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Details Top

Internal ID UUID644047437591b855102523
Scientific name Litsea acutivena
Authority Hayata
First published in Icon. Pl. Formosan. 5: 163 (1915)

Description Top

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Synonyms Top

Scientific name Authority First published in
Litsea naufoensis Hayata ex Kamik. Trans. Nat. Hist. Soc. Formosa 25: 240 (1935)
Actinodaphne acutivena (Hayata) Nakai J. Jap. Bot. 14: 191 (1938)
Actinodaphne nakaii (Hayata) Tang S.Liu & J.C.Liao Sci. Ann. Taiwan Mus. 14: 7 1971
Litsea nakaii Hayata Icon. Pl. Formosan. 5: 168 (1915)
Tetradenia acutivena (Hayata) Makino & Nemoto Fl. Japan., ed. 2 (Makino & Nemoto) 373. 1931
Litsea elongata var. acutivena (Hayata) S.S.Ying et in Mem. Coll. Agric. Nation. Taiwan Univ. 25(1): 99 (April 1985):.
Tetradenia nakaii (Hayata) Makino & Nemoto Fl. Japan., ed. 2 (Makino & Nemoto) 375. 1931

Common names Top

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Language Common/alternative name
Chinese 尖叶木姜子
Chinese 尖脉木姜子
Chinese 銳脈木薑子
Chinese 毛叉树
Chinese 锐脉木姜子
Chinese 长果木姜子
Chinese 黄桂

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
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Taiwan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001070638
Tropicos 17801731
KEW urn:lsid:ipni.org:names:465490-1
The Plant List tro-17801731
Open Tree Of Life 18346
NCBI Taxonomy 344083
IPNI 465490-1
iNaturalist 736723
GBIF 4179081
EOL 5397143

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 complete plastid genome of a medicinal tree Lindera chienii Cheng 1934 (Lauraceae: Laureae) Liu C, Chen H, Cai J, Han L Mitochondrial DNA B Resour 04-Jul-2022
PMCID:PMC9262354
doi:10.1080/23802359.2022.2093675
PMID:35814174
Plastid genome evolution of a monophyletic group in the subtribe Lauriineae (Laureae, Lauraceae) Liu C, Chen HH, Tang LZ, Khine PK, Han LH, Song Y, Tan YH Plant Divers 14-Dec-2021
PMCID:PMC9363652
doi:10.1016/j.pld.2021.11.009
PMID:35967258
Conflicting phylogenetic signals in plastomes of the tribe Laureae (Lauraceae) Xiao TW, Xu Y, Jin L, Liu TJ, Yan HF, Ge XJ PeerJ 15-Oct-2020
PMCID:PMC7568859
doi:10.7717/peerj.10155
PMID:33088627
DNA barcoding evaluation and implications for phylogenetic relationships in Lauraceae from China Liu ZF, Ci XQ, Li L, Li HW, Conran JG, Li J PLoS One 17-Apr-2017
PMCID:PMC5393608
doi:10.1371/journal.pone.0175788
PMID:28414813
Phylogenetic congruence between subtropical trees and their associated fungi Liu X, Liang M, Etienne RS, Gilbert GS, Yu S Ecol Evol 26-Oct-2016
PMCID:PMC5167024
doi:10.1002/ece3.2503
PMID:28031793
Chemical constituents and bioactivity of Formosan lauraceous plants Chang HS, Chen IS J Food Drug Anal 05-Jan-2016
PMCID:PMC9339549
doi:10.1016/j.jfda.2015.10.008
PMID:28911577
Chemical Constituents from the Leaves of <i>Litsea Acutivena</i> Ian‐Lih Tsai, Ming‐Jen Cheng, Hsiu‐Wen Hung, Hsin‐I Cheng, Ih‐Sheng Chen Wiley 01-May-2015
doi:10.1002/JCCS.200700071
New cytotoxic butanolides from Litsea acutivena. Cheng HI, Lin WY, Duh CY, Lee KH, Tsai IL, Chen IS J Nat Prod 01-Dec-2001
doi:10.1021/NP0102298
PMID:11754599

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 / Phenols / Methoxyphenols
N-Trans-feruloyltramine 5280537 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown https://doi.org/10.1002/JCCS.200700071
> 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/10.1002/JCCS.200700071
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown https://doi.org/10.1002/JCCS.200700071
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Triacontanol 68972 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO 438.80 unknown https://doi.org/10.1002/JCCS.200700071
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
2-(3-Hydroxy-3,7,11,15-tetramethylhexadecyl)-3,5,6-trimethylcyclohexa-2,5-diene-1,4-dione 24205 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 https://doi.org/10.1002/JCCS.200700071
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 https://doi.org/10.1002/JCCS.200700071
> Lipids and lipid-like molecules / Prenol lipids / Polyprenols
(2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaen-1-ol 11767678 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C)C 699.20 unknown https://doi.org/10.1002/JCCS.200700071
3,7,11,15,19,23,27,31,35,39-Decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaen-1-ol 53439771 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C)C 699.20 unknown https://doi.org/10.1002/JCCS.200700071
Moraprenol 11 375 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C)C)C 767.30 unknown https://doi.org/10.1002/JCCS.200700071
Undecaprenol 5280474 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C)C)C 767.30 unknown https://doi.org/10.1002/JCCS.200700071
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
Alpha-Tocopherol 14985 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown https://doi.org/10.1002/JCCS.200700071
DL-alpha-Tocopherol 2116 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown https://doi.org/10.1002/JCCS.200700071
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
1,3,3-trimethyl-2-[(1E,3E,5E,7E,9E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohexen-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]cyclohexene 152743364 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C 536.90 unknown https://doi.org/10.1002/JCCS.200700071
Beta-Carotene 5280489 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C 536.90 unknown https://doi.org/10.1002/JCCS.200700071
> 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 https://doi.org/10.1002/JCCS.200700071
Super Squalene; trans-Squalene;AddaVax 1105 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1002/JCCS.200700071
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1002/JCCS.200700071
3-Hydroxystigmast-5-en-7-one 160608 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C 428.70 unknown https://doi.org/10.1002/JCCS.200700071
3beta-Hydroxyporiferast-5-en-7-one 14779505 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C 428.70 unknown https://doi.org/10.1002/JCCS.200700071
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1002/JCCS.200700071
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
(2S,3aS,6aR)-6-decylidene-3a-methyl-2-nonyl-6aH-furo[2,3-d][1,3]dioxol-5-one 163065357 Click to see CCCCCCCCCC=C1C2C(OC(O2)CCCCCCCCC)(OC1=O)C 408.60 unknown https://doi.org/10.1002/JCCS.200700071
(2S,3aS,6E,6aR)-6-decylidene-3a-methyl-2-nonyl-6aH-furo[2,3-d][1,3]dioxol-5-one 163190153 Click to see CCCCCCCCCC=C1C2C(OC(O2)CCCCCCCCC)(OC1=O)C 408.60 unknown https://doi.org/10.1002/JCCS.200700071
3-Decylidene-4-hydroxy-5-methoxy-5-methyloxolan-2-one 75216090 Click to see CCCCCCCCCC=C1C(C(OC1=O)(C)OC)O 284.39 unknown https://doi.org/10.1021/NP0102298
Litseakolide D 10446606 Click to see CCCCCCCCCC=C1C(C(OC1=O)(C)OC)O 284.39 unknown https://doi.org/10.1021/NP0102298
Litseakolide E 5316343 Click to see CCCCCCCCCC=C1C(C(OC1=O)(C)OC)O 284.39 unknown https://doi.org/10.1021/NP0102298
Litseakolide F 10107956 Click to see CCCCCCCCCC=C1C(C(OC1=O)(C)OC)O 284.39 unknown https://doi.org/10.1021/NP0102298
Litseakolide G 10424025 Click to see CCCCCCCCCC=C1C(C(OC1=O)(C)OC)O 284.39 unknown https://doi.org/10.1021/NP0102298
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(5S)-5-nonacosyloxolan-2-one 162977811 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC1CCC(=O)O1 492.90 unknown https://doi.org/10.1002/JCCS.200700071
> Organoheterocyclic compounds / Oxolanes
(3E,4S)-3-dodecylidene-4-hydroxy-5-methylideneoxolan-2-one 11097947 Click to see CCCCCCCCCCCC=C1C(C(=C)OC1=O)O 280.40 unknown https://doi.org/10.1021/NP0102298
3-Decylidene-4-hydroxy-5-methylideneoxolan-2-one 72974352 Click to see CCCCCCCCCC=C1C(C(=C)OC1=O)O 252.35 unknown https://doi.org/10.1002/JCCS.200700071
Isolancifolide 14259072 Click to see CCCCCCCCCC=C1C(C(=C)OC1=O)O 252.35 unknown https://doi.org/10.1002/JCCS.200700071
Isolicomolide D 10356328 Click to see CCCCCCCCCCCC=C1C(C(=C)OC1=O)O 280.40 unknown https://doi.org/10.1021/NP0102298
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Dehydroxymethylailanthoidol 10040210 Click to see COC1=CC(=CC2=C1OC(=C2)C3=CC(=C(C=C3)O)OC)C=C 296.30 unknown https://doi.org/10.1021/NP0102298
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
N-feruloyltyramine; Moupinamide 125213 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown https://doi.org/10.1002/JCCS.200700071

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