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Kayea racemosa

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID68f8f40c66d08466447231
Scientific name Kayea racemosa
Authority Planch. & Triana
First published in Ann. Sci. Nat., Bot. , sér. 4, 15: 297 (1861)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Mesua singaporiana Wall. Numer. List : n.° 4836 (1831)
Mesua racemosa (Planch. & Triana) Kosterm. Reinwardtia 7: 429 (1969)

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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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
KEW urn:lsid:ipni.org:names:428860-1
Open Tree Of Life 774888
NCBI Taxonomy 180120
IPNI 428860-1
GBIF 3711927
World Flora Online wfo-0000356295
KEW urn:lsid:ipni.org:names:428712-1
NCBI Taxonomy 2990930
IPNI 428712-1
GBIF 3714253

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
Two New Pyranoxanthones from Mesua beccariana (Guttiferae) Teh SS, Ee GC, Rahmani M, Sim WC, Mah SH, Teo SH Molecules 27-Sep-2010
PMCID:PMC6259158
doi:10.3390/molecules15106733
New Coumarins from Mesua racemosa: Isolation and Synthesis Pascal Richomme, Cécile Morel, Caroline Dartiguelongue, Thierry Youhana, Jean-Michel Oger, Denis Séraphin, Olivier Duval, Jean Bruneton The Japan Institute of Heterocyclic Chemistry 12-Mar-2009
doi:10.3987/COM-99-8601
6-Acylcoumarins from Mesua racemosa Cécile Morel, David Guilet, Jean-Michel Oger, Denis Séraphin, Thierry Sévenet, Christophe Wiart, A.Hamid A Hadi, Pascal Richomme, Jean Bruneton Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00688-8

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
> Phenylpropanoids and polyketides / Neoflavonoids / Neoflavones
6-Butanoyl-5-hydroxy-4-phenylfuro[2,3-h]chromen-2-one 15407041 Click to see 348.30 unknown https://doi.org/10.3987/COM-99-8601
8-Acetyl-6-butanoyl-5,7-dihydroxy-4-phenylchromen-2-one 15407040 Click to see CCCC(=O)C1=C(C(=C2C(=C1O)C(=CC(=O)O2)C3=CC=CC=C3)C(=O)C)O 366.40 unknown https://doi.org/10.3987/COM-99-8601
> Phenylpropanoids and polyketides / Neoflavonoids / Prenylated neoflavonoids
(8R)-6-butanoyl-5-hydroxy-8-(2-hydroxypropan-2-yl)-4-phenyl-8,9-dihydrofuro[2,3-h]chromen-2-one 162961264 Click to see 408.40 unknown https://doi.org/10.1016/S0031-9422(98)00688-8
(8S)-6-butanoyl-5-hydroxy-8-(2-hydroxypropan-2-yl)-4-phenyl-8,9-dihydrofuro[2,3-h]chromen-2-one 44584740 Click to see 408.40 unknown https://doi.org/10.1016/S0031-9422(98)00688-8
5,7-dihydroxy-6-[(2R)-2-methylbutanoyl]-8-(3-methylbut-2-enyl)-4-phenylchromen-2-one 162892135 Click to see 406.50 unknown https://doi.org/10.1016/S0031-9422(98)00688-8
5,7-dihydroxy-8-[(2R)-2-methylbutanoyl]-6-(3-methylbut-2-enyl)-4-phenylchromen-2-one 162906900 Click to see 406.50 unknown https://doi.org/10.1016/S0031-9422(98)00688-8
6-Butanoyl-5,7-dihydroxy-8-(2-hydroxy-3-methylbut-3-enyl)-4-phenylchromen-2-one 5320883 Click to see 408.40 unknown https://doi.org/10.1016/S0031-9422(98)00688-8
6-butanoyl-5,7-dihydroxy-8-[(2R)-2-hydroxy-3-methylbut-3-enyl]-4-phenylchromen-2-one 162922120 Click to see CCCC(=O)C1=C(C2=C(C(=C1O)CC(C(=C)C)O)OC(=O)C=C2C3=CC=CC=C3)O 408.40 unknown https://doi.org/10.1016/S0031-9422(98)00688-8
6-Butyryl-5-hydroxy-4-phenylseselin 44257540 Click to see 390.40 unknown https://doi.org/10.1016/S0031-9422(98)00688-8
6-Butyryl-5,7-dihydroxy-8-(3',3'-dimethylallyl)-4-phenylcoumarin 44257539 Click to see CCCC(=O)C1=C(C2=C(C(=C1O)C=CC(C)C)OC(=O)C=C2C3=CC=CC=C3)O 392.40 unknown https://doi.org/10.1016/S0031-9422(98)00688-8
8-Butanoyl-5,7-dihydroxy-6-(2-hydroxy-3-methylbut-3-enyl)-4-phenylchromen-2-one 15407043 Click to see 408.40 unknown https://doi.org/10.3987/COM-99-8601
8-Butanoyl-5,7-dihydroxy-6-(3-methylbut-2-enyl)-4-phenylchromen-2-one 15407042 Click to see 392.40 unknown https://doi.org/10.3987/COM-99-8601
8-butanoyl-5,7-dihydroxy-6-[(2R)-2-hydroxy-3-methylbut-3-enyl]-4-phenylchromen-2-one 162983762 Click to see CCCC(=O)C1=C(C(=C(C2=C1OC(=O)C=C2C3=CC=CC=C3)O)CC(C(=C)C)O)O 408.40 unknown https://doi.org/10.3987/COM-99-8601
Mammea A/AB 6483317 Click to see 406.50 unknown https://doi.org/10.1016/S0031-9422(98)00688-8
Mammea A/AC cyclo F 5319254 Click to see 408.40 unknown https://doi.org/10.1016/S0031-9422(98)00688-8
Mammea A/BB 11750116 Click to see 406.50 unknown https://doi.org/10.1016/S0031-9422(98)00688-8
Mammea A/BB, (-)- 53322741 Click to see 406.50 unknown https://doi.org/10.1016/S0031-9422(98)00688-8
Mammeisin 5281419 Click to see CC(C)CC(=O)C1=C(C2=C(C(=C1O)CC=C(C)C)OC(=O)C=C2C3=CC=CC=C3)O 406.50 unknown https://doi.org/10.1016/S0031-9422(98)00688-8
Mesuagin 5319380 Click to see CC(C)C(=O)C1=C2C(=C3C(=C1O)C(=CC(=O)O3)C4=CC=CC=C4)C=CC(O2)(C)C 390.40 unknown https://doi.org/10.1016/S0031-9422(98)00688-8

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