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Cornus walteri

Cornus walteri - 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 UUID644035dea9aaf099431336
Scientific name Cornus walteri
Authority Wangerin
First published in Repert. Spec. Nov. Regni Veg. 6: 99 (1908)

Description Top

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Synonyms Top

Scientific name Authority First published in
Swida coreana (Wangerin) Soják Novit. Bot. Delect. Seminum Horti Bot. Univ. Carol. Prag. 1960: 10 (1960)
Swida walteri (Wangerin) Soják Novit. Bot. Delect. Seminum Horti Bot. Univ. Carol. Prag. 1960: 11 (1960)
Swida walteri var. confertiflora (Fang & W.K.Hu) Fang & W.K.Hu Bull. Bot. Res., Harbin 4(3): 108 (1984)
Swida walteri var. insignis (Fang & W.K.Hu) Fang & W.K.Hu Bull. Bot. Res., Harbin 4(3): 108 (1984)
Thelycrania coreana (Wangerin) Pojark. Fl. URSS 17: 335 (1951)
Cornus coreana Wangerin Repert. Spec. Nov. Regni Veg. 6: 99 (1908)
Cornus henryi Hemsl. ex Wangerin Pflanzenr. , IV, 229: 90 (1910)
Cornus walteri var. confertiflora W.P.Fang & W.K.Hu Fl. Sichuanica 1: 470 (1981)
Cornus walteri var. insignis W.P.Fang & W.K.Hu Fl. Sichuanica 1: 469 (1981)
Cornus yunnanensis H.L.Li J. Arnold Arbor. 25: 312 (1944)

Common names Top

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Language Common/alternative name
English walter's dogwood
Azerbaijani valter zoğalı
Persian زغالاخته کرهای
Korean 말채나무
Chinese 毛棶
Chinese 癞树叶
Chinese 毛梾
Chinese 毛梾枝叶
Chinese 黑椋子

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 North-central
      • China South-central
      • China Southeast
    • Eastern Asia
      • Korea

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000924883
UNII N2F08B55XU
Tropicos 8700427
KEW urn:lsid:ipni.org:names:271706-1
The Plant List kew-47545
Open Tree Of Life 505082
NCBI Taxonomy 16907
IUCN Red List 130050012
IPNI 271706-1
GBIF 7322020
Freebase /m/05w5wt
EPPO CRWWA
USDA GRIN 11578
Wikipedia Cornus_walteri
CMAUP NPO19594

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
Woody plant functional traits and phylogenetic signals correlate with urbanization in remnant forest patches Yang J, Wang Z, Pan Y, Zheng Y Ecol Evol 31-Jul-2023
PMCID:PMC10388403
doi:10.1002/ece3.10366
PMID:37529580
Secondary metabolites related to the resistance of Psidium spp. against the nematode Meloidogyneenterolobii Costa SN, Silva MV, Ribeiro JM, Castro JM, Muzitano MF, Costa RG, Oliveira AE, Fernandes KV Heliyon 04-Jul-2023
PMCID:PMC10395151
doi:10.1016/j.heliyon.2023.e17778
PMID:37539183
Recent Advances Regarding the Molecular Mechanisms of Triterpenic Acids: A Review (Part II) Mioc M, Prodea A, Racoviceanu R, Mioc A, Ghiulai R, Milan A, Voicu M, Mardale G, Șoica C Int J Mol Sci 10-Aug-2022
PMCID:PMC9408012
doi:10.3390/ijms23168896
PMID:36012159
A Review on Carbon Dots: Synthesis, Characterization and Its Application in Optical Sensor for Environmental Monitoring Omar NA, Fen YW, Irmawati R, Hashim HS, Ramdzan NS, Fauzi NI Nanomaterials (Basel) 11-Jul-2022
PMCID:PMC9321155
doi:10.3390/nano12142365
PMID:35889589
Phytochemical Profiling, Anti-Inflammatory, Anti-Oxidant and In-Silico Approach of Cornus macrophylla Bioss (Bark) Khan A, Pervaiz A, Ansari B, Ullah R, Shah SM, Khan H, Saeed Jan M, Hussain F, Ijaz Khan M, Albadrani GM, Altyar AE, Abdel-Daim MM Molecules 24-Jun-2022
PMCID:PMC9268425
doi:10.3390/molecules27134081
PMID:35807324
Recent Advances in Synthesis, Modification, Characterization, and Applications of Carbon Dots Pundi A, Chang CJ Polymers (Basel) 25-May-2022
PMCID:PMC9183192
doi:10.3390/polym14112153
PMID:35683827
Implementation of the visual aesthetic quality of slope forest autumn color change into the configuration of tree species Mu Y, Lin W, Diao X, Zhang Z, Wang J, Lu Z, Guo W, Wang Y, Hu C, Zhao C Sci Rep 20-Jan-2022
PMCID:PMC8776743
doi:10.1038/s41598-021-04317-1
PMID:35058486
Natural and Historical Heritage of the Lisbon Botanical Gardens: An Integrative Approach with Tree Collections Cunha AR, Soares AL, Brilhante M, Arsénio P, Vasconcelos T, Espírito-Santo D, Duarte MC, Romeiras MM Plants (Basel) 04-Jul-2021
PMCID:PMC8309379
doi:10.3390/plants10071367
PMID:34371570
Distribution of Woody Plant Species Among Different Disturbance Regimes of Forests in a Temperate Deciduous Broad-Leaved Forest Xi J, Shao Y, Li Z, Zhao P, Ye Y, Li W, Chen Y, Yuan Z Front Plant Sci 06-Apr-2021
PMCID:PMC8056040
doi:10.3389/fpls.2021.618524
PMID:33889163
Differentiation in stem and leaf traits among sympatric lianas, scandent shrubs and trees in a subalpine cold temperate forest Zhang KY, Yang D, Zhang YB, Ellsworth DS, Xu K, Zhang YP, Chen YJ, He F, Zhang JL Tree Physiol 05-Apr-2021
PMCID:PMC8597974
doi:10.1093/treephys/tpab049
PMID:33823048
Identification of Bioactive Natural Product from the Stems and Stem Barks of Cornus walteri: Benzyl Salicylate Shows Potential Anti-Inflammatory Activity in Lipopolysaccharide-Stimulated RAW 264.7 Macrophages Lee D, Alishir A, Jang TS, Kim KH Pharmaceutics 25-Mar-2021
PMCID:PMC8064495
doi:10.3390/pharmaceutics13040443
PMID:33805999
(-)-Leucophyllone, a Tirucallane Triterpenoid from Cornus walteri, Enhances Insulin Secretion in INS-1 Cells Lee D, Kim KH, Jang T, Kang KS Plants (Basel) 24-Feb-2021
PMCID:PMC7996230
doi:10.3390/plants10030431
PMID:33668330
New Approaches in Urban Forestry to Minimize Invasive Species Impacts: The Case of Xiongan New Area in China Li HP, Wickham JD, Bushley K, Wang ZG, Zhang B, Sun JH Insects 12-May-2020
PMCID:PMC7290593
doi:10.3390/insects11050300
PMID:32408656
Unique Triterpenoid of Jujube Root Protects Cisplatin-induced Damage in Kidney Epithelial LLC-PK1 Cells via Autophagy Regulation Lee D, Kang KB, Kim HW, Park JS, Hwang GS, Kang KS, Choi S, Yamabe N, Kim KH Nutrients 02-Mar-2020
PMCID:PMC7146250
doi:10.3390/nu12030677
PMID:32131519
Benzyl salicylate from the stems and stem barks of Cornus walteri as a nephroprotective agent against cisplatin-induced apoptotic cell death in LLC-PK1 cells Lee D, Lee SR, Kang KS, Kim KH RSC Adv 05-Feb-2020
PMCID:PMC9049590
doi:10.1039/c9ra07009e
PMID:35497438

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 / Phenols / Methoxyphenols
Kompasinol A 102505446 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3C4=C2C(=CC(=C4)O)O)C5=CC(=C(C=C5)O)O 452.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(-)-Leucophyllone 70698253 Click to see CC(CC=CC(C)(C)OC)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 454.70 unknown https://doi.org/10.1021/NP100660V
(10S,13S,14S,17S)-17-[(2S,4S)-4-methoxy-6-methylhept-5-en-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,12,15,16,17-octahydrocyclopenta[a]phenanthren-3-one 53317047 Click to see CC(CC(C=C(C)C)OC)C1CCC2(C1(CC=C3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 452.70 unknown via CMAUP database
(3S,8R,9S,10R,13S,14R,17S)-17-[(E,2S)-6-methoxy-6-methylhept-4-en-2-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 70682451 Click to see CC(CC=CC(C)(C)OC)C1CCC2(C1(CCC3C2CCC4C3(CCC(C4(C)C)O)C)C)C 458.80 unknown via CMAUP database
(3S,9R,10R,13S,14S,17S)-17-[(2S,4R)-4-methoxy-6-methylhept-5-en-2-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 53323674 Click to see CC(CC(C=C(C)C)OC)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 456.70 unknown via CMAUP database
(3S,9R,10R,13S,14S,17S)-17-[(E,2S)-6-methoxy-6-methylhept-4-en-2-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 53319543 Click to see CC(CC=CC(C)(C)OC)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 456.70 unknown via CMAUP database
(8R,9S,10R,13S,14R,17S)-17-[(E,2S)-6-methoxy-6-methylhept-4-en-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 70688780 Click to see CC(CC=CC(C)(C)OC)C1CCC2(C1(CCC3C2CCC4C3(CCC(=O)C4(C)C)C)C)C 456.70 unknown via CMAUP database
(9R,10R,13S,14S,17S)-17-[(2S,4R)-4-methoxy-6-methylhept-5-en-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 53317046 Click to see CC(CC(C=C(C)C)OC)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 454.70 unknown via CMAUP database
(9R,10R,13S,14S,17S)-17-[(2S,4S)-4-methoxy-6-methylhept-5-en-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 53324955 Click to see CC(CC(C=C(C)C)OC)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 454.70 unknown via CMAUP database
(9R,10R,13S,14S,17S)-17-[(E,2S)-6-methoxy-6-methylhept-4-en-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 15241162 Click to see CC(CC=CC(C)(C)OC)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 454.70 unknown via CMAUP database
(9R,10R,13S,14S,17S)-4,4,10,13,14-pentamethyl-17-[(2S,4E)-6-methylhepta-4,6-dien-2-yl]-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 53318193 Click to see CC(CC=CC(=C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 422.70 unknown via CMAUP database
(9R,10R,13S,14S,17S)-4,4,10,13,14-pentamethyl-17-[(2S)-6-methylheptan-2-yl]-5,6,9,11,12,15,16,17-octahydrocyclopenta[a]phenanthren-3-one 53325645 Click to see CC(C)CCCC(C)C1CCC2(C1(CCC3C2=CCC4C3(C=CC(=O)C4(C)C)C)C)C 424.70 unknown via CMAUP database
(9R,10R,13S,14S,17S)-4,4,10,13,14-pentamethyl-17-[(3S,5R)-5-(2-methylprop-1-enyl)oxolan-3-yl]-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 53326248 Click to see CC(=CC1CC(CO1)C2CCC3(C2(CCC4C3=CCC5C4(CCC(=O)C5(C)C)C)C)C)C 438.70 unknown via CMAUP database
(9R,10R,13S,14S,17S)-4,4,10,13,14-pentamethyl-17-[(3S,5S)-5-(2-methylprop-1-enyl)oxolan-3-yl]-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 53319674 Click to see CC(=CC1CC(CO1)C2CCC3(C2(CCC4C3=CCC5C4(CCC(=O)C5(C)C)C)C)C)C 438.70 unknown via CMAUP database
(9S,10S,13S,14S,17S)-4,4,10,13,14-pentamethyl-17-[(2S)-6-methylheptan-2-yl]-5,6,9,11,12,15,16,17-octahydrocyclopenta[a]phenanthren-1-one 53323673 Click to see CC(C)CCCC(C)C1CCC2(C1(CCC3C2=CCC4C3(C(=O)C=CC4(C)C)C)C)C 424.70 unknown via CMAUP database
1-Hydroxy-4,4,10,13,14-pentamethyl-17-(6-methylheptan-2-yl)-1,2,7,8,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 75597769 Click to see CC(C)CCCC(C)C1CCC2(C1(CCC3C2CC=C4C3(C(CC(=O)C4(C)C)O)C)C)C 442.70 unknown https://doi.org/10.1021/NP100660V
17-(4-Methoxy-6-methylhept-5-en-2-yl)-4,4,10,13,14-pentamethyl-1,2,5,6,12,15,16,17-octahydrocyclopenta[a]phenanthren-3-one 75597737 Click to see CC(CC(C=C(C)C)OC)C1CCC2(C1(CC=C3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 452.70 unknown https://doi.org/10.1021/NP100660V
17-(4-Methoxy-6-methylhept-5-en-2-yl)-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 75597736 Click to see CC(CC(C=C(C)C)OC)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 454.70 unknown https://doi.org/10.1021/NP100660V
17-(4-methoxy-6-methylhept-5-en-2-yl)-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 75597738 Click to see CC(CC(C=C(C)C)OC)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 456.70 unknown https://doi.org/10.1021/NP100660V
17-(6-Methoxy-6-methylhept-4-en-2-yl)-4,4,10,13,14-pentamethyl-1,2,5,6,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 75597707 Click to see CC(CC=CC(C)(C)OC)C1CCC2(C1(CCC3C2CCC4C3(CCC(=O)C4(C)C)C)C)C 456.70 unknown https://doi.org/10.1021/NP100660V
17-(6-Methoxy-6-methylhept-4-en-2-yl)-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 73189944 Click to see CC(CC=CC(C)(C)OC)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 454.70 unknown https://doi.org/10.1021/NP100660V
17-(6-methoxy-6-methylhept-4-en-2-yl)-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 75597708 Click to see CC(CC=CC(C)(C)OC)C1CCC2(C1(CCC3C2CCC4C3(CCC(C4(C)C)O)C)C)C 458.80 unknown https://doi.org/10.1021/NP100660V
17-(6-methoxy-6-methylhept-4-en-2-yl)-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 75597706 Click to see CC(CC=CC(C)(C)OC)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 456.70 unknown https://doi.org/10.1021/NP100660V
4,4,10,13,14-Pentamethyl-17-(6-methylhepta-4,6-dien-2-yl)-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 75597709 Click to see CC(CC=CC(=C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 422.70 unknown https://doi.org/10.1021/NP100660V
4,4,10,13,14-Pentamethyl-17-(6-methylheptan-2-yl)-5,6,9,11,12,15,16,17-octahydrocyclopenta[a]phenanthren-1-one 75597735 Click to see CC(C)CCCC(C)C1CCC2(C1(CCC3C2=CCC4C3(C(=O)C=CC4(C)C)C)C)C 424.70 unknown https://doi.org/10.1021/NP100660V
4,4,10,13,14-Pentamethyl-17-(6-methylheptan-2-yl)-5,6,9,11,12,15,16,17-octahydrocyclopenta[a]phenanthren-3-one 75597710 Click to see CC(C)CCCC(C)C1CCC2(C1(CCC3C2=CCC4C3(C=CC(=O)C4(C)C)C)C)C 424.70 unknown https://doi.org/10.1021/NP100660V
4,4,10,13,14-Pentamethyl-17-[5-(2-methylprop-1-enyl)oxolan-3-yl]-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 14830845 Click to see CC(=CC1CC(CO1)C2CCC3(C2(CCC4C3=CCC5C4(CCC(=O)C5(C)C)C)C)C)C 438.70 unknown https://doi.org/10.1021/NP100660V
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown via CMAUP database
Cornusalterin A 50994221 Click to see CC(CC=CC(C)(C)OC)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 456.70 unknown https://doi.org/10.1021/NP100660V
Cornusalterin B 50994222 Click to see CC(CC=CC(C)(C)OC)C1CCC2(C1(CCC3C2CCC4C3(CCC(=O)C4(C)C)C)C)C 456.70 unknown https://doi.org/10.1021/NP100660V
Cornusalterin C 50994223 Click to see CC(CC=CC(C)(C)OC)C1CCC2(C1(CCC3C2CCC4C3(CCC(C4(C)C)O)C)C)C 458.80 unknown https://doi.org/10.1021/NP100660V
Cornusalterin D 50994224 Click to see CC(CC=CC(=C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 422.70 unknown https://doi.org/10.1021/NP100660V
Cornusalterin E 50994225 Click to see CC(C)CCCC(C)C1CCC2(C1(CCC3C2=CCC4C3(C=CC(=O)C4(C)C)C)C)C 424.70 unknown https://doi.org/10.1021/NP100660V
Cornusalterin F 50994305 Click to see CC(C)CCCC(C)C1CCC2(C1(CCC3C2=CCC4C3(C(=O)C=CC4(C)C)C)C)C 424.70 unknown https://doi.org/10.1021/NP100660V
Cornusalterin G 50994306 Click to see CC(CC(C=C(C)C)OC)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 454.70 unknown https://doi.org/10.1021/NP100660V
Cornusalterin H 50994307 Click to see CC(CC(C=C(C)C)OC)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 454.70 unknown https://doi.org/10.1021/NP100660V
Cornusalterin I 50994308 Click to see CC(CC(C=C(C)C)OC)C1CCC2(C1(CC=C3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 452.70 unknown https://doi.org/10.1021/NP100660V
Cornusalterin J 50994309 Click to see CC(CC(C=C(C)C)OC)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 456.70 unknown https://doi.org/10.1021/NP100660V
Cornusalterin K 50994389 Click to see CC(C)CCCC(C)C1CCC2(C1(CCC3C2CC=C4C3(C(CC(=O)C4(C)C)O)C)C)C 442.70 unknown https://doi.org/10.1021/NP100660V
Cornusalterin L 50994390 Click to see CC(=CC1CC(CO1)C2CCC3(C2(CCC4C3=CCC5C4(CCC(=O)C5(C)C)C)C)C)C 438.70 unknown https://doi.org/10.1021/NP100660V
Deoxyflindissone 70698213 Click to see CC(=CC1CC(CO1)C2CCC3(C2(CCC4C3=CCC5C4(CCC(=O)C5(C)C)C)C)C)C 438.70 unknown https://doi.org/10.1021/NP100660V
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
Vincosamide 10163855 Click to see C=CC1C2CC3C4=C(CCN3C(=O)C2=COC1OC5C(C(C(C(O5)CO)O)O)O)C6=CC=CC=C6N4 498.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Catechin 3-rhamnoside 21626704 Click to see CC1C(C(C(C(O1)OC2CC3=C(C=C(C=C3OC2C4=CC(=C(C=C4)O)O)O)O)O)O)O 436.40 unknown via CMAUP database

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