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Sedum crassularia

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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 UUID64405c09b753c786574375
Scientific name Sedum crassularia
Authority Raym.-Hamet
First published in Candollea 4: 27 (1929)

Description Top

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Synonyms Top

Scientific name Authority First published in
Crassula sediformis Schweinf. Beitr. Fl. Aethiop. : 80 (1867)

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
  • Africa
    • East Tropical Africa
      • Kenya
    • Northeast Tropical Africa
      • Ethiopia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001300351
Tropicos 8902860
KEW urn:lsid:ipni.org:names:275279-1
The Plant List tro-8902860
NCBI Taxonomy 2726413
IPNI 275279-1
iNaturalist 739226
GBIF 5689819

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
Two phloroglucinol glucosides, flavan gallates and flavonol glycosides from Sedum sediforme flowers M.Koray Sakar, Frank Petereit, Adolf Nahrstedt Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(93)85416-O

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown https://doi.org/10.1016/0031-9422(93)85416-O
> Benzenoids / Phenols / Methoxyphenols
3-Methoxyphenol 9007 Click to see COC1=CC=CC(=C1)O 124.14 unknown https://doi.org/10.1016/0031-9422(93)85416-O
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
3-methoxy-5-hydroxyphenol-1-O-beta-d-glucopyranoside 91378659 Click to see COC1=CC(=CC(=C1)O)OC2C(C(C(C(O2)CO)O)O)O 302.28 unknown https://doi.org/10.1016/0031-9422(93)85416-O
CID 476785 476785 Click to see C1=C(C=C(C=C1O)OC2C(C(C(C(O2)CO)O)O)O)O 288.25 unknown https://doi.org/10.1016/0031-9422(93)85416-O
Phlorin 12314169 Click to see C1=C(C=C(C=C1O)OC2C(C(C(C(O2)CO)O)O)O)O 288.25 unknown https://doi.org/10.1016/0031-9422(93)85416-O
Picraquassioside D 56776291 Click to see COC1=CC(=CC(=C1)O)OC2C(C(C(C(O2)CO)O)O)O 302.28 unknown https://doi.org/10.1016/0031-9422(93)85416-O
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
[7-hydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-5-methoxy-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate 74977187 Click to see COC1=CC(=CC(=C1O)OC)C2C(CC3=C(O2)C=C(C=C3OC)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 500.40 unknown https://doi.org/10.1016/0031-9422(93)85416-O
Epigallocatechin 5,3',5'-trimethyl ether 3-O-gallate 44257124 Click to see COC1=CC(=CC(=C1O)OC)C2C(CC3=C(O2)C=C(C=C3OC)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 500.40 unknown https://doi.org/10.1016/0031-9422(93)85416-O
Epigallocatechin Gallate 65064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 458.40 unknown https://doi.org/10.1016/0031-9422(93)85416-O
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one 5353915 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/0031-9422(93)85416-O
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 5320854 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/0031-9422(93)85416-O
5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-methoxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 14186852 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC4C(C(C(C(O4)CO)O)O)O)O 508.40 unknown https://doi.org/10.1016/0031-9422(93)85416-O
5,7-dihydroxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one 16103933 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/0031-9422(93)85416-O
kaempferol-3-O-alpha-L-rhamnoside 15558501 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown https://doi.org/10.1016/0031-9422(93)85416-O
Limocitrin 3-O-beta-D-glucopyranoside 5319024 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC4C(C(C(C(O4)CO)O)O)O)O 508.40 unknown https://doi.org/10.1016/0031-9422(93)85416-O
Myricetin 3-rhamnoside 5352000 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/0031-9422(93)85416-O
Myricitrin 5281673 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/0031-9422(93)85416-O
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/0031-9422(93)85416-O

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