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Stauranthus perforatus

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 UUID64404d7f7ca0c755172384
Scientific name Stauranthus perforatus
Authority Liebm.
First published in Vidensk. Meddel. Naturhist. Foren. Kjøbenhavn 1853: 92 (1854)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

No known synonyms.

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Gulf
      • Mexico Southeast
      • Mexico Southwest

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001132730
Tropicos 28100266
KEW urn:lsid:ipni.org:names:775280-1
The Plant List tro-28100266
Open Tree Of Life 6126620
NCBI Taxonomy 2896591
IUCN Red List 151999670
IPNI 775280-1
iNaturalist 279147
GBIF 3837193
EOL 5625485

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
Chalepin and Chalepensin: Occurrence, Biosynthesis and Therapeutic Potential Nahar L, Al-Majmaie S, Al-Groshi A, Rasul A, Sarker SD Molecules 14-Mar-2021
PMCID:PMC7999183
doi:10.3390/molecules26061609
PMID:33799365
Biologically Active Quinoline and Quinazoline Alkaloids Part II Shang XF, Morris-Natschke SL, Yang GZ, Liu YQ, Guo X, Xu XS, Goto M, Li JC, Zhang JY, Lee KH Med Res Rev 27-Feb-2018
PMCID:PMC6105521
doi:10.1002/med.21492
PMID:29485730
Antileishmanial Potential of Tropical Rainforest Plant Extracts Monzote L, Piñón A, Setzer WN Medicines (Basel) 19-Nov-2014
PMCID:PMC5532977
doi:10.3390/medicines1010032
PMID:28933376
Antiprotozoal and Antimycobacterial Activities of Pure Compounds from Aristolochia elegans Rhizomes Jiménez-Arellanes A, León-Díaz R, Meckes M, Tapia A, Molina-Salinas GM, Luna-Herrera J, Yépez-Mulia L Evid Based Complement Alternat Med 16-Feb-2012
PMCID:PMC3292206
doi:10.1155/2012/593403
PMID:22454670
Effects of Naturally Occurring Coumarins on Hepatic Drug Metabolizing Enzymes in Mice Kleiner HE, Xia X, Sonoda J, Zhang J, Pontius E, Abey J, Evans RM, Moore DD, DiGiovanni. J Toxicol Appl Pharmacol 15-Jul-2008
PMCID:PMC2585982
doi:10.1016/j.taap.2008.07.004
PMID:18692084
Allelochemicals from Stauranthus perforatus, a Rutaceous tree of the Yucatan Peninsula, Mexico. Anaya AL, Macías-Rubalcava M, Cruz-Ortega R, García-Santana C, Sánchez-Monterrubio PN, Hernández-Bautista BE, Mata R Phytochemistry 01-Feb-2005
doi:10.1016/J.PHYTOCHEM.2004.12.028
PMID:15694456
HPLC-NMR/HPLC-MS analysis of the bark extract of Stauranthus perforatus. Setzer WN, Vogler B, Bates RB, Schmidt JM, Dicus CW, Nakkiew P, Haber WA Phytochem Anal 01-Jan-2003
doi:10.1002/PCA.687
PMID:12597256
Cytotoxic components from the bark of Stauranthus perforatus from Monteverde, Costa Rica. Setzer WN, Setzer MC, Schmidt JM, Moriarity DM, Vogler B, Reeb S, Holmes AM, Haber WA Planta Med 01-Jun-2000
doi:10.1055/S-2000-8595
PMID:10909280

Phytochemical Profile Top

Add a new one!
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
> Lignans, neolignans and related compounds / Furanoid lignans
(+-)-Fargesin 10926754 Click to see 370.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.028
4-[(3S,3aR,6R,6aR)-3-(1,3-benzodioxol-4-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-1,3-benzodioxole 154496198 Click to see 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.028
5-[(3aR,6aR)-6-(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-1,3-benzodioxole 137705003 Click to see 370.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.028
5-[(3aR,6R,6aR)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-1,3-benzodioxole 102004873 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.028
Episesamin 5204 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.028
Npc268574 5320622 Click to see 370.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.028
Npc67790 233333 Click to see 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.028
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
(2E,4E)-N-[(2R)-butan-2-yl]deca-2,4-dienamide 154497067 Click to see 223.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.028
n-Isobutyl-2,4-decadienamide 3009280 Click to see 223.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.028
Pellitorine 5318516 Click to see 223.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.028
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane 5315723 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.028
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1055/S-2000-8595
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-2000-8595
https://doi.org/10.1016/J.PHYTOCHEM.2004.12.028
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1055/S-2000-8595
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
3-Hexadeca-7,12-dien-9-ynyl-4-hydroxy-5-methylidenefuran-2-one 163033172 Click to see CCCC=CCC#CC=CCCCCCCC1=C(C(=C)OC1=O)O 328.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.028
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1055/S-2000-8595
> Organoheterocyclic compounds / Quinolines and derivatives / Phenylquinolines
5-Hydroxy-1-methyl-2-phenylquinolin-4(1H)-one 71307707 Click to see 251.28 unknown https://doi.org/10.1002/PCA.687
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
2-Hydroxy-4,4,9-trimethyl-3,12,14-trioxa-9-azatetracyclo[8.7.0.02,7.011,15]heptadeca-1(10),6,11(15),16-tetraene-5,8-dione 163105666 Click to see CC1(C(=O)C=C2C(=O)N(C3=C(C2(O1)O)C=CC4=C3OCO4)C)C 317.29 unknown https://doi.org/10.1002/PCA.687
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
10b-Hydroxy-7,8-dimethoxy-2,2,6-trimethylpyrano[3,2-c]quinoline-3,5-dione 163103647 Click to see 333.30 unknown https://doi.org/10.1002/PCA.687
4,4,9-Trimethyl-3,12,14-trioxa-9-azatetracyclo[8.7.0.02,7.011,15]heptadeca-1(10),2(7),5,11(15),16-pentaen-8-one 163104545 Click to see 285.29 unknown https://doi.org/10.1002/PCA.687
Veprisine 338941 Click to see 301.34 unknown https://doi.org/10.1002/PCA.687
https://doi.org/10.1055/S-2000-8595
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(-)-Heraclenol 40429858 Click to see 304.29 unknown https://doi.org/10.1002/PCA.687
(+)-Rutamarin alcohol 5287846 Click to see 314.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.028
(2R)-2-prop-1-en-2-yl-2,3-dihydrofuro[3,2-g]chromen-7-one 759292 Click to see 228.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.028
2-isopropyl-7H-furo[3,2-g]chromen-7-one 677576 Click to see 228.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.028
2,3-Dihydro-2-isopropenyl-7H-furo[3,2-g][1]benzopyran-7-one 611672 Click to see 228.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.028
9-[[(2S)-3,3-dimethyloxiran-2-yl]methoxy]furo[3,2-g]chromen-7-one 17897 Click to see CC1(C(O1)COC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C 286.28 unknown https://doi.org/10.1002/PCA.687
https://doi.org/10.1055/S-2000-8595
Chalepensin 128834 Click to see CC(C)(C=C)C1=CC2=C(C=C3C(=C2)C=CO3)OC1=O 254.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.028
Chalepin 119066 Click to see 314.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.028
Heraclenin 458010 Click to see CC1(C(O1)COC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C 286.28 unknown https://doi.org/10.1002/PCA.687
https://doi.org/10.1055/S-2000-8595
Heraclenol 73253 Click to see CC(C)(C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O)O 304.29 unknown https://doi.org/10.1002/PCA.687
Imperatorin 10212 Click to see 270.28 unknown https://doi.org/10.1002/PCA.687
Oxyimperatorin 182251 Click to see CC1(C(O1)COC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C 286.28 unknown https://doi.org/10.1055/S-2000-8595
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Byakangelicol 3055167 Click to see 316.30 unknown https://doi.org/10.1002/PCA.687
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
8-Methoxypsoralen 4114 Click to see 216.19 unknown https://doi.org/10.1002/PCA.687
https://doi.org/10.1055/S-2000-8595
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown https://doi.org/10.1055/S-2000-8595
https://doi.org/10.1002/PCA.687
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
7-(1,1-Dimethylallyl)-2,2-dimethyl-pyrano[3,2-g]chromen-8-one 14133592 Click to see CC1(C=CC2=C(O1)C=C3C(=C2)C=C(C(=O)O3)C(C)(C)C=C)C 296.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.028
Xanthyletin 65188 Click to see 228.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.12.028

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