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Glycine falcata

Glycine falcata - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Glycine falcata - 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 UUID643fd9c7ea844842593797
Scientific name Glycine falcata
Authority Benth.
First published in Fl. Austral.2: 243 (1864)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Arabic حلوة منجلية

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
  • Australasia
    • Australia
      • Northern Territory
      • Queensland
      • South Australia
      • Western Australia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000187286
USDA Plants GLFA3
Tropicos 13019705
KEW urn:lsid:ipni.org:names:496715-1
The Plant List ild-33813
Open Tree Of Life 952066
NCBI Taxonomy 45690
IPNI 496715-1
GBIF 5359654
EPPO GLXFA
EOL 643706
USDA GRIN 17695
CMAUP NPO12800

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
Complete chloroplast genome of a rare and endangered plant species Osteomeles subrotunda: genomic features and phylogenetic relationships with other Rosaceae plants Jiang M, Wang J, Chen M, Zhang H Mitochondrial DNA B Resour 11-Mar-2021
PMCID:PMC7954488
doi:10.1080/23802359.2021.1881835
PMID:33763572
Amphicarpic plants: definition, ecology, geographic distribution, systematics, life history, evolution and use in agriculture Zhang K, Baskin JM, Baskin CC, Cheplick GP, Yang X, Huang Z Biol Rev Camb Philos Soc 28-May-2020
PMCID:PMC7540684
doi:10.1111/brv.12623
PMID:32462729
Ancestral Reconstruction and Investigations of Genomic Recombination on some Pentapetalae Chloroplasts Guyeux C, Salomon M, Al-Nuaimi B, AlKindy B, Couchot JF J Integr Bioinform 20-Dec-2019
PMCID:PMC7074144
doi:10.1515/jib-2018-0057
PMID:31860470
Intraspecific and heteroplasmic variations, gene losses and inversions in the chloroplast genome of Astragalus membranaceus Lei W, Ni D, Wang Y, Shao J, Wang X, Yang D, Wang J, Chen H, Liu C Sci Rep 22-Feb-2016
PMCID:PMC4761949
doi:10.1038/srep21669
PMID:26899134
The Complete Sequence of the Acacia ligulata Chloroplast Genome Reveals a Highly Divergent clpP1 Gene Williams AV, Boykin LM, Howell KA, Nevill PG, Small I PLoS One 08-May-2015
PMCID:PMC4425659
doi:10.1371/journal.pone.0125768
PMID:25955637
Plastid-LCGbase: a collection of evolutionarily conserved plastid-associated gene pairs Wang D, Yu J Nucleic Acids Res 05-Nov-2014
PMCID:PMC4383908
doi:10.1093/nar/gku1070
PMID:25378306
Molecular and Chromosomal Evidence for Allopolyploidy in Soybean Gill N, Findley S, Walling JG, Hans C, Ma J, Doyle J, Stacey G, Jackson SA Plant Physiol 01-Nov-2009
PMCID:PMC2773056
doi:10.1104/pp.109.137935
PMID:19605552

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
> Benzenoids / Phenanthrenes and derivatives
Isosalviamine A 86226793 Click to see CC1=C2C=CC3=C(C2=CC=C1)C4=C(C5=C3OC=C5C)OC=N4 287.30 unknown via CMAUP database
Isosalviamine B 86226794 Click to see CC1=C2C=CC3=C(C2=CC=C1)C4=C(C5=C3OC=C5C)OC(=N4)C 301.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Ferruginol 442027 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown via CMAUP database
Sugiol 94162 Click to see CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O 300.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
(6S)-6-hydroxy-1,6-dimethyl-8,9-dihydro-7H-naphtho[1,2-g][1]benzofuran-10,11-dione 56967683 Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)O 296.30 unknown via CMAUP database
(8S)-2-Hydroxy-8,9-dihydro-4,8-dimethylphenanthro[3,2-b]furan-7,11-dione 102185094 Click to see CC1COC2=C1C(=O)C3=C(C2=O)C4=C(C=C3)C(=CC(=C4)O)C 294.30 unknown via CMAUP database
(S)-6-(Hydroxymethyl)-1,6-dimethyl-6,7,8,9-tetrahydrophenanthro[1,2-b]furan-10,11-dione 9926694 Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)CO 310.30 unknown via CMAUP database
2-Isopropyl-8-methylphenanthrene-3,4-dione 135872 Click to see CC1=C2C=CC3=C(C2=CC=C1)C(=O)C(=O)C(=C3)C(C)C 264.30 unknown via CMAUP database
Cryptotanshinone 160254 Click to see CC1COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C 296.40 unknown via CMAUP database
Danshenol A 3083514 Click to see CC1COC2=C1C(=O)C(C3=C2C=CC4=C(C=CC=C43)C)(CC(=O)C)O 336.40 unknown via CMAUP database
Dihydrotanshinone I 11425923 Click to see CC1COC2=C1C(=O)C(=O)C3=C2C=CC4=C(C=CC=C43)C 278.30 unknown via CMAUP database
Methylenetanshinquinone 105118 Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4=C 278.30 unknown via CMAUP database
Tanshinone I 114917 Click to see CC1=C2C=CC3=C(C2=CC=C1)C(=O)C(=O)C4=C3OC=C4C 276.30 unknown via CMAUP database
Tanshinone IIA 164676 Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C 294.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
epi-Maslinic acid 25564831 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
Euscaphic acid 471426 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown via CMAUP database
Lup-20(29)-ene-2alpha,3alpha-diol 102090518 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C 442.70 unknown via CMAUP database
Lup-20(29)-ene-2alpha,3beta-diol 15127233 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C 442.70 unknown via CMAUP database
Lupa-20(29)-ene-2alpha,3alpha-diol 3-acetate 46850686 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)OC(=O)C)O)C)C)C 484.80 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Maslinic Acid 73659 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
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 via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid acids / 3-carboxy steroids
Hyptadienic acid 14605533 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=CC5(C)C)CO)C)C)C2C1(C)O)C)C(=O)O 470.70 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 / L-alpha-amino acids
(2S)-2-azaniumyl-4-hydroxybutanoate 6971022 Click to see C(CO)C(C(=O)[O-])[NH3+] 119.12 unknown via CMAUP database

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