Nardia scalaris - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Upload a new image!

Details Top

Internal ID UUID6440501b9ec47716568595
Scientific name Nardia scalaris
Authority (Schrad.) Gray
First published in Nat. Arr. Brit. Pl. 1: 694 1821

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

No known synonyms.

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Czech okružnice schodovitá
Welsh ysgol-lys cyffredin
Finnish ojasiiransammal
Irish aelus dréimreach
Dutch echt vleugelmos
Swedish dikesnardia
Chinese 密叶被蒴苔

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
Name Authority First published in
Nardia scalaris subsp. harae (Amak.) Amak. J. Hattori Bot. Lab. 21: 280 1959

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
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-0001196575
USDA Plants NASC2
Tropicos 35185650
INPN 6424
The Plant List tro-35185650
Open Tree Of Life 94644
Observations.org 17762
NCBI Taxonomy 280838
NBN Atlas NHMSYS0000310228
Nature Serve 2.125091
iNaturalist 165652
GBIF 4277463
EPPO NABSC
EOL 604350
Elurikkus 5851
CMAUP NPO29518

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
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
Lamina Cell Shape and Cell Wall Thickness Are Useful Indicators for Metal Tolerance—An Example in Bryophytes Petschinger K, Adlassnig W, Sabovljevic MS, Lang I Plants (Basel) 31-Jan-2021
PMCID:PMC7911191
doi:10.3390/plants10020274
PMID:33572599
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
Nardiin, a new ent-kaurane diterpenoid from the liverwort Nardia scalaris Ivan Beneš, Tomáš Vaněk, Miloš Buděšínský Institute of Organic Chemistry & Biochemistry 03-Aug-2011
doi:10.1135/CCCC19821873
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
Primary Cell Wall Composition of Bryophytes and Charophytes POPPER ZA, FRY SC Ann Bot 01-Jan-2003
PMCID:PMC4240358
doi:10.1093/aob/mcg013
PMID:12495914
Diterpene malonates and other terpenes from Nardia succulenta and N. scalaris Ulrich Langenbahn, Gunther Burkhardt, Hans Becker Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(93)85044-R

Phytochemical Profile Top

Add a new one!
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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,4R,9R,10S,13R,15R)-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-ol 15478796 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4O)C)C 288.50 unknown https://doi.org/10.1016/0031-9422(93)85044-R
(1R,4R,9R,10S,13R)-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 10334208 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4=O)C)C 286.50 unknown https://doi.org/10.1016/0031-9422(93)85044-R
(1S,4R,9R,10S,13S,16R)-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-16-ol 162975751 Click to see CC1(CCCC2(C1CCC34C2CCC(C3O)C(=C)C4)C)C 288.50 unknown https://doi.org/10.1016/0031-9422(93)85044-R
(1S,4R,9R,13R,15R)-15-hydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadec-10-en-3-one 101690648 Click to see CC1(CCCC2(C1C(=O)CC34C2=CCC(C3)C(=C)C4O)C)C 300.40 unknown https://doi.org/10.1135/CCCC19821873
1-O-(3,7,11,15-tetramethylhexadec-2-enyl) 3-O-(5,5,9-trimethyl-14-methylidene-16-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) propanedioate 163032842 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCOC(=O)CC(=O)OC1C2CCC3C1(CCC4C3(CCCC4(C)C)C)CC2=C)C 653.00 unknown https://doi.org/10.1016/0031-9422(93)85044-R
1-O-(4,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl) 3-O-(5,5,9-trimethyl-14-methylidene-15-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) propanedioate 162947366 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4OC(=O)CC(=O)OC5CC6(CCC5C6(C)C)C)C)C 510.70 unknown https://doi.org/10.1016/0031-9422(93)85044-R
1-O-(4,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl) 3-O-(5,5,9-trimethyl-14-methylidene-16-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) propanedioate 162895114 Click to see CC1(CCCC2(C1CCC34C2CCC(C3OC(=O)CC(=O)OC5CC6(CCC5C6(C)C)C)C(=C)C4)C)C 510.70 unknown https://doi.org/10.1016/0031-9422(93)85044-R
1-O-[(1S,2S,4S)-4,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl] 3-O-[(1R,4R,9R,10S,13R,15R)-5,5,9-trimethyl-14-methylidene-15-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] propanedioate 162947367 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4OC(=O)CC(=O)OC5CC6(CCC5C6(C)C)C)C)C 510.70 unknown https://doi.org/10.1016/0031-9422(93)85044-R
1-O-[(1S,2S,4S)-4,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl] 3-O-[(1S,4R,9R,10S,13S,16R)-5,5,9-trimethyl-14-methylidene-16-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] propanedioate 162895115 Click to see CC1(CCCC2(C1CCC34C2CCC(C3OC(=O)CC(=O)OC5CC6(CCC5C6(C)C)C)C(=C)C4)C)C 510.70 unknown https://doi.org/10.1016/0031-9422(93)85044-R
1-O-[(E,7S,11S)-3,7,11,15-tetramethylhexadec-2-enyl] 3-O-[(1S,4R,9R,10S,13S,16R)-5,5,9-trimethyl-14-methylidene-16-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] propanedioate 163032843 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCOC(=O)CC(=O)OC1C2CCC3C1(CCC4C3(CCCC4(C)C)C)CC2=C)C 653.00 unknown https://doi.org/10.1016/0031-9422(93)85044-R
3-O-(1,3,3-trimethyl-2-bicyclo[2.2.1]heptanyl) 1-O-(5,5,9-trimethyl-14-methylidene-16-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) propanedioate 162908396 Click to see CC1(CCCC2(C1CCC34C2CCC(C3OC(=O)CC(=O)OC5C(C6CCC5(C6)C)(C)C)C(=C)C4)C)C 510.70 unknown https://doi.org/10.1016/0031-9422(93)85044-R
3-O-[(1R,2S,4S)-1,3,3-trimethyl-2-bicyclo[2.2.1]heptanyl] 1-O-[(1S,4R,9R,10S,13S,16R)-5,5,9-trimethyl-14-methylidene-16-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] propanedioate 162908397 Click to see CC1(CCCC2(C1CCC34C2CCC(C3OC(=O)CC(=O)OC5C(C6CCC5(C6)C)(C)C)C(=C)C4)C)C 510.70 unknown https://doi.org/10.1016/0031-9422(93)85044-R
3-Oxo-3-[(5,5,9-trimethyl-14-methylidene-15-tetracyclo[11.2.1.01,10.04,9]hexadecanyl)oxy]propanoic acid 163026146 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4OC(=O)CC(=O)O)C)C 374.50 unknown https://doi.org/10.1016/0031-9422(93)85044-R
3-Oxo-3-[(5,5,9-trimethyl-14-methylidene-16-tetracyclo[11.2.1.01,10.04,9]hexadecanyl)oxy]propanoic acid 163048754 Click to see CC1(CCCC2(C1CCC34C2CCC(C3OC(=O)CC(=O)O)C(=C)C4)C)C 374.50 unknown https://doi.org/10.1016/0031-9422(93)85044-R
3-oxo-3-[[(1S,4R,9R,10S,13S,16R)-5,5,9-trimethyl-14-methylidene-16-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]oxy]propanoic acid 163189443 Click to see CC1(CCCC2(C1CCC34C2CCC(C3OC(=O)CC(=O)O)C(=C)C4)C)C 374.50 unknown https://doi.org/10.1016/0031-9422(93)85044-R
5,5,9-Trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 14635499 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4=O)C)C 286.50 unknown https://doi.org/10.1016/0031-9422(93)85044-R
5,5,9-Trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-16-ol 162975750 Click to see CC1(CCCC2(C1CCC34C2CCC(C3O)C(=C)C4)C)C 288.50 unknown https://doi.org/10.1016/0031-9422(93)85044-R
Bis(5,5,9-trimethyl-14-methylidene-16-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) propanedioate 162858248 Click to see CC1(CCCC2(C1CCC34C2CCC(C3OC(=O)CC(=O)OC5C6CCC7C5(CCC8C7(CCCC8(C)C)C)CC6=C)C(=C)C4)C)C 645.00 unknown https://doi.org/10.1016/0031-9422(93)85044-R
bis[(1S,4R,9R,10S,13S,16R)-5,5,9-trimethyl-14-methylidene-16-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] propanedioate 162858249 Click to see CC1(CCCC2(C1CCC34C2CCC(C3OC(=O)CC(=O)OC5C6CCC7C5(CCC8C7(CCCC8(C)C)C)CC6=C)C(=C)C4)C)C 645.00 unknown https://doi.org/10.1016/0031-9422(93)85044-R
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Isoafricanol 11020495 Click to see CC1CCC2C1(CC(CC3C2(C3)C)(C)C)O 222.37 unknown https://doi.org/10.1016/0031-9422(93)85044-R
(6S,10S)-6,10,14-trimethylpentadecan-2-one 1810797 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=O)C 268.50 unknown https://doi.org/10.1016/0031-9422(93)85044-R
2-Methyl-5-(1,2,2-trimethylcyclopentyl)phenol 586002 Click to see CC1=C(C=C(C=C1)C2(CCCC2(C)C)C)O 218.33 unknown https://doi.org/10.1016/0031-9422(93)85044-R
3,3,5,7b-Tetramethyl-1,1a,2,4,5,6,7,7a-octahydrocyclopropa[h]azulen-4a-ol 5232643 Click to see CC1CCC2C1(CC(CC3C2(C3)C)(C)C)O 222.37 unknown https://doi.org/10.1016/0031-9422(93)85044-R
6,10,14-Trimethylpentadecan-2-one 10408 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=O)C 268.50 unknown https://doi.org/10.1016/0031-9422(93)85044-R
Phenol, 2-methyl-5-(1,2,2-trimethylcyclopentyl)-, (S)- 11790670 Click to see CC1=C(C=C(C=C1)C2(CCCC2(C)C)C)O 218.33 unknown https://doi.org/10.1016/0031-9422(93)85044-R
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
2-Hydroxy-7-methoxy-9H-carbazole-3-carbaldehyde 189687 Click to see COC1=CC2=C(C=C1)C3=C(N2)C=C(C(=C3)C=O)O 241.24 unknown via CMAUP database
2-methoxy-9H-carbazol-3-ol 15182256 Click to see COC1=C(C=C2C3=CC=CC=C3NC2=C1)O 213.23 unknown via CMAUP database
2-methoxy-9H-carbazole-3-carbaldehyde 6483032 Click to see COC1=CC2=C(C=C1C=O)C3=CC=CC=C3N2 225.24 unknown via CMAUP database
3-Formyl-2-hydroxy-6-methoxycarbazole 101508363 Click to see C1=CC2=C(C=C1O)C3=C(N2)C=C(C(=C3)C=O)O 227.21 unknown via CMAUP database
3,3-dimethyl-7H-pyrano[2,3-c]carbazole-10-carbaldehyde 71623858 Click to see CC1(C=CC2=C(O1)C=CC3=C2C4=C(N3)C=CC(=C4)C=O)C 277.30 unknown via CMAUP database
7-Hydroxyheptaphylline 15767846 Click to see CC(=CCC1=C(C(=CC2=C1NC3=C2C=CC(=C3)O)C=O)O)C 295.30 unknown via CMAUP database
7-Methoxyheptaphylline 189688 Click to see CC(=CCC1=C(C(=CC2=C1NC3=C2C=CC(=C3)OC)C=O)O)C 309.40 unknown via CMAUP database
9H-Carbazole-3-carbaldehyde 504067 Click to see C1=CC=C2C(=C1)C3=C(N2)C=CC(=C3)C=O 195.22 unknown via CMAUP database
9H-Carbazole-3-carboxaldehyde, 2,7-dimethoxy- 5317755 Click to see COC1=CC2=C(C=C1)C3=C(N2)C=C(C(=C3)C=O)OC 255.27 unknown via CMAUP database
Clauraila D 51039828 Click to see CC1(C=CC2=C(O1)C=CC3=C2C4=C(N3)C=C(C(=C4)C=O)O)C 293.30 unknown via CMAUP database
Clausenawalline H 71623801 Click to see CC(=CCC1=C(C=CC2=C1C3=C(N2)C=C(C(=C3)C=O)O)O)C 295.30 unknown via CMAUP database
Clausenawalline K 71623860 Click to see CC1(C(C(C2=C(O1)C=CC3=C2C4=C(N3)C=C(C(=C4)C=O)O)O)O)C 327.30 unknown via CMAUP database
Clausine H 5315952 Click to see COC1=CC2=C(C=C1)C3=CC(=C(C=C3N2)OC)C(=O)OC 285.29 unknown via CMAUP database
Clausine K 504070 Click to see COC1=CC2=C(C=C1)C3=CC(=C(C=C3N2)OC)C(=O)O 271.27 unknown via CMAUP database
Clauszoline K 10537169 Click to see COC1=CC2=C(C=C1)C3=C(N2)C=CC(=C3)C=O 225.24 unknown via CMAUP database
Girinimbine 96943 Click to see CC1=CC2=C(C3=C1OC(C=C3)(C)C)NC4=CC=CC=C42 263.30 unknown via CMAUP database
Heptaphylline 5318015 Click to see CC(=CCC1=C(C(=CC2=C1NC3=CC=CC=C32)C=O)O)C 279.30 unknown via CMAUP database
Lansine 5278451 Click to see COC1=CC2=C(C=C1)NC3=C2C=C(C(=C3)O)C=O 241.24 unknown via CMAUP database
methyl 1,6-dihydroxy-5-(3-methylbut-2-enyl)-9H-carbazole-3-carboxylate 71623800 Click to see CC(=CCC1=C(C=CC2=C1C3=C(N2)C(=CC(=C3)C(=O)OC)O)O)C 325.40 unknown via CMAUP database
Methyl 3-carbazolecarboxylate 504069 Click to see COC(=O)C1=CC2=C(C=C1)NC3=CC=CC=C32 225.24 unknown via CMAUP database
methyl 8-hydroxy-3,3-dimethyl-7H-pyrano[2,3-c]carbazole-10-carboxylate 71623859 Click to see CC1(C=CC2=C(O1)C=CC3=C2C4=C(N3)C(=CC(=C4)C(=O)OC)O)C 323.30 unknown via CMAUP database
Mukonal 504068 Click to see C1=CC=C2C(=C1)C3=C(N2)C=C(C(=C3)C=O)O 211.22 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine 68085 Click to see COC1=C2C=COC2=NC3=CC=CC=C31 199.20 unknown via CMAUP database
Gamma-Fagarine 107936 Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3 229.23 unknown via CMAUP database

Biological Material Top ebay Auctions

Please wait .. loading items ..
Loading...

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.