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| - wetenschappelijk artikel (nl)
- наукова стаття (uk)
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| publication date
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| publication date
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| author name string
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| author name string
| - HARUO MEGURI
- MASAAKI KATAI
- TADAMASA TERAI
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| rdfs:label
| - Triterpenoids of the bark of Pieris japonica D. Don (Japanese name: asebi). II. 13C Nuclear magnetic resonance of the .GAMMA.-lactones of ursane- and oleanane-type triterpenes. (en)
- Triterpenoids of the bark of Pieris japonica D. Don (Japanese name: asebi). II. 13C Nuclear magnetic resonance of the .GAMMA.-lactones of ursane- and oleanane-type triterpenes. (nl)
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| skos:prefLabel
| - Triterpenoids of the bark of Pieris japonica D. Don (Japanese name: asebi). II. 13C Nuclear magnetic resonance of the .GAMMA.-lactones of ursane- and oleanane-type triterpenes. (en)
- Triterpenoids of the bark of Pieris japonica D. Don (Japanese name: asebi). II. 13C Nuclear magnetic resonance of the .GAMMA.-lactones of ursane- and oleanane-type triterpenes. (nl)
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| name
| - Triterpenoids of the bark of Pieris japonica D. Don (Japanese name: asebi). II. 13C Nuclear magnetic resonance of the .GAMMA.-lactones of ursane- and oleanane-type triterpenes. (en)
- Triterpenoids of the bark of Pieris japonica D. Don (Japanese name: asebi). II. 13C Nuclear magnetic resonance of the .GAMMA.-lactones of ursane- and oleanane-type triterpenes. (nl)
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| title
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| title
| - Triterpenoids of the bark of Pieris japonica D. Don (Japanese name: asebi). II. 13C Nuclear magnetic resonance of the .GAMMA.-lactones of ursane- and oleanane-type triterpenes. (en)
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| main subject
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| main subject
| - Pieris japonica
- taraxerol
- D-Friedoolean-14-en-3-one
- taraxerone
- beta-Sitosterone
- Acetyl taraxerol
- (1S,4S,5R,8R,10S,13S,14R,17S,18R,19S,20R)-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracos-15-en-10-yl acetate
- (1S,4S,5R,8R,10S,13R,14R,16S,17S,18R)-16-hydroxy-4,5,9,9,13,20,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosan-10-yl acetate
- [(3S,4aR,6aR,6bS,8aS,11R,12S,12aS,14aR,14bR)-8a-formyl-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl] acetate
- Uvaol 3-acetate
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| is about
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| is cites work
of | - Two isomeric epoxysitosterols from Rhododendron formosanum: 1H and 13C NMR chemical shift assignments
- ACE and platelet aggregation inhibitors from Tamarix hohenackeri Bunge (host plant of Herba Cistanches) growing in Xinjiang
- Constituents ofClinopodium Umbrosum
- Dihydrochalcones from the leaves of Pieris japonica
- Cancer chemopreventive activity of oleanane-type triterpenoids from the stem bark of Betula ermanii.
- Triterpenoidal constituents from Eucalyptus camaldulensis var. obtusa leaves
- Studies on cytotoxic constituents from the leaves of Elaeagnus oldhamii Maxim. in non-small cell lung cancer A549 cells.
- Terpenoidal constituents of Eucalyptus loxophleba ssp. lissophloia
- Bismuth triflate-catalyzed Wagner-Meerwein rearrangement in terpenes. Application to the synthesis of the 18alpha-oleanane core and A-neo-18alpha-oleanene compounds from lupanes
- Cladocalol, a pentacyclic 28-nor-triterpene from Eucalyptus cladocalyx with cytotoxic activity
- Efficient oxidation of oleanolic acid derivatives using magnesium bis(monoperoxyphthalate) hexahydrate (MMPP): A convenient 2-step procedure towards 12-oxo-28-carboxylic acid derivatives
- Triterpene saponins from the roots of Ilex asprella
- Tyrosinase inhibitors from the leaves of Eucalyptus globulus
- Triterpenoids from the resin of Shorea robusta
- Spasmolytic constituents from Eucalyptus camaldulensis var. obtusa leaves
- Two triterpenoid lactones from the resin of Bursera delpechiana
- Three New Triterpenoids fromDracocephalum forrestii
- β-Amyrin acetate epoxide from Canarina canariensis
- Colebroside A, a new diglucoside of fatty acid ester of glycerin from Clerodendrum colebrookianum
- One lignanoid compound and four triterpenoid compounds with anti-inflammatory activity from the leaves of Elaeagnus oldhamii maxim.
- Alkylphloroglucinol derivatives and triterpenoids with soluble epoxide hydrolase inhibitory activity from Callistemon citrinus.
- Antinociceptive Grayanane Diterpenoids from the Leaves of Pieris japonica
- UPLC-PDA-Q Exactive Orbitrap-MS profiling of the lipophilic compounds product isolated from <i>Eucalyptus viminalis</i> plants
- (1S*,2R*,4aS*,6aS*,6bR*,10S*,12aR*,14aS*)-10-Hydr-oxy-1,2,6a,6b,9,9,12a-hepta-methyl-perhydro-picene-4a,14a-carbolactone
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