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Bridelia balansae

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643ffa22012e6120085490
Scientific name Bridelia balansae
Authority Tutcher
First published in J. Linn. Soc., Bot. 37: 66 (1905)

Description Top

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Synonyms Top

Scientific name Authority First published in
Bridelia kawakamii Hayata J. Coll. Sci. Imp. Univ. Tokyo 22: 362 (1906)
Bridelia pachinensis Hayata J. Coll. Sci. Imp. Univ. Tokyo 22: 362 (1906)

Common names Top

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Language Common/alternative name
Chinese 禾串树
Chinese 刺杜密
Chinese 刺楠
Chinese 禾串树叶
Chinese 大叶逼迫子
Chinese 禾串土蜜树

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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No germination or propagation data was added yet.

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
      • Nansei-shoto
      • Taiwan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000416150
Tropicos 50002069
KEW urn:lsid:ipni.org:names:340128-1
The Plant List kew-24479
Open Tree Of Life 637987
NCBI Taxonomy 577015
IUCN Red List 147632404
IPNI 340128-1
iNaturalist 741461
GBIF 3076230
EOL 1149099

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
Antibacterial, Antifungal, and Antiviral Bioactive Compounds from Natural Products Song X Molecules 11-Feb-2024
PMCID:PMC10892233
doi:10.3390/molecules29040825
PMID:38398577
Isolation and Anticancer Progression Evaluation of the Chemical Constituents from Bridelia balansae Tutcher Zhao L, Xie WJ, Du YX, Xia YX, Liu KL, Ku CF, Ou Z, Wang MZ, Zhang HJ Molecules 21-Aug-2023
PMCID:PMC10457964
doi:10.3390/molecules28166165
PMID:37630417
Revealing the relative importance among plant species, slope positions, and soil types on rhizosphere microbial communities in northern tropical karst and non-karst seasonal rainforests of China Zhang X, Wang B, Chen T, Guo Y, Li X Front Microbiol 17-Apr-2023
PMCID:PMC10149764
doi:10.3389/fmicb.2023.1103550
PMID:37138641
Shift of Host Range for the Immature Stages of the Lanternfly, Pyrops watanabei (Matsumura) (Hemiptera, Fulgoridae) Native to Taiwan Hsu MH, Yang YL, Wu ML, Wang LJ Insects 12-Sep-2022
PMCID:PMC9500622
doi:10.3390/insects13090826
PMID:36135527
Bridelia ferruginea Benth.; An ethnomedicinal, phytochemical, pharmacological and toxicological review Yeboah GN, Owusu FW, Archer MA, Kyene MO, Kumadoh D, Ayertey F, Mintah SO, Atta-Adjei Junior P, Appiah AA Heliyon 23-Aug-2022
PMCID:PMC9445295
doi:10.1016/j.heliyon.2022.e10366
PMID:36082325
Tree regeneration characteristics in limestone forests of the Cat Ba National Park, Vietnam Pham VV, Ammer C, Annighöfer P, Heinrichs S BMC Ecol Evol 15-Jan-2022
PMCID:PMC8761296
doi:10.1186/s12862-021-01957-9
PMID:35033001
Mutualism favours higher host specificity than does antagonism in plant–herbivore interaction Kawakita A, Okamoto T, Goto R, Kato M Proc Biol Sci 28-Apr-2010
PMCID:PMC2981980
doi:10.1098/rspb.2010.0355
PMID:20427340
Bridelioside, a new lignan glycoside from Bridelia glauca Bl. f. balansae (Tucht.) Hatusima Etsuko Sueyoshi, Hui Liu, Katsuyoshi Matsunami, Hideaki Otsuka, Takakazu Shinzato, Mitsunori Aramoto, Yoshio Takeda Springer Science and Business Media LLC 17-Jul-2007
doi:10.1007/S11418-007-0178-Z
New Long‐Chain Esters and Adenine Analogs from the Leaves of Formosan <i>Bridelia balansae</i> Yeh‐Hsin Tsai, Ih‐Sheng Chen, Ian‐Lih Tsai Wiley 05-Aug-2003
doi:10.1002/HLCA.200390198

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
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3S,4S,5S)-2-[[(2R,3R,4S)-6-hydroxy-4-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]oxane-3,4,5-triol 163067942 Click to see COC1=C(C=C2C(C(C(CC2=C1)COC3C(C(C(CO3)O)O)O)CO)C4=CC(=C(C=C4)O)OC)O 492.50 unknown https://doi.org/10.1007/S11418-007-0178-Z
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Wax esters / Wax monoesters
[(E)-3-methylhexadec-2-enyl] (10S,12R)-10,12,15-trimethylhexadecanoate 163093201 Click to see CCCCCCCCCCCCCC(=CCOC(=O)CCCCCCCCC(C)CC(C)CCC(C)C)C 534.90 unknown https://doi.org/10.1002/HLCA.200390198
[(E)-3-methylhexadec-2-enyl] (6S,8R)-6,8,11-trimethyldodecanoate 162885238 Click to see CCCCCCCCCCCCCC(=CCOC(=O)CCCCC(C)CC(C)CCC(C)C)C 478.80 unknown https://doi.org/10.1002/HLCA.200390198
[(E)-3-methylhexadec-2-enyl] 6,8,11-trimethyldodecanoate 101258553 Click to see CCCCCCCCCCCCCC(=CCOC(=O)CCCCC(C)CC(C)CCC(C)C)C 478.80 unknown https://doi.org/10.1002/HLCA.200390198
3-Methylhexadec-2-enyl 10,12,15-trimethylhexadecanoate 163093200 Click to see CCCCCCCCCCCCCC(=CCOC(=O)CCCCCCCCC(C)CC(C)CCC(C)C)C 534.90 unknown https://doi.org/10.1002/HLCA.200390198
3-Methylhexadec-2-enyl 6,8,11-trimethyldodecanoate 162885237 Click to see CCCCCCCCCCCCCC(=CCOC(=O)CCCCC(C)CC(C)CCC(C)C)C 478.80 unknown https://doi.org/10.1002/HLCA.200390198
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(8-Hydroperoxy-3,10,10-trimethyl-7-methylidenecycloundec-3-en-1-yl) 3-(4-hydroxyphenyl)prop-2-enoate 75058032 Click to see CC1=CCCC(=C)C(CC(CC(C1)OC(=O)C=CC2=CC=C(C=C2)O)(C)C)OO 400.50 unknown https://doi.org/10.1002/HLCA.200390198
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(13S,14R)-4,4,10,13,14-pentamethyl-17-(6-methyl-5-methylidenehept-1-en-2-yl)-1,2,5,6,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 101258555 Click to see CC(C)C(=C)CCC(=C)C1CCC2(C1(CCC3C2CCC4C3(CCC(=O)C4(C)C)C)C)C 438.70 unknown https://doi.org/10.1002/HLCA.200390198
(5R,8R,9S,10S,13S,14R,17R)-4,4,10,13,14-pentamethyl-17-(6-methyl-5-methylidenehept-1-en-2-yl)-1,2,5,6,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 163188520 Click to see CC(C)C(=C)CCC(=C)C1CCC2(C1(CCC3C2CCC4C3(CCC(=O)C4(C)C)C)C)C 438.70 unknown https://doi.org/10.1002/HLCA.200390198
4,4,10,13,14-Pentamethyl-17-(6-methyl-5-methylidenehept-1-en-2-yl)-1,2,5,6,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 163035762 Click to see CC(C)C(=C)CCC(=C)C1CCC2(C1(CCC3C2CCC4C3(CCC(=O)C4(C)C)C)C)C 438.70 unknown https://doi.org/10.1002/HLCA.200390198
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid imides / N-substituted carboxylic acid imides
5-(3-methylbut-2-enyl)-1H-pyrrolo[3,4-d]imidazole-4,6-dione 85913694 Click to see CC(=CCN1C(=O)C2=C(C1=O)N=CN2)C 205.21 unknown https://doi.org/10.1002/HLCA.200390198
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines
1-(3-methylbut-2-enyl)purin-6-amine 101596827 Click to see CC(=CCN1C=NC2=NC=NC2=C1N)C 203.24 unknown https://doi.org/10.1002/HLCA.200390198
3-(3-methylbut-2-enyl)purin-6-amine 45070 Click to see CC(=CCN1C=NC(=C2C1=NC=N2)N)C 203.24 unknown https://doi.org/10.1002/HLCA.200390198
9-(3-Methyl-but-2-enyl)-9H-purin-6-ylamine 10655770 Click to see CC(=CCN1C=NC2=C(N=CN=C21)N)C 203.24 unknown https://doi.org/10.1002/HLCA.200390198
Adenine 190 Click to see C1=NC2=NC=NC(=C2N1)N 135.13 unknown https://doi.org/10.1002/HLCA.200390198
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines / 6-alkylaminopurines
N-(3-Methylbut-2-EN-1-YL)-9H-purin-6-amine 92180 Click to see CC(=CCNC1=NC=NC2=C1NC=N2)C 203.24 unknown https://doi.org/10.1002/HLCA.200390198

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