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Diplotaenia cachrydifolia

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 UUID64401795a7d9e884848911
Scientific name Diplotaenia cachrydifolia
Authority Boiss.
First published in Ann. Sci. Nat., Bot. , sér. 3, 1: 309 (1844)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Diplotaenia cachrydifolia has no documented ethnobotanical uses involving preparations such as infusions, decoctions, tinctures, macerations, or poultices in reliable sources.

(No output generated)

General Uses Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Persian کزل جانشیری

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000650381
Tropicos 100325240
KEW urn:lsid:ipni.org:names:841381-1
The Plant List kew-2771214
Open Tree Of Life 796467
NCBI Taxonomy 325714
IPNI 841381-1
GBIF 3637256
EOL 5048852

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
Analysis of Primary Liquid Chromatography Mass Spectrometry Data by Neural Networks for Plant Samples Classification Turova P, Stavrianidi A, Svekolkin V, Lyskov D, Podolskiy I, Rodin I, Shpigun O, Buryak A Metabolites 19-Oct-2022
PMCID:PMC9611620
doi:10.3390/metabo12100993
PMID:36295895
Brazilian essential oils as source for the discovery of new anti-COVID-19 drug: a review guided by in silico study Amparo TR, Seibert JB, Silveira BM, Costa FS, Almeida TC, Braga SF, da Silva GN, dos Santos OD, de Souza GH Phytochem Rev 13-Apr-2021
PMCID:PMC8042356
doi:10.1007/s11101-021-09754-4
PMID:33867898
Optimization of technological procedure for amygdalin isolation from plum seeds (Pruni domesticae semen) Savic IM, Nikolic VD, Savic-Gajic IM, Nikolic LB, Ibric SR, Gajic DG Front Plant Sci 28-Apr-2015
PMCID:PMC4411975
doi:10.3389/fpls.2015.00276
PMID:25972881
Volatiles from the Root of Diplotaenia cachrydifolia, the First Natural Source of 6-Camphenone K. J. Harkiss, M. H. Slehy Surmaghy American Chemical Society (ACS) 30-May-2007
doi:10.1021/NP50053A047
Constituents of the Essential Oil of the Fruits of Diplotaenia cachrydifolia. Harkiss KJ, Surmaghy MH Planta Med 01-Aug-1988
doi:10.1055/S-2006-962452
PMID:17265282

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Phenol ethers / Anisoles
Elemicin 10248 Click to see 208.25 unknown https://doi.org/10.1021/NP50053A047
https://doi.org/10.1055/S-2006-962452
Isoelemicin 5318557 Click to see CC=CC1=CC(=C(C(=C1)OC)OC)OC 208.25 unknown https://doi.org/10.1055/S-2006-962452
https://doi.org/10.1021/NP50053A047
> Hydrocarbons / Unsaturated hydrocarbons / Acetylenes / Alkynes / Terminal alkynes
4-Decyne 16944 Click to see CCCCCC#CCCC 138.25 unknown https://doi.org/10.1021/NP50053A047
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1021/NP50053A047
https://doi.org/10.1055/S-2006-962452
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(-)-Lavandulol 5464156 Click to see 154.25 unknown https://doi.org/10.1021/NP50053A047
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-962452
https://doi.org/10.1021/NP50053A047
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-962452
https://doi.org/10.1021/NP50053A047
Citral 638011 Click to see 152.23 unknown https://doi.org/10.1021/NP50053A047
https://doi.org/10.1055/S-2006-962452
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1055/S-2006-962452
Lavandulol, (+/-)- 94060 Click to see CC(=CCC(CO)C(=C)C)C 154.25 unknown https://doi.org/10.1021/NP50053A047
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1055/S-2006-962452
Linalyl Acetate 8294 Click to see 196.29 unknown https://doi.org/10.1021/NP50053A047
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-962452
https://doi.org/10.1021/NP50053A047
Neral 643779 Click to see 152.23 unknown https://doi.org/10.1055/S-2006-962452
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1055/S-2006-962452
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1055/S-2006-962452
Thymol 6989 Click to see 150.22 unknown https://doi.org/10.1055/S-2006-962452
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-962452
(+)-cis-Verbenol 164888 Click to see 152.23 unknown https://doi.org/10.1021/NP50053A047
(1S,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-ol 10975683 Click to see 152.23 unknown https://doi.org/10.1021/NP50053A047
[(1R,2R,5S)-6,6-dimethyl-2-bicyclo[3.1.1]heptanyl]methanol 12313061 Click to see 154.25 unknown https://doi.org/10.1055/S-2006-962452
[(1S,2R,4S)-5,5-dimethyl-6-methylidene-2-bicyclo[2.2.1]heptanyl] acetate 13969119 Click to see 194.27 unknown https://doi.org/10.1021/NP50053A047
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1021/NP50053A047
https://doi.org/10.1055/S-2006-962452
4-Methyl-1-propan-2-ylbicyclo[3.1.0]hexan-3-ol 10550 Click to see CC1C2CC2(CC1O)C(C)C 154.25 unknown https://doi.org/10.1055/S-2006-962452
6-Camphenone 14088350 Click to see 150.22 unknown https://doi.org/10.1021/NP50053A047
6,6-Dimethyl-5-methylidenebicyclo[2.2.1]heptan-2-ol 85185505 Click to see 152.23 unknown https://doi.org/10.1021/NP50053A047
Acetic acid 1,7,7-trimethyl-bicyclo(2.2.1)hept-2-yl ester 6448 Click to see 196.29 unknown https://doi.org/10.1021/NP50053A047
alpha Thujene 6451618 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-962452
alpha-Thujene 17868 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-962452
Bergamotene 521569 Click to see 204.35 unknown https://doi.org/10.1055/S-2006-962452
https://doi.org/10.1021/NP50053A047
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1055/S-2006-962452
https://doi.org/10.1021/NP50053A047
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1021/NP50053A047
Camphenol, 6- 526611 Click to see 152.23 unknown https://doi.org/10.1021/NP50053A047
Camphor 2537 Click to see 152.23 unknown https://doi.org/10.1021/NP50053A047
Myrtanol 521314 Click to see CC1(C2CCC(C1C2)CO)C 154.25 unknown https://doi.org/10.1055/S-2006-962452
Myrtenal 61130 Click to see 150.22 unknown https://doi.org/10.1055/S-2006-962452
https://doi.org/10.1021/NP50053A047
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1021/NP50053A047
https://doi.org/10.1055/S-2006-962452
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-cis-Carveol 330573 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1021/NP50053A047
2-Methyl-5-(1-methylethenyl)cyclohexanol 12072 Click to see 154.25 unknown https://doi.org/10.1021/NP50053A047
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1021/NP50053A047
https://doi.org/10.1055/S-2006-962452
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1055/S-2006-962452
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1055/S-2006-962452
Carveol 7438 Click to see 152.23 unknown https://doi.org/10.1055/S-2006-962452
Carvone, (+-)- 7439 Click to see 150.22 unknown https://doi.org/10.1021/NP50053A047
https://doi.org/10.1055/S-2006-962452
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1021/NP50053A047
https://doi.org/10.1055/S-2006-962452
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1021/NP50053A047
https://doi.org/10.1055/S-2006-962452
Pulegone 442495 Click to see CC1CCC(=C(C)C)C(=O)C1 152.23 unknown https://doi.org/10.1021/NP50053A047
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
1,4-Dimethyl-7-(propan-2-ylidene)-1,2,3,4,5,6,7,8-octahydroazulene 6949 Click to see 204.35 unknown https://doi.org/10.1021/NP50053A047
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1055/S-2006-962452
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Alloaromadendren 91746537 Click to see 204.35 unknown https://doi.org/10.1055/S-2006-962452
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
Cedrol 65575 Click to see 222.37 unknown https://doi.org/10.1055/S-2006-962452
> Organic oxygen compounds / Organic oxides
Photocitral B 296248 Click to see 152.23 unknown https://doi.org/10.1055/S-2006-962452
Safranal 61041 Click to see CC1=C(C(CC=C1)(C)C)C=O 150.22 unknown https://doi.org/10.1021/NP50053A047

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Collections Top

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