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Ferulopsis hystrix

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 UUID64401c4933ca5549816442
Scientific name Ferulopsis hystrix
Authority (Bunge ex Ledeb.) Pimenov
First published in Bot. Zhurn. (Moscow & Leningrad) 76: 1391 (1991 publ. 1992)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Johrenia nudiuscula Palib. Bot. Centralbl. 92: 588 (1903)
Libanotis cachroides DC. Prodr. 4: 151 (1830)
Peucedanum cachroides Koso-Pol. Trudy Glavn. Bot. Sada 36: 24 (1920)
Peucedanum nudiusculum Koso-Pol. Trudy Glavn. Bot. Sada 36: 24 (1920)
Peucedanum hystrix Bunge Mém. Acad. Imp. Sci. St.-Pétersbourg Divers Savans 2(6): 538. 1835
Seseli vaginatum Ledeb. Fl. Altaic. 1: 336 (1829)
Peucedanum hystrix Bunge Verz. Altai Pfl. : 23 (1836)
Phlojodicarpus nudiusculus Turcz. ex Besser Flora 17(1 Beibl.): 14 (1834)
Phlojodicarpus turczaninovii Sipliv. Novosti Sist. Vyssh. Rast. 7: 261 (1970 publ. 1971)
Ferulopsis mongolica Kitag. J. Jap. Bot. 46: 284 (1971)
Phlojodicarpus nudiusculus var. major Popov Konspekt Fl. Pober. Baikal 213. 1966

Common names Top

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Language Common/alternative name
Russian Феруловидка щетинистая
Chinese 鞘颈芹

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
    • China
      • Inner Mongolia
    • Mongolia
      • Mongolia
    • Siberia
      • Altay
      • Buryatiya
      • Chita
      • Irkutsk
      • Tuva
      • Yakutskiya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000686991
Tropicos 1704311
KEW urn:lsid:ipni.org:names:842646-1
The Plant List kew-2808820
Open Tree Of Life 3890951
IPNI 842646-1
GBIF 3635090
Tropicos 50185623
KEW urn:lsid:ipni.org:names:963729-1
The Plant List kew-2808819
Open Tree Of Life 972991
Observations.org 128758
NCBI Taxonomy 489386
IPNI 963729-1
iNaturalist 1045107
GBIF 3635099
Elurikkus 4743
Plantarium 16076

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
The Different Composition of Coumarins and Antibacterial Activity of Phlojodicarpus sibiricus and Phlojodicarpus villosus Root Extracts Khandy MT, Grigorchuk VP, Sofronova AK, Gorpenchenko TY Plants (Basel) 22-Feb-2024
PMCID:PMC10933757
doi:10.3390/plants13050601
PMID:38475448
Visnadin—A new component of the plant genus phlojodicarpus G. K. Nikonov, V. V. Vandyshev Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00633290
Khellactone derivatives from Phlojodicarpus sibiricus D. Gantimur, A. I. Syrchina, A. A. Semenov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00574597
New glycosides from plants of the genus Phlojodicarpus D. Gantimur, A. I. Syrchina, A. A. Semenov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00574575
Coumarins fromPhlojodicarpus sibiricus D. Gantimur, A. A. Semenov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00566431
Coumarins of the roots ofPhlojodicarpus sibiricus O. K. Antonova, B. V. Shemeryankin Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00574388
Isoimperatorin from Phlojodicarpus sibiricus D. Gantimur, A. I. Syrchina, A. A. Semenov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00574598

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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Hex-2-ulofuranosyl hexopyranoside 1115 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1007/BF00574388
Sucrose 5988 Click to see 342.30 unknown https://doi.org/10.1007/BF00574388
> Phenylpropanoids and polyketides / Coumarins and derivatives
8-(1,2-Epoxy-3-hydroxy-3-methylbutyl)-7-methoxycoumarin 129881722 Click to see CC(C)(C1C(O1)C2=C(C=CC3=C2OC(=O)C=C3)OC)O 276.28 unknown https://doi.org/10.1007/BF00566431
8-(2,3-Epoxy-1-hydroxy-3-methylbutyl)-7-methoxycoumarin 11231201 Click to see CC1(C(O1)C(C2=C(C=CC3=C2OC(=O)C=C3)OC)O)C 276.28 unknown https://doi.org/10.1007/BF00566431
8-[(2S,3S)-3-(2-hydroxypropan-2-yl)oxiran-2-yl]-7-methoxychromen-2-one 162931186 Click to see 276.28 unknown https://doi.org/10.1007/BF00566431
8-[(R)-[(2S)-3,3-dimethyloxiran-2-yl]-hydroxymethyl]-7-methoxychromen-2-one 163188174 Click to see 276.28 unknown https://doi.org/10.1007/BF00566431
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
7-[6-[[3,4-Dihydroxy-4-(hydroxymethyl)tetrahydrofuran-2-yl]oxymethyl]-3,4,5-trihydroxy-tetrahydropyran-2-yl]oxychromen-2-one 14236612 Click to see 456.40 unknown https://doi.org/10.1007/BF00574598
8-(2,3-Dihydroxy-3-methylbutyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 73019183 Click to see 426.40 unknown https://doi.org/10.1007/BF00574575
8-[(2R)-2,3-dihydroxy-3-methylbutyl]-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 101915811 Click to see 426.40 unknown https://doi.org/10.1007/BF00574575
Apiosylskimmin 14236613 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C3)C=CC(=O)O4)O)O)O)O)(CO)O 456.40 unknown https://doi.org/10.1007/BF00574598
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Isoimperatorin 68081 Click to see 270.28 unknown https://doi.org/10.1007/BF00574598
https://doi.org/10.1007/BF00574597
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1007/BF00574388
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1007/BF00574598
https://doi.org/10.1007/BF00574597
https://doi.org/10.1007/BF00574388
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
(10-Acetyloxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-9-yl) 2-methylbutanoate 10157 Click to see 388.40 unknown https://doi.org/10.1007/BF00574388
https://doi.org/10.1007/BF00633290
(9-Acetoxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl) 2-methylbutanoate 455902 Click to see 388.40 unknown https://doi.org/10.1007/BF00574597
[(9R,10R)-9-acetyloxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] (2R)-2-methylbutanoate 12143978 Click to see 388.40 unknown https://doi.org/10.1007/BF00574597
9-(acetyloxy)-8,8-dimethyl-2-oxo-9,10-dihydro-2H,8H-pyrano[2,3-f]chromen-10-yl 3-methylbutanoate 455909 Click to see 388.40 unknown https://doi.org/10.1007/BF00574597
9-Hydroxy-10-methoxy-8,8-dimethyl-9,10-dihydropyrano[2,3-f]chromen-2-one 73823599 Click to see 276.28 unknown https://doi.org/10.1007/BF00574597
cis-Methylkhellactone 44567006 Click to see 276.28 unknown https://doi.org/10.1007/BF00574597
Dihydrosamidin 442128 Click to see CC(C)CC(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)C 388.40 unknown https://doi.org/10.1007/BF00574388
Khellactone, cis-(-)- 11097348 Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC(=O)C=C3)O)O)C 262.26 unknown https://doi.org/10.1007/BF00574597
rac Dihydro Samidin 2841560 Click to see 388.40 unknown https://doi.org/10.1007/BF00574388
Suksdorfin 72414 Click to see CC(C)CC(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C 388.40 unknown https://doi.org/10.1007/BF00574598
https://doi.org/10.1007/BF00574597
trans-Methylkhellactone 21679806 Click to see 276.28 unknown https://doi.org/10.1007/BF00574597
Visnadine 442151 Click to see 388.40 unknown https://doi.org/10.1007/BF00574388
https://doi.org/10.1007/BF00633290
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
7-O-B-D-Glucopyranoside 5378562 Click to see 462.40 unknown https://doi.org/10.1007/BF00574575
Diosmetin 7-O-beta-D-glucoside 11016019 Click to see 462.40 unknown https://doi.org/10.1007/BF00574575

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