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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

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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

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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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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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Northwest
    • Southwestern U.S.A.
      • Arizona
      • California

Links to other databases Top

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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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
From Plant to Chemistry: Sources of Antinociceptive Non-Opioid Active Principles for Medicinal Chemistry and Drug Design Turnaturi R, Piana S, Spoto S, Costanzo G, Reina L, Pasquinucci L, Parenti C Molecules 09-Feb-2024
PMCID:PMC10892999
doi:10.3390/molecules29040815
PMID:38398566
Argentatin C Analogues with Potential Antinociceptive Activity and Other Triterpenoid Constituents from the Aerial Parts of Parthenium incanum Xu YM, Wijeratne EM, Calderon-Rivera A, Loya-López S, Perez-Miller S, Khanna R, Gunatilaka AA ACS Omega 25-May-2023
PMCID:PMC10249386
doi:10.1021/acsomega.3c02302
PMID:37305315
Plant-derived natural products targeting ion channels for pain Goyal S, Goyal S, Goins AE, Alles SR Neurobiol Pain 17-Apr-2023
PMCID:PMC10160805
doi:10.1016/j.ynpai.2023.100128
PMID:37151956
Antinociceptive effect of plant-based natural products in chemotherapy-induced peripheral neuropathies: A systematic review Santos WB, Guimarães JO, Pina LT, Serafini MR, Guimarães AG Front Pharmacol 19-Sep-2022
PMCID:PMC9527321
doi:10.3389/fphar.2022.1001276
PMID:36199686
Plant and fungi derived analgesic natural products targeting voltage-gated sodium and calcium channels Calderon-Rivera A, Loya-Lopez S, Gomez K, Khanna R Channels (Austin) 26-Aug-2022
PMCID:PMC9423853
doi:10.1080/19336950.2022.2103234
PMID:36017978
The vessel wall thickness–vessel diameter relationship across woody angiosperms Echeverría A, Petrone‐Mendoza E, Segovia‐Rivas A, Figueroa‐Abundiz VA, Olson ME Am J Bot 12-Jun-2022
PMCID:PMC9328290
doi:10.1002/ajb2.1854
PMID:35435252
Health Benefits of the Diverse Volatile Oils in Native Plants of Ancient Ironwood-Giant Cactus Forests of the Sonoran Desert: An Adaptation to Climate Change? Nabhan GP, Daugherty E, Hartung T Int J Environ Res Public Health 10-Mar-2022
PMCID:PMC8950382
doi:10.3390/ijerph19063250
PMID:35328938
Analgesic effects of medicinal plants and phytochemicals on chemotherapy‐induced neuropathic pain through glial modulation Lee JH, Kim N, Park S, Kim SK Pharmacol Res Perspect 22-Oct-2021
PMCID:PMC8532132
doi:10.1002/prp2.819
PMID:34676990
Arbuscular Mycorrhizal Fungal Communities in the Soils of Desert Habitats Vasar M, Davison J, Sepp SK, Öpik M, Moora M, Koorem K, Meng Y, Oja J, Akhmetzhanova AA, Al-Quraishy S, Onipchenko VG, Cantero JJ, Glassman SI, Hozzein WN, Zobel M Microorganisms 22-Jan-2021
PMCID:PMC7912695
doi:10.3390/microorganisms9020229
PMID:33499315
Subtribe Hyptidinae (Lamiaceae): A promising source of bioactive metabolites Bridi H, de Carvalho Meirelles G, Lino von Poser G J Ethnopharmacol 05-Aug-2020
PMCID:PMC7403033
doi:10.1016/j.jep.2020.113225
PMID:32763419
Exchange of medicinal plant information in California missions McBride JR, Cavero RY, Cheshire AL, Calvo MI, McBride DL J Ethnobiol Ethnomed 15-Jun-2020
PMCID:PMC7296748
doi:10.1186/s13002-020-00388-y
PMID:32539795
Taxane‐induced neurotoxicity: Pathophysiology and therapeutic perspectives da Costa R, Passos GF, Quintão NL, Fernandes ES, Maia JR, Campos MM, Calixto JB Br J Pharmacol 03-Jun-2020
PMCID:PMC7312267
doi:10.1111/bph.15086
PMID:32352155
Ecology of the Western Queen Butterfly Danaus gilippus thersippus (Lepidoptera: Nymphalidae) in the Mojave and Sonoran Deserts Saul-Gershenz L, Grodsky SM, Hernandez RR Insects 19-May-2020
PMCID:PMC7290759
doi:10.3390/insects11050315
PMID:32438741
1-O-Acetylgeopyxin A, a derivative of a fungal metabolite, blocks tetrodotoxin-sensitive voltage-gated sodium, calcium channels and neuronal excitability which correlates with inhibition of neuropathic pain Zhou Y, Cai S, Gomez K, Wijeratne EM, Ji Y, Bellampalli SS, Luo S, Moutal A, Gunatilaka AA, Khanna R Mol Brain 11-May-2020
PMCID:PMC7216607
doi:10.1186/s13041-020-00616-2
PMID:32393368
Betulinic acid, derived from the desert lavender Hyptis emoryi, attenuates paclitaxel-, HIV-, and nerve injury-associated peripheral sensory neuropathy via block of N- and T-type calcium channels Bellampalli SS, Ji Y, Moutal A, Cai S, Kithsiri Wijeratne EM, Gandini MA, Yu J, Chefdeville A, Dorame A, Chew LA, Madura CL, Luo S, Molnar G, Khanna M, Streicher JM, Zamponi GW, Leslie Gunatilaka AA, Khanna R Pain 01-Jan-2019
PMCID:PMC6309937
doi:10.1097/j.pain.0000000000001385
PMID:30169422

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

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