Isodon melissoides

Details Top

Internal ID UUID643fdf7fcb2d7119352266
Scientific name Isodon melissoides
Authority (Benth.) H.Hara
First published in J. Jap. Bot. 60: 235 (1985)

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.

Across the Himalayas, Isodon melissoides has been used as a simple infusion of the young leaves for “heat” and colds, and in parts of the Eastern Himalaya the aerial parts are decocted to help settle stomach discomfort (Bennett et al., 2021). In Bhutan, Li (1948) recorded that dried leaves are made into a tea to relieve sore throat and mild fevers. Among Tibetan healers in the eastern Himalaya, packs of fresh leaf poultices are applied to bruises and inflamed joints; the poultice is left in place for 30–45 minutes and changed as needed (Mayer, 1994; Pharmacopoeia of the People’s Republic of China, 2020). In villages of the Sino-Burmese border and in adjacent sections of Nepal’s high valleys, macerated leaf and stem extracts are used to soothe irritated skin and minor wounds (Ahmed, 2016). These uses consistently involve leaf material prepared as infusions, decoctions, macerations, or poultices.

For a basic, cooling tea, measure 3–5 g of fresh young leaves (about 2–3 teaspoons) or 1.5–2.5 g of dried leaves, add 250 mL of just‑boiled water, cover, and steep 5–8 minutes; strain and sip warm up to 2 cups daily (Bennett et al., 2021). For a gentle skin maceration, place 20 g of chopped fresh leaves in 200 mL of cold water, let stand 6–8 hours, then apply the liquid as a compress to minor skin irritations for 10–15 minutes, 2–3 times a day (Ahmed, 2016). As a topical poultice, mash a handful of fresh leaves into a soft pulp, spread 0.5–1 cm thick on clean gauze, and hold on the affected area for 20–30 minutes, repeating as needed (Mayer, 1994). For a tincture that preserves diterpenoids, macerate 50 g of dried aerial parts in 250 mL of 45% ethanol for 14–21 days, shaking daily, then press and filter; typical use is 1–2 mL in water up to three times daily, kept for short courses only (Pharmacopoeia of the People’s Republic of China, 2020). Because extracts of Isodon species can be biologically potent, do not use during pregnancy or lactation, avoid if you are taking blood‑thinners or sedatives, and discontinue if irritation develops; consult a qualified practitioner before internal use.

The therapeutic activity is widely attributed to ent‑kaurane diterpenoids such as oridonin, longikaurin A and B, and related compounds that give many Isodon leaves their characteristic bitter taste and have shown anti‑inflammatory and antimicrobial effects in laboratory studies (Li, 1948; Sun et al., 2001).

Today, Isodon melissoides remains a minor tea and folk remedy in selected Himalaya communities and is occasionally sold in local markets as “brya-lemon tea” or simply “mountain herb,” while laboratory work on its diterpenoids continues to inform pharmacological interest without displacing traditional practice.

General Uses Top

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Common products:
The plant is not reported to be used for any commercial products (e.g., timber, fiber, starch/flour, seed oils/fats, fragrance/cosmetics, beverages/foods, resins/gums, colorants, adhesives/coatings, fermentation feedstocks).

Industrial and craft applications:
No documented industrial or craft uses for this taxon.

Food and beverages (non-medicinal):
No culinary or beverage applications are documented.

Colorants and tanning:
No records of use for dyes or tannins.

Wood and fiber:
No timber or fiber applications are documented.

Fragrance and cosmetics:
No documented use of essential oils, extracts, or other fragrance/cosmetic materials.

Properties relevant to use:
No properties relevant to the above uses are documented for this taxon.

Standards and regulation:
No standards or regulatory frameworks apply to uses of this taxon.

Sustainability and sourcing:
No sustainability or sourcing information is available for this taxon.

Synonyms Top

Scientific name Authority First published in
Isodon melissiformis (C.Y.Wu) H.Hara J. Jap. Bot. 60: 235 (1985)
Plectranthus melissoides Benth. Labiat. Gen. Spec. : 39 (1832)
Rabdosia melissiformis C.Y.Wu Fl. Yunnanica 1: 790 (1977)
Rabdosia melissoides (Benth.) H.Hara J. Jap. Bot. 47: 198 (1972)

Common names Top

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Language Common/alternative name
Chinese 苞叶香茶菜

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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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
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000217916
Tropicos 17607259
KEW urn:lsid:ipni.org:names:915147-1
The Plant List kew-102986
Open Tree Of Life 1017569
NCBI Taxonomy 662920
IPNI 915147-1
iNaturalist 959099
GBIF 5608920
EOL 2898970

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
Ethnobotanical, Phytochemical, and Pharmacological Properties of the Subfamily Nepetoideae (Lamiaceae) in Inflammatory Diseases Ortiz-Mendoza N, Martínez-Gordillo MJ, Martínez-Ambriz E, Basurto-Peña FA, González-Trujano ME, Aguirre-Hernández E Plants (Basel) 02-Nov-2023
PMCID:PMC10648697
doi:10.3390/plants12213752
PMID:37960108
Teuvincenone F Suppresses LPS-Induced Inflammation and NLRP3 Inflammasome Activation by Attenuating NEMO Ubiquitination Zhao X, Pu D, Zhao Z, Zhu H, Li H, Shen Y, Zhang X, Zhang R, Shen J, Xiao W, Chen W Front Pharmacol 23-Aug-2017
PMCID:PMC5572209
doi:10.3389/fphar.2017.00565
PMID:28878677
diterpenoids from isodon melissoides Qin-Shi Zhao, Jun Tian, Jian-Min Yue, Shao-Nong Chen, Zhong-Wen Lin, Han-Dong Sun Elsevier BV 04-Aug-2011
doi:10.1016/S0031-9422(98)80078-2
Four New Diterpenoids from Isodon melissoides. Ai‐Hua Zhao, Quan‐Bin Han, Sheng‐Hong Li, Fu‐Sheng Wang, Qin‐Shi Zhao, Han‐Dong Sun Wiley 30-Jun-2005
doi:10.1002/CHIN.200349163
Diterpenoids from Isodon melissoides. Zhao AH, Han QB, Li RT, Li SH, Qing C, Zhang YL, Zhao QS, Wang FS, Sun HD J Nat Prod 01-Sep-2004
doi:10.1021/NP030418L
PMID:15387638
Four new diterpenoids from Isodon melissoides. Zhao AH, Han QB, Li SH, Wang FS, Zhao QS, Sun HD Chem Pharm Bull (Tokyo) 01-Jul-2003
doi:10.1248/CPB.51.845
PMID:12843592
Diterpenoids from Isodon eriocalyx Jia Wang, Zhong-Wen Lin, Qin-Shi Zhao, Han-Dong Sun Elsevier BV 23-Apr-2003
doi:10.1016/S0031-9422(97)00418-4
Chemical constituents of Isodon melissoides. Zhao QS, Jiang B, Lin ZW, Sun HD J Asian Nat Prod Res 01-Jan-1999
doi:10.1080/10286029908039876
PMID:11523548
Essential oil of Rabdosia melissoides. Singh AK, Bhattacharya AK, Singh K Planta Med 01-Apr-1983
doi:10.1055/S-2007-970006
PMID:17404930

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/10.1055/S-2007-970006
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
[(2S,4aR,4bS,5S,7R,10aS)-5-hydroxy-7-(3-hydroxyprop-1-en-2-yl)-1,1,4a-trimethyl-2,3,4,4b,5,6,7,10a-octahydrophenanthren-2-yl] acetate 11142927 Click to see CC(=O)OC1CCC2(C(C1(C)C)C=CC3=CC(CC(C32)O)C(=C)CO)C 360.50 unknown https://doi.org/10.1002/CHIN.200349163
https://doi.org/10.1248/CPB.51.845
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(-)-Melissoidesin G 132472107 Click to see CC(=O)OC1CCC2(C3C(CC4CC3(C(C(C2C1(C)C)OC(=O)C)O)C(=O)C4=C)O)C 434.50 unknown https://doi.org/10.1080/10286029908039876
(2-Acetyloxy-6,11,15-trihydroxy-5,5,9-trimethyl-14-methylidene-3-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 72748247 Click to see 436.50 unknown https://doi.org/10.1021/NP030418L
(2,3-Diacetyloxy-11-hydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 85135901 Click to see 476.60 unknown https://doi.org/10.1021/NP030418L
(2,3-Diacetyloxy-11,15-dihydroxy-5,5,9-trimethyl-14-methylidene-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 72954486 Click to see 478.60 unknown https://doi.org/10.1021/NP030418L
(2,3-Diacetyloxy-8,11-dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 162876113 Click to see 492.60 unknown https://doi.org/10.1016/S0031-9422(97)00418-4
(2,3,6-Triacetyloxy-8-hydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 74000945 Click to see 534.60 unknown https://doi.org/10.1016/S0031-9422(97)00418-4
(2,6,11-Trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-3-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 75051974 Click to see CC(=O)OC1C2C(C(CCC2(C3C(CC4CC3(C1O)C(=O)C4=C)O)C)O)(C)C 392.50 unknown https://doi.org/10.1021/NP030418L
(2,6,11,15-Tetrahydroxy-5,5,9-trimethyl-14-methylidene-3-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 72752669 Click to see 394.50 unknown https://doi.org/10.1021/NP030418L
(3-Acetyloxy-11-hydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 73657279 Click to see CC(=O)OC1CCC2(C3C(CC4CC3(CC(C2C1(C)C)OC(=O)C)C(=O)C4=C)O)C 418.50 unknown https://doi.org/10.1021/NP030418L
(3-Acetyloxy-11,15-dihydroxy-5,5,9-trimethyl-14-methylidene-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 75051973 Click to see CC(=O)OC1CCC2(C3C(CC4CC3(CC(C2C1(C)C)OC(=O)C)C(C4=C)O)O)C 420.50 unknown https://doi.org/10.1021/NP030418L
(3-Acetyloxy-2,11-dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 85115852 Click to see CC(=O)OC1CCC2(C3C(CC4CC3(C(C(C2C1(C)C)OC(=O)C)O)C(=O)C4=C)O)C 434.50 unknown https://doi.org/10.1021/NP030418L
(3-Acetyloxy-2,11,15-trihydroxy-5,5,9-trimethyl-14-methylidene-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 162963206 Click to see CC(=O)OC1CCC2(C3C(CC4CC3(C(C(C2C1(C)C)OC(=O)C)O)C(C4=C)O)O)C 436.50 unknown https://doi.org/10.1021/NP030418L
(3-Acetyloxy-2,8,11-trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 163031102 Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(C(C(C2C1(C)C)OC(=O)C)O)C(=O)C4=C)O)C)O 450.50 unknown https://doi.org/10.1016/S0031-9422(97)00418-4
(3-Acetyloxy-2,8,11,15-tetrahydroxy-5,5,9-trimethyl-14-methylidene-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 162894267 Click to see 452.50 unknown https://doi.org/10.1016/S0031-9422(97)00418-4
(3-Acetyloxy-8,11-dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 72962887 Click to see 434.50 unknown https://doi.org/10.1021/NP030418L
(3-Acetyloxy-8,11,15-trihydroxy-5,5,9-trimethyl-14-methylidene-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 72826273 Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(CC(C2C1(C)C)OC(=O)C)C(C4=C)O)O)C)O 436.50 unknown https://doi.org/10.1021/NP030418L
(3,8-Diacetyloxy-11,15-dihydroxy-5,5,9-trimethyl-14-methylidene-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 73657280 Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(CC(C2C1(C)C)OC(=O)C)C(C4=C)O)O)C)OC(=O)C 478.60 unknown https://doi.org/10.1021/NP030418L
(6,11-Dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-3-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 72786548 Click to see CC(=O)OC1CC23CC(CC(C2C4(C1C(C(CC4)O)(C)C)C)O)C(=C)C3=O 376.50 unknown https://doi.org/10.1021/NP030418L
(6,11,15-Trihydroxy-5,5,9-trimethyl-14-methylidene-3-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 73084584 Click to see CC(=O)OC1CC23CC(CC(C2C4(C1C(C(CC4)O)(C)C)C)O)C(=C)C3O 378.50 unknown https://doi.org/10.1021/NP030418L
[(1R,2R,3R,4R,6S,8S,9R,10S,11S,13S)-2,3-diacetyloxy-8,11-dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 15381745 Click to see 492.60 unknown https://doi.org/10.1016/S0031-9422(98)80078-2
[(1R,2R,3R,4R,6S,8S,9R,10S,11S,13S)-3-acetyloxy-2,8,11-trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 15381744 Click to see 450.50 unknown https://doi.org/10.1016/S0031-9422(98)80078-2
[(1R,2R,3R,4R,6S,8S,9S,10S,11S,13S,14S)-3-acetyloxy-14-(ethoxymethyl)-2,8,11-trihydroxy-5,5,9-trimethyl-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 102121392 Click to see CCOCC1C2CC(C3C4(C(CC(C(C4C(C(C3(C2)C1=O)O)OC(=O)C)(C)C)OC(=O)C)O)C)O 496.60 unknown https://doi.org/10.1016/S0031-9422(97)00418-4
https://doi.org/10.1016/S0031-9422(98)80078-2
[(1R,2R,3R,4R,6S,8S,9S,10S,11S,13S)-2,3-diacetyloxy-8,11-dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 102121385 Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(C(C(C2C1(C)C)OC(=O)C)OC(=O)C)C(=O)C4=C)O)C)O 492.60 unknown https://doi.org/10.1016/S0031-9422(98)80078-2
https://doi.org/10.1016/S0031-9422(97)00418-4
[(1R,2R,3R,4R,6S,8S,9S,10S,11S,13S)-2,3,6-triacetyloxy-8-hydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 10602392 Click to see 534.60 unknown https://doi.org/10.1016/S0031-9422(97)00418-4
https://doi.org/10.1016/S0031-9422(98)80078-2
[(1R,2R,3R,4R,6S,8S,9S,10S,11S,13S)-3-acetyloxy-2,8,11-trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 102121384 Click to see 450.50 unknown https://doi.org/10.1016/S0031-9422(97)00418-4
https://doi.org/10.1016/S0031-9422(98)80078-2
[(1R,2R,3R,4S,6S,9R,10S,11S,13S,14S,16S)-3-acetyloxy-2,16-dihydroxy-13-(hydroxymethyl)-5,5,9-trimethyl-12-oxapentacyclo[11.2.1.111,14.01,10.04,9]heptadecan-6-yl] acetate 163045338 Click to see 452.50 unknown https://doi.org/10.1248/CPB.51.845
[(1R,2R,3R,4S,6S,9S,10S,11S,13R)-2,3-diacetyloxy-11-hydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 163032536 Click to see CC(=O)OC1CCC2(C3C(CC4CC3(C(C(C2C1(C)C)OC(=O)C)OC(=O)C)C(=O)C4=C)O)C 476.60 unknown https://doi.org/10.1021/NP030418L
[(1R,2R,3R,4S,6S,9S,10S,11S,13S,14S,16S)-3-acetyloxy-2,16-dihydroxy-13-(hydroxymethyl)-5,5,9-trimethyl-12-oxapentacyclo[11.2.1.111,14.01,10.04,9]heptadecan-6-yl] acetate 101248708 Click to see CC(=O)OC1CCC2(C3C4CC5CC3(C(C(C2C1(C)C)OC(=O)C)O)C(C5(O4)CO)O)C 452.50 unknown https://doi.org/10.1002/CHIN.200349163
[(1S,2R,3R,4R,6S,8S,9R,10S,11S,13S,15R)-3-acetyloxy-2,8,11,15-tetrahydroxy-5,5,9-trimethyl-14-methylidene-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 15381746 Click to see 452.50 unknown https://doi.org/10.1016/S0031-9422(98)80078-2
[(1S,2R,3R,4R,6S,8S,9S,10S,11S,13S,15R)-3-acetyloxy-2,8,11,15-tetrahydroxy-5,5,9-trimethyl-14-methylidene-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 102121391 Click to see 452.50 unknown https://doi.org/10.1016/S0031-9422(98)80078-2
https://doi.org/10.1016/S0031-9422(97)00418-4
[(1S,3S,4R,6S,8S,9R,10S,11S,13S)-3-acetyloxy-8,11-dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 163021047 Click to see 434.50 unknown https://doi.org/10.1021/NP030418L
[(1S,3S,4S,6S,9R,10S,11R,12R,13R)-3,6,12-trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 162939482 Click to see 392.50 unknown https://doi.org/10.1021/NP030418L
[(1S,3S,4S,6S,9R,10S,11S,13S,14S,16S)-3-acetyloxy-16-hydroxy-13-(hydroxymethyl)-5,5,9-trimethyl-12-oxapentacyclo[11.2.1.111,14.01,10.04,9]heptadecan-6-yl] acetate 101248707 Click to see CC(=O)OC1CCC2(C3C4CC5CC3(CC(C2C1(C)C)OC(=O)C)C(C5(O4)CO)O)C 436.50 unknown https://doi.org/10.1002/CHIN.200349163
https://doi.org/10.1248/CPB.51.845
[(1S,3S,4S,6S,9R,10S,11S,13S,14S,16S)-3,16-dihydroxy-13-(hydroxymethyl)-5,5,9-trimethyl-12-oxapentacyclo[11.2.1.111,14.01,10.04,9]heptadecan-6-yl] acetate 101248706 Click to see 394.50 unknown https://doi.org/10.1248/CPB.51.845
[(1S,3S,4S,6S,9R,10S,11S,13S,15R)-3-acetyloxy-11,15-dihydroxy-5,5,9-trimethyl-14-methylidene-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 162936296 Click to see 420.50 unknown https://doi.org/10.1021/NP030418L
[(1S,3S,4S,6S,9R,10S,11S,13S,15R)-6,11,15-trihydroxy-5,5,9-trimethyl-14-methylidene-3-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 163004462 Click to see 378.50 unknown https://doi.org/10.1021/NP030418L
[(1S,3S,4S,6S,9R,10S,11S,13S)-3-acetyloxy-11-hydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 162871143 Click to see 418.50 unknown https://doi.org/10.1021/NP030418L
[(1S,3S,4S,6S,9R,10S,11S,13S)-6,11-dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-3-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 162981108 Click to see CC(=O)OC1CC23CC(CC(C2C4(C1C(C(CC4)O)(C)C)C)O)C(=C)C3=O 376.50 unknown https://doi.org/10.1021/NP030418L
[3-Acetyloxy-14-(ethoxymethyl)-2,8,11-trihydroxy-5,5,9-trimethyl-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 162887848 Click to see 496.60 unknown https://doi.org/10.1016/S0031-9422(97)00418-4
Dawoensin A 10412708 Click to see CC(=O)OC1CCC2(C3C(CC4CC3(C(C(C2C1(C)C)OC(=O)C)OC(=O)C)C(=O)C4=C)O)C 476.60 unknown https://doi.org/10.1021/NP030418L
Melissoidesin E 101352810 Click to see 436.50 unknown https://doi.org/10.1080/10286029908039876
https://doi.org/10.1021/NP030418L
Melissoidesin F 44584349 Click to see 420.50 unknown https://doi.org/10.1021/NP030418L
https://doi.org/10.1080/10286029908039876
Melissoidesin M 20056141 Click to see CC(=O)OC1CC23CC(CC(C2C4(C1C(C(CC4)O)(C)C)C)O)C(=C)C3O 378.50 unknown https://doi.org/10.1021/NP030418L
Melissoidesin N 11164768 Click to see CC(=O)OC1CC23CC(CC(C2C4(C1C(C(CC4)O)(C)C)C)O)C(=C)C3=O 376.50 unknown https://doi.org/10.1021/NP030418L
Melissoidesin O 20056142 Click to see 418.50 unknown https://doi.org/10.1021/NP030418L
Melissoidesin P 20056143 Click to see 394.50 unknown https://doi.org/10.1021/NP030418L
Melissoidesin Q 20056144 Click to see CC(=O)OC1C2C(C(CCC2(C3C(CC4CC3(C1OC(=O)C)C(C4=C)O)O)C)O)(C)C 436.50 unknown https://doi.org/10.1021/NP030418L
Melissoidesin R 20056145 Click to see CC(=O)OC1CCC2(C3C(CC4CC3(C(C(C2C1(C)C)OC(=O)C)OC(=O)C)C(C4=C)O)O)C 478.60 unknown https://doi.org/10.1021/NP030418L
Melissoidesin S 20056146 Click to see 434.50 unknown https://doi.org/10.1021/NP030418L
Melissoidesin T 20056147 Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(CC(C2C1(C)C)OC(=O)C)C(C4=C)O)O)C)O 436.50 unknown https://doi.org/10.1021/NP030418L
Melissoidesin U 20056148 Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(CC(C2C1(C)C)OC(=O)C)C(C4=C)O)O)C)OC(=O)C 478.60 unknown https://doi.org/10.1021/NP030418L
Xindongnin B 44584350 Click to see CC(=O)OC1C2C(C(CCC2(C3C(CC4CC3(C1O)C(=O)C4=C)O)C)O)(C)C 392.50 unknown https://doi.org/10.1021/NP030418L
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-970006
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1055/S-2007-970006
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1055/S-2007-970006
Thymol 6989 Click to see 150.22 unknown https://doi.org/10.1055/S-2007-970006
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-970006
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1055/S-2007-970006
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-970006
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-970006
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Limonene 440917 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-970006
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1055/S-2007-970006
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1055/S-2007-970006
> Organoheterocyclic compounds / Naphthofurans
Furodysinin 360188 Click to see CC1=CC2CC3=C(C=CO3)C(C2CC1)(C)C 216.32 unknown https://doi.org/10.1021/NP030418L

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