N-(1-adamantylmethyl)-2,3-dichlorobenzamide

• 常用名: N-(1-adamantylmethyl)-2,3-dichlorobenzamide
• 英文名: N-(1-adamantylmethyl)-2,3-dichlorobenzamide
• CAS号: 227327-54-0
• 分子量: 338.3
• 密度: N/A
• 沸点: N/A
• 分子式: C₁₈H₂₁Cl₂NO
• 熔点: N/A
• 闪点: N/A

名称

• 英文名: N-(1-adamantylmethyl)-2,3-dichlorobenzamide

物理化学性质

• 分子式: C₁₈H₂₁Cl₂NO
• 分子量: 338.3
• InChIKey: OFGFKUJAQALHEW-UHFFFAOYSA-N
• SMILES: C1C2CC3CC1CC(C2)(C3)CNC(=O)C4=C(C(=CC=C4)Cl)Cl

靶点实验

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实验名称：Antagonistic activity against the P2X7 ion channel 来源：ChEMBL 靶标：P2X purinoceptor 7 External Id：CHEMBL882189

实验名称：Antagonist activity at P2X7 receptor in human THP1 cells assessed as inhibition of Bz... 来源：ChEMBL 靶标：P2X purinoceptor 7 External Id：CHEMBL1028693

实验名称：ASTRAZENECA: Octan-1-ol/water (pH7.4) distribution coefficent measured by a shake fl... 来源：ChEMBL 靶标：N/A External Id：CHEMBL3301363

实验名称：Intrinsic clearance in rat hepatocytes was determined 来源：ChEMBL 靶标：Rattus norvegicus External Id：CHEMBL875276

实验名称：Pharmacokinetic property (Vss) in rat 来源：ChEMBL 靶标：Rattus norvegicus External Id：CHEMBL624666

实验名称：Antagonist activity at human P2X7 receptor expressed in human 1321N1 cells assessed a... 来源：ChEMBL 靶标：P2X purinoceptor 7 External Id：CHEMBL870213

实验名称：Ability to block pore formation in human THP1 cells assessed as inhibition of YO-PRO-... 来源：ChEMBL 靶标：THP-1 External Id：CHEMBL869036

实验名称：Intrinsic clearance in human liver microsomes was determined 来源：ChEMBL 靶标：N/A External Id：CHEMBL618998

实验名称：Antagonist activity at human recombinant P2X7 receptor 来源：ChEMBL 靶标：P2X purinoceptor 7 External Id：CHEMBL886454

实验名称：Half life period in rat 来源：ChEMBL 靶标：Rattus norvegicus External Id：CHEMBL618518

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