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Rhanterium epapposum

Rhanterium epapposum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643fd381a7a57103592988
Scientific name Rhanterium epapposum
Authority Oliv.
First published in Hooker's Icon. Pl. 14: t. 1367 (1881)

Description Top

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Synonyms Top

Scientific name Authority First published in
Musilia arabica Velen. Mem. Soc. Sci. Boheme 1921-22(6): 6. 1923

Common names Top

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Language Common/alternative name
English arfaj
Arabic العرفج
Arabic عرفج
Persian عرفج

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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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
  • Asia-temperate
    • Arabian Peninsula
      • Gulf States
      • Kuwait
      • Oman
      • Saudi Arabia
    • Western Asia
      • Iran
      • Iraq

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000132641
KEW urn:lsid:ipni.org:names:241373-1
The Plant List gcc-93476
Open Tree Of Life 705707
NCBI Taxonomy 313948
IPNI 241373-1
iNaturalist 633977
GBIF 3110118
Freebase /m/07hdky
EOL 5123245
Wikipedia Rhanterium_epapposum

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
Camel urine as a potential source of bioactive molecules showing their efficacy against pathogens: A systematic review Amina R, Habiba R, Abouddihaj B Saudi J Biol Sci 25-Feb-2024
PMCID:PMC10940778
doi:10.1016/j.sjbs.2024.103966
PMID:38495380
Country-Wide Ecological Health Assessment Methodology for Air Toxics: Bridging Gaps in Ecosystem Impact Understanding and Policy Foundations Munshed M, Van Griensven Thé J, Fraser R, Matthews B, Elkamel A Toxics 05-Jan-2024
PMCID:PMC10820021
doi:10.3390/toxics12010042
PMID:38250998
Ethnomedicinal evaluation of medicinal plants used for therapies by men and women in rural and urban communities in Makkah district Qari SH, Alqethami A, Qumsani AT Saudi Pharm J 02-Dec-2023
PMCID:PMC10733703
doi:10.1016/j.jsps.2023.101881
PMID:38130903
A Review on Extracts, Chemical Composition and Product Development of Walnut Diaphragma Juglandis Fructus Zhan Y, Ma M, Chen Z, Ma A, Li S, Xia J, Jia Y Foods 08-Sep-2023
PMCID:PMC10529104
doi:10.3390/foods12183379
PMID:37761088
Updates on Biogenic Metallic and Metal Oxide Nanoparticles: Therapy, Drug Delivery and Cytotoxicity Nikolova MP, Joshi PB, Chavali MS Pharmaceutics 03-Jun-2023
PMCID:PMC10301310
doi:10.3390/pharmaceutics15061650
PMID:37376098
Antifungal Potential of Melaleuca alternifolia against Fungal Pathogen Fusarium oxysporum f. sp. cubense Tropical Race 4 Paramalingam P, Baharum NA, Abdullah JO, Hong JK, Saidi NB Molecules 31-May-2023
PMCID:PMC10254191
doi:10.3390/molecules28114456
PMID:37298932
Immunomodulatory Effects of Natural Feed Additives for Meat Chickens Phillips CJ, Hosseintabar-Ghasemabad B, Gorlov IF, Slozhenkina MI, Mosolov AA, Seidavi A Life (Basel) 30-May-2023
PMCID:PMC10301336
doi:10.3390/life13061287
PMID:37374069
Green Synthesis of Bioinspired Nanoparticles Mediated from Plant Extracts of Asteraceae Family for Potential Biological Applications Jaison JP, Balasubramanian B, Gangwar J, James N, Pappuswamy M, Anand AV, Al-Dhabi NA, Valan Arasu M, Liu WC, Sebastian JK Antibiotics (Basel) 08-Mar-2023
PMCID:PMC10044610
doi:10.3390/antibiotics12030543
PMID:36978410
Therapeutic Applications of Biogenic Silver Nanomaterial Synthesized from the Paper Flower of Bougainvillea glabra (Miami, Pink) Oves M, Rauf MA, Qari HA Nanomaterials (Basel) 03-Feb-2023
PMCID:PMC9920917
doi:10.3390/nano13030615
PMID:36770576
Plants from a semi-arid environment as a source of phytochemicals against Fusarium crown and foot rot in zucchini Khalil AM, Saleh AM, Abo El-Souad SM, Mohamed MS AMB Express 17-Jan-2023
PMCID:PMC9845481
doi:10.1186/s13568-023-01515-0
PMID:36648547
In Silico Evaluation of Bioactive Compounds of Artemisia pallens Targeting the Efflux Protein of Multidrug-Resistant Acinetobacter baumannii (LAC-4 Strain) Suvaithenamudhan S, Ananth S, Mariappan V, Dhayabaran VV, Parthasarathy S, Ganesh PS, Shankar EM Molecules 15-Aug-2022
PMCID:PMC9414700
doi:10.3390/molecules27165188
PMID:36014428
Molecular Assessment of Genetic Diversity and Genetic Structure of Rhanterium epapposum Oliv. in Scarce Populations in Some Regions of Western Saudi Arabia Mansour H, Alsamadany H, Al-Hasawi ZM Plants (Basel) 13-Jun-2022
PMCID:PMC9230628
doi:10.3390/plants11121560
PMID:35736710
Genetic Diversity of Rhanterium eppaposum Oliv. Populations in Kuwait as Revealed by GBS Al Salameen F, Habibi N, Al Amad S, Al Doaij B Plants (Basel) 27-May-2022
PMCID:PMC9183190
doi:10.3390/plants11111435
PMID:35684208
Estrogens and Androgens in Plants: The Last 20 Years of Studies Janeczko A Plants (Basel) 16-Dec-2021
PMCID:PMC8705621
doi:10.3390/plants10122783
PMID:34961254
The Essential Oil-Bearing Plants in the United Arab Emirates (UAE): An Overview Shahin SM, Jaleel A, Alyafei MA Molecules 27-Oct-2021
PMCID:PMC8587291
doi:10.3390/molecules26216486
PMID:34770890

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
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown https://doi.org/10.1002/FFJ.2730020106
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown https://doi.org/10.1002/FFJ.2730020106
> Benzenoids / Phenol ethers / Anisoles
Estragole 8815 Click to see COC1=CC=C(C=C1)CC=C 148.20 unknown https://doi.org/10.1002/FFJ.2730020106
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown https://doi.org/10.1002/FFJ.2730020106
> Hydrocarbons / Polycyclic hydrocarbons
Bornylene 10047 Click to see CC1(C2CCC1(C=C2)C)C 136.23 unknown https://doi.org/10.1002/FFJ.2730020106
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Phenethyl valerate 81964 Click to see CCCCC(=O)OCCC1=CC=CC=C1 206.28 unknown https://doi.org/10.1002/FFJ.2730020106
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Neryl propionate 5365982 Click to see CCC(=O)OCC=C(C)CCC=C(C)C 210.31 unknown https://doi.org/10.1002/FFJ.2730020106
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
3-Octanol 11527 Click to see CCCCCC(CC)O 130.23 unknown https://doi.org/10.1002/FFJ.2730020106
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
2,6-Dimethyl-2,4,6-octatriene 5368821 Click to see CC=C(C)C=CC=C(C)C 136.23 unknown https://doi.org/10.1002/FFJ.2730020106
beta-CITRONELLOL, (+/-)- 8842 Click to see CC(CCC=C(C)C)CCO 156.26 unknown https://doi.org/10.1002/FFJ.2730020106
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1002/FFJ.2730020106
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1002/FFJ.2730020106
Linalyl acetate 8294 Click to see CC(=CCCC(C)(C=C)OC(=O)C)C 196.29 unknown https://doi.org/10.1002/FFJ.2730020106
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1002/FFJ.2730020106
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1002/FFJ.2730020106
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1002/FFJ.2730020106
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1002/FFJ.2730020106
Thymol 6989 Click to see CC1=CC(=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1002/FFJ.2730020106
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Isopinocampheol 10524983 Click to see CC1C2CC(C2(C)C)CC1O 154.25 unknown https://doi.org/10.1002/FFJ.2730020106
(1R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-one 6973628 Click to see CC1=CC(=O)C2CC1C2(C)C 150.22 unknown https://doi.org/10.1002/FFJ.2730020106
(1R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-2-ene 6451618 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1002/FFJ.2730020106
(3R)-4-methylidene-1-(propan-2-yl)bicyclo[3.1.0]hexan-3-ol 42626428 Click to see CC(C)C12CC1C(=C)C(C2)O 152.23 unknown https://doi.org/10.1002/FFJ.2730020106
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1002/FFJ.2730020106
2-Carene 79044 Click to see CC1=CC2C(C2(C)C)CC1 136.23 unknown https://doi.org/10.1002/FFJ.2730020106
3-Thujanone 11027 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1002/FFJ.2730020106
alpha-Bergamotene 86608 Click to see CC1=CCC2CC1C2(C)CCC=C(C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730020106
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1002/FFJ.2730020106
alpha-Thujone 12304613 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1002/FFJ.2730020106
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)- 17868 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1002/FFJ.2730020106
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1002/FFJ.2730020106
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1002/FFJ.2730020106
Myrtenal 61130 Click to see CC1(C2CC=C(C1C2)C=O)C 150.22 unknown https://doi.org/10.1002/FFJ.2730020106
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1002/FFJ.2730020106
Verbenone 29025 Click to see CC1=CC(=O)C2CC1C2(C)C 150.22 unknown https://doi.org/10.1002/FFJ.2730020106
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Menthone 443159 Click to see CC1CCC(C(=O)C1)C(C)C 154.25 unknown https://doi.org/10.1002/FFJ.2730020106
(+)-Neomenthol 439263 Click to see CC1CCC(C(C1)O)C(C)C 156.26 unknown https://doi.org/10.1002/FFJ.2730020106
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1002/FFJ.2730020106
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1002/FFJ.2730020106
alpha-Terpinyl acetate 111037 Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C 196.29 unknown https://doi.org/10.1002/FFJ.2730020106
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1002/FFJ.2730020106
Carveol 7438 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1002/FFJ.2730020106
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1002/FFJ.2730020106
Carvone, (+/-)- 7439 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1002/FFJ.2730020106
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1002/FFJ.2730020106
p-Menthan-3-one 6986 Click to see CC1CCC(C(=O)C1)C(C)C 154.25 unknown https://doi.org/10.1002/FFJ.2730020106
Piperitone 6987 Click to see CC1=CC(=O)C(CC1)C(C)C 152.23 unknown https://doi.org/10.1002/FFJ.2730020106
Pulegone 442495 Click to see CC1CCC(=C(C)C)C(=O)C1 152.23 unknown https://doi.org/10.1002/FFJ.2730020106
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1002/FFJ.2730020106
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-beta-Bourbonene 324224 Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730020106
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730020106
(3R,6E)-nerolidol 11241545 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1002/FFJ.2730020106
alpha-Curcumene 92139 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C 202.33 unknown https://doi.org/10.1002/FFJ.2730020106
beta-Bourbonene 62566 Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730020106
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1002/FFJ.2730020106
beta-Ionone 638014 Click to see CC1=C(C(CCC1)(C)C)C=CC(=O)C 192.30 unknown https://doi.org/10.1002/FFJ.2730020106
Bulnesol 90785 Click to see CC1CCC2=C(CCC(CC12)C(C)(C)O)C 222.37 unknown https://doi.org/10.1002/FFJ.2730020106
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730020106
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1002/FFJ.2730020106
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730020106
Cyclohexene, 4-ethenyl-4-methyl-3-(1-methylethenyl)-1-(1-methylethyl)-, (3R-trans)- 89316 Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730020106
delta-Elemene 12309449 Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730020106
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730020106
Nerolidol 8888 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1002/FFJ.2730020106
Sesquichamene 97829 Click to see CC1=CCC2(CCCC(C23C1C3)(C)C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730020106
Thujopsene 442402 Click to see CC1=CCC2(CCCC(C23C1C3)(C)C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730020106
Zingiberene 92776 Click to see CC1=CCC(C=C1)C(C)CCC=C(C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730020106
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7aS,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene 91746456 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1002/FFJ.2730020106
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1002/FFJ.2730020106
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1002/FFJ.2730020106
Aromadendrene 91354 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1002/FFJ.2730020106
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
beta-EUDESMOL 91457 Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown https://doi.org/10.1002/FFJ.2730020106
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
Germacrone 6436348 Click to see CC1=CCC(=C(C)C)C(=O)CC(=CCC1)C 218.33 unknown https://doi.org/10.1002/FFJ.2730020106
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
Chamazulene 10719 Click to see CCC1=CC2=C(C=CC2=C(C=C1)C)C 184.28 unknown https://doi.org/10.1002/FFJ.2730020106
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
Hex-3-enyl acetate 15574 Click to see CCC=CCCOC(=O)C 142.20 unknown https://doi.org/10.1002/FFJ.2730020106
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters / Enol esters
Hex-1-enyl formate 53738491 Click to see CCCCC=COC=O 128.17 unknown https://doi.org/10.1002/FFJ.2730020106
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Decanone 12741 Click to see CCCCCCCCC(=O)C 156.26 unknown https://doi.org/10.1002/FFJ.2730020106
6-Methyl-5-hepten-2-one 9862 Click to see CC(=CCCC(=O)C)C 126.20 unknown https://doi.org/10.1002/FFJ.2730020106
> Phenylpropanoids and polyketides / Cinnamaldehydes
3-Phenyl-propenal 307 Click to see C1=CC=C(C=C1)C=CC=O 132.16 unknown https://doi.org/10.1002/FFJ.2730020106
Cinnamaldehyde 637511 Click to see C1=CC=C(C=C1)C=CC=O 132.16 unknown https://doi.org/10.1002/FFJ.2730020106

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