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Hedera rhombea

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 UUID64403ddb6b4b8163315248
Scientific name Hedera rhombea
Authority (Miq.) Paul
First published in Gard. Chron. 1867: 926 (1867)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Hedera helix var. rhombea Miq. Ann. Mus. Bot. Lugduno-Batavi 1: 13 (1863)
Hedera rhomboidea hort. ex Handl. Trees Kew Pt. i. (Polypet.) 245.
Hedera submarginata hort. ex Gard. Kew i. [Polypet.] (1895) 247.

Common names Top

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Language Common/alternative name
English japanese ivy
Japanese キヅタ
Korean 담장나무
Korean 송악
Chinese 菱叶常春藤

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Hedera rhombea var. formosana (Nakai) H.L.Li Woody Fl. Taiwan : 669 (1963)
Hedera rhombea var. rhombea Unknown

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-0000979881
KEW urn:lsid:ipni.org:names:60453330-2
The Plant List kew-96799
Open Tree Of Life 549542
NCBI Taxonomy 85360
IPNI 60453330-2
iNaturalist 447226
GBIF 3036022
Freebase /m/0h94czg
EPPO HEERH
EOL 1142997
USDA GRIN 18570
Wikipedia Hedera_rhombea
CMAUP NPO23598
PaleoBotany 86297

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
Climbing strategies of Taiwan climbers Chen PH, Chung AC, Lin HC, Yang SZ Bot Stud 22-Sep-2023
PMCID:PMC10516820
doi:10.1186/s40529-023-00399-4
PMID:37736799
Stem cambial variants of Taiwan lianas Yang SZ, Chen PH, Chen JJ Bot Stud 24-Sep-2022
PMCID:PMC9509506
doi:10.1186/s40529-022-00358-5
PMID:36153445
Xanthomonas hortorum – beyond gardens: Current taxonomy, genomics, and virulence repertoires Dia NC, Morinière L, Cottyn B, Bernal E, Jacobs JM, Koebnik R, Osdaghi E, Potnis N, Pothier JF Mol Plant Pathol 23-Jan-2022
PMCID:PMC8995068
doi:10.1111/mpp.13185
PMID:35068051
Hedera rhombea inhibits the biofilm formation of Candida, thereby increases the susceptibility to antifungal agent, and reduces infection Kim D, Kim KY PLoS One 06-Oct-2021
PMCID:PMC8494327
doi:10.1371/journal.pone.0258108
PMID:34614005
Growth Suppression of a Gingivitis and Skin Pathogen Cutibacterium (Propionibacterium) acnes by Medicinal Plant Extracts Choi HA, Ahn SO, Lim HD, Kim GJ Antibiotics (Basel) 09-Sep-2021
PMCID:PMC8465884
doi:10.3390/antibiotics10091092
PMID:34572674
An alcoholic extract of Thuja orientalis L. leaves inhibits autophagy by specifically targeting pro-autophagy PIK3C3/VPS34 complex Jung J, Chun Y, Jang YP, Oh MS, Kim JH, Kim J Sci Rep 06-Sep-2021
PMCID:PMC8421415
doi:10.1038/s41598-021-97216-4
PMID:34489486
In Vitro Screening of East Asian Plant Extracts for Potential Use in Reducing Ruminal Methane Production Bharanidharan R, Arokiyaraj S, Baik M, Ibidhi R, Lee SJ, Lee Y, Nam IS, Kim KH Animals (Basel) 04-Apr-2021
PMCID:PMC8066825
doi:10.3390/ani11041020
PMID:33916571
Bioactive C17 and C18 Acetylenic Oxylipins from Terrestrial Plants as Potential Lead Compounds for Anticancer Drug Development Christensen LP Molecules 31-May-2020
PMCID:PMC7321150
doi:10.3390/molecules25112568
PMID:32486470
The 8.2 ka cooling event in coastal East Asia: High-resolution pollen evidence from southwestern Korea Park J, Park J, Yi S, Kim JC, Lee E, Jin Q Sci Rep 20-Aug-2018
PMCID:PMC6102300
doi:10.1038/s41598-018-31002-7
PMID:30127401
Screening of promising chemotherapeutic candidates from plants extracts Kinjo J, Nakano D, Fujioka T, Okabe H J Nat Med 16-Apr-2016
PMCID:PMC4935755
doi:10.1007/s11418-016-0992-2
PMID:27086008
Ethanol Extract of Cirsium japonicum var. ussuriense Kitamura Exhibits the Activation of Nuclear Factor Erythroid 2-Related Factor 2-dependent Antioxidant Response Element and Protects Human Keratinocyte HaCaT Cells Against Oxidative DNA Damage Yoo OK, Choi BY, Park JO, Lee JW, Park BK, Joo CG, Heo HJ, Keum YS J Cancer Prev 30-Mar-2016
PMCID:PMC4819669
doi:10.15430/JCP.2016.21.1.66
PMID:27051652
Effects of Floral Scents and Their Dietary Experiences on the Feeding Preference in the Blowfly, Phormia regina Maeda T, Tamotsu M, Yamaoka R, Ozaki M Front Integr Neurosci 01-Dec-2015
PMCID:PMC4664696
doi:10.3389/fnint.2015.00059
PMID:26648851
Herbal antioxidant in clinical practice: A review Alok S, Jain SK, Verma A, Kumar M, Mahor A, Sabharwal M Asian Pac J Trop Biomed 01-Jan-2014
PMCID:PMC3819501
doi:10.1016/S2221-1691(14)60213-6
PMID:24144136
Ethnomedicinal Practices for Treating Liver Disorders of Local Communities in the Southern Regions of Korea Kim H, Song MJ Evid Based Complement Alternat Med 08-Sep-2013
PMCID:PMC3782137
doi:10.1155/2013/869176
PMID:24089622
Inhibitory Activities of Cudrania tricuspidata Leaves on Pancreatic Lipase In Vitro and Lipolysis In Vivo Kim YS, Lee Y, Kim J, Sohn E, Kim CS, Lee YM, Jo K, Shin S, Song Y, Kim JH, Kim JS Evid Based Complement Alternat Med 10-Dec-2012
PMCID:PMC3529879
doi:10.1155/2012/878365
PMID:23365603

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 / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(3R,8R,9Z,11Z)-heptadeca-1,9,11-trien-4,6-diyne-3,8-diol 16743556 Click to see CCCCCC=CC=CC(C#CC#CC(C=C)O)O 258.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.03.036
Heptadeca-1,9,11-trien-4,6-diyne-3,8-diol 73318791 Click to see 258.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.03.036
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-6-(acetyloxymethyl)-3,4-dihydroxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 163192005 Click to see 1117.30 unknown https://doi.org/10.1248/CPB.33.3473
[6-[[6-(Acetyloxymethyl)-3,4-dihydroxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] 10-[4,5-dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 14606070 Click to see 1263.40 unknown https://doi.org/10.1248/CPB.33.3473
[6-[[6-(Acetyloxymethyl)-3,4-dihydroxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] 9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-(3,4,5-trihydroxyoxan-2-yl)oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162869287 Click to see 1117.30 unknown https://doi.org/10.1248/CPB.33.3473
Kizuta saponin K11 21636378 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)CO)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)O)O)C)(C)C)O)O)O)COC(=O)C)O)O)O 1263.40 unknown https://doi.org/10.1248/CPB.33.3473
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2R,3R,4S,5S,6S)-2-[(E,6S)-6-[(3S,5R,6S,8R,9R,10R,13S,14R,17S)-3,6-dihydroxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-hydroxy-2-methylhept-2-enoxy]-6-methoxyoxane-3,4,5-triol 162896007 Click to see CC(=CCCC(C)(C1CCC2(C1CCC3C2(CC(C4C3(CCC(C4(C)C)O)C)O)C)C)O)COC5C(C(C(C(O5)OC)O)O)O 638.90 unknown https://doi.org/10.1248/CPB.33.1400
(2R,3R,4S,5S,6S)-2-[(E,6S)-6-hydroxy-2-methyl-6-[(3S,5R,8R,9R,10R,13S,14R,17S)-4,4,8,10,14-pentamethyl-3-[(2R,3R,4S,5S,6S)-3,4,5-trihydroxy-6-methoxyoxan-2-yl]oxy-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]hept-2-enoxy]-6-methoxyoxane-3,4,5-triol 163042230 Click to see 785.00 unknown https://doi.org/10.1248/CPB.33.1400
(5R,6S,8R,9R,10R,13R,14R,17S)-6-hydroxy-17-[(E,2S)-2-hydroxy-6-oxohept-4-en-2-yl]-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 101049767 Click to see 458.70 unknown https://doi.org/10.1007/BF02974009
https://doi.org/10.1016/S0960-894X(97)00139-X
(5R,6S,8R,9R,10R,13S,14R,17S)-6-hydroxy-17-[(E,2S)-2-hydroxy-6-methyl-7-[(2R,3R,4S,5S,6S)-3,4,5-trihydroxy-6-methoxyoxan-2-yl]oxyhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 162926381 Click to see 636.90 unknown https://doi.org/10.1248/CPB.33.1400
(6aS,9R)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 10102176 Click to see 883.10 unknown via CMAUP database
[(3S,5R,6S,8R,9R,10R,13S,14R,17S)-6-hydroxy-17-[(E,2S)-2-hydroxy-6-methyl-7-[(2R,3R,4S,5S,6S)-3,4,5-trihydroxy-6-methoxyoxan-2-yl]oxyhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 162945528 Click to see 680.90 unknown https://doi.org/10.1248/CPB.33.1400
[6-hydroxy-17-[2-hydroxy-6-methyl-7-(3,4,5-trihydroxy-6-methoxyoxan-2-yl)oxyhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 162945527 Click to see 680.90 unknown https://doi.org/10.1248/CPB.33.1400
10-[4,5-Dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 267360 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)O)O 751.00 unknown via CMAUP database
2-[6-(3,6-dihydroxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl)-6-hydroxy-2-methylhept-2-enoxy]-6-methoxyoxane-3,4,5-triol 162896006 Click to see CC(=CCCC(C)(C1CCC2(C1CCC3C2(CC(C4C3(CCC(C4(C)C)O)C)O)C)C)O)COC5C(C(C(C(O5)OC)O)O)O 638.90 unknown https://doi.org/10.1248/CPB.33.1400
2-[6-hydroxy-2-methyl-6-[4,4,8,10,14-pentamethyl-3-(3,4,5-trihydroxy-6-methoxyoxan-2-yl)oxy-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]hept-2-enoxy]-6-methoxyoxane-3,4,5-triol 163042229 Click to see 785.00 unknown https://doi.org/10.1248/CPB.33.1400
6-Hydroxy-17-(2-hydroxy-6-oxohept-4-en-2-yl)-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 162847529 Click to see CC(=O)C=CCC(C)(C1CCC2(C1CCC3C2(CC(C4C3(CCC(=O)C4(C)C)C)O)C)C)O 458.70 unknown https://doi.org/10.1016/S0960-894X(97)00139-X
6-Hydroxy-17-[2-hydroxy-6-methyl-7-(3,4,5-trihydroxy-6-methoxyoxan-2-yl)oxyhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 162926380 Click to see CC(=CCCC(C)(C1CCC2(C1CCC3C2(CC(C4C3(CCC(=O)C4(C)C)C)O)C)C)O)COC5C(C(C(C(O5)OC)O)O)O 636.90 unknown https://doi.org/10.1248/CPB.33.1400
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Methyl Betulinate 73493 Click to see 470.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
Guggulsterone 6450278 Click to see 312.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
[(1S)-1-[(8S,9S,10R,13S,14S,17S)-10,13-dimethyl-3,16-dioxo-2,6,7,8,9,11,12,14,15,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]ethyl] acetate 91597955 Click to see 372.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
[(3R,5S,8R,9S,10S,13S,14S,17R)-17-ethyl-10,13-dimethyl-16-oxo-1,2,3,4,5,6,7,8,9,11,12,14,15,17-tetradecahydrocyclopenta[a]phenanthren-3-yl] acetate 15767893 Click to see 360.50 unknown via CMAUP database
[(8R,9S,10R,13S,14S,16S,17Z)-17-ethylidene-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-16-yl] acetate 101929524 Click to see CC=C1C(CC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)OC(=O)C 356.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
campesterol-3-O-beta-d-glucoside 12895788 Click to see 562.80 unknown https://doi.org/10.1248/CPB.33.3473
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1248/CPB.33.3473
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1248/CPB.33.3473
Stigmasterol Glucoside 6602508 Click to see 574.80 unknown https://doi.org/10.1248/CPB.33.3473
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
isochlorogenic acid A 6474310 Click to see 516.40 unknown https://doi.org/10.1007/BF02977526
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Mannitol 6251 Click to see 182.17 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives / Indole-3-acetic acid derivatives
[(3R,8S,9Z)-3-hydroxyheptadeca-1,9-dien-4,6-diyn-8-yl] 2-(1H-indol-3-yl)acetate 16744766 Click to see 417.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.03.036
3-hydroxyheptadeca-1,9-dien-4,6-diyn-8-yl 2-(1H-indol-3-yl)acetate 73319254 Click to see 417.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.03.036
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.1007/BF02977526
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1007/BF02977526

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