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Internal ID UUID644051305a2b7852582623
Scientific name Liochlaena subulata
Authority (A.Evans) Schljakov
First published in Pečen. Mhi Severa SSSR 4: 71 1981

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Language Common/alternative name
Estonian naaskel-lusiksammal
Swedish spetsig rörsvepemossa
Chinese 锥叶狭叶苔

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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-0001203121
Tropicos 35202526
INPN 786433
The Plant List tro-35202526
Open Tree Of Life 246583
NCBI Taxonomy 463575
Nature Serve 2.126684
iNaturalist 997154
GBIF 2689239
Elurikkus 282509

Genomes (via NCBI) Top

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
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
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
Does Calypogeia azurea (Calypogeiaceae, Marchantiophyta) occur outside Europe? Molecular and morphological evidence Buczkowska K, Bakalin V, Bączkiewicz A, Aguero B, Gonera P, Ślipiko M, Szczecińska M, Sawicki J PLoS One 10-Oct-2018
PMCID:PMC6179228
doi:10.1371/journal.pone.0204561
PMID:30304042
ent-Kaurane-type diterpenoids from a cell suspension culture of the liverwort Jungermannia subulata. Nozaki H, Hayashi K, Okuda K, Kuyama F, Ono K, Matsuo A Planta Med 01-Jun-2007
doi:10.1055/S-2007-981529
PMID:17541881
ent-Kaurane-type diterpenoids produced by cell culture of the liverwort Jungermannia subulata Hiroyuki Tazaki, Takeshi Iwasaki, Izumi Nakasuga, Kimiko Kobayashi, Hiroyuki Koshino, Masayasu Tanaka, Kensuke Nabeta Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(99)00347-7
Subulatin, an antioxidic caffeic acid derivative isolated from the in vitro cultured liverworts, Jungermannia subulata, Lophocolea heterophylla, and Scapania parvitexta. Tazaki H, Ito M, Miyoshi M, Kawabata J, Fukushi E, Fujita T, Motouri M, Furuki T, Nabeta K Biosci Biotechnol Biochem 01-Feb-2002
doi:10.1271/BBB.66.255
PMID:11999396

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
> Alkaloids and derivatives / Corynanthean-type alkaloids
methyl 2-{3-ethenyl-1H,2H,3H,4H,6H,7H,12H,12bH-indolo[2,3-a]quinolizin-2-yl}-3-hydroxypropanoate 5321352 Click to see COC(=O)C(CO)C1CC2C3=C(CCN2CC1C=C)C4=CC=CC=C4N3 354.40 unknown https://doi.org/10.1271/BBB.66.255
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,2S,4R,9R,10S,13R)-2-hydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 162850939 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C)C4=O)O)C)C 302.50 unknown https://doi.org/10.1055/S-2007-981529
(1R,4R,9R,10S,13R,14R)-5,5,9,14-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadecane-6,15-dione 163007000 Click to see CC1C2CCC3C4(CCC(=O)C(C4CCC3(C2)C1=O)(C)C)C 302.50 unknown https://doi.org/10.1016/S0031-9422(99)00347-7
(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/10.1055/S-2007-981529
(1R,4S,6R,9R,10S,13R,14R)-6-hydroxy-5,5,9,14-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 14635518 Click to see CC1C2CCC3C4(CCC(C(C4CCC3(C2)C1=O)(C)C)O)C 304.50 unknown https://doi.org/10.1055/S-2007-981529
(1R,4S,9R,10S,13R,14R)-5,5,9,14-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadecane-6,15-dione 15478795 Click to see CC1C2CCC3C4(CCC(=O)C(C4CCC3(C2)C1=O)(C)C)C 302.50 unknown https://doi.org/10.1055/S-2007-981529
(1R,4S,9R,10S,13R)-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-6,15-dione 102331303 Click to see CC1(C2CCC34CC(CCC3C2(CCC1=O)C)C(=C)C4=O)C 300.40 unknown https://doi.org/10.1055/S-2007-981529
(1R,4S,9R,10S,13S,14R)-13-hydroxy-5,5,9,14-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadecane-6,15-dione 162929583 Click to see CC1C(=O)C23CCC4C(C(=O)CCC4(C2CCC1(C3)O)C)(C)C 318.40 unknown https://doi.org/10.1055/S-2007-981529
(1R,4S,9S,10S,13R,15R)-15-hydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-6-one 21602049 Click to see CC1(C2CCC34CC(CCC3C2(CCC1=O)C)C(=C)C4O)C 302.50 unknown https://doi.org/10.1055/S-2007-981529
(1R,4S,9S,10S,13S,15R)-13,15-dihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-6-one 162954324 Click to see CC1(C2CCC34CC(CCC3C2(CCC1=O)C)(C(=C)C4O)O)C 318.40 unknown https://doi.org/10.1055/S-2007-981529
(5,5,9-Trimethyl-14-methylidene-6,15-dioxo-13-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 162919870 Click to see CC(=O)OC12CCC3C4(CCC(=O)C(C4CCC3(C1)C(=O)C2=C)(C)C)C 358.50 unknown https://doi.org/10.1055/S-2007-981529
[(1R,4S,9R,10S,13S)-5,5,9-trimethyl-14-methylidene-6,15-dioxo-13-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 162919871 Click to see CC(=O)OC12CCC3C4(CCC(=O)C(C4CCC3(C1)C(=O)C2=C)(C)C)C 358.50 unknown https://doi.org/10.1055/S-2007-981529
11-Hydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 14019093 Click to see CC1(CCCC2(C1CCC34C2C(CC(C3)C(=C)C4=O)O)C)C 302.50 unknown https://doi.org/10.1055/S-2007-981529
11beta-Hydroxykaur-16-en-15-one 101831563 Click to see CC1(CCCC2(C1CCC34C2C(CC(C3)C(=C)C4=O)O)C)C 302.50 unknown https://doi.org/10.1055/S-2007-981529
13-Hydroxy-5,5,9,14-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadecane-6,15-dione 162929582 Click to see CC1C(=O)C23CCC4C(C(=O)CCC4(C2CCC1(C3)O)C)(C)C 318.40 unknown https://doi.org/10.1055/S-2007-981529
13,15-Dihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-6-one 162954323 Click to see CC1(C2CCC34CC(CCC3C2(CCC1=O)C)(C(=C)C4O)O)C 318.40 unknown https://doi.org/10.1055/S-2007-981529
15-Hydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-6-one 73798318 Click to see CC1(C2CCC34CC(CCC3C2(CCC1=O)C)C(=C)C4O)C 302.50 unknown https://doi.org/10.1055/S-2007-981529
2-Hydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 78157249 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(=C)C4=O)O)C)C 302.50 unknown https://doi.org/10.1055/S-2007-981529
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/10.1055/S-2007-981529
5,5,9-Trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-6,15-dione 163033660 Click to see CC1(C2CCC34CC(CCC3C2(CCC1=O)C)C(=C)C4=O)C 300.40 unknown https://doi.org/10.1055/S-2007-981529
5,5,9,14-Tetramethyltetracyclo[11.2.1.01,10.04,9]hexadecane-6,15-dione 163006999 Click to see CC1C2CCC3C4(CCC(=O)C(C4CCC3(C2)C1=O)(C)C)C 302.50 unknown https://doi.org/10.1055/S-2007-981529
6-Hydroxy-5,5,9,14-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 14635516 Click to see CC1C2CCC3C4(CCC(C(C4CCC3(C2)C1=O)(C)C)O)C 304.50 unknown https://doi.org/10.1055/S-2007-981529
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Friedelan-3-one 244297 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1055/S-2007-981529
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1055/S-2007-981529
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-2007-981529
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-2007-981529
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(1,2-dihydroxyethyl)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-4-[3-[3-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoyloxy]-3,4-dihydro-2H-pyran-6-carboxylic acid 85052747 Click to see C1=CC(=C(C=C1C=CC(=O)OC2C(C=C(OC2C(CO)O)C(=O)O)OC(=O)C=CC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 706.60 unknown https://doi.org/10.1271/BBB.66.255
Subulatin 9853163 Click to see C1=CC(=C(C=C1C=CC(=O)OC2C(C=C(OC2C(CO)O)C(=O)O)OC(=O)C=CC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 706.60 unknown https://doi.org/10.1271/BBB.66.255
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Phaselic acid, (-)- 92299542 Click to see C1=CC(=C(C=C1C=CC(=O)OC(CC(=O)O)C(=O)O)O)O 296.23 unknown https://doi.org/10.1271/BBB.66.255

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