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Pterocaulon alopecuroides

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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 UUID643fc7b62bad9915822659
Scientific name Pterocaulon alopecuroides
Authority (Lam.) DC.
First published in Prodr. 5: 454 (1836)

Description Top

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Synonyms Top

Scientific name Authority First published in
Pluchea alopecuroides Less. Syn. Gen. Compos. : 207 (1832)
Pterocaulon virgatum f. alopecuroides (Lam.) Arechav. Anales Mus. Nac. Montevideo 6: 268 (1908)
Pterocaulon latifolium Kuntze Revis. Gen. Pl. 3[3]: 169 (1898)
Chlaenobolus alopecuroides (Lam.) Cass. Dict. Sci. Nat., ed. 2. 49: 339 (1827)
Pterocaulon alopecuroides var. mollis Chodat Bull. Herb. Boissier , ser. 2, 2: 387 (1902)
Pterocaulon virgatum var. alopecuroides (Lam.) Griseb. Cat. Pl. Cub. 150. 1866.
Pterocaulon alopecuroides var. glabrescens Chodat Bull. Herb. Boissier , ser. 2, 2: 387 (1902)
Pterocaulon interruptum var. monostachyum DC. Prodr. 5: 454 (1836)
Pterocaulon alopecuroides var. polystachyum DC. Prodr. 5: 454 (1836)
Pterocaulon interruptum var. polystachyum DC. Prodr. 5: 454 (1836)
Pterocaulon virgatum f. subcorymbosa Arechav. Anales Mus. Nac. Montevideo 6: 269 (1908)
Conyza alopecuroides Lam. Encycl. 2: 93 (1786)
Baccharis erioptera Benth. Ann. Nat. Hist. 2(12): 441 (1839)
Pterocaulon interruptum DC. Prodr. 5: 454 (1836)

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
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Puerto Rico
      • Trinidad-Tobago
      • Windward Islands
    • Central America
      • Panamá
    • Northern South America
      • Guyana
      • Suriname
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Paraguay
      • Uruguay
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000016722
Tropicos 2711937
INPN 630518
KEW urn:lsid:ipni.org:names:240147-1
The Plant List gcc-116179
Open Tree Of Life 5920997
NCBI Taxonomy 1548644
IPNI 240147-1
iNaturalist 775412
GBIF 5392221
CMAUP NPO16534

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
Extracts from Argentinian native plants reverse fluconazole resistance in Candida species by inhibiting the efflux transporters Mdr1 and Cdr1 Gil F, Laiolo J, Bayona-Pacheco B, Cannon RD, Ferreira-Pereira A, Carpinella MC BMC Complement Med Ther 12-Oct-2022
PMCID:PMC9555179
doi:10.1186/s12906-022-03745-4
PMID:36224581
The Symbiotic Fungus Leucoagaricus gongylophorus (Möller) Singer (Agaricales, Agaricaceae) as a Target Organism to Control Leaf-Cutting Ants Araújo S, Seibert J, Ruani A, Alcántara-de la Cruz R, Cruz A, Pereira A, Zandonai D, Forim M, Silva MF, Bueno O, Fernandes J Insects 06-Apr-2022
PMCID:PMC9029082
doi:10.3390/insects13040359
PMID:35447801
Reviewing the Etiologic Agents, Microbe-Host Relationship, Immune Response, Diagnosis, and Treatment in Chromoblastomycosis Passero LF, Cavallone IN, Belda W Jr J Immunol Res 01-Nov-2021
PMCID:PMC8575639
doi:10.1155/2021/9742832
PMID:34761009
Natural-Product-Based Solutions for Tropical Infectious Diseases Adegboye O, Field MA, Kupz A, Pai S, Sharma D, Smout MJ, Wangchuk P, Wong Y, Loiseau C Clin Microbiol Rev 08-Sep-2021
PMCID:PMC8673330
doi:10.1128/CMR.00348-20
PMID:34494873
A comprehensive review on tyrosinase inhibitors Zolghadri S, Bahrami A, Hassan Khan MT, Munoz-Munoz J, Garcia-Molina F, Garcia-Canovas F, Saboury AA J Enzyme Inhib Med Chem 03-Jan-2019
PMCID:PMC6327992
doi:10.1080/14756366.2018.1545767
PMID:30734608
Cytotoxic Activity of Extracts from Plants of Central Argentina on Sensitive and Multidrug-Resistant Leukemia Cells: Isolation of an Active Principle from Gaillardia megapotamica González ML, Joray MB, Laiolo J, Crespo MI, Palacios SM, Ruiz GM, Carpinella MC Evid Based Complement Alternat Med 10-May-2018
PMCID:PMC5971282
doi:10.1155/2018/9185935
PMID:29861776
Antibacterial Activity of Polyphenols: Structure-Activity Relationship and Influence of Hyperglycemic Condition Xie Y, Chen J, Xiao A, Liu L Molecules 06-Nov-2017
PMCID:PMC6150409
doi:10.3390/molecules22111913
PMID:29113147
Medicinal Plants from Mexico, Central America, and the Caribbean Used as Immunostimulants Alonso-Castro AJ, Juárez-Vázquez MD, Campos-Xolalpa N Evid Based Complement Alternat Med 03-Mar-2016
PMCID:PMC4794563
doi:10.1155/2016/4017676
PMID:27042188
Distribution of coumarins in the tribe Plucheeae, genus Pterocaulon A. C. Stein, D. Fritz, L. F. Paiva Lima, N. I. Matzenbacher, J. Schripsema, V. Pires, P. Sonnet, G. von Poser Springer Science and Business Media LLC 23-Feb-2008
doi:10.1007/S10600-007-0231-X
Coumarins and a flavonoid from Pterocaulon alopecuroides Wagner Vilegas, Nivaldo Boralle, Alvaro Cabrera, Alberto Carlos Bernardi, Gilberto Luiz Pozetti, Simone Fontes Arantes Elsevier BV 01-May-2003
doi:10.1016/0031-9422(94)00726-A

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
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
(5Z)-9,15-Dioxoprosta-5,8(12)-diene-1-oic acid methyl ester 21609756 Click to see CCCCCC(=O)CCC1=C(C(=O)CC1)CC=CCCCC(=O)OC 348.50 unknown via CMAUP database
methyl (Z)-7-[2-[(E,3S)-3-hydroxyoct-1-enyl]-5-oxocyclopenten-1-yl]hept-5-enoate 21160888 Click to see CCCCCC(C=CC1=C(C(=O)CC1)CC=CCCCC(=O)OC)O 348.50 unknown via CMAUP database
prostaglandin B2 5280881 Click to see CCCCCC(C=CC1=C(C(=O)CC1)CC=CCCCC(=O)O)O 334.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidonic Acid 444899 Click to see CCCCCC=CCC=CCC=CCC=CCCCC(=O)O 304.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Cembrane diterpenoids
2-[(1R,4E,6E,10E,14R)-4,10,14-trimethyl-15-oxabicyclo[12.1.0]pentadeca-4,6,10-trien-7-yl]propan-2-ol 23247586 Click to see CC1=CCCC2(C(O2)CCC(=CC=C(CC1)C(C)(C)O)C)C 304.50 unknown via CMAUP database
dimethyl (1S,4E,6Z,10Z,14S)-14-methyl-7-propan-2-yl-15-oxabicyclo[12.1.0]pentadeca-4,6,10-triene-4,10-dicarboxylate 16091634 Click to see CC(C)C1=CC=C(CCC2C(O2)(CCC=C(CC1)C(=O)OC)C)C(=O)OC 376.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Secogorgosterol 386853 Click to see CC(C)C(C)C1(CC1C(C)C2CCC(C2(C)CCO)C3CC=C4CC(CCC4(C3=O)C)O)C 458.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
methyl (1S,2S,5E,7E)-2-acetyloxy-1-methyl-16-oxo-8-propan-2-yl-15-oxabicyclo[9.3.2]hexadeca-5,7,11-triene-5-carboxylate 16059808 Click to see CC(C)C1=CC=C(CCC(C2(CCC=C(CC1)C(=O)O2)C)OC(=O)C)C(=O)OC 404.50 unknown via CMAUP database
Sarcrassin E 16091635 Click to see CC(C)C1=CC=C(CCC(=O)C2(CCC=C(CC1)C(=O)O2)C)C(=O)OC 360.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones / Cembranolides
Crassocolide B 11995280 Click to see CC1=CCCC(C(CC2C(C(C(=CCC1)C)OC(=O)C)OC(=O)C2=C)OC(=O)C)(C)O 434.50 unknown via CMAUP database
Crassocolide C 11995174 Click to see CC1=CCCC(C(CC2C(CC(=CCC1)C)OC(=O)C2=C)OC(=O)C)(C)O 376.50 unknown via CMAUP database
Crassocolide D 11995281 Click to see CC1=CCCC(C(CC2C(CC(=CCC1)C)OC(=O)C2=C)O)(C)O 334.40 unknown via CMAUP database
Crassolide A 11995173 Click to see CC1=CCCC(C(CC2C(C(C(=CCC1)C)OC(=O)C)OC(=O)C2=C)O)(C)O 392.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,5R,6R,8S,9S,10R,13R,14S,17R)-17-[(2R,5S)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-1,2,3,4,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,5,6-triol 44558918 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC(C4(C3(CCC(C4)O)C)O)O)C 434.70 unknown via CMAUP database
25-Acetoxy-ergosta-3beta,5alpha,6beta-triol 14034721 Click to see CC(CCC(C)C(C)(C)OC(=O)C)C1CCC2C1(CCC3C2CC(C4(C3(CCC(C4)O)C)O)O)C 492.70 unknown via CMAUP database
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Furospirostanes and derivatives
(1S,2S,3'S,4S,6R,7R,8R,9S,12S,13R,16S)-2',2',3',7,9,13-hexamethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,5'-oxolane]-7,16-diol 101007150 Click to see CC1CC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)(C)O)OC1(C)C 444.60 unknown via CMAUP database
(1S,2S,3'S,4S,6S,7R,8R,9S,12S,13R,16S)-2',2',3',7,9,13-hexamethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,5'-oxolane]-7,16-diol 54586888 Click to see CC1CC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)(C)O)OC1(C)C 444.60 unknown via CMAUP database
(22R,24S)-24-Methyl-22,25-epoxyfurosta-5-ene-3beta,20-diol 3-acetate 101007149 Click to see CC1CC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC(=O)C)C)C)(C)O)OC1(C)C 486.70 unknown via CMAUP database
[(1S,2S,3'S,4S,6S,7R,8R,9S,12S,13R,16S)-7-hydroxy-2',2',3',7,9,13-hexamethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,5'-oxolane]-16-yl] acetate 101007148 Click to see CC1CC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC(=O)C)C)C)(C)O)OC1(C)C 486.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Gorgostanes and derivatives
11alpha-Hydroxygorgosterol 10599347 Click to see CC(C)C(C)C1(CC1C(C)C2CCC3C2(CC(C4C3CC=C5C4(CCC(C5)O)C)O)C)C 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
Pregnenolone 8955 Click to see CC(=O)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 316.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
24-Propylidenecholest-5-en-3beta-ol 193212 Click to see CCC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 426.70 unknown via CMAUP database
Fucosterol 5281328 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Isofucosterol 5281326 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans
(1R,2E,6R,8S,11E)-3,8,12,16-tetramethyl-7,18-dioxatricyclo[13.3.0.06,8]octadeca-2,11,15-triene 54585297 Click to see CC1=CCCC2(C(O2)CCC(=CC3C(=C(CO3)C)CC1)C)C 302.50 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Sarcocrassocolide A 70691856 Click to see CC1=CCCC(=C)C2CCC(O2)(C(CC3C(C1OC(=O)C)OC(=O)C3=C)O)C 390.50 unknown via CMAUP database
Sarcocrassocolide B 70696020 Click to see CC1=CCCC(=C)C2CCC(O2)(C(CC3C(C1OC(=O)C)OC(=O)C3=C)O)C 390.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
2H-1-Benzopyran-2-one, 7-[(3,3-dimethyloxiranyl)methoxy]-6-methoxy- 11277378 Click to see CC1(C(O1)COC2=C(C=C3C=CC(=O)OC3=C2)OC)C 276.28 unknown https://doi.org/10.1007/S10600-007-0231-X
7-[(2S)-2,3-dihydroxy-3-methylbutoxy]-6-methoxychromen-2-one 906620 Click to see CC(C)(C(COC1=C(C=C2C=CC(=O)OC2=C1)OC)O)O 294.30 unknown https://doi.org/10.1016/0031-9422(94)00726-A
7-[[(2R)-3,3-dimethyloxiran-2-yl]methoxy]-6-methoxychromen-2-one 26113470 Click to see CC1(C(O1)COC2=C(C=C3C=CC(=O)OC3=C2)OC)C 276.28 unknown https://doi.org/10.1007/S10600-007-0231-X
9-methoxy-6H-[1,3]dioxolo[4,5-g]chromen-6-one 11310556 Click to see COC1=C2C=CC(=O)OC2=CC3=C1OCO3 220.18 unknown https://doi.org/10.1007/S10600-007-0231-X
Obtusinin 3604942 Click to see CC(C)(C(COC1=C(C=C2C=CC(=O)OC2=C1)OC)O)O 294.30 unknown https://doi.org/10.1016/0031-9422(94)00726-A
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
7-(2,3-Dihydroxy-3-methylbutoxy)-5-hydroxy-6-methoxychromen-2-one 101919846 Click to see CC(C)(C(COC1=C(C(=C2C=CC(=O)OC2=C1)O)OC)O)O 310.30 unknown https://doi.org/10.1016/0031-9422(94)00726-A
7-[(2R)-2,3-dihydroxy-3-methylbutoxy]-5-hydroxy-6-methoxychromen-2-one 163022324 Click to see CC(C)(C(COC1=C(C(=C2C=CC(=O)OC2=C1)O)OC)O)O 310.30 unknown https://doi.org/10.1016/0031-9422(94)00726-A
7-[(2S)-2,3-dihydroxy-3-methylbutoxy]-5-hydroxy-6-methoxychromen-2-one 163185581 Click to see CC(C)(C(COC1=C(C(=C2C=CC(=O)OC2=C1)O)OC)O)O 310.30 unknown https://doi.org/10.1016/0031-9422(94)00726-A
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-(3-methylbut-2-enoxy)-2,3-dihydrochromen-4-one 101919845 Click to see CC(=CCOC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC(=C(C=C3)O)O)O)C 372.40 unknown https://doi.org/10.1016/0031-9422(94)00726-A
2-(3,4-Dihydroxyphenyl)-3,5-dihydroxy-7-(3-methylbut-2-enoxy)-2,3-dihydrochromen-4-one 163020087 Click to see CC(=CCOC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC(=C(C=C3)O)O)O)C 372.40 unknown https://doi.org/10.1016/0031-9422(94)00726-A
> Phenylpropanoids and polyketides / Macrolides and analogues
(1aS,4E,8E,10aR,13aR,14aS)-4,8,14a-trimethyl-11-methylene-1a,3,6,7,10,10a,11,13a,14,14a-decahydrooxireno(12,13)cyclotetradeca(1,2-b)furan-12(2H)-one 643720 Click to see CC1=CCCC(=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C)C 316.40 unknown via CMAUP database
(1R,2E,6R,8R,11E)-3,8,12,16-tetramethyl-7,18-dioxatricyclo[13.3.0.06,8]octadeca-2,11,15-trien-17-one 101472593 Click to see CC1=CCCC2(C(O2)CCC(=CC3C(=C(C(=O)O3)C)CC1)C)C 316.40 unknown via CMAUP database
(1R,3R,5R,8E,12E,14S,15R)-14-hydroxy-5,9,13-trimethyl-18-methylidene-4,16-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-17-one 21574172 Click to see CC1=CCCC2(C(O2)CC3C(C(C(=CCC1)C)O)OC(=O)C3=C)C 332.40 unknown via CMAUP database
(1R,3R,5R,8E,12E,15S)-5,9,13-trimethyl-18-methylidene-4,16-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-17-one 643718 Click to see CC1=CCCC2(C(O2)CC3C(CC(=CCC1)C)OC(=O)C3=C)C 316.40 unknown via CMAUP database
[(1R,3R,5R,8E,12E,14S,15R)-5,9,13-trimethyl-18-methylidene-17-oxo-4,16-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-14-yl] acetate 21638415 Click to see CC1=CCCC2(C(O2)CC3C(C(C(=CCC1)C)OC(=O)C)OC(=O)C3=C)C 374.50 unknown via CMAUP database
13-Acetoxysarcocrassolide 21775908 Click to see CC1=CCCC2(C(O2)CC3C(C(C(=CCC1)C)OC(=O)C)OC(=O)C3=C)C 374.50 unknown via CMAUP database
Crassocolide E 11995175 Click to see CC1=CCCC(=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C)C 316.40 unknown via CMAUP database
Crassocolide F 11995282 Click to see CC1=CCC(C(=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C)C)OC(=O)C 374.50 unknown via CMAUP database
Crassocolide N 54764414 Click to see CC1=CCCC(=CC2C(CC3C(O3)(C(=O)CC1)C)C(=C)C(=O)O2)C 330.40 unknown via CMAUP database
Lobophytolide 23425511 Click to see CC1=CCCC(=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C)C 316.40 unknown via CMAUP database
Sarcocrassocolide C 46233394 Click to see CC1=CCCC(=C)C2CCC(O2)(C(CC3C(C1)OC(=O)C3=C)O)C 332.40 unknown via CMAUP database
Sarcocrassocolide D 46233452 Click to see CC1=CCCC(=C)C2CCC(O2)(C(CC3C(C1)OC(=O)C3=C)O)C 332.40 unknown via CMAUP database
Sarcocrassolide 643719 Click to see CC1=CCCC2(C(O2)CC3C(CC(=CCC1)C)OC(=O)C3=C)C 316.40 unknown via CMAUP database

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