METHOD FOR PRODUCING PEPTIDE COMPOUND
A task of the present invention is to provide a method for producing a peptide at high efficiency. In the present invention, there is provided a method for producing a peptide, which comprises the steps of:(1) removing the N-terminal protective group of an amino acid or peptide compound represented...
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creator | NAGAYA, Akihiro MIMORI, Yuji HANDA, Michiharu |
description | A task of the present invention is to provide a method for producing a peptide at high efficiency. In the present invention, there is provided a method for producing a peptide, which comprises the steps of:(1) removing the N-terminal protective group of an amino acid or peptide compound represented by the formula (I):wherein Y represents a residue of an N-protected amino acid or an N-protected peptide, andeach of R1, R2, and R3 independently represents an aliphatic hydrocarbon group which may have a substituent (in which each of 1 to 5 methylene groups in the aliphatic hydrocarbon group may be independently replaced by a structure selected from the group consisting of -O-, -CO-, -N(R6)-, -N(R7)CO-, and -CON(R8)-) or an aromatic hydrocarbon group which may have a substituent, wherein each of R6, R7, and R8 independently represents a hydrogen atom or a C1-6 alkyl group,wherein the total number of carbon atoms in the R1R2R3Si group is 18 to 80, andthe R1R2R3SiCH2CH2 group is bonded to the C-terminus of the amino acid or peptide residue in Y;and(2) causing condensation of an N-protected amino acid or an N-protected peptide and the N-terminus of the C-protected amino acid or C-protected peptide obtained in the step (1). |
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In the present invention, there is provided a method for producing a peptide, which comprises the steps of:(1) removing the N-terminal protective group of an amino acid or peptide compound represented by the formula (I):wherein Y represents a residue of an N-protected amino acid or an N-protected peptide, andeach of R1, R2, and R3 independently represents an aliphatic hydrocarbon group which may have a substituent (in which each of 1 to 5 methylene groups in the aliphatic hydrocarbon group may be independently replaced by a structure selected from the group consisting of -O-, -CO-, -N(R6)-, -N(R7)CO-, and -CON(R8)-) or an aromatic hydrocarbon group which may have a substituent, wherein each of R6, R7, and R8 independently represents a hydrogen atom or a C1-6 alkyl group,wherein the total number of carbon atoms in the R1R2R3Si group is 18 to 80, andthe R1R2R3SiCH2CH2 group is bonded to the C-terminus of the amino acid or peptide residue in Y;and(2) causing condensation of an N-protected amino acid or an N-protected peptide and the N-terminus of the C-protected amino acid or C-protected peptide obtained in the step (1).</description><language>eng ; fre ; ger</language><subject>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM ; CHEMISTRY ; METALLURGY ; ORGANIC CHEMISTRY ; PEPTIDES</subject><creationdate>2024</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20240904&DB=EPODOC&CC=EP&NR=4023661B1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76290</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20240904&DB=EPODOC&CC=EP&NR=4023661B1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>NAGAYA, Akihiro</creatorcontrib><creatorcontrib>MIMORI, Yuji</creatorcontrib><creatorcontrib>HANDA, Michiharu</creatorcontrib><title>METHOD FOR PRODUCING PEPTIDE COMPOUND</title><description>A task of the present invention is to provide a method for producing a peptide at high efficiency. In the present invention, there is provided a method for producing a peptide, which comprises the steps of:(1) removing the N-terminal protective group of an amino acid or peptide compound represented by the formula (I):wherein Y represents a residue of an N-protected amino acid or an N-protected peptide, andeach of R1, R2, and R3 independently represents an aliphatic hydrocarbon group which may have a substituent (in which each of 1 to 5 methylene groups in the aliphatic hydrocarbon group may be independently replaced by a structure selected from the group consisting of -O-, -CO-, -N(R6)-, -N(R7)CO-, and -CON(R8)-) or an aromatic hydrocarbon group which may have a substituent, wherein each of R6, R7, and R8 independently represents a hydrogen atom or a C1-6 alkyl group,wherein the total number of carbon atoms in the R1R2R3Si group is 18 to 80, andthe R1R2R3SiCH2CH2 group is bonded to the C-terminus of the amino acid or peptide residue in Y;and(2) causing condensation of an N-protected amino acid or an N-protected peptide and the N-terminus of the C-protected amino acid or C-protected peptide obtained in the step (1).</description><subject>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM</subject><subject>CHEMISTRY</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><subject>PEPTIDES</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2024</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZFD1dQ3x8HdRcPMPUggI8ncJdfb0c1cIcA0I8XRxVXD29w3wD_Vz4WFgTUvMKU7lhdLcDApuriHOHrqpBfnxqcUFicmpeakl8a4BJgZGxmZmhk6GxkQoAQBfxiLl</recordid><startdate>20240904</startdate><enddate>20240904</enddate><creator>NAGAYA, Akihiro</creator><creator>MIMORI, Yuji</creator><creator>HANDA, Michiharu</creator><scope>EVB</scope></search><sort><creationdate>20240904</creationdate><title>METHOD FOR PRODUCING PEPTIDE COMPOUND</title><author>NAGAYA, Akihiro ; MIMORI, Yuji ; HANDA, Michiharu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_EP4023661B13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng ; fre ; ger</language><creationdate>2024</creationdate><topic>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM</topic><topic>CHEMISTRY</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><topic>PEPTIDES</topic><toplevel>online_resources</toplevel><creatorcontrib>NAGAYA, Akihiro</creatorcontrib><creatorcontrib>MIMORI, Yuji</creatorcontrib><creatorcontrib>HANDA, Michiharu</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>NAGAYA, Akihiro</au><au>MIMORI, Yuji</au><au>HANDA, Michiharu</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>METHOD FOR PRODUCING PEPTIDE COMPOUND</title><date>2024-09-04</date><risdate>2024</risdate><abstract>A task of the present invention is to provide a method for producing a peptide at high efficiency. In the present invention, there is provided a method for producing a peptide, which comprises the steps of:(1) removing the N-terminal protective group of an amino acid or peptide compound represented by the formula (I):wherein Y represents a residue of an N-protected amino acid or an N-protected peptide, andeach of R1, R2, and R3 independently represents an aliphatic hydrocarbon group which may have a substituent (in which each of 1 to 5 methylene groups in the aliphatic hydrocarbon group may be independently replaced by a structure selected from the group consisting of -O-, -CO-, -N(R6)-, -N(R7)CO-, and -CON(R8)-) or an aromatic hydrocarbon group which may have a substituent, wherein each of R6, R7, and R8 independently represents a hydrogen atom or a C1-6 alkyl group,wherein the total number of carbon atoms in the R1R2R3Si group is 18 to 80, andthe R1R2R3SiCH2CH2 group is bonded to the C-terminus of the amino acid or peptide residue in Y;and(2) causing condensation of an N-protected amino acid or an N-protected peptide and the N-terminus of the C-protected amino acid or C-protected peptide obtained in the step (1).</abstract><oa>free_for_read</oa></addata></record> |
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subjects | ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM CHEMISTRY METALLURGY ORGANIC CHEMISTRY PEPTIDES |
title | METHOD FOR PRODUCING PEPTIDE COMPOUND |
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