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Selliguea hastata

Selliguea hastata - 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
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Details Top

Internal ID UUID6440766914141353867159
Scientific name Selliguea hastata
Authority (Thunb.) H.Ohashi & K.Ohashi
First published in J. Jap. Bot. 84(5): 307. 2009 [20 Oct 2009]

Description Top

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Synonyms Top

Scientific name Authority First published in
Phymatopteris similis (Ching) W.M.Chu ex P.S.Wang & X.Y.Wang Pterid. Fl. Guizhou : 501 (2001)
Crypsinus hastatus (Thunb.) Copel. Gen. Fil. : 206 (1947)
Phymatodes hastata (Thunb.) Ching Sinensia 3: 344. 1933
Polypodium hastatum Thunb. Syst. Veg. ed. 14 935 (1784)
Phymatopsis chenkouensis Ching Acta Phytotax. Sin. 9: 188. 1964. (1964)
Phymatopsis hunyaensis Ching Acta Phytotax. Sin. 9: 187. 1964. (1964)
Phymatopsis rotunda Ching Acta Phytotax. Sin. 9: 186. 1964. (1964)
Phymatopsis simplicifolia Ching Acta Phytotax. Sin. 9: 187. 1964. (1964)
Polypodium dolichopodum Diels Bot. Jahrb. Syst. 29(2): 205 (1900)
Polypodium mathewii Tutcher J. Linn. Soc., Bot. 37. 68. 1905 (1905)
Polypodium arenarium Baker Bull. Misc. Inform. Kew 1895: 56 (1895)
Phymatopsis hastata (Thunb.) Kitag. ex H.Ito J. Jap. Bot. 11: 99 (1935)
Polypodium hastatum f. pygmaeum Maxim. Fl. As. Orient. Fragm. : 73 (1879)
Phymatopsis hastata f. pygmaea (Maxim.) H.Itô Nom. Pl. Japan. (Ed. Emend.) 19–20 1939
Phymatopteris chenkouensis (Ching) Pic.Serm. Webbia 28: 461. 1973. (1973)
Phymatopteris hastata (Thunb.) Pic.Serm. Webbia 28: 462. (1973)
Phymatopteris hunyaensis (Ching) Pic.Serm. Webbia 28: 462. 1973. (1973)
Phymatopsis shandongensis J.X.Li & C.Y.Wang Acta Phytotax. Sin. 22(2): 165 (1984)
Phymatopteris rotunda (Ching) Pic.Serm. Webbia 28: 464. 1973. (1973)
Phymatopteris simplicifolia (Ching) Pic.Serm. Webbia 28: 464. 1973. (1973)
Phymatopsis similis Ching Fl. Xizang. 1: 319 (1983)
Phymatopsis tarningensis Ching Wuyi Sci. J. 1: 10 (1981)
Phymatopsis hastata var. pygmaea (Maxim.) Li & J.Z.Wang Bull. Bot. Res., Harbin 9(4): 80 (1989)
Drynaria hastata Fée Mém. Foug., 5. Gen. Filic. : 271 (1852)
Pleopeltis hastata T.Moore Index Fil. : 346 (1862)
Pleopeltis oxyloba Bedd. Ferns S. India t. 175. 1863-65 (1863)
Crypsinus similis (Ching) X.Cheng Fl. Yunnanica 21: 378 (-379) (2005)
Crypsinus hastatus f. pygmaeus (Maxim.) Nakaike New Fl. Jap. Pterid. 840 (1992): (1992)
Phymatopteris hastata f. pygmaea (Maxim.) Nakaike Checkl. Lycophytes Ferns Japan : 33 (2013)

Common names Top

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Language Common/alternative name
Japanese ミツデウラボシ
Korean 고란초
Chinese 三葉茀蕨
Chinese 金鸡脚假瘤蕨
Chinese 维氏假瘤蕨
Chinese 金鸡脚假瘤蕨(金鸡脚）
Chinese 金鸡脚

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Selliguea hastata var. longisquamata (Tagawa) H.Ohashi & K.Ohashi J. Jap. Bot. 84(5): 307 (2009)

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001035140
Tropicos 100356708
KEW urn:lsid:ipni.org:names:77100111-1
The Plant List tro-100354141
NCBI Taxonomy 187376
IPNI 77103143-1
Freebase /m/0cz8d1v
Wikipedia Selliguea_hastata
CMAUP NPO26228

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
Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C J Ethnobiol Ethnomed 30-May-2023
PMCID:PMC10230803
doi:10.1186/s13002-023-00594-4
PMID:37254191
Ethnobotanical study of Hakka traditional medicine in Ganzhou, China and their antibacterial, antifungal, and cytotoxic assessments Hu H, Yang Y, Aissa A, Tekin V, Li J, Panda SK, Huang H, Luyten W BMC Complement Med Ther 19-Sep-2022
PMCID:PMC9484230
doi:10.1186/s12906-022-03712-z
PMID:36123737
Structural Variation of Plastomes Provides Key Insight Into the Deep Phylogeny of Ferns Du XY, Kuo LY, Zuo ZY, Li DZ, Lu JM Front Plant Sci 02-May-2022
PMCID:PMC9134734
doi:10.3389/fpls.2022.862772
PMID:35645990
Hearty recipes for health: the Hakka medicinal soup in Guangdong, China Ding M, Shi S, Luo B J Ethnobiol Ethnomed 25-Jan-2022
PMCID:PMC8787035
doi:10.1186/s13002-022-00502-2
PMID:35078485
Effects of Shade and Planting Methods on the Growth of Heracleum moellendorffii and Adenophora divaricata in Different Soil Moisture and Nutrient Conditions Youn WB, Hernandez JO, Park BB Plants (Basel) 17-Oct-2021
PMCID:PMC8537555
doi:10.3390/plants10102203
PMID:34686011
Study of the independent gametophytes found on Jeju Island in South Korea and the first record of the obligate independent gametophyte of Antrophyum obovatum Baker Park SH, Kim JS, Kim HT Ecol Evol 07-Jul-2020
PMCID:PMC7391314
doi:10.1002/ece3.6510
PMID:32760567
Diversity and use of medicinal plants for soup making in traditional diets of the Hakka in West Fujian, China Luo B, Li F, Ahmed S, Long C J Ethnobiol Ethnomed 28-Nov-2019
PMCID:PMC6883701
doi:10.1186/s13002-019-0335-y
PMID:31779654
Identification of Potential Anticancer Protein Targets in Cytotoxicity Mediated by Tropical Medicinal Fern Extracts Tan ST, Ong HC, Chai TT, Wong FC Pharmacogn Mag 10-Apr-2018
PMCID:PMC5909320
doi:10.4103/pm.pm_282_17
PMID:29720836
Insight into the binding interaction of kaempferol-7-O-α-L-rhamnopyranoside with human serum albumin by multiple fluorescence spectroscopy and molecular modeling Zhang W, Chen C, Zhang C, Duan J, Yao H, Li Y, Meng A, Shi J Exp Ther Med 04-May-2017
PMCID:PMC5450801
doi:10.3892/etm.2017.4427
PMID:28588690
The Relationship between Mating System and Genetic Diversity in Diploid Sexual Populations of Cyrtomium falcatum in Japan Imai R, Tsuda Y, Matsumoto S, Ebihara A, Watano Y PLoS One 05-Oct-2016
PMCID:PMC5051678
doi:10.1371/journal.pone.0163683
PMID:27706257

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 / Aporphines
(-)-Isoboldine 6971182 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC 327.40 unknown via CMAUP database
Isoboldine 133323 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC 327.40 unknown via CMAUP database
> Alkaloids and derivatives / Pavine alkaloids
(-)-Argemonine 442168 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)OC)OC)OC)OC 355.40 unknown via CMAUP database
(+)-Caryachine 12305286 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC5=C(C=C24)OCO5)OC)O 325.40 unknown via CMAUP database
(1R,12R)-16-Methoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-15-ol 3082467 Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC(=C(C=C25)O)OC)OCO4 325.40 unknown via CMAUP database
(1R,12S)-15,16-dimethoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-1-ol 10948236 Click to see CN1C2CC3=CC4=C(C=C3C1(CC5=CC(=C(C=C25)OC)OC)O)OCO4 355.40 unknown via CMAUP database
(1R,12S)-23-methyl-5,7,16,18-tetraoxa-23-azahexacyclo[10.10.1.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaen-1-ol 11110561 Click to see CN1C2CC3=CC4=C(C=C3C1(CC5=CC6=C(C=C25)OCO6)O)OCO4 339.30 unknown via CMAUP database
(1R,9R)-5,12-dimethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4,6,10,12,14-hexaene-4,13-diol 11869664 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)OC)OC)O 327.40 unknown via CMAUP database
(1S,12S,20R)-15-methoxy-20-methyl-20-oxido-5,7-dioxa-20-azoniapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-16-ol 102304441 Click to see C[N+]1(C2CC3=CC(=C(C=C3C1CC4=CC5=C(C=C24)OCO5)OC)O)[O-] 341.40 unknown via CMAUP database
(1S,12S,20R)-16-methoxy-20-methyl-20-oxido-5,7-dioxa-20-azoniapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-15-ol 102304443 Click to see C[N+]1(C2CC3=CC4=C(C=C3C1CC5=CC(=C(C=C25)O)OC)OCO4)[O-] 341.40 unknown via CMAUP database
(1S,12S)-15-methoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-16-ol 11823545 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC5=C(C=C24)OCO5)OC)O 325.40 unknown via CMAUP database
(1S,12S)-5,7,16,18-tetraoxa-23-azahexacyclo[10.10.1.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaene 11012304 Click to see C1C2C3=CC4=C(C=C3CC(N2)C5=CC6=C(C=C51)OCO6)OCO4 309.30 unknown via CMAUP database
(1S,9S)-4,13-dimethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2(7),3,5,10,12,14-hexaene-3,12-diol 92856799 Click to see CN1C2CC3=C(C1CC4=CC(=C(C=C24)O)OC)C(=C(C=C3)OC)O 327.40 unknown via CMAUP database
(1S,9S)-5,12-dimethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4,6,10,12,14-hexaene-4,13-diol 12300156 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)OC)OC)O 327.40 unknown via CMAUP database
Caryachine 44575219 Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC(=C(C=C25)O)OC)OCO4 325.40 unknown via CMAUP database
Crychine 193382 Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC6=C(C=C25)OCO6)OCO4 323.30 unknown via CMAUP database
Escholtzine 12304178 Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC6=C(C=C25)OCO6)OCO4 323.30 unknown via CMAUP database
> Alkaloids and derivatives / Proaporphines
(+)-8,9-Dihydrostepharine 13819281 Click to see COC1=C(C2=C3C(CC24CCC(=O)C=C4)NCCC3=C1)OC 299.40 unknown via CMAUP database
(1'S,2S,4R)-10-methoxy-5-methylspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohex-2-ene]-1',11-diol 10870351 Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC(C=C4)O)O)OC 301.40 unknown via CMAUP database
Isoamuronine 12306127 Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC(=O)C=C4)OC)OC 313.40 unknown via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
Berberine 2353 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC 336.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
alpha-Tocopherolquinone 2734086 Click to see CC1=C(C(=O)C(=C(C1=O)C)CCC(C)(CCCC(C)CCCC(C)CCCC(C)C)O)C 446.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Cryptocaryone 10379026 Click to see C1C2C(C=CC(=O)C2=C(C=CC3=CC=CC=C3)O)OC1=O 282.29 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives
6-Methyl-[1,3]dioxolo[4,5-g]isoquinolin-6-ium 2753983 Click to see C[N+]1=CC2=CC3=C(C=C2C=C1)OCO3 188.20 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
4-(6,7-Dimethoxyisoquinoline-1-ylmethyl)phenol 21814573 Click to see COC1=C(C=C2C(=C1)C=CN=C2CC3=CC=C(C=C3)O)OC 295.30 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
Doryanin 12998814 Click to see CN1C=CC2=CC3=C(C=C2C1=O)OCO3 203.19 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
7-O-Methylcryptochinone A 46939685 Click to see COC1CC2=C(C3C1OC(=O)C3)C(=O)CC(O2)C4=CC=CC=C4 314.30 unknown via CMAUP database
Cryptocaryanone A 10356404 Click to see C1C2C(C=CC3=C2C(=O)CC(O3)C4=CC=CC=C4)OC1=O 282.29 unknown via CMAUP database
Cryptochinone A 46939683 Click to see C1C2C(C(CC3=C2C(=O)CC(O3)C4=CC=CC=C4)O)OC1=O 300.30 unknown via CMAUP database
Cryptochinone B 46939684 Click to see C1C2C(C(CC3=C2C(=O)CC(O3)C4=CC=CC=C4)O)OC1=O 300.30 unknown via CMAUP database
Cryptochinone D 46939686 Click to see COC1CC2=C(C3C1OC(=O)C3)C(=O)CC(O2)C4=CC=CC=C4 314.30 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(1'S,2R,4R)-10,11-dimethoxy-5-methylspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,6'-cyclohex-2-ene]-1'-ol 10914050 Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC=CC4O)OC)OC 315.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Hexacosyl (E)-ferulate 5318033 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 558.90 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-7-hydroxyflavanone 688857 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3 240.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(-)-Epitaxifolin 712318 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4H-1-Benzopyran-4-one, 5-hydroxy-3,7-dimethoxy-2-phenyl- 5748697 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=CC=C3)O 298.29 unknown via CMAUP database
5-Hydroxy-7-methoxy-2-phenylchroman-4-one 73201 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
Mosloflavone 471722 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O)OC 298.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5-Hydroxy-3,7,8-trimethoxyflavone 21632881 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C(=C(O2)C3=CC=CC=C3)OC)OC 328.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Larrein 9993268 Click to see COC1=C(C=CC(=C1O)C(=O)C=CC2=CC=CC=C2)O 270.28 unknown via CMAUP database

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