奥美拉唑镁结构式
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常用名 | 奥美拉唑镁 | 英文名 | Omeprazole magnesium |
|---|---|---|---|---|
| CAS号 | 95382-33-5 | 分子量 | 713.121 | |
| 密度 | N/A | 沸点 | 600ºC at 760mmHg | |
| 分子式 | C17H19MgN3O3S | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 316.7ºC |
奥美拉唑镁用途奥美拉唑镁是一种口服活性质子泵抑制剂(PPI),可以抑制胃酸。奥美拉唑镁可用于酸反流相关症状和频繁烧心的研究[1][2]。 |
| 中文名 | 奥美拉唑镁 |
|---|---|
| 英文名 | Magnesium,bis[6-methoxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl-kO]-1H-benzimidazolato-kN3]-, (T-4) |
| 英文别名 | 更多 |
| 描述 | 奥美拉唑镁是一种口服活性质子泵抑制剂(PPI),可以抑制胃酸。奥美拉唑镁可用于酸反流相关症状和频繁烧心的研究[1][2]。 |
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| 相关类别 | |
| 参考文献 |
[1]. Holt S, et al. Omeprazole. Overview and opinion. Dig Dis Sci. 1991 Apr;36(4):385-93. |
| 沸点 | 600ºC at 760mmHg |
|---|---|
| 分子式 | C17H19MgN3O3S |
| 分子量 | 713.121 |
| 闪点 | 316.7ºC |
| 精确质量 | 712.198792 |
| PSA | 96.31000 |
| LogP | 3.76540 |
| InChIKey | MQEUGMWHWPYFDD-UHFFFAOYSA-N |
| SMILES | COc1ccc2nc(S(=O)Cc3ncc(C)c(OC)c3C)[nH]c2c1.[Mg] |
| 水溶解性 | Very slightly soluble in water, sparingly soluble in methanol, practically insoluble in heptane. |
| 危险品运输编码 | NONH for all modes of transport |
|---|---|
| 海关编码 | 2933990090 |
| 海关编码 | 2933990090 |
|---|---|
| 中文概述 | 2933990090. 其他仅含氮杂原子的杂环化合物. 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 | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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实验名称:Primary cell-based high-throughput screening assay for identification of compounds th...
来源:Johns Hopkins Ion Channel Center
靶标:regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id:JHICC_RGS_Act_HTS
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实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
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实验名称:QFRET-based biochemical primary high throughput screening assay to identify exosite i...
来源:The Scripps Research Institute Molecular Screening Center
靶标:disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
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实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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实验名称:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
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实验名称:Antibacterial activity against Staphylococcus aureus MRSA ATCC 43300 (CO-ADD:GP_020);...
来源:ChEMBL
靶标:Staphylococcus aureus
External Id:CHEMBL4296184
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实验名称:Antibacterial activity against Klebsiella pneumoniae MDR ATCC 70063 (CO-ADD:GN_003); ...
来源:ChEMBL
靶标:Klebsiella pneumoniae
External Id:CHEMBL4296186
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实验名称:Antibacterial activity against Escherichia coli ATCC 25922 (CO-ADD:GN_001); MIC in CA...
来源:ChEMBL
靶标:Escherichia coli
External Id:CHEMBL4296185
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实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
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实验名称:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
来源:Broad Institute
靶标:N/A
External Id:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
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