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Monachosorum maximowiczii

Monachosorum maximowiczii - Unknown
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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 UUID64404cfc2df61546856195
Scientific name Monachosorum maximowiczii
Authority Hayata
First published in Bot. Mag. (Tokyo) 23: 29 (1909)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ptilopteris maximowiczii Hance J. Bot. 22: 139 (1884)
Polypodium maximowiczii Baker Syn. Fil. , ed. 2: 504 (1874)
Monachosorella maximowiczii (Baker) Hayata Bot. Mag. (Tokyo) 41: 540 (1927)
Phegopteris maximowiczii Christ Farnkr. Erde : 271 (1897)
Polystichum maximowiczii (Baker) Diels Nat. Pflanzenfam. 1 [4]. 189. 1899 (1899)

Common names Top

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Language Common/alternative name
Japanese フジシダ
Chinese 岩穴蕨
Chinese 穴子蕨

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Monachosorum maximowiczii var. melanocaulon (Hayata) Hayata Icon. Pl. Formosan. 6: 160 1916

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
    • Eastern Asia
      • Japan
      • Taiwan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001124684
Tropicos 26620882
KEW urn:lsid:ipni.org:names:17254260-1
The Plant List tro-26620882
Open Tree Of Life 365732
NCBI Taxonomy 872622
IPNI 17254260-1
iNaturalist 137329
GBIF 3747258
EOL 6130289
CMAUP NPO29180

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
Light response of gametophyte in Adiantum flabellulatum: transcriptome analysis and identification of key genes and pathways Cai Z, Wang X, Xie Z, Wen Z, Yu X, Xu S, Su X, Luo J Front Plant Sci 07-Sep-2023
PMCID:PMC10513451
doi:10.3389/fpls.2023.1222414
PMID:37746005
Untying the Gordian knot of plastid phylogenomic conflict: A case from ferns Wang T, Li TZ, Chen SS, Yang T, Shu JP, Mu YN, Wang KL, Chen JB, Xiang JY, Yan YH Front Plant Sci 24-Nov-2022
PMCID:PMC9730426
doi:10.3389/fpls.2022.918155
PMID:36507421
Plastome phylogenomic analysis reveals evolutionary divergences of Polypodiales suborder Dennstaedtiineae Lu JM, Du XY, Kuo LY, Ebihara A, Perrie LR, Zuo ZY, Shang H, Chang YH, Li DZ BMC Plant Biol 02-Nov-2022
PMCID:PMC9628275
doi:10.1186/s12870-022-03886-1
PMID:36319964
Full-length transcriptome analysis of Adiantum flabellulatum gametophyte Cai Z, Xie Z, Huang L, Wang Z, Pan M, Yu X, Xu S, Luo J PeerJ 09-Mar-2022
PMCID:PMC8917799
doi:10.7717/peerj.13079
PMID:35287343
Large-scale phylogenomic analysis resolves a backbone phylogeny in ferns Shen H, Jin D, Shu JP, Zhou XL, Lei M, Wei R, Shang H, Wei HJ, Zhang R, Liu L, Gu YF, Zhang XC, Yan YH Gigascience 24-Nov-2017
PMCID:PMC5795342
doi:10.1093/gigascience/gix116
PMID:29186447
Chemical and Chemotaxonomical Studies of Filices. LXVIII. The Distribution of Sesquiterpene Dimers 'Monachosorins' and Its Chemotaxonomic Implication KAZUYUKI HORI, TOSHIKO SATAKE, MASUO YABUUCHI, YASUHISA SAIKI, TAKAO MURAKAMI, CHIUMING CHEN Pharmaceutical Society of Japan 20-Apr-2017
doi:10.1248/YAKUSHI1947.107.7_485

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
> Benzenoids / Indanes / Indanones
Monachosorin B 13854555 Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2)CC3=C(C(=C4C(=C3)CCC4=O)C)CCO 406.50 unknown https://doi.org/10.1248/YAKUSHI1947.107.7_485
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
2-hydroxy-6-methoxy-9H-carbazole-3-carbaldehyde 5278451 Click to see COC1=CC2=C(C=C1)NC3=C2C=C(C(=C3)O)C=O 241.24 unknown via CMAUP database
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-Hydroxy-9H-carbazole-3-carbaldehyde 504068 Click to see C1=CC=C2C(=C1)C3=C(N2)C=C(C(=C3)C=O)O 211.22 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
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-methoxy-9H-carbazole-3-carbaldehyde 10537169 Click to see COC1=CC2=C(C=C1)C3=C(N2)C=CC(=C3)C=O 225.24 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 G 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
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 I 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
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 N 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
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
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
> 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

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