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Internal ID UUID64405a6cc36fa943932775
Scientific name Knema elegans
Authority Warb.
First published in Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 68: 615 (1897)

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Synonyms Top

Scientific name Authority First published in
Myristica elegans Pierre ex Warb. Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 68: 615 (1897)
Knema siamensis Warb. Repert. Spec. Nov. Regni Veg. 16: 254 (1919)

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Language Common/alternative name
Chinese 假广子

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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-0001285888
Tropicos 50333335
KEW urn:lsid:ipni.org:names:585854-1
The Plant List tro-50333335
Open Tree Of Life 5700082
NCBI Taxonomy 1679394
IPNI 585854-1
GBIF 3743588

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
Complete chloroplast genome sequences of Myristicaceae species with the comparative chloroplast genomics and phylogenetic relationships among them Mao C, Zhang F, Li X, Yang T, Zhao Q, Wu Y PLoS One 20-Mar-2023
PMCID:PMC10027215
doi:10.1371/journal.pone.0281042
PMID:36940204
Seed Size Variation of Trees and Lianas in a Tropical Forest of Southeast Asia: Allometry, Phylogeny, and Seed Trait - Plant Functional Trait Relationships Pothasin P, Paradis E, Brockelman WY, Nathalang A, Khemrugka T, Lomwong N, Thripob P, Saenprasert R, Chanthorn W Front Plant Sci 17-May-2022
PMCID:PMC9165448
doi:10.3389/fpls.2022.852167
PMID:35668813
Antimicrobial Properties of Compounds Isolated from Syzygium malaccense (L.) Merr. and L.M. Perry and Medicinal Plants Used in French Polynesia Quenon C, Hennebelle T, Butaud JF, Ho R, Samaillie J, Neut C, Lehartel T, Rivière C, Siah A, Bonneau N, Sahpaz S, Anthérieu S, Lebegue N, Raharivelomanana P, Roumy V Life (Basel) 14-May-2022
PMCID:PMC9147835
doi:10.3390/life12050733
PMID:35629400
Acyl–Acyl Carrier Protein Desaturases and Plant Biotic Interactions Kazaz S, Miray R, Baud S Cells 18-Mar-2021
PMCID:PMC8002970
doi:10.3390/cells10030674
PMID:33803674
Complete chloroplast sequence of Fenerivia ghesquiereana (Annonaceae): a rare and endemic tree from Madagascar Wang Y, Cvetković T, Aritsara AN, Carrion AD, Strijk JS Mitochondrial DNA B Resour 16-Jan-2021
PMCID:PMC7836981
doi:10.1080/23802359.2020.1855604
PMID:33542954
The complete chloroplast genome sequence of Knema conferta (Myristicaceae) Zhang FL, Yang T, Mao CL, Li XQ, Zhao Q, Wu Y Mitochondrial DNA B Resour 13-Nov-2020
PMCID:PMC7671699
doi:10.1080/23802359.2020.1835574
PMID:33367085
The complete chloroplast genome sequence of Knema elegans (Myristicaceae) Mao CL, Li XQ, Zhang FL, Yang T, Zhao Q, Wu Y Mitochondrial DNA B Resour 20-Jan-2020
PMCID:PMC7748504
doi:10.1080/23802359.2020.1715278
PMID:33366723
Targeting DNA Polymerase β for Therapeutic Intervention Goellner EM, Svilar D, Almeida KH, Sobol RW Curr Mol Pharmacol 01-Jan-2012
PMCID:PMC3894524
PMID:22122465
Monocyclic Phenolic Acids; Hydroxy- and Polyhydroxybenzoic Acids: Occurrence and Recent Bioactivity Studies Khadem S, Marles RJ Molecules 08-Nov-2010
PMCID:PMC6259451
doi:10.3390/molecules15117985
PMID:21060304
(+)-Myristinins A and D from Knema elegans, which inhibit DNA polymerase beta and cleave DNA. Deng JZ, Starck SR, Li S, Hecht SM J Nat Prod 01-Nov-2005
doi:10.1021/NP058064G
PMID:16309311
Alkyl and phenylalkyl anacardic acids from Knema elegans seed oil. Spencer GF, Tjarks LW, Kleiman R J Nat Prod 01-Nov-1980
doi:10.1021/NP50012A005
PMID:20707395

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Anacardic acid 167551 Click to see CCCCCCCCCCCCCCCC1=C(C(=CC=C1)O)C(=O)O 348.50 unknown https://doi.org/10.1021/NP50012A005
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Cardanol 11266523 Click to see C=CCC=CCC=CCCCCCCCC1=CC(=CC=C1)O 298.50 unknown https://doi.org/10.1021/NP50012A005
Cardanolmonoene 5315696 Click to see CCCCCCC=CCCCCCCCC1=CC(=CC=C1)O 302.50 unknown https://doi.org/10.1021/NP50012A005
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(-)-Galbacin 11175182 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC5=C(C=C4)OCO5)C 340.40 unknown https://doi.org/10.1021/NP50012A005
Galbacin 234441 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC5=C(C=C4)OCO5)C 340.40 unknown https://doi.org/10.1021/NP50012A005
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
(+)-Myristinin A 497359 Click to see CCCCCCCCCCCC(=O)C1=C(C=C(C(=C1O)C2CC(OC3=C2C=CC(=C3)O)C4=CC=C(C=C4)O)O)O 548.70 unknown https://doi.org/10.1021/NP058064G
(+)-Myristinin D 497362 Click to see C1C(C2=C(C=C(C=C2)O)OC1C3=CC=C(C=C3)O)C4=C(C(=C(C=C4O)O)C(=O)CCCCCCCCC5=CC=CC=C5)O 582.70 unknown https://doi.org/10.1021/NP058064G
1-[2,4,6-trihydroxy-3-[7-hydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]phenyl]dodecan-1-one 132031 Click to see CCCCCCCCCCCC(=O)C1=C(C=C(C(=C1O)C2CC(OC3=C2C=CC(=C3)O)C4=CC=C(C=C4)O)O)O 548.70 unknown https://doi.org/10.1021/NP058064G
9-phenyl-1-[2,4,6-trihydroxy-3-[(2R,4R)-7-hydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]phenyl]nonan-1-one 10054015 Click to see C1C(C2=C(C=C(C=C2)O)OC1C3=CC=C(C=C3)O)C4=C(C(=C(C=C4O)O)C(=O)CCCCCCCCC5=CC=CC=C5)O 582.70 unknown https://doi.org/10.1021/NP058064G
9-phenyl-1-[2,4,6-trihydroxy-3-[7-hydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]phenyl]nonan-1-one 45360379 Click to see C1C(C2=C(C=C(C=C2)O)OC1C3=CC=C(C=C3)O)C4=C(C(=C(C=C4O)O)C(=O)CCCCCCCCC5=CC=CC=C5)O 582.70 unknown https://doi.org/10.1021/NP058064G
Myristinin B 497361 Click to see CCCCCCCCCCCC(=O)C1=C(C=C(C(=C1O)C2CC(OC3=C2C=CC(=C3)O)C4=CC=C(C=C4)O)O)O 548.70 unknown https://doi.org/10.1021/NP058064G

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