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Shorea uliginosa

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID6440046dbe3d7505501410
Scientific name Shorea uliginosa
Authority Foxw.
First published in Malayan Forest Rec. 10: 210 (1932)

Description Top

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Synonyms Top

Scientific name Authority First published in
Shorea rugosa subsp. uliginosa Symington

Common names Top

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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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000499292
KEW urn:lsid:ipni.org:names:321476-1
Open Tree Of Life 6114937
NCBI Taxonomy 2025636
IUCN Red List 33140
IPNI 321476-1
iNaturalist 443658
GBIF 4096571
Freebase /m/02y_hvq
USDA GRIN 468247
Wikipedia Shorea_uliginosa
CMAUP NPO15485

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
Metabolite profiling of Borneo’s Gonystylus bancanus through comprehensive extraction from various polarity of solvents Oktavianawati I, Santoso M, Fatmawati S Sci Rep 14-Sep-2023
PMCID:PMC10502116
doi:10.1038/s41598-023-41494-7
PMID:37709800
Natural and nature-inspired stilbenoids as antiviral agents Mattio LM, Catinella G, Pinto A, Dallavalle S Eur J Med Chem 04-Jul-2020
PMCID:PMC7335248
doi:10.1016/j.ejmech.2020.112541
PMID:32652408
Impact of forest plantation on methane emissions from tropical peatland Deshmukh CS, Julius D, Evans CD, Nardi, Susanto AP, Page SE, Gauci V, Laurén A, Sabiham S, Agus F, Asyhari A, Kurnianto S, Suardiwerianto Y, Desai AR Glob Chang Biol 20-Feb-2020
PMCID:PMC7155032
doi:10.1111/gcb.15019
PMID:31991028
Microbial Community Structure in a Malaysian Tropical Peat Swamp Forest: The Influence of Tree Species and Depth Too CC, Keller A, Sickel W, Lee SM, Yule CM Front Microbiol 04-Dec-2018
PMCID:PMC6288306
doi:10.3389/fmicb.2018.02859
PMID:30564202
Chemistry and Biology of Resveratrol-Derived Natural Products Keylor MH, Matsuura BS, Stephenson CR Chem Rev 02-Apr-2015
PMCID:PMC4566929
doi:10.1021/cr500689b
PMID:25835567
Absolute structures of C-glucosides of resveratrol oligomers from Shorea uliginosa Tetsuro Ito, Naohito Abe, Masayoshi Oyama, Munekazu Iinuma Elsevier BV 14-Mar-2009
doi:10.1016/J.TETLET.2009.03.043
Organic matter dynamics control plant species coexistence in a tropical peat swamp forest Shimamura T, Momose K Proc Biol Sci 28-Jun-2005
PMCID:PMC1559832
doi:10.1098/rspb.2005.3095
PMID:16011926
Rotational isomerism of a resveratrol tetramer, shoreaketone, in Shorea uliginosa Tetsuro Ito, Miyuki Furusawa, Ibrahim Iliya, Toshiyuki Tanaka, Ken-ichi Nakaya, Ryuichi Sawa, Yumiko Kubota, Yoshikazu Takahashi, Soedarsono Riswan, Munekazu Iinuma Elsevier BV 17-Mar-2005
doi:10.1016/J.TETLET.2005.02.165

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
2-Methyl-2-butene 10553 Click to see CC=C(C)C 70.13 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
threo-9,10-Dihydroxystearic acid 12235228 Click to see CCCCCCCCC(C(CCCCCCCC(=O)O)O)O 316.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
cis-9,10-Epoxyoctadecanoic acid 12235227 Click to see CCCCCCCCC1C(O1)CCCCCCCC(=O)O 298.50 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
(2S,3S)-2-ammonio-3-hydroxybutanoate 6995276 Click to see CC(C(C(=O)[O-])[NH3+])O 119.12 unknown via CMAUP database
(2S)-6-amino-2-azaniumylhexanoate 122198194 Click to see C(CCN)CC(C(=O)[O-])[NH3+] 146.19 unknown via CMAUP database
Arginine 6322 Click to see C(CC(C(=O)O)N)CN=C(N)N 174.20 unknown via CMAUP database
L-Cysteic acid 72886 Click to see C(C(C(=O)O)N)S(=O)(=O)O 169.16 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Aspartic acid and derivatives
[3H]L-aspartic acid 44367445 Click to see C(C(C(=O)O)[NH3+])C(=O)[O-] 133.10 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Histidine and derivatives
(2S)-2-azaniumyl-3-(1H-imidazol-5-yl)propanoate 6971009 Click to see C1=C(NC=N1)CC(C(=O)[O-])[NH3+] 155.15 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Isoleucine and derivatives
(2S,3S)-2-ammonio-3-methylpentanoate 7043901 Click to see CCC(C)C(C(=O)[O-])[NH3+] 131.17 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Leucine and derivatives
(2S)-2-azaniumyl-4-methylpentanoate 7045798 Click to see CC(C)CC(C(=O)[O-])[NH3+] 131.17 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Methionine and derivatives
(2S)-2-ammonio-4-(methylsulfanyl)butanoate 6992087 Click to see CSCCC(C(=O)[O-])[NH3+] 149.21 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Serine and derivatives
Serine 5951 Click to see C(C(C(=O)O)N)O 105.09 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
(2S)-2-ammonio-3-(4-hydroxyphenyl)propanoate 6942100 Click to see C1=CC(=CC=C1CC(C(=O)[O-])[NH3+])O 181.19 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Gamma amino acids and derivatives
4-Aminobutanoate 6992099 Click to see C(CC(=O)[O-])C[NH3+] 103.12 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S,3R,4R,5S,6R)-2-[2,6-dihydroxy-4-[(2S,3S)-6-hydroxy-2-(4-hydroxyphenyl)-4-[(E)-2-(4-hydroxyphenyl)ethenyl]-7-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2,3-dihydro-1-benzofuran-3-yl]phenyl]-6-(hydroxymethyl)oxane-3,4,5-triol 102577447 Click to see C1=CC(=CC=C1C=CC2=CC(=C(C3=C2C(C(O3)C4=CC=C(C=C4)O)C5=CC(=C(C(=C5)O)C6C(C(C(C(O6)CO)O)O)O)O)C7C(C(C(C(O7)CO)O)O)O)O)O 778.70 unknown https://doi.org/10.1016/J.TETLET.2009.03.043
(2S,3R,4R,5S,6R)-2-[4-[(2R,3R)-5-[(E)-2-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2,3-dihydro-1-benzofuran-4-yl]ethenyl]-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-3-yl]-2,6-dihydroxyphenyl]-6-(hydroxymethyl)oxane-3,4,5-triol 163191470 Click to see C1=CC(=CC=C1C2C(C3=C(O2)C=CC(=C3)C=CC4=CC(=C(C5=C4C(C(O5)C6=CC=C(C=C6)O)C7=CC(=CC(=C7)O)O)C8C(C(C(C(O8)CO)O)O)O)O)C9=CC(=C(C(=C9)O)C1C(C(C(C(O1)CO)O)O)O)O)O 1005.00 unknown https://doi.org/10.1016/J.TETLET.2009.03.043
(2S,3R,4R,5S,6R)-2-[4-[(2S,3S)-5-[(E)-2-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2,3-dihydro-1-benzofuran-4-yl]ethenyl]-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-3-yl]-2,6-dihydroxyphenyl]-6-(hydroxymethyl)oxane-3,4,5-triol 163195596 Click to see C1=CC(=CC=C1C2C(C3=C(O2)C=CC(=C3)C=CC4=CC(=C(C5=C4C(C(O5)C6=CC=C(C=C6)O)C7=CC(=CC(=C7)O)O)C8C(C(C(C(O8)CO)O)O)O)O)C9=CC(=C(C(=C9)O)C1C(C(C(C(O1)CO)O)O)O)O)O 1005.00 unknown https://doi.org/10.1016/J.TETLET.2009.03.043
2-[2,6-Dihydroxy-4-[6-hydroxy-2-(4-hydroxyphenyl)-4-[2-(4-hydroxyphenyl)ethenyl]-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2,3-dihydro-1-benzofuran-3-yl]phenyl]-6-(hydroxymethyl)oxane-3,4,5-triol 85246308 Click to see C1=CC(=CC=C1C=CC2=CC(=C(C3=C2C(C(O3)C4=CC=C(C=C4)O)C5=CC(=C(C(=C5)O)C6C(C(C(C(O6)CO)O)O)O)O)C7C(C(C(C(O7)CO)O)O)O)O)O 778.70 unknown https://doi.org/10.1016/J.TETLET.2009.03.043
2-[4-[5-[2-[3-(3,5-Dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2,3-dihydro-1-benzofuran-4-yl]ethenyl]-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-3-yl]-2,6-dihydroxyphenyl]-6-(hydroxymethyl)oxane-3,4,5-triol 162958557 Click to see C1=CC(=CC=C1C2C(C3=C(O2)C=CC(=C3)C=CC4=CC(=C(C5=C4C(C(O5)C6=CC=C(C=C6)O)C7=CC(=CC(=C7)O)O)C8C(C(C(C(O8)CO)O)O)O)O)C9=CC(=C(C(=C9)O)C1C(C(C(C(O1)CO)O)O)O)O)O 1005.00 unknown https://doi.org/10.1016/J.TETLET.2009.03.043
3-[3-(3,5-Dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-7,15-dihydroxy-2,11-bis(4-hydroxyphenyl)-10,18-dioxaheptacyclo[11.10.2.15,9.01,19.04,24.017,25.012,26]hexacosa-5(26),6,8,13(25),14,16,22-heptaen-21-one 163004480 Click to see C1C2C3(C=CC1=O)C(C(C4C3C5=C(C=C(C=C5O2)O)C6C(OC7=CC(=CC4=C67)O)C8=CC=C(C=C8)O)C9=C1C(C(OC1=CC(=C9)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)C1=CC=C(C=C1)O 906.90 unknown https://doi.org/10.1016/J.TETLET.2005.02.165
Shoreaketone 12192382 Click to see C1C2C3(C=CC1=O)C(C(C4C3C5=C(C=C(C=C5O2)O)C6C(OC7=CC(=CC4=C67)O)C8=CC=C(C=C8)O)C9=C1C(C(OC1=CC(=C9)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)C1=CC=C(C=C1)O 906.90 unknown https://doi.org/10.1016/J.TETLET.2005.02.165
Uriginoside A 101011050 Click to see C1=CC(=CC=C1C=CC2=CC(=C(C3=C2C(C(O3)C4=CC=C(C=C4)O)C5=CC(=C(C(=C5)O)C6C(C(C(C(O6)CO)O)O)O)O)C7C(C(C(C(O7)CO)O)O)O)O)O 778.70 unknown https://doi.org/10.1016/J.TETLET.2009.03.043

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