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Internal ID UUID644013cea1d33876682454
Scientific name Cotylelobium lanceolatum
Authority Craib
First published in Bull. Misc. Inform. Kew 1913: 113 (1913)

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Synonyms Top

Scientific name Authority First published in
Sunaptea lanceolata (Craib) Kosterm. Proc. Round Table Conf. Dipterocarps 3: 614 (1987)
Cotylelobium malayanum Slooten Bull. Jard. Bot. Buitenzorg , sér. 3, 12: 43 (1932)

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Language Common/alternative name
Spanish cotylelobium malayanum
Spanish sunaptea lanceolata
Thai เคี่ยม

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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-0000624079
Tropicos 100316948
KEW urn:lsid:ipni.org:names:320614-1
The Plant List kew-2740425
Open Tree Of Life 589339
NCBI Taxonomy 152388
IUCN Red List 33069
IPNI 320614-1
iNaturalist 184039
GBIF 4096772
Freebase /m/03cx8ck
EOL 5712967
USDA GRIN 405645
Wikipedia Cotylelobium_lanceolatum

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
Critical Review on the Use of Extractives of Naturally Durable Woods as Natural Wood Protectants Kirker GT, Hassan B, Mankowski ME, Eller FJ Insects 18-Jan-2024
PMCID:PMC10816604
doi:10.3390/insects15010069
PMID:38249075
Sustainable Nipa Palm (Nypa fruticans Wurmb.) Product Utilization in Thailand Cheablam O, Chanklap B Scientifica (Cairo) 25-Sep-2020
PMCID:PMC7533023
doi:10.1155/2020/3856203
PMID:33062377
Resveratrol oligomer structure in Dipterocarpaceaeous plants Ito T J Nat Med 30-Apr-2020
PMCID:PMC7456419
doi:10.1007/s11418-020-01412-x
PMID:32356240
Molecular database for classifying Shorea species (Dipterocarpaceae) and techniques for checking the legitimacy of timber and wood products Tsumura Y, Kado T, Yoshida K, Abe H, Ohtani M, Taguchi Y, Fukue Y, Tani N, Ueno S, Yoshimura K, Kamiya K, Harada K, Takeuchi Y, Diway B, Finkeldey R, Na’iem M, Indrioko S, Ng KK, Muhammad N, Lee SL J Plant Res 15-May-2010
PMCID:PMC3388261
doi:10.1007/s10265-010-0348-z
PMID:20473629
Stilbenoids with One Epoxy Group from Cotylelobium lanceolatum Tetsuro Ito, Zulfiqar Ali, Toshiyuki Tanaka, Ken-ichi Nakaya, Jin Murata, Dedy Darnaedi, Munekazu Iinuma The Japan Institute of Heterocyclic Chemistry 17-Feb-2009
doi:10.3987/COM-06-10769
Resveratrol oligomers and their O-glucosides from Cotylelobium lanceolatum. Ito T, Ali Z, Furusawa M, Iliya I, Tanaka T, Nakaya K, Murata J, Darnaedi D, Iinuma M Chem Pharm Bull (Tokyo) 01-Mar-2006
doi:10.1248/CPB.54.363
PMID:16508193

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 / Dibenzocycloheptenes
(9S,10R,11S,12S)-12-(3,5-dihydroxyphenyl)-5,7,14,16-tetrahydroxy-9,11-bis(4-hydroxyphenyl)tetracyclo[8.6.1.03,8.013,17]heptadeca-1(16),3(8),4,6,13(17),14-hexaen-2-one 102253982 Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C(=O)C5=C(C=C(C(=C35)C2C6=CC(=CC(=C6)O)O)O)O)C7=CC=C(C=C7)O)O 590.60 unknown https://doi.org/10.3987/COM-06-10769
12-(3,5-Dihydroxyphenyl)-5,7,14,16-tetrahydroxy-9,11-bis(4-hydroxyphenyl)tetracyclo[8.6.1.03,8.013,17]heptadeca-1(16),3(8),4,6,13(17),14-hexaen-2-one 162853934 Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C(=O)C5=C(C=C(C(=C35)C2C6=CC(=CC(=C6)O)O)O)O)C7=CC=C(C=C7)O)O 590.60 unknown https://doi.org/10.3987/COM-06-10769
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
3,14-dihydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 628409 Click to see CC12CCC(CC1C(=O)C=C3C2CCC4(C3(CCC4C(C)(C(CCC(C)(C)O)O)O)O)C)O 464.60 unknown https://doi.org/10.1248/CPB.54.363
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(1R,2R,3R,9S,10S,17S)-2,9,17-tris(4-hydroxyphenyl)-3-[3-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaene-5,13,15-triol 21606278 Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=CC(=CC(=C7)OC8C(C(C(C(O8)CO)O)O)O)O)C(=C6)O)C9=CC=C(C=C9)O)C1=CC=C(C=C1)O)O 842.80 unknown https://doi.org/10.1248/CPB.54.363
(1R,2R,3R,9S,10S,17S)-3-[(2R,3S)-3-(3,5-dihydroxyphenyl)-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydro-1-benzofuran-5-yl]-2,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaene-5,13,15-triol 154497656 Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=CC8=C(C(=C7)OC9C(C(C(C(O9)CO)O)O)O)OC(C8C1=CC(=CC(=C1)O)O)C1=CC=C(C=C1)O)C(=C6)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O 1069.10 unknown https://doi.org/10.1248/CPB.54.363
(1R,2R,3R,9S,10S,17S)-3-[(2S,3S)-7-hydroxy-2-(4-hydroxyphenyl)-3-[3-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydro-1-benzofuran-5-yl]-2,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaene-5,13,15-triol 154497655 Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=CC8=C(C(=C7)O)OC(C8C9=CC(=CC(=C9)OC1C(C(C(C(O1)CO)O)O)O)O)C1=CC=C(C=C1)O)C(=C6)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O 1069.10 unknown https://doi.org/10.1248/CPB.54.363
(1R,2S,3S,9S,10S,17R)-2,9,17-tris(4-hydroxyphenyl)-3-[3-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaene-5,13,15-triol 101393390 Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=CC(=CC(=C7)OC8C(C(C(C(O8)CO)O)O)O)O)C(=C6)O)C9=CC=C(C=C9)O)C1=CC=C(C=C1)O)O 842.80 unknown https://doi.org/10.1248/CPB.54.363
(1S,2R,3R,9R,10S,17S)-2,9,17-tris(4-hydroxyphenyl)-3-[3-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaene-5,13,15-triol 163071019 Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=CC(=CC(=C7)OC8C(C(C(C(O8)CO)O)O)O)O)C(=C6)O)C9=CC=C(C=C9)O)C1=CC=C(C=C1)O)O 842.80 unknown https://doi.org/10.1248/CPB.54.363
(1S,2R,3R,9S,10S,17S)-2,9,17-tris(4-hydroxyphenyl)-3-[3-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaene-5,13,15-triol 101393391 Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=CC(=CC(=C7)OC8C(C(C(C(O8)CO)O)O)O)O)C(=C6)O)C9=CC=C(C=C9)O)C1=CC=C(C=C1)O)O 842.80 unknown https://doi.org/10.1248/CPB.54.363
(1S,2S,3R,4R,10R,11S)-4-[(2S,3S)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-3,11-bis(4-hydroxyphenyl)hexacyclo[8.7.6.12,5.012,17.018,23.09,24]tetracosa-5,7,9(24),12(17),13,15,18(23),19,21-nonaene-6,8,14,19,21-pentol 162841987 Click to see C1=CC(=CC=C1C2C3C4C5=C(C=C(C=C5)O)C(C(C6=C4C(=CC(=C6)O)O)C7=C3C(=C(C=C7O)O)C2C8=C9C(C(OC9=CC(=C8)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)C1=CC=C(C=C1)O)O 906.90 unknown https://doi.org/10.1248/CPB.54.363
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
(1R,2R,3S,4R,10R,11R)-3,11-bis(4-hydroxyphenyl)-4-[3-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]hexacyclo[8.7.6.12,5.012,17.018,23.09,24]tetracosa-5(24),6,8,12(17),13,15,18(23),19,21-nonaene-6,8,14,19,21-pentol 154497657 Click to see C1=CC(=CC=C1C2C3C4C5=C(C=C(C=C5)O)C(C(C6=C4C(=CC(=C6)O)O)C7=C(C=C(C(=C37)C2C8=CC(=CC(=C8)OC9C(C(C(C(O9)CO)O)O)O)O)O)O)C1=CC=C(C=C1)O)O 842.80 unknown https://doi.org/10.1248/CPB.54.363
2-[3-Hydroxy-5-[2-(4-hydroxyphenyl)vinyl]phenoxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol 393787 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 390.40 unknown https://doi.org/10.1248/CPB.54.363
Piceid 5281718 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 390.40 unknown https://doi.org/10.1248/CPB.54.363

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