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Pterocaulon polystachyum

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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 UUID643fcc55ee88d361555158
Scientific name Pterocaulon polystachyum
Authority DC.
First published in Prodr. 5: 454 (1836)

Description 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
  • Southern America
    • Brazil
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Southern South America
      • Argentina Northeast
      • Paraguay
      • Uruguay

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000061541
Tropicos 50174565
KEW urn:lsid:ipni.org:names:240171-1
The Plant List gcc-18568
Open Tree Of Life 5921003
NCBI Taxonomy 1548649
IPNI 240171-1
iNaturalist 623066
GBIF 5392232
CMAUP NPO9533

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
Natural Coumarins: Exploring the Pharmacological Complexity and Underlying Molecular Mechanisms Sharifi-Rad J, Cruz-Martins N, López-Jornet P, Lopez EP, Harun N, Yeskaliyeva B, Beyatli A, Sytar O, Shaheen S, Sharopov F, Taheri Y, Docea AO, Calina D, Cho WC Oxid Med Cell Longev 23-Aug-2021
PMCID:PMC8440074
doi:10.1155/2021/6492346
PMID:34531939
In Vitro Growth- and Encystation-Inhibitory Efficacies of Matcha Green Tea and Epigallocatechin Gallate Against Acanthameoba Castellanii Dickson A, Cooper E, Fakae LB, Wang B, Chan KL, Elsheikha HM Pathogens 17-Sep-2020
PMCID:PMC7558711
doi:10.3390/pathogens9090763
PMID:32957663
Drug Discovery against Acanthamoeba Infections: Present Knowledge and Unmet Needs Elsheikha HM, Siddiqui R, Khan NA Pathogens 22-May-2020
PMCID:PMC7281112
doi:10.3390/pathogens9050405
PMID:32456110
Phytochemical Screening and Acanthamoebic Activity of Shoots from in Vitro Cultures and in Vivo Plants of Eryngium alpinum L.—The Endangered and Protected Species Kikowska M, Kruszka D, Derda M, Hadaś E, Thiem B Molecules 20-Mar-2020
PMCID:PMC7144402
doi:10.3390/molecules25061416
PMID:32244952
A Review of the Current Research Trends in the Application of Medicinal Plants as a Source for Novel Therapeutic Agents Against Acanthamoeba Infections Niyyati M, Dodangeh S, Lorenzo-Morales J Iran J Pharm Res 01-Sep-2016
PMCID:PMC5316269
PMID:28243287
Artemisia annua L. as a plant with potential use in the treatment of acanthamoebiasis Derda M, Hadaś E, Cholewiński M, Skrzypczak Ł, Grzondziel A, Wojtkowiak-Giera A Parasitol Res 19-Jan-2016
PMCID:PMC4799240
doi:10.1007/s00436-016-4902-z
PMID:26782959
Lethal Effects of Helianthemum lippii (L.) on Acanthamoeba castellanii Cysts in Vitro Badria FA, Hetta MH, Sarhan RM, Ezz El-Din MH Korean J Parasitol 26-Jun-2014
PMCID:PMC4096634
doi:10.3347/kjp.2014.52.3.243
PMID:25031463
Review on Natural Coumarin Lead Compounds for Their Pharmacological Activity Venugopala KN, Rashmi V, Odhav B Biomed Res Int 24-Mar-2013
PMCID:PMC3622347
doi:10.1155/2013/963248
PMID:23586066
Antifungal Activity and Nail Permeation of Nail Lacquer Containing Piper regnellii (Miq.) C. CD. var. pallescens (C. DC.) Yunck (Piperaceae) Leave Extracts and Derivatives Koroishi AM, Sehn E, Baesso ML, Ueda-Nakamura T, Nakamura CV, Cortez DA, Filho BP Molecules 01-Jun-2010
PMCID:PMC6257596
doi:10.3390/molecules15063920
PMID:20657417
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
Induction of cell differentiation in human leukemia U-937 cells by 5-oxygenated-6,7-methylenedioxycoumarins from Pterocaulon polystachyum M EUGENIARIVEIRO Elsevier BV 25-May-2004
doi:10.1016/S0304-3835(04)00225-3
New coumarins from Pterocaulon polystachyum. Vera N, Bardón A, Catalán CA, Gedris TE, Herz W Planta Med 01-Oct-2001
doi:10.1055/S-2001-17365
PMID:11582550
6,7-Dioxygenated and 5,6,7-Trioxygenated Coumarins from Pterocaulon polystachium. Palacios PS, Rojo AA, Coussio JD, De Kimpe N, Debenedetti SL Planta Med 01-Apr-1999
doi:10.1055/S-2006-960786
PMID:17260310

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
5-[(3R,3aS,6S,6aR)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-1,3-benzodioxole 7059611 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
7-Acetoxy-18-trachylobanol 102239718 Click to see CC(=O)OC1CC2C(CCCC2(C3C14CC5C(C3)C5(C4)C)C)(C)CO 346.50 unknown via CMAUP database
Kaura-11-ene-16alpha,19-diol 19-acetate 101615189 Click to see CC(=O)OCC1(CCCC2(C1CCC34C2C=CC(C3)C(C4)(C)O)C)C 346.50 unknown via CMAUP database
Kaura-11-ene-7beta,16alpha,19-triol 7,19-diacetate 101480806 Click to see CC(=O)OCC1(CCCC2(C1CC(C34C2C=CC(C3)C(C4)(C)O)OC(=O)C)C)C 404.50 unknown via CMAUP database
Kaura-16-ene-7beta,19-diol 7-acetate 101615200 Click to see CC(=O)OC1CC2C(CCCC2(C3C14CC(CC3)C(=C)C4)C)(C)CO 346.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
4-Hydroxy-4-(3-hydroxybut-1-enyl)-3,5,5-trimethylcyclohex-2-en-1-one 440244 Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C 224.30 unknown https://doi.org/10.1055/S-2001-17365
Corchoionol C 137705650 Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C 224.30 unknown https://doi.org/10.1055/S-2001-17365
Dehydrovomifoliol 688492 Click to see CC1=CC(=O)CC(C1(C=CC(=O)C)O)(C)C 222.28 unknown via CMAUP database
Vomifoliol 5280462 Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C 224.30 unknown https://doi.org/10.1055/S-2001-17365
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown via CMAUP database
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
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 / Stigmastanes and derivatives
3-Hydroxystigmast-5-en-7-one 160608 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C 428.70 unknown via CMAUP database
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
Rhoiptelenol 102304204 Click to see CC1CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1C)C)C)CCC(C5(C)C)O)C)C 426.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
(+)-Epiloliolide 44511808 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 unknown https://doi.org/10.1055/S-2001-17365
6-Hydroxy-4,4,7a-trimethyl-5,6,7,7a-tetrahydrobenzofuran-2(4H)-one 14334 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 unknown https://doi.org/10.1055/S-2001-17365
Loliolide 100332 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 unknown https://doi.org/10.1055/S-2001-17365
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Methyl 3,4-dihydroxycinnamate 92202 Click to see COC(=O)C=CC1=CC(=C(C=C1)O)O 194.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
6-(2-Hydroxy-3-methylbut-3-enoxy)-7-methoxychromen-2-one 100936168 Click to see CC(=C)C(COC1=C(C=C2C(=C1)C=CC(=O)O2)OC)O 276.28 unknown https://doi.org/10.1055/S-2001-17365
6-[(2S)-2-hydroxy-3-methylbut-3-enoxy]-7-methoxychromen-2-one 163021498 Click to see CC(=C)C(COC1=C(C=C2C(=C1)C=CC(=O)O2)OC)O 276.28 unknown https://doi.org/10.1055/S-2001-17365
6-Methoxy-7-(3-methylbut-2-enoxy)chromen-2-one 1764914 Click to see CC(=CCOC1=C(C=C2C=CC(=O)OC2=C1)OC)C 260.28 unknown https://doi.org/10.1007/S10600-007-0231-X
https://doi.org/10.1055/S-2001-17365
https://doi.org/10.1055/S-2006-960786
7-(2-Hydroxy-3-methylbut-3-enoxy)-6-methoxychromen-2-one 10636169 Click to see CC(=C)C(COC1=C(C=C2C=CC(=O)OC2=C1)OC)O 276.28 unknown https://doi.org/10.1055/S-2006-960786
https://doi.org/10.1055/S-2001-17365
7-(2-Hydroxy-3-methylbutoxy)-6-methoxychromen-2-one 85800695 Click to see CC(C)C(COC1=C(C=C2C=CC(=O)OC2=C1)OC)O 278.30 unknown https://doi.org/10.1055/S-2001-17365
7-(2-Hydroxyethoxy)-6-methoxychromen-2-one 85800492 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OCCO 236.22 unknown https://doi.org/10.1055/S-2001-17365
7-(4-Hydroxy-3-methylbut-2-enoxy)-6-methoxychromen-2-one 73177491 Click to see CC(=CCOC1=C(C=C2C=CC(=O)OC2=C1)OC)CO 276.28 unknown https://doi.org/10.1055/S-2001-17365
7-[(2R)-2-hydroxy-3-methylbutoxy]-6-methoxychromen-2-one 162973016 Click to see CC(C)C(COC1=C(C=C2C=CC(=O)OC2=C1)OC)O 278.30 unknown https://doi.org/10.1055/S-2001-17365
7-[(2S)-2-hydroxy-3-methylbut-3-enoxy]-6-methoxychromen-2-one 163044953 Click to see CC(=C)C(COC1=C(C=C2C=CC(=O)OC2=C1)OC)O 276.28 unknown https://doi.org/10.1055/S-2001-17365
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/10.1055/S-2001-17365
7-[(E)-4-hydroxy-3-methylbut-2-enoxy]-6-methoxychromen-2-one 12920848 Click to see CC(=CCOC1=C(C=C2C=CC(=O)OC2=C1)OC)CO 276.28 unknown https://doi.org/10.1055/S-2001-17365
8H-1,3-Dioxolo[4,5-h][1]benzopyran-8-one 13704003 Click to see C1OC2=C(O1)C3=C(C=C2)C=CC(=O)O3 190.15 unknown https://doi.org/10.1016/S0304-3835(04)00225-3
9-(2-Hydroxyethoxy)-6H-1,3-dioxolo[4,5-g][1]benzopyran-6-one 91585468 Click to see C1OC2=C(O1)C(=C3C=CC(=O)OC3=C2)OCCO 250.20 unknown https://doi.org/10.1055/S-2001-17365
9-[(2R)-2,3-dihydroxy-3-methylbutoxy]-[1,3]dioxolo[4,5-g]chromen-6-one 162968188 Click to see CC(C)(C(COC1=C2C=CC(=O)OC2=CC3=C1OCO3)O)O 308.28 unknown https://doi.org/10.1055/S-2001-17365
9-[(3-Methylbut-2-en-1-yl)oxy]-2H,6H-[1,3]dioxolo[4,5-g][1]benzopyran-6-one 46226618 Click to see CC(=CCOC1=C2C=CC(=O)OC2=CC3=C1OCO3)C 274.27 unknown https://doi.org/10.1055/S-2001-17365
9-Hydroxy-4-(3-methylbut-2-enyl)-[1,3]dioxolo[4,5-g]chromen-6-one 101142533 Click to see CC(=CCC1=C2C(=C(C3=C1OCO3)O)C=CC(=O)O2)C 274.27 unknown https://doi.org/10.1055/S-2001-17365
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/10.1055/S-2001-17365
Ayapin 3083597 Click to see C1OC2=C(O1)C=C3C(=C2)C=CC(=O)O3 190.15 unknown https://doi.org/10.1055/S-2001-17365
https://doi.org/10.1055/S-2006-960786
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/10.1055/S-2001-17365
Sabandinol 179597 Click to see CC(C)(C(COC1=C2C=CC(=O)OC2=CC3=C1OCO3)O)O 308.28 unknown https://doi.org/10.1055/S-2001-17365
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
(8S)-6-hydroxy-8,9,9-trimethyl-8H-furo[2,3-h]chromen-2-one 162900064 Click to see CC1C(C2=C3C(=CC(=C2O1)O)C=CC(=O)O3)(C)C 246.26 unknown https://doi.org/10.1055/S-2001-17365
6-hydroxy-8,9,9-trimethyl-8H-furo[2,3-h]chromen-2-one 101142534 Click to see CC1C(C2=C3C(=CC(=C2O1)O)C=CC(=O)O3)(C)C 246.26 unknown https://doi.org/10.1055/S-2001-17365
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin 69894 Click to see COC1=C(C=C2C=CC(=O)OC2=C1)O 192.17 unknown https://doi.org/10.1055/S-2001-17365
Prenyletin 3873459 Click to see CC(=CCOC1=C(C=C2C=CC(=O)OC2=C1)O)C 246.26 unknown https://doi.org/10.1007/S10600-007-0231-X
https://doi.org/10.1055/S-2006-960786
https://doi.org/10.1055/S-2001-17365
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 4-hydroxycoumarins
3,4-Dihydroxy-6-methoxy-7-(3-methylbut-2-enoxy)chromen-2-one 162868576 Click to see CC(=CCOC1=C(C=C2C(=C1)OC(=O)C(=C2O)O)OC)C 292.28 unknown https://doi.org/10.1055/S-2001-17365
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O 178.14 unknown https://doi.org/10.1055/S-2006-960786
https://doi.org/10.1055/S-2001-17365
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
7-Hydroxy-6-(2-methylbut-3-en-2-yl)chromen-2-one 86111746 Click to see CC(C)(C=C)C1=C(C=C2C(=C1)C=CC(=O)O2)O 230.26 unknown https://doi.org/10.1055/S-2001-17365
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1055/S-2006-960786
https://doi.org/10.1055/S-2001-17365
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database

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