Language	Common/alternative name
Spanish	ruda bravia
Spanish	ruda bravía
Spanish	ruda silvestre menor
Arabic	سذاب مصري
Catalan	ruda de fulla estreta
French	rue à feuilles étroites
Malay	pokok garuda

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
- Northern Africa
  - Algeria
  - Morocco
  - Tunisia

Europe click to expand
- Southeastern Europe
  - Italy
  - Sicilia
  - Yugoslavia
- Southwestern Europe
  - Baleares
  - Corse
  - France
  - Portugal
  - Sardegna
  - Spain

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000463817
Tropicos	28101495
INPN	119707
Flora of Italy	2987
KEW	urn:lsid:ipni.org:names:775060-1
The Plant List	kew-2527510
Open Tree Of Life	1081358
Observations.org	121611
NCBI Taxonomy	452789
IPNI	775060-1
iNaturalist	82849
GBIF	3832875
EPPO	RUAAN
Elurikkus	420992

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

Furoquinoline Alkaloids: Insights into Chemistry, Occurrence, and Biological Properties

Szewczyk A, Pęczek F

Int J Mol Sci

15-Aug-2023

PMCID:	PMC10454094
doi:	10.3390/ijms241612811
PMID:	37628986

Cytotoxic, Anti-Hemolytic, and Antioxidant Activities of Ruta chalepensis L. (Rutaceae) Extract, Fractions, and Isolated Compounds

Elizondo-Luévano JH, Rodríguez-Garza NE, Bazaldúa-Rodríguez AF, Romo-Sáenz CI, Tamez-Guerra P, Verde-Star MJ, Gomez-Flores R, Quintanilla-Licea R

Plants (Basel)

02-Jun-2023

PMCID:	PMC10255231
doi:	10.3390/plants12112203
PMID:	37299182

Role of phytocompounds as the potential anti-viral agent: an overview

Mohanty SS, Sahoo CR, Paidesetty SK, Padhy RN

Naunyn Schmiedebergs Arch Pharmacol

09-May-2023

PMCID:	PMC10169142
doi:	10.1007/s00210-023-02517-2
PMID:	37160482

Microscopic and physicochemical evaluation of Ruta angustifolia leaves

Wahyuni TS, Khoiriyah N, Tumewu L, Ekasari W, Fuad A, Widyawaruyanti A

J Public Health Afr

16-Mar-2023

PMCID:	PMC10365675
doi:	10.4081/jphia.2023.2520
PMID:	37492534

Promising alkaloids and flavonoids compounds as anti-hepatitis c virus agents: a review

Rizaldi G, Hafid AF, Wahyuni TS

J Public Health Afr

16-Mar-2023

PMCID:	PMC10365654
doi:	10.4081/jphia.2023.2514
PMID:	37492538

Ruta angustifolia Pers. (Narrow-Leaved Fringed Rue): Pharmacological Properties and Phytochemical Profile

Bailly C

Plants (Basel)

13-Feb-2023

PMCID:	PMC9959652
doi:	10.3390/plants12040827
PMID:	36840175

Plastome evolution and phylogeny of the tribe Ruteae (Rutaceae)

Liu Q, Gao Y, Dong W, Zhao L

Ecol Evol

09-Feb-2023

PMCID:	PMC9911629
doi:	10.1002/ece3.9821
PMID:	36789335

Medicinal Plants Used Traditionally for Skin Related Problems in the South Balkan and East Mediterranean Region—A Review

Tsioutsiou EE, Amountzias V, Vontzalidou A, Dina E, Stevanović ZD, Cheilari A, Aligiannis N

Front Pharmacol

05-Jul-2022

PMCID:	PMC9294246
doi:	10.3389/fphar.2022.936047
PMID:	35865952

Essential Oils in Respiratory Mycosis: A Review

Zuzarte M, Salgueiro L

Molecules

28-Jun-2022

PMCID:	PMC9268412
doi:	10.3390/molecules27134140
PMID:	35807386

Ethnoveterinary Medicine and Ethnopharmacology in the Main Transhumance Areas of Castilla-La Mancha (Spain)

Rivera D, Verde A, Fajardo Rodríguez J, Ríos S, Alcaraz F, Cárceles C, Ortíz J, Valdés A, Ruíz-Gallardo JR, García-Flores A, Palazón JA, Obón C

Front Vet Sci

03-May-2022

PMCID:	PMC9113055
doi:	10.3389/fvets.2022.866132
PMID:	35591874

Bioactive Based Nanocarriers for the Treatment of Viral Infections and SARS-CoV-2

Goyal R, Bala R, Sindhu RK, Zehravi M, Madaan R, Ramproshad S, Mondal B, Dey A, Rahman MH, Cavalu S

Nanomaterials (Basel)

01-May-2022

PMCID:	PMC9104170
doi:	10.3390/nano12091530
PMID:	35564239

Niche Variation in Endemic Lilium pomponium on a Wide Altitudinal Gradient in the Maritime Alps

Fontaine N, Gauthier P, Casazza G, Thompson JD

Plants (Basel)

21-Mar-2022

PMCID:	PMC8954139
doi:	10.3390/plants11060833
PMID:	35336714

An in vitro study of an Artocarpus heterophyllus substance as a hepatitis C antiviral and its combination with current anti-HCV drugs

Permanasari AA, Aoki-Utsubo C, Wahyuni TS, Tumewu L, Adianti M, Widyawaruyanti A, Hotta H, Hafid AF

BMC Complement Med Ther

12-Oct-2021

PMCID:	PMC8507375
doi:	10.1186/s12906-021-03408-w
PMID:	34641875

A Systematic Review on the Antimicrobial Properties of Mediterranean Wild Edible Plants: We Still Know Too Little about Them, but What We Do Know Makes Persistent Investigation Worthwhile

Cappelli G, Mariani F

Foods

18-Sep-2021

PMCID:	PMC8471169
doi:	10.3390/foods10092217
PMID:	34574327

Ruta Essential Oils: Composition and Bioactivities

Nahar L, El-Seedi HR, Khalifa SA, Mohammadhosseini M, Sarker SD

Molecules

06-Aug-2021

PMCID:	PMC8400350
doi:	10.3390/molecules26164766
PMID:	34443352

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Nonyl acetate	8918	Click to see CCCCCCCCCOC(=O)C	186.29	unknown	https://doi.org/10.1080/10412905.1991.9697956
Octyl acetate	8164	Click to see CCCCCCCCOC(=O)C	172.26	unknown	https://doi.org/10.1080/10412905.1991.9697956
Undecyl acetate	15605	Click to see CCCCCCCCCCCOC(=O)C	214.34	unknown	https://doi.org/10.1080/10412905.1991.9697956
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Decanol	8174	Click to see CCCCCCCCCCO	158.28	unknown	https://doi.org/10.1080/10412905.1991.9697956
1-Dodecanol	8193	Click to see CCCCCCCCCCCCO	186.33	unknown	https://doi.org/10.1080/10412905.1991.9697956
1-Undecanol	8184	Click to see CCCCCCCCCCCO	172.31	unknown	https://doi.org/10.1080/10412905.1991.9697956
2-Nonanol	12367	Click to see CCCCCCCC(C)O	144.25	unknown	https://doi.org/10.1080/10412905.1991.9697956
2-Undecanol	15448	Click to see CCCCCCCCCC(C)O	172.31	unknown	https://doi.org/10.1080/10412905.1991.9697956
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	https://doi.org/10.1080/10412905.1991.9697956
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1991.9697956
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
(3S,4S)-4-Ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexene	12310053	Click to see CC(=C)C1C=CCCC1(C)C=C	162.27	unknown	https://doi.org/10.1080/10412905.1991.9697956
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1991.9697956
Humulene	5281520	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1991.9697956
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-(4-Ethenyl-4-methyl-3-prop-1-en-2-ylcyclohexyl)propan-2-ol	547972	Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O	222.37	unknown	https://doi.org/10.1080/10412905.1991.9697956
Elemol	92138	Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O	222.37	unknown	https://doi.org/10.1080/10412905.1991.9697956
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
Angustifolin	21575185	Click to see CC12CCCC3(C1C(OC2)OC)COC(=O)C45C3C(CC(C4)C(=C)C5=O)O	376.40	unknown	https://doi.org/10.1016/S0031-9422(00)84991-2 https://doi.org/10.1016/0031-9422(86)80093-0
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Nonanal	31289	Click to see CCCCCCCCC=O	142.24	unknown	https://doi.org/10.1080/10412905.1991.9697956
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
10-Methylundecan-2-one	528743	Click to see CC(C)CCCCCCCC(=O)C	184.32	unknown	https://doi.org/10.1080/10412905.1991.9697956
11-Methyldodecan-2-one	21427346	Click to see CC(C)CCCCCCCCC(=O)C	198.34	unknown	https://doi.org/10.1080/10412905.1991.9697956
2-Decanone	12741	Click to see CCCCCCCCC(=O)C	156.26	unknown	https://doi.org/10.1080/10412905.1991.9697956
2-Dodecanone	22556	Click to see CCCCCCCCCCC(=O)C	184.32	unknown	https://doi.org/10.1080/10412905.1991.9697956
2-Nonanone	13187	Click to see CCCCCCCC(=O)C	142.24	unknown	https://doi.org/10.1080/10412905.1991.9697956
2-Octanone	8093	Click to see CCCCCCC(=O)C	128.21	unknown	https://doi.org/10.1080/10412905.1991.9697956
2-Tridecanone	11622	Click to see CCCCCCCCCCCC(=O)C	198.34	unknown	https://doi.org/10.1080/10412905.1991.9697956
2-Undecanone	8163	Click to see CCCCCCCCCC(=O)C	170.29	unknown	https://doi.org/10.1080/10412905.1991.9697956
7-Methyloctan-2-one	519008	Click to see CC(C)CCCCC(=O)C	142.24	unknown	https://doi.org/10.1080/10412905.1991.9697956
8-Methylnonan-2-one	528744	Click to see CC(C)CCCCCC(=O)C	156.26	unknown	https://doi.org/10.1080/10412905.1991.9697956
9-Methyldecan-2-one	528742	Click to see CC(C)CCCCCCC(=O)C	170.29	unknown	https://doi.org/10.1080/10412905.1991.9697956
> Organoheterocyclic compounds / Benzodioxoles
(2S)-6-(1,3-benzodioxol-5-yl)hexan-2-ol	163014567	Click to see CC(CCCCC1=CC2=C(C=C1)OCO2)O	222.28	unknown	https://doi.org/10.1016/0031-9422(86)80093-0
2-Hexanone, 6-(3,4-methylenedioxyphenyl)	529777	Click to see CC(=O)CCCCC1=CC2=C(C=C1)OCO2	220.26	unknown	https://doi.org/10.1016/0031-9422(86)80093-0
2-Octanone, 8-(3,4-methylenedioxyphenyl)	529778	Click to see CC(=O)CCCCCCC1=CC2=C(C=C1)OCO2	248.32	unknown	https://doi.org/10.1016/0031-9422(86)80093-0
3',4'-(Methylenedioxy)acetophenone	76622	Click to see CC(=O)C1=CC2=C(C=C1)OCO2	164.16	unknown	https://doi.org/10.1016/0031-9422(86)80093-0
moskachan C	44558951	Click to see CC(CCCCC1=CC2=C(C=C1)OCO2)O	222.28	unknown	https://doi.org/10.1016/0031-9422(86)80093-0
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
Graveoline	353825	Click to see CN1C2=CC=CC=C2C(=O)C=C1C3=CC4=C(C=C3)OCO4	279.29	unknown	https://doi.org/10.1016/0031-9422(73)80445-5 https://doi.org/10.1016/S0031-9422(00)84991-2
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone	8417	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC	206.19	unknown	https://doi.org/10.1016/S0031-9422(00)84991-2
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
7-Hydroxy-3-(2-methylbut-3-en-2-yl)chromen-2-one	5363192	Click to see CC(C)(C=C)C1=CC2=C(C=C(C=C2)O)OC1=O	230.26	unknown	https://doi.org/10.1016/S0031-9422(00)84991-2
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	https://doi.org/10.1515/ZNC-1983-1-226

Biological Material Top

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Ruta angustifolia

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