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Derris elliptica

Derris elliptica - 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 UUID643fd9b4d1d5d058908293
Scientific name Derris elliptica
Authority (Wall.) Benth.
First published in J. Proc. Linn. Soc., Bot.4(Suppl.): 111 (1860)

Description Top

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Synonyms Top

Scientific name Authority First published in
Galedupa elliptica (Wall.) Roxb. Fl. Ind. ed. 1832, 3: 242 (1832)
Pongamia elliptica Wall. Pl. Asiat. Rar.3: 20 (1832)
Derris elliptica var. elliptica (Wall.) Benth.
Deguelia elliptica (Wall.) Taub. Bot. Centralbl.47: 386 (1891)
Galactia termimaliflora Blanco
Pongamia volubilis Zoll. & Moritzi A.Moritzi, Syst. Verz. Java: 3 (1846)
Nothoderris purpurea Blume Fl. Ned. Ind.1(1): 149 (1855)
Nothoderris glaucescens Blume Fl. Ned. Ind.1(1): 149 (1855)
Nothoderris elliptica (Wall.) Blume Fl. Ned. Ind.1(1): 148 (1855)
Pongamia horsfieldii Miq. Fl. Ned. Ind.1(1): 149 (1855)
Pongamia hypoleuca Miq. Fl. Ned. Ind.1(1): 148 (1855)
Pongamia grandiflora Vent. Jard. Malmaison: t. 28 (1803)
Dalbergia elliptica Span. Linnaea15: 197 (1841)
Pterocarpus ellipticus Kuntze Revis. Gen. Pl.1: 203 (1891)
Paraderris elliptica (Wall.) Adema Thai Forest Bull., Bot.28: 11 (2000)
Derris elliptica var. glaucophylla (Miq.) Kaneh. & Hatus. Bot. Mag. (Tokyo)56: 364 (1942)
Paraderris elliptica var. chittagongensis (Thoth.) Adema Blumea48: 137 (2003)
Derris elliptica var. chittagongensis Thoth. Bull. Bot. Surv. India3: 195 (1961 publ. 1962)
Pongamia volubilis var. glaucophylla Miq. Fl. Ned. Ind.1(1): 149 (1855)
Derris elliptica var. tonkinensis Gagnep. H.Lecomte (ed.), Fl. Indo-Chine2: 461 (1916)
Millettia elliptica (Roxb.) Steud. Nomencl. Bot., ed. 2, 2: 146 (1841)
Dalbergia glaucescens Zipp. ex Miq. Fl. Ned. Ind.1(1): 149 (1855)
Dalbergia purpurea Reinw. ex Hassk. Flora25(2, Beibl. 1): 53 (1842)

Common names Top

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Language Common/alternative name
English derris
Arabic دريس إهليلجي
Indonesian akar tuba
mad tobbhâ
Malay akar tuba
Thai หางไหล
Chinese 毛鱼藤
Chinese 毒鱼藤
Chinese 魚藤
Chinese 南亚鱼藤

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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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
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Ogasawara-Shoto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • India
      • Nepal
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Christmas Island
      • Jawa
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea
  • Pacific
    • North-central Pacific
      • Hawaii
    • Northwestern Pacific
      • Caroline Islands
      • Marianas
  • Southern America
    • Brazil
      • Brazil Northeast
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Leeward Islands
      • Trinidad-Tobago

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000186905
USDA Plants DEEL3
Tropicos 13018222
INPN 629534
KEW urn:lsid:ipni.org:names:491300-1
The Plant List ild-33408
Open Tree Of Life 170173
NCBI Taxonomy 56063
IPNI 491300-1
iNaturalist 348735
GBIF 5350305
EPPO DRREL
EOL 686011
USDA GRIN 13545
Wikipedia Derris_elliptica

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
Acute rotenone poisoning: A scoping review Tat J, Heskett K, Boss GR Heliyon 21-Mar-2024
PMCID:PMC11021885
doi:10.1016/j.heliyon.2024.e28334
PMID:38633629
Exploring the therapeutic potential of Derris elliptica (Wall.) Benth in Streptozotocin-Induced diabetic Rats: Phytochemical characterization and antidiabetic evaluation Abd Rahman R, Jayasingh Chellammal HS, Ali Shah SA, Mohd Zohdi R, Ramachandran D, Mohsin HF Saudi Pharm J 28-Feb-2024
PMCID:PMC10920961
doi:10.1016/j.jsps.2024.102016
PMID:38463183
Anti-Insect Properties of Penicillium Secondary Metabolites Nicoletti R, Andolfi A, Becchimanzi A, Salvatore MM Microorganisms 16-May-2023
PMCID:PMC10221605
doi:10.3390/microorganisms11051302
PMID:37317276
Inhibitory Effects of Thermolysis Transformation Products of Rotenone on Nitric Oxide Production Jeong GH, Lee H, Lee SS, Chung BY, Bai HW, Kim TH Int J Mol Sci 23-Mar-2023
PMCID:PMC10093917
doi:10.3390/ijms24076095
PMID:37047068
Insect Cell-Based Models: Cell Line Establishment and Application in Insecticide Screening and Toxicology Research He X, Lu L, Huang P, Yu B, Peng L, Zou L, Ren Y Insects 18-Jan-2023
PMCID:PMC9965340
doi:10.3390/insects14020104
PMID:36835673
The protective impact of growth hormone against rotenone-induced apoptotic cell death via acting on endoplasmic reticulum stress and autophagy axis BERRAK RENCÜZOĞULLARI Ö, TORNACI S, ÇELİK Y, CİROĞLU NN, OBAKAN YERLİKAYA P, ARISAN ED, ÇOKER GÜRKAN A Turk J Biol 15-Dec-2022
PMCID:PMC10388008
doi:10.55730/1300-0152.2639
PMID:37529115
Microbial and Plant Derived Low Risk Pesticides Having Nematocidal Activity Evidente A Toxins (Basel) 03-Dec-2022
PMCID:PMC9787815
doi:10.3390/toxins14120849
PMID:36548747
Stem cambial variants of Taiwan lianas Yang SZ, Chen PH, Chen JJ Bot Stud 24-Sep-2022
PMCID:PMC9509506
doi:10.1186/s40529-022-00358-5
PMID:36153445
Identification of Gedunin from a Phytochemical Depository as a Novel Multidrug Resistance-Bypassing Tubulin Inhibitor of Cancer Cells Khalid SA, Dawood M, Boulos JC, Wasfi M, Drif A, Bahramimehr F, Shahhamzehei N, Shan L, Efferth T Molecules 09-Sep-2022
PMCID:PMC9501561
doi:10.3390/molecules27185858
PMID:36144591
The anti‐Trypanosoma activities of medicinal plants: A systematic review of the literature Nekoei S, Khamesipour F, Habtemariam S, de Souza W, Mohammadi Pour P, Hosseini SR Vet Med Sci 29-Aug-2022
PMCID:PMC9677405
doi:10.1002/vms3.912
PMID:36037401
Multivalent Pyrrolidine Iminosugars: Synthesis and Biological Relevance Wang Y, Xiao J, Meng A, Liu C Molecules 24-Aug-2022
PMCID:PMC9457877
doi:10.3390/molecules27175420
PMID:36080188
Occurrence of Macrophomina phaseolina on Chickpea in Italy: Pathogen Identification and Characterization Dell’Olmo E, Tripodi P, Zaccardelli M, Sigillo L Pathogens 27-Jul-2022
PMCID:PMC9415271
doi:10.3390/pathogens11080842
PMID:36014963
Assessing Anti-Social and Aggressive Behavior in a Zebrafish (Danio rerio) Model of Parkinson’s Disease Chronically Exposed to Rotenone Ilie OD, Duta R, Jijie R, Nita IB, Nicoara M, Faggio C, Dobrin R, Mavroudis I, Ciobica A, Doroftei B Brain Sci 08-Jul-2022
PMCID:PMC9313068
doi:10.3390/brainsci12070898
PMID:35884705
A Complete Review of Mexican Plants with Teratogenic Effects Chamorro-Cevallos G, Mojica-Villegas MA, García-Martínez Y, Pérez-Gutiérrez S, Madrigal-Santillán E, Vargas-Mendoza N, Morales-González JA, Cristóbal-Luna JM Plants (Basel) 24-Jun-2022
PMCID:PMC9268836
doi:10.3390/plants11131675
PMID:35807626
Environmental Neurotoxic Pesticide Exposure Induces Gut Inflammation and Enteric Neuronal Degeneration by Impairing Enteric Glial Mitochondrial Function in Pesticide Models of Parkinson’s Disease: Potential Relevance to Gut-Brain Axis Inflammation in Disease Pathogenesis Palanisamy BN, Sarkar S, Malovic E, Samidurai M, Charli A, Zenitsky G, Jin H, Anantharam V, Kanthasamy A, Kanthasamy A Int J Biochem Cell Biol 12-May-2022
PMCID:PMC10411482
doi:10.1016/j.biocel.2022.106225
PMID:35550926

Phytochemical Profile Top

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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
> Organoheterocyclic compounds / Pyrrolidines
(2S,3S,4S,5S)-2,5-bis(hydroxymethyl)pyrrolidine-3,4-diol 11073745 Click to see C(C1C(C(C(N1)CO)O)O)O 163.17 unknown https://doi.org/10.1016/S0031-9422(00)94435-2
2(R), 4(R)-dihydroxypyrrolidine 1472 Click to see C(C1C(C(C(N1)CO)O)O)O 163.17 unknown https://doi.org/10.1016/S0031-9422(00)94435-2
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(-)-Deguelin;(-)-cis-Deguelin 606171 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)C 394.40 unknown https://doi.org/10.1021/JA01326A060
(1S,12S,13S)-16,17-dimethoxy-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),5,9,14,16,18-heptaen-12-ol 162980105 Click to see COC1=C(C=C2C(=C1)C3C(CO2)OC4=C(C3O)C=CC5=C4C=CO5)OC 354.40 unknown https://doi.org/10.1055/S-2006-961936
(1S,13S)-10-hydroxy-16,17-dimethoxy-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),5,9,14,16,18-heptaen-12-one 12312700 Click to see COC1=C(C=C2C(=C1)C3C(CO2)OC4=C(C3=O)C(=CC5=C4C=CO5)O)OC 368.30 unknown https://doi.org/10.1002/RECL.19390580304
5-Hydroxy-8,9-dimethoxy-2-(prop-1-en-2-yl)-1,2,12,12a-tetrahydrofuro[2',3':7,8][1]benzopyrano[2,3-c][1]benzopyran-6(6aH)-one 3665545 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)O 410.40 unknown https://doi.org/10.1002/RECL.19390580304
5'beta-Rotenone 5102 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC 394.40 unknown https://doi.org/10.1016/S0031-9422(00)98664-3
https://doi.org/10.1002/ARDP.19112490408
https://doi.org/10.1248/YAKUSHI1881.1923.491_10
6-Hydroxy-9,10-dimethoxy-3,3-dimethyl-13,13a-dihydro-3H,7aH-pyrano[2,3-c:6,5-f']dichromen-7-one 243723 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)O)C 410.40 unknown https://doi.org/10.1002/RECL.19390580304
alpha-Toxicarol 442826 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)O)C 410.40 unknown https://doi.org/10.1002/RECL.19390580304
Deguelin 107935 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)C 394.40 unknown https://doi.org/10.1055/S-2006-961936
Dehydrotoxicarol 5491616 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC)O)C 408.40 unknown https://doi.org/10.1021/JA01328A504
Derride 13846199 Click to see COC1=C(C=C2C(=C1)C3C(CO2)OC4=C(C3=O)C=CC5=C4C=CO5)OC 352.30 unknown https://doi.org/10.1002/RECL.19390580304
https://doi.org/10.1039/JR9390001099
Elliptinol 44257418 Click to see COC1=C(C=C2C(=C1)C3C(CO2)OC4=C(C3O)C=CC5=C4C=CO5)OC 354.40 unknown https://doi.org/10.1055/S-2006-961936
Elliptone 160477 Click to see COC1=C(C=C2C(=C1)C3C(CO2)OC4=C(C3=O)C=CC5=C4C=CO5)OC 352.30 unknown https://doi.org/10.1002/RECL.19390580304
https://doi.org/10.1039/JR9390001099
Malaccol 5319228 Click to see COC1=C(C=C2C(=C1)C3C(CO2)OC4=C(C3=O)C(=CC5=C4C=CO5)O)OC 368.30 unknown https://doi.org/10.1002/RECL.19390580304
rel-(7aR,13aR)-9,10-Dimethoxy-3,3-dimethyl-13,13a-dihydro-3H-pyrano[2,3-c:6,5-f']dichromen-7(7aH)-one 184223 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)C 394.40 unknown https://doi.org/10.1021/JA01326A060
Rotenone 6758 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC 394.40 unknown https://doi.org/10.1016/S0040-4020(01)93394-0
https://doi.org/10.1002/ARDP.19112490408
https://doi.org/10.1248/YAKUSHI1881.1923.491_10
https://doi.org/10.1016/S0031-9422(99)00098-9
Sumatrol 442824 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)O 410.40 unknown https://doi.org/10.1002/RECL.19390580304
Tephrosin 114909 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)C 410.40 unknown https://doi.org/10.1055/S-2006-961936

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