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Internal ID UUID643fe7cacb468906456820
Scientific name Piranhea mexicana
Authority (Standl.) Radcl.-Sm.
First published in Kew Bull. 51: 546 (1996)

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Synonyms Top

Scientific name Authority First published in
Celaenodendron mexicanum Standl. Contr. Dudley Herb. 1: 76 (1927)

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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-0000273930
Tropicos 50170279
KEW urn:lsid:ipni.org:names:990431-1
The Plant List kew-156646
Open Tree Of Life 3908009
NCBI Taxonomy 1639866
IUCN Red List 126609070
IPNI 990431-1
iNaturalist 209960
GBIF 3075264
EOL 1152437

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
High Density of Tree-Cavities and Snags in Tropical Dry Forest of Western Mexico Raises Questions for a Latitudinal Gradient Vázquez L, Renton K PLoS One 23-Jan-2015
PMCID:PMC4304802
doi:10.1371/journal.pone.0116745
PMID:25615612
Secondary Metabolites from the Stem Bark of Celaenodendron mexicanum Perla Castañeda, Alma Bahena, Eric García, Daniel Chávez, Rachel Mata, Atilano Gutiérrez American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50099A017
Bioactive compounds from Celaenodendron mexicanum. Camacho MR, Mata R, Castaneda P, Kirby GC, Warhurst DC, Croft SL, Phillipson JD Planta Med 01-Jun-2000
doi:10.1055/S-2000-8598
PMID:10909269
Effects of some compounds isolated fromCelaenodendron mexicanum standl (euphorbiaceae) on seeds and phytopathogenic fungi. Castañeda P, Garcia MR, Hernandez BE, Torres BA, Anaya AL, Mata R J Chem Ecol 01-Jul-1992
doi:10.1007/BF00980060
PMID:24254145

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
(4aS,6aS,6aR,6bS,8aS,9R,10S,12aS,14aS,14bS)-10-hydroxy-2,2,4a,6a,6a,8a,9,14a-octamethyl-3,4,6,6b,7,8,9,10,11,12,12a,13,14,14b-tetradecahydro-1H-picen-5-one 101679786 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CC(=O)C5(C4CC(CC5)(C)C)C)C)C)C)C)O 442.70 unknown https://doi.org/10.1055/S-2000-8598
(4R,4aS,6aS,6aS,6bR,8aS,12aS,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,4,5,6,6a,7,9,10,12,12a,13,14,14b-tetradecahydropicene-3,8-dione 21636453 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CC(=O)C5(C4CC(CC5)(C)C)C)C)C)C)C 440.70 unknown https://doi.org/10.1055/S-2000-8598
https://doi.org/10.1007/BF00980060
(Z,6S)-2-methyl-6-[(5R,9S,10R,13S,14S,17S)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]hept-2-enoic acid 51693592 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 454.70 unknown https://doi.org/10.1055/S-2000-8598
(Z,6S)-6-[(3R,5R,9S,10R,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylhept-2-enoic acid 162964137 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 456.70 unknown https://doi.org/10.1055/S-2000-8598
10-hydroxy-2,2,4a,6a,6a,8a,9,14a-octamethyl-3,4,6,6b,7,8,9,10,11,12,12a,13,14,14b-tetradecahydro-1H-picen-5-one 162927537 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CC(=O)C5(C4CC(CC5)(C)C)C)C)C)C)C)O 442.70 unknown https://doi.org/10.1055/S-2000-8598
2-Methyl-6-(4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl)hept-2-enoic acid 346346 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 454.70 unknown https://doi.org/10.1055/S-2000-8598
3-Epioleanolic acid 11869658 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1055/S-2000-8598
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1055/S-2000-8598
4,4a,6a,6b,8a,11,11,14a-Octamethyl-1,2,4,5,6,6a,7,9,10,12,12a,13,14,14b-tetradecahydropicene-3,8-dione 73817656 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CC(=O)C5(C4CC(CC5)(C)C)C)C)C)C)C 440.70 unknown https://doi.org/10.1055/S-2000-8598
6-(3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-methylhept-2-enoic acid 73719044 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 456.70 unknown https://doi.org/10.1055/S-2000-8598
Friedelan-3-one 244297 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1055/S-2000-8598
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1055/S-2000-8598
https://doi.org/10.1021/NP50099A017
https://doi.org/10.1007/BF00980060
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1S,2R,3S,3'R,5R,6S,7R,8S,9S,12S)-2,12-dihydroxy-3'-[(1R)-1-hydroxyethyl]-8-methoxy-7-methyl-12-prop-1-en-2-ylspiro[4,10-dioxatetracyclo[7.2.1.02,7.03,5]dodecane-6,5'-oxolane]-2',11-dione 163188751 Click to see CC(C1CC2(C3C(O3)C4(C2(C(C5C(C4C(=O)O5)(C(=C)C)O)OC)C)O)OC1=O)O 410.40 unknown https://doi.org/10.1055/S-2000-8598
(1S,2R,3S,3'R,5R,6S,7R,8S,9S)-2,12-dihydroxy-3'-[(1R)-1-hydroxyethyl]-8-methoxy-7-methyl-12-prop-1-en-2-ylspiro[4,10-dioxatetracyclo[7.2.1.02,7.03,5]dodecane-6,5'-oxolane]-2',11-dione 101047058 Click to see CC(C1CC2(C3C(O3)C4(C2(C(C5C(C4C(=O)O5)(C(=C)C)O)OC)C)O)OC1=O)O 410.40 unknown https://doi.org/10.1055/S-2000-8598
2,12-Dihydroxy-3'-(1-hydroxyethyl)-8-methoxy-7-methyl-12-prop-1-en-2-ylspiro[4,10-dioxatetracyclo[7.2.1.02,7.03,5]dodecane-6,5'-oxolane]-2',11-dione 162974329 Click to see CC(C1CC2(C3C(O3)C4(C2(C(C5C(C4C(=O)O5)(C(=C)C)O)OC)C)O)OC1=O)O 410.40 unknown https://doi.org/10.1055/S-2000-8598
https://doi.org/10.1021/NP50099A017
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Amentoflavone 5281600 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O 538.50 unknown https://doi.org/10.1055/S-2000-8598
https://doi.org/10.1007/BF00980060
Bilobetin 5315459 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O 552.50 unknown https://doi.org/10.1007/BF00980060
Ginkgetin 5271805 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O 566.50 unknown https://doi.org/10.1007/BF00980060
Podocarpusflavone A 5320644 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O 552.50 unknown https://doi.org/10.1055/S-2000-8598
Podocarpusflavone B 5320646 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)OC)O)O 566.50 unknown https://doi.org/10.1055/S-2000-8598

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