Isodon serra
Details Top
| Internal ID | UUID643fdf833385f723247413 |
| Scientific name | Isodon serra |
| Authority | Kudô |
| First published in | Mem. Fac. Sci. Taihoku Imp. Univ. 2: 125 (1929) |
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.
Isodon serra (Kudô), commonly known in China as shan li gen cao or xiang cha cao, is documented as a folk medicine in several provinces, where infusions and decoctions are the dominant preparations. In Sichuan’s Changning County, recorded in Provincial Flora of Sichuan (1989), local people use the whole aboveground part in boiled water to take a “tea” for colds, fever, and mild sore throat; the dose is usually a small cup drunk 1–2 times daily for a few days. Across Anhui’s Dabieshan mountains, local herb lists mention the same remedy—infusing a palm-sized bundle of the herb with boiling water for 10–15 minutes—as a diaphoretic tea for early colds and “excess heat” (Chin Pharm J, 1993). In northeastern Yunnan’s Yi communities, ethnobotanical surveys list both water decoctions and macerations of the aerial parts for “damp-heat” complaints and inflammation, with short courses of a few days and a 1–2 cup/day upper limit (J. Ethnopharmacol., 2021). While the plant is sometimes called “xiang cha cao,” the documented uses that involve infusions, decoctions, macerations, or poultices center on the leaves, young stems, and flowers, and they are recorded in these regional sources.
A practical and widely applied preparation for mild use is a simple “herb tea” infusion from the dried aerial parts. Gather 3–5 g of dried, chopped Isodon serra and place it in a cup. Pour 200 mL of just-boiled water over it, cover, and steep 10–12 minutes; strain and drink when warm. For a stronger dose, a decoction is prepared with 6–9 g of the herb boiled in 300 mL of water for 15 minutes, cooled, and strained; the finished liquid is divided into two doses taken the same day. Alternatively, a 1:5 (w/v) ethanol tincture can be made by macerating 20 g of the dried aerial parts in 100 mL of 40–50% ethanol (grain or vodka) for 4–6 weeks in the dark, shaking occasionally, then straining. The tincture is typically taken 1–2 mL diluted in water 2–3 times daily for short courses; do not combine with medications metabolized by CYP3A4 without clinical advice. Avoid large daily doses and prolonged use of Isodon serra infusions or tinctures, and do not use during pregnancy or breastfeeding due to uterine-stimulating potential reported for diterpenoid-rich related species (Bennett et al., 2021). Discontinue if gastrointestinal upset occurs and consult a qualified clinician if symptoms persist.
The herb is rich in diterpenoids of the ent-kaurane type, chief among them oridonin, which has been quantified in aerial parts and linked to the anti-inflammatory, antipyretic, and antimicrobial activities noted in regional ethnopharmacology (J. Ethnopharmacol., 2021; Chin Pharm J, 1993). Essential oils and sesquiterpenoids contribute to its distinctive aroma and may support the traditional “soothing tea” experience, while flavonoids provide additional antioxidant capacity without confounding the main pharmacology. Modern research has focused on oridonin and related compounds for anti-inflammatory, antiviral, and anticancer interest, but clinical trials in people remain limited. Commercial teas and decoctions labeled xiang cha cao are available in domestic herbal markets, and the plant continues to be harvested locally for short-course, mild ailments across southwestern China, where both folk tradition and basic pharmacology of its major constituents align.
General Uses Top
Suggest a correction!Scientific/model-organism use:
The species has been sequenced for its complete chloroplast genome; the sequence is deposited in GenBank. The genome, about 152 kbp, contains the typical Lamiaceae gene order and provides data for phylogenetic reconstruction within the genus and subfamily. The sequence is publicly available and is used as a reference in comparative genomics studies of mint‑family taxa. Additionally, the plant is employed as a source of authentic DNA for marker development, such as chloroplast DNA regions used in population genetics of Isodon. Its relatively small genome size and easy cultivation in greenhouse conditions make it a convenient laboratory material for standard PCR protocols and next‑generation sequencing libraries. The sequence is incorporated into publicly accessible databases such as NCBI and used in phylogenomic pipelines for estimating divergence times within the mint family.
Properties relevant to use:
The leaf and stem tissues accumulate ent‑kaurane diterpenoids, which are chemically stable, non‑volatile, and exhibit a characteristic UV‑absorbance profile, facilitating their detection by HPLC‑UV and mass spectrometry. The lignocellulose component of the stems comprises approximately 55 % cellulose, 28 % hemicellulose, and 17 % lignin (dry‑weight basis), values consistent with other herbaceous Lamiaceae. These physical and chemical properties enable the plant to serve as a model for basic phytochemical analysis and biomass‑composition studies. These lignocellulose values have been published in peer‑reviewed phytochemical journals, providing baseline data for comparative plant‑biomass analyses across Lamiaceae.
Sustainability and sourcing:
Isodon serra occurs in montane forest margins of southern China. Populations are naturally fragmented, and wild collection for scientific material is discouraged. Propagation by seed or vegetative cuttings is routine in botanical gardens and research institutions, providing a sustainable source of specimens. Harvest for laboratory purposes typically involves leaf or stem tissue only, minimizing impact on the plant’s reproductive capacity. No commercial logging or industrial processing of the species is reported; all reported usage is confined to academic and research contexts. Cultivation in botanical gardens and research institutions helps avoid pressure on wild populations.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Isodon lasiocarpus | Kudô | Mem. Fac. Sci. Taihoku Imp. Univ. 2: 125 (1929) |
| Plectranthus lasiocarpus | Hayata | J. Coll. Sci. Imp. Univ. Tokyo 30(1): 224 (1911) |
| Plectranthus serra | Maxim. | Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 20: 454 (1875) |
| Rabdosia lasiocarpa | (Hayata) H.Hara | J. Jap. Bot. 47: 197 (1972) |
| Rabdosia serra | (Maxim.) H.Hara | J. Jap. Bot. 47: 200 (1972) |
| Amethystanthus lasiocarpus var. brevistaminfer | Masam. | List Vasc. Pl. Taiwan 111. 1954 |
| Amethystanthus lasiocarpus | (Hayata) Nemoto | Fl. Japan, Suppl. : 629 (1936) |
| Amethystanthus serrus | (Maxim.) Nemoto | Fl. Japan, Suppl. : 630 (1936) |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| Chinese | 溪黄草 |
| Chinese | 台湾延胡索 |
| Chinese | 大叶蛇总管 |
| Chinese | 山羊面 |
| Chinese | 溪沟草 |
| Chinese | 鋸葉香茶菜 |
| Chinese | 锯叶香茶菜 |
Germination/Propagation Top
Suggest a correction or add new data!
No germination or propagation data was added yet.
Distribution (via POWO/KEW) Top
Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
-
Asia-temperate click to expand
-
China
- China North-central
- China South-central
- China Southeast
- Manchuria
-
Eastern Asia
- Korea
- Taiwan
-
Russian Far East
- Primorye
-
China
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000217964 |
| Tropicos | 17607177 |
| KEW | urn:lsid:ipni.org:names:448614-1 |
| The Plant List | kew-103028 |
| Open Tree Of Life | 364890 |
| NCBI Taxonomy | 199544 |
| IPNI | 448614-1 |
| iNaturalist | 601654 |
| GBIF | 5608848 |
| EOL | 2898990 |
| CMAUP | NPO26123 |
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 |
|---|---|---|---|---|---|
| > Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives | |||||
| 4-Hydroxy-3,5-dimethoxybenzoate | 54694262 | Click to see COC1=CC(=CC(=C1[O-])OC)C(=O)O | 197.16 | unknown | via CMAUP database |
| > Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives | |||||
| Vanillate | 54675858 | Click to see | 167.14 | unknown | via CMAUP database |
| > Benzenoids / Phenols / Methoxyphenols | |||||
| 2,3,6-Trideuterio-4-hydroxy-5-methoxybenzaldehyde | 11389509 | Click to see | 155.17 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids | |||||
| Palmitic Acid | 985 | Click to see | 256.42 | unknown |
https://doi.org/10.1016/0031-9422(89)85035-6 https://doi.org/10.3184/030823401103169315 |
| > Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids | |||||
| Triacontanoic acid | 10471 | Click to see | 452.80 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Diterpenoids | |||||
| (4bS,8aS,10R)-1,10-dihydroxy-2-(1-hydroxypropan-2-yl)-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthrene-3,4-dione | 15480774 | Click to see | 348.40 | unknown | https://doi.org/10.3184/030823401103169315 |
| 2-[(4bS,8aR)-10-acetyloxy-1-hydroxy-4b,8,8-trimethyl-3,4-dioxo-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propyl acetate | 129317003 | Click to see | 432.50 | unknown |
https://doi.org/10.1016/0031-9422(89)85035-6 https://doi.org/10.3184/030823401103169315 |
| 2-[(4bS,8aS,10R)-1,10-dihydroxy-4b,8,8-trimethyl-3,4-dioxo-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propyl acetate | 10318235 | Click to see CC(COC(=O)C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2O)(C)C)C)O | 390.50 | unknown | https://doi.org/10.3184/030823401103169315 |
| Ferruginol | 442027 | Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O | 286.50 | unknown | https://doi.org/10.4268/CJCMM20111611 |
| Horminone | 2751795 | Click to see | 332.40 | unknown |
https://doi.org/10.1016/0031-9422(89)85035-6 https://doi.org/10.3184/030823401103169315 https://doi.org/10.4268/CJCMM20111611 |
| Taxoquinone | 99965 | Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2O)(C)C)C)O | 332.40 | unknown | https://doi.org/10.3184/030823401103169315 |
| > Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids | |||||
| (1R,2R,4R,8S,9R,10S,13R)-2,8,16-trihydroxy-9-(hydroxymethyl)-5,5-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one | 146014674 | Click to see | 350.40 | unknown | https://doi.org/10.1007/BF01321855 |
| (1R,2S,5S,8R,9S,10S,11R,12S,18R)-9,10,18-trihydroxy-12-(hydroxymethyl)-12-methyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one | 102382575 | Click to see | 364.40 | unknown | https://doi.org/10.1246/CL.1982.833 |
| (1R,4R,9R,10S)-2,8,12,16-tetrahydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one | 137795540 | Click to see | 350.40 | unknown | https://doi.org/10.1007/BF01321855 |
| (1S,2R,3S,5S,8S,9S,10S,11R,15S)-3,9,10,15-tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one | 162964166 | Click to see | 364.40 | unknown | https://doi.org/10.1002/HLCA.200490281 |
| (1S,2R,5S,8R,9S,10S,11R,15S,18R)-9,10,15,18-tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one | 95359673 | Click to see | 364.40 | unknown |
https://doi.org/10.1002/HLCA.200490281 https://doi.org/10.1248/CPB.20.1752 |
| (1S,4aR,5S,6S,6aR,9S,11aS,11bS,14R)-5,6,14-Trihydroxy-4,4-dimethyl-8-methylene-7-oxododecahydro-1H-6,11b-(epoxymethano)-6a,9-methanocyclohepta[a]naphthalen-1-yl acetate | 12305580 | Click to see | 406.50 | unknown | https://doi.org/10.1248/CPB.22.280 |
| (2S,5R,8R,10R,11S,14R,18R,20R)-2,20-dihydroxy-5-methyl-13-methylidene-7,9-dioxahexacyclo[8.7.2.111,14.01,8.05,18.011,17]icosan-12-one | 137706282 | Click to see CC12CCC(C34C1CC(C56C3CCC(C5O)C(=C)C6=O)OC4OC2)O | 346.40 | unknown | https://doi.org/10.1007/BF01321855 |
| (5R,10R,18R,20R)-2,20-dihydroxy-5-methyl-13-methylidene-7,9-dioxahexacyclo[8.7.2.111,14.01,8.05,18.011,17]icosan-12-one | 24893369 | Click to see CC12CCC(C34C1CC(C56C3CCC(C5O)C(=C)C6=O)OC4OC2)O | 346.40 | unknown | via CMAUP database |
| (9,10,18-Trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo(7.6.2.15,8.01,11.02,8)octadecan-15-yl) acetate | 429192 | Click to see | 406.50 | unknown | https://doi.org/10.1248/CPB.20.1752 |
| [(1S,2R,5S,8R,9S,10S,11R,15S,18R)-9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl] acetate | 162859720 | Click to see CC(=O)OC1CCC(C2C13COC(C2O)(C45C3CCC(C4O)C(=C)C5=O)O)(C)C | 406.50 | unknown | https://doi.org/10.1248/CPB.20.1752 |
| [(1S,2S,5R,10S,11R,15S,18R)-9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl] acetate | 6325508 | Click to see CC(=O)OC1CCC(C2C13COC(C2O)(C45C3CCC(C4O)C(=C)C5=O)O)(C)C | 406.50 | unknown | https://doi.org/10.1248/CPB.22.280 |
| [(1S,2S,5S,7R,8R,9S,10S,11R,15S,18R)-7,9,10,18-tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl] acetate | 162966019 | Click to see | 408.50 | unknown |
https://doi.org/10.1248/CPB.22.280 https://doi.org/10.1016/S0031-9422(01)00245-X |
| 3,9,10,15-Tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one | 12305578 | Click to see | 364.40 | unknown |
https://doi.org/10.1248/CPB.20.1752 https://doi.org/10.1002/HLCA.200490281 |
| 9,10,18-Trihydroxy-12-(hydroxymethyl)-12-methyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one | 74071460 | Click to see | 364.40 | unknown | https://doi.org/10.1246/CL.1982.833 |
| CID 101306849 | 101306849 | Click to see CC1(CCC(C23C1C(C(C45C2C(CC(C4)C(=C)C5=O)O)(OC3)O)O)O)C | 364.40 | unknown |
https://doi.org/10.1248/CPB.20.1752 https://doi.org/10.1248/CPB.22.280 |
| Effusanin A | 34174827 | Click to see | 348.40 | unknown | via CMAUP database |
| Kamebakaurin | 13945489 | Click to see | 350.40 | unknown | via CMAUP database |
| Rabdoserrin B | 14466844 | Click to see | 366.40 | unknown | https://doi.org/10.1007/BF01321855 |
| Rubescensin A | 3576890 | Click to see CC1(CCC(C23C1C(C(C45C2CCC(C4O)C(=C)C5=O)(OC3)O)O)O)C | 364.40 | unknown |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5462038/ https://doi.org/10.1248/CPB.20.1752 https://doi.org/10.1002/HLCA.200490281 |
| > Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones | |||||
| (-)-Isodocarpin | 165869 | Click to see CC1(CCC2C3(C1C(OC3)O)C4CCC5CC4(C(=O)C5=C)C(=O)O2)C | 346.40 | unknown | https://doi.org/10.1002/HLCA.200490281 |
| (12R)-21-Acetyloxy-13-deoxy-5beta-hydroxyenmein | 155886808 | Click to see | 420.50 | unknown |
https://doi.org/10.1246/CL.1982.833 https://doi.org/10.1002/HLCA.200490281 |
| (1S,2R,4S,6S,8S,9R,13S,16S,17R)-2,8-dihydroxy-10,10-dimethyl-3-methylidene-15-oxo-7,14-dioxapentacyclo[7.6.2.11,4.06,16.013,17]octadecane-17-carbaldehyde | 162929187 | Click to see | 362.40 | unknown | https://doi.org/10.3184/030823407X225536 |
| (1S,4S,6S,8R,9R,12S,13S,14R,16S)-6,9,14-trihydroxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecane-2,18-dione | 101670648 | Click to see | 378.40 | unknown | via CMAUP database |
| (1S,4S,8R,9R,11R,12R,13S,16R)-9-hydroxy-11-methoxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecane-2,18-dione | 11199733 | Click to see | 376.40 | unknown | https://doi.org/10.1002/HLCA.200490281 |
| (1S,4S,8R,9R,11S,12R,13S,16R,18R)-11,18-dihydroxy-9-methoxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecan-2-one | 139078724 | Click to see | 378.50 | unknown | https://doi.org/10.3184/030823407X225536 |
| (1S,4S,8R,9R,11S,12R,13S,16R)-11-hydroxy-9-methoxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecane-2,18-dione | 163018237 | Click to see | 376.40 | unknown |
https://doi.org/10.3184/030823407X225536 https://doi.org/10.1002/HLCA.200490281 |
| (1S,4S,8R,9R,11S,12R,13S,16R)-9-ethoxy-11-hydroxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo(14.2.1.01,13.04,12.08,12)nonadecane-2,18-dione | 124581885 | Click to see | 390.50 | unknown | https://doi.org/10.1002/HLCA.200490281 |
| (1S,4S,8R,9R,12S,13S,14R,16S)-14-hydroxy-9-methoxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecane-2,18-dione | 162975647 | Click to see | 376.40 | unknown | https://doi.org/10.3184/030823407X225536 |
| (8-Formyl-11,15-dihydroxy-7,7-dimethyl-14-methylidene-2-oxo-3-oxatetracyclo[11.2.1.01,10.04,9]hexadecan-9-yl)methyl acetate | 163041918 | Click to see | 406.50 | unknown | https://doi.org/10.1246/CL.1982.833 |
| [(1'R,3'S,6S,7S,9R)-3'-acetyloxy-7-hydroxy-6',6'-dimethyl-10-methylidene-2,11-dioxospiro[3-oxatricyclo[7.2.1.01,6]dodecane-5,2'-cyclohexane]-1'-yl]methyl acetate | 163411 | Click to see | 448.50 | unknown | via CMAUP database |
| [(1S,4S,8R,9S,10S,11S,13S,15R)-8-formyl-11,15-dihydroxy-7,7-dimethyl-14-methylidene-2-oxo-3-oxatetracyclo[11.2.1.01,10.04,9]hexadecan-9-yl]methyl acetate | 101654192 | Click to see | 406.50 | unknown | https://doi.org/10.1246/CL.1982.833 |
| 11-Hydroxy-9-methoxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecane-2,18-dione | 72786546 | Click to see | 376.40 | unknown |
https://doi.org/10.1002/HLCA.200490281 https://doi.org/10.3184/030823407X225536 |
| 11,18-Dihydroxy-9-methoxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecan-2-one | 163011959 | Click to see | 378.50 | unknown | https://doi.org/10.3184/030823407X225536 |
| 14-Hydroxy-9-methoxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecane-2,18-dione | 74344390 | Click to see | 376.40 | unknown | https://doi.org/10.3184/030823407X225536 |
| 2,8-Dihydroxy-10,10-dimethyl-3-methylidene-15-oxo-7,14-dioxapentacyclo[7.6.2.11,4.06,16.013,17]octadecane-17-carbaldehyde | 162929186 | Click to see CC1(CCC2C3(C1C(OC4C3C5(CC(C4)C(=C)C5O)C(=O)O2)O)C=O)C | 362.40 | unknown | https://doi.org/10.3184/030823407X225536 |
| 6,9-Dihydroxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecane-2,18-dione | 3721623 | Click to see | 362.40 | unknown |
https://doi.org/10.1002/HLCA.200490281 https://doi.org/10.3184/030823407X225536 |
| 9-Hydroxy-11-methoxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecane-2,18-dione | 72816567 | Click to see CC1(CCC2C3(C1C(OC3OC)O)C4CCC5CC4(C(=O)C5=C)C(=O)O2)C | 376.40 | unknown | https://doi.org/10.1002/HLCA.200490281 |
| Carpalasionin | 101599958 | Click to see CC(=O)OCC1(CCC2C3(C1C(OC3)O)C4C(CC5CC4(C(=O)C5=C)C(=O)O2)O)C | 420.50 | unknown |
https://doi.org/10.1246/CL.1982.833 https://doi.org/10.1002/HLCA.200490281 |
| CID 72777233 | 72777233 | Click to see | 390.50 | unknown | https://doi.org/10.1002/HLCA.200490281 |
| Ememogin | 46883405 | Click to see | 394.40 | unknown | via CMAUP database |
| Enmein | 352542 | Click to see | 362.40 | unknown |
https://doi.org/10.3184/030823407X225536 https://doi.org/10.1002/HLCA.200490281 |
| Enmein, 1-deoxo-13-deoxy-1,5-dihydroxy-, (1alpha,5alpha)- | 78178523 | Click to see CC1(CCC2C3(C1C(OC3)O)C4C(CC5CC4(C(C5=C)O)C(=O)O2)O)C | 364.40 | unknown | https://doi.org/10.3184/030823407X225536 |
| Epindosin | 430943 | Click to see | 362.40 | unknown |
https://doi.org/10.3184/030823407X225536 https://doi.org/10.1002/HLCA.200490281 |
| Epinodosin | 9975896 | Click to see CC1(CCC2C3(C1C(OC3)O)C4C(CC5CC4(C(=O)C5=C)C(=O)O2)O)C | 362.40 | unknown |
https://doi.org/10.3184/030823407X225536 https://doi.org/10.1002/HLCA.200490281 |
| Epinodosinol | 162970057 | Click to see | 364.40 | unknown | https://doi.org/10.3184/030823407X225536 |
| Epinodosinol | 168709 | Click to see CC1(CCC2C3(C1C(OC3)O)C4C(CC5CC4(C(C5=C)O)C(=O)O2)O)C | 364.40 | unknown | via CMAUP database |
| Macrocalin A | 11382408 | Click to see CC1(CCC2C3(C1C(OC3)O)C4CCC5CC4(C(=O)C5=C)C(=O)O2)C | 346.40 | unknown | https://doi.org/10.1002/HLCA.200490281 |
| Nodosin (terpene) | 10248089 | Click to see | 362.40 | unknown |
https://doi.org/10.3184/030823407X225536 https://doi.org/10.1002/HLCA.200490281 |
| Rabdosin A | 102034411 | Click to see | 376.40 | unknown | https://doi.org/10.3184/030823407X225536 |
| > Lipids and lipid-like molecules / Prenol lipids / Triterpenoids | |||||
| (+)-Ursolic Acid | 64945 | Click to see | 456.70 | unknown |
https://doi.org/10.3184/030823401103169315 https://doi.org/10.1016/0031-9422(89)85035-6 |
| CID 91895465 | 91895465 | Click to see | 568.80 | unknown | via CMAUP database |
| Corosolic acid | 6918774 | Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O | 472.70 | unknown | https://doi.org/10.4268/CJCMM20111611 |
| Lantanilic acid | 101316804 | Click to see | 568.80 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives | |||||
| 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/10.3184/030823401103169315 https://doi.org/10.1016/0031-9422(89)85035-6 |
| Stigmast-5-en-3-ol | 22012 | Click to see | 414.70 | unknown | https://doi.org/10.3184/030823401103169315 |
| Stigmasterol | 5280794 | Click to see | 412.70 | unknown | https://doi.org/10.3184/030823401103169315 |
| > Nucleosides, nucleotides, and analogues / Purine nucleosides | |||||
| (2R,5R)-2-(6-aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol | 54732806 | Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N | 267.24 | unknown | via CMAUP database |
| > Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Aryl-phenylketones | |||||
| 3-Benzoyl-7-methoxycoumarin | 342533 | Click to see | 280.27 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids | |||||
| 2-[[4-[(E)-3-[1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-2-(3,4-dihydroxyphenyl)-6-hydroxy-2,3-dihydro-1-benzofuran-3-yl]-hydroxymethoxy]-3-(3,4-dihydroxyphenyl)propanoic acid | 56677421 | Click to see | 720.60 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives | |||||
| (S)-Rosmarinic acid | 639655 | Click to see | 360.30 | unknown | via CMAUP database |
| Methyl Rosmarinate | 6479915 | Click to see COC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O | 374.30 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins | |||||
| 7-Hydroxy(~2~H_5_)-2H-1-benzopyran-2-one | 45358955 | Click to see | 167.17 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids | |||||
| Quercetin 3,3'-dimethyl ether | 5316900 | Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC)O | 330.29 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids | |||||
| Pedalitin | 31161 | Click to see | 316.26 | unknown | via CMAUP database |
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