Ruellia tuberosa in Genus Ruellia

Details Top

Internal ID	UUID643ff87ea2d67227658066
Scientific name	Ruellia tuberosa
Authority	L.
First published in	Sp. Pl. : 635 (1753)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Ruellia clandestina	L.	Sp. Pl. : 634 (1753)
Cryphiacanthus barbadensis	Nees	Index Seminum (WROCL, Wratislaviensi) 1841: [3] (1841)
Dipteracanthus clandestinus	C.Presl	Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 3: 528 (1845)

Common names Top

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Language	Common/alternative name
English	fever root
English	minnieroot
English	wayside tuberose/popping pod
Arabic	رولية
Arabic	رولية برية
Bengali	পটপটি ফুল
Hebrew	רואליה טובורוזה
Indonesian	kencana ungu liar
Japanese	ムラサキルエリア
Malayalam	ശിവകരന്ത
Tamil	உரூலியா டுயூபரோசா
Thai	เป๊าะแป๊ะ
Thai	อังกาบฝรั่ง
Thai	ต้อยติ่ง
Chinese	芦莉草
Chinese	塊莖蘆莉草
Chinese	塊根蘆莉草
Chinese	块根芦莉草
Chinese	块根芦莉

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

Africa click to expand
- East Tropical Africa
  - Kenya
  - Tanzania
- Northeast Tropical Africa
  - Sudan
- Western Indian Ocean
  - Seychelles

Asia-temperate click to expand
- China
  - China South-central
- Eastern Asia
  - Taiwan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - India
  - Nepal
  - Pakistan
  - Sri Lanka
- Indo-China
  - Andaman Islands
  - Cambodia
  - Laos
  - Myanmar
  - Nicobar Nicobar
  - Thailand
  - Vietnam
- Malesia
  - Lesser Sunda Islands
  - Malaya

Northern America click to expand
- Mexico
  - Mexico Gulf
  - Mexico Northeast
  - Mexico Northwest
  - Mexico Southeast
  - Mexico Southwest

Pacific click to expand
- Southwestern Pacific
  - New Caledonia

Southern America click to expand
- Caribbean
  - Aruba
  - Bahamas
  - Cayman Islands
  - Cuba
  - Dominican Republic
  - Haiti
  - Jamaica
  - Leeward Islands
  - Netherlands Antilles
  - Puerto Rico
  - Southwest Caribbean
  - Trinidad-Tobago
  - Turks-caicos Islands
  - Venezuelan Antilles
  - Windward Islands
- Central America
  - Guatemala
  - Honduras
  - Panamá
- Northern South America
  - French Guiana
  - Guyana
  - Suriname
  - Venezuela
- Western South America
  - Colombia
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000401309
USDA Plants	RUTU
Tropicos	103304
INPN	630581
KEW	urn:lsid:ipni.org:names:54671-1
The Plant List	kew-2420650
Plantarium	52765
Open Tree Of Life	390453
Observations.org	198853
NCBI Taxonomy	441035
IPNI	54671-1
iNaturalist	291119
GBIF	5415418
Freebase	/m/0h94zzt
EPPO	RUETU
EOL	590262
USDA GRIN	32511
Wikipedia	Ruellia_tuberosa

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

Multi-functional copper oxide nanoparticles synthesized using Lagerstroemia indica leaf extracts and their applications

Geremew A, Palmer L, Johnson A, Reeves S, Brooks N, Carson L

Heliyon

30-Apr-2024

PMCID:	PMC11078880
doi:	10.1016/j.heliyon.2024.e30178
PMID:	38726176

From Flora to Pharmaceuticals: 100 new additions to angiosperms of Gafargaon subdistrict in Bangladesh and unraveling antidiabetic drug candidates targeting DPP4 through in silico approach

Ahmed SS, Rahman MO

PLoS One

29-Mar-2024

PMCID:	PMC10980240
doi:	10.1371/journal.pone.0301348
PMID:	38551991

Bio-mordants: a review

Benli H

Environ Sci Pollut Res Int

23-Feb-2024

PMCID:	PMC10948525
doi:	10.1007/s11356-024-32174-8
PMID:	38396176

Retracted: Biosynthesis of Iron Oxide Nanoparticles Using Leaf Extract of Ruellia tuberosa: Mechanical and Dynamic Mechanical Behaviour Kevlar-Based Hybrid Epoxy Composites

and Applications BC

Bioinorg Chem Appl

20-Dec-2023

PMCID:	PMC10752721
doi:	10.1155/2023/9869405
PMID:	38152455

Clinacanthus nutans genetic diversity and its association with anti-apoptotic, antioxidant, and anti-bacterial activities

Chiangchin S, Thongyim S, Pandith H, Kaewkod T, Tragoolpua Y, Inta A, Watthana S, Pongamornkul W, Jangsutthivorawat S, Panya A

Sci Rep

10-Nov-2023

PMCID:	PMC10638387
doi:	10.1038/s41598-023-46105-z
PMID:	37949910

Phytosynthesized Iron Oxide Nanoparticles Using Aqueous Extract of Saccharum arundinaceum (Hardy Sugar Cane), Their Characterizations, Antiglycation, and Cytotoxic Activities

Aldossari SM, Rehman LU, Ahmad I, Aslam M, Fozia F, Mohany M, Milošević M, Al-Rejaie SS, Aboul-Soud MA

ACS Omega

23-Oct-2023

PMCID:	PMC10634196
doi:	10.1021/acsomega.3c04484
PMID:	37970030

Tanning Wastewater Sterilization in the Dark and Sunlight Using Psidium guajava Leaf-Derived Copper Oxide Nanoparticles and Their Characteristics

Lakshmaiya N, Surakasi R, Nadh VS, Srinivas C, Kaliappan S, Ganesan V, Paramasivam P, Dhanasekaran S

ACS Omega

09-Oct-2023

PMCID:	PMC10600883
doi:	10.1021/acsomega.3c05588
PMID:	37901496

Application of Iron Nanoparticles Synthesized from a Bioflocculant Produced by Yeast Strain Pichia kudriavzevii Obtained from Kombucha Tea SCOBY in the Treatment of Wastewater

Tsilo PH, Basson AK, Ntombela ZG, Dlamini NG, Pullabhotla RV

Int J Mol Sci

29-Sep-2023

PMCID:	PMC10572716
doi:	10.3390/ijms241914731
PMID:	37834177

The Molluscicidal Activity of Green Synthesized Copper Oxide–Based Annona squamosa Seed Extract Nanoparticles on the Feeding Behavior, Biochemical, Molecular, and Immunohistochemical Alterations of Biomphalaria alexandrina Snails

Hussein AA, Abd El-latif MB, Saad El-Din MI, El-Shenawy NS, Hammam O, Ibrahim AM

Biol Trace Elem Res

30-Aug-2023

PMCID:	PMC10954926
doi:	10.1007/s12011-023-03823-9
PMID:	37648936

Isolation and purification of potential weed inhibitors from Mimosa pigra L.

Khang DT, Quy TN, Dam NP, Tuan NT, Men TT, Van Ay N, Thuy NP

Heliyon

17-Jul-2023

PMCID:	PMC10375793
doi:	10.1016/j.heliyon.2023.e18205
PMID:	37519759

Pharmacological Potential of Betulin as a Multitarget Compound

Adepoju FO, Duru KC, Li E, Kovaleva EG, Tsurkan MV

Biomolecules

12-Jul-2023

PMCID:	PMC10377123
doi:	10.3390/biom13071105
PMID:	37509141

Biogenic Synthesis of Copper Nanoparticles: A Systematic Review of Their Features and Main Applications

Luque-Jacobo CM, Cespedes-Loayza AL, Echegaray-Ugarte TS, Cruz-Loayza JL, Cruz I, de Carvalho JC, Goyzueta-Mamani LD

Molecules

18-Jun-2023

PMCID:	PMC10301071
doi:	10.3390/molecules28124838
PMID:	37375393

An Update on the Use of Natural Pigments and Pigment Nanoparticle Adducts for Metal Detection Based on Colour Response

Mulyaningsih RD, Pratiwi R, Hasanah AN

Biosensors (Basel)

18-May-2023

PMCID:	PMC10216405
doi:	10.3390/bios13050554
PMID:	37232915

Invasive Mechanisms of One of the World’s Worst Alien Plant Species Mimosa pigra and Its Management

Kato-Noguchi H

Plants (Basel)

11-May-2023

PMCID:	PMC10221770
doi:	10.3390/plants12101960
PMID:	37653876

Biosynthesis of Iron Oxide Nanoparticles Using Leaf Extract of Ruellia tuberosa: Mechanical and Dynamic Mechanical Behaviour Kevlar-Based Hybrid Epoxy Composites

Natrayan L, Rao YS, Vaidya G, Bhattacharya S, Kaliappan S, Patil PP, Paramasivam P

Bioinorg Chem Appl

20-Apr-2023

PMCID:	PMC10139801
doi:	10.1155/2023/1731931
PMID:	37125143

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Tritriacontane	12411	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC	464.90	unknown	https://doi.org/10.1002/CHIN.199825276
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3S,5S)-2-[[(6R,7R,8S)-8-(4-hydroxy-3,5-dimethoxyphenyl)-6,7-bis(hydroxymethyl)-1,3-dimethoxy-5,6,7,8-tetrahydronaphthalen-2-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162929172	Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)OC4C(C(C(C(O4)CO)O)O)O)OC)CO)CO	582.60	unknown	https://doi.org/10.1007/S10600-013-0549-5
(2S,3S,5S)-2-[4-[(3S,3aR,6S,6aR)-6-[3,5-dimethoxy-4-[(2R,3S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162941458	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC	742.70	unknown	https://doi.org/10.1007/S10600-013-0549-5
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid	11005	Click to see CCCCCCCCCCCCCC(=O)O	228.37	unknown	https://doi.org/10.1002/LIPI.19780800603
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Capric Acid	2969	Click to see CCCCCCCCCC(=O)O	172.26	unknown	https://doi.org/10.1002/LIPI.19780800603
Lauric Acid	3893	Click to see CCCCCCCCCCCC(=O)O	200.32	unknown	https://doi.org/10.1002/LIPI.19780800603
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Roseoside	9930064	Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C	386.40	unknown	https://doi.org/10.1007/S10600-013-0549-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1007/S10600-013-0549-5
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
Tyrosine	6057	Click to see C1=CC(=CC=C1CC(C(=O)O)N)O	181.19	unknown	https://doi.org/10.1079/9781780642635.0298
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / C-glycosyl compounds
(2R)-2-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-4H-1,4-benzoxazin-3-one	162842377	Click to see C1=CC=C2C(=C1)NC(=O)C(O2)C3C(C(C(C(O3)CO)O)O)O	311.29	unknown	https://doi.org/10.1007/S10600-013-0549-5
(2R)-4-hydroxy-2-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-1,4-benzoxazin-3-one	162817636	Click to see C1=CC=C2C(=C1)N(C(=O)C(O2)C3C(C(C(C(O3)CO)O)O)O)O	327.29	unknown	https://doi.org/10.1007/S10600-013-0549-5
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3R,4S,5S,6R)-2-[3-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-2-[4-(3-hydroxyprop-1-enyl)-2-methoxyphenoxy]propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	91321267	Click to see COC1=C(C=CC(=C1)C=CCO)OC(CO)C(C2=CC(=C(C=C2)O)OC)OC3C(C(C(C(O3)CO)O)O)O	538.50	unknown	https://doi.org/10.1007/S10600-013-0549-5
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
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/10.1007/S10600-013-0549-5
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(1R,2R,3R,4S,5R)-2,3,4-trihydroxy-5-methylcyclohexyl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	101778645	Click to see CC1CC(C(C(C1O)O)O)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O	622.60	unknown	https://doi.org/10.1007/S10600-013-0549-5
Rha(a1-3)[coumaroyl(3-OH)(-4)]b-Glc	21632980	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)O)O)O)O)O	488.40	unknown	https://doi.org/10.1007/S10600-013-0549-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-6-methoxy-7-[(2S,3S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	163008950	Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O	478.40	unknown	https://doi.org/10.1007/S10600-013-0549-5
5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-3-methoxy-7-[(2S,3S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	162978397	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)OC)O	492.40	unknown	https://doi.org/10.1007/S10600-013-0549-5
5-hydroxy-6-methoxy-2-(4-methoxyphenyl)-7-[(2S,3S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	162899715	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)OC)O	476.40	unknown	https://doi.org/10.1007/S10600-013-0549-5

Biological Material Top

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Ruellia tuberosa

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top