PlantaeDB Logo
Login Sign-up

Cotylelobium melanoxylon

We don't have an image yet. Upload an image!

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 UUID644013cec5acd981321727
Scientific name Cotylelobium melanoxylon
Authority (Hook.f.) Pierre
First published in Fl. Forest. Cochinch. : t. 235 (1889)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Vatica harmandii F.Heim Bull. Mens. Soc. Linn. Paris 2: 955 (1891)
Vatica melanoxylon (Hook.f.) Benth. & Hook.f. ex Miq. Ann. Mus. Bot. Lugduno-Batavi 3: 85 (1867)
Vatica leucocarpa Foxw. ex L.G.d.Berger & Endert Meded. Proefstat. Boschw. No. 11, 130 (1925), nomen; v. Slooten in Bull. Jard. Bot. Buitenz. Ser. III. ix. 78 (1927), in syn.
Vatica beccariana F.Heim Bull. Mens. Soc. Linn. Paris 2: 955 (1891)
Sunaptea melanoxylon (Hook.f.) Kosterm. Proc. Round Table Conf. Dipterocarps 3: 617 (1987)
Anisoptera melanoxylon Hook.f. Trans. Linn. Soc. London 23: 160 (1860)
Cotylelobium beccarianum F.Heim Rech. Dipterocarp. : 122 (1892)
Cotylelobium beccarii Pierre Rech. Dipterocarp. (1891) t. 258 b.
Cotylelobium harmandii (F.Heim) F.Heim Rech. Dipterocarp. : 122 (1892)
Cotylelobium leucocarpum Slooten Bull. Jard. Bot. Buitenzorg , sér. 3, 9: 78 (1927)
Vatica melanoxylon subsp. recta F.Heim Bull.Mens.Soc.Linn.Paris 2(120): 956. (1891)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Indonesian cotylelobium
Malay pokok resak tempurong

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indo-China
      • Thailand
    • Malesia
      • Borneo
      • Malaya
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000624083
Tropicos 100316951
KEW urn:lsid:ipni.org:names:320618-1
The Plant List kew-2740429
Open Tree Of Life 6114746
NCBI Taxonomy 2867350
IUCN Red List 33070
IPNI 320618-1
iNaturalist 184040
GBIF 4096722
Freebase /m/0bkrwy
EOL 5712971
USDA GRIN 405646
Wikipedia Cotylelobium_melanoxylon

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
Chemistry, Biosynthesis and Pharmacology of Viniferin: Potential Resveratrol-Derived Molecules for New Drug Discovery, Development and Therapy Fuloria S, Sekar M, Khattulanuar FS, Gan SH, Rani NN, Ravi S, Subramaniyan V, Jeyabalan S, Begum MY, Chidambaram K, Sathasivam KV, Safi SZ, Wu YS, Nordin R, Maziz MN, Kumarasamy V, Lum PT, Fuloria NK Molecules 09-Aug-2022
PMCID:PMC9414909
doi:10.3390/molecules27165072
PMID:36014304
Divergence of hydraulic traits among tropical forest trees across topographic and vertical environment gradients in Borneo Bittencourt PR, Bartholomew DC, Banin LF, Bin Suis MA, Nilus R, Burslem DF, Rowland L New Phytol 26-Jun-2022
PMCID:PMC9545514
doi:10.1111/nph.18280
PMID:35633119
Quantitative Determination of Stilbenoids and Dihydroisocoumarins in Shorea roxburghii and Evaluation of Their Hepatoprotective Activity Ninomiya K, Chaipech S, Kunikata Y, Yagi R, Pongpiriyadacha Y, Muraoka O, Morikawa T Int J Mol Sci 20-Feb-2017
PMCID:PMC5343985
doi:10.3390/ijms18020451
PMID:28230758
Antidiabetogenic constituents from the Thai traditional medicine Cotylelobium melanoxylon. Matsuda H, Asao Y, Nakamura S, Hamao M, Sugimoto S, Hongo M, Pongpiriyadacha Y, Yoshikawa M Chem Pharm Bull (Tokyo) 01-May-2009
doi:10.1248/CPB.57.487
PMID:19420780

Phytochemical Profile Top

Add a new one!
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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1248/CPB.57.487
> Lignans, neolignans and related compounds / Aryltetralin lignans
(1S,8R,9R,16R)-8,16-bis(4-hydroxyphenyl)tetracyclo[7.6.1.02,7.010,15]hexadeca-2(7),3,5,10(15),11,13-hexaene-4,6,12,14-tetrol 101680650 Click to see C1=CC(=CC=C1C2C3C(C4=C(C2C5=C3C=C(C=C5O)O)C=C(C=C4O)O)C6=CC=C(C=C6)O)O 454.50 unknown https://doi.org/10.1248/CPB.57.487
(1S,8R,9R,16S)-8,16-bis(4-hydroxyphenyl)tetracyclo[7.6.1.02,7.010,15]hexadeca-2(7),3,5,10(15),11,13-hexaene-4,6,12,14-tetrol 10961436 Click to see C1=CC(=CC=C1C2C3C(C4=C(C2C5=C3C=C(C=C5O)O)C=C(C=C4O)O)C6=CC=C(C=C6)O)O 454.50 unknown https://doi.org/10.1248/CPB.57.487
Ampelopsin F 102004746 Click to see C1=CC(=CC=C1C2C3C(C4=C(C2C5=C3C=C(C=C5O)O)C=C(C=C4O)O)C6=CC=C(C=C6)O)O 454.50 unknown https://doi.org/10.1248/CPB.57.487
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
(+)-Lyoniresinol 11711453 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)CO 420.50 unknown https://doi.org/10.1248/CPB.57.487
Lyoniresinol 317840 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)CO 420.50 unknown https://doi.org/10.1248/CPB.57.487
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(+/-)-Tricholomalide B 44240398 Click to see CC(C)C1CC(=O)C2=CC(C3(CC(=O)OC3CC12C)C)(C(=C)CO)O 348.40 unknown https://doi.org/10.1248/CPB.57.487
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(+)-cis-epsilon-Viniferin 9911790 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O 454.50 unknown https://doi.org/10.1248/CPB.57.487
(+)-epsilon-Viniferin 5315233 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O 454.50 unknown https://doi.org/10.1248/CPB.57.487
(1R,2R,3R,9S,10S,17S)-3-(3,5-dihydroxyphenyl)-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 44224205 Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=CC(=CC(=C7)O)O)C(=C6)O)C8=CC=C(C=C8)O)C9=CC=C(C=C9)O)O 680.70 unknown https://doi.org/10.1248/CPB.57.487
(1R,8R,16R)-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.02,7.014,17]heptadeca-2(7),3,5,10(17),11,13-hexaene-4,6,12-triol 42642843 Click to see C1C(C2=C(C=C(C=C2O)O)C3C(OC4=CC(=CC1=C34)O)C5=CC=C(C=C5)O)C6=CC=C(C=C6)O 454.50 unknown https://doi.org/10.1248/CPB.57.487
(1S,6R,7R,19S)-6-(3,5-dihydroxyphenyl)-7,11,19-tris(4-hydroxyphenyl)-8,18-dioxapentacyclo[11.6.1.02,10.05,9.017,20]icosa-2,4,9,11,13(20),14,16-heptaene-4,15-diol 42642842 Click to see C1=CC(=CC=C1C2C(C3=C(C=C4C5C(OC6=CC(=CC(=C56)C=C(C4=C3O2)C7=CC=C(C=C7)O)O)C8=CC=C(C=C8)O)O)C9=CC(=CC(=C9)O)O)O 678.70 unknown https://doi.org/10.1248/CPB.57.487
(Z)-epsilon-Viniferin 11236373 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O 454.50 unknown https://doi.org/10.1248/CPB.57.487
3-(3,5-Dihydroxyphenyl)-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 73800061 Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=CC(=CC(=C7)O)O)C(=C6)O)C8=CC=C(C=C8)O)C9=CC=C(C=C9)O)O 680.70 unknown https://doi.org/10.1248/CPB.57.487
5-[6-Hydroxy-2-(4-hydroxyphenyl)-4-[2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol 366354 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC=C(C=C4)O)C5=CC(=CC(=C5)O)O)O 454.50 unknown https://doi.org/10.1248/CPB.57.487
6-(3,5-Dihydroxyphenyl)-7,11,19-tris(4-hydroxyphenyl)-8,18-dioxapentacyclo[11.6.1.02,10.05,9.017,20]icosa-2,4,9,11,13(20),14,16-heptaene-4,15-diol 74835147 Click to see C1=CC(=CC=C1C2C(C3=C(C=C4C5C(OC6=CC(=CC(=C56)C=C(C4=C3O2)C7=CC=C(C=C7)O)O)C8=CC=C(C=C8)O)O)C9=CC(=CC(=C9)O)O)O 678.70 unknown https://doi.org/10.1248/CPB.57.487
8,16-Bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.02,7.014,17]heptadeca-2(7),3,5,10(17),11,13-hexaene-4,6,12-triol 14650100 Click to see C1C(C2=C(C=C(C=C2O)O)C3C(OC4=CC(=CC1=C34)O)C5=CC=C(C=C5)O)C6=CC=C(C=C6)O 454.50 unknown https://doi.org/10.1248/CPB.57.487
vaticanol A 44566412 Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=CC(=CC(=C7)O)O)C(=C6)O)C8=CC=C(C=C8)O)C9=CC=C(C=C9)O)O 680.70 unknown https://doi.org/10.1248/CPB.57.487
Vaticanol E 21606276 Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=CC(=CC(=C7)O)O)C(=C6)O)C8=CC=C(C=C8)O)C9=CC=C(C=C9)O)O 680.70 unknown https://doi.org/10.1248/CPB.57.487
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(1R,2R,3S,4S,10R,11R)-4-(3,5-dihydroxyphenyl)-3,11-bis(4-hydroxyphenyl)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 101115403 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)O)O)O)O)C9=CC=C(C=C9)O)O 680.70 unknown https://doi.org/10.1248/CPB.57.487

Biological Material Top ebay Auctions

Please wait .. loading items ..

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.