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Ferula lapidosa

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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 UUID64401c379cb07549867773
Scientific name Ferula lapidosa
Authority Korovin
First published in Monogr. Ferula : 59 (1947)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 多石阿魏

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
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Kirgizstan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000686642
Tropicos 1700104
KEW urn:lsid:ipni.org:names:842345-1
The Plant List kew-2808498
Open Tree Of Life 823254
Observations.org 131372
NCBI Taxonomy 371357
IPNI 842345-1
GBIF 3637852
EOL 2890688
Elurikkus 388436

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
Terpenoids ofFerula lapidosa A. I. Saidkhodzhaev, V. M. Malikov, S. Melibaev Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00629636
Structures of lapidolin and lapidolinin L. A. Golovina, A. I. Saidkhodzhaev, V. M. Malikov, S. Melibaev Springer Science and Business Media LLC 22-Nov-2004
doi:10.1007/BF00579449
Structure and stereochemistry of lapiferin L. A. Golovina, A. I. Saidkhodzhaev, N. D. Abdullaev, V. M. Malikov, M. R. Yagudaev Springer Science and Business Media LLC 21-Nov-2004
doi:10.1007/BF00579759
The structure of lapidolidin L. A. Golovina, A. I. Saidkhodzhaev, V. M. Malikov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00579086
Structure and stereochemistry of lapidin L. A. Golovina, A. I. Saidkhodzhaev Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00568511
Esters from the roots ofFerula lapidosa G. V. Sagitdinova, A. I. Saidkhodzhaev, G. K. Nikonov, U. Rakhmankulov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00567070

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
(2,3-diacetyloxy-5-hydroxy-2a,7a-dimethyl-5-propan-2-yl-2,3,4,5a,6,7-hexahydro-1aH-azuleno[6,7-b]oxiren-6-yl) 3,4-dimethoxybenzoate 4371509 Click to see CC(C)C1(CC(C2(C1C(CC3(C(C2OC(=O)C)O3)C)OC(=O)C4=CC(=C(C=C4)OC)OC)C)OC(=O)C)O 534.60 unknown https://doi.org/10.1007/BF00629636
(3-acetyloxy-2,5-dihydroxy-2a,7a-dimethyl-5-propan-2-yl-2,3,4,5a,6,7-hexahydro-1aH-azuleno[6,7-b]oxiren-6-yl) 3,4-dimethoxybenzoate 45934331 Click to see CC(C)C1(CC(C2(C1C(CC3(C(C2O)O3)C)OC(=O)C4=CC(=C(C=C4)OC)OC)C)OC(=O)C)O 492.60 unknown https://doi.org/10.1007/BF00579086
https://doi.org/10.1007/BF00629636
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
[(2aS,5R,7aR)-2-acetyloxy-5-hydroxy-2a,7a-dimethyl-5-propan-2-yl-2,3,4,5a,6,7-hexahydro-1aH-azuleno[6,7-b]oxiren-6-yl] (Z)-2-methylbut-2-enoate 54608030 Click to see CC=C(C)C(=O)OC1CC2(C(O2)C(C3(C1C(CC3)(C(C)C)O)C)OC(=O)C)C 394.50 unknown https://doi.org/10.1007/BF00579759
https://doi.org/10.1007/BF00629636
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Lapidin 11872435 Click to see CC=C(C)C(=O)OC1CC(=CC(=O)C2(C1C(CC2)(C(C)C)O)C)C 334.40 unknown https://doi.org/10.1007/BF00568511
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
Ferolin 6370341 Click to see CC1=CC(C(C(CC(=CCC1)C)OC(=O)C2=CC=C(C=C2)O)C(C)C)O 358.50 unknown https://doi.org/10.1007/BF00567070
https://doi.org/10.1007/BF00629636
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
(2,3-diacetyloxy-5-hydroxy-2a,7a-dimethyl-5-propan-2-yl-2,3,4,5a,6,7-hexahydro-1aH-azuleno[6,7-b]oxiren-6-yl) 2-methylbut-2-enoate 75137723 Click to see CC=C(C)C(=O)OC1CC2(C(O2)C(C3(C1C(CC3OC(=O)C)(C(C)C)O)C)OC(=O)C)C 452.50 unknown https://doi.org/10.1007/BF00579449
https://doi.org/10.1007/BF00629636

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