Achyrocline satureioides

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Description

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

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Distribution

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Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID643fca73153d6332038459
Scientific name	Achyrocline satureioides
Authority	(Lam.) DC.
First published in	Prodr. [A. P. de Candolle] 6: 220. 1838 [dt. 1837; publ. early Jan 1838] (as satureioides)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Gnaphalium saturejifolium	Poepp. ex DC.	Prodr. 6: 220 (1838)
Achyrocline candicans	DC.	Prodr. 6: 221 (1838)
Gnaphalium satureioides	Lam.	Encycl. [J. Lamarck & al.] 2(2): 747. 1788 [14 Apr 1788] (as satureioides)
Gnaphalium saturejoides var. candicans	(Kunth) Kuntze	Revis. Gen. Pl. 3(3): 153 (1898)
Gnaphalium rufum	Willd. ex Less.	Linnaea 6: 230, in syn. (1831)
Gnaphalium candicans	Kunth	Nov. Gen. Sp. 4: 62 (1820)

Common names Top

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Language	Common/alternative name
Spanish	marcelita
Spanish	vira vira
Spanish	marcela
Spanish	marcela macho
Spanish	marcela hermbra
Spanish	marcela blanca
Spanish	gnaphalium saturejaefolium
Spanish	gnaphalium candicans
Spanish	achyrocline candicans
Spanish	gnaphalium rufum
Spanish	gnaphalium satureioides
Arabic	أكيروكلين ساتوريويديس
Azerbaijani	achyrocline candicans
gn	jate'ika'a
Portuguese	macela
Quechua	allqu wira-wira
Chinese	巴西甘菊花
Chinese	马赛拉

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000038434
UNII	PGA1AZ433Z
Tropicos	2717100
KEW	urn:lsid:ipni.org:names:174407-1
The Plant List	gcc-13716
Open Tree Of Life	531783
NCBI Taxonomy	746493
IPNI	30187325-2
iNaturalist	511347
GBIF	3139534
Freebase	/m/0275j4p
EPPO	ACOSA
EOL	6238558
USDA GRIN	429392
Wikipedia	Achyrocline_saturejoides
CMAUP	NPO29471

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

Separation Methods of Phenolic Compounds from Plant Extract as Antioxidant Agents Candidate

Susanti I, Pratiwi R, Rosandi Y, Hasanah AN

Plants (Basel)

27-Mar-2024

PMCID:	PMC11013868
doi:	10.3390/plants13070965
PMID:	38611494

Characterizations and effects of pectin-coated nanoliposome loaded with Gijavash (Froriepia subpinnata) extract on the physicochemical properties of cheese

Mohammadi F, Yousefi M

Heliyon

31-Oct-2023

PMCID:	PMC10660039
doi:	10.1016/j.heliyon.2023.e21564
PMID:	38027869

A comprehensive review of ultrasonic assisted extraction (UAE) for bioactive components: Principles, advantages, equipment, and combined technologies

Shen L, Pang S, Zhong M, Sun Y, Qayum A, Liu Y, Rashid A, Xu B, Liang Q, Ma H, Ren X

Ultrason Sonochem

13-Oct-2023

PMCID:	PMC10594638
doi:	10.1016/j.ultsonch.2023.106646
PMID:	37862945

Emergence of Nano-Based Formulations for Effective Delivery of Flavonoids against Topical Infectious Disorders

Dwivedi K, Mandal AK, Afzal O, Altamimi AS, Sahoo A, Alossaimi MA, Almalki WH, Alzahrani A, Barkat MA, Almeleebia TM, Mir Najib Ullah SN, Rahman M

Gels

18-Aug-2023

PMCID:	PMC10453850
doi:	10.3390/gels9080671
PMID:	37623126

Potential use of the Asteraceae family as a cure for diabetes: A review of ethnopharmacology to modern day drug and nutraceuticals developments

Mohanta YK, Mishra AK, Nongbet A, Chakrabartty I, Mahanta S, Sarma B, Panda J, Panda SK

Front Pharmacol

03-Aug-2023

PMCID:	PMC10441548
doi:	10.3389/fphar.2023.1153600
PMID:	37608892

Achyrocline satureioides Hydroalcoholic Extract as a Hypoallergenic Antimicrobial Substitute of Natural Origin for Commonly Used Preservatives in Cosmetic Emulsions

Langová D, Córdoba MA, Sorrechia R, Hoová J, Svoboda Z, Mikulíková R, Correa MA, Pietro RC, Márová I

Plants (Basel)

18-May-2023

PMCID:	PMC10222649
doi:	10.3390/plants12102027
PMID:	37653944

From Hop to Beer: Influence of Different Organic Foliar Fertilisation Treatments on Hop Oil Profile and Derived Beers’ Flavour

Rodolfi M, Valentoni A, Pretti L, Sanna M, Guidotti S, Marchioni I, Ganino T

Plants (Basel)

30-Apr-2023

PMCID:	PMC10180877
doi:	10.3390/plants12091861
PMID:	37176918

In Silico Evaluation of Quercetin Methylated Derivatives on the Interaction with Secretory Phospholipases A2 from Crotalus durissus terrificus and Bothrops jararacussu

Belchor MN, Costa CR, Roggero A, Moraes LL, Samelo R, Annunciato I, de Oliveira MA, Sousa SF, Toyama MH

Pharmaceuticals (Basel)

15-Apr-2023

PMCID:	PMC10143728
doi:	10.3390/ph16040597
PMID:	37111354

Nanotechnology Promoting the Development of Products from the Biodiversity of the Asteraceae Family

Yien RM, Matos AP, Gomes AC, Garófalo DD, Santos-Oliveira R, Simas NK, Ricci-Júnior E

Nutrients

26-Mar-2023

PMCID:	PMC10096939
doi:	10.3390/nu15071610
PMID:	37049452

Quercetin: A Functional Food-Flavonoid Incredibly Attenuates Emerging and Re-Emerging Viral Infections through Immunomodulatory Actions

Shorobi FM, Nisa FY, Saha S, Chowdhury MA, Srisuphanunt M, Hossain KH, Rahman MA

Molecules

17-Jan-2023

PMCID:	PMC9920550
doi:	10.3390/molecules28030938
PMID:	36770606

Effect of Adding Matricaria recutita L., Cymbopogon citratus, or Mentha piperita L. Extracts to Fermented Orange Beverage: Sensory Evaluation, Physicochemical Characterization, and Prediction of Toxic Risks and Biological Activity In Silico

Mascarin LG, Franco FW, Dornelles RC, Figueredo KC, Santos RO, Bauermann LD, Emanuelli T, Somacal S, Sautter CK

Foods

05-Jan-2023

PMCID:	PMC9858046
doi:	10.3390/foods12020243
PMID:	36673335

Protective Role of Natural Compounds under Radiation-Induced Injury

Altomare A, Fiore M, D’Ercole G, Imperia E, Nicolosi RM, Della Posta S, Pasqua G, Cicala M, De Gara L, Ramella S, Guarino MP

Nutrients

17-Dec-2022

PMCID:	PMC9786992
doi:	10.3390/nu14245374
PMID:	36558533

LC-HR/MS Analysis of Lipophilic Extracts from Calendula arvensis (Vaill.) L. Organs: An Unexplored Source in Cosmeceuticals

Gravina C, Fiorentino M, Formato M, Pecoraro MT, Piccolella S, Stinca A, Pacifico S, Esposito A

Molecules

14-Dec-2022

PMCID:	PMC9783063
doi:	10.3390/molecules27248905
PMID:	36558038

Effect of Hydrogel Containing Achyrocline satureioides (Asteraceae) Extract–Loaded Nanoemulsions on Wound Healing Activity

Balestrin LA, Back PI, Marques MD, Araújo GD, Carrasco MC, Batista MM, Silveira T, Rodrigues JL, Fachel FN, Koester LS, Bassani VL, Horn AP, Dora CL, Teixeira HF

Pharmaceutics

06-Dec-2022

PMCID:	PMC9788587
doi:	10.3390/pharmaceutics14122726
PMID:	36559219

Plants as Modulators of Melanogenesis: Role of Extracts, Pure Compounds and Patented Compositions in Therapy of Pigmentation Disorders

Merecz-Sadowska A, Sitarek P, Stelmach J, Zajdel K, Kucharska E, Zajdel R

Int J Mol Sci

26-Nov-2022

PMCID:	PMC9736547
doi:	10.3390/ijms232314787
PMID:	36499134

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 / Aporphines
Roemerine	119204	Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3	279.30	unknown	via CMAUP database
> Alkaloids and derivatives / Proaporphines
(+)-Pronuciferine	200480	Click to see CN1CCC2=CC(=C(C3=C2C1CC34C=CC(=O)C=C4)OC)OC	311.40	unknown	via CMAUP database
(+)-Stepharine	193686	Click to see COC1=C(C2=C3C(CC24C=CC(=O)C=C4)NCCC3=C1)OC	297.30	unknown	via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
2,3,10-trimethoxy-6,7-dihydro-5H-isoquinolino[2,1-b]isoquinolin-7-ium-9-one	101280139	Click to see COC1=CC=C2C=C3C4=CC(=C(C=C4CC[NH+]3C=C2C1=O)OC)OC	338.40	unknown	via CMAUP database
2,3,9,10-Tetramethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-7-ium-11-ol	46216998	Click to see COC1=C(C=C2C(=C1)CC[N+]3=CC4=C(C(=C(C=C4C=C23)O)OC)OC)OC	368.40	unknown	via CMAUP database
D-Tetrahydropalmatine	969488	Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)OC	355.40	unknown	via CMAUP database
Dehydrocorydalmine	3083983	Click to see COC1=C(C=C2C(=C1)CC[N+]3=C2C=C4C=CC(=C(C4=C3)OC)O)OC	338.40	unknown	via CMAUP database
l-Stepholidine	6917970	Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C(=C(C=C4)O)OC)O	327.40	unknown	via CMAUP database
Palmatine	19009	Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)OC)OC)OC	352.40	unknown	via CMAUP database
Stepharanine	10358881	Click to see COC1=C(C=C2C(=C1)CC[N+]3=C2C=C4C=CC(=C(C4=C3)OC)O)O	324.30	unknown	via CMAUP database
Tetrahydropalmatine	72301	Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)OC	355.40	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Butyrophenones
3-[[(2S)-4,6-dihydroxy-7-[(2S)-2-methylbutanoyl]-2-prop-1-en-2-yl-2,3-dihydro-1-benzofuran-5-yl]methyl]-6-ethyl-4-hydroxy-5-methylpyran-2-one	118723637	Click to see CCC1=C(C(=C(C(=O)O1)CC2=C(C(=C3C(=C2O)CC(O3)C(=C)C)C(=O)C(C)CC)O)O)C	442.50	unknown	https://doi.org/10.1021/NP500735F
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
6-Ethyl-4-hydroxy-5-methyl-3-[[2,4,6-trihydroxy-3-(2-methylbutanoyl)-5-(3-methylbut-2-enyl)phenyl]methyl]pyran-2-one	101538377	Click to see CCC1=C(C(=C(C(=O)O1)CC2=C(C(=C(C(=C2O)CC=C(C)C)O)C(=O)C(C)CC)O)O)C	444.50	unknown	https://doi.org/10.1021/NP010374L
6-ethyl-4-hydroxy-5-methyl-3-[[2,4,6-trihydroxy-3-[(2R)-2-methylbutanoyl]-5-(3-methylbut-2-enyl)phenyl]methyl]pyran-2-one	162939050	Click to see CCC1=C(C(=C(C(=O)O1)CC2=C(C(=C(C(=C2O)CC=C(C)C)O)C(=O)C(C)CC)O)O)C	444.50	unknown	https://doi.org/10.1021/NP010374L
6-ethyl-4-hydroxy-5-methyl-3-[[2,4,6-trihydroxy-3-[(2S)-2-methylbutanoyl]-5-(3-methylbut-2-enyl)phenyl]methyl]pyran-2-one	118723639	Click to see CCC1=C(C(=C(C(=O)O1)CC2=C(C(=C(C(=C2O)CC=C(C)C)O)C(=O)C(C)CC)O)O)C	444.50	unknown	https://doi.org/10.1021/NP500735F
> Organic oxygen compounds / Organooxygen compounds / Ethers / Diarylethers
Cycleanine	121313	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C6C(CC7=CC=C(O3)C=C7)N(CCC6=CC(=C5OC)OC)C)OC)OC	622.70	unknown	via CMAUP database
N2'-Demethylcycleanine	21582963	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C6C(CC7=CC=C(O3)C=C7)NCCC6=CC(=C5OC)OC)OC)OC	608.70	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzofurans / Dibenzofurans
(2R)-2-methyl-1-[1,3,7,9-tetrahydroxy-4-[(2R)-2-hydroxy-3-methylbut-3-enyl]-6-[(2R)-2-methylbutanoyl]-8-(3-methylbut-2-enyl)dibenzofuran-2-yl]butan-1-one	162896613	Click to see CCC(C)C(=O)C1=C(C2=C(C(=C1O)CC(C(=C)C)O)OC3=C2C(=C(C(=C3C(=O)C(C)CC)O)CC=C(C)C)O)O	552.70	unknown	https://doi.org/10.1021/NP010374L
(2R)-2-methyl-1-[1,3,7,9-tetrahydroxy-4-[(2S)-2-hydroxy-3-methylbut-3-enyl]-6-[(2R)-2-methylbutanoyl]-8-(3-methylbut-2-enyl)dibenzofuran-2-yl]butan-1-one	636931	Click to see CCC(C)C(=O)C1=C(C2=C(C(=C1O)CC(C(=C)C)O)OC3=C2C(=C(C(=C3C(=O)C(C)CC)O)CC=C(C)C)O)O	552.70	unknown	https://doi.org/10.1021/NP500735F https://doi.org/10.1021/NP010374L
(2S)-2-methyl-1-[1,3,7,9-tetrahydroxy-6-[(2S)-2-methylbutanoyl]-8-(3-methylbut-2-enyl)-4-[(2S)-2-methyl-3-oxobutyl]dibenzofuran-2-yl]butan-1-one	163105502	Click to see CCC(C)C(=O)C1=C(C2=C(C(=C1O)CC(C)C(=O)C)OC3=C2C(=C(C(=C3C(=O)C(C)CC)O)CC=C(C)C)O)O	552.70	unknown	https://doi.org/10.1021/NP010374L
(2S)-2-methyl-1-[6,7,9-trihydroxy-8-(2-hydroxy-3-methylbut-3-enyl)-3,3-dimethyl-5-[(2S)-2-methylbutanoyl]-[1]benzofuro[2,3-f]chromen-10-yl]butan-1-one	101910301	Click to see CCC(C)C(=O)C1=C(C(=C(C2=C1OC3=C4C=CC(OC4=C(C(=C23)O)C(=O)C(C)CC)(C)C)O)CC(C(=C)C)O)O	550.60	unknown	https://doi.org/10.1021/NP500735F
Achyrofuran	11757338	Click to see CCC(C)C(=O)C1=C(C2=C(C(=C1O)CC(C(=C)C)O)OC3=C2C(=C(C(=C3C(=O)C(C)CC)O)CC=C(C)C)O)O	552.70	unknown	https://doi.org/10.1021/NP010374L https://doi.org/10.1021/NP500735F
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
(s)-3-[{5,7-Dihydroxy-2,2-dimethyl-8-(2-methylbutanoyl)-2h-chromen-6-yl}methyl]-6-ethyl-4-hydroxy-5-methyl-2h-pyran-2-one	101910299	Click to see CCC1=C(C(=C(C(=O)O1)CC2=C(C(=C3C(=C2O)C=CC(O3)(C)C)C(=O)C(C)CC)O)O)C	442.50	unknown	https://doi.org/10.1021/NP500735F
6-ethyl-4-hydroxy-5-methyl-3-[[(3S)-3,5,7-trihydroxy-2,2-dimethyl-8-[(2S)-2-methylbutanoyl]-3,4-dihydrochromen-6-yl]methyl]pyran-2-one	118723638	Click to see CCC1=C(C(=C(C(=O)O1)CC2=C(C(=C3C(=C2O)CC(C(O3)(C)C)O)C(=O)C(C)CC)O)O)C	460.50	unknown	https://doi.org/10.1021/NP500735F
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid	689043	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://doi.org/10.1002/PTR.2650050511
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone	8417	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC	206.19	unknown	https://doi.org/10.1002/MRC.1260330913
> Phenylpropanoids and polyketides / Flavonoids / Flavones
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	https://doi.org/10.1002/PTR.2650050511 https://doi.org/10.1002/(SICI)1099-1573(199703)11:2<123::AID-PTR44>3.0.CO;2-W https://doi.org/10.1016/J.JEP.2003.11.012 https://doi.org/10.1016/S0731-7085(01)00693-8
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1016/J.JEP.2003.11.012
Myricetin	5281672	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	318.23	unknown	https://doi.org/10.1016/J.JEP.2003.11.012
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	https://doi.org/10.1016/S0731-7085(01)00693-8 https://doi.org/10.1078/0944711041495182 https://doi.org/10.1016/J.JEP.2003.11.012 https://doi.org/10.1002/PTR.2650050511 https://doi.org/10.1002/(SICI)1099-1573(199703)11:2<123::AID-PTR44>3.0.CO;2-W
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin	5280681	Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O	316.26	unknown	https://doi.org/10.1078/0944711041495182
Chryseriol	5280666	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	https://doi.org/10.1016/S0731-7085(01)00693-8 https://doi.org/10.1016/J.JEP.2003.11.012 https://doi.org/10.1002/(SICI)1099-1573(199703)11:2<123::AID-PTR44>3.0.CO;2-W https://doi.org/10.1002/PTR.2650050511
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Alnustin	14138832	Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=CC=C3)O)OC	328.30	unknown	https://doi.org/10.1016/S0031-9422(00)81599-X

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Achyrocline satureioides

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top