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Flourensia cernua

Flourensia cernua - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fcd4dd6403624111345
Scientific name Flourensia cernua
Authority DC.
First published in Prodr. 5: 593 (1836)

Description Top

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Synonyms Top

Scientific name Authority First published in
Helianthus cernuus Benth. & Hook.f. Gen. Pl. 2(1): 376 (1873)

Common names Top

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Language Common/alternative name
English american tarwort
Persian قیرگیاه آمریکایی
Japanese タールブッシュ

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 Northeast
      • Mexico Northwest
      • Mexico Southwest
    • South-central U.S.A.
      • New Mexico
      • Texas
    • Southwestern U.S.A.
      • Arizona

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000071060
USDA Plants FLCE
Tropicos 2702510
KEW urn:lsid:ipni.org:names:277219-2
The Plant List gcc-27847
Open Tree Of Life 4727351
NCBI Taxonomy 2604028
Nature Serve 2.159974
IPNI 277219-2
iNaturalist 157341
GBIF 3094540
Freebase /m/0hzrj3r
FEIS plants/shrub/flocer
EPPO FLOCE
EOL 467572
USDA GRIN 104237
Wikipedia Flourensia_cernua

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
Characterization of the Worthen Sparrow (Spizella wortheni)’s Nest Building Materials in Northeastern Mexico Suarez EB, Mellado M, Luna M, Lozano EA, Calderon G, Angel Y, Angel O, Medina ML, García JE Animals (Basel) 19-Apr-2024
PMCID:PMC11047681
doi:10.3390/ani14081230
PMID:38672377
Lipid incorporated biopolymer based edible films and coatings in food packaging: A review Devi LS, Jaiswal AK, Jaiswal S Curr Res Food Sci 15-Mar-2024
PMCID:PMC10978484
doi:10.1016/j.crfs.2024.100720
PMID:38559379
Plants from Arid and Semi-Arid Zones of Mexico Used to Treat Respiratory Diseases: A Review Dávila-Rangel IE, Charles-Rodríguez AV, López-Romero JC, Flores-López ML Plants (Basel) 11-Mar-2024
PMCID:PMC10974781
doi:10.3390/plants13060792
PMID:38592789
Recent Highlights in Sustainable Bio-Based Edible Films and Coatings for Fruit and Vegetable Applications Martins VF, Pintado ME, Morais RM, Morais AM Foods 19-Jan-2024
PMCID:PMC10814993
doi:10.3390/foods13020318
PMID:38275685
From Nature to Lab: A Review of Secondary Metabolite Biosynthetic Pathways, Environmental Influences, and In Vitro Approaches Reshi ZA, Ahmad W, Lukatkin AS, Javed SB Metabolites 28-Jul-2023
PMCID:PMC10456650
doi:10.3390/metabo13080895
PMID:37623839
Chemical Constituents and Antimicrobial Activity of a Ganoderma lucidum (Curtis.) P. Karst. Aqueous Ammonia Extract Sánchez-Hernández E, Teixeira A, Pereira C, Cruz A, Martín-Gil J, Oliveira R, Martín-Ramos P Plants (Basel) 11-Jun-2023
PMCID:PMC10305452
doi:10.3390/plants12122271
PMID:37375896
Ultrasound-Assisted Extraction of Verbascoside from Clerodendrum glandulosum Leaves for Analysis of Antioxidant and Antidiabetic Activities Khound P, Sarma H, Sarma PP, Jana UK, Devi R ACS Omega 31-May-2023
PMCID:PMC10268293
doi:10.1021/acsomega.3c00173
PMID:37323385
Milk Composition of Creole Goats Raised at Different Altitudes in an Extensive Production System in Northeast Mexico Peña-Avelino LY, Ceballos-Olvera I, Rosales-Martinez GN, Hernández-Melendez J, Alva-Pérez J Animals (Basel) 24-May-2023
PMCID:PMC10251814
doi:10.3390/ani13111738
PMID:37889663
Recent insights into Nanoemulsions: Their preparation, properties and applications Mushtaq A, Mohd Wani S, Malik AR, Gull A, Ramniwas S, Ahmad Nayik G, Ercisli S, Alina Marc R, Ullah R, Bari A Food Chem X 20-Apr-2023
PMCID:PMC10149285
doi:10.1016/j.fochx.2023.100684
PMID:37131847
Inhibitory effect of natural extract mixtures on microbial growth and lipid oxidation of sausages during storage Woo SH, Sung JM, Park H, Kim J, Kim YJ, Kim TK, Lee H, Choi YS J Anim Sci Technol 31-Jan-2023
PMCID:PMC10119476
doi:10.5187/jast.2022.e92
PMID:37093932
Environmental Factors Regulate Plant Secondary Metabolites Qaderi MM, Martel AB, Strugnell CA Plants (Basel) 18-Jan-2023
PMCID:PMC9920071
doi:10.3390/plants12030447
PMID:36771531
Anti-Fungal Activity of Moutan cortex Extracts against Rice Sheath Blight (Rhizoctonia solani) and Its Action on the Pathogen’s Cell Membrane Zhao Y, Wang X, Zhang L, Wang K, Wu Y, Yao J, Cui B, Chen Z ACS Omega 07-Dec-2022
PMCID:PMC9773796
doi:10.1021/acsomega.2c06150
PMID:36570206
Medicinal plants used by rural communities in the arid zone of Viesca and Parras Coahuila in northeast Mexico Torres-León C, Rebolledo Ramírez F, Aguirre-Joya JA, Ramírez-Moreno A, Chávez-González ML, Aguillón-Gutierrez DR, Camacho-Guerra L, Ramírez-Guzmán N, Hernández Vélez S, Aguilar CN Saudi Pharm J 12-Nov-2022
PMCID:PMC9845112
doi:10.1016/j.jsps.2022.11.003
PMID:36685306
Holm Oak (Quercus ilex subsp. ballota (Desf.) Samp.) Bark Aqueous Ammonia Extract for the Control of Invasive Forest Pathogens Sánchez-Hernández E, Balduque-Gil J, Barriuso-Vargas JJ, Casanova-Gascón J, González-García V, Cuchí-Oterino JA, Lorenzo-Vidal B, Martín-Gil J, Martín-Ramos P Int J Mol Sci 06-Oct-2022
PMCID:PMC9569932
doi:10.3390/ijms231911882
PMID:36233184
Advances in apple packaging: a review Bhat SA, Rizwan D, Mir SA, Wani SM, Masoodi FA J Food Sci Technol 19-Apr-2022
PMCID:PMC10188779
doi:10.1007/s13197-022-05447-8
PMID:37206415

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methyl 2,4-dihydroxy-6-methylbenzoate 76658 Click to see CC1=CC(=CC(=C1C(=O)OC)O)O 182.17 unknown https://doi.org/10.1002/CHIN.200401200
https://doi.org/10.1016/S0031-9422(03)00217-6
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1016/0305-1978(94)90116-3
https://doi.org/10.1016/S0031-9422(00)86634-0
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1016/0305-1978(94)90116-3
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)86634-0
https://doi.org/10.1016/0305-1978(94)90116-3
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1016/0305-1978(94)90116-3
trans-Borneol 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1016/0305-1978(94)90116-3
https://doi.org/10.1016/S0031-9422(00)86634-0
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)86634-0
https://doi.org/10.1016/0305-1978(94)90116-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/0305-1978(94)90116-3
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/0305-1978(94)90116-3
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/0305-1978(94)90116-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4R,4aR,7R,7aS,7bS)-1,1,4,7-Tetramethyldecahydro-1H-cyclopropa[e]azulen-4-ol 91746597 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/0305-1978(94)90116-3
(1R,1aR,4S,4aS,7R,7aS,7bR)-1-(hydroxymethyl)-1,4,7-trimethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol 162892821 Click to see CC1CCC2C1C3C(C3(C)CO)CCC2(C)O 238.37 unknown https://doi.org/10.1016/S0031-9422(03)00217-6
(1R,1aR,4S,4aS,7R,7aS,7bS)-1-(hydroxymethyl)-1,4,7-trimethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol 101277324 Click to see CC1CCC2C1C3C(C3(C)CO)CCC2(C)O 238.37 unknown https://doi.org/10.1016/S0031-9422(03)00217-6
https://doi.org/10.1016/0031-9422(75)83120-7
(1R,1aR,4S,4aS,7R,7aS)-1-(hydroxymethyl)-1,4,7-trimethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol 162892820 Click to see CC1CCC2C1C3C(C3(C)CO)CCC2(C)O 238.37 unknown https://doi.org/10.1016/S0031-9422(03)00217-6
1-(hydroxymethyl)-1,4,7-trimethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol 162892818 Click to see CC1CCC2C1C3C(C3(C)CO)CCC2(C)O 238.37 unknown https://doi.org/10.1016/S0031-9422(03)00217-6
https://doi.org/10.1016/0031-9422(75)83120-7
Globulol 101716 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/0305-1978(94)90116-3
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(00)86634-0
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1R,2R,3R,6E,10S)-3,7,11,11-tetramethylbicyclo[8.1.0]undec-6-en-2-ol 162977886 Click to see CC1CCC=C(CCC2C(C1O)C2(C)C)C 222.37 unknown https://doi.org/10.1016/0031-9422(75)83120-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
2-(8,8a-Dimethyl-4-oxo-1,2,3,4a,5,6,7,8-octahydronaphthalen-2-yl)prop-2-enoic acid 78173225 Click to see CC1CCCC2C1(CC(CC2=O)C(=C)C(=O)O)C 250.33 unknown https://doi.org/10.1016/0031-9422(75)83120-7
2-(8,8a-Dimethyl-4-oxo-1,2,3,6,7,8-hexahydronaphthalen-2-yl)prop-2-enoic acid 22298388 Click to see CC1CCC=C2C1(CC(CC2=O)C(=C)C(=O)O)C 248.32 unknown https://doi.org/10.1016/S0031-9422(03)00217-6
Dihydroflourensic acid 641673 Click to see CC1CCC=C2C1(CC(CC2=O)C(=C)C(=O)O)C 248.32 unknown https://doi.org/10.1016/S0031-9422(03)00217-6
Flourensic acid 186172 Click to see CC1CCCC2C1(CC(CC2=O)C(=C)C(=O)O)C 250.33 unknown https://doi.org/10.1016/0031-9422(75)83120-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
alpha-Eudesmol 92762 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1016/S0031-9422(00)86634-0
beta-EUDESMOL 91457 Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(00)86634-0
gamma-EUDESMOL 6432005 Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(00)86634-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
(3S,5S,6S,8S,9R,10S,13R,14S,15R,16R,17R)-17-[(2R)-4-[(1S,2R)-2-(hydroxymethyl)cyclopropyl]butan-2-yl]-10,13-dimethyl-1,2,3,4,5,6,7,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,6,8,15,16-pentol 163047822 Click to see CC(CCC1CC1CO)C2C(C(C3C2(CCC4C3(CC(C5C4(CCC(C5)O)C)O)O)C)O)O 466.60 unknown https://doi.org/10.1016/0031-9422(75)83120-7
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
3,3,6-Trimethylhepta-1,5-dien-4-ol 100197 Click to see CC(=CC(C(C)(C)C=C)O)C 154.25 unknown https://doi.org/10.1016/S0031-9422(00)86634-0
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Jasmone 1549018 Click to see CCC=CCC1=C(CCC1=O)C 164.24 unknown https://doi.org/10.1016/0305-1978(94)90116-3
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(5S)-5-hexacosyloxolan-2-one 10983249 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC1CCC(=O)O1 450.80 unknown https://doi.org/10.1016/S0031-9422(03)00217-6
(5S)-5-pentacosyloxolan-2-one 11102176 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC1CCC(=O)O1 436.80 unknown https://doi.org/10.1016/S0031-9422(03)00217-6
(5S)-5-tetracosyloxolan-2-one 11048118 Click to see CCCCCCCCCCCCCCCCCCCCCCCCC1CCC(=O)O1 422.70 unknown https://doi.org/10.1016/S0031-9422(03)00217-6
(5S)-5-tricosyloxolan-2-one 10982443 Click to see CCCCCCCCCCCCCCCCCCCCCCCC1CCC(=O)O1 408.70 unknown https://doi.org/10.1016/S0031-9422(03)00217-6
5-Docosyldihydrofuran-2(3H)-one 85358949 Click to see CCCCCCCCCCCCCCCCCCCCCCC1CCC(=O)O1 394.70 unknown https://doi.org/10.1016/S0031-9422(03)00217-6
https://doi.org/10.1002/CHIN.200401200
5-Henicosyldihydrofuran-2(3H)-one 85292662 Click to see CCCCCCCCCCCCCCCCCCCCCC1CCC(=O)O1 380.60 unknown https://doi.org/10.1002/CHIN.200401200
https://doi.org/10.1016/S0031-9422(03)00217-6
5-Hexacosyloxolan-2-one 85355295 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC1CCC(=O)O1 450.80 unknown https://doi.org/10.1002/CHIN.200401200
https://doi.org/10.1016/S0031-9422(03)00217-6
5-Icosyloxolan-2-one 21575626 Click to see CCCCCCCCCCCCCCCCCCCCC1CCC(=O)O1 366.60 unknown https://doi.org/10.1002/CHIN.200401200
https://doi.org/10.1016/S0031-9422(03)00217-6
5-Pentacosyloxolan-2-one 85399497 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC1CCC(=O)O1 436.80 unknown https://doi.org/10.1016/S0031-9422(03)00217-6
https://doi.org/10.1002/CHIN.200401200
5-Tetracosyloxolan-2-one 85379733 Click to see CCCCCCCCCCCCCCCCCCCCCCCCC1CCC(=O)O1 422.70 unknown https://doi.org/10.1002/CHIN.200401200
https://doi.org/10.1016/S0031-9422(03)00217-6
5-Tricosyloxolan-2-one 85354940 Click to see CCCCCCCCCCCCCCCCCCCCCCCC1CCC(=O)O1 408.70 unknown https://doi.org/10.1002/CHIN.200401200
https://doi.org/10.1016/S0031-9422(03)00217-6
Hexacosan-4-olide 10992904 Click to see CCCCCCCCCCCCCCCCCCCCCCC1CCC(=O)O1 394.70 unknown https://doi.org/10.1016/S0031-9422(03)00217-6
Pentacosan-4-olide 10861829 Click to see CCCCCCCCCCCCCCCCCCCCCC1CCC(=O)O1 380.60 unknown https://doi.org/10.1016/S0031-9422(03)00217-6
Tetracosan-4-olide 11143096 Click to see CCCCCCCCCCCCCCCCCCCCC1CCC(=O)O1 366.60 unknown https://doi.org/10.1016/S0031-9422(03)00217-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(2S,3S,4S,5S)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one 154496799 Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O 564.50 unknown https://doi.org/10.1016/S0031-9422(00)84420-9
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Ermanin 5352001 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC 314.29 unknown https://doi.org/10.1016/S0031-9422(03)00217-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1016/S0031-9422(00)86634-0
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown https://doi.org/10.1016/S0031-9422(00)86634-0

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