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Drimia elata

Drimia elata - Unknown
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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
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Details Top

Internal ID UUID644025f76d9aa545610350
Scientific name Drimia elata
Authority Jacq. ex Willd.
First published in Sp. Pl., ed. 4 , 2: 185 (1799)

Description Top

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Synonyms Top

Scientific name Authority First published in
Hyacinthus ciliaris (Jacq. ex Willd.) Poir. Encycl. , Suppl. 3: 120 (1813)
Hyacinthus elatus (Jacq. ex Willd.) Poir. Encycl. , Suppl. 3: 120 (1813)
Hyacinthus pusillus Thunb. ex Lam. Encycl. 3: 194 (1789)
Idothea burchellii (Baker) Kuntze Revis. Gen. Pl. 2: 712 (1891)
Idothea ciliaris (Jacq. ex Willd.) Kunth Enum. Pl. 4: 343 (1843)
Idothea concolor (Baker) Kuntze Revis. Gen. Pl. 2: 712 (1891)
Idothea elata (Jacq. ex Willd.) Kunth Enum. Pl. 4: 343 (1843)
Idothea humilis Kunth Enum. Pl. 4: 344 (1843)
Idothea purpurascens (J.Jacq.) Kunth Enum. Pl. 4: 342 (1843)
Idothea pusilla (Jacq. ex Willd.) Kunth Enum. Pl. 4: 344 (1843)
Idothea robusta (Baker) Kuntze Revis. Gen. Pl. 2: 712 (1891)
Idothea villosa (Lindl.) Kunth Enum. Pl. 4: 343 (1843)
Idothearia ciliaris (Jacq. ex Willd.) C.Presl Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 3: 584 (1845)
Idothearia elata (Jacq. ex Willd.) C.Presl Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 3: 584 (1845)
Idothearia humilis (Kunth) C.Presl Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 3: 584 (1845)
Idothearia purpurascens (J.Jacq.) C.Presl Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 3: 584 (1845)
Idothearia pusilla (Jacq. ex Willd.) C.Presl Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 3: 584 (1845)
Idothearia villosa (Lindl.) C.Presl Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 3: 584 (1845)
Strepsiphyla villosa (Lindl.) Raf. Fl. Tellur. 3: 50 (1837)
Drimia alta R.A.Dyer Fl. Pl. South Africa 23: t. 890 (1943)
Drimia burchellii Baker Refug. Bot. 2(App.): 2 (1872)
Drimia ciliaris Jacq. ex Willd. Sp. Pl., ed. 4 2: 165. 1799 (1799)
Drimia concolor Baker J. Linn. Soc., Bot. 11: 422 (1870)
Drimia eckloniana Schult. & Schult.f. Syst. Veg., ed. 15 bis 7: 1710 (1830)
Drimia elgonica Bullock Bull. Misc. Inform. Kew 1932: 504 (1932)
Drimia humilis Bergius ex Eckl. Topogr. Verz. Pflanzensamml. Ecklon : 2 (1827)
Drimia purpurascens J.Jacq. Ecl. Pl. Rar. : t. 30 (1812)
Drimia pusilla Jacq. ex Willd. Sp. Pl., ed. 4 , 2: 165 (1799)
Drimia robusta Baker Refug. Bot. 3: t. 190 (1870)
Drimia rudatisii Schltr. Bot. Jahrb. Syst. 40: 89 (1907)
Drimia villosa Lindl. Edwards's Bot. Reg. 16: t. 1346 (1830)
Drimia zombensis Baker Fl. Trop. Afr. 7: 525 (1898)

Common names Top

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Namibia
      • Northern Provinces
      • Swaziland

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000766104
Tropicos 100183380
KEW urn:lsid:ipni.org:names:534510-1
The Plant List kew-304979
Open Tree Of Life 391902
Observations.org 284191
NCBI Taxonomy 65775
IPNI 534510-1
iNaturalist 507050
GBIF 2776601
EOL 1087726
Elurikkus 301599
Wikipedia Drimia_elata

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
Impact of Heavy Metal Pollution in the Environment on the Metabolic Profile of Medicinal Plants and Their Therapeutic Potential Asiminicesei DM, Fertu DI, Gavrilescu M Plants (Basel) 21-Mar-2024
PMCID:PMC10976221
doi:10.3390/plants13060913
PMID:38592933
Cadmium toxicity in medicinal plants: An overview of the tolerance strategies, biotechnological and omics approaches to alleviate metal stress Al-Khayri JM, Banadka A, Rashmi R, Nagella P, Alessa FM, Almaghasla MI Front Plant Sci 17-Jan-2023
PMCID:PMC9887195
doi:10.3389/fpls.2022.1047410
PMID:36733604
The fate of secondary metabolites in plants growing on Cd-, As-, and Pb-contaminated soils—a comprehensive review Asare MO, Száková J, Tlustoš P Environ Sci Pollut Res Int 19-Dec-2022
PMCID:PMC9760545
doi:10.1007/s11356-022-24776-x
PMID:36529801
Ethnopharmacological Study of Medicinal Plants Used for the Treatment of Cardiovascular Diseases and Their Associated Risk Factors in sub-Saharan Africa Odukoya JO, Odukoya JO, Mmutlane EM, Ndinteh DT Plants (Basel) 23-May-2022
PMCID:PMC9143319
doi:10.3390/plants11101387
PMID:35631812
Medicinal Plants for Mitigating Pain and Inflammatory-Related Conditions: An Appraisal of Ethnobotanical Uses and Patterns in South Africa Aremu AO, Pendota SC Front Pharmacol 22-Oct-2021
PMCID:PMC8569556
doi:10.3389/fphar.2021.758583
PMID:34744737
A Review of Plant-Based Therapies for the Treatment of Urinary Tract Infections in Traditional Southern African Medicine Cock I, Mavuso N, Van Vuuren S Evid Based Complement Alternat Med 29-Jul-2021
PMCID:PMC8346297
doi:10.1155/2021/7341124
PMID:34367307
Anti-SARS-CoV Natural Products With the Potential to Inhibit SARS-CoV-2 (COVID-19) Verma S, Twilley D, Esmear T, Oosthuizen CB, Reid AM, Nel M, Lall N Front Pharmacol 25-Sep-2020
PMCID:PMC7546787
doi:10.3389/fphar.2020.561334
PMID:33101023
Antimicrobial Activity, Antioxidant Potential, Cytotoxicity and Phytochemical Profiling of Four Plants Locally Used against Skin Diseases Asong JA, Amoo SO, McGaw LJ, Nkadimeng SM, Aremu AO, Otang-Mbeng W Plants (Basel) 15-Sep-2019
PMCID:PMC6783968
doi:10.3390/plants8090350
PMID:31540194
Bufadienolides from Drimia robusta BAK L. Krenn, V. Stapf, B. Kopp MDPI AG 03-May-2019
doi:10.3797/SCIPHARM.AUT-00-38
Medicinal Plants Traded in Informal Herbal Medicine Markets of the Limpopo Province, South Africa Rasethe MT, Semenya SS, Maroyi A Evid Based Complement Alternat Med 16-Apr-2019
PMCID:PMC6500648
doi:10.1155/2019/2609532
PMID:31118951
Medicinal Uses, Phytochemistry and Pharmacological Properties of Elaeodendron transvaalense Maroyi A, Semenya SS Nutrients 04-Mar-2019
PMCID:PMC6470740
doi:10.3390/nu11030545
PMID:30836643
Plants Used by Bapedi Traditional Healers to Treat Asthma and Related Symptoms in Limpopo Province, South Africa Semenya SS, Maroyi A Evid Based Complement Alternat Med 19-Jul-2018
PMCID:PMC6077574
doi:10.1155/2018/2183705
PMID:30108649
Effect of Cadmium and Copper Exposure on Growth, Secondary Metabolites and Antioxidant Activity in the Medicinal Plant Sambung Nyawa (Gynura procumbens (Lour.) Merr) Ibrahim MH, Chee Kong Y, Mohd Zain NA Molecules 12-Oct-2017
PMCID:PMC6151666
doi:10.3390/molecules22101623
PMID:29023367
Evaluation of Herbal Concoctions Sold at Ga Maja (Limpopo Province) in South Africa and In Vitro Pharmacological Evaluation of Plants Used to Manufacture the Concoctions Matotoka MM, Masoko P J Evid Based Complementary Altern Med 28-Sep-2017
PMCID:PMC5871308
doi:10.1177/2156587217727112
PMID:29228818
From Traditional Usage to Pharmacological Evidence: Systematic Review of Gunnera perpensa L. Maroyi A Evid Based Complement Alternat Med 07-Dec-2016
PMCID:PMC5174174
doi:10.1155/2016/1720123
PMID:28053640

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 / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1016/J.BSE.2004.11.009
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Bufanolides and derivatives
(3S,5S,8R,9S,10S,13R,14S,16S,17R)-3,5,14,16-tetrahydroxy-13-methyl-17-(6-oxopyran-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde 14888410 Click to see CC12CCC3C(C1(CC(C2C4=COC(=O)C=C4)O)O)CCC5(C3(CCC(C5)O)C=O)O 432.50 unknown https://doi.org/10.3797/SCIPHARM.AUT-00-38
(3S,5S,8R,9S,10S,13R,14S,16S,17R)-5,14,16-trihydroxy-13-methyl-17-(6-oxopyran-3-yl)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde 14888414 Click to see CC12CCC3C(C1(CC(C2C4=COC(=O)C=C4)O)O)CCC5(C3(CCC(C5)OC6C(C(C(C(O6)CO)O)O)O)C=O)O 594.60 unknown https://doi.org/10.3797/SCIPHARM.AUT-00-38
12beta-Hydroxyscillirosidin 637392 Click to see CC(=O)OC1CC2(C(CC(C3(C2(CCC3C4=COC(=O)C=C4)O)C)O)C5(C1=CC(CC5)O)C)O 474.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.051
3,5,14,16-tetrahydroxy-13-methyl-17-(6-oxopyran-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde 14888409 Click to see CC12CCC3C(C1(CC(C2C4=COC(=O)C=C4)O)O)CCC5(C3(CCC(C5)O)C=O)O 432.50 unknown https://doi.org/10.3797/SCIPHARM.AUT-00-38
5-[(3S,5S,8R,9S,10R,13R,14S,16S,17R)-5,14,16-trihydroxy-10,13-dimethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]pyran-2-one 163018399 Click to see CC12CCC(CC1(CCC3C2CCC4(C3(CC(C4C5=COC(=O)C=C5)O)O)C)O)OC6C(C(C(C(O6)CO)O)O)O 580.70 unknown https://doi.org/10.3797/SCIPHARM.AUT-00-38
5-[14-Hydroxy-3-[3-hydroxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-10,13-dimethyl-1,2,3,6,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]pyran-2-one 78172248 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(C(C(O3)CO)O)O)O)C)OC4CCC5(C6CCC7(C(CCC7(C6CCC5=C4)O)C8=COC(=O)C=C8)C)C)O)O)O)O 838.90 unknown https://doi.org/10.1016/S0031-9422(01)00225-4
5-[5,14,16-trihydroxy-10,13-dimethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]pyran-2-one 14888416 Click to see CC12CCC(CC1(CCC3C2CCC4(C3(CC(C4C5=COC(=O)C=C5)O)O)C)O)OC6C(C(C(C(O6)CO)O)O)O 580.70 unknown https://doi.org/10.3797/SCIPHARM.AUT-00-38
5,14-dihydroxy-13-methyl-17-(6-oxopyran-3-yl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde 14888411 Click to see CC12CCC3C(C1(CCC2C4=COC(=O)C=C4)O)CCC5(C3(CCC(C5)OC6C(C(C(C(O6)CO)O)O)O)C=O)O 578.60 unknown https://doi.org/10.3797/SCIPHARM.AUT-00-38
5,14,16-trihydroxy-13-methyl-17-(6-oxopyran-3-yl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde 14888413 Click to see CC12CCC3C(C1(CC(C2C4=COC(=O)C=C4)O)O)CCC5(C3(CCC(C5)OC6C(C(C(C(O6)CO)O)O)O)C=O)O 594.60 unknown https://doi.org/10.3797/SCIPHARM.AUT-00-38
6beta-Acetoxy-3beta,8beta,14beta-trihydroxy-12-oxobufa-4,20,22-trienolide 12137075 Click to see CC(=O)OC1CC2(C(CC(=O)C3(C2(CCC3C4=COC(=O)C=C4)O)C)C5(C1=CC(CC5)O)C)O 472.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.051
Hellebrigenin glucoside 3055779 Click to see CC12CCC3C(C1(CCC2C4=COC(=O)C=C4)O)CCC5(C3(CCC(C5)OC6C(C(C(C(O6)CO)O)O)O)C=O)O 578.60 unknown https://doi.org/10.3797/SCIPHARM.AUT-00-38
Urginin 202218 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(C(C(O3)CO)O)O)O)C)OC4CCC5(C6CCC7(C(CCC7(C6CCC5=C4)O)C8=COC(=O)C=C8)C)C)O)O)O)O 838.90 unknown https://doi.org/10.1016/S0031-9422(01)00225-4
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.051
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.051

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