6,8-二异戊烯基金雀异黄素结构式
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常用名 | 6,8-二异戊烯基金雀异黄素 | 英文名 | 6,8-diprenylgenistein |
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| CAS号 | 51225-28-6 | 分子量 | 406.47 | |
| 密度 | 1.2±0.1 g/cm3 | 沸点 | 627.4±55.0 °C at 760 mmHg | |
| 分子式 | C25H26O5 | 熔点 | N/A | |
| MSDS | 美版 | 闪点 | 214.6±25.0 °C |
6,8-二异戊烯基金雀异黄素用途6,8-Diprenylgenistein 是从杜仲中分离得到的一种异黄酮类化合物。6,8-Diprenylgenistein 具有抗微生物和抗肥胖活性。6,8-Diprenylgenistein 可抑制重组人血管内皮生长因子-A 诱导的 HLMEC 的增殖、迁移和管状形成。6,8-Diprenylgenistein 可用于研究预防和治疗口腔癌转移的新型治疗药物。 |
| 中文名 | 6,8-二异戊烯基金雀异黄素 |
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| 英文名 | 5,7,4'-trihydroxy-6,8-diprenylisoflavone |
| 英文别名 | 更多 |
| 描述 | 6,8-Diprenylgenistein 是从杜仲中分离得到的一种异黄酮类化合物。6,8-Diprenylgenistein 具有抗微生物和抗肥胖活性。6,8-Diprenylgenistein 可抑制重组人血管内皮生长因子-A 诱导的 HLMEC 的增殖、迁移和管状形成。6,8-Diprenylgenistein 可用于研究预防和治疗口腔癌转移的新型治疗药物。 |
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| 相关类别 | |
| 参考文献 |
| 密度 | 1.2±0.1 g/cm3 |
|---|---|
| 沸点 | 627.4±55.0 °C at 760 mmHg |
| 分子式 | C25H26O5 |
| 分子量 | 406.47 |
| 闪点 | 214.6±25.0 °C |
| 精确质量 | 406.178009 |
| PSA | 90.90000 |
| LogP | 7.14 |
| InChIKey | UCHYSPNEUSDFQR-UHFFFAOYSA-N |
| SMILES | CC(C)=CCc1c(O)c(CC=C(C)C)c2occ(-c3ccc(O)cc3)c(=O)c2c1O |
| 外观性状 | 黄色粉末 |
| 蒸汽压 | 0.0±1.9 mmHg at 25°C |
| 折射率 | 1.634 |
| 储存条件 | -20℃,密封,干燥 |
| 危险品运输编码 | NONH for all modes of transport |
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| 海关编码 | 2932999099 |
| 6,8-二异戊烯基金雀异黄素上游产品 0 | |
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| 6,8-二异戊烯基金雀异黄素下游产品 2 | |
| 海关编码 | 2932999099 |
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| 中文概述 | 2932999099. 其他仅含氧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 |
| Summary | 2932999099. other heterocyclic compounds with oxygen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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A new prenylated flavanone from Derris trifoliata Lour.
Molecules 17(1) , 657-63, (2012) A new flavanone, 4',5,7-trihydroxy-6,8-di-(2-hydroxy-3-methylbut-3-enyl)- flavanone, was isolated from the aerial parts of Derris trifoliate, together with eleven known compounds: rotenone, tephrosin,... |
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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:Inhibition of porcine pancreatic lipase assessed as hydrolysis of p-NPB to p-nitrophe...
来源:ChEMBL
靶标:Pancreatic triacylglycerol lipase
External Id:CHEMBL3266917
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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:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
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| 6,8-Diprenylgenistein |
| 5,7-Dihydroxy-3-(4-hydroxyphenyl)-6,8-bis(3-methyl-2-buten-1-yl)-4H-chromen-4-one |