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Gymnospermium smirnovii

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 UUID64401f5732f88056445267
Scientific name Gymnospermium smirnovii
Authority (Trautv.) Takht.
First published in Bot. Zhurn. (Moscow & Leningrad) 55: 1193 (1970)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Leontice smirnowii Trautv. Trudy Imp. S.-Peterburgsk. Bot. Sada 7: 405 (1880)

Common names Top

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Language Common/alternative name
Georgian მრგვალი წამალი

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-0000712823
KEW urn:lsid:ipni.org:names:107336-1
The Plant List kew-2836011
Observations.org 416536
IPNI 107336-1
GBIF 3981673
Elurikkus 445253
Open Tree Of Life 5727749

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
New triterpenoid saponins from Leontice smirnowii. Tabatadze N, Bun SS, Tabidze B, Mshvildadze V, Dekanosidze G, Ollivier E, Elias R Fitoterapia 01-Oct-2010
doi:10.1016/J.FITOTE.2010.05.021
PMID:20554004
Triterpene glycosides from the tubers of Leontice smirnowii N. Tabatadze, B. Tabidze, V. Mshvildadze, R. Elias, G. Dekanosidze, G. Balansard, E. Kemertelidze Springer Science and Business Media LLC 12-Aug-2009
doi:10.1007/S10600-009-9313-2
Alkaloids of Leontice darvasica A. Zunnunzhanov, S. Iskandarov, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00563895

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
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
Hydrorhombinine 7018997 Click to see 248.36 unknown https://doi.org/10.1007/BF00563895
> Alkaloids and derivatives / Pavine alkaloids
(+)-Argemonine 1551634 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)OC)OC)OC)OC 355.40 unknown https://doi.org/10.1007/BF00563895
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
[6-[[3,4-Dihydroxy-6-(hydroxymethyl)-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] 10-[5-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-6a,6b,9,9,12a-pentamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 163008283 Click to see 1337.40 unknown https://doi.org/10.1016/J.FITOTE.2010.05.021
3-O-beta-D-glucopyranosyl-(1->3)-[beta-D-xylopyranosyl-(1->2)]-alpha-L-arabinopyranosyl-28-O-[alpha-L-rhamnopyranosyl-(1->4)-beta-D-glucopyranosyl-(1->6)-beta-D-glucopyranosyl]-3beta-hydroxy-30-norolean-12,20(29)-dien-28-oic acid 163008284 Click to see 1337.40 unknown https://doi.org/10.1016/J.FITOTE.2010.05.021
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[3,4,5-Trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] 10-[4,5-dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 14284457 Click to see 1059.20 unknown https://doi.org/10.1007/S10600-009-9313-2
Anhuienoside C 101718869 Click to see 1059.20 unknown https://doi.org/10.1007/S10600-009-9313-2
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-5-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-6a,6b,9,9,12a-pentamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 101683943 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(CO4)O)OC5C(C(C(C(O5)CO)O)O)O)OC6C(C(C(CO6)O)O)O)C)CC=C7C3(CCC8(C7CC(=C)CC8)C(=O)O)C)C)C 867.00 unknown https://doi.org/10.1007/S10600-009-9313-2
10-[5-Hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-6a,6b,9,9,12a-pentamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 163049811 Click to see 867.00 unknown https://doi.org/10.1007/S10600-009-9313-2

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