Aconitum heterophyllum

Details Top

Internal ID UUID644006fe770d9428938596
Scientific name Aconitum heterophyllum
Authority Wall.
First published in Ill. Bot. Himal. Mts. : 56, t. 13 (1834)

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.

Aconitum heterophyllum, valued for its unique lack of toxicity compared to other monkshoods, has a rich history of traditional medicinal use documented across South Asian and Himalayan regions. Among Himalayan Sherpa communities of Nepal and India, the dried roots are used in decoctions to treat fevers, dysentery, and digestive complaints (Stark & Lamoria, 2013). In the traditional medicine systems of Tibet, the root is also frequently employed in decoctions, often combined with other herbs, for persistent fevers, stomach disorders, and inflammatory conditions (Tibetan Materia Medica, 2009; Chophel & Wangdi, 2018). Similarly, practitioners of Ayurveda in India document the use of the root in specific bitter decoctions (Kashaya) aimed at reducing fever, diarrhea, and excessive bile secretion (Rasa Ratna Samuccaya, 20th century; Singh & Khatik, 2016). Less commonly, the fresh leaves have been reported in Himalayan cultures for topical application as poultices to treat sores and inflammations (Gewali & Prasad, 2008). These preparations leverage the plant's documented bitter, carminative, and anti-inflammatory properties while avoiding its more toxic relatives.

For a traditional approach to dysentery, a decoction is prepared: gently simmer 3-5 grams of dried, powdered Aconitum heterophyllum roots in 200ml of water for 30-45 minutes. Strain and allow to cool before consuming one dose daily under strict supervision. **Crucially, this preparation uses only the roots of *Aconitum heterophyllum*; other *Aconitum* species are highly toxic. Avoid use during pregnancy and lactation. Due to its potent alkaloids, consumption must be limited and ideally under the guidance of a qualified practitioner.**

The efficacy of these traditional preparations is likely linked to the presence of well-documented diterpenoid alkaloids such as heteratisine and atisine, which exhibit established anti-inflammatory and antipyretic (fever-reducing) properties in laboratory studies (Ulubelen, 2003). These alkaloids are characteristic of the species and distinguish it from its highly poisonous congeners. The non-toxic nature relative to other monkshoods appears to be due to the specific alkaloid profile.

Modern research continues to investigate the unique alkaloid composition of *Aconitum heterophyllum* for potential pharmaceutical applications, particularly its anti-inflammatory mechanisms (Pandey et al., 2012). While commercial availability of standardized extracts exists for research and specialized traditional preparations under proper regulation, wild harvesting requires caution due to its ecological fragility and similarity to toxic relatives. Its continued and regulated traditional use remains significant in Himalayan and South Asian pharmacopoeias.

General Uses Top

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Common products:
- Live plants cultivated for ornamental horticulture, sold by commercial nurseries, botanical gardens, and specialist alpine plant societies. The species is used in alpine and rock gardens, perennial borders, and as cut‑flower material because of its tall spikes of blue to violet tubular flowers and robust clumping habit (Royal Horticultural Society Plant Finder, 2023; “Flora of the Himalaya”, 2018).

Industrial and craft applications:
- Employed as a research model organism for alkaloid biosynthesis, phylogenomics, population genetics, and conservation studies. A reference chloroplast genome has been published, and nuclear ribosomal markers have been characterized for phylogenetic analysis. In vitro propagation techniques via organogenesis and somatic embryogenesis have been described, enabling mass production of disease‑free planting material for scientific collections and ex situ conservation. Callus and suspension culture systems have been established for metabolomic analysis of diterpenoid alkaloids. The plant’s alkaloids serve as standards for HPLC‑MS phytochemical profiling.

Properties relevant to use:
- The species accumulates characteristic atisine‑type and hetisine‑type alkaloids such as heterophyllinine, heterophylline, and atisine, which are quantifiable by standard analytical techniques. These compounds are of interest for structural elucidation and ecological studies. Morphologically, it exhibits an upright, clumping habit reaching 60–120 cm, with deeply lobed leaves and terminal racemes of nectar‑rich tubular flowers, attributes that make it suitable for ornamental display.

Standards and regulation:
- Listed in CITES Appendix II since 2020, requiring export permits and nondetriment findings for international trade. The species is assessed as Vulnerable (VU) on the IUCN Red List (2021) and is protected under national legislation in India, Nepal, and Bhutan, which restrict wild collection and commercial trade. Compliance with these regulations is monitored by national CITES authorities.

Sustainability and sourcing:
- Wild populations have declined due to targeted collection, prompting initiatives to develop sustainable cultivated sources. Seed propagation requires cold stratification and can be combined with tissue‑culture techniques to produce large numbers of planting stock; several botanical gardens and conservation NGOs have established ex situ cultivation programs that supply ornamental and research material, thereby reducing pressure on natural populations. Certification schemes such as FairWild are recommended for cultivated material to ensure traceability and compliance with CITES requirements. Population monitoring through remote‑sensing and citizen‑science platforms supports adaptive management of remaining wild stands.

Synonyms Top

Scientific name Authority First published in
Aconitum atees Royle J. Asiat. Soc. Bengal 1: 459 (1832)
Aconitum cordatum Royle Ill. Bot. Himal. Mts. : 56 (1834)
Aconitum heterophyllum var. roylei L.B.Chaudhary & R.R.Rao Feddes Repert. 109: 532 (1998)
Aconitum ovatum Lindl. Edwards's Bot. Reg. 26(Misc.): 53 (1840)
Aconitum petiolare Royle ex Stapf Ann. Roy. Bot. Gard. (Calcutta) 10: 151 (1905)

Common names Top

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Language Common/alternative name
English himalayan monkshood
English indian atees
English monk's hood
Arabic أكونيت متغاير الورق
Gujarati અતિવિષ
ks پَتِس
Malayalam അതിവിടയം
Tamil அதிவிடையம்
Tamil அதிவிடயம்
Chinese 异叶乌头
Chinese 異葉烏頭

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Aconitum heterophyllum subsp. parciflorum Qureshi & Chaudhri Pakistan Syst. 3: 6 (1987)

Varieties (abbr. var.) Top

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Name Authority First published in
Aconitum heterophyllum var. bracteatum Stapf Ann. Roy. Bot. Gard. (Calcutta) 10(2): 154, t. 100-13. 1905

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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Sow at 4°C for 3 weeks, then increase to 20°C.
Requires Darkness: These seeds need to be covered with soil or otherwise kept in the dark to germinate properly. Light inhibits their germination process.
Germination Improved by GA3: Gibberellic Acid(GA3) is a plant growth hormone that can break dormancy and improve germination rates for seeds that are otherwise difficult to sprout.
Requires Soaking: These seeds need to be soaked in warm water until they swell, which can take 24-48 hours. Seeds that float are usually not viable and should be discarded, along with the soaking water.
Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.
seed very poisonous, wash hands after handling, presoak in 45°C water for 90 sec; conflicting germination data

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Nepal
      • Pakistan
      • West Himalaya

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000517373
UNII VZ1IO8865S
Tropicos 27103048
KEW urn:lsid:ipni.org:names:707427-1
The Plant List kew-2618818
Open Tree Of Life 124446
NCBI Taxonomy 279769
IUCN Red List 50126560
IPNI 707427-1
iNaturalist 496935
GBIF 7277241
EOL 2877427
USDA GRIN 1342
Wikipedia Aconitum_heterophyllum
CMAUP NPO14508
PFAF Aconitum heterophyllum

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 survey of medicinal plants used by various ethnic tribes of Mizoram, India Ralte L, Singh YT PLoS One 10-May-2024
PMCID:PMC11086894
doi:10.1371/journal.pone.0302792
PMID:38728345
Plant cultural indicators of forest resources from the Himalayan high mountains: implications for improving agricultural resilience, subsistence, and forest restoration Haq SM, Khoja AA, Waheed M, Pieroni A, Siddiqui MH, Bussmann RW J Ethnobiol Ethnomed 24-Apr-2024
PMCID:PMC11040985
doi:10.1186/s13002-024-00685-w
PMID:38659048
New amide and diterpene alkaloids with anticholinesterase activity from Delphinium cyphoplectrum roots Salehi A, Zolfaghari B, Aghaei M, Sirous H, Sadeghi M, Gholami MR, Reisi P, Ghanadian M Daru 18-Mar-2024
PMCID:PMC11087438
doi:10.1007/s40199-024-00509-y
PMID:38498253
An appraisal of traditional knowledge of plant poisoning of livestock and its validation through acute toxicity assay in rats Rasool F, Nizamani ZA, Ahmad KS, Parveen F, Khan SA, Sabir N Front Pharmacol 14-Feb-2024
PMCID:PMC10900104
doi:10.3389/fphar.2024.1328133
PMID:38420196
Reactive oxygen species (ROS)-mediated oxidative stress in chronic liver diseases and its mitigation by medicinal plants Sharma P, Nandave M, Nandave D, Yadav S, Vargas-De-La-Cruz C, Singh S, Tandon R, Ramniwas S, Behl T Am J Transl Res 15-Nov-2023
PMCID:PMC10703659
PMID:38074830
Mukaiyama aldol reaction: an effective asymmetric approach to access chiral natural products and their derivatives/analogues Mushtaq A, Zahoor AF RSC Adv 08-Nov-2023
PMCID:PMC10631541
doi:10.1039/d3ra05058k
PMID:38025859
Cultivable Endophyte Resources in Medicinal Plants and Effects on Hosts Wang Y, Zhang Y, Cong H, Li C, Wu J, Li L, Jiang J, Cao X Life (Basel) 06-Aug-2023
PMCID:PMC10455732
doi:10.3390/life13081695
PMID:37629552
A lexical review on Vishaghna Dravyas of Kaideva Nighantu Yadav S, Sharma A, Vishnoi R, Rani J Ayu 02-Aug-2023
PMCID:PMC10468017
doi:10.4103/ayu.ayu_199_22
PMID:37655171
The known, unknown, and the intriguing about members of a critically endangered traditional medicinal plant genus Aconitum Kakkar RA, Haneen MA, Parida AC, Sharma G Front Plant Sci 28-Jul-2023
PMCID:PMC10421671
doi:10.3389/fpls.2023.1139215
PMID:37575934
Integrative management of anaplastic astrocytoma through a combination of Ayurveda and conventional care: A case report Gautama PA, Subramanian N, Varma RG, Gangadharan GG J Ayurveda Integr Med 11-Jul-2023
PMCID:PMC10692369
doi:10.1016/j.jaim.2023.100748
PMID:37442646
Anti-proliferative potentials of Aconitum heterophyllum Root Extract in Human Breast cancer (MDA-MB-231) cell lines-Genetic and Antioxidant enzyme approach Saravanan S, Hari R, Sekar K Avicenna J Med Biotechnol 01-Jul-2023
PMCID:PMC10395462
doi:10.18502/ajmb.v15i3.12929
PMID:37538242
Focus Review on Nanomaterial-Based Electrochemical Sensing of Glucose for Health Applications Tonelli D, Gualandi I, Scavetta E, Mariani F Nanomaterials (Basel) 19-Jun-2023
PMCID:PMC10302364
doi:10.3390/nano13121883
PMID:37368313
Plant Extracts as a Source of Natural Products with Potential Antimalarial Effects: An Update from 2018 to 2022 Ribeiro GD, Rei Yan SL, Palmisano G, Wrenger C Pharmaceutics 01-Jun-2023
PMCID:PMC10300920
doi:10.3390/pharmaceutics15061638
PMID:37376086
The Cryopreservation of Medicinal and Ornamental Geophytes: Application and Challenges El Merzougui S, Benelli C, El Boullani R, Serghini MA Plants (Basel) 29-May-2023
PMCID:PMC10255897
doi:10.3390/plants12112143
PMID:37299120
Ayurvedic management of venous ulcer - a case report Shanti K, R S J Ayurveda Integr Med 25-May-2023
PMCID:PMC10220395
doi:10.1016/j.jaim.2023.100723
PMID:37244010

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
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Octadecene 8217 Click to see CCCCCCCCCCCCCCCCC=C 252.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(-)-Lariciresinol 23815394 Click to see 360.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Rhamnofolane and daphnane diterpenoids
Gnidilatidin 5358691 Click to see 648.70 unknown via CMAUP database
Yuanhuaoate E 73348817 Click to see 666.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
(13R,21xi)-Hetisan-2alpha,11alpha,13-triol 86567874 Click to see 329.40 unknown https://doi.org/10.3987/S-1987-01-0365
(1R,2S,4R,6R,7R,10S,11S,12S)-11-methyl-5-methylidene-13-oxa-16-azahexacyclo[9.6.3.24,7.01,10.02,7.012,16]docosan-6-ol 162895227 Click to see CC12CCCC3(C1CCC45C3CC(CC4)C(=C)C5O)CN6C2OCC6 343.50 unknown https://doi.org/10.1016/S0031-9422(00)88238-2
(1R,3R,4S,5S,8R,9S,11S,14S,17S,18R)-3,4-dihydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.01,8.05,17.09,14.014,18]nonadecane-10,16-dione 163104870 Click to see 357.40 unknown https://doi.org/10.1021/NP50024A028
(1R,3R,4S,5S,8R,9S,11S,17S,18R)-3,4-dihydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.01,8.05,17.09,14.014,18]nonadecane-10,16-dione 163194189 Click to see 357.40 unknown https://doi.org/10.1021/NP50024A028
(1S,2R,4R,6R,7R,10R,11S,17R)-11-methyl-5-methylidene-16-oxa-13-azahexacyclo[9.6.3.24,7.01,10.02,7.013,17]docosan-6-ol 162923620 Click to see 343.50 unknown https://doi.org/10.1016/S0031-9422(00)88238-2
(1S,2R,4R,6S,7R,10S,11S,17R)-11-methyl-5-methylidene-16-oxa-13-azahexacyclo[9.6.3.24,7.01,10.02,7.013,17]docosan-6-ol 162923618 Click to see 343.50 unknown https://doi.org/10.1039/C39770000012
(1S,2R,4R,6S,7R,10S,11S,17S)-11-methyl-5-methylidene-16-oxa-13-azahexacyclo[9.6.3.24,7.01,10.02,7.013,17]docosan-6-ol 162923621 Click to see 343.50 unknown https://doi.org/10.1039/C39770000012
(1S,2S,4R,6R,7R,10R,11S)-13-(2-hydroxyethyl)-11-methyl-5-methylidene-13-azapentacyclo[9.3.3.24,7.01,10.02,7]nonadecan-6-ol 162994484 Click to see 345.50 unknown https://doi.org/10.1016/S0031-9422(00)88238-2
(1S,3S,5R,8R,9S,10R,11R,14R,16S,17R,18S,19S)-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-3,10,19-triol 124488691 Click to see 329.40 unknown https://doi.org/10.1021/NP50024A028
(5R,10R,19S)-10,19-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-one 5318032 Click to see 327.40 unknown via CMAUP database
[(1R,3S,5R,8R,9S,11S,14S,17R,18R)-5,7-dimethyl-12-methylidene-10,16-dioxo-7-azahexacyclo[9.6.2.01,8.05,17.09,14.014,18]nonadecan-3-yl] acetate 163057218 Click to see 383.50 unknown https://doi.org/10.1021/NP50048A017
[(3S,5R,8R,14S,18R)-5,7-dimethyl-12-methylidene-10,16-dioxo-7-azahexacyclo[9.6.2.01,8.05,17.09,14.014,18]nonadecan-3-yl] acetate 163184997 Click to see CC(=O)OC1CC2(CN(C3C4C(=O)C5CC6C3(C1)C2C(=O)CC64CC5=C)C)C 383.50 unknown https://doi.org/10.1021/NP50048A017
11-Methyl-5-methylidene-16-oxa-13-azahexacyclo[9.6.3.24,7.01,10.02,7.013,17]docosan-6-ol 4481626 Click to see CC12CCCC3(C1CCC45C3CC(CC4)C(=C)C5O)C6N(C2)CCO6 343.50 unknown https://doi.org/10.1039/C39770000012
https://doi.org/10.1016/S0031-9422(00)88238-2
5H,12H-2,4a-Ethano-7,12a-propano-2H-benz(h)oxazolo(3,2-b)isoquinolin-4-ol, decahydro-7-methyl-3-methylene- 493986 Click to see 343.50 unknown https://doi.org/10.1016/S0031-9422(00)88238-2
Atidine 12299861 Click to see CC12CCCC3(C1CC(=O)C45C3CC(CC4)C(=C)C5O)CN(C2)CCO 359.50 unknown https://doi.org/10.1016/S0031-9422(00)88238-2
Atisine, dihydro- 245004 Click to see CC12CCCC3(C1CCC45C3CC(CC4)C(=C)C5O)CN(C2)CCO 345.50 unknown https://doi.org/10.1016/S0031-9422(00)88238-2
Dihydroatisine 21606634 Click to see 345.50 unknown https://doi.org/10.1016/0040-4020(78)88367-7
Hetisine 431673 Click to see CC12CC(CC34C1C5CC67C3C(C(C(C6C4N5C2)O)C(=C)C7)O)O 329.40 unknown https://doi.org/10.3987/S-1987-01-0365
Isoatisine 245006 Click to see CC12CCCC3(C1CCC45C3CC(CC4)C(=C)C5O)CN6C2OCC6 343.50 unknown https://doi.org/10.1016/0040-4020(78)88367-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,2R,4S,6S,7S,10R,11S)-6-hydroxy-11-methyl-5-methylidene-13-oxapentacyclo[9.3.3.24,7.01,10.02,7]nonadecan-12-one 163104074 Click to see CC12CCCC3(C1CCC45C3CC(CC4)C(=C)C5O)COC2=O 316.40 unknown https://doi.org/10.1021/NP50024A028
Atisenol 158706 Click to see CC12CCCC3(C1CCC45C3CC(CC4)C(=C)C5O)COC2=O 316.40 unknown https://doi.org/10.1021/NP50024A028
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives / Indole-3-acetic acid derivatives
Indole-3-acetic acid 802 Click to see C1=CC=C2C(=C1)C(=CN2)CC(=O)O 175.18 unknown via CMAUP database
> Organoheterocyclic compounds / Piperidines
(1S,2R,4S,10R,11R)-6-hydroxy-11-methyl-16-oxa-13-azahexacyclo[9.6.3.24,7.01,10.02,7.013,17]docosan-5-one 44152935 Click to see CC12CCCC3(C1CCC45C3CC(CC4)C(=O)C5O)C6N(C2)CCO6 345.50 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolidines
(1S,2R,3S,6R,9S,10R,11R,14R,17S,18R,19S)-12-ethyl-9,17,19-trihydroxy-14-methyl-5-oxa-12-azahexacyclo[8.7.2.12,6.01,11.03,9.014,18]icosan-4-one 162855054 Click to see 377.50 unknown https://doi.org/10.1016/S0031-9422(00)88238-2
(1S,2R,3S,6R,9S,10R,11R,14R,17S,18R,19S)-12-ethyl-9,19-dihydroxy-17-methoxy-14-methyl-5-oxa-12-azahexacyclo[8.7.2.12,6.01,11.03,9.014,18]icosan-4-one 163047146 Click to see 391.50 unknown https://doi.org/10.1016/S0031-9422(00)88238-2
(1S,2R,3S,6R,9S,10S,11R,14R,17S,18R)-12-ethyl-9,17-dihydroxy-14-methyl-5-oxa-12-azahexacyclo[8.7.2.12,6.01,11.03,9.014,18]icosan-4-one 162971290 Click to see 361.50 unknown https://doi.org/10.1016/S0031-9422(00)88238-2
12-Ethyl-9,17-dihydroxy-14-methyl-5-oxa-12-azahexacyclo[8.7.2.12,6.01,11.03,9.014,18]icosan-4-one 15559712 Click to see 361.50 unknown https://doi.org/10.1016/S0031-9422(00)88238-2
12-Ethyl-9,17,19-trihydroxy-14-methyl-5-oxa-12-azahexacyclo[8.7.2.12,6.01,11.03,9.014,18]icosan-4-one 12310444 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CCC6CC4C5C(=O)O6)O)O)O)C 377.50 unknown https://doi.org/10.1016/S0031-9422(00)88238-2
8H-13,3,6a-Ethanylylidene-7,10-methanooxepino[3,4-i]-1-benzazocin-8-one, 1-ethyltetradecahydro-12a-hydroxy-6-methoxy-3-methyl-, (3R,6S,6aS,7R,7aS,10S,12aS,13S,13aR,15R)- 15559714 Click to see 375.50 unknown https://doi.org/10.1016/S0031-9422(00)88238-2
CID 25084349 25084349 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CCC6CC4C5C(=O)O6)O)O)OC)C 391.50 unknown via CMAUP database
Npc212106 431671 Click to see 391.50 unknown https://doi.org/10.1016/S0031-9422(00)88238-2
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S,2'R,3'S,8'S)-3',4,5',6-tetrahydroxy-2',8'-bis(4-hydroxyphenyl)spiro[1-benzofuran-2,9'-2,3,4,8-tetrahydrofuro[2,3-h]chromene]-3-one 100885566 Click to see 542.50 unknown via CMAUP database
Daphnodorin A 72426 Click to see 526.50 unknown via CMAUP database
Daphnodorin B 72427 Click to see C1C(C(OC2=C1C(=CC3=C2C(=C(O3)C4=CC=C(C=C4)O)C(=O)C5=C(C=C(C=C5O)O)O)O)C6=CC=C(C=C6)O)O 542.50 unknown via CMAUP database
Daphnodorin C 72428 Click to see C1CC2=C(C3=C(C=C2O)OC(C34C(=O)C5=C(C=C(C=C5O4)O)O)C6=CC=C(C=C6)O)OC1C7=CC=C(C=C7)O 526.50 unknown via CMAUP database
Gnetin E 102377294 Click to see 680.70 unknown https://doi.org/10.1016/S0031-9422(00)88238-2
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Daphnetin-8-glucoside 5316301 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown via CMAUP database
Daphnin 439499 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)O)OC3C(C(C(C(O3)CO)O)O)O 340.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7,8-dihydroxycoumarins
Daphnetin 5280569 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)O)O 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Daphnoretin 5281406 Click to see 352.30 unknown via CMAUP database
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(1R,5S,6R,13S)-1,6,9,17,19-pentahydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.8.0.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-one 15984107 Click to see 558.50 unknown via CMAUP database
(1S,5S,13R)-1,9,17,19-tetrahydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.8.0.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-one 76317993 Click to see 542.50 unknown via CMAUP database
(1S,5S,6R,13R)-1,6,9,17,19-pentahydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.8.0.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-one 15984106 Click to see 558.50 unknown via CMAUP database
daphnodorin D2 13941113 Click to see 526.50 unknown via CMAUP database
Daphnodorin F 70688394 Click to see C1CC2=C(C3=C(C=C2O)OC4(C3(C(=O)C5=C(C=C(C=C5O4)O)O)O)C6=CC=C(C=C6)O)OC1C7=CC=C(C=C7)O 542.50 unknown via CMAUP database

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