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Beilschmiedia tsangii

Beilschmiedia tsangii - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID64400c95a1d4b129220208
Scientific name Beilschmiedia tsangii
Authority Merr.
First published in Lingnan Sci. J. 13: 27 (1934)

Description Top

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Synonyms Top

Scientific name Authority First published in
Beilschmiedia formosana C.E.Chang Bull. Taiwan Prov. Pingt. Inst. Agr. 7: 87 1966

Common names Top

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Language Common/alternative name
Chinese 网脉琼楠
Chinese 華河瓊楠
Chinese 牛奶奶果

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

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 Southeast
      • Hainan
    • Eastern Asia
      • Taiwan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000562137
Tropicos 17802322
KEW urn:lsid:ipni.org:names:462970-1
The Plant List kew-2672685
Open Tree Of Life 5699365
NCBI Taxonomy 1603694
IUCN Red List 145295420
IPNI 462970-1
iNaturalist 736729
GBIF 7304706
CMAUP NPO9339

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
Chemical characteristics of the sesquiterpenes and diterpenes from Lauraceae family and their multifaceted health benefits: A review Feng H, Jiang Y, Cao H, Shu Y, Yang X, Zhu D, Shao M Heliyon 07-Dec-2022
PMCID:PMC9801090
doi:10.1016/j.heliyon.2022.e12013
PMID:36590503
Alcohol extracts of Chinese bayberry branch induce S‐phase arrest and apoptosis in HepG2 cells Zheng Y, Yu Z, Li Y, Zhong S, Sun Y, Sun L, Zheng X, Qi X, Zhang S Food Sci Nutr 02-Oct-2022
PMCID:PMC9834848
doi:10.1002/fsn3.3080
PMID:36655066
Lignans: a versatile source of anticancer drugs Mukhija M, Joshi BC, Bairy PS, Bhargava A, Sah AN Beni Suef Univ J Basic Appl Sci 04-Jun-2022
PMCID:PMC9166195
doi:10.1186/s43088-022-00256-6
PMID:35694188
Traditional Medicinal Plants as a Source of Antituberculosis Drugs: A System Review Xu Y, Liang B, Kong C, Sun Z Biomed Res Int 08-Sep-2021
PMCID:PMC8448615
doi:10.1155/2021/9910365
PMID:34541000
Essential Oil and Major Non-Volatile Secondary Metabolites from the Leaves of Amazonian Piper subscutatum Ramírez J, Andrade MD, Vidari G, Gilardoni G Plants (Basel) 09-Jun-2021
PMCID:PMC8228786
doi:10.3390/plants10061168
PMID:34207495
Identification of Beilschmiedia tsangii Root Extract as a Liver Cancer Cell–Normal Keratinocyte Dual-Selective NRF2 Regulator Chen YS, Chang HS, Hsiao HH, Chen YF, Kuo YP, Yen FL, Yen CH Antioxidants (Basel) 01-Apr-2021
PMCID:PMC8066689
doi:10.3390/antiox10040544
PMID:33915987
Molecular Docking Suggests the Targets of Anti-Mycobacterial Natural Products Baptista R, Bhowmick S, Shen J, Mur LA Molecules 18-Jan-2021
PMCID:PMC7831053
doi:10.3390/molecules26020475
PMID:33477495
Unusual constituents from the medicinal mushroom Ganoderma lingzhi Zhao ZZ, Liang XB, Feng WS, Wu Y, Zhi YL, Xue GM, Chen HP, Liu JK RSC Adv 13-Nov-2019
PMCID:PMC9075120
doi:10.1039/c9ra08566a
PMID:35539093
The potential of plant systems to break the HIV‐TB link Habibi P, Daniell H, Soccol CR, Grossi‐de‐Sa MF Plant Biotechnol J 18-Jul-2019
PMCID:PMC6737023
doi:10.1111/pbi.13110
PMID:30908823
Chemical Structures of Lignans and Neolignans Isolated from Lauraceae Li Y, Xie S, Ying J, Wei W, Gao K Molecules 30-Nov-2018
PMCID:PMC6321345
doi:10.3390/molecules23123164
PMID:30513687
Plants in our combating strategies against Mycobacterium tuberculosis: progress made and obstacles met Gupta VK, Kumar MM, Bisht D, Kaushik A Pharm Biol 07-Apr-2017
PMCID:PMC6130758
doi:10.1080/13880209.2017.1309440
PMID:28385088
Secondary Metabolites from the Roots of Beilschmiedia tsangii and Their Anti-Inflammatory Activities Huang YT, Chang HS, Wang GJ, Lin CH, Chen IS Int J Mol Sci 03-Dec-2012
PMCID:PMC3546699
doi:10.3390/ijms131216430
PMID:23208379
Anti-inflammatory endiandric acid analogues from the roots of Beilschmiedia tsangii. Huang YT, Chang HS, Wang GJ, Cheng MJ, Chen CH, Yang YJ, Chen IS J Nat Prod 23-Sep-2011
doi:10.1021/NP200279R
PMID:21846089
Novel epoxyfuranoid lignans and antitubercular constituents from the leaves of Beilschmiedia tsangii. Chen JJ, Chou ET, Peng CF, Chen IS, Yang SZ, Huang HY Planta Med 01-Jun-2007
doi:10.1055/S-2007-967195
PMID:17520523
New cytotoxic tetrahydrofuran- and dihydrofuran-type lignans from the stem of Beilschmiedia tsangii. Chen JJ, Chou ET, Duh CY, Yang SZ, Chen IS Planta Med 01-Mar-2006
doi:10.1055/S-2005-916220
PMID:16557477

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
[(1R,2R)-1-(7-methoxy-1,3-benzodioxol-5-yl)-2-methyl-3-oxobutyl] 3,4,5-trimethoxybenzoate 11859073 Click to see CC(C(C1=CC2=C(C(=C1)OC)OCO2)OC(=O)C3=CC(=C(C(=C3)OC)OC)OC)C(=O)C 446.40 unknown https://doi.org/10.1055/S-2005-916220
[(1S,2R)-2-methyl-3-oxo-1-(3,4,5-trimethoxyphenyl)butyl] 7-methoxy-1,3-benzodioxole-5-carboxylate 11859072 Click to see CC(C(C1=CC(=C(C(=C1)OC)OC)OC)OC(=O)C2=CC3=C(C(=C2)OC)OCO3)C(=O)C 446.40 unknown https://doi.org/10.1055/S-2005-916220
[1-(7-Methoxy-1,3-benzodioxol-5-yl)-2-methyl-3-oxobutyl] 3,4,5-trimethoxybenzoate 73129348 Click to see CC(C(C1=CC2=C(C(=C1)OC)OCO2)OC(=O)C3=CC(=C(C(=C3)OC)OC)OC)C(=O)C 446.40 unknown https://doi.org/10.1055/S-2005-916220
[2-Methyl-3-oxo-1-(3,4,5-trimethoxyphenyl)butyl] 7-methoxy-1,3-benzodioxole-5-carboxylate 73129347 Click to see CC(C(C1=CC(=C(C(=C1)OC)OC)OC)OC(=O)C2=CC3=C(C(=C2)OC)OCO3)C(=O)C 446.40 unknown https://doi.org/10.1055/S-2005-916220
Tsangin C 56661913 Click to see CC(C(C1=CC(=C(C(=C1)OC)OC)OC)OC(=O)C2=CC(=C(C(=C2)OC)OC)OC)C(=O)C 462.50 unknown https://doi.org/10.1021/NP200279R
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown https://doi.org/10.1021/NP200279R
https://doi.org/10.1055/S-2005-916220
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
4-Methoxy-6-[1-(7-methoxy-1,3-benzodioxol-5-yl)-4,5-dimethyl-2,6-dioxabicyclo[3.1.0]hexan-3-yl]-1,3-benzodioxole 78073384 Click to see CC1C(OC2(C1(O2)C)C3=CC4=C(C(=C3)OC)OCO4)C5=CC6=C(C(=C5)OC)OCO6 414.40 unknown https://doi.org/10.1055/S-2007-967195
4,5-Dimethyl-1,3-bis(3,4,5-trimethoxyphenyl)-2,6-dioxabicyclo[3.1.0]hexane 78074716 Click to see CC1C(OC2(C1(O2)C)C3=CC(=C(C(=C3)OC)OC)OC)C4=CC(=C(C(=C4)OC)OC)OC 446.50 unknown https://doi.org/10.1055/S-2007-967195
4Alpha,5Alpha-Epoxybeilschmin A 71454057 Click to see CC1C(OC2(C1(O2)C)C3=CC4=C(C(=C3)OC)OCO4)C5=CC(=C(C(=C5)OC)OC)OC 430.40 unknown https://doi.org/10.1055/S-2007-967195
4Alpha,5Alpha-Epoxybeilschmin B 71459474 Click to see CC1C(OC2(C1(O2)C)C3=CC(=C(C(=C3)OC)OC)OC)C4=CC(=C(C(=C4)OC)OC)OC 446.50 unknown https://doi.org/10.1055/S-2007-967195
6-[4,5-Dimethyl-3-(3,4,5-trimethoxyphenyl)-2,6-dioxabicyclo[3.1.0]hexan-1-yl]-4-methoxy-1,3-benzodioxole 78072744 Click to see CC1C(OC2(C1(O2)C)C3=CC4=C(C(=C3)OC)OCO4)C5=CC(=C(C(=C5)OC)OC)OC 430.40 unknown https://doi.org/10.1055/S-2007-967195
Beilschmin D 71455792 Click to see CC1C(OC2(C1(O2)C)C3=CC4=C(C(=C3)OC)OCO4)C5=CC6=C(C(=C5)OC)OCO6 414.40 unknown https://doi.org/10.1055/S-2007-967195
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
3,4-Dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)oxolane 4485701 Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)OC)OC)C3=CC(=C(C(=C3)OC)OC)OC)C 432.50 unknown https://doi.org/10.1055/S-2007-967195
https://doi.org/10.1055/S-2005-916220
6-[3,4-Dimethyl-5-(3,4,5-trimethoxyphenyl)oxolan-2-yl]-4-methoxy-1,3-benzodioxole 22297612 Click to see CC1C(C(OC1C2=CC3=C(C(=C2)OC)OCO3)C4=CC(=C(C(=C4)OC)OC)OC)C 416.50 unknown https://doi.org/10.1055/S-2007-967195
https://doi.org/10.1055/S-2005-916220
Beilschmin A 22297613 Click to see CC1C(C(OC1C2=CC3=C(C(=C2)OC)OCO3)C4=CC(=C(C(=C4)OC)OC)OC)C 416.50 unknown https://doi.org/10.1055/S-2005-916220
https://doi.org/10.1055/S-2007-967195
Beilschmin B 14352170 Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)OC)OC)C3=CC(=C(C(=C3)OC)OC)OC)C 432.50 unknown https://doi.org/10.1055/S-2005-916220
https://doi.org/10.1055/S-2007-967195
beilschminol A, rel- 54671632 Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)OC)O)C3=CC4=C(C(=C3)OC)OCO4)C 402.40 unknown https://doi.org/10.1021/NP200279R
rel-(7R,8R,7'R,8'R)-3,4,3',4'-dimethylene-dioxy-5,5'-dimethoxy-7,7'-epoxylignan 641713 Click to see CC1C(C(OC1C2=CC3=C(C(=C2)OC)OCO3)C4=CC5=C(C(=C4)OC)OCO5)C 400.40 unknown https://doi.org/10.1021/NP200279R
rel-(7R,8R,7'R,8'R)-3',4'-methylenedioxy-3,4,5,5'-tetramethoxy-7,7'-epoxylignan 11080226 Click to see CC1C(C(OC1C2=CC3=C(C(=C2)OC)OCO3)C4=CC(=C(C(=C4)OC)OC)OC)C 416.50 unknown https://doi.org/10.1021/NP200279R
rel-(7S,8S,7'R,8'R)-3,3',4,4',5,5'-hexamethoxy-7.O.7',8.8'-lignan 21827796 Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)OC)OC)C3=CC(=C(C(=C3)OC)OC)OC)C 432.50 unknown https://doi.org/10.1055/S-2005-916220
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Methyl linoleate 5284421 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OC 294.50 unknown https://doi.org/10.1055/S-2007-967195
Methyl octadeca-9,12-dienoate 8203 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OC 294.50 unknown https://doi.org/10.1055/S-2007-967195
> 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/10.1055/S-2007-967195
https://doi.org/10.1055/S-2005-916220
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/10.1055/S-2005-916220
https://doi.org/10.1055/S-2007-967195
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
2,6,11-Trimethyl-dodeca-2,6,10-triene 54304141 Click to see CC(=CCCC=C(C)CCC=C(C)C)C 206.37 unknown https://doi.org/10.1055/S-2005-916220
Tanacetene 5321610 Click to see CC(=CCCC=C(C)CCC=C(C)C)C 206.37 unknown https://doi.org/10.1055/S-2005-916220
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
(2S,5R,9S)-9-Acetyl-9-hydroxy-2,7,8-trimethyl-2-((4R,8R)-4,8,12-trimethyltridecyl)-1-oxaspiro[4.4]non-7-en-6-one 73821792 Click to see CC1=C(C(C2(C1=O)CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)(C(=O)C)O)C 462.70 unknown https://doi.org/10.1055/S-2005-916220
alpha-Tocospiro-B 21674157 Click to see CC1=C(C(C2(C1=O)CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)(C(=O)C)O)C 462.70 unknown https://doi.org/10.1055/S-2005-916220
> 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/10.1055/S-2007-967195
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/10.1055/S-2007-967195
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
17-(5,6-Dimethylhept-3-en-2-yl)-10,13-dimethyl-1,2,9,11,12,15,16,17-octahydrocyclopenta[a]phenanthren-3-one 622723 Click to see CC(C)C(C)C=CC(C)C1CCC2=C3C=CC4=CC(=O)CCC4(C3CCC12C)C 392.60 unknown https://doi.org/10.1055/S-2005-916220
Ergosta-4,6,8(14),22-tetraen-3-one 6441416 Click to see CC(C)C(C)C=CC(C)C1CCC2=C3C=CC4=CC(=O)CCC4(C3CCC12C)C 392.60 unknown https://doi.org/10.1055/S-2005-916220
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(6beta,24R)-6-Hydroxystigmast-4-en-3-one 14769504 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C 428.70 unknown https://doi.org/10.1021/NP200279R
https://doi.org/10.1055/S-2005-916220
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/10.1055/S-2007-967195
https://doi.org/10.1055/S-2005-916220
https://doi.org/10.1021/NP200279R
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1021/NP200279R
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/10.1055/S-2005-916220
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/10.1055/S-2005-916220
6alpha-Hydroxystigmast-4-en-3-one 9867274 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C 428.70 unknown https://doi.org/10.1055/S-2005-916220
6beta-Hydroxystigmast-4-en-3-one 9823926 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C 428.70 unknown https://doi.org/10.1021/NP200279R
https://doi.org/10.1055/S-2005-916220
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/10.1055/S-2007-967195
https://doi.org/10.1021/NP200279R
https://doi.org/10.1055/S-2005-916220
Sitostenone 579897 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown https://doi.org/10.1055/S-2005-916220
Stigmast-4-ee-3,6-dione 14308881 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(=O)C4=CC(=O)CCC34C)C)C(C)C 426.70 unknown https://doi.org/10.1055/S-2005-916220
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown https://doi.org/10.1055/S-2005-916220
Stigmast-4-ene-3,6-dione 5490007 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(=O)C4=CC(=O)CCC34C)C)C(C)C 426.70 unknown https://doi.org/10.1055/S-2005-916220
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see C1=CC(=CC=C1C=O)O 122.12 unknown https://doi.org/10.1055/S-2005-916220
> Organoheterocyclic compounds / Benzodioxoles
6-[(2S,3S)-3,4-dimethyl-2-(3,4,5-trimethoxyphenyl)-2,3-dihydrofuran-5-yl]-4-methoxy-1,3-benzodioxole 162897991 Click to see CC1C(OC(=C1C)C2=CC3=C(C(=C2)OC)OCO3)C4=CC(=C(C(=C4)OC)OC)OC 414.40 unknown https://doi.org/10.1055/S-2005-916220
6-[3,4-Dimethyl-2-(3,4,5-trimethoxyphenyl)-2,3-dihydrofuran-5-yl]-4-methoxy-1,3-benzodioxole 162897990 Click to see CC1C(OC(=C1C)C2=CC3=C(C(=C2)OC)OCO3)C4=CC(=C(C(=C4)OC)OC)OC 414.40 unknown https://doi.org/10.1055/S-2005-916220
Endiandramide A 54669853 Click to see CC(C)CNC(=O)C1C=CC2CC3C(C4C3C2C1C=C4)CC5=CC6=C(C=C5)OCO6 405.50 unknown https://doi.org/10.1021/NP200279R
endiandramide B, rel- 56658431 Click to see CC(C)CNC(=O)C1C2CC3C(C4C1C=CC2C34)CCCC5=CC6=C(C=C5)OCO6 407.50 unknown https://doi.org/10.1021/NP200279R
endiandric acid K, rel- 56675688 Click to see C1C2C3C=CC(C2C(=O)O)C4C3C1C4CCCC5=CC6=C(C=C5)OCO6 352.40 unknown https://doi.org/10.1021/NP200279R
endiandric acid L, rel- 56678990 Click to see C1C2C3C=CC(C2C=CC(=O)O)C4C3C1C4CCCCCC5=CC6=C(C=C5)OCO6 406.50 unknown https://doi.org/10.1021/NP200279R
tsangibeilin A, rac- 54671628 Click to see C1C2C=CC(C3C2C4C1C(C4C=C3)CCCC5=CC6=C(C=C5)OCO6)C(=O)O 378.50 unknown https://doi.org/10.1021/NP200279R
tsangibeilin B, rel- 54671629 Click to see C1C2C=CC(C3C2C4C1C(C4C=C3)CC5=CC6=C(C=C5)OCO6)C(=O)O 350.40 unknown https://doi.org/10.1021/NP200279R

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