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Pleurolobus gangeticus

Pleurolobus gangeticus - 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
Collections

Details Top

Internal ID UUID643fd6d0a7533878327760
Scientific name Pleurolobus gangeticus
Authority (L.) J.St.-Hil. ex H.Ohashi & K.Ohashi
First published in J. Jap. Bot.93: 184 (2018)

Description Top

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Synonyms Top

Scientific name Authority First published in
Desmodium cavaleriei H.Lév.
Meibomia gangetica (L.) Kuntze Revis. Gen. Pl.1: 196 (1891)
Meibomia polygonodes (Welw. ex Baker) Kuntze Revis. Gen. Pl.1: 198 (1891)
Hedysarum gangeticum L. Sp. Pl.: 746 (1753)
Hedysarum maculatum L. Sp. Pl.: 746 (1753)
Desmodium lanceolatum (Schumach. & Thonn.) Walp. Repert. Bot. Syst.1: 737 (1842)
Desmodium polygonoides Welw. ex Baker D.Oliver & auct. suc. (eds.), Fl. Trop. Afr.2: 161 (1871)
Desmodium gangeticum (L.) DC. Prodr.2: 327 (1825)
Desmodium gangeticum var. maculatum (L.) Baker J.D.Hooker, Fl. Brit. India2: 168 (1876)
Desmodium natalitium Sond. Linnaea23: 32 (1850)
Desmodium maculatum (L.) DC. Prodr.2: 327 (1825)
Hedysarum pseudogangeticum Miq.
Aeschynomene gangetica Poir. J.B.A.M.de Lamarck, Encycl., Suppl. 4: 453 (1816)
Aeschynomene maculata Poir. J.B.A.M.de Lamarck, Encycl., Suppl. 4: 452 (1816)
Desmodium gangeticum var. ramnagari Haines
Hedysarum lanceolatum Schumach. & Thonn. C.F.Schumacher, Beskr. Guin. Pl.: 360 (1827)
Desmodium cavaleriei H.Lév. Fl. Kouy-Tchéou: 232 (1915)
Meibomia natalita (Sond.) Kuntze Revis. Gen. Pl.1: 198 (1891)
Desmodium collinum Wight Icon. Pl. Orient.1(14): [1], t. 272 (1840)

Common names Top

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Language Common/alternative name
Arabic عرقيص غانجي
Bambara cɛganakunsigi
Bengali শালপর্ণী
dag wookpargu
Kannada ಮೂರೆಲೆ ಹೊನ್ನೆ
mad kalkal otek
Malayalam ഓരില
Burmese ကျေးမြီးဖို
sd شالپرڻي
Swedish desmodium gangeticum
Tamil மூவிலை
Chinese 蝉豆
Chinese 大葉山螞蝗
Chinese 大葉山螞蟥
Chinese 大叶山蚂蝗

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
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Chad
      • Eritrea
      • Ethiopia
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Kwazulu-Natal
      • Northern Provinces
    • West Tropical Africa
      • Benin
      • Burkina
      • Gambia
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Mali
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Congo
      • Equatorial Guinea
      • Gabon
      • Gulf Of Guinea Islands
      • Rwanda
      • Zaïre
    • Western Indian Ocean
      • Madagascar
      • Réunion
  • Asia-temperate
    • Arabian Peninsula
      • Yemen
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Nansei-shoto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Laccadive Islands
      • Maldives
      • Nepal
      • Pakistan
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sumatera
    • Papuasia
      • Bismarck Archipelago
      • New Guinea
  • Australasia
    • Australia
      • New South Wales
      • Northern Territory
      • Queensland
      • Western Australia
  • Pacific
    • Northwestern Pacific
      • Caroline Islands
      • Marianas
    • South-central Pacific
      • Cook Islands
      • Society Islands
      • Tuamotu
      • Tubuai Islands
    • Southwestern Pacific
      • Fiji

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000170608
Tropicos 13048308
INPN 929304
KEW urn:lsid:ipni.org:names:515302-1
NCBI Taxonomy 670324
IPNI 515302-1
GBIF 2967305
Freebase /m/043m2db
Wikipedia Pleurolobus_gangeticus
CMAUP NPO7804

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
Regulation of virulence in Chromobacterium violaceum and strategies to combat it Venkatramanan M, Nalini E Front Microbiol 24-Jan-2024
PMCID:PMC10847564
doi:10.3389/fmicb.2024.1303595
PMID:38328423
Functional Properties and Acceptability of Potentially Medicinal Tea Infusions Based on Equisetum arvense, Desmodium molliculum, and Mentha piperita Salazar-Campos J, Salazar-Campos O, Gálvez-Ruiz O, Gavidia-Chávez H, Gavidia-Chávez M, Irigoin-Guevara L, Obregón-Domínguez J Prev Nutr Food Sci 31-Dec-2023
PMCID:PMC10764227
doi:10.3746/pnf.2023.28.4.444
PMID:38188091
Medicinal plants of the upper Aswa River catchment of northern Uganda - a cultural crossroads Masters ET J Ethnobiol Ethnomed 27-Oct-2023
PMCID:PMC10605377
doi:10.1186/s13002-023-00620-5
PMID:37884931
Innovative Bioactive Nanofibrous Materials Combining Medicinal and Aromatic Plant Extracts and Electrospinning Method Stoyanova N, Nachev N, Spasova M Membranes (Basel) 21-Oct-2023
PMCID:PMC10608671
doi:10.3390/membranes13100840
PMID:37888012
Implementation of machine learning in DNA barcoding for determining the plant family taxonomy Riza LS, Zain MI, Izzuddin A, Prasetyo Y, Hidayat T, Abu Samah KA Heliyon 21-Sep-2023
PMCID:PMC10520734
doi:10.1016/j.heliyon.2023.e20161
PMID:37767518
Dandelion flower-fabricated Ag nanoparticles versus synthetic ones with characterization and determination of photocatalytic, antioxidant, antibacterial, and α-glucosidase inhibitory activities Yousefzadeh-Valendeh S, Fattahi M, Asghari B, Alizadeh Z Sci Rep 18-Sep-2023
PMCID:PMC10507034
doi:10.1038/s41598-023-42756-0
PMID:37723218
Targeting NF-κB pathway for the anti-inflammatory potential of Bhadradarvadi kashayam on stimulated RAW 264.7 macrophages Ali A M MT, Narayana S DS, Lulu S S, Nag S, Sundararajan V Heliyon 19-Aug-2023
PMCID:PMC10469766
doi:10.1016/j.heliyon.2023.e19270
PMID:37664699
Revisiting the Green Synthesis of Nanoparticles: Uncovering Influences of Plant Extracts as Reducing Agents for Enhanced Synthesis Efficiency and Its Biomedical Applications Singh H, Desimone MF, Pandya S, Jasani S, George N, Adnan M, Aldarhami A, Bazaid AS, Alderhami SA Int J Nanomedicine 18-Aug-2023
PMCID:PMC10444627
doi:10.2147/IJN.S419369
PMID:37621852
A lexical review on Vishaghna Dravyas of Kaideva Nighantu Yadav S, Sharma A, Vishnoi R, Rani J Ayu 02-Aug-2023
PMCID:PMC10468017
doi:10.4103/ayu.ayu_199_22
PMID:37655171
Effects of Ayurveda interventions on acute pain and quality of life of a trigeminal neuralgia patient - A case report De Silva UM, Mangal G, Attanayake AM, Upadhyay A, Vedpathak SM J Ayurveda Integr Med 25-Jul-2023
PMCID:PMC10382661
doi:10.1016/j.jaim.2023.100743
PMID:37494834
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
Anti‑tumor effects of an aqueous extract of Ecklonia cava in BALB/cKorl syngeneic mice using colon carcinoma CT26 cells Gong JE, Kim JE, Park SH, Lee SJ, Choi YJ, Choi SI, Choi YW, Lee HS, Hong JT, Hwang DY Oncol Rep 08-May-2023
PMCID:PMC10196738
doi:10.3892/or.2023.8565
PMID:37165874
Corrigendum to “Development and evaluation of aphrodisiac potential of a classical ayurvedic formulation, ‘Kaamdev ghrita’ in rat model” [J Ayurveda Integr Med 12 (2021) 294–301] Gurav N, Gurav S, Wanjari M, Prasad S, Wayal S, Rarokar N J Ayurveda Integr Med 17-Feb-2023
PMCID:PMC10334120
doi:10.1016/j.jaim.2023.100687
PMID:36801157
Synthesis, biomedical applications, and toxicity of CuO nanoparticles Naz S, Gul A, Zia M, Javed R Appl Microbiol Biotechnol 13-Jan-2023
PMCID:PMC9838533
doi:10.1007/s00253-023-12364-z
PMID:36635395
A review on phytochemical and pharmacological facets of tropical ethnomedicinal plants as reformed DPP-IV inhibitors to regulate incretin activity Chhabria S, Mathur S, Vadakan S, Sahoo DK, Mishra P, Paital B Front Endocrinol (Lausanne) 11-Nov-2022
PMCID:PMC9691845
doi:10.3389/fendo.2022.1027237
PMID:36440220

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
> Alkaloids and derivatives / Harmala alkaloids
1,2,8-Trimethyl-1,3,4,9-tetrahydropyrido[3,4-b]indole 5319783 Click to see CC1C2=C(CCN1C)C3=CC=CC(=C3N2)C 214.31 unknown via CMAUP database
> Alkaloids and derivatives / Phthalide isoquinolines
5-([1,3]dioxolo[4,5-g]isoquinolin-5-yl)-5H-furo[3,4-f][1,3]benzodioxol-7-one 5318389 Click to see C1OC2=C(O1)C=C3C(=C2)C=CN=C3C4C5=CC6=C(C=C5C(=O)O4)OCO6 349.30 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
Hordenine 68313 Click to see CN(C)CCC1=CC=C(C=C1)O 165.23 unknown via CMAUP database
Hydrogen sulfate;2-(4-hydroxyphenyl)ethyl-dimethylazanium 44655713 Click to see C[NH+](C)CCC1=CC=C(C=C1)O.OS(=O)(=O)[O-] 263.31 unknown via CMAUP database
N-methyltyraminium 25202330 Click to see C[NH2+]CCC1=CC=C(C=C1)O 152.21 unknown via CMAUP database
Phenethylamine 1001 Click to see C1=CC=C(C=C1)CCN 121.18 unknown via CMAUP database
> Homogeneous metal compounds / Homogeneous transition metal compounds
Copper 23978 Click to see [Cu] 63.55 unknown via CMAUP database
> Mixed metal/non-metal compounds / Transition metal organides / Transition metal sulfides
Cadmium sulfide 14783 Click to see S=[Cd] 144.48 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
3-(1H-indol-3-yl)-2-(trimethylazaniumyl)propanoate 3861164 Click to see C[N+](C)(C)C(CC1=CNC2=CC=CC=C21)C(=O)[O-] 246.30 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
Hovenine A 5318090 Click to see CCC(C)C(C(=O)NC1C(OC2=CC=C(C=C2)C=CNC(=O)C(NC1=O)CC(C)C)C(C)C)NC 486.60 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
Acetate 175 Click to see CC(=O)[O-] 59.04 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3S,4R,5R,6S)-2-methyl-6-[4-[2-(methylamino)ethyl]phenoxy]oxane-3,4,5-triol 11972414 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CCNC)O)O)O 297.35 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives
2-(1H-indol-3-yl)ethyl-trimethylazanium 5316904 Click to see C[N+](C)(C)CCC1=CNC2=CC=CC=C21 203.30 unknown via CMAUP database
Dimethyltryptamine 6089 Click to see CN(C)CCC1=CNC2=CC=CC=C21 188.27 unknown via CMAUP database
N,N-Dimethyl-5-methoxytryptamine 1832 Click to see CN(C)CCC1=CNC2=C1C=C(C=C2)OC 218.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(Z)-3-(3,4-Dihydroxyphenyl)propenoic acid 2-phenylethyl ester 6603789 Click to see C1=CC=C(C=C1)CCOC(=O)C=CC2=CC(=C(C=C2)O)O 284.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
5-Methoxy-1,7-diphenyl-3-heptanone 5319430 Click to see COC(CCC1=CC=CC=C1)CC(=O)CCC2=CC=CC=C2 296.40 unknown via CMAUP database

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