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Odontoschisma denudatum

Odontoschisma denudatum - Unknown
Part: Unknown
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 UUID6440501cbf6d6486751435
Scientific name Odontoschisma denudatum
Authority (Nees) Dumort.
First published in Recueil Observ. Jungerm. 19 1835

Description Top

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Synonyms Top

Scientific name Authority First published in
Jungermannia denudata Nees Fl. Crypt. Erlang. 14 1817

Common names Top

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Language Common/alternative name
Belarusian адантасхізма аголеная
Czech slatinatka obnažená
Welsh fflaplys penbinc
German entblößtes schlitzkelch-lebermoos
German nacktes schlitzkelchmoos
Estonian paljas hammassammal
Finnish itupyörösammal
Dutch zanddubbeltjesmos
Swedish kornknutmossa
Chinese 裂齿苔
Chinese 合叶裂齿苔

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Odontoschisma denudatum subsp. elongatum (Lindb.) Potemkin Arctoa 7: 200 1998

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

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Database ID/link to page
World Flora Online wfo-0001196588
Florida Plant Atlas 4693
USDA Plants ODDE3
Tropicos 35185664
INPN 6598
The Plant List tro-35185664
Open Tree Of Life 33998
Observations.org 17764
NCBI Taxonomy 280636
NBN Atlas NHMSYS0000310236
Nature Serve 2.1035819
iNaturalist 165775
GBIF 2689177
EOL 607018
Elurikkus 5917

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
New Diterpenes with Potential Antitumoral Activity Isolated from Plants in the Years 2017–2022 Forzato C, Nitti P Plants (Basel) 29-Aug-2022
PMCID:PMC9460660
doi:10.3390/plants11172240
PMID:36079622
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
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
Comparative Proteomic Analysis of Differentially Expressed Proteins Induced by Hydrogen Sulfide in Spinacia oleracea Leaves Chen J, Liu TW, Hu WJ, Simon M, Wang WH, Chen J, Liu X, Zheng HL PLoS One 02-Sep-2014
PMCID:PMC4152154
doi:10.1371/journal.pone.0105400
PMID:25181351
(+)-ACETOXYODONTOSCHISMENOL, A NEW DOLABELLANE DITERPENOID FROM THE LIVERWORT <i>ODONTOSCHISMA DENUDATUM</i> Akihiko Matsuo, Katsumi Uohama, Shtûchi Hayashi, Joseph D Connolly Oxford University Press (OUP) 25-Jul-2006
doi:10.1246/CL.1984.599
Two novel skeletal diterpenoids, neodenudatenones A and B, from the liverwort Odontoschisma denudatum Toshihiro Hashimoto, Akari Kikkawa, Mayumi Yoshida, Masami Tanaka, Yoshinori Asakawa Elsevier BV 26-Jul-2002
doi:10.1016/S0040-4039(98)00618-2
Novel ent-vibsane- and dolabellane-type diterpenoids from the liverwort Odontoschisma denudatum Toshihiro Hashimoto, Masao Toyota, Hiroki Koyama, Akari Kikkawa, Mayumi Yoshida, Masani Tanaka, Shigeru Takaoka, Yoshinori Asakawa Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(97)10611-6
Dolabellane diterpenoids from the liverwort Odontoschisma denudatum Akihiko Matsuo, Ki-ichiro Kamio, Katsumi Uohama, Ken-ichiro Yoshida, Joseph D. Connolly, George A. Sim Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80293-0

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 / Diterpenoids
(2E,5E,7R,9E)-3,7,10-trimethyl-7-(4-methyl-3-oxopentyl)cycloundeca-2,5,9-trien-1-one 101936179 Click to see CC1=CC(=O)CC(=CCC(C=CC1)(C)CCC(=O)C(C)C)C 302.50 unknown https://doi.org/10.1016/S0040-4039(98)00618-2
https://doi.org/10.1016/S0040-4039(97)10611-6
(2Z,5E,7R,9E)-3,7,10-trimethyl-7-(4-methyl-3-oxopentyl)cycloundeca-2,5,9-trien-1-one 101936180 Click to see CC1=CC(=O)CC(=CCC(C=CC1)(C)CCC(=O)C(C)C)C 302.50 unknown https://doi.org/10.1016/S0040-4039(98)00618-2
https://doi.org/10.1016/S0040-4039(97)10611-6
1-(7-Hydroxy-1,5,9-trimethylcycloundeca-2,5,9-trien-1-yl)-4-methylpentan-3-one 162876095 Click to see CC1=CC(CC(=CCC(C=CC1)(C)CCC(=O)C(C)C)C)O 304.50 unknown https://doi.org/10.1016/S0040-4039(97)10611-6
1-[(1R,2E,5E,7R,9E)-7-hydroxy-1,5,9-trimethylcycloundeca-2,5,9-trien-1-yl]-4-methylpentan-3-one 101936178 Click to see CC1=CC(CC(=CCC(C=CC1)(C)CCC(=O)C(C)C)C)O 304.50 unknown https://doi.org/10.1016/S0040-4039(98)00618-2
https://doi.org/10.1016/S0040-4039(97)10611-6
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Dolabellane and neodolabellane diterpenoids
(1-Hydroxy-3a,6,10-trimethyl-1-propan-2-yl-2,3,4,7,8,11,12,12a-octahydrocyclopenta[11]annulen-8-yl) acetate 72752148 Click to see CC1=CC(CC(=CCC2(CCC(C2CC1)(C(C)C)O)C)C)OC(=O)C 348.50 unknown https://doi.org/10.1016/0031-9422(88)80293-0
https://doi.org/10.1246/CL.1984.599
(1R,3aR,5E,8S,9E,12aR)-3a,6,10-trimethyl-1-propan-2-yl-2,3,4,7,8,11,12,12a-octahydrocyclopenta[11]annulene-1,8-diol 162964550 Click to see CC1=CC(CC(=CCC2(CCC(C2CC1)(C(C)C)O)C)C)O 306.50 unknown https://doi.org/10.1016/0031-9422(88)80293-0
[(1R,3aR,5E,8S,9E,12aR)-1-hydroxy-3a,6,10-trimethyl-1-propan-2-yl-2,3,4,7,8,11,12,12a-octahydrocyclopenta[11]annulen-8-yl] acetate 11163880 Click to see CC1=CC(CC(=CCC2(CCC(C2CC1)(C(C)C)O)C)C)OC(=O)C 348.50 unknown https://doi.org/10.1016/0031-9422(88)80293-0
[(1R,3aR,5Z,8R,9E,12R)-1,12-dihydroxy-6-(hydroxymethyl)-3a,10-dimethyl-1-propan-2-yl-2,3,4,7,8,11,12,12a-octahydrocyclopenta[11]annulen-8-yl] acetate 101936181 Click to see CC1=CC(CC(=CCC2(CCC(C2C(C1)O)(C(C)C)O)C)CO)OC(=O)C 380.50 unknown https://doi.org/10.1016/S0040-4039(97)10611-6
[(1R,3aR,5Z,8S,9E,12aR)-1-hydroxy-6-(hydroxymethyl)-3a,10-dimethyl-1-propan-2-yl-2,3,4,7,8,11,12,12a-octahydrocyclopenta[11]annulen-8-yl] acetate 162882665 Click to see CC1=CC(CC(=CCC2(CCC(C2CC1)(C(C)C)O)C)CO)OC(=O)C 364.50 unknown https://doi.org/10.1016/0031-9422(88)80293-0
[(1R,3aR,5Z,8S,9E,12R,12aS)-1,12-dihydroxy-6-(hydroxymethyl)-3a,10-dimethyl-1-propan-2-yl-2,3,4,7,8,11,12,12a-octahydrocyclopenta[11]annulen-8-yl] acetate 162865637 Click to see CC1=CC(CC(=CCC2(CCC(C2C(C1)O)(C(C)C)O)C)CO)OC(=O)C 380.50 unknown https://doi.org/10.1016/S0040-4039(97)10611-6
[(1S,3aR,5E,8S,9E,12aR)-1-hydroxy-3a,6,10-trimethyl-1-propan-2-yl-2,3,4,7,8,11,12,12a-octahydrocyclopenta[11]annulen-8-yl] acetate 163193750 Click to see CC1=CC(CC(=CCC2(CCC(C2CC1)(C(C)C)O)C)C)OC(=O)C 348.50 unknown https://doi.org/10.1246/CL.1984.599
[1-Hydroxy-6-(hydroxymethyl)-3a,10-dimethyl-1-propan-2-yl-2,3,4,7,8,11,12,12a-octahydrocyclopenta[11]annulen-8-yl] acetate 162882663 Click to see CC1=CC(CC(=CCC2(CCC(C2CC1)(C(C)C)O)C)CO)OC(=O)C 364.50 unknown https://doi.org/10.1016/0031-9422(88)80293-0
[1,12-Dihydroxy-6-(hydroxymethyl)-3a,10-dimethyl-1-propan-2-yl-2,3,4,7,8,11,12,12a-octahydrocyclopenta[11]annulen-8-yl] acetate 162865636 Click to see CC1=CC(CC(=CCC2(CCC(C2C(C1)O)(C(C)C)O)C)CO)OC(=O)C 380.50 unknown https://doi.org/10.1016/S0040-4039(97)10611-6
3a,6,10-Trimethyl-1-propan-2-yl-2,3,4,7,8,11,12,12a-octahydrocyclopenta[11]annulene-1,8-diol 162964549 Click to see CC1=CC(CC(=CCC2(CCC(C2CC1)(C(C)C)O)C)C)O 306.50 unknown https://doi.org/10.1016/0031-9422(88)80293-0
Acetoxyodontoschismenol 11210243 Click to see CC1=CC(CC(=CCC2(CCC(C2CC1)(C(C)C)O)C)C)OC(=O)C 348.50 unknown https://doi.org/10.1016/0031-9422(88)80293-0
https://doi.org/10.1246/CL.1984.599
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(2R,3S,4R)-3-[(E)-2,6-dimethyl-5-oxohept-1-enyl]-4-ethenyl-4-methyl-2-prop-1-en-2-ylcyclopentan-1-one 102121226 Click to see CC(C)C(=O)CCC(=CC1C(C(=O)CC1(C)C=C)C(=C)C)C 302.50 unknown https://doi.org/10.1016/S0040-4039(98)00618-2
(2S,3R,4S)-3-[(E)-2,6-dimethyl-5-oxohept-1-enyl]-4-ethenyl-4-methyl-2-prop-1-en-2-ylcyclopentan-1-one 102121235 Click to see CC(C)C(=O)CCC(=CC1C(C(=O)CC1(C)C=C)C(=C)C)C 302.50 unknown https://doi.org/10.1016/S0040-4039(98)00618-2
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(5-Formyl-13-hydroxy-1,9-dimethyl-13-propan-2-yl-4-oxatricyclo[10.3.0.03,5]pentadec-8-en-7-yl) acetate 162995192 Click to see CC1=CC(CC2(C(O2)CC3(CCC(C3CC1)(C(C)C)O)C)C=O)OC(=O)C 378.50 unknown https://doi.org/10.1016/0031-9422(88)80293-0
[(1R,3S,5S,7R,8E,12R,13R)-5-formyl-13-hydroxy-1,9-dimethyl-13-propan-2-yl-4-oxatricyclo[10.3.0.03,5]pentadec-8-en-7-yl] acetate 14036789 Click to see CC1=CC(CC2(C(O2)CC3(CCC(C3CC1)(C(C)C)O)C)C=O)OC(=O)C 378.50 unknown https://doi.org/10.1016/0031-9422(88)80293-0

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