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Chironia krebsii

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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 UUID644010e350d01340169366
Scientific name Chironia krebsii
Authority Griseb.
First published in Gen. Sp. Gent. : 98 (1838)

Description Top

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Synonyms Top

Scientific name Authority First published in
Chironia densiflora Scott Elliot J. Bot. 29: 69 (1891)

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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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
      • Tanzania
    • South Tropical Africa
      • Malawi
      • Mozambique
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Lesotho
      • Northern Provinces
      • Swaziland

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000602727
Tropicos 13800891
KEW urn:lsid:ipni.org:names:366831-1
The Plant List kew-2718790
Open Tree Of Life 6068539
IPNI 366831-1
iNaturalist 578531
GBIF 5595784

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)!
Title Authors Publication Released IDs
Search for Bitter Principles in Chironia Species by LC-MS and Isolation of a New Secoiridoid Diglycoside from Chironia krebsii Jean-Luc Wolfender, Matthias Hamburger, Kurt Hostettmann, Jerôme D. Msonthi, Steven Mavi American Chemical Society (ACS) 31-May-2007
doi:10.1021/NP50095A004
Xanthones fromChironia krebsii Jean-luc Wolfender, Matthias Hamburger, Jerome D. Msonthi, Kurt Hostettmann Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)80080-K

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 / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Swertiamarin 442435 Click to see C=CC1C(OC=C2C1(CCOC2=O)O)OC3C(C(C(C(O3)CO)O)O)O 374.34 unknown https://doi.org/10.1021/NP50095A004
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1-hydroxy-3-methoxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyxanthen-9-one 15714467 Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)C=CC=C3OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O 552.50 unknown https://doi.org/10.1016/0031-9422(91)80080-K
1-Hydroxy-3-methoxy-5-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxyxanthen-9-one 162855314 Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)C=CC=C3OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O 552.50 unknown https://doi.org/10.1016/0031-9422(91)80080-K
1-Hydroxy-3,5-dimethoxy-xanthen-9-one 5479773 Click to see COC1=CC=CC2=C1OC3=CC(=CC(=C3C2=O)O)OC 272.25 unknown https://doi.org/10.1016/0031-9422(91)80080-K
1,2-Dihydroxy-6-methoxy-8-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxyxanthen-9-one 85446566 Click to see COC1=CC2=C(C(=C1)OC3C(C(C(C(O3)COC4C(C(C(CO4)O)O)O)O)O)O)C(=O)C5=C(O2)C=CC(=C5O)O 568.50 unknown https://doi.org/10.1016/0031-9422(91)80080-K
1,2,3,4,6-pentamethoxy-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyxanthen-9-one 15714469 Click to see COC1=CC2=C(C(=C1)OC3C(C(C(C(O3)COC4C(C(C(CO4)O)O)O)O)O)O)C(=O)C5=C(O2)C(=C(C(=C5OC)OC)OC)OC 656.60 unknown https://doi.org/10.1016/0031-9422(91)80080-K
1,2,3,4,6-Pentamethoxy-8-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxyxanthen-9-one 162935708 Click to see COC1=CC2=C(C(=C1)OC3C(C(C(C(O3)COC4C(C(C(CO4)O)O)O)O)O)O)C(=O)C5=C(O2)C(=C(C(=C5OC)OC)OC)OC 656.60 unknown https://doi.org/10.1016/0031-9422(91)80080-K
1,8-Dihydroxy-3,5,6,7-tetramethoxyxanthone 5487631 Click to see COC1=CC(=C2C(=C1)OC3=C(C(=C(C(=C3C2=O)O)OC)OC)OC)O 348.30 unknown https://doi.org/10.1016/0031-9422(91)80080-K
3,5-Dimethoxy-1-[(6-O-beta-D-xylopyranosyl-beta-D-glucopyranosyl)oxy]-9H-xanthen-9-one 14189395 Click to see COC1=CC=CC2=C1OC3=C(C2=O)C(=CC(=C3)OC)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O 566.50 unknown https://doi.org/10.1016/0031-9422(91)80080-K
3,5-Dimethoxy-1-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxyxanthen-9-one 14189393 Click to see COC1=CC=CC2=C1OC3=C(C2=O)C(=CC(=C3)OC)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O 566.50 unknown https://doi.org/10.1016/0031-9422(91)80080-K
3,5-Dimethoxy-1,6-dihydroxyxanthone 5281630 Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)C=CC(=C3OC)O)O 288.25 unknown https://doi.org/10.1016/0031-9422(91)80080-K
3,8-Dihydroxy-1,2,4,6-tetramethoxyxanthen-9-one 5491389 Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)C(=C(C(=C3OC)O)OC)OC)O 348.30 unknown https://doi.org/10.1016/0031-9422(91)80080-K
5-hydroxy-3-methoxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 15714465 Click to see COC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(O2)C(=CC=C4)O 420.40 unknown https://doi.org/10.1016/0031-9422(91)80080-K
5-Hydroxy-3-methoxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 162842729 Click to see COC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(O2)C(=CC=C4)O 420.40 unknown https://doi.org/10.1016/0031-9422(91)80080-K
5-Hydroxy-3-methoxyxanthone 57490839 Click to see COC1=CC2=C(C=C1)C(=O)C3=C(O2)C(=CC=C3)O 242.23 unknown https://doi.org/10.1016/0031-9422(91)80080-K
9H-Xanthen-9-one, 1,3,8-trihydroxy-2,4,6-trimethoxy- 5488734 Click to see COC1=CC(=C2C(=C1)OC3=C(C(=C(C(=C3C2=O)O)OC)O)OC)O 334.28 unknown https://doi.org/10.1016/0031-9422(91)80080-K
Decussatin 5378284 Click to see COC1=C(C2=C(C=C1)OC3=CC(=CC(=C3C2=O)O)OC)OC 302.28 unknown https://doi.org/10.1016/0031-9422(91)80080-K
Gentisin 5281636 Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O 258.23 unknown https://doi.org/10.1016/0031-9422(91)80080-K
Isogentiakochianoside 15714468 Click to see COC1=CC2=C(C(=C1)OC3C(C(C(C(O3)COC4C(C(C(CO4)O)O)O)O)O)O)C(=O)C5=C(O2)C=CC(=C5O)O 568.50 unknown https://doi.org/10.1016/0031-9422(91)80080-K
Mesuaxanthone A 5281651 Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)C=CC=C3O)O 258.23 unknown https://doi.org/10.1016/0031-9422(91)80080-K
Norswertianin 5281658 Click to see C1=CC2=C(C(=C1O)O)C(=O)C3=C(C=C(C=C3O2)O)O 260.20 unknown https://doi.org/10.1016/0031-9422(91)80080-K
Swertianin 5281661 Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)C(=C(C=C3)O)O)O 274.22 unknown https://doi.org/10.1016/0031-9422(91)80080-K
Xanthen-9-one, 1-hydroxy-3-methoxy- 5491377 Click to see COC1=CC(=C2C(=C1)OC3=CC=CC=C3C2=O)O 242.23 unknown https://doi.org/10.1016/0031-9422(91)80080-K

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