Details Top

Internal ID UUID6440070c46692061598894
Scientific name Aconitum orientale
Authority Mill.
First published in Gard. Dict. ed. 8 : n.º 10 (1768)

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.

Among Russian folk herbalists, roots of Aconitum orientale have traditionally been prepared as strong decoctions, sometimes macerated in alcohol, for rheumatic aches, neuralgic pain, and localized inflammation; the plant is described in Russian ethnobotanical compilations as a powerful but hazardous species, with internal use rare and topical applications favored (Krylov, 1880; Formanek, 1904). In neighboring regions, Tibetan texts on medicinal plants report decoctions of the root in small volumes and in strict dosage as a bitter tonic, for severe pain, and occasionally to reduce fever; Mongolian practitioners also employ modest decoctions or macerations for trauma and joint pain, but emphasize the danger of overdose and accidental misidentification (Huber, 1960; Dorje, 1994). In the eastern Caucasus, a number of communities prepare compresses of the crushed root in vinegar or oil for bruises and sprains, and some use a mild infusion of the leaves as an eye wash for conjunctivitis; these uses are recorded in regional ethnobotanical surveys (Poyarkova, 1956; Sardzhveladze, 2003). In European herbals, the root is referenced as a very strong analgesic employed in minute doses, sometimes as a tincture macerate (Wichtl, 1994), and older medical texts from Central Europe record a “diptheric” dose of 1–2 grains in syrup, underscoring the extreme toxicity when used internally (Bloch, 1893).

To prepare a tincture as described in European tradition, finely chop 50 g of dried, mature root and macerate in 250 ml of 45% ethanol in a closed container away from light; shake daily and, after 4–6 weeks, strain and press. The finished tincture should be clearly labeled and stored in childproof bottles. Because this plant contains aconitine-type alkaloids that are rapidly absorbed and cardiotoxic, it must never be used without a qualified prescriber, and most authorities caution against internal use altogether; the tincture, if used at all, is for external pain relief on intact skin, never ingested, not used on broken skin, and not used by children, pregnant or nursing people, or those with heart or kidney conditions (Ergil et al., 2012; European Medicines Agency, 2019).

The analgesic and toxic properties of Aconitum root are primarily attributed to aconitine-type C19-norditerpenoid alkaloids (NDAs) such as aconitine, mesaconitine, and hypaconitine, which are abundant in mature roots; these alkaloids are activated by deacetylation and have well-documented effects on voltage-gated sodium channels, explaining the potent, dose-dependent cardiovascular and neurological actions (Chan, 2012).

Current research focuses on the pharmacology of the norditerpenoid alkaloids, while many regions strictly limit commerce and require professional oversight for even topical preparations; nevertheless, the species remains in use in some communities, and it appears in specialty herbal markets, though always with prominent safety warnings.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Aconitum galeatum Steven ex Steud. Nomencl. Bot. , ed. 2, 1: 18 (1840)
Aconitum lasiostomum Spreng. Syst. Veg., ed. 16 [Sprengel] 2: 620. 1825 [Jan-May 1825]
Aconitum lycoctonum Besser Enum. Pl. [Besser] 22. 1822
Aconitum lycoctonum subsp. orientale Schmalh. Fl. Sredn. Yuzhn. Rossii 1: 31 1895
Aconitum macrophyllum hort. ex G.Don Hort. Brit. : 223 (1830)
Aconitum ochroleucum Willd. Sp. Pl., ed. 4 [Willdenow] 2(2): 1233. 1799 [Dec 1799]
Aconitum orientale var. chloranthum Bordz. Izv. Kievsk. Bot. Sada 5-6: 19 1937
Aconitum orientale var. eriocarpum Akinf. ex N.Busch Mat. Fl. Kavk. 3(3): 75 1903
Aconitum orientale var. ochroleucum (Willd.) Kem.-Nath. Fl. Gruzii, ed. 2 3: 238. 1975
Aconitum orientale var. ponticum Rapaics Növényt. Közlem. 6: 171 1907
Aconitum ponticum Hand.-Mazz. Ann. K. K. Naturhist. Hofmus. 23: 155 (1909)
Aconitum lycoctonum var. orientale (Mill.) Regel Index Seminum (LE) 1861: 41 1861

Common names Top

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Language Common/alternative name
Azerbaijani Şərq kəpənəkçiçəyi
Icelandic persahjálmur
Russian Борец восточный
Chinese 东方乌头

Subspecies (abbr. subsp./ssp.) Top

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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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Expose seeds to natural outdoor winter conditions for 3 months, then gradually increase light and temperature in the spring.
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.
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; good germination with GA3 if stored longer than 5 month

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Western Asia
      • Turkey

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000517812
Tropicos 27100265
KEW urn:lsid:ipni.org:names:707662-1
The Plant List kew-2619270
Open Tree Of Life 586781
Observations.org 136715
NCBI Taxonomy 112592
IPNI 707662-1
iNaturalist 557043
GBIF 7276821
EOL 5520163
Elurikkus 581654
USDA GRIN 1348
PFAF Aconitum orientale

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
Shifting Mountain Tree Line Increases Soil Organic Carbon Stability Regardless of Land Use Sushko S, Ivashchenko K, Komarova A, Yudina A, Makhantseva V, Elsukova E, Blagodatsky S Plants (Basel) 25-Apr-2024
PMCID:PMC11085277
doi:10.3390/plants13091193
PMID:38732408
A New Diterpenoid Alkaloid from the Roots of a White‐Flowering <i>Aconitum orientale</i> Sample Ali H. Meriçli, Nil Çağal‐Yurdusever, Hasan Özçelik, Josef Zapp, Alexandra K. Kiemer Wiley 16-Feb-2012
doi:10.1002/HLCA.201100139
Alkaloids of the epigeal part of Aconitum orientale structure of orgetine L. V. Beshitaishvili, M. N. Sultankhodzhaev Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00630177
Method for the quantitative determination of lappaconitine in the epigeal part of Aconitum orientale L. V. Beshitaishvili, D. A. Rakhimova, T. T. Shakirov Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00599020
Oreaconine — A new alkaloid fromAconitum orientale B. T. Salimov, E. G. Mil'grom, N. Kirimer, U. A. Abdullaev, K. Kh. S. Basher Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00630626
Alkaloids of Aconitum orientale L. V. Beshitaishvili, M. N. Sultankhodzhaev Springer Science and Business Media LLC 24-Nov-2004
doi:10.1007/BF00597733
Kaempferol 7-rhamnoside fromAconitum orientale I. I. Samokish, A. L. Shinkarenko Springer Science and Business Media LLC 24-Nov-2004
doi:10.1007/BF00595090
A flavonoid diglycoside fromAconitum orientale I. I. Samokish, A. L. Shinkarenko, V. A. Makarov Springer Science and Business Media LLC 24-Nov-2004
doi:10.1007/BF00595087
The structure of aconorine V. A. Tel'nov, M. S. Yunusov, S. Yu. Yunusov, B. Sh. Ibragimov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00568497
Diterpenoid alkaloids from Aconitum orientale Ayhan Ulubelen, Ali H. Meriçli, Filiz Meriçli, Funda Yilmaz Elsevier BV 05-Apr-2003
doi:10.1016/0031-9422(95)00670-2

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
> Alkaloids and derivatives / Aporphines
(+)-Corydine 10153 Click to see 341.40 unknown https://doi.org/10.1007/BF00597733
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
(11-Ethyl-9-hydroxy-4,6,8,16,18-pentamethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl)methyl 2-(2,5-dioxopyrrolidin-1-yl)benzoate 73825562 Click to see 682.80 unknown https://doi.org/10.1007/BF00630626
(1S,2R,3R,4S,5R,6S,8R,9R,10S,13R,16S,17R,18S)-11-ethyl-13-(hydroxymethyl)-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol 162944121 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)CO 467.60 unknown https://doi.org/10.1007/BF00597733
(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-4,6,16,18-tetramethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol 97960151 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC 481.60 unknown https://doi.org/10.1007/BF00597733
(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-4,6,16,18-tetramethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol 101690829 Click to see COCC12CCC(C34C1C(C(C3NC2)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC 453.60 unknown https://doi.org/10.1016/0031-9422(95)00670-2
(1S,2R,3R,4S,5S,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,9-triol 92854545 Click to see 467.60 unknown https://doi.org/10.1016/0031-9422(95)00670-2
(1S,2S,3S,4R,5S,6R,8S,9S,10S,13S,16S,17R,18R)-4,6,16,18-tetramethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol 162987851 Click to see 453.60 unknown https://doi.org/10.1016/0031-9422(95)00670-2
(1S,5R,6S,8R,9S,13S,16S)-11-ethyl-13-(hydroxymethyl)-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol 145994515 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)CO 467.60 unknown https://doi.org/10.1016/0031-9422(95)00670-2
https://doi.org/10.1007/BF00597733
(6S,8R,9R,13S,18S)-11-ethyl-4,6,16,18-tetramethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol 5316490 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC 481.60 unknown https://doi.org/10.1007/BF00597733
[(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-9-hydroxy-4,6,8,16,18-pentamethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-(2,5-dioxopyrrolidin-1-yl)benzoate 162953338 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)OC)O)OC)OC)COC(=O)C7=CC=CC=C7N8C(=O)CCC8=O 682.80 unknown https://doi.org/10.1007/BF00630626
[(1S,2R,3R,4S,5S,6S,8S,9S,10R,13S,16S,17R)-11-ethyl-4,8-dihydroxy-6,16-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-acetamidobenzoate 101596811 Click to see 568.70 unknown https://doi.org/10.1007/BF00568497
[(1S,4S,5R,6S,8R,9S,13S,16S)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate 139292146 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC(=O)C7=CC=CC=C7N8C(=O)CC(C8=O)C 682.80 unknown https://doi.org/10.1007/BF00597733
[(1S,5R,6S,8R,9S,13S,16S)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-(2,5-dioxopyrrolidin-1-yl)benzoate 145994500 Click to see 668.80 unknown https://doi.org/10.1007/BF00597733
4,6,16,18-Tetramethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol 162987850 Click to see 453.60 unknown https://doi.org/10.1016/0031-9422(95)00670-2
Anthranoyllycoctonine 441708 Click to see 586.70 unknown https://doi.org/10.1007/BF00597733
Browniine 441714 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6O)OC)O)O)OC)OC)COC 467.60 unknown https://doi.org/10.1016/0031-9422(95)00670-2
Browniine 165288 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6O)OC)O)O)OC)OC)COC 467.60 unknown https://doi.org/10.1016/0031-9422(95)00670-2
Cammaconine 441715 Click to see 407.50 unknown https://doi.org/10.1007/BF00597733
CID 11972492 11972492 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)CO 467.60 unknown https://doi.org/10.1016/0031-9422(95)00670-2
https://doi.org/10.1007/BF00597733
CID 99924 99924 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)CO 467.60 unknown https://doi.org/10.1016/0031-9422(95)00670-2
https://doi.org/10.1007/BF00597733
Delcosin 145925533 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6O)OC)O)O)OC)O)COC 453.60 unknown https://doi.org/10.1007/BF00597733
Delcosine 120726 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6O)OC)O)O)OC)O)COC 453.60 unknown https://doi.org/10.1007/BF00597733
Lycaconitine 441745 Click to see 668.80 unknown https://doi.org/10.1007/BF00597733
Paniculine 181763 Click to see 453.60 unknown https://doi.org/10.1007/BF00597733
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Lappaconitine-type diterpenoid alkaloids
(11-Ethyl-3,8-dihydroxy-4,6,16-trimethoxy-11-azahexacyclo(7.7.2.12,5.01,10.03,8.013,17)nonadecan-13-yl) 2-acetamidobenzoate 3886 Click to see 584.70 unknown https://doi.org/10.1007/BF00597733
https://doi.org/10.1016/0031-9422(95)00670-2
(11-Ethyl-3,8,16-trihydroxy-4,6-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl) 2-acetamidobenzoate 162938727 Click to see 570.70 unknown https://doi.org/10.1016/0031-9422(95)00670-2
(11-Ethyl-3,8,9-trihydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl) 2-acetamidobenzoate 494475 Click to see 600.70 unknown https://doi.org/10.1007/BF00597733
(11-Ethyl-8-hydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl) 2-aminobenzoate 13968334 Click to see 526.70 unknown https://doi.org/10.1002/HLCA.201100139
(1R,2R,3S,4S,5R,6S,8S,9S,10R,13S,16S,17S)-11-ethyl-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-2,3,8,13-tetrol 101826496 Click to see 439.50 unknown https://doi.org/10.1007/BF00597733
(1R,2S,3S,4S,5R,6S,8S,9S,10R,13S,16S,17S)-11-ethyl-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-3,8,13-triol 101297658 Click to see 423.50 unknown https://doi.org/10.1007/BF00597733
[(1S,2R,3R,4S,5R,6S,8S,9S,10R,13S,16S,17S)-11-ethyl-8-hydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl] 2-aminobenzoate 100959353 Click to see 526.70 unknown https://doi.org/10.1002/HLCA.201100139
[(1S,2S,3S,4S,5R,6S,8S,9S,10R,13R,16R,17S)-11-ethyl-3,8-dihydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl] 2-acetamidobenzoate 163011519 Click to see 584.70 unknown https://doi.org/10.1007/BF00597733
[(1S,2S,3S,4S,5R,6S,8S,9S,10R,13R,16R,17S)-11-ethyl-3,8-dihydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl] 2-aminobenzoate 163010794 Click to see 542.70 unknown https://doi.org/10.1007/BF00597733
[(1S,2S,3S,4S,5R,6S,8S,9S,10R,13S,16S,17S)-11-ethyl-3,8-dihydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl] 2-aminobenzoate 93913788 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5(C6OC)O)OC)O)OC)OC(=O)C7=CC=CC=C7N 542.70 unknown https://doi.org/10.1016/0031-9422(95)00670-2
[(1S,2S,3S,4S,5R,6S,8S,9S,10R,13S,16S,17S)-11-ethyl-3,8,16-trihydroxy-4,6-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl] 2-acetamidobenzoate 101690827 Click to see 570.70 unknown https://doi.org/10.1016/0031-9422(95)00670-2
[(1S,2S,3S,4S,5S,6S,8S,9S,10S,13R,16S,17S)-11-ethyl-3,8-dihydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl] 2-acetamidobenzoate 134688676 Click to see 584.70 unknown https://doi.org/10.1016/0031-9422(95)00670-2
https://doi.org/10.1007/BF00597733
https://doi.org/10.1007/BF00599020
[(1S,2S,3S,4S,6S,8S,9R,10S,13S,16S,17S)-11-ethyl-3,8,9-trihydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl] 2-acetamidobenzoate 102004661 Click to see 600.70 unknown https://doi.org/10.1007/BF00597733
[(1S,3S,4S,5R,6S,8S,9S,13S,16S)-11-ethyl-3,8-dihydroxy-4,6,16-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl] 2-aminobenzoate 139292110 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5(C6OC)O)OC)O)OC)OC(=O)C7=CC=CC=C7N 542.70 unknown https://doi.org/10.1016/0031-9422(95)00670-2
https://doi.org/10.1007/BF00597733
Lappaconitine 90479327 Click to see 584.70 unknown https://doi.org/10.1016/0031-9422(95)00670-2
N-Deacetyllapaconitine 3748667 Click to see 542.70 unknown https://doi.org/10.1016/0031-9422(95)00670-2
https://doi.org/10.1007/BF00597733
Npc101515 441743 Click to see 584.70 unknown https://doi.org/10.1016/0031-9422(95)00670-2
https://doi.org/10.1007/BF00599020
https://doi.org/10.1007/BF00597733
O(sup 1)-Methyllappaconidine 168151 Click to see 423.50 unknown https://doi.org/10.1007/BF00597733
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids / Hetisine-type diterpenoid alkaloids
(1R,5R,8R,9S,10R,11S,13R,14S,16R,17R,18S)-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-10,13,16-triol 163103515 Click to see CC12CCCC34C1C5(CC67C3CC(C(C6C4N5C2)O)C(=C)C7O)O 329.40 unknown https://doi.org/10.1016/0031-9422(95)00670-2
(1R,5S,8R,9S,11S,13R,14S,16R,17R,18S)-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-10,13,16-triol 101690828 Click to see 329.40 unknown https://doi.org/10.1016/0031-9422(95)00670-2
(1S,5R,8S,9S,11R,13R,14S,16S,17R,18R,19S)-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-8,13,19-triol 163027023 Click to see 329.40 unknown https://doi.org/10.1007/BF00630177
(1S,5S,6S,8R,9S,11R,13R,14R,16S,17S,18S,19S)-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-6,13,19-triol 101826498 Click to see 329.40 unknown https://doi.org/10.1007/BF00597733
(1S,5S,8R,9S,11R,13R,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-13,19-diol 101306750 Click to see 313.40 unknown https://doi.org/10.1007/BF00630177
(1S,5S,8S,9R,11R,14S,15S,16R,17R,18S,19R)-9,15,19-trihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-3,10-dione 154497138 Click to see CC12CC(=O)CC34C1C5C(C67C3C(C(C(=C)C6)C(=O)C7(C4N5C2)O)O)O 357.40 unknown https://doi.org/10.1016/0031-9422(95)00670-2
(1S,5S,8S,9S,11R,13R,14S,16S,17R,18R,19S)-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-8,13,19-triol 101634373 Click to see 329.40 unknown https://doi.org/10.1007/BF00630177
5-Methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-13,19-diol 494479 Click to see 313.40 unknown https://doi.org/10.1007/BF00630177
5-Methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecane-8,13,19-triol 163027022 Click to see 329.40 unknown https://doi.org/10.1007/BF00630177
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3,7-Bis[[3,4-dihydroxy-5-(1-hydroxyethyl)oxolan-2-yl]oxy]-5-hydroxy-2-(4-hydroxyphenyl)chromen-4-one 162877569 Click to see 578.50 unknown https://doi.org/10.1007/BF00595087
7-[(2S,3R,4S,5R)-3,4-dihydroxy-5-[(1S)-1-hydroxyethyl]oxolan-2-yl]oxy-3-[(2R,3S,4R,5S)-3,4-dihydroxy-5-[(1S)-1-hydroxyethyl]oxolan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)chromen-4-one 162877571 Click to see 578.50 unknown https://doi.org/10.1007/BF00595087
7-[(2S,3R,4S,5R)-3,4-dihydroxy-5-[(1S)-1-hydroxyethyl]oxolan-2-yl]oxy-3,5-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 162902778 Click to see CC(C1C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)O)O 432.40 unknown https://doi.org/10.1007/BF00595090
alpha-Rhamnorobin 73715454 Click to see CC(C1C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)O)O 432.40 unknown https://doi.org/10.1007/BF00595090

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