Amentotaxus argotaenia - Unknown
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Internal ID UUID644008c8ac921518584742
Scientific name Amentotaxus argotaenia
Authority (Hance) Pilg.
First published in Bot. Jahrb. Syst. 54: 41 (1916)

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Synonyms Top

Scientific name Authority First published in
Nageia argotaenia Kuntze Revis. Gen. Pl. 2: 800 (1891)
Nageia insignis Kuntze Revis. Gen. Pl. 2: 800. 1891 [5 Nov 1891]
Podocarpus argotaenia Hance J. Bot. 21: 357 (1883)
Cephalotaxus argotaenia (Hance) Pilg. Pflanzenr. , IV, 5: 104 (1903)
Amentotaxus argotaenia var. cathayensis (H.L.Li) Keng f. Rep. 1957 Anniv. Nanjing Univ. 7(2): 451. 1957

Common names Top

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Language Common/alternative name
English catkin yew
Chinese 华西穗花杉
Chinese 穗花杉
Chinese 穗花杉叶
Chinese 穗花杉根
Chinese 穗花杉种子

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Amentotaxus argotaenia var. argotaenia Unknown
Amentotaxus argotaenia var. brevifolia K.M.Lan & F.H.Zhang Acta Phytotax. Sin. 22: 492 (1984)

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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
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Tibet

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000530835
Tropicos 31200004
KEW urn:lsid:ipni.org:names:828260-1
The Plant List kew-2633471
Open Tree Of Life 684229
NCBI Taxonomy 25625
IUCN Red List 42545
IPNI 828260-1
iNaturalist 136237
GBIF 2685171
Freebase /m/02vty55
EPPO AMTAR
EOL 330198
USDA GRIN 415409
Wikipedia Amentotaxus_argotaenia
CMAUP NPO3762

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
A Comprehensive Review of the Classification, Sources, Phytochemistry, and Pharmacology of Norditerpenes Zeng N, Zhang Q, Yao Q, Fu G, Su W, Wang W, Li B Molecules 21-Dec-2023
PMCID:PMC10780140
doi:10.3390/molecules29010060
PMID:38202643
Distribution Patterns of Gymnosperm Species along Elevations on the Qinghai–Tibet Plateau: Effects of Climatic Seasonality, Energy–Water, and Physical Tolerance Variables Umair M, Hu X, Cheng Q, Ali S, Ni J Plants (Basel) 04-Dec-2023
PMCID:PMC10708526
doi:10.3390/plants12234066
PMID:38068701
Recent Developments with Icetexane Natural Products Naeini AA, Ziegelmeier AA, Chain WJ Chem Biodivers 08-Nov-2022
PMCID:PMC11067433
doi:10.1002/cbdv.202200793
PMID:36215180
Unlocking the Hidden Genetic Diversity of Varicosaviruses, the Neglected Plant Rhabdoviruses Bejerman N, Dietzgen RG, Debat H Pathogens 29-Sep-2022
PMCID:PMC9608074
doi:10.3390/pathogens11101127
PMID:36297184
New Diterpenes with Potential Antitumoral Activity Isolated from Plants in the Years 2017–2022 Forzato C, Nitti P Plants (Basel) 29-Aug-2022
PMCID:PMC9460660
doi:10.3390/plants11172240
PMID:36079622
Morpho-histology, endogenous hormone dynamics, and transcriptome profiling in Dacrydium pectinatum during female cone development Wang E, Lu W, Liang H, Zhang X, Huo S, Song X, Wang J, Zhao Y Front Plant Sci 17-Aug-2022
PMCID:PMC9428629
doi:10.3389/fpls.2022.954788
PMID:36061797
Transcriptome Analysis and Identification of a Female-Specific SSR Marker in Pistacia chinensis Based on Illumina Paired-End RNA Sequencing Cheng X, Wang F, Luo W, Kuang J, Huang X Genes (Basel) 07-Jun-2022
PMCID:PMC9222763
doi:10.3390/genes13061024
PMID:35741786
Loss of the IR region in conifer plastomes: Changes in the selection pressure and substitution rate of protein‐coding genes Ping J, Hao J, Li J, Yang Y, Su Y, Wang T Ecol Evol 12-Jan-2022
PMCID:PMC8809450
doi:10.1002/ece3.8499
PMID:35136556
EST‐SSR‐based landscape genetics of Pseudotaxus chienii, a tertiary relict conifer endemic to China Li S, Wang Z, Su Y, Wang T Ecol Evol 15-Jun-2021
PMCID:PMC8293779
doi:10.1002/ece3.7769
PMID:34306638
Distribution of adenylyl cyclase/cAMP phosphodiesterase gene, CAPE, in streptophytes reproducing via motile sperm Yamamoto C, Takahashi F, Ooe Y, Shirahata H, Shibata A, Kasahara M Sci Rep 12-May-2021
PMCID:PMC8115329
doi:10.1038/s41598-021-89539-z
PMID:33980894
Local patterns of arbuscular mycorrhizal fungal diversity and community structure in a natural Toona ciliata var. pubescens forest in South Central China Pan J, Wang Q, Guo X, Jiang X, Cheng Q, Fu L, Liu W, Zhang L PeerJ 03-May-2021
PMCID:PMC8101450
doi:10.7717/peerj.11331
PMID:33987014
Molecular evolution and SSRs analysis based on the chloroplast genome of Callitropsis funebris Ping J, Feng P, Li J, Zhang R, Su Y, Wang T Ecol Evol 20-Mar-2021
PMCID:PMC8093713
doi:10.1002/ece3.7381
PMID:33976848
Characterization and Development of Microsatellite Markers in Pseudotaxus chienii (Taxaceae) Based on Transcriptome Sequencing Xu R, Wang Z, Su Y, Wang T Front Genet 15-Oct-2020
PMCID:PMC7593448
doi:10.3389/fgene.2020.574304
PMID:33193679
A computer-aided method for identifying the presence of softwood growth ring boundaries Lin Q, He T, Sun Y, He X, Qiu J PLoS One 18-Sep-2020
PMCID:PMC7500654
doi:10.1371/journal.pone.0235727
PMID:32946443
Characteristics of Microsatellites Mined from Transcriptome Data and the Development of Novel Markers in Paeonia lactiflora Wan Y, Zhang M, Hong A, Zhang Y, Liu Y Genes (Basel) 19-Feb-2020
PMCID:PMC7073652
doi:10.3390/genes11020214
PMID:32092852

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidic Acid 10467 Click to see CCCCCCCCCCCCCCCCCCCC(=O)O 312.50 unknown via CMAUP database
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown via CMAUP database
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown via CMAUP database
Hexacosanoic acid 10469 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 396.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aS,10aS)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-ol 40522879 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)O)C 272.40 unknown via CMAUP database
(1R,4aS,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid 7075030 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown via CMAUP database
(1R,4aS,9R,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1,9-diol 21604174 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)O)C 288.40 unknown via CMAUP database
(1R,4aS,9R,10aR)-9-hydroxy-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carbaldehyde 10425915 Click to see CC1(CCCC2(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)C)C=O 316.40 unknown via CMAUP database
(1R,4aS,9S,10aR)-1-(hydroxymethyl)-7-(1-hydroxy-1-methyl-ethyl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-9-ol 3009626 Click to see CC1(CCCC2(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)C)CO 318.40 unknown via CMAUP database
(1R,4aS,9S,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1,9-diol 100982592 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)O)C 288.40 unknown via CMAUP database
(1S,4aS,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-ol 26183496 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)O)C 272.40 unknown via CMAUP database
(1S,4aS,10aS)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-ol 26183495 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)O)C 272.40 unknown via CMAUP database
(2R,3R)-1-[(1S,3R,4aS,5S,8aR)-3-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-4-ene-2,3-diol 163024729 Click to see CC1(CCCC2(C1CC(C(=C)C2CC(C(C)(C=C)O)O)O)C)CO 338.50 unknown https://doi.org/10.1002/HLCA.200790123
1-[3-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-4-ene-2,3-diol 163024728 Click to see CC1(CCCC2(C1CC(C(=C)C2CC(C(C)(C=C)O)O)O)C)CO 338.50 unknown https://doi.org/10.1002/HLCA.200790123
15-Hydroxy-7-oxodehydroabietic acid 14017925 Click to see CC12CCCC(C1CC(=O)C3=C2C=CC(=C3)C(C)(C)O)(C)C(=O)O 330.40 unknown via CMAUP database
15-Hydroxydehydroabietic Acid 14487943 Click to see CC12CCCC(C1CCC3=C2C=CC(=C3)C(C)(C)O)(C)C(=O)O 316.40 unknown via CMAUP database
15,18-Dihydroxyabieta-8,11,13-trien-7-one 3009631 Click to see CC1(CCCC2(C1CC(=O)C3=C2C=CC(=C3)C(C)(C)O)C)CO 316.40 unknown via CMAUP database
18-Nor-4,15-dihydroxyabieta-8,11,13-trien-7-one 3009629 Click to see CC12CCCC(C1CC(=O)C3=C2C=CC(=C3)C(C)(C)O)(C)O 302.40 unknown via CMAUP database
18-Norabieta-8,11,13-trien-4-ol 15605917 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)O)C 272.40 unknown via CMAUP database
7-Oxodehydroabietinol 15715176 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)CO)C 300.40 unknown via CMAUP database
7alpha-Hydroxydehydroabieticacid 13370053 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C(=O)O)C 316.40 unknown via CMAUP database
7alpha,15-Dihydroxydehydroabietic acid 12047563 Click to see CC12CCCC(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)(C)C(=O)O 332.40 unknown via CMAUP database
7Beta-Hydroxydehydroabietic Acid 13370052 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C(=O)O)C 316.40 unknown via CMAUP database
7beta,15-Dihydroxydehydroabietic acid 21626423 Click to see CC12CCCC(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)(C)C(=O)O 332.40 unknown via CMAUP database
Aquilarabietic acid H 71578077 Click to see CC(=C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C(=O)O)C 314.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(E)-4-[(1R,3S,4aR,5R,8aS)-3-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]but-3-en-2-one 102472834 Click to see CC(=O)C=CC1C(=C)C(CC2C1(CCCC2(C)CO)C)O 292.40 unknown https://doi.org/10.1002/HLCA.200790123
4-[3-hydroxy-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]but-3-en-2-one 162945259 Click to see CC(=O)C=CC1C(=C)C(CC2C1(CCCC2(C)CO)C)O 292.40 unknown https://doi.org/10.1002/HLCA.200790123
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, octadecyl ester 149044 Click to see CCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 446.70 unknown via CMAUP database
Docosylferulate 54370069 Click to see CCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 502.80 unknown via CMAUP database
Hexacosyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 20980932 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 558.90 unknown via CMAUP database
Icosyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 149045 Click to see CCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 474.70 unknown via CMAUP database
Tetracosyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 54412038 Click to see CCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 530.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Pinobanksin 73202 Click to see C1=CC=C(C=C1)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
3,5-Dimethoxystilbene 5316874 Click to see COC1=CC(=CC(=C1)C=CC2=CC=CC=C2)OC 240.30 unknown via CMAUP database
Cis-3,5-Dimethoxystilbene 13556468 Click to see COC1=CC(=CC(=C1)C=CC2=CC=CC=C2)OC 240.30 unknown via CMAUP database
Pinosylvin methyl ether 5281719 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2 226.27 unknown via CMAUP database

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