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Khaya madagascariensis

Khaya madagascariensis - Unknown
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Author: Public Domain - WikiMedia
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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 UUID6440494348036196157929
Scientific name Khaya madagascariensis
Authority Jum. & H.Perrier
First published in Compt. Rend. Hebd. Séances Acad. Sci. 142: 901 (1906)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Chinese 马达加斯加非洲楝

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-0001083717
Tropicos 20400890
INPN 807352
KEW urn:lsid:ipni.org:names:578861-1
The Plant List tro-20400890
Open Tree Of Life 6124939
NCBI Taxonomy 2590898
IUCN Red List 34888
IPNI 578861-1
iNaturalist 439306
GBIF 3851956
Freebase /m/02xb3gk
USDA GRIN 411844
Wikipedia Khaya_madagascariensis

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
Chloroplast genome skimming of a potential agroforestry species Melia dubia. Cav and its comparative phylogenetic analysis with major Meliaceae members Samji A, Eashwarlal K, Shanmugavel S, Kumar S, Warrier RR 3 Biotech 31-Dec-2022
PMCID:PMC9805483
doi:10.1007/s13205-022-03447-1
PMID:36597460
Complete chloroplast genome of an endangered endemic tree, handeliodendron bodinieri (levl.) rehder (sapindaceae) from karst forests of southwest China Tian X, Li X, Miao H, Xue C, Wang B, Guo Y, Zhang G Mitochondrial DNA B Resour 27-Sep-2019
PMCID:PMC7707296
doi:10.1080/23802359.2019.1671251
PMID:33365952
Limonoids from Khaya madagascariensis Jumelle et Perrier D. A. H. Taylor Royal Society of Chemistry (RSC) 20-Apr-2004
doi:10.1039/J39700000336

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 / Triterpenoids / Limonoids
[(1S,2R,4S,7S,8S,10S,11R,12S,13S,15R,17S,19R)-10,13,15-triacetyloxy-7-(furan-3-yl)-1,8,12,16,16-pentamethyl-5-oxo-3,6-dioxapentacyclo[9.8.0.02,4.02,8.012,17]nonadecan-19-yl] acetate 21596332 Click to see CC(=O)OC1CC2C(C(CC(C2(C3C1(C45C(O4)C(=O)OC(C5(CC3OC(=O)C)C)C6=COC=C6)C)C)OC(=O)C)OC(=O)C)(C)C 644.70 unknown https://doi.org/10.1039/J39700000336
[10,13,15-Triacetyloxy-7-(furan-3-yl)-1,8,12,16,16-pentamethyl-5-oxo-3,6-dioxapentacyclo[9.8.0.02,4.02,8.012,17]nonadecan-19-yl] acetate 3898666 Click to see CC(=O)OC1CC2C(C(CC(C2(C3C1(C45C(O4)C(=O)OC(C5(CC3OC(=O)C)C)C6=COC=C6)C)C)OC(=O)C)OC(=O)C)(C)C 644.70 unknown https://doi.org/10.1039/J39700000336
methyl 2-[(1R,2R,5R,6R,13S,14S,16S)-14-acetyloxy-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.02,11.05,10]heptadec-10-en-16-yl]acetate 51398100 Click to see CC(=O)OC1C2CC3=C4CC(=O)OC(C4(CCC3C(C2=O)(C(C1(C)C)CC(=O)OC)C)C)C5=COC=C5 512.60 unknown https://doi.org/10.1039/J39700000336
methyl 2-[(1R,2S,5R,6R,10S,11S,13R,14S,16S)-14-acetyloxy-6-(furan-3-yl)-13-hydroxy-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.02,11.05,10]heptadecan-16-yl]acetate 21596316 Click to see CC(=O)OC1C(C(C2(C3CCC4(C(C3CC1(C2=O)O)CC(=O)OC4C5=COC=C5)C)C)CC(=O)OC)(C)C 530.60 unknown https://doi.org/10.1039/J39700000336
methyl 2-[(1S,2R,5R,6R,13R,14S,16S)-14-acetyloxy-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.02,11.05,10]heptadec-10-en-16-yl]acetate 162926776 Click to see CC(=O)OC1C2CC3=C4CC(=O)OC(C4(CCC3C(C2=O)(C(C1(C)C)CC(=O)OC)C)C)C5=COC=C5 512.60 unknown https://doi.org/10.1039/J39700000336
Methyl 2-[14-acetyloxy-6-(furan-3-yl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.02,11.05,10]heptadec-10-en-16-yl]acetate 3988487 Click to see CC(=O)OC1C2CC3=C4CC(=O)OC(C4(CCC3C(C2=O)(C(C1(C)C)CC(=O)OC)C)C)C5=COC=C5 512.60 unknown https://doi.org/10.1039/J39700000336
Methyl 2-[14-acetyloxy-6-(furan-3-yl)-13-hydroxy-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.02,11.05,10]heptadecan-16-yl]acetate 73811191 Click to see CC(=O)OC1C(C(C2(C3CCC4(C(C3CC1(C2=O)O)CC(=O)OC4C5=COC=C5)C)C)CC(=O)OC)(C)C 530.60 unknown https://doi.org/10.1039/J39700000336

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