Diplotaenia cachrydifolia

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Scientific Literature

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Details Top

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

Description Top

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Synonyms Top

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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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Distribution (via POWO/KEW) Top

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Legend for the distribution data:

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- Extinct

- Introduced

- Native

Asia-temperate click to expand
- Western Asia
  - Iran

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!
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Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Phenol ethers / Anisoles
Elemicin	10248	Click to see COC1=CC(=CC(=C1OC)OC)CC=C	208.25	unknown	https://doi.org/10.1055/S-2006-962452 https://doi.org/10.1021/NP50053A047
Isoelemicin	5318557	Click to see CC=CC1=CC(=C(C(=C1)OC)OC)OC	208.25	unknown	https://doi.org/10.1021/NP50053A047 https://doi.org/10.1055/S-2006-962452
> 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 CC1=CCC(=CC1)C(C)C	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
beta-OCIMENE, (3E)-	5281553	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1021/NP50053A047 https://doi.org/10.1055/S-2006-962452
beta-Ocimene, (3Z)-	5320250	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1021/NP50053A047 https://doi.org/10.1055/S-2006-962452
Citral	638011	Click to see CC(=CCCC(=CC=O)C)C	152.23	unknown	https://doi.org/10.1055/S-2006-962452 https://doi.org/10.1021/NP50053A047
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1055/S-2006-962452
Lavandulol	5464156	Click to see CC(=CCC(CO)C(=C)C)C	154.25	unknown	https://doi.org/10.1021/NP50053A047
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 CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1055/S-2006-962452
Linalyl acetate	8294	Click to see CC(=CCCC(C)(C=C)OC(=O)C)C	196.29	unknown	https://doi.org/10.1021/NP50053A047
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1021/NP50053A047 https://doi.org/10.1055/S-2006-962452
Neral	643779	Click to see CC(=CCCC(=CC=O)C)C	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 CC1=CC=C(C=C1)C(C)C	134.22	unknown	https://doi.org/10.1055/S-2006-962452
Thymol	6989	Click to see CC1=CC(=C(C=C1)C(C)C)O	150.22	unknown	https://doi.org/10.1055/S-2006-962452
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-2-ene	6451618	Click to see CC1=CCC2(C1C2)C(C)C	136.23	unknown	https://doi.org/10.1055/S-2006-962452
(1S,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-ol	10975683	Click to see CC1=CC(C2CC1C2(C)C)O	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 CC1(C2CCC(C1C2)CO)C	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 CC(=O)OC1CC2CC1C(=C)C2(C)C	194.27	unknown	https://doi.org/10.1021/NP50053A047
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol	64685	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	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 CC1(C2CC(C1=C)CC2=O)C	150.22	unknown	https://doi.org/10.1021/NP50053A047
6,6-Dimethyl-5-methylidenebicyclo[2.2.1]heptan-2-ol	85185505	Click to see CC1(C2CC(C1=C)CC2O)C	152.23	unknown	https://doi.org/10.1021/NP50053A047
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1055/S-2006-962452
Bergamotene	521569	Click to see CC(=CCCC1(C2CCC(=C)C1C2)C)C	204.35	unknown	https://doi.org/10.1055/S-2006-962452 https://doi.org/10.1021/NP50053A047
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1055/S-2006-962452 https://doi.org/10.1021/NP50053A047
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)-	17868	Click to see CC1=CCC2(C1C2)C(C)C	136.23	unknown	https://doi.org/10.1055/S-2006-962452
Bornyl acetate	6448	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	https://doi.org/10.1021/NP50053A047
Camphenol, 6-	526611	Click to see CC1(C2CC(C1=C)C(C2)O)C	152.23	unknown	https://doi.org/10.1021/NP50053A047
Camphor	2537	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	https://doi.org/10.1021/NP50053A047
cis-Verbenol	164888	Click to see CC1=CC(C2CC1C2(C)C)O	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 CC1(C2CC=C(C1C2)C=O)C	150.22	unknown	https://doi.org/10.1021/NP50053A047 https://doi.org/10.1055/S-2006-962452
Sabinen	18818	Click to see CC(C)C12CCC(=C)C1C2	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
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 CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1055/S-2006-962452
Carveol	7438	Click to see CC1=CCC(CC1O)C(=C)C	152.23	unknown	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
Carvone, (+/-)-	7439	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
Dihydrocarveol	12072	Click to see CC1CCC(CC1O)C(=C)C	154.25	unknown	https://doi.org/10.1021/NP50053A047
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
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1055/S-2006-962452
Guaiene	6949	Click to see CC1CCC(=C(C)C)CC2=C1CCC2C	204.35	unknown	https://doi.org/10.1021/NP50053A047
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Alloaromadendren	91746537	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	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 CC1CCC2C13CCC(C(C3)C2(C)C)(C)O	222.37	unknown	https://doi.org/10.1055/S-2006-962452
> Organic oxygen compounds / Organic oxides
Photocitral B	296248	Click to see CC1(C2CCC1(C2C=O)C)C	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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Diplotaenia cachrydifolia

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Area

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top