水合氧化前胡素结构式
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常用名 | 水合氧化前胡素 | 英文名 | Oxypeucedanin hydrate |
|---|---|---|---|---|
| CAS号 | 2643-85-8 | 分子量 | 304.295 | |
| 密度 | 1.4±0.1 g/cm3 | 沸点 | 544.3±50.0 °C at 760 mmHg | |
| 分子式 | C16H16O6 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 283.0±30.1 °C |
水合氧化前胡素用途Oxypeucedanin hydrate ((+)-Oxypeucedanin hydrate) 是从 D. anethifolia 中分离出的一种天然产物。 Prangol 对成纤维细胞和母淋巴瘤细胞有轻微毒性。 |
| 中文名 | 水合氧化前胡素 |
|---|---|
| 英文名 | Oxypeucedanin hydrate |
| 英文别名 | 更多 |
| 描述 | Oxypeucedanin hydrate ((+)-Oxypeucedanin hydrate) 是从 D. anethifolia 中分离出的一种天然产物。 Prangol 对成纤维细胞和母淋巴瘤细胞有轻微毒性。 |
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| 相关类别 | |
| 参考文献 |
| 密度 | 1.4±0.1 g/cm3 |
|---|---|
| 沸点 | 544.3±50.0 °C at 760 mmHg |
| 分子式 | C16H16O6 |
| 分子量 | 304.295 |
| 闪点 | 283.0±30.1 °C |
| 精确质量 | 304.094696 |
| PSA | 93.04000 |
| LogP | 1.31 |
| InChIKey | PEWFWDOPJISUOK-CYBMUJFWSA-N |
| SMILES | CC(C)(O)C(O)COc1c2ccoc2cc2oc(=O)ccc12 |
| 蒸汽压 | 0.0±1.5 mmHg at 25°C |
| 折射率 | 1.630 |
| 储存条件 | 2-8℃ |
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~92%
水合氧化前胡素 2643-85-8 |
| 文献:Row; Brown; Stachulski; Lennard Organic and Biomolecular Chemistry, 2006 , vol. 4, # 8 p. 1604 - 1610 |
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~%
水合氧化前胡素 2643-85-8 |
| 文献:Row; Brown; Stachulski; Lennard Organic and Biomolecular Chemistry, 2006 , vol. 4, # 8 p. 1604 - 1610 |
|
~%
水合氧化前胡素 2643-85-8 |
| 文献:Row; Brown; Stachulski; Lennard Organic and Biomolecular Chemistry, 2006 , vol. 4, # 8 p. 1604 - 1610 |
|
~%
水合氧化前胡素 2643-85-8 |
| 文献:Row; Brown; Stachulski; Lennard Organic and Biomolecular Chemistry, 2006 , vol. 4, # 8 p. 1604 - 1610 |
|
~%
水合氧化前胡素 2643-85-8 |
| 文献:Row; Brown; Stachulski; Lennard Organic and Biomolecular Chemistry, 2006 , vol. 4, # 8 p. 1604 - 1610 |
| 水合氧化前胡素上游产品 5 | |
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| 水合氧化前胡素下游产品 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:High throughput fluorescence intensity-based biochemical assay to screen for small mo...
来源:University of Pittsburgh Molecular Library Screening Center
靶标:furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id:MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
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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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实验名称:Cytotoxicity against human PSN1 cells in DMEM measured after 24 hrs by WST8 assay
来源:ChEMBL
靶标:PSN1
External Id:CHEMBL4200163
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实验名称:Cytotoxicity against human MIAPaCa2 cells in DMEM measured after 24 hrs by WST8 assay
来源:ChEMBL
靶标:MIA PaCa-2
External Id:CHEMBL4200162
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| 4-[(2R)-2,3-Dihydroxy-3-methylbutoxy]-7H-furo[3,2-g]chromen-7-one |
| oxypeucedaninhydrate |