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Osbeckia chinensis

Osbeckia chinensis - 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 UUID64404935015ca897174582
Scientific name Osbeckia chinensis
Authority L.
First published in Sp. Pl. : 345 (1753)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Persian اسبکیا چایننسیس
Chinese 天香炉
Chinese 小朝天罐
Chinese 金錦香
Chinese 金锦香
Chinese 张天缸
Chinese 杯子草
Chinese 装天甕

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Osbeckia chinensis var. chinensis L. Ginkgoana (1973)
Osbeckia chinensis var. procumbens C.Hansen Ginkgoana 4: 60 (1977)
Osbeckia chinensis var. pusilla (Zoll. & Moritzi) Triana Trans. Linn. Soc. London 28: 53. 1872 (1872)

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
      • Japan
      • Nansei-shoto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
      • India
      • Nepal
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Malaya
      • Philippines

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001083278
Tropicos 20305206
KEW urn:lsid:ipni.org:names:574035-1
The Plant List tro-20305206
Open Tree Of Life 391271
NCBI Taxonomy 113475
IPNI 574035-1
iNaturalist 570716
GBIF 3866460
Freebase /m/0j7mb0t
EPPO OSBCH
USDA GRIN 423488
Wikipedia Osbeckia_chinensis

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
Ethnobotany and phytochemistry of plants used to treat musculoskeletal disorders among Skaw Karen, Thailand Kantasrila R, Pandith H, Balslev H, Wangpakapattanawong P, Panyadee P, Inta A Pharm Biol 22-Dec-2023
PMCID:PMC10763916
doi:10.1080/13880209.2023.2292261
PMID:38131672
Towards further understanding the applications of endophytes: enriched source of bioactive compounds and bio factories for nanoparticles Choudhary N, Dhingra N, Gacem A, Yadav VK, Verma RK, Choudhary M, Bhardwaj U, Chundawat RS, Alqahtani MS, Gaur RK, Eltayeb LB, Al Abdulmonem W, Jeon BH Front Plant Sci 10-Jul-2023
PMCID:PMC10364642
doi:10.3389/fpls.2023.1193573
PMID:37492778
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
Therapeutic Potential of Phenolic Compounds in Medicinal Plants—Natural Health Products for Human Health Sun W, Shahrajabian MH Molecules 15-Feb-2023
PMCID:PMC9960276
doi:10.3390/molecules28041845
PMID:36838831
Extracellular Enzyme of Endophytic Fungi Isolated from Ziziphus spina Leaves as Medicinal Plant Hawar SN Int J Biomater 06-Jul-2022
PMCID:PMC9279100
doi:10.1155/2022/2135927
PMID:35845475
Fungal Endophytes as Efficient Sources of Plant-Derived Bioactive Compounds and Their Prospective Applications in Natural Product Drug Discovery: Insights, Avenues, and Challenges Singh A, Singh DK, Kharwar RN, White JF, Gond SK Microorganisms 19-Jan-2021
PMCID:PMC7833388
doi:10.3390/microorganisms9010197
PMID:33477910
Medicinal Plants for Treating Musculoskeletal Disorders among Karen in Thailand Kantasrila R, Pandith H, Balslev H, Wangpakapattanawong P, Panyadee P, Inta A Plants (Basel) 28-Jun-2020
PMCID:PMC7412036
doi:10.3390/plants9070811
PMID:32605228
Diversity and use of medicinal plants for soup making in traditional diets of the Hakka in West Fujian, China Luo B, Li F, Ahmed S, Long C J Ethnobiol Ethnomed 28-Nov-2019
PMCID:PMC6883701
doi:10.1186/s13002-019-0335-y
PMID:31779654
Forest characteristics and population structure of Glyptostrobus pensilis, a globally endangered relict species of southeastern China Tang CQ, Yang Y, Momohara A, Wang HC, Luu HT, Li S, Song K, Qian S, LePage B, Dong YF, Han PB, Ohsawa M, Le BT, Tran HD, Dang MT, Peng MC, Wang CY Plant Divers 25-Jun-2019
PMCID:PMC6742968
doi:10.1016/j.pld.2019.06.007
PMID:31528783
A Novel Antioxidative Synergist Isolated from<i>Osbeckia chinensis</i>L. Jeng-De Su, Toshihiko Osawa, Shunro Kawakishi, Mitsuo Namiki Oxford University Press (OUP) 06-Jun-2016
doi:10.1080/00021369.1987.10868552
Antioxidative Flavonoids Isolated from<i>Osbeckia chinensis</i>L. Jeng-De Su, Toshihiko Osawa, Shunro Kawakishi, Mitsuo Namiki Oxford University Press (OUP) 06-Jun-2016
doi:10.1080/00021369.1987.10868448
Chemical constituents of Lobelia chinensis. Yang S, Shen T, Zhao L, Li C, Zhang Y, Lou H, Ren D Fitoterapia 01-Mar-2014
doi:10.1016/J.FITOTE.2014.01.007
PMID:24444893
Antioxidant capacity of chewing stick miswak Salvadora persica Mohamed SA, Khan JA BMC Complement Altern Med 21-Feb-2013
PMCID:PMC3607854
doi:10.1186/1472-6882-13-40
PMID:23432926
Antioxidative flavonoids isolated from Osbeckia chinensis L. Jeng-De SU, Toshihiko OSAWA, Shunro KAWAKISHI, Mitsuo NAMKI Oxford University Press (OUP) 13-Jul-2011
doi:10.1271/BBB1961.51.2801
A novel antioxidative synergist isolated from Osbeckia chinensis L. Jeng-De SU, Toshihiko OSAWA, Shunro KAWAKISHI, Mitsuo NAMIKI Oxford University Press (OUP) 13-Jul-2011
doi:10.1271/BBB1961.51.3449

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 / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown https://doi.org/10.1016/0031-9422(88)80184-5
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl gallate 7428 Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O 184.15 unknown https://doi.org/10.1016/0031-9422(88)80184-5
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/J.FITOTE.2014.01.007
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/J.FITOTE.2014.01.007
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/J.FITOTE.2014.01.007
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Succinic Acid 1110 Click to see C(CC(=O)O)C(=O)O 118.09 unknown https://doi.org/10.1016/J.FITOTE.2014.01.007
> Organoheterocyclic compounds / Furans / Furoic acid and derivatives / Furoic acids
2-Furoic acid 6919 Click to see C1=COC(=C1)C(=O)O 112.08 unknown https://doi.org/10.1016/J.FITOTE.2014.01.007
5-[(S)-carboxy(hydroxy)methyl]furan-2-carboxylic acid 13965144 Click to see C1=C(OC(=C1)C(=O)O)C(C(=O)O)O 186.12 unknown https://doi.org/10.1080/00021369.1987.10868552
Osbeckic acid 13965143 Click to see C1=C(OC(=C1)C(=O)O)C(C(=O)O)O 186.12 unknown https://doi.org/10.1080/00021369.1987.10868552
https://doi.org/10.1271/BBB1961.51.3449
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
1-(6-Oxo-2,3-dihydropyran-2-yl)hept-4-en-2-yl acetate 162908381 Click to see CCC=CCC(CC1CC=CC(=O)O1)OC(=O)C 252.31 unknown https://doi.org/10.1016/0031-9422(88)80184-5
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]methoxy]chromen-4-one 162919940 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OCC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O 640.50 unknown https://doi.org/10.1080/00021369.1987.10868448
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]methoxy]chromen-4-one 162964697 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OCC4C(C(C(C(O4)CO)O)O)O)O)O 478.40 unknown https://doi.org/10.1080/00021369.1987.10868448
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]methoxy]chromen-4-one 162964696 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OCC4C(C(C(C(O4)CO)O)O)O)O)O 478.40 unknown https://doi.org/10.1080/00021369.1987.10868448
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-[[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]methoxy]chromen-4-one 162919939 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OCC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O 640.50 unknown https://doi.org/10.1080/00021369.1987.10868448
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]methoxy]chromen-4-one 162907664 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OCC4C(C(C(C(O4)CO)O)O)O)O 462.40 unknown https://doi.org/10.1080/00021369.1987.10868448
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]methoxy]chromen-4-one 162907663 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OCC4C(C(C(C(O4)CO)O)O)O)O 462.40 unknown https://doi.org/10.1080/00021369.1987.10868448
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1271/BBB1961.51.2801
https://doi.org/10.1080/00021369.1987.10868448
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1080/00021369.1987.10868448
https://doi.org/10.1016/J.FITOTE.2014.01.007
https://doi.org/10.1271/BBB1961.51.2801
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1271/BBB1961.51.2801
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1271/BBB1961.51.2801
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(10S,11R,12R,13R,15R)-3,4,5,11,12,13,21,22,23-nonahydroxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaene-8,18-dione 14035459 Click to see C1C2C(C(C(C(O2)O)O)O)OC(=O)C3=CC(=C(C(=C3C4=C(C(=C(C=C4C(=O)O1)O)O)O)O)O)O 482.30 unknown https://doi.org/10.1016/0031-9422(88)80184-5
(14S,15R,19R)-2,3,4,7,8,9,19-heptahydroxy-14-[(1R,2R)-1,2,3-trihydroxypropyl]-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaene-12,17-dione 162945306 Click to see C1=C2C(=C(C(=C1O)O)O)C3=C4C(=C(C(=C3O)O)O)C(C(C(OC2=O)C(C(CO)O)O)OC4=O)O 482.30 unknown https://doi.org/10.1016/0031-9422(88)80184-5
[(10R,11R)-10-[(15S,19S)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 101601178 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 936.60 unknown https://doi.org/10.1016/0031-9422(88)80184-5
[(10R,11S)-10-[(14R,15S,19S)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 17999934 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 936.60 unknown https://doi.org/10.1016/0031-9422(88)80184-5
[(1R,2R)-1-[(15S,19S)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-1,3-dihydroxypropan-2-yl] 3,4,5-trihydroxybenzoate 101630966 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC(CO)C(C2C3C(C4=C(C(=C(C(=C4C(=O)O3)C5=C(C(=C(C=C5C(=O)O2)O)O)O)O)O)O)O)O 634.50 unknown https://doi.org/10.1016/0031-9422(88)80184-5
[(1R,2S)-1-[(14S,15R,19R)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-1,3-dihydroxypropan-2-yl] 3,4,5-trihydroxybenzoate 162994708 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC(CO)C(C2C3C(C4=C(C(=C(C(=C4C(=O)O3)C5=C(C(=C(C=C5C(=O)O2)O)O)O)O)O)O)O)O 634.50 unknown https://doi.org/10.1016/0031-9422(88)80184-5
[1-(2,3,4,7,8,9,19-Heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl)-1,3-dihydroxypropan-2-yl] 3,4,5-trihydroxybenzoate 14035445 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC(CO)C(C2C3C(C4=C(C(=C(C(=C4C(=O)O3)C5=C(C(=C(C=C5C(=O)O2)O)O)O)O)O)O)O)O 634.50 unknown https://doi.org/10.1016/0031-9422(88)80184-5
14-(3,4,5,11,17,18,19-Heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl)-2,3,4,7,8,9,19-heptahydroxy-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaene-12,17-dione 14035439 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)O 784.50 unknown https://doi.org/10.1016/0031-9422(88)80184-5
2-O,3-O-[4,4',5,5',6,6'-Hexahydroxy-1,1'-biphenyl-2,2'-diylbis(carbonyl)]-beta-D-glucopyranose 11754973 Click to see C1=C2C(=C(C(=C1O)O)O)C3=C(C(=C(C=C3C(=O)OC4C(C(C(OC4O)CO)O)OC2=O)O)O)O 482.30 unknown https://doi.org/10.1016/0031-9422(88)80184-5
2,3-(S)-hexahydroxydiphenoyl-D-glucose 492390 Click to see C1=C2C(=C(C(=C1O)O)O)C3=C(C(=C(C=C3C(=O)OC4C(C(C(OC4O)CO)O)OC2=O)O)O)O 482.30 unknown https://doi.org/10.1016/0031-9422(88)80184-5
2,3,4,7,8,9,19-Heptahydroxy-14-(1,2,3-trihydroxypropyl)-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaene-12,17-dione 14035450 Click to see C1=C2C(=C(C(=C1O)O)O)C3=C4C(=C(C(=C3O)O)O)C(C(C(OC2=O)C(C(CO)O)O)OC4=O)O 482.30 unknown https://doi.org/10.1016/0031-9422(88)80184-5
5-Desgalloylstachyurin 10417809 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)O 784.50 unknown https://doi.org/10.1016/0031-9422(88)80184-5
Casuariin 14035442 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)O 784.50 unknown https://doi.org/10.1016/0031-9422(88)80184-5
Casuarinin 442673 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 936.60 unknown https://doi.org/10.1016/0031-9422(88)80184-5
Ellagic Acid 5281855 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O 302.19 unknown https://doi.org/10.1016/0031-9422(88)80184-5
Stachyurin 157395 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 936.60 unknown https://doi.org/10.1016/0031-9422(88)80184-5

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