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1-(4-(4-Iodophenoxy)butyl)-1H-imidazole

更新时间:2026-03-03 20:40:39

1-(4-(4-Iodophenoxy)butyl)-1H-imidazole结构式
1-(4-(4-Iodophenoxy)butyl)-1H-imidazole结构式
委托求购
常用名 1-(4-(4-Iodophenoxy)butyl)-1H-imidazole 英文名 1-(4-(4-Iodophenoxy)butyl)-1H-imidazole
CAS号 415722-32-6 分子量 342.18
密度 N/A 沸点 N/A
分子式 C13H15IN2O 熔点 N/A
MSDS N/A 闪点 N/A

 1-(4-(4-Iodophenoxy)butyl)-1H-imidazole名称

英文名 1-(4-(4-Iodophenoxy)butyl)-1H-imidazole

 1-(4-(4-Iodophenoxy)butyl)-1H-imidazole物理化学性质

分子式 C13H15IN2O
分子量 342.18
InChIKey OLXWUOZHYJJJSP-UHFFFAOYSA-N
SMILES C1=CC(=CC=C1OCCCCN2C=CN=C2)I

 1-(4-(4-Iodophenoxy)butyl)-1H-imidazole靶点实验

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实验名称:Inhibition of heme oxygenase 1 in human K562R cell lysates assessed as decrease in bi...
来源:ChEMBL
靶标:Heme oxygenase 1
External Id:CHEMBL4268725
实验名称:Chemical Probes of Kaposi's Sarcoma Herpes Virus Latent Infection
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:ORF 73 [Human herpesvirus 8 type M]
External Id:HMS791
实验名称:Small-molecule inhibitors of ST2 (IL1RL1)
来源:20881
靶标:interleukin-1 receptor-like 1 isoform [homo sapiens]
External Id:ST2_IL33_Inhibitors_Primary_Screening_77700
实验名称:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
实验名称:Induction of ROS production in human K562R cells at 10 uM by DCFH-DA dye based spectr...
来源:ChEMBL
靶标:K-562R
External Id:CHEMBL4268728
实验名称:Inhibition of heme oxygenase 1 in Sprague-Dawley rat spleen microsomal fraction asses...
来源:ChEMBL
靶标:Heme oxygenase 1
External Id:CHEMBL4268715
实验名称:Cytotoxicity against imatinib-sensitive human K562 cells assessed as decrease in cell...
来源:ChEMBL
靶标:K562
External Id:CHEMBL4268714
实验名称:High-throughput screen for inhibitors of the GIV GBA-motif interaction with Galpha-i ...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS1303
实验名称:Cytotoxicity against human K562R cells assessed as decrease in cell viability after 2...
来源:ChEMBL
靶标:K-562R
External Id:CHEMBL4268716
实验名称:Cytotoxicity against MDCK cells incubated for 72 hrs by sulforhodamine B assay
来源:ChEMBL
靶标:MDCK
External Id:CHEMBL3420446
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