Ladyginia bucharica

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Internal ID UUID64404711e6786580639013
Scientific name Ladyginia bucharica
Authority Lipsky
First published in Trudy Imp. S.-Peterburgsk. Bot. Sada 23: 150 (1904)

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Synonyms Top

Scientific name Authority First published in
Ferula bucharica Koso-Pol. Vestn. Tiflissk. Bot. Sada 11: 137 (1916)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Middle Asia
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Western Asia
      • Afghanistan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001068538
Tropicos 1702712
KEW urn:lsid:ipni.org:names:843928-1
Open Tree Of Life 3888349
Observations.org 119184
NCBI Taxonomy 2184474
IPNI 843928-1
iNaturalist 823588
GBIF 3631252
Elurikkus 387297

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)!
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Title Authors Publication Released IDs
Triterpene glycosides of ladyginia bucharica III. Structure of ladyginoside C M. Patkhullaeva, L. G. Mzhel'skaya, N. K. Abubakirov Springer Science and Business Media LLC 22-Nov-2004
doi:10.1007/BF00580884
Triterpene glycosides of Ladyginia bucharica IV. Structure of ladyginosides D and F M. Patkhullaeva, L. G. Mzhel'skaya, N. K. Abubakirov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00565790
Triterpene glycosides ofLadyginia bucharica M. Patkhullaeva, L. G. Mzhel'skaya, N. K. Abubakirov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00564279

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 / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
6-[[8a-[6-[[3,4-Dihydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxymethyl]oxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxycarbonyl-4-(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4,5-dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid 163103394 Click to see 1621.70 unknown https://doi.org/10.1007/BF00565790
6-[[8a-[6-[[3,4-Dihydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxymethyl]oxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxycarbonyl-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4,5-dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid 163104971 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)OC7C(C(C(C(O7)CO)O)O)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)COC9C(C(C(C(O9)COC1C(C(C(C(O1)COC1C(C(C(C(O1)CO)O)O)O)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)O)O)O)C 1605.70 unknown https://doi.org/10.1007/BF00564279
https://doi.org/10.1007/BF00580884
6-[[8a-[6-[[3,4-Dihydroxy-6-(hydroxymethyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxycarbonyl-4-(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4,5-dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid 163104413 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(C(O6)C(=O)O)OC7C(C(C(C(O7)CO)O)O)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)OC1C(C(C(C(O1)CO)O)O)O)O)O)O)O)O)C 1297.40 unknown https://doi.org/10.1007/BF00564279
https://doi.org/10.1007/BF00565790
Calendulaglycoside E 13919550 Click to see 795.00 unknown https://doi.org/10.1007/BF00564279

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