BMS-193884结构式
|
常用名 | BMS-193884 | 英文名 | BMS-193884 |
|---|---|---|---|---|
| CAS号 | 176960-47-7 | 分子量 | 395.43200 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C20H17N3O4S | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
BMS-193884用途BMS-193884是一种选择性、口服活性和竞争性ETA拮抗剂,对人类ETA受体(Ki=1.4nM)的亲和力是ETB受体的10000倍[1]。 |
| 英文名 | N-(3,4-dimethyl-1,2-oxazol-5-yl)-2-[4-(1,3-oxazol-2-yl)phenyl]benzenesulfonamide |
|---|
| 描述 | BMS-193884是一种选择性、口服活性和竞争性ETA拮抗剂,对人类ETA受体(Ki=1.4nM)的亲和力是ETB受体的10000倍[1]。 |
|---|---|
| 相关类别 | |
| 靶点实验 |
ETA:1.4 nM (Ki) ETB:18700 nM (Ki) |
| 参考文献 |
| 分子式 | C20H17N3O4S |
|---|---|
| 分子量 | 395.43200 |
| 精确质量 | 395.09400 |
| PSA | 106.61000 |
| LogP | 5.56800 |
| InChIKey | LJGUZUROJOJEMI-UHFFFAOYSA-N |
| SMILES | Cc1noc(NS(=O)(=O)c2ccccc2-c2ccc(-c3ncco3)cc2)c1C |
|
~53%
BMS-193884 176960-47-7 |
| 文献:Journal of Medicinal Chemistry, , vol. 43, # 16 p. 3111 - 3117 |
|
~%
BMS-193884 176960-47-7 |
| 文献:Journal of Medicinal Chemistry, , vol. 43, # 16 p. 3111 - 3117 |
|
~%
BMS-193884 176960-47-7 |
| 文献:Journal of Medicinal Chemistry, , vol. 43, # 16 p. 3111 - 3117 |
|
~%
BMS-193884 176960-47-7 |
| 文献:Journal of Medicinal Chemistry, , vol. 43, # 16 p. 3111 - 3117 |
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实验名称:Percent oral bioavailability at dose of 50 umol/kg in monkey
来源:ChEMBL
靶标:N/A
External Id:CHEMBL633870
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实验名称:Tested for volume distribution at intravenous dose of 50 umol/kg in monkey
来源:ChEMBL
靶标:N/A
External Id:CHEMBL642530
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实验名称:Inhibitory activity against human endothelin B receptor expressed in CHO cells
来源:ChEMBL
靶标:Endothelin receptor type B
External Id:CHEMBL673234
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实验名称:Binding affinity to CHO cells stably expressing human Endothelin B receptor.
来源:ChEMBL
靶标:Endothelin receptor type B
External Id:CHEMBL672283
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实验名称:Half life in monkey at intravenous dose of 50 umol/kg
来源:ChEMBL
靶标:N/A
External Id:CHEMBL633886
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实验名称:Inhibitory activity against human endothelin A receptor expressed in CHO cells
来源:ChEMBL
靶标:Endothelin-1 receptor
External Id:CHEMBL678072
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实验名称:Compound was evaluated for oral bioavailability in rats
来源:ChEMBL
靶标:N/A
External Id:CHEMBL621775
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