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(2-Chloro-3-(trifluoromethyl)phenyl)(1-(5-fluoropyridin-2-YL)-1,4,6,7-tetrahydro-5H-imidazo[4,5-C]pyridin-5-YL)methanone

更新时间:2025-10-16 11:05:29

(2-Chloro-3-(trifluoromethyl)phenyl)(1-(5-fluoropyridin-2-YL)-1,4,6,7-tetrahydro-5H-imidazo[4,5-C]pyridin-5-YL)methanone结构式
(2-Chloro-3-(trifluoromethyl)phenyl)(1-(5-fluoropyridin-2-YL)-1,4,6,7-tetrahydro-5H-imidazo[4,5-C]pyridin-5-YL)methanone结构式
委托求购
常用名 (2-Chloro-3-(trifluoromethyl)phenyl)(1-(5-fluoropyridin-2-YL)-1,4,6,7-tetrahydro-5H-imidazo[4,5-C]pyridin-5-YL)methanone 英文名 (2-Chloro-3-(trifluoromethyl)phenyl)(1-(5-fluoropyridin-2-YL)-1,4,6,7-tetrahydro-5H-imidazo[4,5-C]pyridin-5-YL)methanone
CAS号 1627904-11-3 分子量 424.8
密度 N/A 沸点 N/A
分子式 C19H13ClF4N4O 熔点 N/A
MSDS N/A 闪点 N/A

 名称

英文名 (2-Chloro-3-(trifluoromethyl)phenyl)(1-(5-fluoropyridin-2-YL)-1,4,6,7-tetrahydro-5H-imidazo[4,5-C]pyridin-5-YL)methanone

 物理化学性质

分子式 C19H13ClF4N4O
分子量 424.8
InChIKey YWVQILGNCOWLGD-UHFFFAOYSA-N
SMILES O=C(c1cccc(C(F)(F)F)c1Cl)N1CCc2c(ncn2-c2ccc(F)cn2)C1

 靶点实验

查看更多实验

实验名称:Ca2+ flux assay from US Patent US10112937: "P2X7 modulators and methods of use"
来源:BindingDB
靶标:N/A
External Id:BindingDB_879_2
实验名称:Extraction ratio in rat liver microsomes at 1 uM upto 60 mins in presence of NDPH by ...
来源:ChEMBL
靶标:NON-PROTEIN TARGET
External Id:CHEMBL3858375
实验名称:FLIPR Ca2+ Flux Assay from US Patent US10150765: "P2X7 modulators"
来源:BindingDB
靶标:N/A
External Id:BindingDB_1127_2
实验名称:Radioligand Binding from US Patent US10112937: "P2X7 modulators and methods of use"
来源:BindingDB
靶标:N/A
External Id:BindingDB_879_1
实验名称:Antagonist activity at recombinant human P2X7 receptor expressed in human 1321N1 cell...
来源:ChEMBL
靶标:P2X purinoceptor 7
External Id:CHEMBL3858376
实验名称:Radioligand Binding assay from US Patent US10150765: "P2X7 modulators"
来源:BindingDB
靶标:N/A
External Id:BindingDB_1127_1
实验名称:FLIPR Assay from US Patent US9464084: "P2X7 modulators"
来源:BindingDB
靶标:N/A
External Id:BindingDB_8504_1
实验名称:Radioligand Binding from US Patent US10703749: "P2X7 modulators"
来源:BindingDB
靶标:N/A
External Id:BindingDB_9212_1
实验名称:Antagonist activity at P2X7 receptor in LPS-stimulated human PBMC assessed as inhibit...
来源:ChEMBL
靶标:P2X purinoceptor 7
External Id:CHEMBL3858372
实验名称:Antagonist activity at recombinant rat P2X7 receptor expressed in human 1321N1 cells ...
来源:ChEMBL
靶标:P2X purinoceptor 7
External Id:CHEMBL3858373
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