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Pyrrosia petiolosa

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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 UUID644075083221c764483428
Scientific name Pyrrosia petiolosa
Authority (Christ) Ching
First published in Bull. Chin. Bot. Soc. 1: 59 (1935)

Description Top

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Synonyms Top

Scientific name Authority First published in
Polypodium petiolosum Christ Nuovo Giorn. Bot. Ital. , n.s., 4: 96 (1897)
Cyclophorus petiolosus (Christ) C.Chr. Index Filic. : 200 (1905)
Niphobolus petiolosus (Christ) Diels Bot. Jahrb. Syst. 29: 207 (1900)

Common names Top

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Language Common/alternative name
Chinese 石韦
Chinese 有柄石韦
Chinese 有柄石韋

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
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Korea
    • Mongolia
      • Mongolia
    • Russian Far East
      • Khabarovsk
      • Primorye

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000748144
UNII 3N68O0948D
Tropicos 26624119
KEW urn:lsid:ipni.org:names:17416510-1
The Plant List kew-2902273
Open Tree Of Life 666233
Observations.org 138396
NCBI Taxonomy 746522
IPNI 17416510-1
iNaturalist 701646
GBIF 5647926
EOL 6118920
USDA GRIN 423513
CMAUP NPO24078

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
Quinces (Cydonia oblonga, Chaenomeles sp., and Pseudocydonia sinensis) as Medicinal Fruits of the Rosaceae Family: Current State of Knowledge on Properties and Use Kostecka-Gugała A Antioxidants (Basel) 03-Jan-2024
PMCID:PMC10812678
doi:10.3390/antiox13010071
PMID:38247495
Semisynthesis, Biological Evaluation and Molecular Docking Studies of Barbatic Acid Derivatives as Novel Diuretic Candidates Yu X, Sui Y, Xi Y, Zhang Y, Luo G, Long Y, Yang W Molecules 10-May-2023
PMCID:PMC10222548
doi:10.3390/molecules28104010
PMID:37241751
Variation in flavonoid and antioxidant activities of Pyrrosia petiolosa (Christ) Ching from different geographic origins Chen J, Ning S, Lu X, Xiang W, Zhou X, Bu Y, Li L, Huang R Front Plant Sci 14-Apr-2023
PMCID:PMC10140315
doi:10.3389/fpls.2023.1173489
PMID:37123848
Lichen Depsides and Tridepsides: Progress in Pharmacological Approaches Ureña-Vacas I, González-Burgos E, Divakar PK, Gómez-Serranillos MP J Fungi (Basel) 14-Jan-2023
PMCID:PMC9866793
doi:10.3390/jof9010116
PMID:36675938
Antitumor effects of Chinese herbal medicine compounds and their nano-formulations on regulating the immune system microenvironment Sun K, Wu L, Wang S, Deng W Front Oncol 23-Sep-2022
PMCID:PMC9540406
doi:10.3389/fonc.2022.949332
PMID:36212483
Pyrrosia petiolosa Extract Ameliorates Ethylene Glycol-Induced Urolithiasis in Rats by Inhibiting Oxidative Stress and Inflammatory Response Zhou F, Wang X Dis Markers 05-Aug-2022
PMCID:PMC9374559
doi:10.1155/2022/1913067
PMID:35968503
Traditional Chinese Medicine is an Alternative Therapeutic Option for Treatment of Pseudomonas aeruginosa Infections Pang Z, Zhu Q Front Pharmacol 27-Aug-2021
PMCID:PMC8429605
doi:10.3389/fphar.2021.737252
PMID:34512364
The first complete chloroplast genome of Drynaria acuminata (Polypodiaceae), a local rare fern species Wang K, Liu H Mitochondrial DNA B Resour 27-Jan-2021
PMCID:PMC7850416
doi:10.1080/23802359.2020.1860709
PMID:33553636
Vascular Epiphytic Medicinal Plants as Sources of Therapeutic Agents: Their Ethnopharmacological Uses, Chemical Composition, and Biological Activities Nugraha AS, Triatmoko B, Wangchuk P, Keller PA Biomolecules 24-Jan-2020
PMCID:PMC7072150
doi:10.3390/biom10020181
PMID:31991657
Screening for Neuraminidase Inhibitory Activity in Traditional Chinese Medicines Used to Treat Influenza Yang XY, Liu AL, Liu SJ, Xu XW, Huang LF Molecules 27-Aug-2016
PMCID:PMC6273436
doi:10.3390/molecules21091138
PMID:27618892
Flavonoids, Antioxidant Potential, and Acetylcholinesterase Inhibition Activity of the Extracts from the Gametophyte and Archegoniophore of Marchantia polymorpha L. Wang X, Cao J, Wu Y, Wang Q, Xiao J Molecules 17-Mar-2016
PMCID:PMC6273606
doi:10.3390/molecules21030360
PMID:26999088
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
Chaihuang-Yishen Granule Inhibits Diabetic Kidney Disease in Rats through Blocking TGF-β/Smad3 Signaling Zhao TT, Zhang HJ, Lu XG, Huang XR, Zhang WK, Wang H, Lan HY, Li P PLoS One 19-Mar-2014
PMCID:PMC3960111
doi:10.1371/journal.pone.0090807
PMID:24646636
Chemical constituents of Pyrrosia petiolosa. Yang C, Shi JG, Mo SY, Yang YC J Asian Nat Prod Res 01-Jun-2003
doi:10.1080/1028602031000066843
PMID:12765199

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1080/1028602031000066843
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
Diploptene 92155 Click to see CC(=C)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C 410.70 unknown https://doi.org/10.1080/1028602031000066843
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
Covi-ox 6560141 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown https://doi.org/10.1080/1028602031000066843
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(25R)-5alpha-spirostan-3beta,6alpha-diol 52931478 Click to see CCC1C(CC2C1(CCC3C2CC(C4C3(CCC(C4)O)C)O)C)OC5(CCC(CO5)C)C 448.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
Cycloeucalenol 101690 Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1O)C)C(C)CCC(=C)C(C)C)C 426.70 unknown https://doi.org/10.1080/1028602031000066843
> 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/10.1080/1028602031000066843
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1080/1028602031000066843
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(-)-Quinate 1560034 Click to see C1C(C(C(CC1(C(=O)[O-])O)O)O)O 191.16 unknown via CMAUP database
(+)-Quinic acid 37439 Click to see C1C(C(C(CC1(C(=O)O)O)O)O)O 192.17 unknown via CMAUP database
1-Caffeoylquinic acid 10155076 Click to see C1C(C(C(CC1(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O)O 354.31 unknown via CMAUP database
3,4-Dicaffeoylquinic acid 6474309 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown via CMAUP database
4-p-Coumaroylquinic acid 5281766 Click to see C1C(C(C(CC1(C(=O)O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O 338.31 unknown via CMAUP database
4,5-Dicaffeoyl quinic acid 13887346 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown via CMAUP database
5-p-Coumaroylquinic acid, (Z)- 90478782 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O)O 338.31 unknown via CMAUP database
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
Chlorogensaure 12310830 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
Cinnamic acid, 3,4-dihydroxy-, (-)-1-carboxy-3,4,5-trihydroxycyclohexyl ester 6451212 Click to see C1C(C(C(CC1(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O)O 354.31 unknown via CMAUP database
cis-Chlorogenic acid 1794425 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
Cryptochlorogenic acid 9798666 Click to see C1C(C(C(CC1(C(=O)O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O 354.31 unknown via CMAUP database
Isochlorogenic acid A 6474310 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O 516.40 unknown via CMAUP database
Neochlorogenic acid 5280633 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
Quinic acid 6508 Click to see C1C(C(C(CC1(C(=O)O)O)O)O)O 192.17 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
Protocatechualdehyde 8768 Click to see C1=CC(=C(C=C1C=O)O)O 138.12 unknown https://doi.org/10.1080/1028602031000066843
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Isomangiferin 5318597 Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=CC(=C3C4C(C(C(C(O4)CO)O)O)O)O)O 422.30 unknown via CMAUP database
Mangiferin 5281647 Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O 422.30 unknown via CMAUP database
Norathyriol 5281656 Click to see C1=C(C=C2C(=C1O)C(=O)C3=CC(=C(C=C3O2)O)O)O 260.20 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
4-o-Caffeoylshikimic acid 49821869 Click to see C1C(C(C(C=C1C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O 336.29 unknown via CMAUP database
5-Caffeoylshikimic acid 5281762 Click to see C1C(C(C(C=C1C(=O)O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O 336.29 unknown via CMAUP database
5-O-caffeoylshikimate 25243950 Click to see C1C(C(C(C=C1C(=O)[O-])O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O 335.28 unknown via CMAUP database
> 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/10.1080/1028602031000066843
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isoorientin 114776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
Isovitexin 162350 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
(1S)-1,5-anhydro-2-O-(6-deoxy-beta-L-mannopyranosyl)-1-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-8-yl]-D-glucitol 86289611 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2C3=C(C=C(C4=C3OC(=CC4=O)C5=CC=C(C=C5)O)O)O)CO)O)O)O)O)O 578.50 unknown via CMAUP database
Apigenin-8-C-glucoside-2'-rhamnoside 20055288 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2C3=C(C=C(C4=C3OC(=CC4=O)C5=CC=C(C=C5)O)O)O)CO)O)O)O)O)O 578.50 unknown via CMAUP database
Lucenin-2 442615 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O 610.50 unknown via CMAUP database
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown via CMAUP database
Vitexin 5280441 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown via CMAUP database
Vitexin 2''-O-rhamnoside 5282151 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2C3=C(C=C(C4=C3OC(=CC4=O)C5=CC=C(C=C5)O)O)O)CO)O)O)O)O)O 578.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Luteolin 7-glucuronide 5280601 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O 462.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Quercetin 3-rutinoside-7-glucoside 10190763 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)O)O)C6=CC(=C(C=C6)O)O)O)O)O)O)O)O 772.70 unknown via CMAUP database
Quercetin-7-o-rutinoside 101764560 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=C(C4=O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-(3,4-Dihydroxyphenyl)propionic acid 348154 Click to see C1=CC(=C(C=C1CCC(=O)O)O)O 182.17 unknown https://doi.org/10.1080/1028602031000066843

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