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Ophiopogon jaburan

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64401ac003742847381078
Scientific name Ophiopogon jaburan
Authority (Siebold) G.Lodd.
First published in Bot. Cab. 19: t. 1876 (1832)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Slateria jaburan Siebold Verh. Batav. Genootsch. Kunsten 12: 15 (1830)
Mondo jaburan (Siebold) L.H.Bailey Gentes Herbarum 2: 27 (1929)
Mondo taquetii (H.Lév.) Farw. Amer. Midl. Naturalist 7: 43 (1921)
Ophiopogon taquetii H.Lév. Repert. Spec. Nov. Regni Veg. 8: 171 (1910)
Flueggea jaburan (Siebold) Kunth Enum. Pl. [Kunth] 5: 303. 1850 [10-11 Jun 1850]
Convallaria japonica var. major Thunb. Fl. Jap. 159. 1784
Mondo jaburan var. major (Thunb.) Nakai Bull. Natl. Sci. Mus. Tokyo 31: 144 1952
Flueggea japonica var. major (Thunb.) Schult. & Schult.f. Syst. Veg. 7: 309 1829
Mondo japonicum var. major (Thunb.) Farw. Amer. Midl. Naturalist 7: 42 1921

Common names Top

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Language Common/alternative name
English lilyturf
Japanese ノシラン
Chinese 剑叶沿阶草
Chinese 劍葉沿階草

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000673566
USDA Plants OPJA3
Tropicos 18404335
INPN 630268
KEW urn:lsid:ipni.org:names:429779-1
The Plant List kew-279474
Open Tree Of Life 725824
NCBI Taxonomy 100505
Nature Serve 2.151419
IPNI 429779-1
iNaturalist 165862
GBIF 2774214
EPPO OPPJB
EOL 1002092
USDA GRIN 25787

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
Plastome structure, phylogenomic analyses and molecular dating of Arecaceae Chen DJ, Landis JB, Wang HX, Sun QH, Wang Q, Wang HF Front Plant Sci 27-Sep-2022
PMCID:PMC9552784
doi:10.3389/fpls.2022.960588
PMID:36237503
Liriopogons (Genera Ophiopogon and Liriope, Asparagaceae): A Critical Review of the Phytochemical and Pharmacological Research Lei F, Weckerle CS, Heinrich M Front Pharmacol 03-Dec-2021
PMCID:PMC8678496
doi:10.3389/fphar.2021.769929
PMID:34925027
An Exploration of Traditional Chinese Medicinal Plants with Anti-Inflammatory Activities Fan C, Jin HZ, Wu L, Zhang Y, Ye RD, Zhang W, Zhang Y Evid Based Complement Alternat Med 04-Apr-2017
PMCID:PMC5394394
doi:10.1155/2017/1231820
PMID:28473862
Networks in a Large-Scale Phylogenetic Analysis: Reconstructing Evolutionary History of Asparagales (Lilianae) Based on Four Plastid Genes Chen S, Kim DK, Chase MW, Kim JH PLoS One 18-Mar-2013
PMCID:PMC3605904
doi:10.1371/journal.pone.0059472
PMID:23544071
Comparative studies on the constituents of ophiopogonis tuber and its congeners. III. Studies on the constituents of the subterranean part of Ophiopogon ohwii Okuyama and O. jaburan (Kunth) Lodd. YOSHIAKI WATANABE, SHUICHI SANADA, YOSHITERU IDA, JUNZO SHOJI Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.32.3994
Molecular phylogenetics of Ruscaceae sensu lato and related families (Asparagales) based on plastid and nuclear DNA sequences Kim JH, Kim DK, Forest F, Fay MF, Chase MW Ann Bot 07-Oct-2010
PMCID:PMC2958784
doi:10.1093/aob/mcq167
PMID:20929900
Isolation of a new flavonol glycoside and its effects on the blue color of seed coats ofOphiopogon jaburan Kunijiro Yoshitama, Tomoyuki Kawasoe, Nariyuki Ishikura Springer Science and Business Media LLC 15-Mar-2006
doi:10.1007/BF02344589
Effect of Ethylene on Flower Abscission: a Survey VAN DOORN WG Ann Bot 01-Jun-2002
PMCID:PMC4233834
doi:10.1093/aob/mcf124
PMID:12102524
Anthocyanin-Flavonol Co-pigmentation in Blue Seed Coats of Ophiopogon jaburan. Ishikura N, Yoshitama K J Plant Physiol 01-May-1984
doi:10.1016/S0176-1617(84)80064-4
PMID:23196143

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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
[(2R,3R,4R,5R,6R)-4-hydroxy-2-methyl-6-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,14R,16R)-5',7,9,13-tetramethyl-16-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] hydrogen sulfate 162895833 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)C)OS(=O)(=O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1 965.10 unknown https://doi.org/10.1248/CPB.32.3994
[(2R,3R,4R,5R,6R)-4-hydroxy-6-[[(1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16R)-6-hydroxy-7,9,13-trimethyl-16-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[3-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]but-3-enyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-14-yl]oxy]-2-methyl-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] hydrogen sulfate 162852096 Click to see 1143.20 unknown https://doi.org/10.1248/CPB.32.3994
[(2R,3R,4R,5R,6R)-4-hydroxy-6-[[(1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16R)-6-hydroxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-16-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-14-yl]oxy]-2-methyl-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] hydrogen sulfate 162897698 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)OC6C(C(C(C(O6)CO)O)O)O)OC7C(C(C(C(O7)C)OS(=O)(=O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O 1145.30 unknown https://doi.org/10.1248/CPB.32.3994
[(3S,4R,5R,6S)-4-hydroxy-6-[[(1S,2S,4S,6S,7S,8R,9S,12S,13R,14R,16R)-6-hydroxy-7,9,13-trimethyl-16-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[3-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]but-3-enyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-14-yl]oxy]-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] hydrogen sulfate 162944161 Click to see 1129.20 unknown https://doi.org/10.1248/CPB.32.3994
[4-Hydroxy-2-methyl-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-6-[7,9,13-trimethyl-5'-methylidene-16-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxyoxan-3-yl] hydrogen sulfate 78302661 Click to see 963.10 unknown https://doi.org/10.1248/CPB.32.3994
[4-Hydroxy-2-methyl-6-[5',7,9,13-tetramethyl-16-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] hydrogen sulfate 162895832 Click to see 965.10 unknown https://doi.org/10.1248/CPB.32.3994
[4-Hydroxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-6-[7,9,13-trimethyl-5'-methylidene-16-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxyoxan-3-yl] hydrogen sulfate 78302662 Click to see 949.10 unknown https://doi.org/10.1248/CPB.32.3994
[4-Hydroxy-6-[[6-hydroxy-7,9,13-trimethyl-16-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[3-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]but-3-enyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-14-yl]oxy]-2-methyl-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] hydrogen sulfate 162852095 Click to see 1143.20 unknown https://doi.org/10.1248/CPB.32.3994
[4-Hydroxy-6-[[6-hydroxy-7,9,13-trimethyl-16-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[3-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]but-3-enyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-14-yl]oxy]-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] hydrogen sulfate 162944160 Click to see 1129.20 unknown https://doi.org/10.1248/CPB.32.3994
[4-Hydroxy-6-[[6-hydroxy-7,9,13-trimethyl-6-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-16-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-14-yl]oxy]-2-methyl-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] hydrogen sulfate 162897697 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)OC6C(C(C(C(O6)CO)O)O)O)OC7C(C(C(C(O7)C)OS(=O)(=O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O 1145.30 unknown https://doi.org/10.1248/CPB.32.3994
Glycoside J-3 3086405 Click to see 963.10 unknown https://doi.org/10.1248/CPB.32.3994
Glycoside J-4 3086406 Click to see 949.10 unknown https://doi.org/10.1248/CPB.32.3994
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Ophionin 44256959 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C(=C5)OC6C(C(C(C(O6)CO)O)O)O)O)OC)O)O)OC7C(C(C(C(O7)CO)O)O)O)O)O)O)O)O 949.80 unknown https://doi.org/10.1016/S0176-1617(84)80064-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-dihydroxy-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 162910336 Click to see 610.50 unknown https://doi.org/10.1007/BF02344589

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