Reseda muricata

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Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

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Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID643fffd2c0576831446120
Scientific name	Reseda muricata
Authority	C.Presl
First published in	Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 3: 438 (1845)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Reseda patzakiana	Rech.f.	Anz. Österr. Akad. Wiss., Math.-Naturwiss. Kl. 98: 246 (1961)

Common names Top

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Language	Common/alternative name
Arabic	بليحاء بنفسجية
Arabic	دنبان

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Reseda muricata var. intermedia	Abdallah & de Wit	Meded. Landbouwhoogeschool 78(14): 283 (1978)

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
- Northern Africa
  - Egypt

Asia-temperate click to expand
- Arabian Peninsula
  - Gulf States
  - Kuwait
  - Oman
  - Saudi Arabia
- Western Asia
  - Iraq
  - Lebanon-Syria
  - Palestine
  - Sinai

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000462739
KEW	urn:lsid:ipni.org:names:715559-1
The Plant List	kew-2526115
Open Tree Of Life	359598
NCBI Taxonomy	415816
IPNI	715559-1
iNaturalist	447866
GBIF	7275919
EOL	5164119

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)!
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Title

Authors

Publication

Released

IDs

GC-MS Analysis, Heavy Metals, Biological, and Toxicological Evaluation of Reseda muricata and Marrubium vulgare Methanol Extracts

Ullah R, Alqahtani AS

Evid Based Complement Alternat Med

21-Mar-2022

PMCID:	PMC8959963
doi:	10.1155/2022/2284328
PMID:	35356243

A review on ethno-medicinal plants used in traditional medicine in the Kingdom of Saudi Arabia

Ullah R, Alqahtani AS, Noman OM, Alqahtani AM, Ibenmoussa S, Bourhia M

Saudi J Biol Sci

20-Jun-2020

PMCID:	PMC7499296
doi:	10.1016/j.sjbs.2020.06.020
PMID:	32994730

Floristic diversity and vegetation analysis of Wadi Arar: A typical desert Wadi of the Northern Border region of Saudi Arabia

Osman AK, Al-Ghamdi F, Bawadekji A

Saudi J Biol Sci

18-Feb-2014

PMCID:	PMC4250517
doi:	10.1016/j.sjbs.2014.02.001
PMID:	25473364

Evaluation of the effects of 80% methanolic leaf extract of Caylusea abyssinica (fresen.) fisch. & Mey. on glucose handling in normal, glucose loaded and diabetic rodents

Tamiru W, Engidawork E, Asres K

BMC Complement Altern Med

11-Sep-2012

PMCID:	PMC3495218
doi:	10.1186/1472-6882-12-151
PMID:	22967092

Vegetation analysis of Wadi Al-Jufair, a hyper-arid region in Najd, Saudi Arabia

Alatar A, El-Sheikh MA, Thomas J

Saudi J Biol Sci

17-May-2012

PMCID:	PMC3730721
doi:	10.1016/j.sjbs.2012.04.003
PMID:	23961197

Kaempferol triosides from Reseda muricata.

El-Sayed NH, Omara NM, Yousef AK, Farag AM, Mabry TJ

Phytochemistry

01-Jun-2001

doi:	10.1016/S0031-9422(00)00479-9
PMID:	11394860

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	https://doi.org/10.1016/S0031-9422(00)00479-9
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-{[3-(3,4-Dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid	348159	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1016/S0031-9422(00)00479-9
Chlorogenic Acid	1794427	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1016/S0031-9422(00)00479-9
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoic acid	709	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1016/S0031-9422(00)00479-9
3,4-Dihydroxy cinnamic acid	2518	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://doi.org/10.1016/S0031-9422(00)00479-9
4-Hydroxycinnamic acid	322	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	https://doi.org/10.1016/S0031-9422(00)00479-9
Caffeic Acid	689043	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://doi.org/10.1016/S0031-9422(00)00479-9
Ferulic acid	445858	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1016/S0031-9422(00)00479-9
p-Coumaric acid	637542	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	https://doi.org/10.1016/S0031-9422(00)00479-9
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	https://doi.org/10.1016/S0031-9422(00)00479-9
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1016/S0031-9422(00)00479-9
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1016/S0031-9422(00)00479-9
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/10.1016/S0031-9422(00)00479-9
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Afzelin	5316673	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O	432.40	unknown	https://doi.org/10.1016/S0031-9422(00)00479-9
Kaempferol-3-O-rhamnoside	5835713	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O	432.40	unknown	https://doi.org/10.1016/S0031-9422(00)00479-9
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3R,4S,5R,6S)-6-[3-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate	163190079	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)COC(=O)C=CC5=CC=C(C=C5)O)O)O)O)C6=CC=C(C=C6)O)O)O)OC7C(C(C(C(O7)CO)O)O)O	902.80	unknown	https://doi.org/10.1016/S0031-9422(00)00479-9
[(2R,3S,4S,5S,6S)-6-[3-[(2S,3S,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate	163103701	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)COC(=O)C=CC5=CC=C(C=C5)O)O)O)O)C6=CC=C(C=C6)O)OC7C(C(C(C(O7)CO)O)O)O)O)O	902.80	unknown	https://doi.org/10.1016/S0031-9422(00)00479-9
[6-[3-[3,4-Dihydroxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate	162854580	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)COC(=O)C=CC5=CC=C(C=C5)O)O)O)O)C6=CC=C(C=C6)O)O)O)OC7C(C(C(C(O7)CO)O)O)O	902.80	unknown	https://doi.org/10.1016/S0031-9422(00)00479-9
2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-[(2S,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	44259225	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O	464.40	unknown	https://doi.org/10.1016/S0031-9422(00)00479-9
3-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	162900907	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)OC6C(C(C(C(O6)CO)O)O)O	756.70	unknown	https://doi.org/10.1016/S0031-9422(00)00479-9
3-[3,4-Dihydroxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	162900906	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)OC6C(C(C(C(O6)CO)O)O)O	756.70	unknown	https://doi.org/10.1016/S0031-9422(00)00479-9
kaempferol 7-O-beta-D-galactopyranoside	72551439	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1016/S0031-9422(00)00479-9
kaempferol 7-O-glucoside	10095180	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1016/S0031-9422(00)00479-9
Kaempferol-7-o-glucoside	5480982	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1016/S0031-9422(00)00479-9
Quercetin 7-O-glucoside	5381351	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O	464.40	unknown	https://doi.org/10.1016/S0031-9422(00)00479-9
Quercimeritrin	5282160	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O	464.40	unknown	https://doi.org/10.1016/S0031-9422(00)00479-9

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Reseda muricata

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