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
Suggest a correction!
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
Suggest a correction!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
Add a new one! Suggest a correction!| 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
Add a new one! Suggest a correction!| Name | Authority | First published in |
|---|---|---|
| Aconitum heterophyllum subsp. parciflorum | Qureshi & Chaudhri | Pakistan Syst. 3: 6 (1987) |
Varieties (abbr. var.) Top
Add a new one! Suggest a correction!| Name | Authority | First published in |
|---|---|---|
| Aconitum heterophyllum var. bracteatum | Stapf | Ann. Roy. Bot. Gard. (Calcutta) 10(2): 154, t. 100-13. 1905 |
Germination/Propagation Top
Suggest a correction or add new data!| 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 click to expand
-
Indian Subcontinent
- Nepal
- Pakistan
- West Himalaya
-
Indian Subcontinent
Links to other databases Top
Suggest others/fix!| 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.
If you wish to see all the related articles click here.
Phytochemical Profile Top
Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
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 / 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 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |