Results 11 to 20 of about 894 (155)

3D documentation and classification of incense tree Aquilaria sinensis (Lour.) Spreng. wounds by photogrammetry and its potential conservation applications [PDF]

open access: yesEcology and Evolution
In recent years, illegal felling of and damage to the incense tree Aquilaria sinensis (Lour.) Spreng. have been reported in Hong Kong. Their native populations are under increasingly severe threat.
Ho Lam Wang   +4 more
doaj   +3 more sources

Dynamic Environmental Interactions Shape the Volatile Compounds of Agarwood Oils Extracted from Aquilaria sinensis Using Supercritical Carbon Dioxide [PDF]

open access: yesMolecules
Aquilaria spp. are a highly valuable plant species found in the Chinese herbal medicine and agarwood fragrance supplement industries for fumigation, combustion and perfume.
Wenxian Zhang   +5 more
doaj   +2 more sources

Repeated mechanical damage enhanced Aquilaria sinensis resistance to Heortia vitessoides through jasmonic acid [PDF]

open access: yesFrontiers in Plant Science, 2023
IntroductionThe leaf-chewing pest Heortia vitessoides severely threatens the growth and development of Aquilaria sinensis. In our previous study, we found that mechanical damage (MD) to stem enhanced A. sinensis sapling resistance to H.
Yingying Chen   +13 more
doaj   +2 more sources

Floral Biology of Aquilaria sinensis (Lour.) Spreng

open access: yesHorticulturae
Aquilaria sinensis (Lour.) Spreng is a known medicinal plant producing agarwood. To date, studies on the floral biology of A. sinensis have been limited.
Bin Wang   +8 more
doaj   +2 more sources

Development and Application of SSR Markers for Aquilaria sinensis on the Basis of Whole-Genome Resequencing Data [PDF]

open access: yesPlants
Aquilaria sinensis (Lour.) Spreng. is an economically important tree specie that produces agarwood, a valuable medicinal and aromatic resin, when injured.
Yu Chen   +9 more
doaj   +2 more sources

Bioassay-guided isolation of cytotoxic constituents from the flowers of Aquilaria sinensis. [PDF]

open access: yesNat Prod Bioprospect, 2022
AbstractBioassay-guided fractionation of the EtOH extract from the flowers of Aquilaria sinensis (Lour.) Spreng. (Thymelaeaceae) led to the isolation of a new cucurbitane-type triterpenoid, aquilarolide A (1), along with five known compounds (2–6). The structure of 1 was elucidated by extensive 1D and 2D nuclear magnetic resonance (NMR) experiments and
Yang J   +5 more
europepmc   +4 more sources

2-(2-Phenylethyl)chromones increase in Aquilaria sinensis with the formation of agarwood. [PDF]

open access: yesFront Plant Sci
Obtained from Aquilaria Lam. and Gyrinops Gaertn., agarwood is a prestigious perfume and medicinal material in the world. Its primary chemical constituents and indicators of agarwood's development are 2-(2-phenylethyl)chromones (PECs). However, how PECs affect its quality, accumulation, and transformation pattern is still unclear.
Sun Y   +5 more
europepmc   +4 more sources

Comparative Analysis of Metabolome and Transcriptome in Different Tissue Sites of Aquilaria sinensis (Lour.) Gilg [PDF]

open access: yesMolecules
The resinous stem of Aquilaria sinensis (Lour.) Gilg is the sole legally authorized source of agarwood in China. However, whether other tissue parts can be potential substitutes for agarwood requires further investigation.
Anjun Wang, Juan Liu, Luqi Huang
doaj   +2 more sources

GC-MS Study of the Chemical Components of Different Aquilaria sinensis (Lour.) Gilgorgans and Agarwood from Different Asian Countries

open access: yesMolecules, 2018
As a traditional medicinal herb and valuable natural spice in China, Aquilaria sinensis (Lour.) Gilg has many significant pharmacological effects. Agarwood is the resinous heartwood acquired from wounded A.
Shouxin Liu, , Xin Zhao
exaly   +3 more sources

Flavonoid and a Rare Benzophenone Glycoside from the Leaves of Aquilaria sinensis

open access: yesChemical and Pharmaceutical Bulletin, 2009
From the leaves of Aquilaria sinensis (LOUR.) GILG, a novel benzophenone glucoside, designated as aquilarinoside A (1), and a new flavonoid, as 7-beta-D-glucoside of 5-O-methylapigenin (2), along with eight known compounds (3-10) were isolated. The structures of 1 and 2 were fully characterized by spectroscopic methods (1D, 2D NMR and MS) and the ...
Boyang Yu, Wenling Dai
exaly   +4 more sources

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