About: Biosynthesis of oleanene- and ursene-type triterpenes from [4-13C]mevalonolactone and sodium [1,2-13C2]acetate in tissue cultures of Isodon japonicus Hara

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About: Biosynthesis of oleanene- and ursene-type triterpenes from [4-13C]mevalonolactone and sodium [1,2-13C2]acetate in tissue cultures of Isodon japonicus Hara Goto Sponge NotDistinct Permalink

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Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття (uk) article scientifique publié en 2005 (fr)
publication date	wds:Q104415713-51DCEF66-21E6-4055-A412-0C516A10E185
publication date	1981-04-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q104415713-1B4640D7-369A-4BF1-8743-5D1A39CA8FEB wds:Q104415713-98525505-D7D9-48A4-AEEE-D7ECB63A165D wds:Q104415713-BFE8D044-B3E5-47AD-84FD-1F0B1DA49F4F
author name string	Shujiro Seo Yutaka Tomita Kazuo Tori
rdfs:label	Biosynthesis of oleanene- and ursene-type triterpenes from [4-13C]mevalonolactone and sodium [1,2-13C2]acetate in tissue cultures of Isodon japonicus Hara (en) Biosynthesis of oleanene- and ursene-type triterpenes from [4-13C]mevalonolactone and sodium [1,2-13C2]acetate in tissue cultures of Isodon japonicus Hara (nl)
skos:prefLabel	Biosynthesis of oleanene- and ursene-type triterpenes from [4-13C]mevalonolactone and sodium [1,2-13C2]acetate in tissue cultures of Isodon japonicus Hara (en) Biosynthesis of oleanene- and ursene-type triterpenes from [4-13C]mevalonolactone and sodium [1,2-13C2]acetate in tissue cultures of Isodon japonicus Hara (nl)
name	Biosynthesis of oleanene- and ursene-type triterpenes from [4-13C]mevalonolactone and sodium [1,2-13C2]acetate in tissue cultures of Isodon japonicus Hara (en) Biosynthesis of oleanene- and ursene-type triterpenes from [4-13C]mevalonolactone and sodium [1,2-13C2]acetate in tissue cultures of Isodon japonicus Hara (nl)
title	wds:Q104415713-96C22ACD-4F4A-4984-BBE0-B133FD5B6DD4
title	Biosynthesis of oleanene- and ursene-type triterpenes from [4-13C]mevalonolactone and sodium [1,2-13C2]acetate in tissue cultures of Isodon japonicus Hara (en)
page(s)	wds:Q104415713-D0251CC9-263D-4A95-B8D1-700EF848C21F
page(s)	2075-2080
instance of	wds:Q104415713-7112B0E2-6431-4952-8B98-E021DAA34680
instance of	scholarly article
main subject	wds:Q104415713-03DE18EE-158A-418E-9E50-50A36618F7D5 wds:Q104415713-04CCD37F-D819-4601-967F-AAB9FB635FA4 wds:Q104415713-363ADABB-43AF-4219-A96D-CDE5ADF127CB wds:Q104415713-403F7764-F63A-4FB9-81F3-F14A0D1E592E wds:Q104415713-46A4D52D-D9F9-4C62-8AEF-3645713E94DF wds:Q104415713-79342460-5392-4048-B4D4-B56978E02B4B wds:Q104415713-938926D9-1195-4933-9CBD-D38503D298B7 wds:Q104415713-A98D428C-1118-45BC-97EF-06D55D34F7E9
main subject	stigmastanol Isodon japonicus 17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol Methyl ursolate Methyl oleanolate Maslinic acid methyl ester Methyl 3-epimaslinate methyl (1R,2R,4S,5R,6S,11S,14R,15R,18R,20S,23S)-20-hydroxy-8,8,14,15,19,19,23-heptamethyl-3-oxahexacyclo[13.8.0.02,4.05,14.06,11.018,23]tricosane-11-carboxylate
published in	wds:Q104415713-7F33AA66-A55A-411C-A181-559D1F2A8924
published in	Journal of the American Chemical Society
issue	wds:Q104415713-BA14015C-4C85-402E-B661-8482B8B21E4B
volume	wds:Q104415713-EA1F42A9-9A4A-4003-94D2-EDCF36E71A39
issue	8
volume	103
DOI	wds:Q104415713-25327F9F-8E0E-416A-AA0E-8ED588EEDB71
DOI	http://dx.doi.org/10.1021/JA00398A034
DOI	10.1021/JA00398A034
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q104415713
is cites work of	Chemical Constituents from the Root and Aerial Parts ofRosa taiwanensis Advances in triterpenoid research, 1990-1994. Antiproliferative constituents from Umbelliferae plants VII. Active triterpenes and rosmarinic acid from Centella asiatica Revisited after 50 Years: The ‘Stereochemical Interpretation of the Biogenetic Isoprene Rule for the Triterpenes’ Triterpenoidal Secondary Metabolites fromLantana CamaraLinn. Pentacyclic triterpenoids from the aerial parts of Lantana camara. Triterpenoids from Desfontainia spinosa Investigation of the biosynthesis of 3α-hydroxy triterpenoids, ganoderic acids T and S, by application of a feeding experiment using [1,2-13C2]acetate Ganoderic acid derivatives, highly oxygenated lanostane-type triterpenoids, from Ganoderma lucidum Triterpenoids from enkianthus campanulatus Triterpenoids from Eucalyptus perriniana cultured cells Structural and spectral assignment of three forskolin-like diterpenoids isolated from Plectranthus ornatus. Bacchara-12,21-dien-3β-ol from the seeds of Glycine max
is cites work of	wds:Q104415183-4A002D21-3E11-497B-AA67-8DA6B2DA45EB wds:Q104384024-19976D13-3167-487D-A4F1-8FDEF7933D47 wds:Q104884511-DA3238A8-9941-4C13-92CD-1E89C68C3965 wds:Q56489906-9B73DEAB-270F-4025-A7C6-80B6DC305D9E wds:Q104924008-515A7543-32ED-40F7-BC11-ACB4FE0F4817 wds:Q104989324-1D7A34E9-E1D3-4BDF-82E6-3BC9B575BF5A wds:Q46517144-A5CF49B8-869E-4E00-B0D9-90A34D1BCD9B wds:Q45213614-5C9601AE-868B-4496-AF7F-ECE15FB3EBB7 wds:Q44308612-5D71018E-7784-41DD-901E-6E775ECECCB7 wds:Q104917087-0BE9B40E-0939-4736-88A2-769003344D75 wds:Q41442227-7ACB913C-2DB3-420B-96BD-CCDB54B452FC wds:Q58239804-243B3483-CAB4-444E-9C06-59DF035D0B7A wds:Q104850663-C13026DD-2C3E-4542-A267-3AEC6C452834
is pr:P248 of	wdref:6225998aaa1405a0360ed333acba58fe7bfd2c38

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