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Anemoclema glaucifolium

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID6440094ed6b28141839668
Scientific name Anemoclema glaucifolium
Authority (Franch.) W.T.Wang
First published in Acta Phytotax. Sin. 9: 106 (1964)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Pulsatilloides glaucifolia (Franch.) Starod. Vetrenitsy: Sist. i Evol. : 124 (1991)
Anemone glaucifolia Franch. Bull. Soc. Bot. France 33: 363 (1886)
Pulsatilla glauciifolia Huth Bot. Jahrb. Syst. 22: 588 (1897)

Common names Top

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Language Common/alternative name
Chinese 罂粟莲花

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000534996
Tropicos 27103121
KEW urn:lsid:ipni.org:names:708173-1
The Plant List kew-2637946
Open Tree Of Life 274594
NCBI Taxonomy 640772
IPNI 708173-1
GBIF 3928312
EOL 2899803
USDA GRIN 105304

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
Comparative analysis of chloroplast genomes of Pulsatilla species reveals evolutionary and taxonomic status of newly discovered endangered species Pulsatilla saxatilis Xue H, Xing Y, Bian C, Hou W, Men W, Zheng H, Yang Y, Ying X, Kang T, Xu L BMC Plant Biol 17-Apr-2024
PMCID:PMC11022354
doi:10.1186/s12870-024-04940-w
Complete Plastid Genomes of Nine Species of Ranunculeae (Ranunculaceae) and Their Phylogenetic Inferences Ji J, Luo Y, Pei L, Li M, Xiao J, Li W, Wu H, Luo Y, He J, Cheng J, Xie L Genes (Basel) 27-Nov-2023
PMCID:PMC10742492
doi:10.3390/genes14122140
PMID:38136961
Complete chloroplast genome sequence of Eranthis byunsanensis B.Y. Sun (Ranunculaceae), an endemic species in Korea Park JM, Oh A, Koo J Mitochondrial DNA B Resour 15-May-2023
PMCID:PMC10187104
doi:10.1080/23802359.2023.2209383
PMID:37200680
Diversity of Cationic Antimicrobial Peptides in Black Cumin (Nigella sativa L.) Seeds Barashkova AS, Smirnov AN, Zorina ES, Rogozhin EA Int J Mol Sci 29-Apr-2023
PMCID:PMC10179141
doi:10.3390/ijms24098066
PMID:37175769
Phylogeny and Historical Biogeography of the East Asian Clematis Group, Sect. Tubulosae, Inferred from Phylogenomic Data Lyu R, Xiao J, Li M, Luo Y, He J, Cheng J, Xie L Int J Mol Sci 03-Feb-2023
PMCID:PMC9917980
doi:10.3390/ijms24033056
PMID:36769378
Genome-partitioning strategy, plastid and nuclear phylogenomic discordance, and its evolutionary implications of Clematis (Ranunculaceae) Xiao J, Lyu R, He J, Li M, Ji J, Cheng J, Xie L Front Plant Sci 14-Nov-2022
PMCID:PMC9703796
doi:10.3389/fpls.2022.1059379
PMID:36452086
Characterization of the complete chloroplast genome of the Helleborus atrorubens Waldst. & Kit. (Ranunculaceae) Shi X, Mao L, Jin L, Ma G Mitochondrial DNA B Resour 07-Sep-2022
PMCID:PMC9467529
doi:10.1080/23802359.2022.2119105
PMID:36106185
Natural Hybrid Origin of the Controversial “Species” Clematis × pinnata (Ranunculaceae) Based on Multidisciplinary Evidence Lyu R, He J, Luo Y, Lin L, Yao M, Cheng J, Xie L, Pei L, Yan S, Li L Front Plant Sci 12-Oct-2021
PMCID:PMC8545901
doi:10.3389/fpls.2021.745988
PMID:34712260
Comparative chloroplast genomes and phylogenetic analysis of Aquilegia Zhang W, Wang H, Dong J, Zhang T, Xiao H Appl Plant Sci 16-Mar-2021
PMCID:PMC8027367
doi:10.1002/aps3.11412
PMID:33854846
The complete chloroplast genome of Stauntonia chinensis and compared analysis revealed adaptive evolution of subfamily Lardizabaloideae species in China Wen F, Wu X, Li T, Jia M, Liu X, Liao L BMC Genomics 06-Mar-2021
PMCID:PMC7937279
doi:10.1186/s12864-021-07484-7
PMID:33676415
Chloroplast genomes elucidate diversity, phylogeny, and taxonomy of Pulsatilla (Ranunculaceae) Li QJ, Su N, Zhang L, Tong RC, Zhang XH, Wang JR, Chang ZY, Zhao L, Potter D Sci Rep 13-Nov-2020
PMCID:PMC7666119
doi:10.1038/s41598-020-76699-7
PMID:33188288
Comparative analysis of the complete chloroplast genome sequences of six species of Pulsatilla Miller, Ranunculaceae Zhang T, Xing Y, Xu L, Bao G, Zhan Z, Yang Y, Wang J, Li S, Zhang D, Kang T Chin Med 28-Nov-2019
PMCID:PMC6883693
doi:10.1186/s13020-019-0274-5
PMID:31798674
Structural variation of the complete chloroplast genome and plastid phylogenomics of the genus Asteropyrum (Ranunculaceae) He J, Yao M, Lyu RD, Lin LL, Liu HJ, Pei LY, Yan SX, Xie L, Cheng J Sci Rep 25-Oct-2019
PMCID:PMC6814708
doi:10.1038/s41598-019-51601-2
PMID:31653891
Efficient Identification of Pulsatilla (Ranunculaceae) Using DNA Barcodes and Micro-Morphological Characters Li QJ, Wang X, Wang JR, Su N, Zhang L, Ma YP, Chang ZY, Zhao L, Potter D Front Plant Sci 09-Oct-2019
PMCID:PMC6794950
doi:10.3389/fpls.2019.01196
PMID:31649688
The complete chloroplast genome of Menispermum dauricum (Menispermaceae, Ranunculales) Hina F, Jin Z, Yang Z, Li P, Fu C Mitochondrial DNA B Resour 17-Aug-2018
PMCID:PMC7800853
doi:10.1080/23802359.2018.1501306
PMID:33474364

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 / Indolonaphthyridine alkaloids
8-Hydroxy-4-methylsulfinyl-1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-3,5(16),7,9,11,14-hexaene-2,13-dione 101370302 Click to see CS(=O)C1=CC(=O)N2C3=CC(=O)C=CC3=C4C2=C1NC=C4O 314.30 unknown https://doi.org/10.1016/0031-9422(95)00107-I
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,5S,7R,10R,11R,14R,15S,18S,23S)-2,10,14,15,21,21-hexamethyl-7-[(1R,2S,3S)-1,2,3,4-tetrahydroxybutyl]-6,8-dioxahexacyclo[12.12.0.02,11.05,10.015,24.018,23]hexacos-24-ene-18-carboxylic acid 15225942 Click to see 604.80 unknown https://doi.org/10.1016/0031-9422(95)00107-I
(1R,2R,5S,7R,10R,11R,14R,15S,18S,23S)-2,10,14,15,21,21-hexamethyl-7-[(1R,2S,3S)-2,3,4-trihydroxy-1-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxybutyl]-6,8-dioxahexacyclo[12.12.0.02,11.05,10.015,24.018,23]hexacos-24-ene-18-carboxylic acid 11399996 Click to see 751.00 unknown https://doi.org/10.1016/0031-9422(95)00107-I
(1R,2R,5S,7R,10R,11R,14R,15S,18S,23S)-2,10,14,15,21,21-hexamethyl-7-[(1R,2S,3S)-2,3,4-trihydroxy-1-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxybutyl]-6,8-dioxahexacyclo[12.12.0.02,11.05,10.015,24.018,23]hexacos-24-ene-18-carboxylic acid 101927628 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC6C5(COC(O6)C(C(C(CO)O)O)OC7C(C(C(CO7)O)O)O)C)C)C)C2C1)C)C(=O)O)C 736.90 unknown https://doi.org/10.1016/0031-9422(95)00107-I
(1R,2R,5S,7S,10R,11R,14R,15S,18S,23S)-2,10,14,15,21,21-hexamethyl-7-[(1R,2S,3S)-1,2,3,4-tetrahydroxybutyl]-6,8-dioxahexacyclo[12.12.0.02,11.05,10.015,24.018,23]hexacos-24-ene-18-carboxylic acid 163024278 Click to see 604.80 unknown https://doi.org/10.1016/0031-9422(95)00107-I
10-[4,5-Dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 4483449 Click to see 735.00 unknown https://doi.org/10.1016/0031-9422(95)00107-I
10-[4,5-Dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 267360 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)O)O 751.00 unknown https://doi.org/10.1016/0031-9422(95)00107-I
2,10,14,15,21,21-Hexamethyl-7-(1,2,3,4-tetrahydroxybutyl)-6,8-dioxahexacyclo[12.12.0.02,11.05,10.015,24.018,23]hexacos-24-ene-18-carboxylic acid 163024277 Click to see 604.80 unknown https://doi.org/10.1016/0031-9422(95)00107-I
2,10,14,15,21,21-Hexamethyl-7-[2,3,4-trihydroxy-1-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxybutyl]-6,8-dioxahexacyclo[12.12.0.02,11.05,10.015,24.018,23]hexacos-24-ene-18-carboxylic acid 72832442 Click to see 751.00 unknown https://doi.org/10.1016/0031-9422(95)00107-I
9-(Hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-(3,4,5-trihydroxyoxan-2-yl)oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 4483448 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(CO6)O)O)O)C)C)C2C1)C)C(=O)O)C 604.80 unknown https://doi.org/10.1016/0031-9422(95)00107-I
Alpha-Hederin 73296 Click to see 751.00 unknown https://doi.org/10.1016/0031-9422(95)00107-I
Beta-Hederin 441929 Click to see 735.00 unknown https://doi.org/10.1016/0031-9422(95)00107-I
Cauloside A 441928 Click to see 604.80 unknown https://doi.org/10.1016/0031-9422(95)00107-I
Hederagenin 73299 Click to see 472.70 unknown https://doi.org/10.1016/0031-9422(95)00107-I

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