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Phlomidoschema parviflorum

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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 UUID643fe6ffcb0d5113829416
Scientific name Phlomidoschema parviflorum
Authority (Benth.) Vved.
First published in Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 9: 55 (1941)

Description Top

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Synonyms Top

Scientific name Authority First published in
Stachys parviflora Benth. Prodr. 12: 490 (1848)

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
  • Asia-temperate
    • Middle Asia
      • Tadzhikistan
    • Western Asia
      • Afghanistan
      • Iran
  • Asia-tropical
    • Indian Subcontinent
      • India
      • Pakistan
      • West Himalaya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000269164
Tropicos 17604190
KEW urn:lsid:ipni.org:names:453773-1
The Plant List kew-152105
Open Tree Of Life 298391
Observations.org 137744
NCBI Taxonomy 194202
IPNI 453773-1
iNaturalist 919254
GBIF 7824617

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
Genus Stachys: A Review of Traditional Uses, Phytochemistry and Bioactivity Tomou EM, Barda C, Skaltsa H Medicines (Basel) 29-Sep-2020
PMCID:PMC7601302
doi:10.3390/medicines7100063
PMID:33003416
New terpenoids from Stachys parviflora Benth. Ahmad VU, Arshad S, Bader S, Iqbal S, Khan A, Khan SS, Hussain J, Tareen RB, Ahmed A Magn Reson Chem 01-Oct-2008
doi:10.1002/MRC.2277
PMID:18698563
Stachyfloroside E: A New Acylated Flavone Glycoside from Stachys parviflora V. U. Ahmad, S. Arshad, S. Bader, S. Iqbal, R. B. Tareen Wiley 17-Nov-2005
doi:10.1002/CHIN.200550183

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
(3S,4aR,6S,6aR,6aS,6bR,8aR,10R,11S,12aR,14bS)-11-[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-6-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-3,10-bis[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 163030406 Click to see CC1(CC2C3=CCC4C(C3(C(CC2(CC1OC5C(C(C(C(O5)CO)O)O)O)C(=O)O)O)C)(CCC6C4(CC(C(C6(C)C)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(O8)CO)O)O)C)C)C 961.10 unknown https://doi.org/10.1002/MRC.2277
11-[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-6-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-3,10-bis[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 163030404 Click to see CC1(CC2C3=CCC4C(C3(C(CC2(CC1OC5C(C(C(C(O5)CO)O)O)O)C(=O)O)O)C)(CCC6C4(CC(C(C6(C)C)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(O8)CO)O)O)C)C)C 961.10 unknown https://doi.org/10.1002/MRC.2277
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,3R,4R,4aS,6S,6aR,6aS,6bR,8aR,10S,12aR,14bS)-4-[(2R,3R,4S,5R,6R)-4-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-10-[(2R,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-1,3,6-trihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162976458 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(C(CC7(C6C(C(C(C7OC8C(C(C(C(O8)CO)O)OC9C(C(C(O9)CO)O)O)O)O)(C)C)O)C(=O)O)O)C)C)C)CO)O)O)O)O 1123.20 unknown https://doi.org/10.1002/MRC.2277
4-[4-[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-10-[3,5-dihydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-1,3,6-trihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162976456 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(C(CC7(C6C(C(C(C7OC8C(C(C(C(O8)CO)O)OC9C(C(C(O9)CO)O)O)O)O)(C)C)O)C(=O)O)O)C)C)C)CO)O)O)O)O 1123.20 unknown https://doi.org/10.1002/MRC.2277
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3R,4S,5R,6S)-6-[(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-6,8-dihydroxy-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 163047745 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C=C4C(=O)C=C(OC4=C3O)C5=CC(=C(C=C5)O)O)O)CO)O)O)O)O)O 668.60 unknown https://doi.org/10.1002/CHIN.200550183
[6-[2-[2-(3,4-Dihydroxyphenyl)-6,8-dihydroxy-4-oxochromen-7-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 163047744 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C=C4C(=O)C=C(OC4=C3O)C5=CC(=C(C=C5)O)O)O)CO)O)O)O)O)O 668.60 unknown https://doi.org/10.1002/CHIN.200550183

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