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Osmanthus armatus

Osmanthus armatus - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64402b0499751834709970
Scientific name Osmanthus armatus
Authority Diels
First published in Bot. Jahrb. Syst. 29: 532 (1900)

Description Top

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Synonyms Top

Scientific name Authority First published in
Osmanthus armatus var. microcarpus J.L.Liu Bull. Bot. Res., Harbin 21: 337 (2001)
Osmanthus obtusifolius H.T.Chang Acta Sci. Nat. Univ. Sunyatseni 1982(2): 12 (1982)

Common names Top

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Language Common/alternative name
Chinese 罐子草
Chinese 红柄木樨
Chinese 红柄木犀
Chinese 小果木犀

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000817169
Tropicos 23000784
KEW urn:lsid:ipni.org:names:610852-1
The Plant List kew-355019
Missouri Botanical Garden 301075
Open Tree Of Life 752431
NCBI Taxonomy 424903
IUCN Red List 152840236
IPNI 610852-1
iNaturalist 502501
GBIF 7326088
EPPO OSUAR
USDA GRIN 26119
Wikipedia Osmanthus_armatus

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Plastid genomes reveal evolutionary shifts in elevational range and flowering time of Osmanthus (Oleaceae) Li Y, Li X, Sylvester SP, Zhang M, Wang X, Duan Y Ecol Evol 01-Apr-2022
PMCID:PMC8975774
doi:10.1002/ece3.8777
PMID:35386867
Complete plastome sequence of Osmanthus armatus and phylogenetic implications in Oleaceae Du Y, Li R, Zhang Q Mitochondrial DNA B Resour 19-Sep-2019
PMCID:PMC7706894
doi:10.1080/23802359.2019.1666686
PMID:33365865
Rapid, Effective DNA Isolation from Osmanthus via Modified Alkaline Lysis Alexander L J Biomol Tech 18-Jan-2016
PMCID:PMC4719223
doi:10.7171/jbt.16-2702-001
PMID:26816495
Community Structure and Survival of Tertiary Relict Thuja sutchuenensis (Cupressaceae) in the Subtropical Daba Mountains, Southwestern China Tang CQ, Yang Y, Ohsawa M, Momohara A, Yi SR, Robertson K, Song K, Zhang SQ, He LY PLoS One 30-Apr-2015
PMCID:PMC4415794
doi:10.1371/journal.pone.0125307
PMID:25928845
Constituents from the heartwoods of Osmanthus armatus. Yin RJ, Huang XF, Kong LY Nat Prod Res 01-Jun-2010
doi:10.1080/14786410802689713
PMID:20496233

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Anthracenes
Anthrone, 1,8-dihydroxy-3-methoxy-6-methyl- 19132 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2)C=C(C=C3O)OC 270.28 unknown https://doi.org/10.1080/14786410802689713
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin 3220 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)O 270.24 unknown https://doi.org/10.1080/14786410802689713
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
5-Methoxy-3-methyl-2,7-bis(prop-2-enoxy)-9,10-dihydrophenanthrene 163003263 Click to see CC1=CC2=C(CCC3=C2C(=CC(=C3)OCC=C)OC)C=C1OCC=C 336.40 unknown https://doi.org/10.1080/14786410802689713
> Lignans, neolignans and related compounds / Furanoid lignans
3,6-Bis(4-hydroxy-3-methoxyphenyl)-1,3,4,6-tetrahydrofuro[3,4-c]furan-3a,6a-diol 14890536 Click to see COC1=C(C=CC(=C1)C2C3(COC(C3(CO2)O)C4=CC(=C(C=C4)O)OC)O)O 390.40 unknown https://doi.org/10.1080/14786410802689713
Prinsepiol 3010931 Click to see COC1=C(C=CC(=C1)C2C3(COC(C3(CO2)O)C4=CC(=C(C=C4)O)OC)O)O 390.40 unknown https://doi.org/10.1080/14786410802689713
> Lignans, neolignans and related compounds / Lignan glycosides
(+)-Phylliroside 21722933 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)OC 534.60 unknown https://doi.org/10.1080/14786410802689713
Forsythin 12314162 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)OC 534.60 unknown https://doi.org/10.1080/14786410802689713
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 2371 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1080/14786410802689713
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1080/14786410802689713
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(6beta,24R)-6-Hydroxystigmast-4-en-3-one 14769504 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C 428.70 unknown https://doi.org/10.1080/14786410802689713
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1080/14786410802689713
6beta-Hydroxystigmast-4-en-3-one 9823926 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C 428.70 unknown https://doi.org/10.1080/14786410802689713
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1080/14786410802689713
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2-methoxyphenoxy]oxane-3,4,5-triol 3496897 Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O 342.34 unknown https://doi.org/10.1080/14786410802689713
2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 323959 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown https://doi.org/10.1080/14786410802689713
4-O-[[4-(6-ethyl-3,4,5-trihydroxyoxan-2-yl)oxyphenyl]methyl] 1-O-[[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl] 2-butan-2-yl-2-hydroxybutanedioate 162914675 Click to see CCC1C(C(C(C(O1)OC2=CC=C(C=C2)COC(=O)CC(C(C)CC)(C(=O)OCC3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 724.70 unknown https://doi.org/10.1080/14786410802689713
4-O-[[4-[(2S,3R,4S,5S,6R)-6-ethyl-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]methyl] 1-O-[[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl] (2S)-2-[(2S)-butan-2-yl]-2-hydroxybutanedioate 162914676 Click to see CCC1C(C(C(C(O1)OC2=CC=C(C=C2)COC(=O)CC(C(C)CC)(C(=O)OCC3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 724.70 unknown https://doi.org/10.1080/14786410802689713
4-O-butyl 1-O-[[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl] (2R)-2-hydroxy-2-(2-methylpropyl)butanedioate 163007573 Click to see CCCCOC(=O)CC(CC(C)C)(C(=O)OCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)O 514.60 unknown https://doi.org/10.1080/14786410802689713
4-O-butyl 1-O-[[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl] 2-hydroxy-2-(2-methylpropyl)butanedioate 163007572 Click to see CCCCOC(=O)CC(CC(C)C)(C(=O)OCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)O 514.60 unknown https://doi.org/10.1080/14786410802689713
Coniferin 5280372 Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O 342.34 unknown https://doi.org/10.1080/14786410802689713
Eleutheroside B 5316860 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown https://doi.org/10.1080/14786410802689713
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
1,3-Dihydroxy-8,9-dimethoxy-[1]benzofuro[3,2-c]chromen-6-one 11602329 Click to see COC1=C(C=C2C(=C1)C3=C(O2)C4=C(C=C(C=C4OC3=O)O)O)OC 328.27 unknown https://doi.org/10.1080/14786410802689713

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