- 相似结构搜索
- InChIKey: OYULCCKKLJPNPU-PIGZYNQJSA-N
- InChI=1S/C19H19NO5/c1-11(21)17(18(22)23)20-19(24)25-10-16-14-8-4-2-6-12(14)13-7-3-5-9-15(13)16/h2-9,11,16-17,21H,10H2,1H3,(H,20,24)(H,22,23)/t11-,17-/m1/s1
- 计算化学: 氢键受体数4.0氢键供体数3可旋转键数5
相似化合物
120791-76-6 73724-48-8 253595-72-1欧盟法规
C&L通报上下游产品
D-allo-threonine α-(9-Fluorenylmethoxycarbonyl)-D-allothreonine t-butyl etherNα-(9-Fluorenylmethoxycarbonyl)-D-allothreonine t-butyl ether N-(9H-fluoren-2-ylmethoxycarbonyloxy)succinimideL-threonine N-methyl threonine N,N-dimethyl-threonine Nα-(9-fluorenylmethoxycarbonyl)-3-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-L-threonine 📜D-别苏氨酸 反应生成芴甲氧羰基-L-苏氨酸
参考文献:Solid-Phase Synthesis Of Viscosin,A Cyclic Depsipeptide With Antibacterial And Antiviral Properties
标题:Solid-Phase Synthesis Of Viscosin,A Cyclic Depsipeptide With Antibacterial And Antiviral Properties
摘要:
Doi:10.1016/s0040-4039(00)95242-0
海关参考信息
- 2902600000-乙苯
2905122000-异丙醇
2905399001-1,3-丙二醇
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:US-8569452-B2
优先权日:2011-02-17
标题:Preparation of phalloidin and its derivatives
发明人:LIU BAOSHENG; ZHANG JIANHENG
权利人:LIU BAOSHENG; ZHANG JIANHENG; AMERICAN PEPTIDE COMPANY INC
摘要:The present invention relates to novel phalloidin derivatives and their fluorescent dye conjugates. These new compounds may be used in studies of actin dynamics in living systems. The present invention also relates to methods for preparing such compounds. The synthesis routes combine solid-phase and solution phase peptide synthesis, and has great advantage for efficient preparation of a diverse library of the phalloidin derivatives, especially for the synthesis of phalloidin.
专利号:US-2025011366-A1
优先权日:2021-09-08
标 题:Prodrugs of Antibiotic Teixobactin
发明人:JONES CHELSEA R; NOWICK JAMES S
权利人:UNIV CALIFORNIA
摘要:Prodrugs of antibiotic teixobactin, methods of their synthesis, and methods of their use as antimicrobial treatments are described. The teixobactin prodrugs incorporate one or more O-acyl linkages. The O-acyl linkages can be utilized in substitution of amide peptide bonds between an amino acid containing an alcohol side chain and the immediately preceding amino acid.
专利号:JP-2008506633-A
优先权日:2004-04-22
标题 :Convergent synthesis of kahalalide compounds
专利号:US-11897970-B2
优先权日:2017-03-09
标 题 :Antibacterial products
发明人:SINGH ISHWAR; TAYLOR EDWARD
权利人:UNIV LIVERPOOL
摘要:The invention provides novel antibacterial compounds of formulae IA, IB and IC as defined herein. Optionally, the antibacterial compounds can be bonded to a delivery agent that is capable of bonding to one or more structures on a bacterial cell membrane. The invention also provides the use of such compounds in treating or preventing bacterial infections, and processes for their synthesis.