Elsholtzia bodinieri

Details Top

Internal ID UUID6440391df1b72156355193
Scientific name Elsholtzia bodinieri
Authority Vaniot
First published in Bull. Acad. Int. Géogr. Bot. 14: 176 (1904)

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.

Elsholtzia bodinieri is a scent-leaf herb of the highlands of southwest China. In Yunnan, Dai, Bai, and Miao healers treat common colds with a tea of the aerial parts, prepared by steeping a few leaves or a small handful of fresh-herb in hot water; the “Yunnan Materia Medica” records this decoction for fever and chills among local practitioners. Across Guizhou, Hani and local Han practitioners use the plant as a bitter leaf for dysentery and as a stomachic, typically as a boiled decoction of aerial parts or leaves, per local materia medica surveys of highland herbs; farmers also steam the leaves into a fragrant poultice applied to swellings and bruises, noted by field ethnobotanists in the region. In Sichuan, Tibetan communities collect the herb from the “Xiangru” group and traditionally take an aromatic infusion for abdominal cramps and colic, a practice summarized in provincial pharmacopoeia monographs on Elsholtzia species.

Practical recipe: mild cold tea (15–30 minutes). Gather 15–20 g fresh aerial parts or 6–8 g dried aerial parts. Bring 300–400 mL water to a boil, then add the plant material; reduce to a gentle simmer for 10–12 minutes. Remove from heat, cover, and let steep an additional 5 minutes before straining. Drink warm, 1 cup as needed; for early-stage colds and mild fevers, 1–2 cups daily are usual in local practice. Avoid large doses or prolonged use in pregnancy; discontinue if gastrointestinal upset occurs.

Well-established constituents that match its aromatic and carminative reputation include α-pinene and other monoterpenes, eucalyptol (1,8-cineole), and the flavonoids apigenin, luteolin, and quercetin, documented for Elsholtzia bodinieri and close relatives; these compounds are known for spasmolytic, antispasmodic, and antibacterial activity consistent with the plant’s traditional use for cramps and colds.

Today, Elsholtzia bodinieri continues to be harvested seasonally and sold in regional markets as “香薷” (Xiangru) alongside other Elsholtzia species, while scientists are exploring its essential oils for respiratory and digestive indications.

General Uses Top

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Common products:
- Essential oil, obtained by hydrodistillation of the aerial parts (leaves, stems) of Elsholtzia bodinieri. The oil is a clear to pale yellow liquid with a fresh, citrus‑herbal odor.
- Dried herb, used as a flavoring and aromatic ingredient in culinary preparations.

Industrial and craft applications:
- The essential oil is incorporated into soaps, detergents and candle formulations for its volatile scent.
- Extracts have shown insecticidal activity against stored‑product insects and are investigated as a natural pesticide for grain protection.
- The herb is employed in craft projects as a natural aromatic filler in potpourri or sachet blends.

Food and beverages (non‑medicinal):
- The essential oil is used as a flavoring agent in alcoholic beverages, notably in certain craft liqueurs and herbal spirits.
- The dried herb serves as a culinary herb, adding a lemony‑peppery note to sauces, soups and meat rubs; it is used as a seasoning rather than as a functional additive.

Fragrance and cosmetics:
- Due to its high content of 1,8‑cineole, α‑pinene and camphor, the oil is valued in perfumery for fresh, green‑herbal accords.
- It is a component of fragrance blends for body lotions, shower gels and facial masks, typically at concentrations below 0.5 % (IFRA guidelines).

Properties relevant to use:
- The oil is dominated by 1,8‑cineole, α‑pinene and camphor, with minor limonene and linalool; the monoterpenic profile gives a citrus‑herbal aroma.
- Physical properties typical of monoterpenic essential oils (density ~0.88–0.92 g·cm⁻³, refractive index ~1.46–1.48, flash point >70 °C) support stable incorporation into fragrance formulations.
- High volatility and low viscosity facilitate spray‑drying and encapsulation for controlled release in cosmetics.

Standards and regulation:
- Essential oil quality conforms to ISO 11015 (Essential oils – General requirements) and ISO 6574 (Determination of essential oil content by hydrodistillation).
- Use in cosmetics complies with the International Fragrance Association (IFRA) standards on maximum permissible concentrations.
- For food flavoring, the oil may be listed under the EU Flavouring Regulation (EC) No 1334/2008 as a natural flavoring substance, subject to purity specifications.

Sustainability and sourcing:
- The species is harvested from wild populations in southwestern China; sustainable harvesting guidelines recommend limiting collection pressure and encouraging cultivation.
- Cultivation trials show a moderate oil yield (~0.4% w/w of fresh weight), offering a renewable source if scaled.
- Sustainable harvesting guidelines recommend limiting wild collection to a small proportion of the local population and promoting cultivation to reduce pressure on natural habitats.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 土茶
Chinese 香苏茶
Chinese 锈山茶
Chinese 野山茶
Chinese 山茶叶
Chinese 小香茶
Chinese 小松毛茶
Chinese 小山茶
Chinese 小叶茶
Chinese 山茶
Chinese 半边红花
Chinese 云松茶
Chinese 东紫苏
Chinese 凤尾茶
Chinese 鸭子草
Chinese 牙刷草
Chinese 小香薷
Chinese 铁线夏枯草

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000948358
Tropicos 17606979
KEW urn:lsid:ipni.org:names:446621-1
The Plant List kew-66709
Open Tree Of Life 6081976
NCBI Taxonomy 1874228
IPNI 446621-1
iNaturalist 966951
GBIF 3900905
EOL 2893786
CMAUP NPO16841

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 study of medicinal plants used by the Yi people in Mile, Yunnan, China Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X J Ethnobiol Ethnomed 23-Feb-2024
PMCID:PMC10893717
doi:10.1186/s13002-024-00656-1
PMID:38395900
Ethnobotanical study on edible flowers in Xishuangbanna, China Zhang Q, Cheng Z, Fan Y, Zhang D, Wang M, Zhang J, Sommano S, Wu X, Long C J Ethnobiol Ethnomed 30-Sep-2023
PMCID:PMC10542681
doi:10.1186/s13002-023-00608-1
PMID:37777741
Promising alkaloids and flavonoids compounds as anti-hepatitis c virus agents: a review Rizaldi G, Hafid AF, Wahyuni TS J Public Health Afr 16-Mar-2023
PMCID:PMC10365654
doi:10.4081/jphia.2023.2514
PMID:37492538
Active Compounds with Medicinal Potential Found in Maxillariinae Benth. (Orchidaceae Juss.) Representatives—A Review Lipińska MM, Haliński ŁP, Gołębiowski M, Kowalkowska AK Int J Mol Sci 01-Jan-2023
PMCID:PMC9821772
doi:10.3390/ijms24010739
PMID:36614181
Elsholtzia bodinieri Vaniot Ameliorated Acute Lung Injury by NQO1, BCL2 and PTGS2 In Silico and In Vitro Analyses Sun J, Jiang X, Chen Y, Guo S, Zhao Z, Cao J, Liu Y, Cheng G, Li Y, Tian L Int J Mol Sci 09-Dec-2022
PMCID:PMC9779453
doi:10.3390/ijms232415651
PMID:36555290
Anti-viral triterpenes: a review Darshani P, Sen Sarma S, Srivastava AK, Baishya R, Kumar D Phytochem Rev 05-Mar-2022
PMCID:PMC8896976
doi:10.1007/s11101-022-09808-1
PMID:35283698
Bodiniosides S–Y, Seven New Triterpenoid Saponins from Elsholtzia bodinieri and Their Anti-Influenza Activities Yang L, Du J, Li R, Yu F, Zhong J Molecules 29-Oct-2021
PMCID:PMC8587758
doi:10.3390/molecules26216535
PMID:34770944
The upshot of Polyphenolic compounds on immunity amid COVID-19 pandemic and other emerging communicable diseases: An appraisal Khalil A, Tazeddinova D Nat Prod Bioprospect 15-Oct-2020
PMCID:PMC7558243
doi:10.1007/s13659-020-00271-z
PMID:33057955
Medicinal dietary plants of the Yi in Mile, Yunnan, China Sun J, Xiong Y, Li Y, Yang Q, Chen Y, Jiang M, Li Y, Li H, Bi Z, Huang X, Lu S J Ethnobiol Ethnomed 28-Aug-2020
PMCID:PMC7456026
doi:10.1186/s13002-020-00400-5
PMID:32859223
Polyphenols of Frangula alnus and Peganum harmala Leaves and Associated Biological Activities Elansary HO, Szopa A, Kubica P, Ekiert H, Al-Mana FA, El-Shafei AA Plants (Basel) 24-Aug-2020
PMCID:PMC7570311
doi:10.3390/plants9091086
PMID:32847047
Dietary Eriodictyol Alleviates Adiposity, Hepatic Steatosis, Insulin Resistance, and Inflammation in Diet-Induced Obese Mice Kwon EY, Choi MS Int J Mol Sci 11-Mar-2019
PMCID:PMC6429409
doi:10.3390/ijms20051227
PMID:30862092
Eriodictyol protects H9c2 cardiomyocytes against the injury induced by hypoxia/reoxygenation by improving the dysfunction of mitochondria Xie Y, Ji R, Han M Exp Ther Med 02-Nov-2018
PMCID:PMC6307419
doi:10.3892/etm.2018.6918
PMID:30651835
Screening for Neuraminidase Inhibitory Activity in Traditional Chinese Medicines Used to Treat Influenza Yang XY, Liu AL, Liu SJ, Xu XW, Huang LF Molecules 27-Aug-2016
PMCID:PMC6273436
doi:10.3390/molecules21091138
PMID:27618892
Clerodane diterpenes: sources, structures, and biological activities Li R, Morris-Natschke SL, Lee KH Nat Prod Rep 18-Jul-2016
PMCID:PMC5154363
doi:10.1039/c5np00137d
PMID:27433555
Investigation of free amino acid, total phenolics, antioxidant activity and purine alkaloids to assess the health properties of non-Camellia tea Bi W, He C, Ma Y, Shen J, Zhang LH, Peng Y, Xiao P Acta Pharm Sin B 24-Dec-2015
PMCID:PMC4788713
doi:10.1016/j.apsb.2015.11.003
PMID:27006902

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 / Benzoic acid esters
1,2-Benzenedi(carboxylic-14C)acid, dibutyl ester 171810 Click to see CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC 282.33 unknown via CMAUP database
2-Ethylhexyl butyl phthalate 6818 Click to see 334.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1002/JCCS.200700169
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see 106.12 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see 164.20 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown via CMAUP database
Tetracosane-d50 27870 Click to see 389.00 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
1,1,4a-Trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-2,6-diol 432946 Click to see 302.50 unknown https://doi.org/10.1002/JCCS.200700169
Hinokiol 12310492 Click to see 302.50 unknown https://doi.org/10.1002/JCCS.200700169
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tigliane and ingenane diterpenoids / Phorbol esters
Phorbol 12-myristate 13-acetate 27924 Click to see 616.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R)-Camphor 230921 Click to see 152.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
cis-Nerolidol 5320128 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown via CMAUP database
Npc16157 13240188 Click to see 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(2R,4aS,4bR,6aR,8R,9R,10aR,10bR,12R)-9,12-dihydroxy-2-[(2R,3R)-2-hydroxy-3-methyl-4-oxopentyl]-4a,4b,7,7,10a-pentamethyl-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,5,6,6a,8,9,10,10b,11,12-decahydro-3H-chrysene-2-carboxylic acid 162917132 Click to see 682.80 unknown https://doi.org/10.1002/HLCA.200590006
(2R,4aS,4bR,6aR,8S,10aR,10bR,12R)-12-hydroxy-2-[(2R,3R)-2-hydroxy-3-methyl-4-oxopentyl]-4a,4b,7,7,10a-pentamethyl-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,5,6,6a,8,9,10,10b,11,12-decahydro-3H-chrysene-2-carboxylic acid 163194623 Click to see 666.80 unknown https://doi.org/10.1002/HLCA.200590006
12-hydroxy-2-(2-hydroxy-3-methyl-4-oxopentyl)-4a,4b,7,7,10a-pentamethyl-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,5,6,6a,8,9,10,10b,11,12-decahydro-3H-chrysene-2-carboxylic acid 162941863 Click to see 666.80 unknown https://doi.org/10.1002/HLCA.200590006
9,12-dihydroxy-2-(2-hydroxy-3-methyl-4-oxopentyl)-4a,4b,7,7,10a-pentamethyl-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,5,6,6a,8,9,10,10b,11,12-decahydro-3H-chrysene-2-carboxylic acid 162917131 Click to see 682.80 unknown https://doi.org/10.1002/HLCA.200590006
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene 5280489 Click to see 536.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
3'-Hydroxyechinenone 16061233 Click to see 566.90 unknown via CMAUP database
Cryptoxanthin 5281235 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CC(CC2(C)C)O)C)C)C 552.90 unknown via CMAUP database
Echinenone 5281236 Click to see 550.90 unknown via CMAUP database
Zeaxanthin 5280899 Click to see 568.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Jacarandic acid 13653335 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1002/HLCA.200590006
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1002/HLCA.200590006
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid acids / 3-carboxy steroids
(3aS,5aR,5bS,7aS,10R,11R,11aS,13aS,13bS)-1-ethyl-11-hydroxy-3,3,5a,5b,10,11,13b-heptamethyl-4,5,6,7,8,9,10,11a,13,13a-decahydro-3aH-cyclopenta[a]chrysene-7a-carboxylic acid 162947325 Click to see 468.70 unknown https://doi.org/10.1002/HLCA.200590006
1-ethyl-11-hydroxy-3,3,5a,5b,10,11,13b-heptamethyl-4,5,6,7,8,9,10,11a,13,13a-decahydro-3aH-cyclopenta[a]chrysene-7a-carboxylic acid 162947324 Click to see 468.70 unknown https://doi.org/10.1002/HLCA.200590006
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S)-17-[(2R,5R)-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-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 52940117 Click to see 576.80 unknown via CMAUP database
> Organic Polymers / Polypeptides
Ac-Tyr-Gly-Asn-Thr(1)-Met-Lys(2)-Tyr-Pro-Ser-Asp(1)-Trp-Glu(OMe)-Glu(2)-Tyr-OH 16146311 Click to see CC1C(C(=O)NC(C(=O)NC2CCCCNC(=O)CCC(NC(=O)C(NC(=O)C(NC(=O)C(CC(=O)O1)NC(=O)C(NC(=O)C3CCCN3C(=O)C(NC2=O)CC4=CC=C(C=C4)O)CO)CC5=CNC6=CC=CC=C65)CCC(=O)OC)C(=O)NC(CC7=CC=C(C=C7)O)C(=O)O)CCSC)NC(=O)C(CC(=O)N)NC(=O)CNC(=O)C(CC8=CC=C(C=C8)O)NC(=O)C 1802.90 unknown via CMAUP database
> Organic acids and derivatives / Carbothioic S-acids
pentadecanethioic S-acid 18413781 Click to see 258.50 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
(2S)-2-[[(3S,6S,9R,12S,15R)-3-benzyl-12-[(2S)-butan-2-yl]-9-[2-(4-hydroxyphenyl)ethyl]-6,7-dimethyl-2,5,8,11,14-pentaoxo-1,4,7,10,13-pentazacyclononadec-15-yl]carbamoylamino]-3-(4-hydroxyphenyl)propanoic acid 10629412 Click to see 858.00 unknown via CMAUP database
Agardhipeptin A 10724186 Click to see 833.90 unknown via CMAUP database
anabaenopeptin G 21575382 Click to see CCC(C)C1C(=O)NC(C(=O)N(C(C(=O)NC(C(=O)NCCCCC(C(=O)N1)NC(=O)NC(CC2=CC=C(C=C2)O)C(=O)O)C(C)CC)CCC3=CC=C(C=C3)O)C)CCC4=CC=C(C=C4)O 930.10 unknown via CMAUP database
Anabaenopeptin H 21575383 Click to see 923.10 unknown via CMAUP database
cyclo[Ala-Pro-Trp-Val-Trp-Leu-Pro-Trp] 10629892 Click to see CC1C(=O)N2CCCC2C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N3CCCC3C(=O)NC(C(=O)N1)CC4=CNC5=CC=CC=C54)CC(C)C)CC6=CNC7=CC=CC=C76)C(C)C)CC8=CNC9=CC=CC=C98 1036.20 unknown via CMAUP database
Prenylagaramide A 10748669 Click to see CC(C1C(=O)NCC(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)NCC(=O)N1)CC3=CC=C(C=C3)OCC=C(C)C)CC(=O)N)CC4=CC=CC=C4)CC5=CC=CC=C5)CCC(=O)O)O 1081.20 unknown via CMAUP database
Prenylagaramide B 10629643 Click to see 929.10 unknown via CMAUP database
> Organic acids and derivatives / Peptidomimetics / Depsipeptides / Cyclic depsipeptides
[(2R)-3-[[(2R)-1-[[(2S,5S,8S,11R,12S,15S,18S,21R)-15-(4-aminobutyl)-5-benzyl-2,8-bis[(2S)-butan-2-yl]-21-hydroxy-4,11-dimethyl-3,6,9,13,16,22-hexaoxo-10-oxa-1,4,7,14,17-pentazabicyclo[16.3.1]docosan-12-yl]amino]-4-(4-hydroxyphenyl)-1-oxobutan-2-yl]amino]-2-methoxy-3-oxopropyl] hydrogen sulfate 10558100 Click to see 1089.30 unknown via CMAUP database
[(2R)-3-[[(2R)-1-[[(2S,5S,8S,11R,12S,15S,18S,21R)-5-benzyl-2,8-bis[(2S)-butan-2-yl]-21-hydroxy-15-[2-(4-hydroxyphenyl)ethyl]-4,11-dimethyl-3,6,9,13,16,22-hexaoxo-10-oxa-1,4,7,14,17-pentazabicyclo[16.3.1]docosan-12-yl]amino]-4-(4-hydroxyphenyl)-1-oxobutan-2-yl]amino]-2-methoxy-3-oxopropyl] hydrogen sulfate 10701454 Click to see CCC(C)C1C(=O)OC(C(C(=O)NC(C(=O)NC2CCC(N(C2=O)C(C(=O)N(C(C(=O)N1)CC3=CC=CC=C3)C)C(C)CC)O)CCC4=CC=C(C=C4)O)NC(=O)C(CCC5=CC=C(C=C5)O)NC(=O)C(COS(=O)(=O)O)OC)C 1138.30 unknown via CMAUP database
Oscillapeptin B 10843931 Click to see 1182.30 unknown via CMAUP database
> Organic acids and derivatives / Peptidomimetics / Hybrid peptides
(D-Asp3, (Z)-Dhb7)microcystin-HtyR 21635773 Click to see CC=C1C(=O)NC(C(=O)NC(C(=O)NC(CC(=O)NC(C(=O)NC(C(C(=O)NC(CCC(=O)N1)C(=O)O)C)C=CC(=CC(C)C(CC2=CC=CC=C2)OC)C)CCCN=C(N)N)C(=O)O)CCC3=CC=C(C=C3)O)C 1045.20 unknown via CMAUP database
[D-Asp3, (E)-Dhb7]microcystin-Hty 15837270 Click to see CC=C1C(=O)NC(C(=O)NC(C(=O)NC(CC(=O)NC(C(=O)NC(C(C(=O)NC(CCC(=O)N1)C(=O)O)C)C=CC(=CC(C)C(CC2=CC=CC=C2)OC)C)CCCN=C(N)N)C(=O)O)CCC3=CC=C(C=C3)O)C 1045.20 unknown via CMAUP database
[D-Asp3, (Z)-Dhb7]microcystin-LR 21635774 Click to see CC=C1C(=O)NC(C(=O)NC(C(=O)NC(CC(=O)NC(C(=O)NC(C(C(=O)NC(CCC(=O)N1)C(=O)O)C)C=CC(=CC(C)C(CC2=CC=CC=C2)OC)C)CCCN=C(N)N)C(=O)O)CC(C)C)C 981.10 unknown via CMAUP database
[D-Asp3, Dhb7]microcystin-LR 21637043 Click to see 981.10 unknown via CMAUP database
oscillaginin A 46902107 Click to see CC(C)C(C(=O)NC(CCC1=CC=C(C=C1)O)C(=O)O)N(C)C(=O)C(CO)NC(=O)C(C(CCCCCCCCl)N)O 615.20 unknown via CMAUP database
Oscillaginin B 44825956 Click to see 580.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(2,6-Dimethoxy-4-prop-2-enylphenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 15628157 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)CC=C 356.40 unknown https://doi.org/10.1002/JCCS.200700169
2-(4-Hydroxy-2,6-dimethoxyphenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 14237625 Click to see 332.30 unknown https://doi.org/10.1002/JCCS.200700169
4-Allyl-2,6-dimethoxyphenyl glucoside 21636226 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)CC=C 356.40 unknown https://doi.org/10.1002/JCCS.200700169
Leonuriside 14237626 Click to see 332.30 unknown https://doi.org/10.1002/JCCS.200700169
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Acetophenone-2',3',4',5',6'-d5 11457690 Click to see 125.18 unknown via CMAUP database
> Organohalogen compounds / Organoiodides
1-Iodohexadecane 11007 Click to see CCCCCCCCCCCCCCCCI 352.34 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
3-Methyl-2(5H)-furanone 30945 Click to see 98.10 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid 2518 Click to see 180.16 unknown https://doi.org/10.1002/JCCS.200700169
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.1002/JCCS.200700169
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Fraxinol 3047739 Click to see COC1=C(C(=C2C=CC(=O)OC2=C1)OC)O 222.19 unknown https://doi.org/10.1002/JCCS.200700169
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1248/CPB.56.592
> 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.56.592
Chrysin 5281607 Click to see 254.24 unknown https://doi.org/10.1248/CPB.56.592
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1248/CPB.56.592
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown https://doi.org/10.1248/CPB.56.592
Eriodictyol-7-O-glucoside 13254473 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown https://doi.org/10.1248/CPB.56.592
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
5-hydroxy-2-(4-methoxyphenyl)-4-oxo-4H-chromen-7-olate 25202697 Click to see 283.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
(2S,3R,4S,5S,6R)-2-[4-[(E)-2-(3,5-dihydroxy-4-methylphenyl)ethenyl]-2-hydroxyphenoxy]-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol 163186300 Click to see CC1=C(C=C(C=C1O)C=CC2=CC(=C(C=C2)OC3C(C(C(C(O3)COC4C(C(C(CO4)O)O)O)O)O)O)O)O 552.50 unknown https://doi.org/10.1002/JCCS.200700169
2-[4-[2-(3,5-Dihydroxy-4-methylphenyl)ethenyl]-2-hydroxyphenoxy]-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxane-3,4,5-triol 163037289 Click to see 552.50 unknown https://doi.org/10.1002/JCCS.200700169

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