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Retinoylserine and retinoylalanine, new natural products of the moth, Trichoplusia ni
Insect cells convert vitamin A into a number of retinoids that are evolutionarily conserved with those of mammalian cells. However, insect cells also produce additional natural retinoids. Namely, two retinoic acid peptides, N- trans -retinoylserine ( 1 ) and N- trans -retinoylalanine ( 2 ) ( Figure...
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Published in: | Journal of natural products (Washington, D.C.) D.C.), 2005-10, Vol.68 (10), p.1536-1540 |
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container_title | Journal of natural products (Washington, D.C.) |
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creator | Rogge, Barbara Itagaki, Yasuhiro Fishkin, Nathan Levi, Ester Rühl, Ralph Yi, San-San Nakanishi, Koji Hammerling, Ulrich |
description | Insect cells convert vitamin A into a number of retinoids that are evolutionarily conserved with those of mammalian cells. However, insect cells also produce additional natural retinoids. Namely, two retinoic acid peptides, N-
trans
-retinoylserine (
1
) and N-
trans
-retinoylalanine (
2
) (
Figure 1
), have been isolated from a cell line of the common cabbage looper,
Trichoplusia ni
. These are the first examples of naturally occurring retinoic acid linked to amino acids through an amide bond; the amino acid moieties are depicted in the more common L-configuration although the absolute configuration was not determined due to the minuscule sample amount. |
doi_str_mv | 10.1021/np0496791 |
format | article |
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trans
-retinoylserine (
1
) and N-
trans
-retinoylalanine (
2
) (
Figure 1
), have been isolated from a cell line of the common cabbage looper,
Trichoplusia ni
. These are the first examples of naturally occurring retinoic acid linked to amino acids through an amide bond; the amino acid moieties are depicted in the more common L-configuration although the absolute configuration was not determined due to the minuscule sample amount.</description><identifier>ISSN: 0163-3864</identifier><identifier>EISSN: 1520-6025</identifier><identifier>DOI: 10.1021/np0496791</identifier><identifier>PMID: 16252921</identifier><language>eng</language><ispartof>Journal of natural products (Washington, D.C.), 2005-10, Vol.68 (10), p.1536-1540</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27903,27904</link.rule.ids></links><search><creatorcontrib>Rogge, Barbara</creatorcontrib><creatorcontrib>Itagaki, Yasuhiro</creatorcontrib><creatorcontrib>Fishkin, Nathan</creatorcontrib><creatorcontrib>Levi, Ester</creatorcontrib><creatorcontrib>Rühl, Ralph</creatorcontrib><creatorcontrib>Yi, San-San</creatorcontrib><creatorcontrib>Nakanishi, Koji</creatorcontrib><creatorcontrib>Hammerling, Ulrich</creatorcontrib><title>Retinoylserine and retinoylalanine, new natural products of the moth, Trichoplusia ni</title><title>Journal of natural products (Washington, D.C.)</title><description>Insect cells convert vitamin A into a number of retinoids that are evolutionarily conserved with those of mammalian cells. However, insect cells also produce additional natural retinoids. Namely, two retinoic acid peptides, N-
trans
-retinoylserine (
1
) and N-
trans
-retinoylalanine (
2
) (
Figure 1
), have been isolated from a cell line of the common cabbage looper,
Trichoplusia ni
. These are the first examples of naturally occurring retinoic acid linked to amino acids through an amide bond; the amino acid moieties are depicted in the more common L-configuration although the absolute configuration was not determined due to the minuscule sample amount.</description><issn>0163-3864</issn><issn>1520-6025</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqlzLFOwzAUhWELgWgoDLzBfYAGru3a4IUFgZhRmS03cYlRcm3ZDqhvT4YuzExH-o_0MXbL8Y6j4PeUcGv0g-FnrOFKYKtRqHPWINeylY96u2JXpXwhokSjLtmKa6GEEbxhH---BorHsfgcyIOjHvIpudHR0jZA_gfI1Tm7EVKO_dzVAvEAdfAwxTpsYJdDN8Q0ziU4oHDNLg5uIW9Ou2ZPry-757c2zfvJ952nulg25TC5fLTRBfv3oTDYz_hthZJCGSH_DfwC8jVfcQ</recordid><startdate>20051001</startdate><enddate>20051001</enddate><creator>Rogge, Barbara</creator><creator>Itagaki, Yasuhiro</creator><creator>Fishkin, Nathan</creator><creator>Levi, Ester</creator><creator>Rühl, Ralph</creator><creator>Yi, San-San</creator><creator>Nakanishi, Koji</creator><creator>Hammerling, Ulrich</creator><scope>5PM</scope></search><sort><creationdate>20051001</creationdate><title>Retinoylserine and retinoylalanine, new natural products of the moth, Trichoplusia ni</title><author>Rogge, Barbara ; Itagaki, Yasuhiro ; Fishkin, Nathan ; Levi, Ester ; Rühl, Ralph ; Yi, San-San ; Nakanishi, Koji ; Hammerling, Ulrich</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmedcentral_primary_oai_pubmedcentral_nih_gov_25325923</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rogge, Barbara</creatorcontrib><creatorcontrib>Itagaki, Yasuhiro</creatorcontrib><creatorcontrib>Fishkin, Nathan</creatorcontrib><creatorcontrib>Levi, Ester</creatorcontrib><creatorcontrib>Rühl, Ralph</creatorcontrib><creatorcontrib>Yi, San-San</creatorcontrib><creatorcontrib>Nakanishi, Koji</creatorcontrib><creatorcontrib>Hammerling, Ulrich</creatorcontrib><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of natural products (Washington, D.C.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rogge, Barbara</au><au>Itagaki, Yasuhiro</au><au>Fishkin, Nathan</au><au>Levi, Ester</au><au>Rühl, Ralph</au><au>Yi, San-San</au><au>Nakanishi, Koji</au><au>Hammerling, Ulrich</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Retinoylserine and retinoylalanine, new natural products of the moth, Trichoplusia ni</atitle><jtitle>Journal of natural products (Washington, D.C.)</jtitle><date>2005-10-01</date><risdate>2005</risdate><volume>68</volume><issue>10</issue><spage>1536</spage><epage>1540</epage><pages>1536-1540</pages><issn>0163-3864</issn><eissn>1520-6025</eissn><abstract>Insect cells convert vitamin A into a number of retinoids that are evolutionarily conserved with those of mammalian cells. However, insect cells also produce additional natural retinoids. Namely, two retinoic acid peptides, N-
trans
-retinoylserine (
1
) and N-
trans
-retinoylalanine (
2
) (
Figure 1
), have been isolated from a cell line of the common cabbage looper,
Trichoplusia ni
. These are the first examples of naturally occurring retinoic acid linked to amino acids through an amide bond; the amino acid moieties are depicted in the more common L-configuration although the absolute configuration was not determined due to the minuscule sample amount.</abstract><pmid>16252921</pmid><doi>10.1021/np0496791</doi></addata></record> |
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source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
title | Retinoylserine and retinoylalanine, new natural products of the moth, Trichoplusia ni |
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