4-咪唑-1-基丁酸结构式
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常用名 | 4-咪唑-1-基丁酸 | 英文名 | 4-IMIDAZOL-1-YL-BUTYRIC ACID |
|---|---|---|---|---|
| CAS号 | 72338-58-0 | 分子量 | 154.16600 | |
| 密度 | 1.21g/cm3 | 沸点 | 406ºC at 760 mmHg | |
| 分子式 | C7H10N2O2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 199.3ºC |
| 中文名 | 4-咪唑-1-基丁酸 |
|---|---|
| 英文名 | 4-imidazol-1-ylbutanoic acid |
| 英文别名 | 更多 |
| 密度 | 1.21g/cm3 |
|---|---|
| 沸点 | 406ºC at 760 mmHg |
| 分子式 | C7H10N2O2 |
| 分子量 | 154.16600 |
| 闪点 | 199.3ºC |
| 精确质量 | 154.07400 |
| PSA | 55.12000 |
| LogP | 0.74790 |
| InChIKey | ZCWMZLARYIDEEZ-UHFFFAOYSA-N |
| SMILES | O=C(O)CCCn1ccnc1 |
| 折射率 | 1.56 |
| 危害码 (欧洲) | Xi: Irritant; |
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| 海关编码 | 2933290090 |
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~72%
4-咪唑-1-基丁酸 72338-58-0 |
| 文献:Takeda Chemical Industries, Ltd. Patent: US5719157 A1, 1998 ; |
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~91%
4-咪唑-1-基丁酸 72338-58-0 |
| 文献:Lahue, Brian R.; Lo, Sie-Mun; Wan, Zhao-Kui; Woo, Grace H. C.; Snyder, John K. Journal of Organic Chemistry, 2004 , vol. 69, # 21 p. 7171 - 7182 |
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~%
4-咪唑-1-基丁酸 72338-58-0 |
| 文献:Varasi; Tarzia; Luzzani; Gallico; Barone Farmaco, Edizione Scientifica, 1987 , vol. 42, # 6 p. 425 - 435 |
| 4-咪唑-1-基丁酸上游产品 3 | |
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| 4-咪唑-1-基丁酸下游产品 2 | |
| 海关编码 | 2933290090 |
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| 中文概述 | 2933290090. 其他结构含非稠合咪唑环的化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0% |
| 申报要素 | 品名, 成分含量, 用途, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期 |
| Summary | 2933290090. other compounds containing an unfused imidazole ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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实验名称:Selectivity ratio of pIC50 for mouse GAT3 to pIC50 for mouse GAT4
来源:ChEMBL
靶标:N/A
External Id:CHEMBL1776004
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实验名称:Selectivity ratio of pIC50 for mouse GAT3 to pIC50 for mouse GAT2
来源:ChEMBL
靶标:N/A
External Id:CHEMBL1776003
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实验名称:Discovery of Small Molecules to Inhibit Human Cytomegalovirus Nuclear Egress
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:HCMV UL50
External Id:HMS1262
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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
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实验名称:Inhibition of mouse GAT1-mediated [3H]GABA uptake expressed in human HEK cells
来源:ChEMBL
靶标:Sodium- and chloride-dependent GABA transporter 1
External Id:CHEMBL1775994
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实验名称:Inhibition of mouse GAT3-mediated [3H]GABA uptake expressed in human HEK cells
来源:ChEMBL
靶标:Sodium- and chloride-dependent GABA transporter 3
External Id:CHEMBL1775996
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实验名称:Inhibition of mouse GAT2-mediated [3H]GABA uptake expressed in human HEK cells
来源:ChEMBL
靶标:Sodium- and chloride-dependent GABA transporter 2
External Id:CHEMBL1775995
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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
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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
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实验名称:Selectivity ratio of pIC50 for mouse GAT3 topIC50 for mouse GAT1
来源:ChEMBL
靶标:N/A
External Id:CHEMBL1776030
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| 4-imidazolylbutanoic acid |
| 1H-imidazole-1-butanoic acid |
| 4-Imidazol-1-yl-butyric acid |
| Imidazole-1-butyric acid |
| 4-imidazole-1-yl butyric acid |