetase (LTC4S, glutathione S-transferase II) inhibitor, with an IC50 of 0.28 nM. AZD9898 has the potential to treat asthma. AZD9898 mitigates the GABA binding and hepatic toxicity signal.(In Vivo):AZD9898 (10 and 100 mg/kg; oral) is well tolerated and shows no safety concerns.
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In Vitro——
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In VivoAZD9898 with the single dose of 100 mg/kg is well tolerated and no safety concerns are raised. Animal Model:Rat 6M/group.Dosage:10 and 100 mg/kg (for Toxicology Study).Administration:Sing oral dose.Result:Showed no signs of testicular toxicity, and only adaptive changes in the liver due to cytochrome P450 induction which were not judged adverse, providing a 200 fold margin between the no adverse effect level and the predicted human exposure at the predicted therapeutic dose.
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorAntifungal
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Research Area——
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Indication——
Chemical Information
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CAS Number2042347-69-1
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Formula Weight457.83
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Molecular FormulaC20H19ClF3N3O4
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : ≥ 250 mg/mL (546.05 mM)
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SMILESCOc1nc(cnc1C(=O)[C@H]1C[C@@H]1C(O)=O)N(CC(C)(C)F)c1cc(Cl)c(F)cc1F
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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
1.S Boukaew, et al. Efficacy of volatile compounds from Streptomyces philanthi RL-1-178 as a biofumigant for controlling growth and aflatoxin production of the two aflatoxin-producing fungi on stored soybean seeds. J Appl Microbiol. 2020 Sep;129(3):652-664.
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