Chiloscyphus pallescens - Unknown
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Internal ID UUID6440500101595744472659
Scientific name Chiloscyphus pallescens
Authority (Ehrh. ex Hoffm.) Dumort.
First published in Syll. Jungerm. Europ. 67 1831

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Synonyms Top

Scientific name Authority First published in
Jungermannia pallescens Ehrh. ex Hoffm. Fl. Allemagne 2: 87 1795

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Language Common/alternative name
Welsh afuad gwelw gwenffrewi
German bleiches lippenbechermoos
Estonian kahkjas peekersammal
Finnish hetealvesammal
Swedish skogsblekmossa
Chinese 淡色裂萼苔

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Varieties (abbr. var.) Top

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Name Authority First published in
Chiloscyphus pallescens var. fragilis (Roth) K.Müller Ber. Deutsch. Bot. Ges. 59: 429 1942

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001196254
USDA Plants CHPA43
Tropicos 35185046
INPN 6479
The Plant List tro-35185046
Open Tree Of Life 744348
NCBI Taxonomy 95762
NBN Atlas NHMSYS0000309622
Nature Serve 2.126534
iNaturalist 56503
GBIF 2689488
EOL 605065
Elurikkus 3695

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
Liverworts of Magadan: Life on the Edge of Beringia Bakalin VA, Klimova KG, Bakalin DA, Choi SS Plants (Basel) 22-Nov-2023
PMCID:PMC10708503
doi:10.3390/plants12233928
PMID:38068565
The Bryophyte Flora of Vienna Zechmeister HG, Kropik M Plants (Basel) 20-Aug-2023
PMCID:PMC10458201
doi:10.3390/plants12163002
PMID:37631214
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 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
Different from tracheophytes, liverworts commonly have mixed 35S and 5S arrays Sousa A, Bechteler J, Temsch EM, Renner SS Ann Bot 17-Feb-2020
PMCID:PMC7262461
doi:10.1093/aob/mcaa027
PMID:32064492
Relating Bryophyte Assemblages to a Remotely Sensed Depth-to-Water Index in Boreal Forests Bartels SF, Caners RT, Ogilvie J, White B, Macdonald SE Front Plant Sci 25-Jun-2018
PMCID:PMC6026670
doi:10.3389/fpls.2018.00858
PMID:29988528
Vascular plant and bryophyte species richness in response to water quality in lowland spring niches with different anthropogenic impacts Puczko K, Zieliński P, Jusik S, Kołakowska A, Jekatierynczuk-Rudczyk E Environ Monit Assess 10-May-2018
PMCID:PMC5945798
doi:10.1007/s10661-018-6703-6
PMID:29748822
The structure of chiloscypholone, a sesquiterpenoid with a novel carbon skeleton, from the liverwort Chiloscyphus pallescens. A revised structure for chiloscyphone Joseph D. Connolly, Leslie J. Harrison, David S. Rycroft Royal Society of Chemistry (RSC) 30-Mar-2004
doi:10.1039/C39820001236
Oppositane and chiloscyphane sesquiterpenoids from the liverwortChiloscyphus pallescens Leslie J. Harrison, Yoshinori Asakawa Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)80117-J

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
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
CID 11447401 11447401 Click to see CC1(CCCC2(C3C1C(C2(CC3)C)O)C)C 222.37 unknown https://doi.org/10.1039/C39820001236
Longiborneol 521200 Click to see CC1(CCCC2(C3C1C(C2(CC3)C)O)C)C 222.37 unknown https://doi.org/10.1039/C39820001236
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
(3a-hydroxy-7,7a-dimethyl-2,3,4,5,6,7-hexahydro-1H-inden-1-yl)-(2-methyloxiran-2-yl)methanone 162881944 Click to see CC1CCCC2(C1(C(CC2)C(=O)C3(CO3)C)C)O 252.35 unknown https://doi.org/10.1016/0031-9422(91)80117-J
[(1R,3aS,7R,7aR)-3a-hydroxy-7,7a-dimethyl-2,3,4,5,6,7-hexahydro-1H-inden-1-yl]-[(2R)-2-methyloxiran-2-yl]methanone 162881945 Click to see CC1CCCC2(C1(C(CC2)C(=O)C3(CO3)C)C)O 252.35 unknown https://doi.org/10.1016/0031-9422(91)80117-J
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/10.1039/C39820001236
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/10.1016/0031-9422(91)80117-J
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/10.1039/C39820001236
1-[(1R,7R,7aR)-7,7a-dimethyl-1,2,3,5,6,7-hexahydroinden-1-yl]-2-methylprop-2-en-1-one 14414083 Click to see CC1CCC=C2C1(C(CC2)C(=O)C(=C)C)C 218.33 unknown https://doi.org/10.1016/0031-9422(91)80117-J
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/10.1016/0031-9422(91)80117-J
https://doi.org/10.1039/C39820001236
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
1-(7-hydroxy-3a,7-dimethyl-2,3,4,5,6,7a-hexahydro-1H-inden-1-yl)-2-methylpropan-1-one 72828806 Click to see CC(C)C(=O)C1CCC2(C1C(CCC2)(C)O)C 238.37 unknown https://doi.org/10.1016/0031-9422(91)80117-J
1-[(1R,3aS,7S,7aS)-7-hydroxy-3a,7-dimethyl-2,3,4,5,6,7a-hexahydro-1H-inden-1-yl]-2-methylpropan-1-one 15715077 Click to see CC(C)C(=O)C1CCC2(C1C(CCC2)(C)O)C 238.37 unknown https://doi.org/10.1016/0031-9422(91)80117-J
Chiloscyphone 534993 Click to see CC1=CCC(C2C1CCC(=C)C2=O)C(C)C 218.33 unknown https://doi.org/10.1016/0031-9422(91)80117-J
> 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/10.1039/C39820001236
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/10.1039/C39820001236

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