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Lepidozia fauriana

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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 UUID6440521cc7f31299366037
Scientific name Lepidozia fauriana
Authority Stephani
First published in Sp. Hepat. 3: 631 1908

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Chinese 东亚指叶苔

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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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-0001208208
Tropicos 35209157
The Plant List tro-35209157
Open Tree Of Life 169569
NCBI Taxonomy 989928
iNaturalist 1205477
GBIF 8017752

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
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
Farnesoid X receptor regulators from natural products and their biological function PENG W, NI H, GUO D, DENG Y, DAI M J Tradit Chin Med 04-Apr-2023
PMCID:PMC10133962
doi:10.19852/j.cnki.jtcm.20230404.002
PMID:37147766
Natural Products Targeting Liver X Receptors or Farnesoid X Receptor She J, Gu T, Pang X, Liu Y, Tang L, Zhou X Front Pharmacol 05-Jan-2022
PMCID:PMC8766425
doi:10.3389/fphar.2021.772435
PMID:35069197
Antiproliferative and Antimicrobial Activities of Selected Bryophytes Vollár M, Gyovai A, Szűcs P, Zupkó I, Marschall M, Csupor-Löffler B, Bérdi P, Vecsernyés A, Csorba A, Liktor-Busa E, Urbán E, Csupor D Molecules 23-Jun-2018
PMCID:PMC6099959
doi:10.3390/molecules23071520
PMID:29937511
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
Amorphane- and Eudesmane-type Sesquiterpenoids from Liverworts Y.-F Shu, H.-C. Wei, C.-L. Wu Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1997.9699475
Ring strain and total syntheses of modified macrocycles of the isoplagiochin type Speicher A, Backes T, Hesidens K, Kolz J Beilstein J Org Chem 01-Dec-2009
PMCID:PMC2839535
doi:10.3762/bjoc.5.71
PMID:20300508
Sesquiterpenoids from liverworts Lepidozia vitrea and L. Fauriana Yi-Fang Shu, Han-Chao Wei, Chia-Li Wu Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)90356-X
Sesquiterpenoid constituents of the liverworts Lepidozia fauriana and Lepidozia vitrea. Paul C, König WA, Wu CL Phytochemistry 01-Nov-2001
doi:10.1016/S0031-9422(01)00322-3
PMID:11672745

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 / Polycyclic hydrocarbons
(1aR,4R,7R,7bS)-1,1,4,7-Tetramethyl-1a,2,3,4,5,6,7,7b-octahydro-1H-cyclopropa[e]azulene 15431199 Click to see CC1CCC2C(C2(C)C)C3=C1CCC3C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
Isoledene 530426 Click to see CC1CCC2C(C2(C)C)C3=C1CCC3C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
(4S)-1,4-dimethyl-4-[(1R)-1-methyl-2-methylidenecyclopentyl]cyclohexene 12444487 Click to see CC1=CCC(CC1)(C)C2(CCCC2=C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://doi.org/10.1016/S0031-9422(00)90356-X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R,2R,7S,8R)-2,6,6-trimethyl-9-methylidenetricyclo[5.4.0.02,8]undecane 154495921 Click to see CC1(CCCC2(C3C1C2C(=C)CC3)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
(1R,8R)-2,6,6-trimethyl-9-methylidenetricyclo[5.4.0.02,8]undecane 163185614 Click to see CC1(CCCC2(C3C1C2C(=C)CC3)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
beta-Longipinene 25203064 Click to see CC1(CCCC2(C3C1C2C(=C)CC3)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
Dihydrochiloscypholone 15275881 Click to see CC1CCCC2(C1(C(CC2)C(=O)C(C)C)C)O 238.37 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
Dihydrochiloscypholone 91747870 Click to see CC1CCCC2(C1(C(CC2)C(=O)C(C)C)C)O 238.37 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+/-)-alpha-Cadinene 96843146 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
(1S,2S,6S,7R,8R)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 101607926 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
https://doi.org/10.1016/S0031-9422(01)00322-3
(1S,3R,6R,7S,8S)-3-methyl-2-methylidene-6-propan-2-yltricyclo[5.2.1.03,8]decane 131851742 Click to see CC(C)C1CCC2(C3C1CC(C3)C2=C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
(1S,4R,5R,6R,7S,10S)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]decane 163059581 Click to see CC1CCC23C1C2C(CCC3C)C(C)C 206.37 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
(6R)-3-Methylidene-6-(1,2,2-trimethylcyclopentyl)cyclohex-1-ene 71375071 Click to see CC1(CCCC1(C)C2CCC(=C)C=C2)C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
(R)-3-Methylene-6-((S)-1,2,2-trimethylcyclopentyl)cyclohex-1-ene 25202927 Click to see CC1(CCCC1(C)C2CCC(=C)C=C2)C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
1,4-Methanoindan, hexahydro-7-isopropyl-4-methyl-8-methylene- 530427 Click to see CC(C)C1CCC2(C3C1C(C2=C)CC3)C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
delta-Elemene 12309449 Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
Isosativene 565045 Click to see CC(C)C1CCC2(C3C1CC(C3)C2=C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
Thujopsen 97829 Click to see CC1=CCC2(CCCC(C23C1C3)(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
Thujopsene 442402 Click to see CC1=CCC2(CCCC(C23C1C3)(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4aR,7R,7aS,7bS)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene 12305246 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
(1aR,4R,4aR,7R,7aR,7bS)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol 124305339 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
(1aR,4R,4aR,7R,7aS,7bS)-1,1,4,7-Tetramethyldecahydro-1H-cyclopropa[e]azulen-4-ol 91746597 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
(1aR,4S,4aS,7R,7aR,7bS)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol 131705161 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
(1aR,7S,7aS,7bR)-1,1,4,7-Tetramethyl-1a,2,3,5,6,7,7a,7b-octahydro-1H-cyclopropa[e]azulen-7-ol 14038848 Click to see CC1=C2CCC(C2C3C(C3(C)C)CC1)(C)O 220.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
(1aS,4aS,7aS,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene 91746456 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)90356-X
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)90356-X
Alloaromadendren 91746537 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
Alloaromadendrene 12305247 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
Aromadendrene 91354 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
Globulol 101716 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
Viridiflorol (incomplete stereochemistry) 94174 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
> 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/S0031-9422(01)00322-3
cis-Bicyclogermacradiene 91747210 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(+)-beta-Cedrene 102432 Click to see CC1CCC2C13CCC(=C)C(C3)C2(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
beta-Cedrene 11106485 Click to see CC1CCC2C13CCC(=C)C(C3)C2(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
Cedrol 65575 Click to see CC1CCC2C13CCC(C(C3)C2(C)C)(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Maalialcohol 10944069 Click to see CC1(C2C1C3C(CCCC3(C)O)(CC2)C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(01)00322-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1S,7R,8S,12S)-10-methyl-7-propan-2-yl-2-oxatricyclo[6.3.1.04,12]dodeca-4,10-dien-3-one 10376656 Click to see CC1=CC2C3C(C1)C(CC=C3C(=O)O2)C(C)C 232.32 unknown https://doi.org/10.1080/10412905.1997.9699475
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
Stachatranone B 145721048 Click to see CC1=CC(CC2(C(O2)CC3(C(CC1)C(=CC(=O)O3)C(C)C)C)C)O 334.40 unknown https://doi.org/10.1016/S0031-9422(01)00322-3

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