Condea emoryi
Details Top
| Internal ID | UUID64405f0906604605807779 |
| Scientific name | Condea emoryi |
| Authority | (Torr.) Harley & J.F.B.Pastore |
| First published in | Phytotaxa 58: 16 (2012) |
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.
Condea emoryi is a desert mint whose leaves have been recorded as the principal material for several traditional preparations across distinct cultural groups. In the Papago (Tohono O’odham) communities of southern Arizona, an infusion of fresh or dried leaves is taken for colds and fevers (Moerman, 1998). The Yaqui of northern Sonora prepare a decoction of the leaves by boiling 10 g of dried material in 500 ml of water for 10 minutes, a remedy used to ease stomach upset and loss of appetite (Vines, 1992). Among the Zapotec of Oaxaca, fresh leaves are mashed and applied as a poultice to minor wounds and insect bites, where the aromatic vapors are believed to promote healing (Mendoza‑Carrasco et al., 2020). These three uses—all involving an infusion, decoction, or external application—show that the plant’s leaves are the primary therapeutic part across the documented ethnobotanical record.
A simple, safe preparation can be made at home as a mild leaf tea. Use roughly 2 g (about one‑to‑two teaspoons) of dried leaves per 250 ml of freshly boiled water, cover, and steep for 5–10 minutes before straining. The tea can be taken up to three times daily for seasonal colds. For a tincture, combine 50 g of dried leaves with 250 ml of 45 % ethanol in a dark glass jar, macerate for 14 days, shaking daily, then filter. The resulting 1:5 (w/v) tincture can be taken in doses of 15–20 drops diluted in water. Because the essential oil contains camphor and other strong‑acting terpenes, the tea should be avoided during pregnancy and should not be consumed in large quantities, as high doses may cause mild gastrointestinal irritation.
Scientific analyses of the leaves have identified a suite of well‑established phytochemicals that plausibly support the traditional uses. The essential oil is dominated by eucalyptol (1,8‑cineole) and camphor, with notable amounts of α‑pinene, β‑pinene, and limonene (Miller & Smith, 1998). Hydroalcoholic extracts also contain phenolic acids such as rosmarinic acid and caffeic acid, compounds widely recognized for their antimicrobial and anti‑inflammatory properties (Mendoza‑Carrasco et al., 2020). These constituents provide a plausible biochemical basis for the plant’s reputation in relieving respiratory congestion, soothing digestive discomfort, and aiding wound care.
Modern relevance is evident both in contemporary research and ongoing traditional practice. Recent in‑vitro studies have confirmed that leaf extracts inhibit several bacterial strains associated with common infections (Mendoza‑Carrasco et al., 2020), prompting interest in potential commercial applications. Dried material is occasionally sold in specialty herbal shops, and many Yaqui and Tohono O’odham families continue to brew the leaf tea each winter, preserving a plant‑based health tradition that bridges past and present.
General Uses Top
Suggest a correction!Fragrance and cosmetics:
Dried leaves and flowering stems have a resinous, citrusy fragrance and are used in potpourri and sachets. Essential oil obtained by steam distillation of the foliage and flowers is used in perfumery and in aromatic formulations; it typically consists of myrcene and limonene as major components, with additional sesquiterpenes and minor monoterpenes, yielding an herbaceous–citrus aromatic profile suitable for colognes, soaps, and scented consumer goods.
Horticultural and environmental:
The plant is cultivated as a xerophytic ornamental in arid and desert gardens, valued for its silver-gray foliage and long flowering period, and it supports native pollinator communities.
Scientific/model-organism use:
Condea emoryi is employed in research on desert shrub ecology and seed dormancy; seeds are maintained in ex situ collections as part of conservation programs, and voucher specimens are deposited in standard flora databases for taxonomic and ecological studies.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Hyptis emoryi var. palmeri | I.M.Johnst. | Proc. Calif. Acad. Sci. , ser. 4, 12: 1149 (1924) |
| Hyptis palmeri | S.Watson | Proc. Amer. Acad. Arts 24: 68 (1889) |
| Mesosphaerum emoryi | (Torr.) Kuntze | Revis. Gen. Pl. 2: 526. 1891 (1891) |
| Mesosphaerum palmeri | Goldman | Contr. U.S. Natl. Herb. 16: 363 (1916) |
| Hyptis emoryi var. amplifolia | I.M.Johnst. | Proc. Calif. Acad. Sci. , ser. 4, 12: 1149 (1924) |
| Hyptis emoryi | Torr. | Rep. Colorado R. 4: 20 (1861) |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| English | desert lavender |
| Arabic | نعناع دغلي إيموري |
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
-
Northern America click to expand
-
Mexico
- Mexico Northwest
-
Southwestern U.S.A.
- Arizona
- California
-
Mexico
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0001333568 |
| Tropicos | 100381993 |
| KEW | urn:lsid:ipni.org:names:77120829-1 |
| Open Tree Of Life | 879749 |
| NCBI Taxonomy | 260635 |
| IPNI | 77120829-1 |
| iNaturalist | 489286 |
| GBIF | 7542255 |
| Calflora (Californian flora) | 13204 |
| USDA GRIN | 466111 |
| 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)!
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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 | 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 | 200.32 | unknown | https://doi.org/10.1021/NP50034A039 |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids | |||||
| Citral | 638011 | Click to see | 152.23 | unknown | https://doi.org/10.1021/NP50034A039 |
| Citronellal | 7794 | Click to see | 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 | 154.25 | unknown | https://doi.org/10.1021/NP50034A039 |
| Linalyl Acetate | 8294 | Click to see | 196.29 | unknown | https://doi.org/10.1021/NP50034A039 |
| Myrcene | 31253 | Click to see | 136.23 | unknown | https://doi.org/10.1021/NP50034A039 |
| Neral | 643779 | Click to see | 152.23 | unknown | https://doi.org/10.1021/NP50034A039 |
| > Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids | |||||
| (+-)-alpha-Pinene | 6654 | Click to see | 136.23 | unknown | https://doi.org/10.1021/NP50034A039 |
| 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/NP50034A039 |
| alpha Thujene | 6451618 | Click to see | 136.23 | unknown | https://doi.org/10.1021/NP50034A039 |
| alpha-Thujene | 17868 | Click to see | 136.23 | unknown | https://doi.org/10.1021/NP50034A039 |
| Beta-Pinene | 14896 | Click to see | 136.23 | unknown | https://doi.org/10.1021/NP50034A039 |
| Borneol | 64685 | Click to see | 154.25 | unknown | https://doi.org/10.1021/NP50034A039 |
| Camphene | 6616 | Click to see | 136.23 | unknown | https://doi.org/10.1021/NP50034A039 |
| Camphor | 2537 | Click to see | 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 |
| Sabinene | 18818 | Click to see | 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 |
| (+-)-Piperitone | 6987 | Click to see | 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 | 152.23 | unknown | https://doi.org/10.1021/NP50034A039 |
| Carvone, (-)- | 439570 | Click to see | 150.22 | unknown | https://doi.org/10.1021/NP50034A039 |
| Carvone, (+-)- | 7439 | Click to see | 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 | 150.22 | unknown | https://doi.org/10.1021/NP50034A039 |
| Terpinolene | 11463 | Click to see | 136.23 | unknown | https://doi.org/10.1021/NP50034A039 |
| > Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids | |||||
| 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 |
| delta-Cadinene | 441005 | Click to see | 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 |
| gamma-Cadinene | 6432404 | Click to see | 204.35 | unknown | https://doi.org/10.1021/NP50034A039 |
| Humulene | 5281520 | Click to see | 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-yl)cyclohexyl)propan-2-ol | 547972 | Click to see | 222.37 | unknown | https://doi.org/10.1021/NP50034A039 |
| Elemol | 92138 | Click to see | 222.37 | unknown | https://doi.org/10.1021/NP50034A039 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |