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Mammea punctata

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 UUID64405b84d97f7760355728
Scientific name Mammea punctata
Authority (H.Perrier) P.F.Stevens
First published in Harvard Pap. Bot. 9: 432 (2005)

Ethnobotanical Use Top

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General Uses Top

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Scientific and model organism uses:
The species is a focal taxon for phylogenetic and taxonomic research in the Clusiaceae, providing morphological and molecular data for comparative systematics and for community databases (e.g., World Flora Online, GBIF). Studies utilize leaf architecture, flower micromorphology, and DNA sequences to reconstruct relationships, and herbarium specimens support morphological analyses relevant to species delimitation and conservation.

Properties relevant to use:
Leaves and bark synthesize benzophenone xanthones and mammea coumarins characteristic of the genus, and wood contains extractives typical of Clusiaceae heartwoods that can inhibit certain fungal taxa; these chemistries are studied for chemosystematics rather than for commercial application. No industrial or culinary uses are documented.

Standards and regulation:
There are no established international product standards or regulatory frameworks directly addressing Mammea punctata as a commercial species.

Sustainability and sourcing:
The conservation status of M. punctata has been evaluated in national Red List processes (e.g., Madagascar). Its inclusion in conservation assessments reflects limited occurrence and habitat sensitivity; no recognized harvest or trade routes for industrial or consumer products have been documented. Continued monitoring via herbarium and field records underpins the status assessments.

Synonyms Top

Scientific name Authority First published in
Ochrocarpos punctatus H.Perrier Mém. Mus. Hist. Nat., Paris n.s., xxiv. 104 (1948).

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Mammea punctata var. rubrifolia P.F.Stevens Harvard Pap. Bot. 9: 432 (2005)
Mammea punctata var. punctata Unknown

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

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-0001296094
Tropicos 7801328
KEW urn:lsid:ipni.org:names:60439832-2
The Plant List tro-7801328
Open Tree Of Life 6099186
NCBI Taxonomy 2899635
IPNI 60439832-2
iNaturalist 709438
GBIF 7879906

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
Sleeping and Ranging Behavior of the Sambirano Mouse Lemur, Microcebus sambiranensis Hending D, McCabe G, Holderied M Int J Primatol 28-Oct-2017
PMCID:PMC5730628
doi:10.1007/s10764-017-9997-2
PMID:29263564
Biodiversity conservation and drug discovery: Can they be combined? The Suriname and Madagascar experiences Cao S, Kingston DG Pharm Biol 01-Aug-2009
PMCID:PMC2746688
doi:10.1080/13880200902988629
PMID:20161050
New cytotoxic coumarins and prenylated benzophenone derivatives from the bark of Ochrocarpos punctatus from the Madagascar rainforest. Chaturvedula VS, Schilling JK, Kingston DG J Nat Prod 01-Jul-2002
doi:10.1021/NP020030A
PMID:12141854

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
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(1R,2S,4R,6R,8S,10R)-1-benzoyl-4-(2-hydroxypropan-2-yl)-11,11-dimethyl-8,10-bis(3-methylbut-2-enyl)-3-oxatricyclo[6.3.1.02,6]dodecane-7,12-dione 163104220 Click to see 520.70 unknown https://doi.org/10.1021/NP020030A
(1R,2S,4R,6S,8S,10S)-8-benzoyl-4-(2-hydroxypropan-2-yl)-9,9-dimethyl-1,10-bis(3-methylbut-2-enyl)-3-oxatricyclo[6.3.1.02,6]dodecane-7,12-dione 163105992 Click to see 520.70 unknown https://doi.org/10.1021/NP020030A
(1R,5R,9R,11S)-9-benzoyl-5-hydroperoxy-4,4,10,10-tetramethyl-1,11-bis(3-methylbut-2-enyl)-3-oxatricyclo[7.3.1.02,7]tridec-2(7)-ene-8,13-dione 162962705 Click to see 534.70 unknown https://doi.org/10.1021/NP020030A
(1S,4R,8R,10S)-1-benzoyl-4-(2-hydroxypropan-2-yl)-11,11-dimethyl-8,10-bis(3-methylbut-2-enyl)-3-oxatricyclo[6.3.1.02,6]dodec-2(6)-ene-7,12-dione 132594786 Click to see CC(=CCC1CC2(C(=O)C3=C(C(C2=O)(C1(C)C)C(=O)C4=CC=CC=C4)OC(C3)C(C)(C)O)CC=C(C)C)C 518.70 unknown https://doi.org/10.1021/NP020030A
(1S,4R,8S,10R)-8-benzoyl-4-(2-hydroxypropan-2-yl)-9,9-dimethyl-1,10-bis(3-methylbut-2-enyl)-3-oxatricyclo[6.3.1.02,6]dodec-2(6)-ene-7,12-dione 9984117 Click to see CC(=CCC1CC2(C3=C(CC(O3)C(C)(C)O)C(=O)C(C2=O)(C1(C)C)C(=O)C4=CC=CC=C4)CC=C(C)C)C 518.70 unknown https://doi.org/10.1021/NP020030A
(1S,4S,8S,10S)-8-benzoyl-4-(2-hydroxypropan-2-yl)-9,9-dimethyl-1,10-bis(3-methylbut-2-enyl)-3-oxatricyclo[6.3.1.02,6]dodec-2(6)-ene-7,12-dione 636668 Click to see CC(=CCC1CC2(C3=C(CC(O3)C(C)(C)O)C(=O)C(C2=O)(C1(C)C)C(=O)C4=CC=CC=C4)CC=C(C)C)C 518.70 unknown https://doi.org/10.1021/NP020030A
(1S,5R,9R,11S)-1-benzoyl-5-hydroperoxy-4,4,12,12-tetramethyl-9,11-bis(3-methylbut-2-enyl)-3-oxatricyclo[7.3.1.02,7]tridec-2(7)-ene-8,13-dione 162940652 Click to see 534.70 unknown https://doi.org/10.1021/NP020030A
(1S,5S,9S,11R)-9-benzoyl-5-hydroperoxy-4,4,10,10-tetramethyl-1,11-bis(3-methylbut-2-enyl)-3-oxatricyclo[7.3.1.02,7]tridec-2(7)-ene-8,13-dione 162962704 Click to see 534.70 unknown https://doi.org/10.1021/NP020030A
1-Benzoyl-5-hydroperoxy-4,4,12,12-tetramethyl-9,11-bis(3-methylbut-2-enyl)-3-oxatricyclo[7.3.1.02,7]tridec-2(7)-ene-8,13-dione 44559882 Click to see CC(=CCC1CC2(C(=O)C3=C(C(C2=O)(C1(C)C)C(=O)C4=CC=CC=C4)OC(C(C3)OO)(C)C)CC=C(C)C)C 534.70 unknown https://doi.org/10.1021/NP020030A
Ochrocarpinone A 10347061 Click to see 534.70 unknown https://doi.org/10.1021/NP020030A
Ochrocarpinone B 10459280 Click to see 518.70 unknown https://doi.org/10.1021/NP020030A
Ochrocarpinone C 10256066 Click to see 518.70 unknown https://doi.org/10.1021/NP020030A
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
[(1R)-1-[(8R)-5-hydroxy-8-(2-hydroxypropan-2-yl)-6-[(2S)-2-methylbutanoyl]-2-oxo-8,9-dihydrofuro[2,3-h]chromen-4-yl]propyl] acetate 162885731 Click to see 446.50 unknown https://doi.org/10.1021/NP020030A
[(1R)-1-[(8S)-5-hydroxy-8-(2-hydroxypropan-2-yl)-6-[(2S)-2-methylbutanoyl]-2-oxo-8,9-dihydrofuro[2,3-h]chromen-4-yl]propyl] acetate 162885732 Click to see 446.50 unknown https://doi.org/10.1021/NP020030A
[(1S)-1-[(8S)-5-hydroxy-8-(2-hydroxypropan-2-yl)-6-[(2S)-2-methylbutanoyl]-2-oxo-8,9-dihydrofuro[2,3-h]chromen-4-yl]propyl] acetate 162885733 Click to see 446.50 unknown https://doi.org/10.1021/NP020030A
1-[5-Hydroxy-8-(2-hydroxypropan-2-yl)-6-(2-methylbutanoyl)-2-oxo-8,9-dihydrofuro[2,3-h]chromen-4-yl]propyl acetate 73805541 Click to see CCC(C)C(=O)C1=C2C(=C3C(=C1O)C(=CC(=O)O3)C(CC)OC(=O)C)CC(O2)C(C)(C)O 446.50 unknown https://doi.org/10.1021/NP020030A
Ochrocarpin F 10388861 Click to see CCC(C)C(=O)C1=C2C(=C3C(=C1O)C(=CC(=O)O3)C(CC)OC(=O)C)CC(O2)C(C)(C)O 446.50 unknown https://doi.org/10.1021/NP020030A
Ochrocarpin F 10343524 Click to see 446.50 unknown https://doi.org/10.1021/NP020030A
> Phenylpropanoids and polyketides / Neoflavonoids / Neoflavones
5-hydroxy-8-(2-hydroxypropan-2-yl)-6-[(2R)-2-methylbutanoyl]-4-phenylfuro[2,3-h]chromen-2-one 162937531 Click to see 420.50 unknown https://doi.org/10.1021/NP020030A
5-Hydroxy-8-(2-methoxypropan-2-yl)-6-(2-methylbutanoyl)-4-phenylfuro[2,3-h]chromen-2-one 10025917 Click to see 434.50 unknown https://doi.org/10.1021/NP020030A
5-hydroxy-8-(2-methoxypropan-2-yl)-6-[(2R)-2-methylbutanoyl]-4-phenylfuro[2,3-h]chromen-2-one 163067521 Click to see 434.50 unknown https://doi.org/10.1021/NP020030A
Lpgfebxrfjlodr-uhfffaoysa- 10454802 Click to see 420.50 unknown https://doi.org/10.1021/NP020030A
Ochrocarpin A 44559918 Click to see 420.50 unknown https://doi.org/10.1021/NP020030A
Ochrocarpin C 11742055 Click to see 406.40 unknown https://doi.org/10.1021/NP020030A
Ochrocarpin D 44559858 Click to see 434.50 unknown https://doi.org/10.1021/NP020030A
> Phenylpropanoids and polyketides / Neoflavonoids / Prenylated neoflavonoids
(2R)-4-hydroxy-2-(2-hydroxypropan-2-yl)-5-(2-methylpropanoyl)-9-phenyl-2,3-dihydrofuro[2,3-f]chromen-7-one 163027970 Click to see 408.40 unknown https://doi.org/10.1021/NP020030A
(2S)-4-hydroxy-2-(2-hydroxypropan-2-yl)-5-(2-methylpropanoyl)-9-phenyl-2,3-dihydrofuro[2,3-f]chromen-7-one 163027969 Click to see 408.40 unknown https://doi.org/10.1021/NP020030A
(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/10.1021/NP020030A
(8S)-5-hydroxy-8-(1-hydroxy-1-methyl-ethyl)-6-(3-methylbutanoyl)-4-phenyl-8,9-dihydrofuro[2,3-h]chromen-2-one 6483323 Click to see 422.50 unknown https://doi.org/10.1021/NP020030A
(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/10.1021/NP020030A
5-Hydroxy-6'',6''-dimethyl-6-(2-methylbutyryl)-4-phenylpyrano[2'',3'':7,8]coumarin 15223665 Click to see 404.50 unknown https://doi.org/10.1021/NP020030A
5-hydroxy-8,8-dimethyl-6-[(2R)-2-methylbutanoyl]-4-phenylpyrano[2,3-h]chromen-2-one 26176279 Click to see 404.50 unknown https://doi.org/10.1021/NP020030A
Cyclomammeisin 21592420 Click to see CC(C)CC(=O)C1=C2C(=C3C(=C1O)C(=CC(=O)O3)C4=CC=CC=C4)CC(O2)C(C)(C)O 422.50 unknown https://doi.org/10.1021/NP020030A
Mammea A/AC cyclo F 5319254 Click to see 408.40 unknown https://doi.org/10.1021/NP020030A
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/10.1021/NP020030A
Ochrocarpin B 10387413 Click to see 420.50 unknown https://doi.org/10.1021/NP020030A
Ochrocarpin E 10250876 Click to see CC(C)C(=O)C1=C2C(=C3C(=C1O)CC(O3)C(C)(C)O)C(=CC(=O)O2)C4=CC=CC=C4 408.40 unknown https://doi.org/10.1021/NP020030A

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