CAS: 119831-72-0; Fmoc-Arg(Pmc)-Oh

相似化合物

154445-77-9 187618-60-6 2124196-74-1

上下游产品

CAS号82911-69-1 9-芴甲基-N-琥珀酰亚胺碳酸酯 | CAS号112160-37-9 N5-[[[(3,4-二氢-2... | CAS号55646-01-0 2,2,5,7,8-五甲基色满 | CAS号697-82-5 2,3,5-三甲基苯酚 | CAS号112160-39-1 2,2,5,7,8-五甲基苯并... | CAS号112160-32-4 Nα-benzyloxycar... | CAS号78-79-5 异戊二烯 | CAS号2387-23-7 N,N’-二环己基脲 | CAS号2791-05-1 促肾上腺皮质激素片段 (1-10),人 | CAS号700377-76-0 Fm°C-L-β-homoar...

📜2,3,5-三甲基苯酚置于palladium On Activated Charcoal 氯磺酸,Sodium Hydroxide,氢气,Sodium Carbonate,Zinc(II) Chloride体系中,用 甲醇,氯仿,溶剂黄146,N,N-二甲基甲酰胺,丙酮 用作溶剂,化学反应 25.25H,反应生成Nα-Fmoc-Nω-(2,2,5,7,8-五甲基苯并二氢吡喃-6-磺酰基)-L-精氨酸
参考文献:用于肽合成的酸不稳定的精氨酸衍生物:N G-2,2,2,5,7,8-五甲基苯并吡喃-6-磺酰基-L-精氨酸
标题:用于肽合成的酸不稳定的精氨酸衍生物:N G-2,2,2,5,7,8-五甲基苯并吡喃-6-磺酰基-L-精氨酸
摘要:已经开发出用于精氨酸的胍侧链功能的三氟乙酸(tfa)不稳定的保护基.ñ ģ-(2,2,5,7,8-五甲基-6-磺酰基-L-精氨酸在室温下迅速裂解以tfa或50%tfa的二氯甲烷溶液fmoc.Arg(pmc).oh的制剂和描述了bnpeoc.Arg(pmc).Oh.
Doi:10.1016/s0040-4020(01)86564-9

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-6316593-B1
优先权日:1996-02-09
标题:Synthesis of VIP analog
发明人：BOLIN DAVID ROBERT; DANHO WALEED; FELIX ARTHUR M
权利人:HOFFMANN LA ROCHE
摘要:This invention relates to a novel process for the synthesis of vasoactive intestinal peptide analog Ac(1-31)-NH2 from four protected peptide fragments.

专利号:WO-9106558-A1
优先权日:1989-10-25
标题 :Process for peptide synthesis and vehicles therefor
发明人：FRANK RONALD; KRAUSE SUSANNE
权利人:BIOTECHNOLOG FORSCHUNG GMBH
摘要:The invention concerns a process for the fast and, where appropriate, simultaneous synthesis of peptides and suitable rod-like vehicles therefor.

专利号:US-6316595-B1
优先权日:1994-03-14
标题 :PNA synthesis using a base-labile amino protecting group
发明人：BREIPOHL GERHARD; UHLMANN EUGEN; KNOLLE JOCHEN
权利人:AVENTIS PHARMA GMBH
摘要:The invention provides compounds and processes for synthesis of peptide nucleic acids (PNA). The compounds include temporary amino protecting groups that are base-labile, and protection groups for the exocyclic amino function of the nucleotide base that is compatible with the base-labile amino protecting group. Cleavage of an oligomer comprising these compounds from a solid support can be achieved using weak or medium strength acids.

专利号:US-2005100968-A1
优先权日:2000-02-23
标题 :Self-encoded combinatorial synthesis of compound multiplets
发明人：GALLOP MARK A; DOWER WILLIAM J; BARRETT RON W
权利人:XENOPORT INC
摘要:The present invention provides a variety of methods for synthesizing, encoding and decoding compounds in a combinatorial library. One step or cycle in the synthetic methods of the invention is a self-encoding step in which different pairs of components, each pair with a known and different molecular weight difference, are reacted with supports, whereby two compounds differing in molecular weight are formed on each support. The molecular weight difference between the two compounds on the support encodes for a particular component pair. Libraries of compounds formed according to the methods of the invention are also provided.

专利号:US-6569993-B1
优先权日:1998-04-15
标题 :Process for the preparation of resin-bound cyclic peptides
发明人：SLEDESKI ADAM W; MENCEL JAMES J
权利人:AVENTIS PHARMA SA
摘要:This invention is directed to a process for the solid phase, fragment-based synthesis of resin-bound cyclic peptide analogs of parathyroid hormones and analogs of parathyroid hormone-related proteins, which analogs contain at least one bridge between the side chains of two non-adjacent amino acid residues, and to peptide fragments useful therefor.