Hyptis emoryi - Unknown
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Internal ID UUID643fdf64dbdf7145786393
Scientific name Hyptis emoryi
Authority Torr.
First published in Rep. Colorado R. 4: 20 (1861)

Description Top

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Condea emoryi, also known as desert lavender, is a large shrub species in the mint family, Lamiaceae. It is a favored plant of honeybees in the early spring in the southwest deserts of North America. This multi-stemmed shrub can reach up to 18 feet and has violet-blue flowers that are highly attractive to bees. It is found in dry washes and rocky slopes in Arizona, Nevada, California, and northwestern Mexico. It is evergreen or cold deciduous depending on its location. Recently, it was transferred from the Hyptis genus to Condea due to evidence from DNA analysis. Desert lavender is commonly found in areas with a water source and is often intermixed with other species in the desert. In Arizona, it is found in the Sonoran and Mojave Deserts, while in southern California and Nevada it is found in the Mojave and Colorado Deserts.

Synonyms Top

Scientific name Authority First published in
Mesosphaerum emoryi (Torr.) Kuntze Revis. Gen. Pl. 2: 526. 1891 (1891)

Common names Top

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Language Common/alternative name
English desert lavender
Arabic نعناع دغلي إيموري

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) 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

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000216646
USDA Plants HYEM
Tropicos 17601467
KEW urn:lsid:ipni.org:names:448076-1
The Plant List kew-101758
Nature Serve 2.136925
IPNI 448076-1
iNaturalist 50172
GBIF 2926808
Freebase /m/03qclbg
EOL 579580
Calflora (Californian flora) 4315
USDA GRIN 454208
Wikipedia Condea_emoryi

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)!
Title Authors Publication Released IDs
Terpenoids of Hyptis emoryi. Tanowitz BD, Junak SA, Smith DM J Nat Prod 01-Jul-1984
doi:10.1021/NP50034A039
PMID:6491687

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
> 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/NP50034A039
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Decyl acetate 8167 Click to see CCCCCCCCCCOC(=O)C 200.32 unknown https://doi.org/10.1021/NP50034A039
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Citral 638011 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1021/NP50034A039
Citronellal 7794 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown https://doi.org/10.1021/NP50034A039
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1021/NP50034A039
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1021/NP50034A039
Linalyl acetate 8294 Click to see CC(=CCCC(C)(C=C)OC(=O)C)C 196.29 unknown https://doi.org/10.1021/NP50034A039
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1021/NP50034A039
Neral 643779 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1021/NP50034A039
> 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/10.1021/NP50034A039
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/NP50034A039
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1021/NP50034A039
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1021/NP50034A039
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/10.1021/NP50034A039
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1021/NP50034A039
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1021/NP50034A039
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1021/NP50034A039
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1021/NP50034A039
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1021/NP50034A039
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-trans-Carveol 94221 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1021/NP50034A039
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1021/NP50034A039
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1021/NP50034A039
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1021/NP50034A039
Carveol 7438 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1021/NP50034A039
Carvone, (-)- 439570 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1021/NP50034A039
Carvone, (+/-)- 7439 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1021/NP50034A039
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1021/NP50034A039
Piperitenone 381152 Click to see CC1=CC(=O)C(=C(C)C)CC1 150.22 unknown https://doi.org/10.1021/NP50034A039
Piperitone 6987 Click to see CC1=CC(=O)C(CC1)C(C)C 152.23 unknown https://doi.org/10.1021/NP50034A039
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1021/NP50034A039
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1021/NP50034A039
(+)-Gamma-cadinene 6432404 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1021/NP50034A039
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1021/NP50034A039
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1021/NP50034A039
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1021/NP50034A039
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1021/NP50034A039
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1021/NP50034A039
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-(4-Ethenyl-4-methyl-3-prop-1-en-2-ylcyclohexyl)propan-2-ol 547972 Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O 222.37 unknown https://doi.org/10.1021/NP50034A039
Elemol 92138 Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O 222.37 unknown https://doi.org/10.1021/NP50034A039

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