Lavandula stoechas subsp. luisieri

We don't have an image yet. Upload an image!
You are now on a "subspecies" page! Please be sure to also check the "species" page for compounds!

Details Top

Internal ID UUID643fe0939c3ca243701914
Scientific name Lavandula stoechas subsp. luisieri
Authority (Rozeira) Rozeira
First published in Agron. Lusit. 24: 173 (1964)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Chinese 卢氏薰衣草

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000224249
Tropicos 17604970
KEW urn:lsid:ipni.org:names:77188229-1
The Plant List kew-109099
Open Tree Of Life 5810583
Observations.org 145956
NCBI Taxonomy 1461649
GBIF 7660687
EPPO LAVSL
USDA GRIN 453631

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
Necrodane (1,2,2,3,4-pentamethylcyclopentane) derivatives in Lavandula luisieri, new compounds to the plant kingdom M.C. M.I. García-Vallejo, García-Vallejo, J. Sanz, M. Bernabe, A. Velasco-Negueruela Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97009-2

Phytochemical Profile Top

Add a new one!
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 / Benzene and substituted derivatives / Phenylpropanes
2-(4-Methylphenyl)propan-2-ol 14529 Click to see CC1=CC=C(C=C1)C(C)(C)O 150.22 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
[(2R)-1-hydroxy-5-methyl-2-prop-1-en-2-ylhex-4-enyl] acetate 129819800 Click to see CC(=CCC(C(O)OC(=O)C)C(=C)C)C 212.28 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
beta-Ocimene, (3Z)- 5320250 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
Lavandulol 5464156 Click to see CC(=CCC(CO)C(=C)C)C 154.25 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
Lavandulol, (+/-)- 94060 Click to see CC(=CCC(CO)C(=C)C)C 154.25 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
Linalyl acetate 8294 Click to see CC(=CCCC(C)(C=C)OC(=O)C)C 196.29 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
> 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/10.1016/S0031-9422(00)97009-2
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1S,2R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-ol 88298 Click to see CC1=CC(C2CC1C2(C)C)O 152.23 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
(1S,3R,5S)-6,6-Dimethyl-2-methylenebicyclo[3.1.1]heptan-3-ol 12314318 Click to see CC1(C2CC1C(=C)C(C2)O)C 152.23 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
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/10.1016/S0031-9422(00)97009-2
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
Fenchone 14525 Click to see CC1(C2CCC(C2)(C1=O)C)C 152.23 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
Myrtenol 10582 Click to see CC1(C2CC=C(C1C2)CO)C 152.23 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
Pinocarveol 102667 Click to see CC1(C2CC1C(=C)C(C2)O)C 152.23 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
trans-Borneol 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315592 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
(2R)-6-methyl-2-(4-methylcyclohex-3-en-1-yl)hept-5-en-2-ol 6506009 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
(3R,6E)-nerolidol 11241545 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
alpha-Bisabolol 10586 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
Nerolidol 8888 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
alpha-Gurjunene 15560276 Click to see CC1CCC2C(C2(C)C)C3=C(CCC13)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(00)97009-2
Viridiflorol (incomplete stereochemistry) 94174 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(00)97009-2

Biological Material Top ebay Auctions

Please wait .. loading items ..
Loading...

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.