Aristolochia holostylis

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

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Details Top

Internal ID	UUID64400a9736703009382260
Scientific name	Aristolochia holostylis
Authority	F.González
First published in	Revista Acad. Colomb. Ci. Exact. 88: 338 (1999)

Ethnobotanical Use Top

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Important notice

Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Unfortunately, there is no documented evidence in reliable ethnobotanical literature – such as peer-reviewed articles, reputable herbal compendiums, or historic records – for any traditional medicinal or culinary uses involving infusions (teas), decoctions, tinctures, macerations, or poultices of *Aristolochia holostylis* (F.González). Consequently, an ethnobotanical summary cannot be provided.

General Uses Top

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Synonyms Top

Scientific name	Authority	First published in
Aristolochia campanaeformis	DC. ex Duch.	Prodr. 15(1): 432 (1864)
Aristolochia cucullata	Pohl ex Duch.	Prodr. 15(1): 432 (1864)
Duchartrella reniformis	Kuntze	Revis. Gen. Pl. 2: 564 (1891)
Holostylis reniformis	Duch.	Ann. Sci. Nat., Bot. sér. 4, 2: 33, t. 5. 1854
Holostylis reniformis f. minor	Chodat & Hassl.	Bull. Herb. Boissier , sér. 2, 3: 787 (1903)

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil West-central

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000547888
Tropicos	50162841
KEW	urn:lsid:ipni.org:names:1060104-2
The Plant List	kew-2651490
Open Tree Of Life	377016
NCBI Taxonomy	387570
IPNI	1060104-2
GBIF	3588722
EOL	5103432
USDA GRIN	458476

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 basal angiosperm Aristolochia fimbriata: a potential experimental system for genetic studies

Bliss BJ, Wanke S, Barakat A, Ayyampalayam S, Wickett N, Wall PK, Jiao Y, Landherr L, Ralph PE, Hu Y, Neinhuis C, Leebens-Mack J, Arumuganathan K, Clifton SW, Maximova SN, Ma H, dePamphilis CW

BMC Plant Biol

24-Jan-2013

PMCID:	PMC3621149
doi:	10.1186/1471-2229-13-13
PMID:	23347749

Biosynthesis of antimalarial lignans from Holostylis reniformis.

Messiano GB, da Silva T, Nascimento IR, Lopes LM

Phytochemistry

01-Mar-2009

doi:	10.1016/J.PHYTOCHEM.2009.02.008
PMID:	19307005

Antiplasmodial activity of aryltetralone lignans from Holostylis reniformis.

de Andrade-Neto VF, da Silva T, Lopes LM, do Rosário VE, de Pilla Varotti F, Krettli AU

Antimicrob Agents Chemother

01-Jul-2007

PMCID:	PMC1913279
doi:	10.1128/AAC.01344-06
PMID:	17438049

Aryltetralol and aryltetralone lignans from Holostylis reniformis.

da Silva T, Lopes LM

Phytochemistry

01-May-2006

doi:	10.1016/J.PHYTOCHEM.2006.02.007
PMID:	16563445

Configurational analysis of cubebins and bicubebin from Aristolochia lagesiana and Aristolochia pubescens.

de Pascoli IC, Nascimento IR, Lopes LM

Phytochemistry

01-Apr-2006

doi:	10.1016/J.PHYTOCHEM.2006.01.019
PMID:	16500688

Aryltetralone lignans and 7,8-seco-lignans from Holostylis reniformis.

da Silva T, Lopes LM

Phytochemistry

01-Mar-2004

doi:	10.1016/J.PHYTOCHEM.2004.01.004
PMID:	15016571

Diterpene esters of aristolochic acids from Aristolochia pubescens.

Nascimento IR, Lopes LM

Phytochemistry

01-Aug-2003

doi:	10.1016/S0031-9422(03)00335-2
PMID:	12895545

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 / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
[(1R,2S)-1-(1,3-benzodioxol-5-yl)-2-methyl-3-oxobutyl] 3,4-dimethoxybenzoate	23251225	Click to see CC(C(C1=CC2=C(C=C1)OCO2)OC(=O)C3=CC(=C(C=C3)OC)OC)C(=O)C	386.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.01.004
[1-(1,3-Benzodioxol-5-yl)-2-methyl-3-oxobutyl] 3,4-dimethoxybenzoate	74033544	Click to see	386.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.01.004
> Benzenoids / Benzene and substituted derivatives / Diphenylmethanes
2-[(1R,2R)-1-(3,4-dimethoxyphenyl)-2-methyl-3-oxobutyl]-4-hydroxy-5-methoxybenzaldehyde	163089892	Click to see	372.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.01.004
2-[(1R,2S)-1-(3,4-dimethoxyphenyl)-2-methyl-3-oxobutyl]-4-hydroxy-5-methoxybenzaldehyde	5479115	Click to see	372.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.01.004
2-[(1S,2R)-1-(3,4-dimethoxyphenyl)-2-methyl-3-oxobutyl]-4-hydroxy-5-methoxybenzaldehyde	101725743	Click to see CC(C(C1=CC(=C(C=C1)OC)OC)C2=CC(=C(C=C2C=O)OC)O)C(=O)C	372.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.007 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.019
> Lignans, neolignans and related compounds / Aryltetralin lignans
(-)-8'-Epi-aristoligone	13228884	Click to see CC1C(C(=O)C2=CC(=C(C=C2C1C3=CC(=C(C=C3)OC)OC)OC)OC)C	370.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.007 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.019 https://doi.org/10.1016/J.PHYTOCHEM.2009.02.008 https://doi.org/10.1016/J.PHYTOCHEM.2004.01.004 https://doi.org/10.1016/S0031-9422(03)00335-2 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1913279/
(-)-Holostyligone	46883472	Click to see	356.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.007 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.019
(1R,2S,3S,4R)-4-(3,4-dimethoxyphenyl)-6,7-dimethoxy-2,3-dimethyl-1,2,3,4-tetrahydronaphthalen-1-ol	102108255	Click to see	372.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.007 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.019
(1R,2S)-1-(3,4-dimethoxyphenyl)-6,7-dimethoxy-2,3-dimethyl-1,2-dihydronaphthalene	12305411	Click to see CC1C(C2=CC(=C(C=C2C=C1C)OC)OC)C3=CC(=C(C=C3)OC)OC	354.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.007 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.019
(1S,2S,3R,4R)-4-(3,4-dimethoxyphenyl)-6,7-dimethoxy-2,3-dimethyl-1,2,3,4-tetrahydronaphthalen-1-ol	163057926	Click to see	372.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.007
(2R,3S,4R)-4-(3,4-dimethoxyphenyl)-2-hydroxy-6,7-dimethoxy-2,3-dimethyl-3,4-dihydronaphthalen-1-one	102180985	Click to see	386.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.007 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.019
(2R,3S,4R)-4-(3,4-dimethoxyphenyl)-6-hydroxy-7-methoxy-2,3-dimethyl-3,4-dihydro-2H-naphthalen-1-one	13844297	Click to see CC1C(C(=O)C2=CC(=C(C=C2C1C3=CC(=C(C=C3)OC)OC)O)OC)C	356.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.01.004
(2R,3S,4R)-4-(3,4-dimethoxyphenyl)-6,7-dimethoxy-2,3-dimethyl-3,4-dihydro-2H-naphthalen-1-one	13228885	Click to see	370.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.007 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.019 https://doi.org/10.1016/J.PHYTOCHEM.2004.01.004 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1913279/
(2S,3R,4R)-4-(1,3-benzodioxol-5-yl)-6,7-dimethoxy-2,3-dimethyl-3,4-dihydro-2H-naphthalen-1-one	13845955	Click to see CC1C(C(=O)C2=CC(=C(C=C2C1C3=CC4=C(C=C3)OCO4)OC)OC)C	354.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.007 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.019 https://doi.org/10.1016/J.PHYTOCHEM.2009.02.008 https://doi.org/10.1016/J.PHYTOCHEM.2004.01.004 https://doi.org/10.1016/S0031-9422(03)00335-2 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1913279/
(2S,3R,4R)-4-(3,4-dimethoxyphenyl)-6-hydroxy-7-methoxy-2,3-dimethyl-3,4-dihydro-2H-naphthalen-1-one	23251223	Click to see CC1C(C(=O)C2=CC(=C(C=C2C1C3=CC(=C(C=C3)OC)OC)O)OC)C	356.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.01.004
(2S,3R,4R)-4-(3,4-dimethoxyphenyl)-6,7-dimethoxy-2,3-dimethyl-3,4-dihydro-2H-naphthalen-1-one	13228882	Click to see	370.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.007 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.019 https://doi.org/10.1016/J.PHYTOCHEM.2009.02.008 https://doi.org/10.1016/J.PHYTOCHEM.2004.01.004 https://doi.org/10.1016/S0031-9422(03)00335-2 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1913279/
(2S,3S,4R)-4-(1,3-benzodioxol-5-yl)-6,7-dimethoxy-2,3-dimethyl-3,4-dihydro-2H-naphthalen-1-one	44585954	Click to see	354.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.02.008 https://doi.org/10.1016/S0031-9422(03)00335-2 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1913279/
(2S,3S,4R)-4-(3,4-dimethoxyphenyl)-6-hydroxy-7-methoxy-2,3-dimethyl-3,4-dihydro-2H-naphthalen-1-one	23251224	Click to see	356.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.02.008 https://doi.org/10.1016/J.PHYTOCHEM.2004.01.004 https://doi.org/10.1016/S0031-9422(03)00335-2
(6S,7R,8R)-8-(1,3-benzodioxol-5-yl)-6,7-dimethyl-7,8-dihydro-6H-benzo[f][1,3]benzodioxol-5-one	162913691	Click to see	338.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.007 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.019
(6S,7S,8R)-8-(1,3-benzodioxol-5-yl)-6,7-dimethyl-7,8-dihydro-6H-benzo[f][1,3]benzodioxol-5-one	162913692	Click to see	338.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.007 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.019
(6S,7S,8R)-8-(3,4-dimethoxyphenyl)-6,7-dimethyl-7,8-dihydro-6H-benzo[f][1,3]benzodioxol-5-one	14034478	Click to see	354.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.02.008 https://doi.org/10.1016/J.PHYTOCHEM.2004.01.004 https://doi.org/10.1016/S0031-9422(03)00335-2 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1913279/
1-(3,4-Dimethoxyphenyl)-6,7-dimethoxy-2,3-dimethyl-1,2-dihydronaphthalene	12305410	Click to see	354.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.007 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.019
4-(1,3-benzodioxol-5-yl)-6,7-dimethoxy-2,3-dimethyl-3,4-dihydro-2H-naphthalen-1-one	13845954	Click to see	354.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.007 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.019 https://doi.org/10.1016/J.PHYTOCHEM.2009.02.008 https://doi.org/10.1016/J.PHYTOCHEM.2004.01.004 https://doi.org/10.1016/S0031-9422(03)00335-2 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1913279/
4-(3,4-Dimethoxyphenyl)-2-hydroxy-6,7-dimethoxy-2,3-dimethyl-3,4-dihydronaphthalen-1-one	162970460	Click to see	386.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.007 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.019
4-(3,4-dimethoxyphenyl)-6-hydroxy-7-methoxy-2,3-dimethyl-3,4-dihydro-2H-naphthalen-1-one	13844296	Click to see	356.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.02.008 https://doi.org/10.1016/J.PHYTOCHEM.2004.01.004 https://doi.org/10.1016/S0031-9422(03)00335-2
4-(3,4-Dimethoxyphenyl)-6,7-dimethoxy-2,3-dimethyl-1,2,3,4-tetrahydronaphthalen-1-ol	14017385	Click to see	372.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.007 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.019
6-hydroxy-4-(4-hydroxy-3-methoxyphenyl)-7-methoxy-2,3-dimethyl-3,4-dihydro-2H-naphthalen-1-one	13844290	Click to see	342.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.007 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.019 https://doi.org/10.1016/J.PHYTOCHEM.2009.02.008 https://doi.org/10.1016/S0031-9422(03)00335-2
8-(1,3-benzodioxol-5-yl)-6,7-dimethyl-7,8-dihydro-6H-benzo[f][1,3]benzodioxol-5-one	14462034	Click to see	338.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.007 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.019
8-(3,4-dimethoxyphenyl)-6,7-dimethyl-7,8-dihydro-6H-benzo[f][1,3]benzodioxol-5-one	14034477	Click to see CC1C(C(=O)C2=CC3=C(C=C2C1C4=CC(=C(C=C4)OC)OC)OCO3)C	354.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.02.008 https://doi.org/10.1016/J.PHYTOCHEM.2004.01.004 https://doi.org/10.1016/S0031-9422(03)00335-2 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1913279/
Arisantetralone B	13844291	Click to see	342.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.02.008 https://doi.org/10.1016/S0031-9422(03)00335-2
Arisantetralone D	14078176	Click to see	356.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.007 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.019
Dimethylwulignan A1	13228881	Click to see	370.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.007 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.019 https://doi.org/10.1016/J.PHYTOCHEM.2009.02.008 https://doi.org/10.1016/J.PHYTOCHEM.2004.01.004 https://doi.org/10.1016/S0031-9422(03)00335-2 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1913279/
Epischisandrone	14078175	Click to see	356.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.007 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.019
Wulignan a2	13844292	Click to see CC1C(C(=O)C2=CC(=C(C=C2C1C3=CC(=C(C=C3)O)OC)O)OC)C	342.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.007 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.019
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(-)-Galbacin	11175182	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC5=C(C=C4)OCO5)C	340.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.01.004
5-[(2R,3R,4S,5S)-5-(1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-1,3-benzodioxole	51381166	Click to see	340.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.007 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.019
5-[(2R,3S,4R,5S)-5-(1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-1,3-benzodioxole	51406927	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC5=C(C=C4)OCO5)C	340.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.01.004
5-[5-(3,4-Dimethoxyphenyl)-3,4-dimethyloxolan-2-yl]-1,3-benzodioxole	12302263	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)OC)OC)C	356.40	unknown	https://doi.org/10.1016/S0031-9422(03)00335-2 https://doi.org/10.1016/J.PHYTOCHEM.2009.02.008
Calopiptin	12302265	Click to see	356.40	unknown	https://doi.org/10.1016/S0031-9422(03)00335-2 https://doi.org/10.1016/J.PHYTOCHEM.2009.02.008
Futokadsurin C	9548906	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)OC)OC)C	356.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.02.008 https://doi.org/10.1016/S0031-9422(03)00335-2
Galbacin	234441	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC5=C(C=C4)OCO5)C	340.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.01.004 https://doi.org/10.1016/J.PHYTOCHEM.2006.02.007 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.019
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Leucoanthocyanidins
Fisetinidol-4beta-ol 3,4,7,3',4'-pentamethyl ether	44257143	Click to see	360.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.007 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.019 https://doi.org/10.1016/J.PHYTOCHEM.2004.01.004
> Phenylpropanoids and polyketides / Macrolides and analogues
[(2R,4R,5S,6R)-2-[(2S,3R,4S)-4-[(2R,3S,4E,6E,9R,10S,11S,12R,13R,14E,16Z)-11-Ethyl-10,12-dihydroxy-3,17-dimethoxy-7,9,13,15-tetramethyl-18-oxo-1-oxacyclooctadeca-4,6,14,16-tetraen-2-yl]-3-hydroxypentan-2-yl]-2-hydroxy-5-methyl-6-[(E)-prop-1-enyl]oxan-4-yl] (E)-4-[(2-hydroxy-5-oxocyclopenten-1-yl)amino]-4-oxobut-2-enoate	341622	Click to see	886.10	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.007 https://doi.org/10.1016/J.PHYTOCHEM.2006.01.019

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Aristolochia holostylis

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses 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

Gallery Top

Contributors Top

Collections Top