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Saccogyna viticulosa

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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 UUID644051eeabd5c792750933
Scientific name Saccogyna viticulosa
Authority (L.) Dumort.
First published in Syll. Jungerm. Europ. : 74. 1831

Description Top

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Synonyms Top

Scientific name Authority First published in
Sykorea viticulosa (L.) Corda Naturalientausch 12: 653 1829

Common names Top

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Language Common/alternative name
Welsh codlys traphlith
Chinese 囊萼苔

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-0001207079
Tropicos 35207884
INPN 6502
The Plant List tro-35207884
Open Tree Of Life 379644
NCBI Taxonomy 362792
NBN Atlas NHMSYS0000310458
iNaturalist 461377
GBIF 2689016
EPPO ZCGVI
EOL 6071167

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
Desiccation tolerance in bryophytes relates to elasticity but is independent of cell wall thickness and photosynthesis Perera‐Castro AV, Flexas J Physiol Plant 16-Mar-2022
PMCID:PMC9314017
doi:10.1111/ppl.13661
PMID:35249226
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
Chemotypes and Biomarkers of Seven Species of New Caledonian Liverworts from the Bazzanioideae Subfamily Métoyer B, Lebouvier N, Hnawia E, Herbette G, Thouvenot L, Asakawa Y, Nour M, Raharivelomanana P Molecules 05-Jun-2018
PMCID:PMC6100190
doi:10.3390/molecules23061353
PMID:29874780
Modeling Species Distributions from Heterogeneous Data for the Biogeographic Regionalization of the European Bryophyte Flora Mateo RG, Vanderpoorten A, Muñoz J, Laenen B, Désamoré A PLoS One 11-Feb-2013
PMCID:PMC3569459
doi:10.1371/journal.pone.0055648
PMID:23409015
ChemInform Abstract: Two Novel Zierane Sesquiterpenoids from the Liverwort Saccogyna viticulosa. J. D. CONNOLLY, L. J. HARRISON, D. S. RYCROFT Wiley 25-Aug-2010
doi:10.1002/CHIN.199446220
Conservative ecological and evolutionary patterns in liverwort–fungal symbioses Bidartondo MI, Duckett JG Proc Biol Sci 07-Oct-2009
PMCID:PMC2842645
doi:10.1098/rspb.2009.1458
PMID:19812075
Isogermacrene A, a Proposed Intermediate in Sesquiterpene Biosynthesis. Thomas Hackl, Wilfried A. Koenig, Hermann Muhle Wiley 22-Dec-2004
doi:10.1002/CHIN.200503177
Are Bryophytes Shade Plants? Photosynthetic Light Responses and Proportions of Chlorophyll a, Chlorophyll b and Total Carotenoids MARSCHALL M, PROCTOR MC Ann Bot 19-Aug-2004
PMCID:PMC4242232
doi:10.1093/aob/mch178
PMID:15319230
Isogermacrene A, a proposed intermediate in sesquiterpene biosynthesis. Hackl T, König WA, Muhle H Phytochemistry 01-Aug-2004
doi:10.1016/J.PHYTOCHEM.2004.05.024
PMID:15587711

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
(1Z,4Z,8Z)-1,3,3,8-tetramethylcycloundeca-1,4,8-triene 101349815 Click to see CC1=CCCC(=CC(C=CCC1)(C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.05.024
(1Z,5Z,7S)-1,5-dimethyl-7-prop-1-en-2-ylcyclodeca-1,5-diene 101349813 Click to see CC1=CCCC(=CC(CCC1)C(=C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.05.024
(4Z,10R)-4-methyl-9-methylidenebicyclo[8.2.1]trideca-1(13),4-diene 101349816 Click to see CC1=CCCCC(=C)C2CCC(=C2)CC1 202.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.05.024
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1S,3aR,4R,6R,8aS)-1,4-dimethyl-6-(6-methylhepta-1,5-dien-2-yl)-2,3,3a,5,6,7,8,8a-octahydro-1H-azulen-4-ol 101349817 Click to see CC1CCC2C1CCC(CC2(C)O)C(=C)CCC=C(C)C 290.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.05.024
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1002/CHIN.200503177
https://doi.org/10.1016/J.PHYTOCHEM.2004.05.024
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1002/CHIN.200503177
https://doi.org/10.1016/J.PHYTOCHEM.2004.05.024
Tricyclene 79035 Click to see CC1(C2CC3C1(C3C2)C)C 136.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.05.024
https://doi.org/10.1002/CHIN.200503177
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
(1S,2S,3S)-1-ethenyl-2,3-bis(prop-1-en-2-yl)cyclohexane 101349814 Click to see CC(=C)C1CCCC(C1C(=C)C)C=C 190.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.05.024
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Eudesma-5,7(11)-diene 6428860 Click to see CC1CCCC2(C1=CC(=C(C)C)CC2)C 204.35 unknown https://doi.org/10.1002/CHIN.200503177
(4S,4aR,8aS)-5,8a-dimethyl-4-prop-1-en-2-yl-2,3,4,4a,7,8-hexahydro-1H-naphthalene 21579271 Click to see CC1=CCCC2(C1C(CCC2)C(=C)C)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.05.024
(4S,4aS,8aS)-8a-methyl-5-methylidene-4-prop-1-en-2-yl-1,2,3,4,4a,6,7,8-octahydronaphthalene 12310323 Click to see CC(=C)C1CCCC2(C1C(=C)CCC2)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.05.024
> 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/J.PHYTOCHEM.2004.05.024
Calarene 28481 Click to see CC1CCC=C2C1(C3C(C3(C)C)CC2)C 204.35 unknown https://doi.org/10.1002/CHIN.200503177
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Anastreptene 91746864 Click to see CC1=CCC2C13C2(CCC4C3C4(C)C)C 202.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.05.024
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 44583886 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.05.024
Bicyclogermacrene 5315347 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1002/CHIN.200503177
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
(1R,2R,3R,6R)-3-ethenyl-3,7,7-trimethyl-2-prop-1-en-2-ylbicyclo[4.1.0]heptane 101973934 Click to see CC(=C)C1C2C(C2(C)C)CCC1(C)C=C 204.35 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.05.024
Beta-Elemene 6918391 Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C 204.35 unknown https://doi.org/10.1002/CHIN.200503177
https://doi.org/10.1016/J.PHYTOCHEM.2004.05.024
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
3,8-Dimethylidene-4-prop-1-en-2-yl-1,2,3a,4,5,6,7,8a-octahydroazulen-2-ol 73803984 Click to see CC(=C)C1CCCC(=C)C2C1C(=C)C(C2)O 218.33 unknown https://doi.org/10.1002/CHIN.199446220
https://doi.org/10.1016/J.PHYTOCHEM.2004.05.024
> Organoheterocyclic compounds / Oxolanes
(-)-Maalioxide 12085452 Click to see CC1(C2CCCC3(C2C(O1)(CCC3)C)C)C 222.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.05.024

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