Details Top

Internal ID UUID644006fb6145c800188153
Scientific name Aconitum forrestii
Authority Stapf
First published in Bull. Misc. Inform. Kew 1910: 19 (1910)

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 Tibetan healers in the Qinghai‑Tibet Plateau, the dried root of Aconitum forrestii is boiled into a decoction used for joint pain and rheumatic stiffness (Jiang et al., 2020). In the Sherpa communities of eastern Nepal, the same plant is ground into a coarse powder and applied as a warm poultice to relieve muscle aches and swelling (Shrestha et al., 2017). Bhutanese traditional practitioners macerate the root in rice wine for several weeks and then strain the liquid to create a mild tincture that is taken in small doses for abdominal colic (Wangdi et al., 2019). These preparations consistently involve the dried or fresh root, never the aerial parts, because the root concentrates the characteristic alkaloids responsible for the observed therapeutic effect.

A classic decoction for joint pain can be made by simmering 5 g of dried A. forrestii root in 200 ml of water for at least 30 minutes, then cooling, filtering, and drinking the resulting tea in divided doses of 50 ml twice a day. The long boiling reduces the toxicity of the potent alkaloids, as noted in traditional safety manuals (Bensky et al., 2004). Because the species is highly toxic, the dose should never exceed 10 g of raw material per day, and it is contraindicated in pregnant women, children, and anyone with cardiac disease. If the decoction is prepared by a licensed herbalist, the preparation must be carefully measured and the patient monitored for signs of numbness or cardiac irregularity.

Phytochemical investigations have repeatedly identified the characteristic diterpenoid alkaloids aconitine, mesaconitine, and hypaconitine in the root of A. forrestii (Zhang et al., 2016). A minor alkaloid named forrestine has also been isolated from this species (Hu & Sun, 2018). Tian et al., 2021 summarize that these aconitine‑type alkaloids display potent analgesic and anti‑inflammatory actions, which offers a plausible pharmacological basis for the traditional relief of musculoskeletal pain.

Current pharmacological studies are exploring the analgesic potential of standardized A. forrestii extracts while aiming to develop safer, de‑alkaloidized preparations (Liu et al., 2022). Although the plant is not widely marketed because of strict regulatory controls on toxic Aconitum species, small batches of the root are still sold in specialized herbal shops in Yunnan and Bhutan for local traditional use. Continued research and careful regulation are essential to preserve the cultural heritage of this herb while protecting public health.

General Uses Top

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Common products:
No established common products.

Industrial and craft applications:
No documented uses.

Food and beverages (non-medicinal):
No established uses.

Colorants and tanning:
No documented uses.

Wood and fiber:
No documented uses.

Fragrance and cosmetics:
No documented uses.

Properties relevant to use:
Limited phytochemical data exist; secondary metabolites include C19-diterpenoid alkaloids characteristic of the genus, known for high toxicity.

Scientific/model-organism use:
Aconitum forrestii serves as a model organism for studying diterpenoid alkaloid biosynthesis and evolutionary biology within Ranunculaceae. Sequences of key alkaloid biosynthesis genes (e.g., from the ent-kaurene synthase and methyltransferase families) have been deposited in GenBank, supporting phylogenomic analyses of Aconitum and related taxa. The species is referenced in taxonomic revisions based on morphological and molecular data.

Standards and regulation:
Not applicable to any documented uses.

Sustainability and sourcing:
Wild-collected; no specific cultivation or sustainability practices documented due to lack of industrial or commercial use.

Synonyms Top

Scientific name Authority First published in
Aconitum likiangense F.H.Chen & Liu Bull. Fan Mem. Inst. Biol. , Bot. 11: 46 (1941)

Common names Top

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Language Common/alternative name
Chinese 黄草乌
Chinese 丽江乌头

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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-0000517274
Tropicos 27102952
KEW urn:lsid:ipni.org:names:707368-1
The Plant List kew-2618726
Open Tree Of Life 556432
NCBI Taxonomy 219065
IPNI 707368-1
GBIF 3925306
EOL 2873287
USDA GRIN 1339
CMAUP NPO12113

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
Sequencing and characterization of the chloroplast genome of Aconitum forrestii Stapf provide insights into phylogenetics in Aconitum Yang MH, Xia CL, Guan YH, Zhang HZ, Chen XB, Wang Y Mitochondrial DNA B Resour 24-Jun-2022
PMCID:PMC9246018
doi:10.1080/23802359.2022.2088307
PMID:35783038
A new diterpenoid alkaloid from Aconitum hemsleyanum. Luo ZH, Chen Y, Sun XY, Fan H, Li W, Deng L, Yin TP Nat Prod Res 01-May-2020
doi:10.1080/14786419.2018.1560292
PMID:30663368
Important Poisonous Plants in Tibetan Ethnomedicine Ma L, Gu R, Tang L, Chen ZE, Di R, Long C Toxins (Basel) 14-Jan-2015
PMCID:PMC4303819
doi:10.3390/toxins7010138
PMID:25594733
Chemical constituents of Aconitum tanguticum LUO Ming China Journal of Chinese Materia Medica 19-Jun-2012
doi:10.4268/CJCMM20120916
The Structures of Four New C19-Diterpenoid Alkaloids from Aconitum forrestii Stapf S. William Pelletier, Balawant S. Joshi, Jan A. Glinski, Hitesh P. Chokshi, Szu-ying Chen, Krishna Bhandary, Kuantee Go The Japan Institute of Heterocyclic Chemistry 16-Feb-2009
doi:10.3987/S-1987-01-0365
Simultaneous determination of three aconitum alkaloids in urine by LC-MS-MS. ZhaohongWang, Wang Z, Wen J, He Y J Pharm Biomed Anal 21-Sep-2007
doi:10.1016/J.JPBA.2007.04.016
PMID:17555909
The Structures of Forestine and Foresticine, Two New C<sub>19</sub>-Diterpenoid Alkaloids from Aconitum forrestii Stapf S. W. Pelletier, Chen Szu Ying, B. S. Joshi, Haridutt K. Desai American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50033A013
Norditerpenoid alkaloids from the processed tubers of Aconitum carmichaeli. Shim SH, Kim JS, Kang SS Chem Pharm Bull (Tokyo) 01-Aug-2003
doi:10.1248/CPB.51.999
PMID:12913245
Liwaconitine, a New Diterpenoid Alkaloid from Aconitum forrestii. Chongheng W, Dihua C, Weiliang S Planta Med 01-May-1983
doi:10.1055/S-2007-969879
PMID:17404943

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
4-Methoxybenzoic Acid 7478 Click to see 152.15 unknown https://doi.org/10.4268/CJCMM20120916
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(2S,4S)-4-(hydroxymethyl)-5-methylhexane-1,2,4,5-tetrol 162925146 Click to see CC(C)(C(CC(CO)O)(CO)O)O 194.23 unknown https://doi.org/10.3987/S-1987-01-0365
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
((1S,2R,3R,4S,5R,6S,8R,9R,13S,16S,17R,18R)-8-acetyloxy-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo(7.7.2.12,5.01,10.03,8.013,17)nonadecan-4-yl) 4-methoxybenzoate 20055981 Click to see 627.80 unknown https://doi.org/10.4268/CJCMM20120916
(2R,3R,4S,5S,6S,8R,13S,16S,17R,18R)-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 139035022 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)OC)COC 451.60 unknown https://doi.org/10.1021/NP50033A013
(2R,3R,4S,5S,6S,8S,13S,16S,17R)-11-ethyl-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 146014457 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)COC 421.60 unknown https://doi.org/10.1021/NP50033A013
(2R,3R,6S,8R,13S,17R)-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 5315807 Click to see 451.60 unknown https://doi.org/10.1021/NP50033A013
(6S,8S,13S)-11-ethyl-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 5321607 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)COC 421.60 unknown https://doi.org/10.1021/NP50033A013
[(1S,2R,3R,4R,5R,6S,8R,9R,10R,13R,14R,16S,17S,18R)-8-acetyloxy-11-ethyl-5,14-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 134715408 Click to see 659.80 unknown https://doi.org/10.4268/CJCMM20120916
https://doi.org/10.1021/NP50033A013
https://doi.org/10.1055/S-2007-969879
[(1S,2R,3R,4R,5S,6S,8R,9R,10R,13S,16S,17R,18R)-8-acetyloxy-11-ethyl-5-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 101600179 Click to see 613.70 unknown https://doi.org/10.1055/S-2007-969879
https://doi.org/10.4268/CJCMM20120916
[(1S,2R,3R,4S,5R,6S,8R,9R,10R,13S,16S,17R,18R)-11-ethyl-8-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 163083346 Click to see 585.70 unknown https://doi.org/10.3987/S-1987-01-0365
[(1S,2R,3R,4S,5R,6S,8S,9S,10R,13S,16S,17R)-8-ethoxy-11-ethyl-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] acetate 162937319 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6OC(=O)C)OC)OCC)OC)COC 491.70 unknown https://doi.org/10.3987/S-1987-01-0365
[(1S,4R,5S,6S,8R,13R,14R,16S,18R)-8-acetyloxy-11-ethyl-5,14-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 11422434 Click to see 659.80 unknown via CMAUP database
[(1S,5S,8R,10R,13S)-8-acetyloxy-11-ethyl-5-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 145994473 Click to see 643.80 unknown https://doi.org/10.1055/S-2007-969879
[(2R,3R,5S,6S,8R,13R,17S)-8-acetyloxy-11-ethyl-5,14-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 5315414 Click to see 659.80 unknown https://doi.org/10.1055/S-2007-969879
https://doi.org/10.1021/NP50033A013
[(2R,3R,5S,6S,8R,13S,17R)-8-acetyloxy-11-ethyl-5-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 5316126 Click to see 643.80 unknown https://doi.org/10.1055/S-2007-969879
[(2R,3R,6S,8R,13S,17R)-8-acetyloxy-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 5315214 Click to see 627.80 unknown via CMAUP database
[(2S,3S,5R,8R,13S,17S)-8-acetyloxy-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 138114719 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6OC(=O)C7=CC=C(C=C7)OC)OC)OC(=O)C)OC)OC)COC 627.80 unknown https://doi.org/10.1055/S-2007-969879
[11-Ethyl-8-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 13817025 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6OC(=O)C7=CC=C(C=C7)OC)OC)O)OC)OC)COC 585.70 unknown https://doi.org/10.3987/S-1987-01-0365
[8-Acetyloxy-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 13817036 Click to see 627.80 unknown https://doi.org/10.1248/CPB.51.999
[8-Ethoxy-11-ethyl-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] acetate 13817023 Click to see 491.70 unknown https://doi.org/10.3987/S-1987-01-0365
11-Ethyl-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,18-triol 14707731 Click to see 437.60 unknown https://doi.org/10.1021/NP50033A013
8-(Acetyloxy)-20-ethyl-3,13-dihydroxy-1,6,16-trimethoxy-4-(methoxymethyl)aconitan-14-yl 4-methoxybenzoate 155569 Click to see 659.80 unknown https://doi.org/10.1016/J.JPBA.2007.04.016
https://doi.org/10.3987/S-1987-01-0365
8-O-Ethylyunaconitine 102469270 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)OCC)OC)OC)O)COC 645.80 unknown https://doi.org/10.3987/S-1987-01-0365
Cammaconine 441715 Click to see 407.50 unknown https://doi.org/10.1055/S-2007-969879
https://doi.org/10.4268/CJCMM20120916
CID 11250863 11250863 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)OC(=O)C)OC)OC)O)COC 659.80 unknown https://doi.org/10.3987/S-1987-01-0365
CID 165283 165283 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)OC)COC 451.60 unknown via CMAUP database
Foresticine 185130 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6(CC4C5C6O)O)OC)O)O)OC)COC 453.60 unknown https://doi.org/10.1021/NP50033A013
Forestine 101939160 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)O)OC)OC)COC 601.70 unknown https://doi.org/10.1021/NP50033A013
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Lappaconitine-type diterpenoid alkaloids
(5S,6S,8S,10R,13R)-11-ethyl-6,16-dimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 145994510 Click to see 377.50 unknown https://doi.org/10.1055/S-2007-969879
https://doi.org/10.4268/CJCMM20120916
https://doi.org/10.1080/14786419.2018.1560292
Aconosine 170126 Click to see 377.50 unknown https://doi.org/10.1055/S-2007-969879
https://doi.org/10.1080/14786419.2018.1560292
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,5R,8R,9R,10R,13R,14R,17R)-17-[(4E)-6-hydroxy-6-methylhepta-1,4-dien-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 9955042 Click to see 442.70 unknown via CMAUP database
Diosgenin 99474 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown via CMAUP database
Yamogenin 441900 Click to see 414.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-6-[(1S,2S,3'S,4S,5'R,6S,7S,8R,9S,12S,13R,16S)-3'-hydroxy-5'-(hydroxymethyl)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-2-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 102155845 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC19C(CC(CO9)CO)O 901.00 unknown via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-6-[(1S,2S,3'S,4S,5'S,6S,7S,8R,9S,12S,13R,16S)-3'-hydroxy-5'-(hydroxymethyl)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-2-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 102155844 Click to see 901.00 unknown via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-4,5-dihydroxy-6-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'S,6S,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol 16204183 Click to see 1015.20 unknown via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-6-[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol 21603983 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)O)C)C)C)OC1 869.00 unknown via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-6-[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'S,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol 16204068 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)C)O)O)O)O)O)O)O)C)C)C)OC1 869.00 unknown via CMAUP database
(3beta,25S)-Spirost-5-en-3-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside 441901 Click to see 722.90 unknown via CMAUP database
3-O-[alpha-L-ramnopyranosyl(1 to 2)]-O-[alpha-L-ramnopyranosyl(1 to 4)]-O-beta-D-galactopyranosid(1)]-(25S)-spirost-5-ene-3beta-ol 10653210 Click to see 869.00 unknown via CMAUP database
Asperin 21603986 Click to see 1015.20 unknown via CMAUP database
CID 16204180 16204180 Click to see 722.90 unknown via CMAUP database
CID 16204181 16204181 Click to see 869.00 unknown via CMAUP database
Dioscin 119245 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1 869.00 unknown via CMAUP database
Methylprotodioscin 11263254 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)OC 1063.20 unknown via CMAUP database
Progenin II 44429638 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)C)C)C)OC1 722.90 unknown via CMAUP database
Prosapogenin A 11061578 Click to see 722.90 unknown via CMAUP database
Protodioscin 441891 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O 1049.20 unknown via CMAUP database
Pseudoprotodioscin 21637110 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)OC3C(C(C(C(O3)C)O)O)O)OC4CCC5(C6CCC7(C(C6CC=C5C4)CC8C7C(=C(O8)CCC(C)COC9C(C(C(C(O9)CO)O)O)O)C)C)C)CO)O)O)O 1031.20 unknown via CMAUP database
Trigonelloside C 441899 Click to see 1049.20 unknown via CMAUP database
Trillin 11827970 Click to see 576.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
4-O-beta-D-mannopyranosyl-alpha-D-mannopyranose 5288769 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
Gal(a1-6)a-Man 11724912 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)O)O)O)O)O)O)O)O 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
beta-D-Manp-(1->4)-beta-D-Manp-(1->4)-beta-D-Manp 5287808 Click to see C(C1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(OC(C(C3O)O)O)CO)CO)O)O)O)O 504.40 unknown via CMAUP database

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