Sambucus williamsii - Unknown
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Internal ID UUID64405aeb40d4f597296047
Scientific name Sambucus williamsii
Authority Hance
First published in Ann. Sci. Nat., Bot. , sér. 5, 5: 217 (1866)

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Synonyms Top

Scientific name Authority First published in
Sambucus microsperma Nakai Kamik.-Tennenk.-Chosahok. : 40 (1928)
Sambucus latipinna Nakai Bot. Mag. (Tokyo) 30: 290 (1916)
Sambucus barbinervis Nakai Bot. Mag. (Tokyo) 40: 477 (1926)
Sambucus sieboldiana var. buergeriana Nakai J. Coll. Sci. Imp. Univ. Tokyo 42(Art. 2): 9 (1921)
Sambucus junnanica J.J.Vassil. Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 8: 200 (1940)
Sambucus peninsularis Kitag. Rep. Inst. Sci. Res. Manchoukuo 3(App. 1): 409 (1939)
Sambucus potaninii J.J.Vassil. Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 8: 199 (1940)
Sambucus racemosa subsp. manshurica (Kitag.) Vorosch. Florist. Issl. Razn. Raionakh SSSR : 192 (1985)
Sambucus foetidissima f. flava Skvortsov & W.Wang Ill. Fl. Lign. Pl. N.-E. China 567 1955
Sambucus manshurica Kitag. Rep. Inst. Sci. Res. Manchoukuo 4: 117 (1940)
Sambucus foetidissima Nakai Rep. Exped. Manchoukuo Sect. IV 1: 12 (1934)
Sambucus latipinna var. pendula Skv. Ill. Man. Woody Pl. N.-E. Forest. Inst. 576 1955
Sambucus buergeriana (Nakai) Blume ex Nakai Bot. Mag. (Tokyo) 40: 474 (1926)

Common names Top

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Language Common/alternative name
lzh 接骨木
Chinese 接骨木花
Chinese 九节风
Chinese 欧接骨木
Chinese 接骨木
Chinese 木蒴藋
Chinese 续骨草
Chinese 接骨木叶
Chinese 接骨木根
Chinese 扦扦活

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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 North-central
      • China South-central
      • China Southeast
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Primorye
    • Siberia
      • Buryatiya
      • Chita
      • Irkutsk
      • Yakutskiya

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001290841
UNII XS87VM9688
Tropicos 6000520
KEW urn:lsid:ipni.org:names:149409-1
The Plant List tro-6000520
Open Tree Of Life 589181
NCBI Taxonomy 180062
IPNI 149409-1
iNaturalist 538220
GBIF 7272554
USDA GRIN 33007
CMAUP NPO17434

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
Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X J Ethnobiol Ethnomed 23-Feb-2024
PMCID:PMC10893717
doi:10.1186/s13002-024-00656-1
PMID:38395900
Exploring the mechanism of traditional Chinese medicine in regulating gut-derived 5-HT for osteoporosis treatment Sun K, Wang Y, Du J, Wang Y, Liu B, Li X, Zhang X, Xu X Front Endocrinol (Lausanne) 17-Oct-2023
PMCID:PMC10616894
doi:10.3389/fendo.2023.1234683
PMID:37916145
Modern drug discovery using ethnobotany: A large-scale cross-cultural analysis of traditional medicine reveals common therapeutic uses Domingo-Fernández D, Gadiya Y, Mubeen S, Bollerman TJ, Healy MD, Chanana S, Sadovsky RG, Healey D, Colluru V iScience 25-Aug-2023
PMCID:PMC10494464
doi:10.1016/j.isci.2023.107729
PMID:37701812
Evaluation of How Methacrylate Gelatin Hydrogel Loaded with Ximenia americana L. Extract (Steam Bark) Effects Bone Repair Activity Using Rats as Models Leal SS, Gusmão GO, Uchôa VT, Figueiredo-Silva J, Pinto LS, Tim CR, Assis L, Maia-Filho AL, de Oliveira RA, Lobo AO, Pavinatto A J Funct Biomater 23-Aug-2023
PMCID:PMC10531560
doi:10.3390/jfb14090438
PMID:37754851
Identification of the Microbial Transformation Products of Secoisolariciresinol Using an Untargeted Metabolomics Approach and Evaluation of the Osteogenic Activities of the Metabolites Yu WX, Tang HH, Ye JJ, Xiao HH, Lam CY, Shum TF, Sun ZK, Li YZ, Zang XY, Du WC, Zhang JP, Kong TH, Zhou LP, Chiou JC, Kung CF, Mok KW, Hu J, Wong MS Molecules 29-Jul-2023
PMCID:PMC10420892
doi:10.3390/molecules28155742
PMID:37570714
Comparative chloroplast genome analysis of Sambucus L. (Viburnaceae): inference for phylogenetic relationships among the closely related Sambucus adnata Wall. ex DC Sambucus javanica Blume Waswa EN, Mkala EM, Odago WO, Amenu SG, Mutinda ES, Muthui SW, Ding SX, Hu GW, Wang QF Front Plant Sci 16-Jun-2023
PMCID:PMC10313135
doi:10.3389/fpls.2023.1179510
PMID:37396648
High‐molecular‐weight DNA extraction for long‐read sequencing of plant genomes: An optimization of standard methods Kang M, Chanderbali A, Lee S, Soltis DE, Soltis PS, Kim S Appl Plant Sci 13-Jun-2023
PMCID:PMC10278927
doi:10.1002/aps3.11528
PMID:37342161
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
Antioxidant Activity of Crocodile Oil (Crocodylus siamensis) on Cognitive Function in Rats Srisuksai K, Parunyakul K, Santativongchai P, Phaonakrop N, Roytrakul S, Tulayakul P, Fungfuang W Foods 13-Feb-2023
PMCID:PMC9956878
doi:10.3390/foods12040791
PMID:36832865
Ontogeny influences tree growth response to soil fertility and neighbourhood crowding in an old-growth temperate forest Ren J, Fang S, Wang QW, Liu H, Lin F, Ye J, Hao Z, Wang X, Fortunel C Ann Bot 01-Dec-2022
PMCID:PMC10457036
doi:10.1093/aob/mcac146
PMID:36454654
Effects of a mouthwash containing Lespedeza cuneata extract on risk of dental caries: a randomized, placebo-controlled clinical trial Kim YR, Nam SH Sci Rep 01-Dec-2022
PMCID:PMC9715620
doi:10.1038/s41598-022-25162-w
PMID:36456715
The Lignan-Rich Fraction from Sambucus williamsii Hance Exerts Bone Protective Effects via Altering Circulating Serotonin and Gut Microbiota in Rats Xiao HH, Zhu YX, Lu L, Zhou LP, Poon CC, Chan CO, Wang LJ, Cao S, Yu WX, Wong KY, Mok DK, Wong MS Nutrients 08-Nov-2022
PMCID:PMC9692752
doi:10.3390/nu14224718
PMID:36432403
Antimicrobial activities and mechanisms of extract and components of herbs in East Asia Liang J, Huang X, Ma G RSC Adv 12-Oct-2022
PMCID:PMC9554739
doi:10.1039/d2ra02389j
PMID:36320733
Insight into Recent Progress and Perspectives in Improvement of Antioxidant Machinery upon PGPR Augmentation in Plants under Drought Stress: A Review Gowtham HG, Singh SB, Shilpa N, Aiyaz M, Nataraj K, Udayashankar AC, Amruthesh KN, Murali M, Poczai P, Gafur A, Almalki WH, Sayyed RZ Antioxidants (Basel) 07-Sep-2022
PMCID:PMC9495777
doi:10.3390/antiox11091763
PMID:36139837
Extraction, isolation, structural characterization, and antioxidant activity of polysaccharides from elderberry fruit Wei X, Yao J, Wang F, Wu D, Zhang R Front Nutr 19-Jul-2022
PMCID:PMC9343709
doi:10.3389/fnut.2022.947706
PMID:35928842

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 / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
cis-Coniferyl alcohol 1549094 Click to see COC1=C(C=CC(=C1)C=CCO)O 180.20 unknown via CMAUP database
Coniferyl alcohol 1549095 Click to see COC1=C(C=CC(=C1)C=CCO)O 180.20 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
(-)-Lyoniresinol 9888378 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)CO 420.50 unknown via CMAUP database
(+)-Lyoniresinol 11711453 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)CO 420.50 unknown via CMAUP database
(2R,3R,4R)-4-(4-hydroxy-3-methoxy-phenyl)-2,3-bis(hydroxymethyl)-7-methoxy-tetralin-6-ol 11631864 Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown via CMAUP database
5-Methoxy-isolarisiresinol, (+)- 21574504 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C=C23)O)OC)CO)CO 390.40 unknown via CMAUP database
Isolariciresinol, (+)- 160521 Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown via CMAUP database
Isoolivil 5316262 Click to see COC1=C(C=C2C(C(C(CC2=C1)(CO)O)CO)C3=CC(=C(C=C3)O)OC)O 376.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(-) Syringaresinol 332426 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
(-)-Pinoresinol 12309636 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown via CMAUP database
(-)-Syringaresinol 11604108 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
4-[(3R,3aR,6R,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 12309637 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown via CMAUP database
4-[6-(4-Hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 234817 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257477/
CID 17750970 17750970 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown via CMAUP database
Epipinoresinol 637584 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown via CMAUP database
Episyringaresinol 12309694 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257477/
Syringaresinol 100067 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
Syringaresinol, (+)- 443023 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(-)-Lariciresinol 23815394 Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown via CMAUP database
Lariciresinol 332427 Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown via CMAUP database
Tetrahydro-2-(4-hydroxy-3-methoxyphenyl)-4-((4-hydroxy-3-methoxyphenyl)methyl)-3-furanmethanol 134203 Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O 360.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(E,8R,11S,12R)-8,11,12-trihydroxyoctadec-9-enoic acid 162989952 Click to see CCCCCCC(C(C=CC(CCCCCCC(=O)O)O)O)O 330.50 unknown https://doi.org/10.1248/CPB.54.676
(E,8R,11S,12S)-8,11,12-trihydroxyoctadec-9-enoic acid 162989953 Click to see CCCCCCC(C(C=CC(CCCCCCC(=O)O)O)O)O 330.50 unknown https://doi.org/10.1248/CPB.54.676
8,11,12-Trihydroxyoctadec-9-enoic acid 78385598 Click to see CCCCCCC(C(C=CC(CCCCCCC(=O)O)O)O)O 330.50 unknown https://doi.org/10.1248/CPB.54.676
Tianshic acid 5321949 Click to see CCCCCCC(C(C=CC(CCCCCCC(=O)O)O)O)O 330.50 unknown https://doi.org/10.1248/CPB.54.676
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
methyl (E,8R,11S,12S)-8,11,12-trihydroxyoctadec-9-enoate 162927921 Click to see CCCCCCC(C(C=CC(CCCCCCC(=O)OC)O)O)O 344.50 unknown https://doi.org/10.1248/CPB.54.676
Methyl 8,11,12-trihydroxyoctadec-9-enoate 73067298 Click to see CCCCCCC(C(C=CC(CCCCCCC(=O)OC)O)O)O 344.50 unknown https://doi.org/10.1248/CPB.54.676
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1S,4S,4aS,6S,8aS)-6-(3-hydroxyprop-1-en-2-yl)-4,8a-dimethyl-1,2,3,4a,5,6,7,8-octahydronaphthalene-1,4-diol 162904722 Click to see CC12CCC(CC1C(CCC2O)(C)O)C(=C)CO 254.36 unknown https://doi.org/10.1248/CPB.54.676
6-(3-Hydroxyprop-1-en-2-yl)-4,8a-dimethyl-1,2,3,4a,5,6,7,8-octahydronaphthalene-1,4-diol 73066948 Click to see CC12CCC(CC1C(CCC2O)(C)O)C(=C)CO 254.36 unknown https://doi.org/10.1248/CPB.54.676
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)icosahydro-1H-cyclopenta[a]chrysen-9-ol 51340201 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see C1=CC(=CC=C1C=O)O 122.12 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
D-ascorbic acid 54690394 Click to see C(C(C1C(=C(C(=O)O1)O)O)O)O 176.12 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(-)-Dehydrodiconiferyl Alcohol 11078843 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CCO 358.40 unknown via CMAUP database
(+)-Balanophonin 23252258 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CC=O 356.40 unknown via CMAUP database
(+)-Dehydrodiconiferyl alcohol 11824478 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CCO 358.40 unknown via CMAUP database
4-[3-(Hydroxymethyl)-5-(3-hydroxypropyl)-7-methoxy-2,3-dihydrobenzofuran-2-yl]-2-methoxy-phenol 4365980 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCO 360.40 unknown via CMAUP database
5-Methoxy-trans-dihydrodehydrodiconiferyl alcohol 56838440 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)O)OC)CCCO 390.40 unknown via CMAUP database
Dehydrodiconiferyl alcohol 5372367 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CCO 358.40 unknown via CMAUP database
Dihydrodehydroconiferyl alcohol, (7R,8S)-(-)- 5274623 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCO 360.40 unknown via CMAUP database
Dihydrodehydrodiconiferyl alcohol 384679 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCO 360.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Acide tannique [French] 16133892 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2=CC(=CC(=C2O)O)C(=O)OCC3C(C(C(C(O3)OC(=O)C4=CC(=C(C(=C4)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6)OC(=O)C7=CC(=C(C(=C7)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)OC(=O)C9=CC(=C(C(=C9)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O 1701.20 unknown via CMAUP database

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