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Chiloscyphus polyanthos

Chiloscyphus polyanthos - Unknown
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Author: Public Domain - WikiMedia
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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 UUID6440500161220807144781
Scientific name Chiloscyphus polyanthos
Authority (L.) Corda
First published in Naturalientausch 12: 651 1829

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Welsh afuad gwenffrewi
Estonian roheline peekersammal
Dutch lippenmos
Swedish bäckblekmossa
Chinese 裂萼苔

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001196257
USDA Plants CHPO14
Tropicos 35185049
INPN 6483
The Plant List tro-35185049
Open Tree Of Life 663872
Observations.org 17712
NCBI Taxonomy 70557
NBN Atlas NHMSYS0000309624
Nature Serve 2.123332
iNaturalist 56506
iNaturalist 490108
GBIF 2689491
EPPO QLSPO
EOL 605033
Elurikkus 3696

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
The Type Specimens of Plectocolea and Solenostoma (Marchantiophyta) in Some Japanese and European Herbaria Bakalin VA, Choi SS Plants (Basel) 22-Nov-2023
PMCID:PMC10708210
doi:10.3390/plants12233935
PMID:38068572
The Bryophyte Flora of Vienna Zechmeister HG, Kropik M Plants (Basel) 20-Aug-2023
PMCID:PMC10458201
doi:10.3390/plants12163002
PMID:37631214
The Liverwort and Hornwort Flora of Jeju Island, Republic of Korea: A Volcanic Island with a Unique Mixture of Subtropical, Temperate, Boreal, and Arctomontane Taxa Choi SS, Bakalin VA, Bum HM, Park SJ, Kim DS, Ahn US, Moon MO Plants (Basel) 20-Jun-2023
PMCID:PMC10301385
doi:10.3390/plants12122384
PMID:37376013
Liverwort and Hornwort Flora of Hoàng Liên National Park and the Adjacent Areas (North Vietnam, Indochina) Bakalin VA, Klimova KG, Nguyen VS, Nguyen HM, Bakalin DA, Choi SS Plants (Basel) 29-Apr-2023
PMCID:PMC10181137
doi:10.3390/plants12091841
PMID:37176900
Germacrene B – a central intermediate in sesquiterpene biosynthesis Xu H, Dickschat JS Beilstein J Org Chem 20-Feb-2023
PMCID:PMC9972886
doi:10.3762/bjoc.19.18
PMID:36865023
Ecological Preferences and Indication Potential of Freshwater Bryophytes–Insights from Croatian Watercourses Rimac A, Alegro A, Šegota V, Vuković N, Koletić N Plants (Basel) 09-Dec-2022
PMCID:PMC9788454
doi:10.3390/plants11243451
PMID:36559560
The Taxonomically Richest Liverwort Hemiboreal Flora in Eurasia Is in the South Kurils Bakalin VA, Klimova KG, Bakalin DA, Choi SS Plants (Basel) 25-Aug-2022
PMCID:PMC9460601
doi:10.3390/plants11172200
PMID:36079582
Environmental ranges discriminating between macrophytes groups in European rivers Kaijser W, Birk S, Hering D PLoS One 14-Jun-2022
PMCID:PMC9197031
doi:10.1371/journal.pone.0269744
PMID:35700165
Environmental Gradients Shaping the Freshwater Bryophyte Communities of Croatia (Western Balkans) Rimac A, Alegro A, Šegota V, Vuković N, Koletić N Plants (Basel) 09-Jun-2022
PMCID:PMC9230072
doi:10.3390/plants11121542
PMID:35736693
The distribution and evolution of fungal symbioses in ancient lineages of land plants Rimington WR, Duckett JG, Field KJ, Bidartondo MI, Pressel S Mycorrhiza 04-Mar-2020
PMCID:PMC7062687
doi:10.1007/s00572-020-00938-y
PMID:32130512
Nor-Lignans: Occurrence in Plants and Biological Activities—A Review Frezza C, Venditti A, Toniolo C, De Vita D, Franceschin M, Ventrone A, Tomassini L, Foddai S, Guiso M, Nicoletti M, Serafini M, Bianco A Molecules 03-Jan-2020
PMCID:PMC6983269
doi:10.3390/molecules25010197
PMID:31947789
Unusual and Highly Bioactive Sesterterpenes Synthesized by Pleurotus ostreatus during Coculture with Trametes robiniophila Murr Shen XT, Mo XH, Zhu LP, Tan LL, Du FY, Wang QW, Zhou YM, Yuan XJ, Qiao B, Yang S Appl Environ Microbiol 01-Jul-2019
PMCID:PMC6606861
doi:10.1128/AEM.00293-19
PMID:31053589
9-Norlignans: Occurrence, Properties and Their Semisynthetic Preparation from Hydroxymatairesinol Eklund P, Raitanen JE Molecules 09-Jan-2019
PMCID:PMC6358742
doi:10.3390/molecules24020220
PMID:30634427
Bryophytes: Hoard of remedies, an ethno-medicinal review Chandra S, Chandra D, Barh A, Pankaj, Pandey RK, Sharma IP J Tradit Complement Med 04-Apr-2016
PMCID:PMC5198817
doi:10.1016/j.jtcme.2016.01.007
PMID:28053893
The absolute configuration of eudesmane-type sesquiterpenoids found in the Japanese liverwort Chiloscyphus polyanthos M Toyota, T Saito, Y Asakawa Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(99)00159-4

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 / Naphthalenes / Naphthalenecarboxylic acids and derivatives / Naphthalenecarboxylic acids
(2R)-2-[4-(3,4-dihydroxyphenyl)-6,7-dihydroxynaphthalene-2-carbonyl]oxybutanedioic acid 162964254 Click to see C1=CC(=C(C=C1C2=C3C=C(C(=CC3=CC(=C2)C(=O)OC(CC(=O)O)C(=O)O)O)O)O)O 428.30 unknown https://doi.org/10.1016/S0031-9422(99)00279-4
4-(3,4-Dihydroxyphenyl)-6,7-dihydroxynaphthalene-2-carboxylic acid 195328 Click to see C1=CC(=C(C=C1C2=C3C=C(C(=CC3=CC(=C2)C(=O)O)O)O)O)O 312.27 unknown https://doi.org/10.1016/S0031-9422(99)00279-4
4-(3,4-Dihydroxyphenyl)-6,7-dihydroxynaphthalene-2-carboxylic acid 1,2-dicarboxyethyl ester 101006811 Click to see C1=CC(=C(C=C1C2=C3C=C(C(=CC3=CC(=C2)C(=O)OC(CC(=O)O)C(=O)O)O)O)O)O 428.30 unknown https://doi.org/10.1016/S0031-9422(99)00279-4
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
beta-Barbatene 14109421 Click to see CC12CCC(=C)C(C1)C3(C2(CCC3)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(99)00159-4
> Lignans, neolignans and related compounds / Aryltetralin lignans
1-(3,4-Dihydroxyphenyl)-6,7-dihydroxy-1,2-dihydronaphthalene-2,3-dicarboxylic acid 3035586 Click to see C1=CC(=C(C=C1C2C(C(=CC3=CC(=C(C=C23)O)O)C(=O)O)C(=O)O)O)O 358.30 unknown https://doi.org/10.1016/S0031-9422(99)00279-4
Epiphyllic acid 44383640 Click to see C1=CC(=C(C=C1C2C(C(=CC3=CC(=C(C=C23)O)O)C(=O)O)C(=O)O)O)O 358.30 unknown https://doi.org/10.1016/S0031-9422(99)00279-4
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
1-(3a-hydroxy-7,7a-dimethyl-2,3,4,5,6,7-hexahydro-1H-inden-1-yl)-2-methylprop-2-en-1-one 14414079 Click to see CC1CCCC2(C1(C(CC2)C(=O)C(=C)C)C)O 236.35 unknown https://doi.org/10.1016/S0031-9422(99)00159-4
1-(7,7a-Dimethyl-1,2,3,5,6,7-hexahydroinden-1-yl)-2-methylprop-2-en-1-one 14414082 Click to see CC1CCC=C2C1(C(CC2)C(=O)C(=C)C)C 218.33 unknown https://doi.org/10.1016/S0031-9422(99)00159-4
1-[(1R,3aS,7R,7aR)-3a-hydroxy-7,7a-dimethyl-2,3,4,5,6,7-hexahydro-1H-inden-1-yl]-2-methylprop-2-en-1-one 14414078 Click to see CC1CCCC2(C1(C(CC2)C(=O)C(=C)C)C)O 236.35 unknown https://doi.org/10.1016/S0031-9422(99)00159-4
1-[(1S,3aR,7S,7aS)-3a-hydroxy-7,7a-dimethyl-2,3,4,5,6,7-hexahydro-1H-inden-1-yl]-2-methylprop-2-en-1-one 101696495 Click to see CC1CCCC2(C1(C(CC2)C(=O)C(=C)C)C)O 236.35 unknown https://doi.org/10.1016/S0031-9422(99)00159-4
1-[(1S,7S,7aS)-7,7a-dimethyl-1,2,3,5,6,7-hexahydroinden-1-yl]-2-methylprop-2-en-1-one 11830932 Click to see CC1CCC=C2C1(C(CC2)C(=O)C(=C)C)C 218.33 unknown https://doi.org/10.1016/S0031-9422(99)00159-4
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,4aR,8aR)-1,4a-dimethyl-7-propan-2-ylidene-3,4,5,6,8,8a-hexahydro-2H-naphthalen-1-ol 5318734 Click to see CC(=C1CCC2(CCCC(C2C1)(C)O)C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(99)00159-4
Juniper camphor 521214 Click to see CC(=C1CCC2(CCCC(C2C1)(C)O)C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(99)00159-4
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Chamigranes
(-)-beta-Chamigrene 442353 Click to see CC1=CCC2(CC1)C(=C)CCCC2(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(99)00159-4
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R,2R,4aR,8aS)-4a-methyl-8-methylidene-2-propan-2-yl-3,4,5,6,7,8a-hexahydro-1H-naphthalene-1,2-diol 100938040 Click to see CC(C)C1(CCC2(CCCC(=C)C2C1O)C)O 238.37 unknown https://doi.org/10.1016/S0031-9422(99)00159-4
(2S,4aR,8aR)-4a,8-dimethyl-2-propan-2-yl-1,3,4,5,6,8a-hexahydronaphthalen-2-ol 15786170 Click to see CC1=CCCC2(C1CC(CC2)(C(C)C)O)C 222.37 unknown https://doi.org/10.1016/S0031-9422(99)00159-4
(2S,4aR,8aS)-4a-methyl-8-methylidene-2-propan-2-yl-3,4,5,6,7,8a-hexahydro-1H-naphthalen-2-ol 15786172 Click to see CC(C)C1(CCC2(CCCC(=C)C2C1)C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(99)00159-4
4a-methyl-8-methylidene-2-propan-2-yl-3,4,5,6,7,8a-hexahydro-1H-naphthalen-2-ol 101417780 Click to see CC(C)C1(CCC2(CCCC(=C)C2C1)C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(99)00159-4
4a-methyl-8-methylidene-2-propan-2-yl-3,4,5,6,7,8a-hexahydro-1H-naphthalene-1,2-diol 162852551 Click to see CC(C)C1(CCC2(CCCC(=C)C2C1O)C)O 238.37 unknown https://doi.org/10.1016/S0031-9422(99)00159-4
4a,8-Dimethyl-2-propan-2-yl-1,3,4,5,6,8a-hexahydronaphthalen-2-ol 78384906 Click to see CC1=CCCC2(C1CC(CC2)(C(C)C)O)C 222.37 unknown https://doi.org/10.1016/S0031-9422(99)00159-4
alpha-Selinene 10856614 Click to see CC1=CCCC2(C1CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(99)00159-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3aR,4aS,8aS,9aS)-3a-hydroxy-5,8a-dimethyl-3-methylidene-4,4a,7,8,9,9a-hexahydrobenzo[f][1]benzofuran-2-one 163049584 Click to see CC1=CCCC2(C1CC3(C(C2)OC(=O)C3=C)O)C 248.32 unknown https://doi.org/10.1016/0031-9422(83)85030-4
(3aS,4aR,8aS,9aS)-4a-hydroxy-5,8a-dimethyl-3-methylidene-3a,4,7,8,9,9a-hexahydrobenzo[f][1]benzofuran-2-one 163103367 Click to see CC1=CCCC2(C1(CC3C(C2)OC(=O)C3=C)O)C 248.32 unknown https://doi.org/10.1016/S0031-9422(00)91465-1
(3aS,4aS,8aS,9aS)-5,8a-dimethyl-3-methylidene-4,4a,7,8,9,9a-hexahydro-3aH-benzo[f][1]benzofuran-2-one 11053496 Click to see CC1=CCCC2(C1CC3C(C2)OC(=O)C3=C)C 232.32 unknown https://doi.org/10.1016/0031-9422(83)85030-4
(3aS,8aS,9aS)-5,8a-dimethyl-3-methylidene-3a,4,7,8,9,9a-hexahydrobenzo[f][1]benzofuran-2,6-dione 101313327 Click to see CC1=C2CC3C(CC2(CCC1=O)C)OC(=O)C3=C 246.30 unknown https://doi.org/10.1016/0031-9422(83)85030-4
(3aS,8aS,9aS)-5,8a-dimethyl-3-methylidene-4,6,7,8,9,9a-hexahydro-3aH-benzo[f][1]benzofuran-2-one 6545095 Click to see CC1=C2CC3C(CC2(CCC1)C)OC(=O)C3=C 232.32 unknown https://doi.org/10.1016/0031-9422(83)85030-4
3a-Hydroxy-5,8a-dimethyl-3-methylidene-4,4a,7,8,9,9a-hexahydrobenzo[f][1]benzofuran-2-one 163049583 Click to see CC1=CCCC2(C1CC3(C(C2)OC(=O)C3=C)O)C 248.32 unknown https://doi.org/10.1016/0031-9422(83)85030-4
5,8a-dimethyl-3-methylidene-2H,3H,3aH,4H,6H,7H,8H,8aH,9H,9aH-naphtho[2,3-b]furan-2-one 315677 Click to see CC1=C2CC3C(CC2(CCC1)C)OC(=O)C3=C 232.32 unknown https://doi.org/10.1016/0031-9422(83)85030-4
5,8a-Dimethyl-3-methylidene-3a,4,7,8,9,9a-hexahydrobenzo[f][1]benzofuran-2,6-dione 13889963 Click to see CC1=C2CC3C(CC2(CCC1=O)C)OC(=O)C3=C 246.30 unknown https://doi.org/10.1016/0031-9422(83)85030-4
ent-Diplophyllolide-A 318811 Click to see CC1=CCCC2(C1CC3C(C2)OC(=O)C3=C)C 232.32 unknown https://doi.org/10.1016/0031-9422(83)85030-4

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