Alysicarpus monilifer - Unknown
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Internal ID UUID643fd7eeebf31693036996
Scientific name Alysicarpus monilifer
Authority (L.) DC.
First published in Prodr.2: 353 (1825)

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Synonyms Top

Scientific name Authority First published in
Hedysarum moniliferum L. Mant. Pl.1: 102 (1767)
Alysicarpus narimanii S.M.Almeida & M.R.Almeida J. Bombay Nat. Hist. Soc.85: 394 (1988)
Alysicarpus mahbubnagarensis Ragh.Rao, Rajagopal & Ram.Chary Asian J. Pl. Sci.1: 97 (1989)
Fabricia monilifera (L.) Kuntze Revis. Gen. Pl.1: 182 (1891)
Alysicarpus monilifer var. mahbubnagarensis (Ragh.Rao, Rajagopal & Ram.Chary) Pokle Bull. Pure Appl. Sci., Modinagar, B17: 32 (1998)
Alysicarpus monilifer var. cuddapahensis S.M.Almeida & M.R.Almeida J. Bombay Nat. Hist. Soc.85: 402 (1988)

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) 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
    • Northeast Tropical Africa
      • Ethiopia
      • Socotra
      • Somalia
      • Sudan
    • West Tropical Africa
      • Benin
      • Niger
    • Western Indian Ocean
      • Madagascar
      • Mauritius
      • Réunion
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Laccadive Islands
      • Maldives
      • Pakistan
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Myanmar

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000176832
Tropicos 13046385
INPN 705806
KEW urn:lsid:ipni.org:names:473535-1
The Plant List ild-2296
Open Tree Of Life 3927164
NCBI Taxonomy 1766240
IPNI 473535-1
iNaturalist 495569
GBIF 2948685
EPPO ALZMO
EOL 642359
USDA GRIN 2735

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)!
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Title Authors Publication Released IDs
Nanomedicine for the Treatment of Viral Diseases: Smaller Solution to Bigger Problems Ghorai S, Shand H, Patra S, Panda K, Santiago MJ, Rahman MS, Chinnapaiyan S, Unwalla HJ Pharmaceutics 16-Mar-2024
PMCID:PMC10975899
doi:10.3390/pharmaceutics16030407
PMID:38543301
Silver Nanoparticle-Based Therapy: Can It Be Useful to Combat Multi-Drug Resistant Bacteria? Mateo EM, Jiménez M Antibiotics (Basel) 06-Sep-2022
PMCID:PMC9495113
doi:10.3390/antibiotics11091205
PMID:36139984
Silver nanomaterials: synthesis and (electro/photo) catalytic applications Sharma RK, Yadav S, Dutta S, Kale HB, Warkad IR, Zbořil R, Varma RS, Gawande MB Chem Soc Rev 18-Oct-2021
PMCID:PMC8942099
doi:10.1039/d0cs00912a
PMID:34661205
Therapeutic potential of medicinal plants against COVID-19: The role of antiviral medicinal metabolites Khan T, Khan MA, Mashwani ZU, Ullah N, Nadhman A Biocatal Agric Biotechnol 11-Dec-2020
PMCID:PMC7831775
doi:10.1016/j.bcab.2020.101890
PMID:33520034
GC–MS analysis of phytoconstituents from Amomum nilgiricum and molecular docking interactions of bioactive serverogenin acetate with target proteins Konappa N, Udayashankar AC, Krishnamurthy S, Pradeep CK, Chowdappa S, Jogaiah S Sci Rep 02-Oct-2020
PMCID:PMC7532471
doi:10.1038/s41598-020-73442-0
PMID:33009462
Effect of nitrogen (N) deposition on soil-N processes: a holistic approach Verma P, Sagar R Sci Rep 26-Jun-2020
PMCID:PMC7320165
doi:10.1038/s41598-020-67368-w
PMID:32591625
Elemental Silver Nanoparticles: Biosynthesis and Bio Applications Mikhailov OV, Mikhailova EO Materials (Basel) 27-Sep-2019
PMCID:PMC6803994
doi:10.3390/ma12193177
PMID:31569794
Qualitative and quantitative ethnobotanical study of the Pangkhua community in Bilaichari Upazilla, Rangamati District, Bangladesh Faruque MO, Feng G, Khan MN, Barlow JW, Ankhi UR, Hu S, Kamaruzzaman M, Uddin SB, Hu X J Ethnobiol Ethnomed 05-Feb-2019
PMCID:PMC6364474
doi:10.1186/s13002-019-0287-2
PMID:30722779
Alpinia calcarata: potential source for the fabrication of bioactive silver nanoparticles Khandel P, Shahi SK, Soni DK, Yadaw RK, Kanwar L Nano Converg 06-Dec-2018
PMCID:PMC6281549
doi:10.1186/s40580-018-0167-9
PMID:30519797
Potential antibacterial mechanism of silver nanoparticles and the optimization of orthopedic implants by advanced modification technologies Qing Y, Cheng L, Li R, Liu G, Zhang Y, Tang X, Wang J, Liu H, Qin Y Int J Nanomedicine 05-Jun-2018
PMCID:PMC5993028
doi:10.2147/IJN.S165125
PMID:29892194
Green synthesis of silver nanoparticles with the Arial part of Dorema ammoniacum D. extract by antimicrobial analysis Zandpour F, Allafchian AR, Vahabi MR, Jalali SA IET Nanobiotechnol 20-Mar-2018
PMCID:PMC8675994
doi:10.1049/iet-nbt.2017.0216
PMID:29768235
Ultramafic geoecology of South and Southeast Asia Galey ML, van der Ent A, Iqbal MC, Rajakaruna N Bot Stud 03-Apr-2017
PMCID:PMC5432931
doi:10.1186/s40529-017-0167-9
PMID:28510201
Alysinol--a new triterpene from Alysicarpus monolifer. Riaz N, Anis I, Khan PM, Shah R, Malik A Nat Prod Lett 01-Dec-2002
doi:10.1080/10575630290034258
PMID:12462347

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 / Acetophenones
Usnic acid 5646 Click to see CC1=C(C(=C2C(=C1O)C3(C(=CC(=O)C(C3=O)C(=O)C)O2)C)C(=O)C)O 344.30 unknown https://doi.org/10.1080/10575630290034258
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3-Hydroxybenzoic acid 7420 Click to see C1=CC(=CC(=C1)O)C(=O)O 138.12 unknown https://doi.org/10.1080/10575630290034258
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1080/10575630290034258
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Poriferasterol 5281330 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1080/10575630290034258
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1080/10575630290034258

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