- 英文名称(E)-5-((1S,4Ar,6S,8Ar)-6-Hydroxy-5,5,8A-Trimethyl-2-Methylenedecahydronaphthalen-1-yl)-3-Methylpent-2-Enoic Acid
- 中文名称紫背金牛酸
- IUPAC名称(E)-5-((1S,4aR,6S,8aR)-6-hydroxy-5,5,8a-trimethyl-2-methylenedecahydronaphthalen-1-yl)-3-methylpent-2-enoic acid
- 其它别名Alepterolic Acid; Purple-Backed Taurine; 2-Pentenoic Acid, 5-(Decahydro-6-Hydroxy-5,5,8A-Trimethyl-2-Methylene-1-Naphthalenyl)-3-Methyl-, [1S-(1α,4Aβ,6α,8Aα)]- (9Ci)
- CAS编号63399-38-2
- MFCD编号:MFCD17214872
- 分子式:C20H32O3分子量:320.47
- 产品CID: 1615546
- 产品分类天然产物 → 萜类
- 相似结构搜索
- 产品信息参考
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- InChIKey: LNWOKEZJIRLIDO-ZJGHDVHGSA-N
- InChI=1S/C20H32O3/c1-13(12-18(22)23)6-8-15-14(2)7-9-16-19(3,4)17(21)10-11-20(15,16)5/h12,15-17,21H,2,6-11H2,1,3-5H3,(H,22,23)/b13-12+/t15-,16-,17-,20+/m0/s1
- 计算化学: 氢键受体数3.0氢键供体数2.0可旋转键数4.0
上下游产品
methyl(E)-3-methyl-5-(trans-decahydro-5',5',8a'β-trimethyl-2'-methylene-6'β-hydroxy-1'β-naphthalenyl)-2-pentenoate -5',5',8a'β-trimethyl-2'-methylene-1'β-naphthalenyl>-3-oxo-pentanoatemethyl 5--5',5',8a'β-trimethyl-2'-methylene-1'β-naphthalenyl-3-oxo-pentanoate Trifluoro-methanesulfonic acid (1S,4aR,6S,8aS)-6-(tert-butyl-dimethyl-silanyloxy)-5,5,8a-trimethyl-2-methylene-decahydro-naphthalen-1-ylmethyl ester (Z)-5-[(1S,4aR,6S,8aR)-6-(tert-Butyl-dimethyl-silanyloxy)-5,5,8a-trimethyl-2-methylene-decahydro-naphthalen-1-yl]-3-(diethoxy-phosphoryloxy)-pent-2-enoic acid methyl ester 海关参考信息
- 2901210000-乙烯
2901220000-丙烯
2905122000-异丙醇
2912110000-甲醛 - 💡 提示:海关信息按照顺序优先匹配,如需确认的海关信息,请参考相关资料。
- 详情请参考:📖 海关编码查询和海关进出口税则
专利信息
专利号:CN-111393318-B
优先权日:2020-04-13
标题 :Synthesis of aleuritopteris forbesii acid amide derivative and application of aleuritopteris forbesii acid amide derivative in antitumor drugs供应商参考报价(招募中)
品牌试剂参考报价(招募中)
📌 第三方产品分析报告
✅ COA系统入驻 | 共享模式
合成参考文献
参考文献:10.5281/zenodo.5794106
摘要:The LOTUS Initiative for Open Natural Products Research: frozen dataset union wikidata (with metadata) | DOI:10.5281/zenodo.5794106
参考文献:10.1016/s0031-9422(00)84783-4
摘要:Zinkel DF, Magee TV. Diterpene resin acids from the needle oleoresin of pinus strobus. Phytochemistry. 1987 Jan;26(3):769–74. doi: 10.1016/s0031-9422(00)84783-4.