Dysoxylum gotadhora

Details Top

Internal ID UUID644005d77d3ed248787818
Scientific name Dysoxylum gotadhora
Authority (Buch.-Ham.) Mabb.
First published in Fl. China 11: 127 (2008)

Ethnobotanical Use Top

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Synonyms Top

Scientific name Authority First published in
Alliaria golodhara Kuntze Revis. Gen. Pl. 1: 109. 1891 [5 Nov 1891]
Amoora ficiformis Wight Ill. Ind. Bot. 1: 147 1840
Dysoxylum binectariferum Hook.f. ex Bedd. Trans. Linn. Soc. London 25: 212 (1865)
Dysoxylum binectariferum var. coriaceum C.DC. Monogr. Phan. 1: 492 1878
Dysoxylum binectariferum var. punctulatum C.DC. Monogr. Phan. 1: 492 1878
Dysoxylum binectariferum var. pyyriforme Thwaites ex Trimen Handb. Fl. Ceylon 1: 247 1893
Dysoxylum binectarifolium C.DC. Monogr. Phan. 1: 592 (1878)
Dysoxylum grandifolium H.L.Li J. Arnold Arbor. 25: 302. 1944
Dysoxylum translucidum Pierre Fl. Forest. Cochinch. : t. 350 B (1897)
Dysoxylum zeylanicum Kosterm. Acta Bot. Neerl. 31: 324 (1982)
Epicharis gotadhora M.Roem. Fam. Nat. Syn. Monogr. 1: 103 (1846)
Guarea amaris Buch.-Ham. Mem. Wern. Nat. Hist. Soc. 6: 308 (1832)
Guarea binectarifera Roxb. Fl. Ind. 2: 240 (1824)
Guarea gotadhora Buch.-Ham. Mem. Wern. Nat. Hist. Soc. 6: 307 (1832)
Dysoxylum cupuliforme H.L.Li J. Arnold Arbor. 25: 301 (1944)
Dysoxylum pyriforme (Trimen) Kosterm. Acta Bot. Neerl. 31(4): 323 (1982):.

Common names Top

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Language Common/alternative name
Assamese বান্দৰডিমা
Bengali বড গোটাধরা
Bengali লস্সুনি
Kannada ಕಾಡುಗಂಧ
Malayalam അകിൽ (dysoxylum gotadhora)
Burmese အောက်ချင်းစာနီပင်
Chinese 杯萼樫木
Chinese 杯萼葱臭木
Chinese 红罗
Chinese 红果樫木
Chinese 杯萼蔥臭木

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000509125
Tropicos 50002009
KEW urn:lsid:ipni.org:names:578105-1
The Plant List kew-2779929
IPNI 578105-1
GBIF 3850503
EOL 26723075
Tropicos 50322459
KEW urn:lsid:ipni.org:names:77091051-1
The Plant List kew-2607025
Open Tree Of Life 5747800
NCBI Taxonomy 1679391
IPNI 77091051-1
iNaturalist 915088
GBIF 3850114
USDA GRIN 460883
Wikipedia Dysoxylum_gotadhora

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
Fungal endophyte bioinoculants as a green alternative towards sustainable agriculture Sharma I, Raina A, Choudhary M, Apra, Kaul S, Dhar MK Heliyon 25-Aug-2023
PMCID:PMC10472071
doi:10.1016/j.heliyon.2023.e19487
PMID:37662754
A wound inducible chalcone synthase gene from Dysoxylum gotadhora (DbCHS) regulates flavonoid biosynthesis Mahajan V, Chouhan R, Jamwal VL, Kapoor N, Gandhi SG Physiol Mol Biol Plants 21-Aug-2023
PMCID:PMC10462589
doi:10.1007/s12298-023-01344-2
PMID:37649885
Inhibition and potential treatment of colorectal cancer by natural compounds via various signaling pathways Wang M, Liu X, Chen T, Cheng X, Xiao H, Meng X, Jiang Y Front Oncol 08-Sep-2022
PMCID:PMC9496650
doi:10.3389/fonc.2022.956793
PMID:36158694
Exogenously Applied Rohitukine Inhibits Photosynthetic Processes, Growth and Induces Antioxidant Defense System in Arabidopsis thaliana Ahmed S, Asgher M, Kumar A, Gandhi SG Antioxidants (Basel) 03-Aug-2022
PMCID:PMC9404761
doi:10.3390/antiox11081512
PMID:36009231
Rugosic acid A, derived from Rosa rugosa Thunb., is novel inhibitory agent for NF‐κB and IL‐6/STAT3 axis in acute lung injury model Kim K, Park Y, Jang H, Lee S, Lee S, Yun B, Lee SW, Rho M Phytother Res 21-Jul-2020
PMCID:PMC7404680
doi:10.1002/ptr.6767
PMID:32779813
Flavonoids and Other Phenolic Compounds from Medicinal Plants for Pharmaceutical and Medical Aspects: An Overview Tungmunnithum D, Thongboonyou A, Pholboon A, Yangsabai A Medicines (Basel) 25-Aug-2018
PMCID:PMC6165118
doi:10.3390/medicines5030093
PMID:30149600
Natural Products Research in China From 2015 to 2016 Liu H, Zhu G, Fan Y, Du Y, Lan M, Xu Y, Zhu W Front Chem 20-Mar-2018
PMCID:PMC5869933
doi:10.3389/fchem.2018.00045
PMID:29616210
Dysoxylum binectariferum Hook.f (Meliaceae), a rich source of rohitukine. Mohanakumara P, Sreejayan N, Priti V, Ramesha BT, Ravikanth G, Ganeshaiah KN, Vasudeva R, Mohan J, Santhoshkumar TR, Mishra PD, Ram V, Shaanker RU Fitoterapia 01-Mar-2010
doi:10.1016/J.FITOTE.2009.08.010
PMID:19686817
A new alkaloid from Dysoxylum binectariferum. Yang DH, Cai SQ, Zhao YY, Liang H J Asian Nat Prod Res 01-Sep-2004
doi:10.1080/10286020310001608930
PMID:15224423
Dysobinin, a new tetranortriterpene from Dysoxylum binectariferum S. Singh, H.S. Garg, N.M. Khanna Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)88877-9
An antiinflammatory cum immunomodulatory piperidinylbenzopyranone from dysoxylum binectariferum : isolation, structure and total synthesis Ramachandra G. Naik, S.L. Kattige, S.V. Bhat, B. Alreja, N.J. de Souza, R.H. Rupp Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4020(01)90352-7

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 / Gallic acid and derivatives
Methyl 3,4,5-trimethoxybenzoate 15956 Click to see 226.23 unknown https://doi.org/10.1016/S0031-9422(00)88877-9
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
[(5R,6S,7S,8R,9R,10R,13R,17R)-7-acetyloxy-17-(furan-3-yl)-4,4,8,10,13-pentamethyl-3-oxo-5,6,7,9,11,12,16,17-octahydrocyclopenta[a]phenanthren-6-yl] acetate 162964716 Click to see CC(=O)OC1C2C(C(=O)C=CC2(C3CCC4(C(CC=C4C3(C1OC(=O)C)C)C5=COC=C5)C)C)(C)C 494.60 unknown https://doi.org/10.1016/S0031-9422(00)88877-9
> Organoheterocyclic compounds / Piperidines / Phenylpiperidines
5,7-Dihydroxy-8-(3-hydroxy-1-methyl-4-piperidinyl)-2-methyl-4H-1-benzopyran-4-one 5387431 Click to see 305.32 unknown https://doi.org/10.1016/S0040-4020(01)90352-7
https://doi.org/10.1016/J.FITOTE.2009.08.010
https://doi.org/10.1080/10286020310001608930
5,7-dihydroxy-8-[(3S,4R)-3-hydroxy-1-methyl-1-oxidopiperidin-1-ium-4-yl]-2-methylchromen-4-one 102223361 Click to see 321.32 unknown https://doi.org/10.1080/10286020310001608930
CID 13422576 13422576 Click to see 305.32 unknown https://doi.org/10.1016/J.FITOTE.2009.08.010
https://doi.org/10.1016/S0040-4020(01)90352-7
Rohitukine 13422573 Click to see CC1=CC(=O)C2=C(O1)C(=C(C=C2O)O)C3CCN(CC3O)C 305.32 unknown https://doi.org/10.1016/S0040-4020(01)90352-7
https://doi.org/10.1080/10286020310001608930

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