Impatiens edgeworthii - Unknown
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Internal ID UUID64404f223f170794729157
Scientific name Impatiens edgeworthii
Authority Hook.f.
First published in Fl. Brit. India 1: 476 (1875)

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Synonyms Top

Scientific name Authority First published in
Impatiens chrysantha Hook.f. Bot. Mag. 127: t. 7786 (1901)

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) 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
  • Asia-tropical
    • Indian Subcontinent
      • Nepal
      • Pakistan
      • West Himalaya

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001141842
Tropicos 3100048
KEW urn:lsid:ipni.org:names:374069-1
The Plant List tro-3100048
PFAF Impatiens edgeworthii
Open Tree Of Life 1074031
NCBI Taxonomy 342012
IPNI 374069-1
iNaturalist 602376
GBIF 4936345
EPPO IPAED
EOL 2878518
USDA GRIN 19818
CMAUP NPO7779

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
Keeping Healthy in Your Skin—Plants and Fungi Used by Indigenous Himalayan Communities to Treat Dermatological Ailments Haq SM, Khoja AA, Lone FA, Waheed M, Bussmann RW, Casini R, Mahmoud EA, Elansary HO Plants (Basel) 06-Apr-2023
PMCID:PMC10097107
doi:10.3390/plants12071575
PMID:37050200
Edible wild plant species used by different linguistic groups of Kohistan Upper Khyber Pakhtunkhwa (KP), Pakistan Amin M, Aziz MA, Pieroni A, Nazir A, Al-Ghamdi AA, Kangal A, Ahmad K, Abbasi AM J Ethnobiol Ethnomed 13-Feb-2023
PMCID:PMC9923922
doi:10.1186/s13002-023-00577-5
PMID:36782205
Phyto-ecological studies and distribution pattern of plant species and communities of Dhirkot, Azad Jammu and Kashmir, Pakistan Mumshad M, Ahmad I, Khan SM, Abdullah, Rehman K, Islam M, Sakhi S, Khan SU, Afridi SG, Shams S, Azam S, Ahmad I, Afza R, Ahmad Z PLoS One 06-Oct-2021
PMCID:PMC8494300
doi:10.1371/journal.pone.0257493
PMID:34614011
Impacts of the Invasive Impatiens glandulifera: Lessons Learned from One of Europe’s Top Invasive Species Coakley S, Petti C Biology (Basel) 03-Jul-2021
PMCID:PMC8301180
doi:10.3390/biology10070619
PMID:34356476
Ethnobotanical survey of the medicinal flora of Harighal, Azad Jammu & Kashmir, Pakistan Amjad MS, Zahoor U, Bussmann RW, Altaf M, Gardazi SM, Abbasi AM J Ethnobiol Ethnomed 27-Oct-2020
PMCID:PMC7590686
doi:10.1186/s13002-020-00417-w
PMID:33109243
Ethnomedicinal knowledge of the rural communities of Dhirkot, Azad Jammu and Kashmir, Pakistan Farooq A, Amjad MS, Ahmad K, Altaf M, Umair M, Abbasi AM J Ethnobiol Ethnomed 30-Aug-2019
PMCID:PMC6716831
doi:10.1186/s13002-019-0323-2
PMID:31470868
A Comprehensive Review of Chemistry, Sources and Bioavailability of Omega-3 Fatty Acids Cholewski M, Tomczykowa M, Tomczyk M Nutrients 04-Nov-2018
PMCID:PMC6267444
doi:10.3390/nu10111662
PMID:30400360
Sustainable utilization and conservation of plant biodiversity in montane ecosystems: the western Himalayas as a case study Khan SM, Page SE, Ahmad H, Harper DM Ann Bot 03-Jul-2013
PMCID:PMC3718215
doi:10.1093/aob/mct125
PMID:23825353
Stereochemistry of alpha-parinaric acid fromImpatiens edgeworthii seed oil. Bagby MO, Smith CR Jr, Wolff IA Lipids 01-Jan-1970
doi:10.1007/BF02531613
PMID:17805627

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
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(6R,9R)-3-Oxo-alpha-ionol glucoside 9820702 Click to see CC1=CC(=O)CC(C1C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C 370.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
cis-Parinaric acid 5460995 Click to see CCC=CC=CC=CC=CCCCCCCCC(=O)O 276.40 unknown https://doi.org/10.1007/BF02531613
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Camphene 440966 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown via CMAUP database
(-)-Camphor 444294 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown via CMAUP database
(+)-Chrysanthenone 11789373 Click to see CC1=CCC2C(=O)C1C2(C)C 150.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
(1R,2S,3S,6S,7R,10S,11R,14S,15S,17S,20S,21S,24S)-3,24-dihydroxy-3,7,12,15,20,24-hexamethyl-9,18-dioxaheptacyclo[13.10.1.02,11.02,14.06,10.016,25.017,21]hexacosa-12,16(25)-diene-8,19-dione 162913451 Click to see CC1C2CCC(C34C5CC(C3C=C(C4C2OC1=O)C)(C6=C5C(CCC7C6OC(=O)C7C)(C)O)C)(C)O 496.60 unknown https://doi.org/10.1007/BF02531613
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3R,4S,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxycyclohexane-1-carboxylic acid 91492 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 via CMAUP database
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 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 via CMAUP database
(1S,3R,4R,5R)-3,4-Bis[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,5-dihydroxycyclohexane-1-carboxylic acid 153946 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown via CMAUP database
1,3-Dicaffeoylquinic acid 6474640 Click to see C1C(C(C(CC1(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O 516.40 unknown via CMAUP database
3,4-Di-O-caffeoylquinic acid methyl ester 10392218 Click to see COC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O 530.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
Protocatechualdehyde 8768 Click to see C1=CC(=C(C=C1C=O)O)O 138.12 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Caffeic acid methyl ester 689075 Click to see COC(=O)C=CC1=CC(=C(C=C1)O)O 194.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown via CMAUP database
> 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 via CMAUP database
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
Tilianin 5321954 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)O 446.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3'-O-methyltricetin 11267045 Click to see COC1=CC(=CC(=C1O)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 316.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
5,7-Dihydroxy-3',4',5'-trimethoxyflavone 5379265 Click to see COC1=CC(=CC(=C1OC)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 344.30 unknown via CMAUP database
Acacetin 5280442 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 284.26 unknown via CMAUP database
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
5,7,3'-Trihydroxy-6,4',5'-trimethoxyflavone 5496475 Click to see COC1=CC(=CC(=C1OC)O)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 360.30 unknown via CMAUP database
6-Methoxytricin 14034284 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 360.30 unknown via CMAUP database
Eupafolin 5317284 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O 316.26 unknown via CMAUP database
Jaceidin 5464461 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O 360.30 unknown via CMAUP database

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