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Cyclopia falcata

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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 UUID643fdbd09f548317830108
Scientific name Cyclopia falcata
Authority (Harv.) Kies
First published in Bothalia6: 168 (1951)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cyclopia brachypoda Hofmeyr & E.Phillips Bothalia1: 108 (1922)
Cyclopia vogelii var. falcata Harv. W.H.Harvey & auct. suc. (eds.), Fl. Cap.2: 7 (1862)

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000197696
Tropicos 13057634
KEW urn:lsid:ipni.org:names:489288-1
The Plant List ild-4423
Open Tree Of Life 786749
NCBI Taxonomy 337839
IPNI 489288-1
iNaturalist 583170
GBIF 5341865
EOL 685832
USDA GRIN 436010

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
Biogenic Phytochemicals Modulating Obesity: From Molecular Mechanism to Preventive and Therapeutic Approaches Kumar V, Singh DD, Lakhawat SS, Yasmeen N, Pandey A, Singla RK Evid Based Complement Alternat Med 27-Mar-2022
PMCID:PMC8977300
doi:10.1155/2022/6852276
PMID:35388304
Patterns of Variation and Chemosystematic Significance of Phenolic Compounds in the Genus Cyclopia (Fabaceae, Podalyrieae) Stander MA, Redelinghuys H, Masike K, Long H, Van Wyk BE Molecules 26-Jun-2019
PMCID:PMC6651507
doi:10.3390/molecules24132352
PMID:31247917
Nodulation of Cyclopia spp. (Leguminosae, Papilionoideae) by Burkholderia tuberum Elliott GN, Chen WM, Bontemps C, Chou JH, Young JP, Sprent JI, James EK Ann Bot 19-Sep-2007
PMCID:PMC2759218
doi:10.1093/aob/mcm227
PMID:17881339
Phenolic metabolites from honeybush tea (Cyclopia subternata). Kamara BI, Brand DJ, Brandt EV, Joubert E J Agric Food Chem 25-Aug-2004
doi:10.1021/JF040097Z
PMID:15315375

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
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
3,4,5-Trihydroxy-1-cyclohexene-1-carboxylic acid 1094 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown https://doi.org/10.1021/JF040097Z
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
6-Methoxycyclohexane-1,2,3,4,5-pentol 230881 Click to see COC1C(C(C(C(C1O)O)O)O)O 194.18 unknown https://doi.org/10.1021/JF040097Z
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Icariside D2 10614148 Click to see C1=CC(=CC=C1CCO)OC2C(C(C(C(O2)CO)O)O)O 300.30 unknown https://doi.org/10.1021/JF040097Z
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,3,6,7-Tetrahydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-one 5358385 Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O 422.30 unknown https://doi.org/10.1021/JF040097Z
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1021/JF040097Z
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
[(2R,3S)-7-hydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)-2,3-dihydrochromen-3-yl] 3,4,5-trihydroxybenzoate 162946468 Click to see C1=CC2=C(C=C1O)OC(C(C2=O)OC(=O)C3=CC(=C(C(=C3)O)O)O)C4=CC(=C(C(=C4)O)O)O 456.40 unknown https://doi.org/10.1021/JF040097Z
[7-Hydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)-2,3-dihydrochromen-3-yl] 3,4,5-trihydroxybenzoate 162946467 Click to see C1=CC2=C(C=C1O)OC(C(C2=O)OC(=O)C3=CC(=C(C(=C3)O)O)O)C4=CC(=C(C(=C4)O)O)O 456.40 unknown https://doi.org/10.1021/JF040097Z
> Phenylpropanoids and polyketides / Flavonoids / Flavones
7,3',4'-Trihydroxyflavone 5322065 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C=C3)O)O)O 270.24 unknown https://doi.org/10.1021/JF040097Z
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
3,5,7-trihydroxy-2-(4-hydroxyphenyl)-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 24721625 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/JF040097Z
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2S,3R,4S,5S,6R)-2-[[(2S)-2-(3,4-dihydroxyphenyl)-7-hydroxy-3,4-dihydro-2H-chromen-5-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 21576516 Click to see C1CC2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)O)OC1C4=CC(=C(C=C4)O)O 436.40 unknown https://doi.org/10.1021/JF040097Z
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[2-acetyloxy-4-[5-hydroxy-4-oxo-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-2-yl]phenyl] acetate 162878068 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)OC(=O)C)OC(=O)C)O)O)O)O)O)O)O 678.60 unknown https://doi.org/10.1021/JF040097Z
4H-1-Benzopyran-4-one, 7-[[6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-2,3-dihydro-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-, (S)- 3594 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 610.60 unknown https://doi.org/10.1021/JF040097Z
Eriocitrin 83489 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O 596.50 unknown https://doi.org/10.1021/JF040097Z
Hesperidin 10621 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 610.60 unknown https://doi.org/10.1021/JF040097Z
Naringenin 7-rutinoside 85704 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)O)O)O)O)O)O 580.50 unknown https://doi.org/10.1021/JF040097Z

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