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Aristolochia arcuata

Table of Contents

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
Collections

Details Top

Internal ID UUID64400a8470b36930741082
Scientific name Aristolochia arcuata
Authority Mast.
First published in Fl. Bras. 4(2): 101 (1875)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Portuguese cipó-mil-homens

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000547533
Tropicos 50263993
KEW urn:lsid:ipni.org:names:92744-1
The Plant List kew-2651163
Open Tree Of Life 708565
NCBI Taxonomy 158533
IPNI 92744-1
GBIF 3589027
EPPO ARPAR
USDA GRIN 4079

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
Advances in the roles and mechanisms of lignans against Alzheimer’s disease Han N, Wen Y, Liu Z, Zhai J, Li S, Yin J Front Pharmacol 12-Oct-2022
PMCID:PMC9596774
doi:10.3389/fphar.2022.960112
PMID:36313287
New Users of Herbal Medicine Containing Aristolochic Acids and the Risk of Dementia in the Elderly: A Nationwide, Population-Based Study in Taiwan Chiou YE, Chien WC, Chung CH, Chang HA, Kao YC, Tsay PK, Tzeng NS Neuropsychiatr Dis Treat 12-Jun-2020
PMCID:PMC7297452
doi:10.2147/NDT.S250659
PMID:32606702
Chemistry and Neurotrophic Activities of (–)-Talaumidin and Its Derivatives Harada K, Kubo M, Fukuyama Y Front Chem 23-Apr-2020
PMCID:PMC7192021
doi:10.3389/fchem.2020.00301
PMID:32391327
Biomimetic Phosphate-Catalyzed Pictet–Spengler Reaction for the Synthesis of 1,1′-Disubstituted and Spiro-Tetrahydroisoquinoline Alkaloids Zhao J, Méndez-Sánchez D, Ward JM, Hailes HC J Org Chem 16-May-2019
PMCID:PMC7007230
doi:10.1021/acs.joc.9b00527
PMID:31095375
Applications of Friedel–Crafts reactions in total synthesis of natural products Heravi MM, Zadsirjan V, Saedi P, Momeni T RSC Adv 03-Dec-2018
PMCID:PMC9091380
doi:10.1039/c8ra07325b
PMID:35558228
Oxidative Stress and Renal Fibrosis: Recent Insights for the Development of Novel Therapeutic Strategies Lv W, Booz GW, Fan F, Wang Y, Roman RJ Front Physiol 16-Feb-2018
PMCID:PMC5820314
doi:10.3389/fphys.2018.00105
PMID:29503620
Review of Herbal Traditional Chinese Medicine for the Treatment of Diabetic Nephropathy Sun GD, Li CY, Cui WP, Guo QY, Dong CQ, Zou HB, Liu SJ, Dong WP, Miao LN J Diabetes Res 15-Nov-2015
PMCID:PMC4662991
doi:10.1155/2016/5749857
PMID:26649322
The betrayed thief – the extraordinary strategy of Aristolochia rotunda to deceive its pollinators Oelschlägel B, Nuss M, von Tschirnhaus M, Pätzold C, Neinhuis C, Dötterl S, Wanke S New Phytol 08-Dec-2014
PMCID:PMC4357391
doi:10.1111/nph.13210
PMID:25488155
Neurotrophic Natural Products: Chemistry and Biology Xu J, Lacoske MH, Theodorakis EA Angew Chem Int Ed Engl 18-Dec-2013
PMCID:PMC3945720
doi:10.1002/anie.201302268
PMID:24353244
Herbal constituent sequoyitol improves hyperglycemia and glucose intolerance by targeting hepatocytes, adipocytes, and β-cells Shen H, Shao M, Cho KW, Wang S, Chen Z, Sheng L, Wang T, Liu Y, Rui L Am J Physiol Endocrinol Metab 31-Jan-2012
PMCID:PMC3330724
doi:10.1152/ajpendo.00479.2011
PMID:22297305
Neurotrophic effects of talaumidin, a neolignan from Aristolochia arcuata, in primary cultured rat cortical neurons. Zhai H, Nakatsukasa M, Mitsumoto Y, Fukuyama Y Planta Med 01-Jul-2004
doi:10.1055/S-2004-827179
PMID:15303251
Alkaloids from Aristolochia arcuata Lilian Y Watanabe, Lucia M.X Lopes Elsevier BV 01-May-2003
doi:10.1016/0031-9422(95)00341-4
Tetrahydroisoquinoline alkaloids and 2-deoxyribonolactones from Aristolochia arcuata. Francisco MC, Nasser AL, Lopes LM Phytochemistry 01-Apr-2003
doi:10.1016/S0031-9422(02)00655-6
PMID:12648549

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
> 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/10.1016/0031-9422(95)00341-4
Talaumidin, (-)- 11573701 Click to see 342.40 unknown https://doi.org/10.1055/S-2004-827179
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aristolane sesquiterpenoids
1H-Cyclopropa(a)naphthalene, 1a,2,3,5,6,7,7a,7b-octahydro-1,1,7,7a-tetramethyl-, (1aR-(1aalpha,7alpha,7aalpha,7balpha))- 15560278 Click to see CC1CCC=C2C1(C3C(C3(C)C)CC2)C 204.35 unknown https://doi.org/10.1016/0031-9422(95)00341-4
Calarene 28481 Click to see CC1CCC=C2C1(C3C(C3(C)C)CC2)C 204.35 unknown https://doi.org/10.1016/0031-9422(95)00341-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(95)00341-4
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(95)00341-4
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
6-Methoxycyclohexane-1,2,3,4,5-pentol 230881 Click to see COC1C(C(C(C(C1O)O)O)O)O 194.18 unknown https://doi.org/10.1016/S0031-9422(02)00655-6
Sequoyitol 439990 Click to see 194.18 unknown https://doi.org/10.1016/S0031-9422(02)00655-6
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see 342.30 unknown https://doi.org/10.1016/S0031-9422(02)00655-6
https://doi.org/10.1016/0031-9422(95)00341-4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
D-(-)-Fructose 5984 Click to see 180.16 unknown https://doi.org/10.1016/S0031-9422(02)00655-6
https://doi.org/10.1016/0031-9422(95)00341-4
D-Fructose 2723872 Click to see 180.16 unknown https://doi.org/10.1016/S0031-9422(02)00655-6
https://doi.org/10.1016/0031-9422(95)00341-4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Glycerin 753 Click to see C(C(CO)O)O 92.09 unknown https://doi.org/10.1016/S0031-9422(02)00655-6
> Organoheterocyclic compounds / Tetrahydroisoquinolines
Salsolinol 91588 Click to see 179.22 unknown https://doi.org/10.1016/S0031-9422(02)00655-6

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Collections Top

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