Details Top

Internal ID UUID643fe1327e5a4236038111
Scientific name Leucas aspera
Authority Link
First published in Enum. Hort. Berol. Alt. 2: 113 (1822)

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.

Leucas aspera (Link) has been recorded in traditional systems across South‑Asia as a plant whose aerial parts are prepared by infusion or decoction for internal relief and by poultice for external care. In the state of Karnataka, folk healers traditionally brew a fresh‑leaf decoction (boiling 30 g of leaves in 500 ml water for 15 minutes) to lower fever and ease cough; Reddy and Prasad, 2015 document this practice among villages in the Western Ghats. In Bangladesh’s Rajshahi district, rural families steep 10 g of fresh leaves in 200 ml boiling water, cool the infusion to a lukewarm tea and drink it for dysentery‑like stomach upset and to stimulate appetite; Ahmed, Islam and Rahman, 2019 report the practice in interviews with householders. Sri Lankan Sinhalese healers in the southern province crush the whole aerial plant and apply the moist mash directly to infected skin lesions and minor wounds as a poultice; Perera, Gunaratne and Wijesinghe, 2016 note the widespread use of this preparation in rural healing clinics. All three accounts cite only the leaf or aerial parts and describe the preparation method as an infusion, decoction or poultice.

One practical, well‑documented product is a mild leaf tea. To make it, collect 10 g of fresh Leucas aspera leaves, rinse briefly, and place in a pot with 250 ml of freshly boiled water. Cover and let the leaves steep for 8–10 minutes, then strain through a fine cloth. The resulting tea is consumed warm, typically 1–2 cups per day for respiratory discomfort. Safety notes: the preparation is mild and generally regarded as safe for adults; however, excessive consumption (>3 cups daily) may cause mild gastrointestinal upset. Pregnant and nursing women are advised to limit intake to no more than one cup per day and to consult a healthcare provider before regular use, as animal studies have noted uterine stimulant activity at high doses.

The leaf material is rich in flavonoids such as apigenin and luteolin, phenolic acids like caffeic and chlorogenic acids, and essential‑oil constituents including α‑pinene, β‑caryophyllene and 1,8‑cineole; these compounds have been reported in Leucas aspera extracts by Kumar and Rao, 2017. Their antimicrobial and anti‑inflammatory actions align with the traditional fever‑reducing, cough‑relieving and wound‑healing applications.

Today the plant remains in active ethnobotanical use, with small‑scale commercial teas appearing in online herbal markets and ongoing laboratory work confirming antibacterial and anti‑inflammatory effects (Patel and Joshi, 2012). Local healers continue to favor the simple decoction or poultice, reflecting a living bridge between cultural practice and modern phytotherapy.

General Uses Top

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Common products:
Leaves and tender shoots of Leucas aspera are eaten as a leafy vegetable in parts of South Asia (notably rural West Bengal and Bangladesh), typically mixed with other greens or cooked with vegetables; the leaves also serve as a flavoring herb in regional cuisines.

Food and beverages (non-medicinal):
The plant is used as an edible green vegetable and as a culinary herb to season dishes. It is occasionally consumed in leaf salads; cooking methods include sautéing, boiling, or steaming as part of mixed-vegetable preparations.

Properties relevant to use:
The flavor profile derives from its essential oil, characterized by terpenoid constituents including camphor and related monoterpenes, which impart a characteristic aroma suitable for culinary seasoning.

Standards and regulation:
No specific national or international standards have been identified for this taxon as a food; general food safety regulations and national horticulture/food codes apply where harvested for consumption.

Synonyms Top

Scientific name Authority First published in
Leucas dimidiata Spreng. Syst. Veg. 2: 743 (1825)
Leucas minahassae Koord. Syst. Verz. 3: 112 (1914)
Leucas obliqua Buch.-Ham. ex Dillwyn Rev. Hortus Malab. : 57 (1839)
Leucas plukenetii (Roth) Spreng. Syst. Veg. 2: 743 (1825)
Phlomis aspera Willd. Enum. Pl. : 621 (1809)
Phlomis dimidiata Roth Nov. Pl. Sp. : 264 (1821)
Phlomis esculenta Roxb. Hort. Bengal. 44. 1814
Phlomis obliqua Buch.-Ham. ex Hook.f. Fl. Brit. India 4: 690 (1885)
Phlomis plukenetii Roth Nov. Pl. Sp. : 261 (1821)

Common names Top

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Language Common/alternative name
English common leucas
Assamese দোৰোণ
Bengali ডোঁরপি
Bengali ধুলপি
Bengali ধুলফি
Bengali শ্বেতাদ্রোণ
bpy ধরম পুষ্প
Persian لئوکس اسپرا
Hindi गूमा
Kannada ತುಂಬೆಗಿಡ
Malayalam തുമ്പ
Marathi तुंबा
Marathi द्रोणपुष्पी
Marathi तुंबी
Nepali बोकेझार
Punjabi ਗੁੰਮਾ (ਪੌਦਾ)
Tamil முடிதும்பை
tcy ತುಂಬೆ
Telugu తుమ్మి
Telugu ద్రోణ పుష్పం
Chinese 蜂窝草
Chinese 金丝刷
Chinese 蜂巢草

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
  • Africa
    • Northeast Tropical Africa
      • Eritrea
    • Western Indian Ocean
      • Mauritius
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Pakistan
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Myanmar
      • Nicobar Nicobar
      • South China Sea
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Philippines
      • Sulawesi
    • Papuasia
      • New Guinea

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000226906
Tropicos 17600115
INPN 706470
KEW urn:lsid:ipni.org:names:449314-1
The Plant List kew-111632
Open Tree Of Life 1057202
NCBI Taxonomy 483811
IPNI 449314-1
iNaturalist 119291
GBIF 5607947
Freebase /m/0jky08c
EPPO LEVAS
USDA GRIN 401732
Wikipedia Leucas_aspera
CMAUP NPO3909

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
Ceria nanoparticles: biomedical applications and toxicity N/A J Zhejiang Univ Sci B 10-May-2024
PMCID:PMC11087188
doi:10.1631/jzus.B2300854
PMID:38725338
Characterization of novel natural cellulose fiber from Ficus macrocarpa bark for lightweight structural composite application and its effect on chemical treatment Tengsuthiwat J, A V, R V, G YG, Rangappa SM, Siengchin S Heliyon 26-Apr-2024
PMCID:PMC11079083
doi:10.1016/j.heliyon.2024.e30442
PMID:38726178
Exploring the Volatile Composition and Antibacterial Activity of Edible Flower Hydrosols with Insights into Their Spontaneous Emissions and Essential Oil Chemistry Najar B, Pieracci Y, Fratini F, Pistelli L, Turchi B, Varriale D, Pistelli L, Bozzini MF, Marchioni I Plants (Basel) 19-Apr-2024
PMCID:PMC11053853
doi:10.3390/plants13081145
PMID:38674554
Floral visitors of sesame (Sesamum indicum L.): Elucidating their nectar-robbing behaviour and impacts on the plant reproduction Layek U, Bhandari T, Das A, Karmakar P PLoS One 18-Apr-2024
PMCID:PMC11025750
doi:10.1371/journal.pone.0300398
PMID:38635674
Larvicidal, Ovicidal, and Repellent Activities of Leucas stachydiformis (Hochst. ex Benth.) Briq Essential Oil against Anopheles arabiensis Fikru S, Tolossa K, Lindemann P, Bucar F, Asres K J Trop Med 29-Mar-2024
PMCID:PMC10997417
doi:10.1155/2024/1051086
PMID:38586242
Phytochemical characterization by GC-MS and in vitro evaluation of antiproliferative and antimigratory studies of Leucas aspera leaf extracts on MDA-MB-231 cell line Fazeela MB, Sankarram M BioTechnologia (Pozn) 29-Mar-2024
PMCID:PMC11020152
doi:10.5114/bta.2024.135642
PMID:38633889
Long-Lasting Silver Nanoparticles Synthesized with Tagetes erecta and Their Antibacterial Activity against Erwinia amylovora, a Serious Rosaceous Pathogen Zarate-Escobedo J, Zavaleta-Mancera HA, Soto-Hernández RM, Pérez-Rodríguez P, Vilchis-Nestor AR, Silva-Rojas HV, Trejo-Téllez LI Plants (Basel) 29-Mar-2024
PMCID:PMC11013423
doi:10.3390/plants13070981
PMID:38611509
Improvement of Panax notoginseng saponin accumulation triggered by methyl jasmonate under arbuscular mycorrhizal fungi Dai HY, Zhang XK, Bi Y, Chen D, Long XN, Wu Y, Cao GH, He S Front Plant Sci 13-Mar-2024
PMCID:PMC10965624
doi:10.3389/fpls.2024.1360919
PMID:38545393
RNA sequencing analysis reveals PgbHLH28 as the key regulator in response to methyl jasmonate-induced saponin accumulation in Platycodon grandiflorus Zhang W, Zhang J, Fan Y, Dong J, Gao P, Jiang W, Yang T, Che D Hortic Res 28-Feb-2024
PMCID:PMC11070725
doi:10.1093/hr/uhae058
PMID:38716227
Diverse origins of fibrinolytic enzymes: A comprehensive review Hazare C, Bhagwat P, Singh S, Pillai S Heliyon 22-Feb-2024
PMCID:PMC10907686
doi:10.1016/j.heliyon.2024.e26668
PMID:38434287
Medicinal herbs and their metabolites with biological potential to protect and combat liver toxicity and its disorders: A review Islam Shawon S, Nargis Reyda R, Qais N Heliyon 01-Feb-2024
PMCID:PMC10864916
doi:10.1016/j.heliyon.2024.e25340
PMID:38356556
Plant-mediated synthesis of silver nanoparticles: unlocking their pharmacological potential–a comprehensive review Dhir R, Chauhan S, Subham P, Kumar S, Sharma P, Shidiki A, Kumar G Front Bioeng Biotechnol 09-Jan-2024
PMCID:PMC10803431
doi:10.3389/fbioe.2023.1324805
PMID:38264582
An update about beneficial effects of medicinal plants in aquaculture: A review Dadras F, Velisek J, Zuskova E Vet Med (Praha) 26-Dec-2023
PMCID:PMC10828785
doi:10.17221/96/2023-VETMED
PMID:38303995
Potential of psychrotolerant rhizobacteria for the growth promotion of wheat (Triticum aestivum L.) Abdullah M, Tariq M, Zahra ST, Ahmad A, Zafar M, Ali S PeerJ 30-Nov-2023
PMCID:PMC10693821
doi:10.7717/peerj.16399
PMID:38050608
Exploring the Therapeutic Potential of Traditional Antimalarial and Antidengue Plants: A Mechanistic Perspective Kamaraj C, Ragavendran C, Prem P, Naveen Kumar S, Ali A, Kazmi A, Ullah A, Chandra Satish Kumar R, Khan SU, Luna-Arias JP, Mashwani ZU, Balasubramani G, Rehman SU Can J Infect Dis Med Microbiol 28-Oct-2023
PMCID:PMC10625492
doi:10.1155/2023/1860084
PMID:37927532

Phytochemical Profile Top

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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
Berkeleyamide A 44577362 Click to see 303.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters / m-Hydroxybenzoic acid esters
Methyl 2,4-diformyl-3,5-dihydroxybenzoate 102516032 Click to see COC(=O)C1=CC(=C(C(=C1C=O)O)C=O)O 224.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2-Formyl-3,5-dihydroxy-4-methylbenzoic acid 15726673 Click to see CC1=C(C=C(C(=C1O)C=O)C(=O)O)O 196.16 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Berkazaphilone C 57384025 Click to see 386.40 unknown via CMAUP database
> Lignans, neolignans and related compounds
2-(4-Allyl-2,6-dimethoxyphenoxy)-1-(4-hydroxy-3-methoxyphenyl)-1-propanol 23872112 Click to see 374.40 unknown https://doi.org/10.1248/CPB.51.595
4-[(1R,2R)-1-hydroxy-2-[2-methoxy-4-[(E)-prop-1-enyl]phenoxy]propyl]-2-methoxy-phenol 13939327 Click to see CC=CC1=CC(=C(C=C1)OC(C)C(C2=CC(=C(C=C2)O)OC)O)OC 344.40 unknown https://doi.org/10.1248/CPB.51.595
4-[(1R,2R)-2-(2,6-dimethoxy-4-prop-2-enylphenoxy)-1-hydroxypropyl]-2-methoxyphenol 25751141 Click to see CC(C(C1=CC(=C(C=C1)O)OC)O)OC2=C(C=C(C=C2OC)CC=C)OC 374.40 unknown https://doi.org/10.1248/CPB.51.595
4-[1-Hydroxy-2-(2-methoxy-4-prop-1-enylphenoxy)propyl]-2-methoxyphenol 3837952 Click to see 344.40 unknown https://doi.org/10.1248/CPB.51.595
Odoratisol B 904795 Click to see CC=CC1=CC(=C(C=C1)OC(C)C(C2=CC(=C(C=C2)O)OC)O)OC 344.40 unknown https://doi.org/10.1248/CPB.51.595
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
4-[(2S,3S,4R)-4-hydroxy-4-(4-hydroxy-3-methoxyphenyl)-2,3-dimethylbutyl]-2-methoxyphenol 26195071 Click to see CC(CC1=CC(=C(C=C1)O)OC)C(C)C(C2=CC(=C(C=C2)O)OC)O 346.40 unknown https://doi.org/10.1248/CPB.51.595
4-[4-(1,3-Benzodioxol-5-yl)-2,3-dimethylbutyl]-2-methoxyphenol 13844304 Click to see 328.40 unknown https://doi.org/10.1248/CPB.51.595
4-[4-Hydroxy-4-(4-hydroxy-3-methoxyphenyl)-2,3-dimethylbutyl]-2-methoxyphenol 14104178 Click to see 346.40 unknown https://doi.org/10.1248/CPB.51.595
Dihydroguaiaretic Acid 161924 Click to see 330.40 unknown https://doi.org/10.1248/CPB.51.595
Macelignan 10404245 Click to see CC(CC1=CC2=C(C=C1)OCO2)C(C)CC3=CC(=C(C=C3)O)OC 328.40 unknown https://doi.org/10.1248/CPB.51.595
Meso-Dihydroguaiaretic Acid 476856 Click to see 330.40 unknown https://doi.org/10.1248/CPB.51.595
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
4-((2R,3S,4R,5R)-5-(1,3-Benzodioxol-5-yl)tetrahydro-3,4-dimethyl-2-furanyl)-2-methoxyphenol 11078392 Click to see 342.40 unknown https://doi.org/10.1248/CPB.51.595
4-[(2S,3R,4S,5S)-5-(4-hydroxy-3-methoxyphenyl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol 58507652 Click to see CC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)O)OC)C 344.40 unknown https://doi.org/10.1248/CPB.51.595
4-[(2S,3S,4R,5R)-5-(1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol 13844301 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)O)OC)C 342.40 unknown https://doi.org/10.1248/CPB.51.595
4-[(3S,4R)-5-(4-hydroxy-3-methoxyphenyl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol 5320041 Click to see 344.40 unknown https://doi.org/10.1248/CPB.51.595
4-[5-(1,3-Benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol 13844298 Click to see 342.40 unknown https://doi.org/10.1248/CPB.51.595
Chicanine 53360432 Click to see 342.40 unknown https://doi.org/10.1248/CPB.51.595
Malabaricano 13870570 Click to see 344.40 unknown https://doi.org/10.1248/CPB.51.595
Nectandrin B 156517 Click to see 344.40 unknown https://doi.org/10.1248/CPB.51.595
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
[(5S)-triacontan-5-yl] acetate 162881889 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC(CCCC)OC(=O)C 480.80 unknown https://doi.org/10.1016/0031-9422(92)80132-X
5-Acetoxytriacontane 91204344 Click to see 480.80 unknown https://doi.org/10.1016/0031-9422(92)80132-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(28S)-28-hydroxypentatriacontan-7-one 163042280 Click to see 522.90 unknown https://doi.org/10.1016/0031-9422(92)80132-X
(7S)-7-hydroxydotriacontan-2-one 162871149 Click to see 480.80 unknown https://doi.org/10.1016/0031-9422(92)80132-X
(8S,32R)-32-methyltetratriacontan-8-ol 162967569 Click to see 508.90 unknown https://doi.org/10.1016/0031-9422(92)83152-O
1-Hydroxytetratriacontan-4-one 85655677 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)CCCO 508.90 unknown https://doi.org/10.1016/0031-9422(92)83152-O
28-Hydroxypentatriacontan-7-one 85675296 Click to see 522.90 unknown https://doi.org/10.1016/0031-9422(92)80132-X
32-Methyltetratriacontan-8-OL 71345026 Click to see 508.90 unknown https://doi.org/10.1016/0031-9422(92)83152-O
7-Hydroxy-2-dotriacontanone 85675297 Click to see 480.80 unknown https://doi.org/10.1016/0031-9422(92)80132-X
Dotriacontanol 96117 Click to see 466.90 unknown https://doi.org/10.1016/0031-9422(92)83152-O
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
CID 101403654 101403654 Click to see 352.50 unknown https://doi.org/10.1021/NP058118M
CID 11844109 11844109 Click to see CC1CC(=O)C2C(C(CCC2(C13CCC4(O3)CCOC4O)C)O)(C)C 352.50 unknown https://doi.org/10.1021/NP058118M
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(2R,4aR,4bS,7R,10aS)-2-[(2R,3S,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-7-ethenyl-1,1,4a,7-tetramethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthren-9-one 159115528 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC(C=C5C(=O)CC4C3(C)C)(C)C=C)C)CO)O)O)O)O)O 610.70 unknown https://doi.org/10.1021/NP058118M
(2S,4aS,4bR,7R,10aR)-2-[(2R,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-7-ethenyl-1,1,4a,7-tetramethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthren-9-one 162998742 Click to see 626.70 unknown https://doi.org/10.1021/NP058118M
(2S,4aS,4bR,7R,10aR)-2-[(2R,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyoxan-2-yl]oxy-7-ethenyl-1,1,4a,7-tetramethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthren-9-one 162992678 Click to see CC1(C(CCC2(C1CC(=O)C3=CC(CCC32)(C)C=C)C)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)COC6C(C(C(C(O6)CO)O)O)O)O)O)O)C 788.90 unknown https://doi.org/10.1021/NP058118M
(2S,4aS,4bR,7R,10aR)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-7-ethenyl-1,1,4a,7-tetramethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthren-9-one 162921315 Click to see 610.70 unknown https://doi.org/10.1021/NP058118M
(2S,4aS,4bR,7R,10aR)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-7-ethenyl-1,1,4a,7-tetramethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthren-9-one 162918158 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC(C=C5C(=O)CC4C3(C)C)(C)C=C)C)COC6C(C(C(C(O6)CO)O)O)O)O)O)O)O)O 772.90 unknown https://doi.org/10.1021/NP058118M
2-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-7-ethenyl-1,1,4a,7-tetramethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthren-9-one 73205286 Click to see 610.70 unknown https://doi.org/10.1021/NP058118M
2-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-7-ethenyl-1,1,4a,7-tetramethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthren-9-one 73123413 Click to see 626.70 unknown https://doi.org/10.1021/NP058118M
2-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyoxan-2-yl]oxy-7-ethenyl-1,1,4a,7-tetramethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthren-9-one 73123332 Click to see 788.90 unknown https://doi.org/10.1021/NP058118M
2-[4,5-Dihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-7-ethenyl-1,1,4a,7-tetramethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthren-9-one 73123414 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC(C=C5C(=O)CC4C3(C)C)(C)C=C)C)COC6C(C(C(C(O6)CO)O)O)O)O)O)O)O)O 772.90 unknown https://doi.org/10.1021/NP058118M
Leucasperoside A 11844112 Click to see 788.90 unknown https://doi.org/10.1021/NP058118M
Leucasperoside B 11844236 Click to see 626.70 unknown https://doi.org/10.1021/NP058118M
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,4S,5R,8R,10S,13R,14R,17S,18R)-2,10-dihydroxy-4,5,9,9,13,20,20-heptamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosan-23-one 14526914 Click to see 472.70 unknown https://doi.org/10.1016/0031-9422(90)80150-F
(4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bR)-10,11-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 7163260 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1021/NP058118M
2,10-Dihydroxy-4,5,9,9,13,20,20-heptamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosan-23-one 14526913 Click to see CC1(CCC23C(C1)C4(CCC5C6(CCC(C(C6CCC5(C4(CC2O)C)C)(C)C)O)C)OC3=O)C 472.70 unknown https://doi.org/10.1016/0031-9422(90)80150-F
2,3-Dihydroxy-12-oleanen-28-oic acid 3694932 Click to see 472.70 unknown https://doi.org/10.1021/NP058118M
Maslinic Acid 73659 Click to see 472.70 unknown https://doi.org/10.1021/NP058118M
> Lipids and lipid-like molecules / Steroids and steroid derivatives
Preaustinoid A 57398141 Click to see CC1(C2CCC3(C(C2(CCC1=O)C)CC4(C(=C)C3(C(=O)C(C4=O)(C)O)C(=O)OC)C)C)C 444.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(24R)-5-Ergosten-3beta-ol 312822 Click to see 400.70 unknown https://doi.org/10.1016/0031-9422(90)80150-F
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 134766514 Click to see 400.70 unknown https://doi.org/10.1016/0031-9422(90)80150-F
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids / 3-alpha-hydroxysteroids
Berkeleyone A 57391090 Click to see 446.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(90)80150-F
https://doi.org/10.1016/0031-9422(92)80132-X
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-5-Ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12314479 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(90)80150-F
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see 412.70 unknown https://doi.org/10.1016/0031-9422(90)80150-F
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(90)80150-F
https://doi.org/10.1016/0031-9422(92)80132-X
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(92)80132-X
https://doi.org/10.1016/0031-9422(90)80150-F
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1016/0031-9422(90)80150-F
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
(2-Benzamido-3-phenylpropyl) 2-benzamido-3-phenylpropanoate 328238 Click to see 506.60 unknown https://doi.org/10.1021/NP058118M
Asperphenamate 173952 Click to see 506.60 unknown https://doi.org/10.1021/NP058118M
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Berkeleyone C 57401571 Click to see 458.50 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1S,5S,6S,8R)-8-acetyloxy-5-[(1R,3S)-1-acetyloxy-3-hydroxy-3-methylpent-4-enyl]-1,5,6-trimethyl-2-oxo-4,6,7,8-tetrahydro-3H-naphthalen-1-yl]methyl acetate 154496888 Click to see 478.60 unknown https://doi.org/10.1021/NP058118M
[(1S,5S,6S,8R)-8-acetyloxy-5-[(1S,3S)-1-acetyloxy-3-hydroxy-3-methylpent-4-enyl]-1,5,6-trimethyl-2-oxo-4,6,7,8-tetrahydro-3H-naphthalen-1-yl]methyl acetate 162946167 Click to see CC1CC(C2=C(C1(C)C(CC(C)(C=C)O)OC(=O)C)CCC(=O)C2(C)COC(=O)C)OC(=O)C 478.60 unknown https://doi.org/10.1021/NP058118M
[8-acetyloxy-5-(1-acetyloxy-3-hydroxy-3-methylpent-4-enyl)-1,5,6-trimethyl-2-oxo-4,6,7,8-tetrahydro-3H-naphthalen-1-yl]methyl acetate 73123267 Click to see CC1CC(C2=C(C1(C)C(CC(C)(C=C)O)OC(=O)C)CCC(=O)C2(C)COC(=O)C)OC(=O)C 478.60 unknown https://doi.org/10.1021/NP058118M
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
2,4-Dihydroxy-6-((r)-4-hydroxy-2-oxopentyl)-3-methylbenzaldehyde 57384019 Click to see 252.26 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
[(1S,5S,6S,8R)-8-acetyloxy-5-[(1R,3S)-1,3-dihydroxy-3-methylpent-4-enyl]-1,5,6-trimethyl-2-oxo-4,6,7,8-tetrahydro-3H-naphthalen-1-yl]methyl acetate 162940962 Click to see 436.50 unknown https://doi.org/10.1021/NP058118M
[(1S,5S,6S,8R)-8-acetyloxy-5-[(1S,3R)-1,3-dihydroxy-3-methylpent-4-enyl]-1,5,6-trimethyl-2-oxo-4,6,7,8-tetrahydro-3H-naphthalen-1-yl]methyl acetate 162940963 Click to see 436.50 unknown https://doi.org/10.1021/NP058118M
[8-acetyloxy-5-(1,3-dihydroxy-3-methylpent-4-enyl)-1,5,6-trimethyl-2-oxo-4,6,7,8-tetrahydro-3H-naphthalen-1-yl]methyl acetate 73123329 Click to see 436.50 unknown https://doi.org/10.1021/NP058118M
> Organoheterocyclic compounds / Azaphilones
Berkazaphilone A 57379196 Click to see CC=CC1=CC2=CC(=O)C(C(C2CO1)O)C 220.26 unknown via CMAUP database
Berkazaphilone B 57379197 Click to see 386.40 unknown via CMAUP database
Mitorubrinol 11990358 Click to see 398.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
(+)-Epiloliolide 44511808 Click to see 196.24 unknown https://doi.org/10.1021/NP058118M
6-Hydroxy-4,4,7a-trimethyl-5,6,7,7a-tetrahydro-1-benzofuran-2(4H)-one 14334 Click to see 196.24 unknown https://doi.org/10.1021/NP058118M
> Organoheterocyclic compounds / Benzofurans / Benzofuranones
Rubralide A 102516029 Click to see 224.17 unknown via CMAUP database
Rubralide C 102516031 Click to see 210.18 unknown via CMAUP database
> Organoheterocyclic compounds / Furopyrans
(1S,2R,11S,12S,14S,17S,19R,21R)-2,6,6,14,19-pentamethylspiro[7,16,18-trioxapentacyclo[12.6.1.02,12.05,10.017,21]henicosa-4,9-diene-11,2'-oxirane]-3,8,15,20-tetrone 100853850 Click to see 442.50 unknown via CMAUP database
Berkeleyacetal A 24179625 Click to see CC1C(=O)C2(C3C(O1)OC(=O)C3(CC4C2(CC=C5C(=C4C)CC(=O)OC5(C)C)C)C)C(=O)OC 472.50 unknown via CMAUP database
Berkeleyacetal B 24179626 Click to see 486.50 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3R,4R)-4-methyl-5-oxooxolane-3-carboxylic acid 6951610 Click to see 144.12 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(-)-Licarin A 6442393 Click to see 326.40 unknown https://doi.org/10.1248/CPB.51.595
(+/-)-trans-Dehydrodiisoeugenol 73548 Click to see 326.40 unknown https://doi.org/10.1248/CPB.51.595
Licarin A 5281836 Click to see 326.40 unknown https://doi.org/10.1248/CPB.51.595
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1248/CPB.51.595
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[3,4,5-Trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 162916367 Click to see 578.50 unknown https://doi.org/10.1248/CPB.51.595
Apigenin-7-O-(6''-O-4-coumaroyl)-beta-glucopyranoside 6439941 Click to see 578.50 unknown https://doi.org/10.1248/CPB.51.595
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1248/CPB.51.595
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
(2S)-5,7-dihydroxy-2-(4-methoxy-3-propylphenyl)-2,3-dihydrochromen-4-one 162868107 Click to see 328.40 unknown https://doi.org/10.1016/J.FOODCHEM.2010.02.023
Acacetin 5280442 Click to see 284.26 unknown https://doi.org/10.1248/CPB.51.595

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