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Phlojodicarpus villosus

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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 UUID644046ee3721a392927413
Scientific name Phlojodicarpus villosus
Authority Turcz.
First published in Fl. Ross. 2: 331 (1844)

Description Top

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Synonyms Top

Scientific name Authority First published in
Libanotis petrophila Korovin Trudy Inst. Bot. Akad. Nauk Kazakhst. S.S.R. 13: 255 (1962)
Phlojodicarpus sibiricus var. villosus (Turcz. ex Fisch. & C.A.Mey.) Chu Fl. Pl. Herb. Chin. Bor.-Or. 6: 287. 1977
Stenocoelium villosum Koso-Pol. Bull. Soc. Imp. Naturalistes Moscou , n.s., 29: 132 (1915 publ. 1916)
Libanotis villosa Turcz. ex Fisch. & C.A.Mey. Index Seminum [St.Petersburg (Petropolitanus)] i. 31.
Phlojodicarpus sibiricus subsp. villosus (Turcz. ex Fisch. & C.A.Mey.) Vorosch. Florist. Issl. Razn. Raionakh SSSR : 184 (1985)

Common names Top

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Language Common/alternative name
Azerbaijani tükcüklü şişmeyvə
Chinese 柔毛胀果芹
Chinese 毛序燥芹
Chinese 柔毛脹果芹

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • Inner Mongolia
    • Middle Asia
      • Kazakhstan
    • Mongolia
      • Mongolia
    • Russian Far East
      • Kamchatka
      • Khabarovsk
      • Magadan
      • Sakhalin
    • Siberia
      • Altay
      • Buryatiya
      • Chita
      • Irkutsk
      • Krasnoyarsk
      • Tuva
      • West Siberia
      • Yakutskiya

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001067695
USDA Plants PHVI20
Tropicos 1700192
KEW urn:lsid:ipni.org:names:846578-1
The Plant List tro-1700192
Open Tree Of Life 1085702
Observations.org 149921
NCBI Taxonomy 669776
IPNI 846578-1
iNaturalist 870438
GBIF 5831982

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
Phytochemicals as Antimicrobials: Prospecting Himalayan Medicinal Plants as Source of Alternate Medicine to Combat Antimicrobial Resistance Ashraf MV, Pant S, Khan MA, Shah AA, Siddiqui S, Jeridi M, Alhamdi HW, Ahmad S Pharmaceuticals (Basel) 15-Jun-2023
PMCID:PMC10302623
doi:10.3390/ph16060881
PMID:37375828
Coumarins ofPhlojodicarpus villosus D. Gantimur, A. A. Semenov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00575771
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 of the roots ofPhlojodicarpus villosus Turcz. F. V. Babilev, G. K. Nikonov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00563704

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
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
7-hydroxy-4H-chromen-4-one 5409279 Click to see C1=CC2=C(C=C1O)OC=CC2=O 162.14 unknown https://doi.org/10.1007/BF00575771
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
7-[6-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxychromen-2-one 14236612 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/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/BF00574575
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
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/BF00563704
rac Dihydro Samidin 2841560 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/BF00563704
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
(9,9-dimethyl-2-oxo-3,4-dihydropyrano[2,3-g]chromen-3-yl) (Z)-2-methylbut-2-enoate 15596603 Click to see CC=C(C)C(=O)OC1CC2=CC3=C(C=C2OC1=O)C(C=CO3)(C)C 328.40 unknown https://doi.org/10.1007/BF00575771
[(3S)-9,9-dimethyl-2-oxo-3,4-dihydropyrano[2,3-g]chromen-3-yl] (E)-2-methylbut-2-enoate 163187939 Click to see CC=C(C)C(=O)OC1CC2=CC3=C(C=C2OC1=O)C(C=CO3)(C)C 328.40 unknown https://doi.org/10.1007/BF00575771
[(3S)-9,9-dimethyl-2-oxo-3,4-dihydropyrano[2,3-g]chromen-3-yl] 2-methylbut-2-enoate 162853176 Click to see CC=C(C)C(=O)OC1CC2=CC3=C(C=C2OC1=O)C(C=CO3)(C)C 328.40 unknown https://doi.org/10.1007/BF00575771
Aegelinol 600671 Click to see CC1(C(CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O)C 246.26 unknown https://doi.org/10.1007/BF00575771
Decursin 442126 Click to see CC(=CC(=O)OC1CC2=C(C=C3C(=C2)C=CC(=O)O3)OC1(C)C)C 328.40 unknown https://doi.org/10.1007/BF00575771
Decursinol 442127 Click to see CC1(C(CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O)C 246.26 unknown https://doi.org/10.1007/BF00575771

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