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Dipcadi glaucum

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID644025e0ca58d164528924
Scientific name Dipcadi glaucum
Authority (Burch. ex Ker Gawl.) Baker
First published in J. Linn. Soc., Bot. 11: 401 (1870)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Lachenalia speciosa F.Dietr. Vollst. Lex. Gärtn. 9: 358 (1809)
Urginea lorata Baker Bull. Herb. Boissier Ser. II. iii. 664.
Uropetalon glaucum Burch. Bot. Reg. 2: t. 156. 1816 [1 Nov 1816]
Dipcadi gracilipes K.Krause Bot. Jahrb. Syst. 48: 357 (1912)
Dipcadi longibracteatum Schinz Verh. Bot. Vereins Prov. Brandenburg 31: 218 (1890)
Dipcadi magnum Baker Fl. Trop. Afr. 7: 522 (1898)

Common names Top

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Language Common/alternative name
Afrikaans malkop-ui
Arabic بريط غلوكي

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
  • Africa
    • Southern Africa
      • Botswana
      • Cape Provinces
      • Free State
      • Namibia
      • Northern Provinces

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000765410
Tropicos 18402899
KEW urn:lsid:ipni.org:names:533935-1
The Plant List kew-304316
Open Tree Of Life 65963
NCBI Taxonomy 480435
IPNI 533935-1
iNaturalist 583896
GBIF 2768304
EPPO DPDGL
EOL 1087523
USDA GRIN 14333

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
D N/A Saunders Comprehensive Veterinary Dictionary 16-Oct-2020
PMCID:PMC9771679
doi:10.1016/B978-0-7020-7463-9.50012-4
Diseases of the Alimentary Tract: Nonruminant N/A Veterinary Medicine 10-Feb-2017
PMCID:PMC7167529
doi:10.1016/B978-0-7020-5246-0.00007-3
Molecular phylogenetics of subfamily Ornithogaloideae (Hyacinthaceae) based on nuclear and plastid DNA regions, including a new taxonomic arrangement Martínez-Azorín M, Crespo MB, Juan A, Fay MF Ann Bot 01-Jan-2010
PMCID:PMC3002468
doi:10.1093/aob/mcq207
PMID:21163815
Cardenolides of the seeds of Ornithogalum magnum N. F. Komissarenko Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00563769
Cardenolides of the flowers and bulbs of Ornithogalum gussonii N. F. Komissarenko, P. E. Krivenchuk Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00563646

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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
3,14-Dihydroxycarda-16,20(22)-dienolide 293736 Click to see 372.50 unknown https://doi.org/10.1007/BF00563646
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives
Sarmentogenin 6437 Click to see 390.50 unknown https://doi.org/10.1007/BF00563646
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
3-[(3S,5R,8R,9S,10S,11S,13R,14S,17S)-11,14-dihydroxy-10,13-dimethyl-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 162949415 Click to see 536.70 unknown https://doi.org/10.1007/BF00563769
3-[(3S,5R,8R,9S,10S,13R,14S,16S,17S)-14,16-dihydroxy-10,13-dimethyl-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 163003402 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CC(C5C6=CC(=O)OC6)O)O)C)C)O)O)O 536.70 unknown https://doi.org/10.1007/BF00563769
3-[(3S,5R,8S,9S,10S,11R,13R,14S,17S)-3-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3S,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-11,14-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 162964976 Click to see 698.80 unknown https://doi.org/10.1007/BF00563769
3-[3-[3,4-dihydroxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-11,14-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 78076507 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3C(CC5(C4(CCC5C6=CC(=O)OC6)O)C)O)C)O)O)OC7C(C(C(C(O7)CO)O)O)O 698.80 unknown https://doi.org/10.1007/BF00563769
Card-20(22)-enolide,3-[(6-deoxy-a-L-mannopyranosyl)oxy]-11,14-dihydroxy-, (3b,5b,11a)- 4482831 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3C(CC5(C4(CCC5C6=CC(=O)OC6)O)C)O)C)O)O)O 536.70 unknown https://doi.org/10.1007/BF00563769
Gitoxigenin,16-propionyl 293734 Click to see 536.70 unknown https://doi.org/10.1007/BF00563769
Rhodexin A 441868 Click to see 536.70 unknown https://doi.org/10.1007/BF00563646
Rhodexoside 123131910 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3C(CC5(C4(CCC5C6=CC(=O)OC6)O)C)O)C)O)O)OC7C(C(C(C(O7)CO)O)O)O 698.80 unknown https://doi.org/10.1007/BF00563646

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