- 相似结构搜索
- InChIKey: IHXHBYFWSOYYTR-ZDUSSCGKSA-N
- InChI=1S/C17H20N2O5/c1-17(2,3)24-16(23)18-13(15(21)22)8-11-9-19(10-20)14-7-5-4-6-12(11)14/h4-7,9-10,13H,8H2,1-3H3,(H,18,23)(H,21,22)/t13-/m0…
- 计算化学: 氢键受体数5.0氢键供体数2.0可旋转键数5.0
相似化合物
143824-78-6 144599-95-1 163619-04-3上下游产品
CAS号73-22-3 L-色氨酸 | CAS号23446-11-9 B°C-MET-GLY-TRP... | CAS号121062-08-6 美拉诺坦 II | CAS号137668-62-3 MSH (5-10), cyclic | CAS号74257-18-4 (2S)-2-amino-3-... | CAS号54-12-6 色氨酸二碳酸二叔丁酯,Nin-Formyl-L-Tryptophan置于三乙胺体系中,用 N,N-二甲基甲酰胺 作为反应溶剂,化学反应 48.0H,以61%的收率获得产物n-叔丁氧羰基-N'-醛基-L-色氨酸
参考文献:Tert-Butoxycarbonylation Of Amino Acids And Their Derivatives: N-Tert-Butoxycarbonyl-L-Phenylalanine
标题:Tert-Butoxycarbonylation Of Amino Acids And Their Derivatives: N-Tert-Butoxycarbonyl-L-Phenylalanine
摘要:
DOI:10.15227/orgsyn.063.0160
海关参考信息
- 2902200000-苯
2905122000-异丙醇
2905143000-叔丁醇
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。
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专利信息
专利号:US-2007179279-A1
优先权日:2005-12-30
标题:Methods for the synthesis of arginine-containing peptides
发明人:CHEN LIN; ROBERTS CHRISTOPHER R
权利人:CHEN LIN; ROBERTS CHRISTOPHER R
摘要:Methods for the synthesis of arginine-containing peptides are provided. The methods include a step that minimizes contact of side chain protected arginine with base prior to the coupling step.
专利号:US-7038037-B2
优先权日:2002-06-20
标题 :Method for sequential support-bound synthesis of conjugated oligomeric compounds
发明人:MAIER MARTIN A; GUZAEV ANDREI P; MANOHARAN MUTHIAH
权利人:ISIS PHARMACEUTICALS INC
摘要:A sequential support-bound synthesis method is disclosed for preparing a conjugated oligomeric compound, preferably a PNA-peptide conjugate or an oligonucleotide-peptide conjugate, using a bridging molecule having at least two N-protecting amino groups. A conjugated oligomeric compound for therapeutic or prophylactic delivery is also disclosed.
专利号:US-2004110228-A1
优先权日:2002-04-01
标 题:Combinatorial organic synthesis of unique biologically active compounds
发明人:MCALPINE SHELLI R; TAYLOR RACHEL E; BOLLA MEGAN L; SEGALL ANCA M
摘要:The invention provides a method for making a combinatorial library of cyclic compounds, such as Holliday junction-trapping compounds, comprising the steps of (a) obtaining a plurality of trimers according to the generic structure X 1- X 2- X 3 , wherein X 1 , X 2 and X 3 can be independently any naturally or nonnaturally occurring amino acids or peptidomimetics thereof; (b) optionally coupling a spacer S to the trimer at either end; (c) cyclizing two trimers or trimer-spacer conjugates in a head-to-tail orientation; thereby obtaining a combinatorial library of compounds, wherein the library does not include an unmodifed or naturally occurring Holliday Junction-trapping compounds. The invention additionally provides methods macrocyclic compounds that are synergimycin derivatives.
专利号:US-2004006203-A1
优先权日:2002-06-20
标题 :Method for sequential support-bound synthesis of conjugated oligomeric compounds
专利号:EP-1968995-A1
优先权日:2005-12-30
标 题:Methods for the synthesis of arginine-containing peptides
专利号:CN-102686601-A
优先权日:2009-11-16
标 题 :Synthesis of Ac-Arg-cyclo(Cys-D-Ala-His-D-Phe-Arg-Trp-Cys)-NH2