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Picrasma crenata

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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 UUID64404ee540c8a005822622
Scientific name Picrasma crenata
Authority Engl.
First published in Nat. Pflanzenfam. 3(4): 222 (1896)

Description Top

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Picrasma crenata, also known as pau-amargo, pau-tenente, or tenente-josé, is a tree from the Simaroubaceae family. It is found in Brazil, specifically in the Atlantic Forest region, in the states of Bahia, Minas Gerais, São Paulo, Rio de Janeiro, Paraná, Santa Catarina, and Rio Grande do Sul.

Synonyms Top

Scientific name Authority First published in
Thevetia pinnata Vell. Fl. Flumin. 57. 1829 [1825 publ. 7 Sep-28 Nov 1829] ; see also Fl. Flumin. Icon. 1: t. 151. 1831. [1827 publ. 29 Oct 1831]
Aeschrion crenata Vell. Fl. Flumin. 1: 58, t. 152 (1829)
Picraena vellozoi Engl. Fl. Bras. (Martius) 12(2): 227. 1874 [1 Sep 1874]
Picrasma vellozoi Planch. London J. Bot. 5: 574. 1846
Picrasma palo-amargo Speg. Physis (Buenos Aires) iii. 173 (1917).
Picraena palo-amargo Speg. Physis (Buenos Aires) 7: 93 (1923)
Picramnia crenata (Vell.) Hassl. Ind. Fl. Dendr. Arg. 1: 59 1935

Common names Top

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Language Common/alternative name
Portuguese pau-amargo

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
  • Southern America
    • Brazil
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
    • Southern South America
      • Argentina Northeast
      • Paraguay

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001140378
Tropicos 29400137
KEW urn:lsid:ipni.org:names:195994-2
The Plant List tro-29400137
Open Tree Of Life 858643
NCBI Taxonomy 459138
IPNI 195994-2
iNaturalist 1078996
GBIF 3708970
Freebase /m/0gyrfm6
EOL 5310444
Wikipedia Picrasma_crenata

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
Phylogenomic analyses of Sapindales support new family relationships, rapid Mid-Cretaceous Hothouse diversification, and heterogeneous histories of gene duplication Joyce EM, Appelhans MS, Buerki S, Cheek M, de Vos JM, Pirani JR, Zuntini AR, Bachelier JB, Bayly MJ, Callmander MW, Devecchi MF, Pell SK, Groppo M, Lowry PP II, Mitchell J, Siniscalchi CM, Munzinger J, Orel HK, Pannell CM, Nauheimer L, Sauquet H, Weeks A, Muellner-Riehl AN, Leitch IJ, Maurin O, Forest F, Nargar K, Thiele KR, Baker WJ, Crayn DM Front Plant Sci 07-Mar-2023
PMCID:PMC10028101
doi:10.3389/fpls.2023.1063174
PMID:36959945
Quassinoids and Other Constituents from Picrasma crenata H. C. Krebs, P. J. Schilling, R. Wartchow, M. Bolte Walter de Gruyter GmbH 17-Feb-2015
doi:10.1515/ZNB-2001-0316
Honey-Based Mixtures Used in Home Medicine by Nonindigenous Population of Misiones, Argentina Kujawska M, Zamudio F, Hilgert NI Evid Based Complement Alternat Med 22-Jan-2012
PMCID:PMC3270538
doi:10.1155/2012/579350
PMID:22315632
Exploring the Links between Ethnobotany, Local Therapeutic Practices, and Protected Areas in Santa Catarina Coastline, Brazil Zank S, Hanazaki N Evid Based Complement Alternat Med 17-Nov-2011
PMCID:PMC3235720
doi:10.1155/2012/563570
PMID:22203874
Quassinoids from Picrasma crenata. Novello CR, Ferreira AG, Marques LC, Cortez DA Nat Prod Res 01-Jun-2003
doi:10.1080/1478641031000104082
PMID:12737395
Quassinoids from Aeschrion crenata J.C. Vitagliano, J. Comin Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(72)80052-9
Two new β-carboline alkaloids from aeschrion crenata E. Sánchez, J. Comin Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97212-1

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
> Alkaloids and derivatives / Harmala alkaloids
1-Ethyl-4-methoxy-9H-pyrido[3,4-b]indole 5317256 Click to see CCC1=NC=C(C2=C1NC3=CC=CC=C32)OC 226.27 unknown https://doi.org/10.1016/S0031-9422(00)97212-1
1-Ethyl-4,8-dimethoxy-beta-carboline 5317243 Click to see CCC1=NC=C(C2=C1NC3=C2C=CC=C3OC)OC 256.30 unknown https://doi.org/10.1016/S0031-9422(00)97212-1
methyl 9H-pyrido[3,4-b]indole-1-carboxylate 597266 Click to see COC(=O)C1=NC=CC2=C1NC3=CC=CC=C23 226.23 unknown https://doi.org/10.1016/S0031-9422(00)97212-1
> Alkaloids and derivatives / Indolonaphthyridine alkaloids
Canthin-6-One 97176 Click to see C1=CC=C2C(=C1)C3=C4N2C(=O)C=CC4=NC=C3 220.23 unknown https://doi.org/10.1515/ZNB-2001-0316
> Benzenoids / Phenols / Methoxyphenols
4-Hydroxy-3-methoxycinnamaldehyde 5280536 Click to see COC1=C(C=CC(=C1)C=CC=O)O 178.18 unknown https://doi.org/10.1515/ZNB-2001-0316
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(+)-Neoolivil 9976812 Click to see COC1=C(C=CC(=C1)C2C(C(C(O2)C3=CC(=C(C=C3)O)OC)CO)CO)O 376.40 unknown https://doi.org/10.1515/ZNB-2001-0316
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
(1R,2S,6R,7R,9R,13R,17S)-15-hydroxy-4-methoxy-2,6,14,17-tetramethyl-10-oxatetracyclo[7.7.1.02,7.013,17]heptadeca-4,14-diene-3,11,16-trione 162945843 Click to see CC1C=C(C(=O)C2(C1CC3C4(C2C(=O)C(=C(C4CC(=O)O3)C)O)C)C)OC 374.40 unknown https://doi.org/10.1016/0031-9422(72)80052-9
(1R,2S,6S,7S,9R,13R,17S)-15-hydroxy-4-methoxy-2,6,14,17-tetramethyl-10-oxatetracyclo[7.7.1.02,7.013,17]heptadeca-4,14-diene-3,11,16-trione 162945842 Click to see CC1C=C(C(=O)C2(C1CC3C4(C2C(=O)C(=C(C4CC(=O)O3)C)O)C)C)OC 374.40 unknown https://doi.org/10.1016/0031-9422(72)80052-9
(1R,2S,6S,7S,9R,13S,14R,15S,17S)-15-hydroxy-4-methoxy-2,6,14,17-tetramethyl-10-oxatetracyclo[7.7.1.02,7.013,17]heptadec-4-ene-3,11,16-trione 162915027 Click to see CC1C=C(C(=O)C2(C1CC3C4(C2C(=O)C(C(C4CC(=O)O3)C)O)C)C)OC 376.40 unknown https://doi.org/10.1016/0031-9422(72)80052-9
(1S,2S,6S,7R,9R,13S,14R,16S,17S)-16-hydroxy-4-methoxy-2,6,14,17-tetramethyl-10-oxatetracyclo[7.7.1.02,7.013,17]heptadec-4-ene-3,11,15-trione 162931712 Click to see CC1C=C(C(=O)C2(C1CC3C4(C2C(C(=O)C(C4CC(=O)O3)C)O)C)C)OC 376.40 unknown https://doi.org/10.1016/0031-9422(72)80052-9
(1S,2S,6S,7S,9R,11S,13R,17S)-11-ethoxy-4,15-dimethoxy-2,6,14,17-tetramethyl-10-oxatetracyclo[7.7.1.02,7.013,17]heptadeca-4,14-diene-3,16-dione 101100881 Click to see CCOC1CC2C(=C(C(=O)C3C2(C(O1)CC4C3(C(=O)C(=CC4C)OC)C)C)OC)C 418.50 unknown https://doi.org/10.1515/ZNB-2001-0316
(1S,2S,6S,7S,9R,13S,14R,16S,17S)-16-hydroxy-4-methoxy-2,6,14,17-tetramethyl-10-oxatetracyclo[7.7.1.02,7.013,17]heptadec-4-ene-3,11,15-trione 102059849 Click to see CC1C=C(C(=O)C2(C1CC3C4(C2C(C(=O)C(C4CC(=O)O3)C)O)C)C)OC 376.40 unknown https://doi.org/10.1016/0031-9422(72)80052-9
11-Ethoxy-4,15-dimethoxy-2,6,14,17-tetramethyl-10-oxatetracyclo[7.7.1.02,7.013,17]heptadeca-4,14-diene-3,16-dione 163011626 Click to see CCOC1CC2C(=C(C(=O)C3C2(C(O1)CC4C3(C(=O)C(=CC4C)OC)C)C)OC)C 418.50 unknown https://doi.org/10.1515/ZNB-2001-0316
15-Hydroxy-4-methoxy-2,6,14,17-tetramethyl-10-oxatetracyclo[7.7.1.02,7.013,17]heptadec-4-ene-3,11,16-trione 162915026 Click to see CC1C=C(C(=O)C2(C1CC3C4(C2C(=O)C(C(C4CC(=O)O3)C)O)C)C)OC 376.40 unknown https://doi.org/10.1016/0031-9422(72)80052-9
15-Hydroxy-4-methoxy-2,6,14,17-tetramethyl-10-oxatetracyclo[7.7.1.02,7.013,17]heptadeca-4,14-diene-3,11,16-trione 162945841 Click to see CC1C=C(C(=O)C2(C1CC3C4(C2C(=O)C(=C(C4CC(=O)O3)C)O)C)C)OC 374.40 unknown https://doi.org/10.1016/0031-9422(72)80052-9
16-Methyl-epi-nigakihemiacetal B 85234534 Click to see CC1C=C(C(=O)C2(C1CC3C4(C2C(=O)C(=C(C4CC(O3)OC)C)OC)C)C)OC 404.50 unknown https://doi.org/10.1515/ZNB-2001-0316
Methylneoquassin 10692599 Click to see CC1C=C(C(=O)C2(C1CC3C4(C2C(=O)C(=C(C4CC(O3)OC)C)OC)C)C)OC 404.50 unknown https://doi.org/10.1515/ZNB-2001-0316
Quassin 65571 Click to see CC1C=C(C(=O)C2(C1CC3C4(C2C(=O)C(=C(C4CC(=O)O3)C)OC)C)C)OC 388.50 unknown https://doi.org/10.1080/1478641031000104082
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
(1S,3'aR,4R,5R,8R,9R,12R,13S)-4-(furan-3-yl)-4',4',5,9,12-pentamethylspiro[3,10,14-trioxatetracyclo[7.4.1.01,5.08,12]tetradecane-13,2'-3,3a-dihydrofuro[3,2-c]pyran]-2,6',11-trione 102202714 Click to see CC1(C2CC3(C4(C5CCC6(C3(C(=O)OC6C7=COC=C7)OC5(OC4=O)C)C)C)OC2=CC(=O)O1)C 484.50 unknown https://doi.org/10.1016/0031-9422(72)80052-9
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Coniferin 5280372 Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O 342.34 unknown https://doi.org/10.1515/ZNB-2001-0316
> Organoheterocyclic compounds / Oxanes
8-Acetyl-9,13-dihydroxy-4,13-dimethyl-6,11-dioxatetracyclo[7.4.0.03,7.010,12]trideca-1,3-dien-5-one 162789741 Click to see CC1=C2C=C3C(C4C(C3(C(C2OC1=O)C(=O)C)O)O4)(C)O 292.28 unknown https://doi.org/10.1080/1478641031000104082

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