Irdabisant (CEP-26401) 是一种具有选择性、口服活性和血脑屏障渗透性的组胺 H3 受体 (histamine H3 receptor, H3R) 拮抗剂/逆激动剂,对大鼠 H3R 和人 H3R 的 Ki 分别为 7.2 nM 和 2.0 nM。Irdabisant 对 hERG 电流的抑制活性相对较低,IC50 为 13.8 μM。Irdabisant 在大鼠社会认知模型中具有认知增强和唤醒作用。 Irdabisant (CEP-26401) is a selective, orally active and blood-brain barrier (BBB) penetrant histamine H3 receptor (H3R) inverse agonist/inverse agonist with Ki values of 7.2 nM and 2.0 nM for rat H3R and human H3R, respectively. Irdabisant has relatively low inhibitory activity against hERG current with an IC50 of 13.8 μM. Irdabisant has cognition-enhancing and wake-promoting activities in the rat social recognition model. Irdabisant can be used to research schizophrenia or cognitive impairment
All
Chemical Reagents
Biomedicine
Organic raw materials
Inorganic chemical industry
intermediate
Agricultural chemicals
Auxiliaries and catalysts
Fragrances and Flavors
Dyes and Pigments
Daily chemical industry
Irdabisant
CAS number:1005402-19-6 molecular formula:C18H23N3O2
overview
compound introduction
Specs
| Chinese alias | 伊尔达比桑特 | ||
| English alias | Irdabisant | IRDABISANT [WHO-DD] | CEP26401 | BDBM50350021 | Irdabisant [USAN:INN] | DTXSID50143375 | 3-[4-[3-[(2R)-2-methylpyrrolidin-1-yl]propoxy]phenyl]-1H-pyridazin-6-one | HY-109968 | 1005402-19-6 | Q27292641 | CHEMBL1813052 | IRDABISANT [USAN] | AT3 | ||
| CAS number | 1005402-19-6 | molecular formula | C18H23N3O2 |
| molecular weight | 313.39 g/mol | Exact mass | ≥98% |
| PSA | 53.900 Ų | logp | 2.5 |
numbering system
No numbering system information yet
physicochemical properties
No physical and chemical property information yet
Safety information
No safety information yet
Production methods and uses
No production method and use information yet
Related
upstream information
No upstream information yet
downstream information
No downstream information yet
MSDS
Found 0 shareMSDS





