Aesculus indica - Unknown
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Internal ID UUID644007b505682320418265
Scientific name Aesculus indica
Authority (Wall. ex Cambess.) Hook.
First published in Bot. Mag. 85: t. 5117 (1859)

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Synonyms Top

Scientific name Authority First published in
Pawia indica Kuntze Revis. Gen. Pl. 1: 146 (1891)
Pavia indica Wall. ex Cambess. Voy. Inde 4: 31 (1841)

Common names Top

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Language Common/alternative name
Bulgarian Индийски конски кестен
Czech jírovec indický
Welsh castanwydden-y-meirch indiaidd
German indische rosskastanie
Persian شاهبلوط هیمالیایی
French marronnier de l'himalaya
Hungarian indiai vadgesztenye
Punjab بن کھوڑ
Ukrainian Гіркокаштан індійський
Chinese 印度七叶树
Chinese 印度七葉樹

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Aesculus indica var. concolor Browicz Fl. Iranica 92: 2 (1972)

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
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
      • Nepal
      • Pakistan
      • West Himalaya

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000522293
Tropicos 50276950
KEW urn:lsid:ipni.org:names:60450399-2
The Plant List kew-2624522
PFAF Aesculus indica
Open Tree Of Life 255757
Observations.org 159225
NCBI Taxonomy 531823
NBN Atlas NHMSYS0000455626
IUCN Red List 150283250
IPNI 60450399-2
iNaturalist 367294
GBIF 7323143
Freebase /m/0fpjrpt
EPPO AECIN
EOL 2905431
Elurikkus 588422
USDA GRIN 1631
Wikipedia Aesculus_indica

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
Vegetation–edaphic correlation and importance value index in himalayan ‘ecotone’ temperate conifer forest using the multivariate technique Ali F, Zeb M, Amin M, Rajpar MN, Hidayat S, Khan WR Saudi J Biol Sci 24-Mar-2024
PMCID:PMC11000104
doi:10.1016/j.sjbs.2024.103983
PMID:38590389
Flavonoids: A treasure house of prospective pharmacological potentials Hasnat H, Shompa SA, Islam MM, Alam S, Richi FT, Emon NU, Ashrafi S, Ahmed NU, Chowdhury MN, Fatema N, Hossain MS, Ghosh A, Ahmed F Heliyon 09-Mar-2024
PMCID:PMC10944245
doi:10.1016/j.heliyon.2024.e27533
PMID:38496846
Effect of Crown Layers on Reproductive Effort and Success in Andromonoecious Aesculus indica (Wall. ex Camb.) Hook (Sapindaceae) in a Temperate Forest of Garhwal Himalaya Pradhan P, Sukumaran A, Khanduri VP, Singh B, Rawat D, Riyal MK, Kumar M, Pinto MM Plants (Basel) 10-Jan-2024
PMCID:PMC10818387
doi:10.3390/plants13020183
PMID:38256737
The local medicinal plant knowledge in Kashmir Western Himalaya: a way to foster ecological transition via community-centred health seeking strategies Manzoor M, Ahmad M, Zafar M, Gillani SW, Shaheen H, Pieroni A, Al-Ghamdi AA, Elshikh MS, Saqib S, Makhkamov T, Khaydarov K J Ethnobiol Ethnomed 30-Nov-2023
PMCID:PMC10688143
doi:10.1186/s13002-023-00631-2
PMID:38037066
Impact of moisture content on microstructural, thermal, and techno-functional characteristics of extruded whole-grain-based breakfast cereal enriched with Indian horse chestnut flour Allai FM, Junaid PM, Azad ZR, Gul K, Dar BN, Siddiqui SA, Manuel Loenzo J Food Chem X 28-Oct-2023
PMCID:PMC10739762
doi:10.1016/j.fochx.2023.100959
PMID:38144831
Phytochemical analysis and bioactivity assessment of five medicinal plants from Pakistan: Exploring polyphenol contents, antioxidant potential, and antibacterial activities Rao H, Rao I, Saeed L, Aati HY, Aati S, Zeeshan M, ur Rehman Khan K Saudi J Biol Sci 22-Aug-2023
PMCID:PMC10480623
doi:10.1016/j.sjbs.2023.103783
PMID:37680976
Commodity risk assessment of Fagus sylvatica plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 28-Jul-2023
PMCID:PMC10375364
doi:10.2903/j.efsa.2023.8118
PMID:37522095
Systematic analyses with genomic and metabolomic insights reveal a new species, Ophiocordyceps indica sp. nov. from treeline area of Indian Western Himalayan region Sharma A, Kaur E, Joshi R, Kumari P, Khatri A, Swarnkar MK, Kumar D, Acharya V, Nadda G Front Microbiol 20-Jul-2023
PMCID:PMC10399244
doi:10.3389/fmicb.2023.1188649
PMID:37547690
Commodity risk assessment of Acer campestre plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 06-Jul-2023
PMCID:PMC10323733
doi:10.2903/j.efsa.2023.8071
PMID:37427018
Bioprospection of Selected Plant Secondary Metabolites as Modulators of the Proteolytic Activity of Plasmodium falciparum Plasmepsin V Sulyman AO, Aje OO, Ajani EO, Abdulsalam RA, Balogun FO, Sabiu S Biomed Res Int 21-Jun-2023
PMCID:PMC10307063
doi:10.1155/2023/6229503
PMID:37388365
Detection, Diagnosis, and Preventive Management of the Bacterial Plant Pathogen Pseudomonas syringae Yang P, Zhao L, Gao YG, Xia Y Plants (Basel) 25-Apr-2023
PMCID:PMC10181079
doi:10.3390/plants12091765
PMID:37176823
Keeping Healthy in Your Skin—Plants and Fungi Used by Indigenous Himalayan Communities to Treat Dermatological Ailments Haq SM, Khoja AA, Lone FA, Waheed M, Bussmann RW, Casini R, Mahmoud EA, Elansary HO Plants (Basel) 06-Apr-2023
PMCID:PMC10097107
doi:10.3390/plants12071575
PMID:37050200
Traditional foraging for ecological transition? Wild food ethnobotany among three ethnic groups in the highlands of the eastern Hindukush, North Pakistan Khan AH, Adil M, Aziz MA, Sõukand R, Pieroni A J Ethnobiol Ethnomed 31-Mar-2023
PMCID:PMC10064566
doi:10.1186/s13002-023-00581-9
PMID:37004043
Exploring soil bacterial diversity in different micro-vegetational habitats of Dachigam National Park in North-western Himalaya Mushtaq H, Ganai BA, Jehangir A Sci Rep 22-Feb-2023
PMCID:PMC9947166
doi:10.1038/s41598-023-30187-w
PMID:36813837
Therapeutic Potential of Phenolic Compounds in Medicinal Plants—Natural Health Products for Human Health Sun W, Shahrajabian MH Molecules 15-Feb-2023
PMCID:PMC9960276
doi:10.3390/molecules28041845
PMID:36838831

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ethyl heptadecanoate 26397 Click to see CCCCCCCCCCCCCCCCC(=O)OCC 298.50 unknown https://doi.org/10.1021/NP50061A026
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl heptadecanoate 15609 Click to see CCCCCCCCCCCCCCCCC(=O)OC 284.50 unknown https://doi.org/10.1021/NP50061A026
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5R)-6-[[(3S,4S,4aR,6aR,6bS,8R,8aR,9R,10R,12aS,14aR,14bR)-9-acetyloxy-8-hydroxy-4,8a-bis(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-10-[(E)-2-methylbut-2-enoyl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4-hydroxy-3,5-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]oxane-2-carboxylic acid 123134563 Click to see CC=C(C)C(=O)OC1C(C2(C(CC1(C)C)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)CO)OC6C(C(C(C(O6)C(=O)O)OC7C(C(C(C(O7)CO)O)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)CO)OC(=O)C 1131.30 unknown https://doi.org/10.3109/13880209509065390
CID 10724706 10724706 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C2(C(C1O)O)CO)O)C)C)(C)CO)OC6C(C(C(C(O6)C(=O)O)OC7C(C(C(C(O7)CO)O)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C 1007.10 unknown https://doi.org/10.1021/NP50053A001
Escin 16211024 Click to see CC=C(C)C(=O)OC1C(C2(C(CC1(C)C)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)CO)OC6C(C(C(C(O6)C(=O)O)OC7C(C(C(C(O7)CO)O)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)CO)OC(=O)C 1131.30 unknown https://doi.org/10.3109/13880209509065390
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,4R,4aR,5R,6aR,6aS,6bR,9S,10S,12aR,14bR)-4a,9-bis(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-3,4,5,10-tetrol 131636595 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C2(C(C1O)O)CO)O)C)C)(C)CO)O)C)C 506.70 unknown https://doi.org/10.1016/S0031-9422(00)83042-3
[(3R,4R,4aR,5S,6R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-3,5,6,10-tetrahydroxy-4a-(hydroxymethyl)-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicen-4-yl] (Z)-2-methylbut-2-enoate 122194856 Click to see CC=C(C)C(=O)OC1C(C(CC2C1(C(C(C3(C2=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)O)O)CO)(C)C)O 588.80 unknown https://doi.org/10.3109/13880208709060921
[3,5,6,10-Tetrahydroxy-4a-(hydroxymethyl)-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicen-4-yl] 2-methylbut-2-enoate 77509161 Click to see CC=C(C)C(=O)OC1C(C(CC2C1(C(C(C3(C2=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)O)O)CO)(C)C)O 588.80 unknown https://doi.org/10.3109/13880208709060921
[4,5,10-Trihydroxy-4a-(hydroxymethyl)-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicen-3-yl] 2-methylbut-2-enoate 558044 Click to see CC=C(C)C(=O)OC1C(C2(C(CC1(C)C)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)CO)O 572.80 unknown https://doi.org/10.3109/13880208709060921
[5,10-Dihydroxy-4a-(hydroxymethyl)-2,2,6a,6b,9,9,12a-heptamethyl-4-(2-methylbut-2-enoyloxy)-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicen-3-yl] 2-methylbut-2-enoate 73817653 Click to see CC=C(C)C(=O)OC1C(C2(C(CC1(C)C)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)CO)OC(=O)C(=CC)C 654.90 unknown https://doi.org/10.3109/13880208709060921
21,22-O-Diangeloyl-3beta,16alpha,28-trihydroxyolean-12-ene 21636448 Click to see CC=C(C)C(=O)OC1C(C2(C(CC1(C)C)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)CO)OC(=O)C(=CC)C 654.90 unknown https://doi.org/10.3109/13880208709060921
8,22-Bis(hydroxymethyl)-3,4,8,12,19,19-hexamethyl-23-oxahexacyclo[18.2.1.03,16.04,13.07,12.017,22]tricos-15-ene-9,21-diol 15558430 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC6C2(C(C1O6)O)CO)C)C)(C)CO)O)C)C 488.70 unknown https://doi.org/10.3109/13880208709060921
Aescigenin 44144285 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC6C2(C(C1O6)O)CO)C)C)(C)CO)O)C)C 488.70 unknown https://doi.org/10.1016/S0031-9422(00)83042-3
Barringtogenol B 21633166 Click to see CC=C(C)C(=O)OC1C(C2(C(CC1(C)C)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)CO)O 572.80 unknown https://doi.org/10.3109/13880208709060921
Barringtogenol C 435277 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C2(C(C1O)O)CO)O)C)C)(C)C)O)C)C 490.70 unknown https://doi.org/10.3109/13880208709060921
Escigenin 15558431 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC6C2(C(C1O6)O)CO)C)C)(C)CO)O)C)C 488.70 unknown https://doi.org/10.3109/13880208709060921
Protoaescigenin 612009 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C2(C(C1O)O)CO)O)C)C)(C)CO)O)C)C 506.70 unknown https://doi.org/10.3109/13880208709060921
Protoescigenin 15560300 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C2(C(C1O)O)CO)O)C)C)(C)CO)O)C)C 506.70 unknown https://doi.org/10.3109/13880208709060921
Saniculagenin D 89508569 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C2(C(C1O)O)CO)O)C)C)(C)C)O)C)C 490.70 unknown https://doi.org/10.1016/S0031-9422(00)83042-3
Theasapogenol B 185465 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C2(C(C1O)O)CO)O)C)C)(C)C)O)C)C 490.70 unknown https://doi.org/10.3109/13880208709060921
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.3109/13880208209083302

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