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水合氧化前胡素

更新时间:2025-08-24 19:58:21

水合氧化前胡素结构式
水合氧化前胡素结构式
品牌特惠专场
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。

 水合氧化前胡素名称

中文名 水合氧化前胡素
英文名 Oxypeucedanin hydrate
英文别名 更多

 水合氧化前胡素生物活性

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。
相关类别
参考文献

[1]. Mottaghipisheh J, et al. Antiproliferative and cytotoxic activities of furocoumarins of Ducrosia anethifolia. Pharm Biol. 2018 Dec;56(1):658-664.

 水合氧化前胡素物理化学性质

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℃

 水合氧化前胡素合成线路

~92%

水合氧化前胡素结构式

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

~%

水合氧化前胡素结构式

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

~%

水合氧化前胡素结构式

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

~%

水合氧化前胡素结构式

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

~%

水合氧化前胡素结构式

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

 水合氧化前胡素靶点实验

查看更多实验

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
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
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
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
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
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.
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
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
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
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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 水合氧化前胡素英文别名

4-[(2R)-2,3-Dihydroxy-3-methylbutoxy]-7H-furo[3,2-g]chromen-7-one
oxypeucedaninhydrate
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