Acacia auriculiformis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Acacia auriculiformis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID643fd740e0e61702747024
Scientific name Acacia auriculiformis
Authority A.Cunn. ex Benth.
First published in London J. Bot.1: 377 (1842)

Description Top

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Acacia auriculiformis, also known as auri, karuvel, and aakashmani, is a fast-growing tree in the Fabaceae family. It is native to Australia, Philippines, Indonesia, and Papua New Guinea and can grow up to 30 meters tall. The tree has dense foliage, with leaves that are 10-16 cm long and 1.5-2.5 cm wide. Its flowers are creamy yellow and have a sweet scent, while its pods are flat and cartilaginous. The wood of Acacia auriculiformis is used for making paper, furniture, and tools, and its bark contains tannin for animal hide tanning. The tree also has various functional uses, such as erosion control, shade or shelter, and soil improvement. However, it is susceptible to pests and diseases, such as a rust fungus and root rot. Efforts are being made to breed resistant strains of the tree to combat these issues.

Synonyms Top

Scientific name Authority First published in
Acacia auriculaeformis Benth.
Racosperma auriculiforme (A.Cunn. ex Benth.) Pedley Bot. J. Linn. Soc.92: 247 (1986)

Common names Top

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Language Common/alternative name
English earleaf acacia
English northern black wattle
English papuan wattle
English tan wattle
English ear-leaf acacia
Bengali আকাশমণি
Persian آکاکیا آریکالیفرمیس
Malayalam അക്കേഷ്യ
Malay pokok akasia
sat ᱟᱠᱟᱥᱢᱚᱱᱤ ᱫᱟᱨᱮ
Telugu అకేషియా అరికులిఫోర్మిస్
Thai กระถินณรงค์
Vietnamese keo lá tràm
Chinese 阿列克栲
Chinese 大葉相思
Chinese 大蘂相思
Chinese 耳葉相思
Chinese 耳莢相思
Chinese 耳荚相思
Chinese 耳果相思
Chinese 耳叶相思
Chinese 澳洲相思
Chinese 大叶相思树
Chinese 大叶相思

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
  • Africa
    • East Tropical Africa
      • Tanzania
    • West Tropical Africa
      • Benin
      • Nigeria
    • West-central Tropical Africa
      • Zaïre
    • Western Indian Ocean
      • Mauritius
      • Réunion
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Pakistan
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Vietnam
    • Malesia
      • Borneo
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
    • Papuasia
      • New Guinea
      • Solomon Islands
  • Pacific
    • North-central Pacific
      • Hawaii
    • Northwestern Pacific
      • Caroline Islands
    • South-central Pacific
      • Cook Islands
  • Southern America
    • Caribbean
      • Bahamas
      • Trinidad-Tobago
    • Central America
      • Panamá

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000173754
Florida Plant Atlas 43
USDA Plants ACAU
Tropicos 13023667
INPN 705750
KEW urn:lsid:ipni.org:names:469784-1
The Plant List ild-19892
PFAF Acacia auriculiformis
Open Tree Of Life 214682
NCBI Taxonomy 205027
Nature Serve 2.146783
IUCN Red List 19891902
IPNI 469784-1
iNaturalist 52445
GBIF 2981001
Freebase /m/025rzbt
EPPO ACAAF
EOL 639977
USDA GRIN 781
Wikipedia Acacia_auriculiformis

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
Effect of organic biostimulants on cannabis productivity and soil microbial activity under outdoor conditions Da Cunha Leme Filho JF, Chim BK, Bermand C, Diatta AA, Thomason WE J Cannabis Res 26-Mar-2024
PMCID:PMC10964707
doi:10.1186/s42238-024-00214-2
PMID:38532457
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Comparative Bioactivity Analysis of Green-Synthesized Metal (Cobalt, Copper, and Selenium) Nanoparticles Ryntathiang I, Dharmalingam Jothinathan MK, Behera A, Saravanan S, Murugan R Cureus 11-Mar-2024
PMCID:PMC11004841
doi:10.7759/cureus.55933
PMID:38601374
Commodity risk assessment of Ligustrum ovalifolium and Ligustrum vulgare 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, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 07-Mar-2024
PMCID:PMC10918603
doi:10.2903/j.efsa.2024.8648
PMID:38455154
Characterization of carbon fluxes, stock and nutrients in the sacred forest groves and invasive vegetation stands within the human dominated landscapes of a tropical semi-arid region Akil Prasath RV, Mohanraj R, Balaramdas KR, Jhony Kumar Tagore A, Raja P, Rajasekaran A Sci Rep 24-Feb-2024
PMCID:PMC10894248
doi:10.1038/s41598-024-55294-0
PMID:38402350
Synergistic interactions of assorted ameliorating agents to enhance the potential of heavy metal phytoremediation Sanjana S, Jazeel K, Janeeshma E, Nair SG, Shackira AM Stress Biol 16-Feb-2024
PMCID:PMC10873264
doi:10.1007/s44154-024-00153-1
PMID:38363436
Biosynthesis and characterization of Ocimum sanctum green silver nanoparticles and unravelling their enhanced anti-filarial activity through a HRAMS proteomics approach Mishra A, Kumar S, Singh A RSC Adv 14-Feb-2024
PMCID:PMC10866198
doi:10.1039/d3ra08702f
PMID:38362069
The Potential of Wood Vinegar to Replace Antimicrobials Used in Animal Husbandry—A Review Gama GS, Pimenta AS, Feijó FM, de Azevedo TK, de Melo RR, de Andrade GS Animals (Basel) 25-Jan-2024
PMCID:PMC10854697
doi:10.3390/ani14030381
PMID:38338024
Use of Trichoderma in the Production of Forest Seedlings Ferreira NC, Ramos ML, Gatto A Microorganisms 23-Jan-2024
PMCID:PMC10893047
doi:10.3390/microorganisms12020237
PMID:38399641
Geometric entropy of plant leaves: A measure of morphological complexity Muraleedharan V, Rajan SC, R J PLoS One 02-Jan-2024
PMCID:PMC10760904
doi:10.1371/journal.pone.0293596
PMID:38166118
Enhancing landslide risk reduction strategies in Southeast Bangladesh Alam E, Islam MK Jamba 22-Dec-2023
PMCID:PMC10784180
doi:10.4102/jamba.v15i1.1541
PMID:38223543
Phenolic Compounds from By-Products for Functional Textiles Afonso TB, Bonifácio-Lopes T, Costa EM, Pintado ME Materials (Basel) 20-Nov-2023
PMCID:PMC10672813
doi:10.3390/ma16227248
PMID:38005176
Plant-Associated Neoscytalidium dimidiatum—Taxonomy, Host Range, Epidemiology, Virulence, and Management Strategies: A Comprehensive Review Derviş S, Özer G J Fungi (Basel) 26-Oct-2023
PMCID:PMC10672476
doi:10.3390/jof9111048
PMID:37998855
Microbial controls over soil priming effects under chronic nitrogen and phosphorus additions in subtropical forests Li J, Liu ZF, Jin MK, Zhang W, Lambers H, Hui D, Liang C, Zhang J, Wu D, Sardans J, Peñuelas J, Petticord DF, Frey DW, Zhu YG ISME J 29-Sep-2023
PMCID:PMC10689846
doi:10.1038/s41396-023-01523-9
PMID:37773438
Implementation of machine learning in DNA barcoding for determining the plant family taxonomy Riza LS, Zain MI, Izzuddin A, Prasetyo Y, Hidayat T, Abu Samah KA Heliyon 21-Sep-2023
PMCID:PMC10520734
doi:10.1016/j.heliyon.2023.e20161
PMID:37767518

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 acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown https://doi.org/10.1007/BF02636360
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://doi.org/10.1007/BF02636360
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown https://doi.org/10.1007/BF02636360
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown https://doi.org/10.1007/BF02636360
Lignoceric Acid 11197 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O 368.60 unknown https://doi.org/10.1007/BF02636360
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(1R,2R,4S,5R,8R,10S,13R,14R,18S,21S)-10-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-2-hydroxy-4,5,9,9,13,20,20-heptamethyl-22-oxahexacyclo[19.2.1.01,18.04,17.05,14.08,13]tetracos-16-en-23-one 102446076 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C26CC1OC6=O)O)C)C)(C)C)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(CO8)O)O)O)C)C 764.90 unknown https://doi.org/10.1016/S0031-9422(96)00399-8
(1R,2R,4S,5R,8R,10S,13R,14R,18S,21S)-10-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-2-hydroxy-4,5,9,9,13,20,20-heptamethyl-22-oxahexacyclo[19.2.1.01,18.04,17.05,14.08,13]tetracos-16-en-23-one 102446682 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C26CC1OC6=O)O)C)C)(C)C)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)OC9C(C(C(CO9)O)O)O)C)C 927.10 unknown https://doi.org/10.1016/S0031-9422(96)00399-8
https://doi.org/10.1016/0031-9422(89)85039-3
(1R,2R,4S,5R,8R,10S,13R,14R,18S,21S)-2-hydroxy-4,5,9,9,13,20,20-heptamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-22-oxahexacyclo[19.2.1.01,18.04,17.05,14.08,13]tetracos-16-en-23-one 102446075 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C26CC1OC6=O)O)C)C)(C)C)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)O)C)C 795.00 unknown https://doi.org/10.1016/S0031-9422(96)00399-8
(1R,2S,4S,5R,8R,10S,13R,14R,18R,21S)-10-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-2-hydroxy-4,5,9,9,13,20,20-heptamethyl-22-oxahexacyclo[19.2.1.01,18.04,17.05,14.08,13]tetracos-16-en-23-one 163026398 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C26CC1OC6=O)O)C)C)(C)C)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(CO8)O)O)O)C)C 764.90 unknown https://doi.org/10.1016/S0031-9422(96)00399-8
(1R,2S,4S,5R,8R,10S,13R,14R,18R,21S)-10-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3-[(2S,3R,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-2-hydroxy-4,5,9,9,13,20,20-heptamethyl-22-oxahexacyclo[19.2.1.01,18.04,17.05,14.08,13]tetracos-16-en-23-one 163021266 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C26CC1OC6=O)O)C)C)(C)C)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)OC9C(C(C(CO9)O)O)O)C)C 927.10 unknown https://doi.org/10.1016/0031-9422(89)85039-3
(1R,2S,4S,5R,8R,10S,13R,14R,18R,21S)-2-hydroxy-4,5,9,9,13,20,20-heptamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-22-oxahexacyclo[19.2.1.01,18.04,17.05,14.08,13]tetracos-16-en-23-one 162867816 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C26CC1OC6=O)O)C)C)(C)C)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)O)C)C 795.00 unknown https://doi.org/10.1016/S0031-9422(96)00399-8
(1R,2S,4S,5R,8R,10S,13R,14R,18R,21S)-2-hydroxy-4,5,9,9,13,20,20-heptamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxy-22-oxahexacyclo[19.2.1.01,18.04,17.05,14.08,13]tetracos-16-en-23-one 162901689 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C26CC1OC6=O)O)C)C)(C)C)OC7C(C(C(C(O7)COC8C(C(C(CO8)O)O)O)O)O)O)C)C 764.90 unknown https://doi.org/10.1016/S0031-9422(96)00399-8
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl] (3S,4aR,5S,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3-[(2E,6S)-2,6-dimethyl-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyocta-2,7-dienoyl]oxy-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 102094666 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC(=O)C34CC(C(CC3C5=CCC6C7(CCC(C(C7CCC6(C5(CC4O)C)C)(C)C)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)OC1C(C(C(CO1)O)O)O)C)(C)C)OC(=O)C(=CCCC(C)(C=C)OC1C(C(C(C(O1)CO)O)O)O)C)OC1C(C(C(CO1)O)O)O)O)O)O)O)O 1713.80 unknown https://doi.org/10.1254/JJP.75.451
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl] (3S,4aR,5S,6aR,6aS,6bR,8aR,10S,12aR,14bS)-3-[(2E,6S)-6-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-2,6-dimethylocta-2,7-dienoyl]oxy-10-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 102094667 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC(=O)C34CC(C(CC3C5=CCC6C7(CCC(C(C7CCC6(C5(CC4O)C)C)(C)C)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)OC1C(C(C(CO1)O)O)O)C)(C)C)OC(=O)C(=CCCC(C)(C=C)OC1C(C(C(C(O1)CO)O)O)OC1C(C(C(CO1)O)O)O)C)OC1C(C(C(CO1)O)O)O)O)O)O)O)O 1846.00 unknown https://doi.org/10.1254/JJP.75.451
10-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-2-hydroxy-4,5,9,9,13,20,20-heptamethyl-22-oxahexacyclo[19.2.1.01,18.04,17.05,14.08,13]tetracos-16-en-23-one 163026397 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C26CC1OC6=O)O)C)C)(C)C)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(CO8)O)O)O)C)C 764.90 unknown https://doi.org/10.1016/S0031-9422(96)00399-8
10-[4,5-Dihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-2-hydroxy-4,5,9,9,13,20,20-heptamethyl-22-oxahexacyclo[19.2.1.01,18.04,17.05,14.08,13]tetracos-16-en-23-one 14194033 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C26CC1OC6=O)O)C)C)(C)C)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)OC9C(C(C(CO9)O)O)O)C)C 927.10 unknown https://doi.org/10.1016/0031-9422(89)85039-3
2-Hydroxy-4,5,9,9,13,20,20-heptamethyl-10-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxy-22-oxahexacyclo[19.2.1.01,18.04,17.05,14.08,13]tetracos-16-en-23-one 85286777 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C26CC1OC6=O)O)C)C)(C)C)OC7C(C(C(C(O7)COC8C(C(C(CO8)O)O)O)O)O)O)C)C 764.90 unknown https://doi.org/10.1016/S0031-9422(96)00399-8
2-Hydroxy-4,5,9,9,13,20,20-heptamethyl-10-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-22-oxahexacyclo[19.2.1.01,18.04,17.05,14.08,13]tetracos-16-en-23-one 162867815 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C26CC1OC6=O)O)C)C)(C)C)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)O)C)C 795.00 unknown https://doi.org/10.1016/S0031-9422(96)00399-8
N-[(2R,3R,4R,5S,6R)-4,5-dihydroxy-2-[[(1R,2R,4S,5R,8R,10S,13R,14R,18S,21S)-2-hydroxy-4,5,9,9,13,20,20-heptamethyl-23-oxo-22-oxahexacyclo[19.2.1.01,18.04,17.05,14.08,13]tetracos-16-en-10-yl]oxy]-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-3-yl]acetamide 15812666 Click to see CC(=O)NC1C(C(C(OC1OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(CC(C67C5CC(C(C6)OC7=O)(C)C)O)C)C)C)COC8C(C(C(CO8)O)O)O)O)O 806.00 unknown https://doi.org/10.1016/S0031-9422(96)00399-8
N-[(2R,3R,4R,5S,6R)-4,5-dihydroxy-2-[[(1R,2S,4S,5R,8R,10S,13R,14R,18R,21S)-2-hydroxy-4,5,9,9,13,20,20-heptamethyl-23-oxo-22-oxahexacyclo[19.2.1.01,18.04,17.05,14.08,13]tetracos-16-en-10-yl]oxy]-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-3-yl]acetamide 163018966 Click to see CC(=O)NC1C(C(C(OC1OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(CC(C67C5CC(C(C6)OC7=O)(C)C)O)C)C)C)COC8C(C(C(CO8)O)O)O)O)O 806.00 unknown https://doi.org/10.1016/S0031-9422(96)00399-8
N-[4,5-dihydroxy-2-[(2-hydroxy-4,5,9,9,13,20,20-heptamethyl-23-oxo-22-oxahexacyclo[19.2.1.01,18.04,17.05,14.08,13]tetracos-16-en-10-yl)oxy]-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-3-yl]acetamide 85262931 Click to see CC(=O)NC1C(C(C(OC1OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(CC(C67C5CC(C(C6)OC7=O)(C)C)O)C)C)C)COC8C(C(C(CO8)O)O)O)O)O 806.00 unknown https://doi.org/10.1016/S0031-9422(96)00399-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,5R,9R,10S,13R,14R,17R)-17-[(E,2R,5R)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12300085 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(80)80226-3
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 521229 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(80)80226-3
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(2R,3R)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 101382379 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C(=C(C=C3)O)O)O)O 288.25 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1264869/
3,4',7,8-Tetrahydroxyflavanone 54452199 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C(=C(C=C3)O)O)O)O 288.25 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1264869/
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Leucoanthocyanidins
Epioritin-4alpha-ol 44187798 Click to see C1=CC(=CC=C1C2C(C(C3=C(O2)C(=C(C=C3)O)O)O)O)O 290.27 unknown https://doi.org/10.1016/S0031-9422(00)85959-2
Epioritin-4beta-ol 12304590 Click to see C1=CC(=CC=C1C2C(C(C3=C(O2)C(=C(C=C3)O)O)O)O)O 290.27 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1264869/
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2R,3R,4S,5S,6R)-2-[3-hydroxy-5-[(2S)-7-hydroxy-3,4-dihydro-2H-chromen-2-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162950040 Click to see COC1=C(C=C(C=C1OC2C(C(C(C(O2)CO)O)O)O)C3CCC4=C(O3)C=C(C=C4)O)O 450.40 unknown https://doi.org/10.1016/0031-9422(80)80226-3
2-[3-hydroxy-5-(7-hydroxy-3,4-dihydro-2H-chromen-2-yl)-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 3482904 Click to see COC1=C(C=C(C=C1OC2C(C(C(C(O2)CO)O)O)O)C3CCC4=C(O3)C=C(C=C4)O)O 450.40 unknown https://doi.org/10.1016/0031-9422(80)80226-3

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