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Details Top

Internal ID UUID644037756eb21730007681
Scientific name Alangium kurzii
Authority Craib
First published in Bull. Misc. Inform. Kew 1911: 60 (1911)

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Synonyms Top

Scientific name Authority First published in
Marlea tomentosa Endl. ex Hassk. Flora 27: 605 (1844)
Alangium begoniifolium var. typicum Wangerin Pflanzenr. IV, 220b: 21. 1910
Alangium chinense var. tomentosum (Blume) Merr. Philipp. J. Sci. 21: 505. 1922
Alangium handelii Schnarf Anz. Akad. Wiss. Wien, Math.-Naturwiss. Kl. 59: 107 (1922)
Alangium kurzii var. handelii (Schnarf) W.P.Fang J. Sichuan Univ., Nat. Sci. Ed. 2: 97 (1979)
Alangium kurzii var. laxiflorum (Y.C.Wu) W.P.Fang J. Sichuan Univ., Nat. Sci. Ed. 2: 98 1979
Alangium kurzii var. pachyphyllum W.P.Fang & H.Y.Su J. Sichuan Univ., Nat. Sci. Ed. 2: 96 (1979)
Alangium kurzii var. umbellatum (Yen C.Yang) W.P.Fang J. Sichuan Univ., Nat. Sci. Ed. 2: 97 (1979)
Alangium kwangsiense Melch. Notizbl. Bot. Gart. Berlin-Dahlem 10: 823 (1929)
Alangium rotundifolium var. laxifolium Y.C.Wu Bot. Jahrb. Syst. 71: 199. 1940
Alangium umbellatum Yen C.Yang Contr. Biol. Lab. Sci. Soc. China, Bot. Ser. 12: 135. 1942 (1942)
Diacicarpium tomentosum Blume Bijdr. Fl. Ned. Ind. : 657 (1826)
Alangium rotundifolium var. laxiflorum Y.C.Wu Bot. Jahrb. Syst. 71: 199 1940
Alangium begoniifolium subsp. tomentosum (Blume) Palm Meded. Deli Proefstat. 42: 19. 1925
Alangium kurzii var. laxifolium (Y.C.Wu) W.P.Fang Sichuan Daxue Xuebao, Zir. Kexue 1979(2): 98.

Common names Top

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Language Common/alternative name
Chinese 毛八角枫
Chinese 长毛八角枫

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Hainan
  • Asia-tropical
    • Indo-China
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Malaya
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000937206
Tropicos 8700385
KEW urn:lsid:ipni.org:names:271414-1
The Plant List kew-5589
Open Tree Of Life 221641
NCBI Taxonomy 161874
IUCN Red List 136141950
IPNI 271414-1
GBIF 7326260
Freebase /m/0105jv23
EOL 2890146
Wikipedia Alangium_kurzii

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
“Realistic strategies” and neutral processes drive the community assembly based on leaf functional traits in a subtropical evergreen broad‐leaved forest Zhao L, Xiang W, Li J, Liu W, Hu Y, Wu H, Zhang Y, Cheng X, Wang W, Wang W, Ouyang S Ecol Evol 17-Sep-2022
PMCID:PMC9482003
doi:10.1002/ece3.9323
PMID:36177111
Seed rain and soil seed bank in Chinese fir plantations and an adjacent natural forest in southern China: Implications for the regeneration of native species Liu B, Liu Q, Zhu C, Liu Z, Huang Z, Tigabu M, He Z, Liu Y, Wang Z Ecol Evol 26-Jan-2022
PMCID:PMC8796942
doi:10.1002/ece3.8539
PMID:35127042
Diaporthe taoicola and D. siamensis, Two New Records on Citrus sinensis in China Cui MJ, Wei X, Xia PL, Yi JP, Yu ZH, Deng JX, Li QL Mycobiology 17-May-2021
PMCID:PMC8259869
doi:10.1080/12298093.2021.1912254
PMID:34290550
The complete chloroplast genome sequences of Cornus elliptica (Cornaceae) Lu H, Tang J, Li D Mitochondrial DNA B Resour 16-Mar-2021
PMCID:PMC7971275
doi:10.1080/23802359.2021.1888333
PMID:33796687
Morphology Characterization, Molecular Phylogeny, and Pathogenicity of Diaporthe passifloricola on Citrus reticulata cv. Nanfengmiju in Jiangxi Province, China Chaisiri C, Liu XY, Yin WX, Luo CX, Lin Y Plants (Basel) 23-Jan-2021
PMCID:PMC7911537
doi:10.3390/plants10020218
PMID:33498730
Combined LM and SEM study of the middle Miocene (Sarmatian) palynoflora from the Lavanttal Basin, Austria: Part V. Magnoliophyta 3 – Myrtales to Ericales Grímsson F, Bouchal JM, Xafis A, Zetter R Grana 14-Feb-2020
PMCID:PMC7195176
doi:10.1080/00173134.2019.1696400
PMID:32406427
High Genetic Diversity and Species Complexity of Diaporthe Associated With Grapevine Dieback in China Manawasinghe IS, Dissanayake AJ, Li X, Liu M, Wanasinghe DN, Xu J, Zhao W, Zhang W, Zhou Y, Hyde KD, Brooks S, Yan J Front Microbiol 02-Sep-2019
PMCID:PMC6732904
doi:10.3389/fmicb.2019.01936
PMID:31543868
An Exploration of Traditional Chinese Medicinal Plants with Anti-Inflammatory Activities Fan C, Jin HZ, Wu L, Zhang Y, Ye RD, Zhang W, Zhang Y Evid Based Complement Alternat Med 04-Apr-2017
PMCID:PMC5394394
doi:10.1155/2017/1231820
PMID:28473862
Leaf Trait-Environment Relationships in a Subtropical Broadleaved Forest in South-East China Kröber W, Böhnke M, Welk E, Wirth C, Bruelheide H PLoS One 23-Apr-2012
PMCID:PMC3335070
doi:10.1371/journal.pone.0035742
PMID:22539999
Alkaloids from Alangium javanicum and Alangium grisolleoides that mediate Cu2+-dependent DNA strand scission. Pham VC, Ma J, Thomas SJ, Xu Z, Hecht SM J Nat Prod 01-Aug-2005
doi:10.1021/NP058013J
PMID:16124751
The biosynthesis of beta-carboline and quinolizidine alkaloids of Alangium lamarckii. Jain S, Sinha A, Bhakuni DS Phytochemistry 01-Aug-2002
doi:10.1016/S0031-9422(02)00057-2
PMID:12150812
A tetrahydroisoquinoline-monoterpene glucoside and an iridoid glucoside from Alangium kurzii. Tanahashi T, Kobayashi C, Itoh A, Nagakura N, Inoue K, Kuwajima H, Wu HX Chem Pharm Bull (Tokyo) 01-Mar-2000
doi:10.1248/CPB.48.415
PMID:10726868
CHEMICAL INVESTIGATIONS OF ALANGIUM LAMARCKII. I. ISOLATION OF A NEW ALKALOID, ANKORINE, FROM THE LEAVES. DASGUPTA B J Pharm Sci 01-Jan-1970
doi:10.1002/JPS.2600540340
PMID:14301596

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 / Prenol lipids / Terpene glycosides
(2S,3R,4S)-3-ethenyl-4-[[(1R)-7-hydroxy-6-methoxy-1,2,3,4-tetrahydroisoquinolin-1-yl]methyl]-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylic acid 10649711 Click to see COC1=C(C=C2C(NCCC2=C1)CC3C(C(OC=C3C(=O)O)OC4C(C(C(C(O4)CO)O)O)O)C=C)O 523.50 unknown https://doi.org/10.1248/CPB.48.415
3-ethenyl-4-[(7-hydroxy-6-methoxy-1,2,3,4-tetrahydroisoquinolin-1-yl)methyl]-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylic acid 20979945 Click to see COC1=C(C=C2C(NCCC2=C1)CC3C(C(OC=C3C(=O)O)OC4C(C(C(C(O4)CO)O)O)O)C=C)O 523.50 unknown https://doi.org/10.1248/CPB.48.415
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aS,7S,7aS)-7-(benzoyloxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid 10790879 Click to see C1CC2C(C1COC(=O)C3=CC=CC=C3)C(OC=C2C(=O)O)OC4C(C(C(C(O4)CO)O)O)O 480.50 unknown https://doi.org/10.1248/CPB.48.415
7-(Benzoyloxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid 85269007 Click to see C1CC2C(C1COC(=O)C3=CC=CC=C3)C(OC=C2C(=O)O)OC4C(C(C(C(O4)CO)O)O)O 480.50 unknown https://doi.org/10.1248/CPB.48.415
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
Uridine 6029 Click to see C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O 244.20 unknown https://doi.org/10.1248/CPB.48.415
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(2S,3S,4R)-4-methoxy-6-oxo-2-[(E,3S,5R,6S)-3,5,6-triacetyloxyhept-1-enyl]oxan-3-yl] acetate 101267306 Click to see CC(C(CC(C=CC1C(C(CC(=O)O1)OC)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 458.50 unknown https://doi.org/10.1248/CPB.48.415
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(1R,16R,17S)-16-ethenyl-4-hydroxy-5-methoxy-15-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-14-oxa-10-azatetracyclo[8.8.0.02,7.012,17]octadeca-2,4,6,12-tetraen-11-one 44143717 Click to see COC1=C(C=C2C3CC4C(C(OC=C4C(=O)N3CCC2=C1)OC5C(C(C(C(O5)CO)O)O)O)C=C)O 505.50 unknown https://doi.org/10.1248/CPB.48.415
16-Ethenyl-4-hydroxy-5-methoxy-15-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-14-oxa-10-azatetracyclo[8.8.0.02,7.012,17]octadeca-2,4,6,12-tetraen-11-one 5089480 Click to see COC1=C(C=C2C3CC4C(C(OC=C4C(=O)N3CCC2=C1)OC5C(C(C(C(O5)CO)O)O)O)C=C)O 505.50 unknown https://doi.org/10.1248/CPB.48.415
16-Ethenyl-4,5-dihydroxy-15-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-14-oxa-10-azatetracyclo[8.8.0.02,7.012,17]octadeca-2,4,6,12-tetraen-11-one 4491372 Click to see C=CC1C2CC3C4=CC(=C(C=C4CCN3C(=O)C2=COC1OC5C(C(C(C(O5)CO)O)O)O)O)O 491.50 unknown https://doi.org/10.1248/CPB.48.415
Alangiside 442161 Click to see COC1=C(C=C2C3CC4C(C(OC=C4C(=O)N3CCC2=C1)OC5C(C(C(C(O5)CO)O)O)O)C=C)O 505.50 unknown https://doi.org/10.1248/CPB.48.415
Demethylalangiside 443418 Click to see C=CC1C2CC3C4=CC(=C(C=C4CCN3C(=O)C2=COC1OC5C(C(C(C(O5)CO)O)O)O)O)O 491.50 unknown https://doi.org/10.1248/CPB.48.415
Isoalangiside 443420 Click to see COC1=C(C=C2C3CC4C(C(OC=C4C(=O)N3CCC2=C1)OC5C(C(C(C(O5)CO)O)O)O)C=C)O 505.50 unknown https://doi.org/10.1021/NP058013J
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 2,6-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]benzoate 102066456 Click to see C1=CC=C(C(=C1)COC(=O)C2=C(C=CC=C2OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 746.70 unknown https://doi.org/10.1248/CPB.48.415
[2-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 2,6-bis[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]benzoate 162891304 Click to see C1=CC=C(C(=C1)COC(=O)C2=C(C=CC=C2OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 746.70 unknown https://doi.org/10.1248/CPB.48.415
> Organoheterocyclic compounds / Quinolizidines
3-ethyl-2-(2-hydroxyethyl)-9,10-dimethoxy-2,3,4,6,7,11b-hexahydro-1H-benzo[a]quinolizin-8-ol 3462223 Click to see CCC1CN2CCC3=C(C(=C(C=C3C2CC1CCO)OC)OC)O 335.40 unknown https://doi.org/10.1002/JPS.2600540340
https://doi.org/10.1016/S0031-9422(02)00057-2
Ankorine 442166 Click to see CCC1CN2CCC3=C(C(=C(C=C3C2CC1CCO)OC)OC)O 335.40 unknown https://doi.org/10.1002/JPS.2600540340
https://doi.org/10.1016/S0031-9422(02)00057-2
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[(2S,3R,4S,5R,6R)-4,5-Dihydroxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 10919701 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)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 740.70 unknown https://doi.org/10.1248/CPB.48.415
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 14825575 Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)CO)O)O)O)O)O 596.50 unknown https://doi.org/10.1248/CPB.48.415
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 13647412 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 610.50 unknown https://doi.org/10.1248/CPB.48.415
4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2-O-beta-D-xylopyranosyl-beta-D-galactopyranosyl)oxy]- 5274586 Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)CO)O)O)O)O)O 596.50 unknown https://doi.org/10.1248/CPB.48.415
4H-1-Benzopyran-4-one, 5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2-O-beta-D-xylopyranosyl-beta-D-galactopyranosyl)oxy]- 10438202 Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)O 580.50 unknown https://doi.org/10.1248/CPB.48.415
Mauritianin 5459192 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)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 740.70 unknown https://doi.org/10.1248/CPB.48.415
Panasenoside 9986191 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 610.50 unknown https://doi.org/10.1248/CPB.48.415
Rustoside 74977996 Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)O 580.50 unknown https://doi.org/10.1248/CPB.48.415

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