Dendrobium chrysotoxum - Unknown
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Details Top

Internal ID UUID644037bcb3a6e900310576
Scientific name Dendrobium chrysotoxum
Authority Lindl.
First published in Edwards's Bot. Reg. 33: t. 19 (1847)

Description Top

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Synonyms Top

Scientific name Authority First published in
Callista chrysotoxa Kuntze Revis. Gen. Pl. 2: 654 (1891)
Callista suavissima Kuntze Revis. Gen. Pl. 2: 655 (1891)
Dendrobium chrysotoxum var. suavissimum (Rchb.f.) A.H.Kent Man. Orchid. Pl. 3: 29. 1888
Dendrobium suavissimum Rchb.f. Gard. Chron. , n.s., 1: 406 (1874)
Callista chrysotoxa (Lindl.) Brieger Orchideen (Schlechter) 1(11-12): 704. 1981

Common names Top

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Language Common/alternative name
English golden arch dendrobium
English golden bow dendrobium
Azerbaijani callista chrysotoxa
Azerbaijani callista suavissima
Azerbaijani dendrobium suavissimum
mni ꯈꯣꯉꯨꯃꯦꯂꯩ
Vietnamese kim điệp thân phình
Chinese 鼓槌石斛
Chinese 金弓石斛
Chinese 束花石斛

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000938772
Tropicos 23500679
INPN 629527
KEW urn:lsid:ipni.org:names:627099-1
The Plant List kew-57402
Open Tree Of Life 371870
Observations.org 473398
NCBI Taxonomy 161865
IPNI 627099-1
iNaturalist 493666
GBIF 5317521
Freebase /m/065_syh
EPPO DENCH
EOL 1100343
Elurikkus 513681
USDA GRIN 312705
Wikipedia Dendrobium_chrysotoxum
CMAUP NPO20900

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_019925795.1 ASM1992579v1 Chromosome The Orchid Conservation and Research Center of Shenzhen 2021-09-10 96.0x 1.27 Gb

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
Recent advances in the potential effects of natural products from traditional Chinese medicine against respiratory diseases targeting ferroptosis Chen T, Ding L, Zhao M, Song S, Hou J, Li X, Li M, Yin K, Li X, Wang Z Chin Med 22-Mar-2024
PMCID:PMC10958864
doi:10.1186/s13020-024-00918-w
PMID:38519984
Identification and Characterization of the AREB/ABF Gene Family in Three Orchid Species and Functional Analysis of DcaABI5 in Arabidopsis Xie X, Lin M, Xiao G, Wang Q, Li Z Plants (Basel) 08-Mar-2024
PMCID:PMC10974128
doi:10.3390/plants13060774
PMID:38592811
Erianin promotes apoptosis and inhibits Akt-mediated aerobic glycolysis of cancer cells Han S, Chen S, Wang J, Huang S, Xiao Y, Deng G J Cancer 04-Mar-2024
PMCID:PMC10937289
doi:10.7150/jca.92780
PMID:38495480
Identification of Fusarium oxysporum Causing Leaf Blight on Dendrobium chrysotoxum in Yunnan Province, China Yang J, Ahmed W, Zhang J, Gao S, Wang Z, Yang H, Bai X, Luo K, Xu C, Ji G Life (Basel) 20-Feb-2024
PMCID:PMC10970817
doi:10.3390/life14030285
PMID:38541611
Erianin promotes endogenous neurogenesis in traumatic brain injury rats Li Q, Gan X, Zhang M, Zhang G, Li Y, Gao L Sci Rep 19-Feb-2024
PMCID:PMC10876537
doi:10.1038/s41598-023-50573-8
PMID:38374284
Identification and Analysis of PEPC Gene Family Reveals Functional Diversification in Orchidaceae and the Regulation of Bacterial-Type PEPC Li R, Gao X, Wu Y, Wei C, Li MH, Liu DK, Liu ZJ Int J Mol Sci 08-Feb-2024
PMCID:PMC10888551
doi:10.3390/ijms25042055
PMID:38396732
Genome-Wide Identification and Expression Profile Analysis of Sugars Will Eventually Be Exported Transporter (SWEET) Genes in Zantedeschia elliottiana and Their Responsiveness to Pectobacterium carotovora subspecies Carotovora (Pcc) Infection Li Z, Guo Y, Jin S, Wu H Int J Mol Sci 07-Feb-2024
PMCID:PMC10888187
doi:10.3390/ijms25042004
PMID:38396683
Genome-wide identification and characterization of TCP gene family in Dendrobium nobile and their role in perianth development Wei X, Yuan M, Zheng BQ, Zhou L, Wang Y Front Plant Sci 05-Feb-2024
PMCID:PMC10875090
doi:10.3389/fpls.2024.1352119
PMID:38375086
Hypoglycemic Effects and Quality Marker Screening of Dendrobium nobile Lindl. at Different Growth Years Luo Y, Yang D, Xu Y, Wu D, Tan D, Qin L, Wu X, Lu Y, He Y Molecules 02-Feb-2024
PMCID:PMC10856227
doi:10.3390/molecules29030699
PMID:38338442
A review of natural products targeting tumor immune microenvironments for the treatment of lung cancer Yao P, Liang S, Liu Z, Xu C Front Immunol 01-Feb-2024
PMCID:PMC10867126
doi:10.3389/fimmu.2024.1343316
PMID:38361933
Elimination of detached Listeria monocytogenes from the biofilm on stainless steel surfaces during milk and cheese processing using natural plant extracts El-sawy YN, Abdel-Salam AB, Abd-Elhady HM, Abou-Taleb KA, Ahmed RF Sci Rep 27-Jan-2024
PMCID:PMC10821901
doi:10.1038/s41598-024-52394-9
PMID:38280925
Genome-Wide Identification of bZIP Transcription Factors in Cymbidium ensifolium and Analysis of Their Expression under Low-Temperature Stress Lai H, Wang M, Yan L, Feng C, Tian Y, Tian X, Peng D, Lan S, Zhang Y, Ai Y Plants (Basel) 12-Jan-2024
PMCID:PMC10818551
doi:10.3390/plants13020219
PMID:38256772
Destructive Phytophthora on orchids: current knowledge and future perspectives Bag TK, Dutta P, Hubballi M, Kaur R, Mahanta M, Chakraborty A, Das G, Kataky M, Waghunde R Front Microbiol 05-Jan-2024
PMCID:PMC10810131
doi:10.3389/fmicb.2023.1139811
PMID:38274767
Genome-wide identification and expression analysis of growth-regulating factors in Dendrobium officinale and Dendrobium chrysotoxum Zhu S, Wang H, Xue Q, Zou H, Liu W, Xue Q, Ding XY PeerJ 15-Dec-2023
PMCID:PMC10726744
doi:10.7717/peerj.16644
PMID:38111654
Genome-Wide Identification of PEBP Gene Family in Two Dendrobium Species and Expression Patterns in Dendrobium chrysotoxum Zhang MM, Zhao X, He X, Zheng Q, Huang Y, Li Y, Ke S, Liu ZJ, Lan S Int J Mol Sci 14-Dec-2023
PMCID:PMC10743876
doi:10.3390/ijms242417463
PMID:38139293

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 / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
Rhein 10168 Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)C(=O)O 284.22 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
Physcione 10639 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OC 284.26 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoate 54675866 Click to see C1=CC(=C(C=C1C(=O)O)O)[O-] 153.11 unknown via CMAUP database
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1007/S10600-009-9329-7
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown via CMAUP database
> 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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
3,4-Dimethoxybenzoic acid 7121 Click to see COC1=C(C=C(C=C1)C(=O)O)OC 182.17 unknown via CMAUP database
Methyl 3,4-dimethoxybenzoate 16522 Click to see COC1=C(C=C(C=C1)C(=O)OC)OC 196.20 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
2-Amino-3,5-dibromobenzaldehyde 688305 Click to see C1=C(C=C(C(=C1C=O)N)Br)Br 278.93 unknown via CMAUP database
> Benzenoids / Fluorenes
(9R)-4-methoxy-9H-fluorene-2,5,9-triol 11425067 Click to see COC1=CC(=CC2=C1C3=C(C2O)C=CC=C3O)O 244.24 unknown https://doi.org/10.1002/HLCA.200490037
1,4,7-trihydroxy-5-methoxy-9H-fluoren-9-one 44418788 Click to see COC1=CC(=CC2=C1C3=C(C=CC(=C3C2=O)O)O)O 258.23 unknown https://doi.org/10.1007/S10600-009-9329-7
2,5-Dihydroxy-4-methoxy-9H-fluoren-9-one 10879298 Click to see COC1=CC(=CC2=C1C3=C(C2=O)C=CC=C3O)O 242.23 unknown https://doi.org/10.1007/S10600-009-9329-7
4-methoxy-9H-fluorene-2,5,9-triol 5248146 Click to see COC1=CC(=CC2=C1C3=C(C2O)C=CC=C3O)O 244.24 unknown https://doi.org/10.1002/HLCA.200490037
> Benzenoids / Phenanthrenes and derivatives
2,3,4,7-Tetramethoxyphenanthrene 11437978 Click to see COC1=CC2=C(C=C1)C3=C(C(=C(C=C3C=C2)OC)OC)OC 298.30 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
2,4,7-Trihydroxy-9,10-dihydrophenanthrene 21678577 Click to see C1CC2=C(C3=C1C=C(C=C3)O)C(=CC(=C2)O)O 228.24 unknown via CMAUP database
Erianthridin 10401022 Click to see COC1=C(C=C2CCC3=C(C2=C1OC)C=CC(=C3)O)O 272.29 unknown https://doi.org/10.1007/S10600-009-9329-7
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
1,5,6-Trimethoxyphenanthrene-2,7-diol 11983285 Click to see COC1=C(C=CC2=C1C=CC3=CC(=C(C(=C32)OC)OC)O)O 300.30 unknown via CMAUP database
2,4-Dimethoxyphenanthrene-3,5-diol 44445443 Click to see COC1=C(C(=C2C(=C1)C=CC3=C2C(=CC=C3)O)OC)O 270.28 unknown via CMAUP database
2,7-Dihydroxy-8-methoxy-5H-phenanthro[4,5-bcd]pyran-5-one 11737608 Click to see COC1=C(C=C2C3=C1C=CC4=CC(=CC(=C43)OC2=O)O)O 282.25 unknown https://doi.org/10.1002/HLCA.200490037
2,7-Phenanthrenediol, 3,4-dimethoxy- 158975 Click to see COC1=C(C=C2C=CC3=C(C2=C1OC)C=CC(=C3)O)O 270.28 unknown via CMAUP database
7-Hydroxy-2,3,4,8-tetramethoxyphenanthrene 5315859 Click to see COC1=C(C(=C2C(=C1)C=CC3=C2C=CC(=C3OC)O)OC)OC 314.30 unknown https://doi.org/10.1007/S10600-009-9329-7
Denbinobin 10423984 Click to see COC1=CC(=C2C(=C1)C=CC3=C2C(=O)C(=CC3=O)OC)O 284.26 unknown via CMAUP database
Dendrochrysanene 11964533 Click to see COC1=C2C(=C3C=CC(=CC3=C1)O)C(=CC4=C2C5(CC(=O)C6=C7C=CC(=CC7=CC(=C65)OC)O)C(=O)O4)O 508.50 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane 12410 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 436.80 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
(-)-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
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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Heptadecanoic acid 10465 Click to see CCCCCCCCCCCCCCCCC(=O)O 270.50 unknown via CMAUP database
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 1-monoacylglycerols
1-Heptadecanoyl-rac-glycerol 107036 Click to see CCCCCCCCCCCCCCCCC(=O)OCC(CO)O 344.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(Z,6S)-2-methyl-6-[(5R,9S,10R,13S,14S,17S)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]hept-2-enoic acid 51693592 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 454.70 unknown via CMAUP database
3-Epioleanolic acid 11869658 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
3beta-Hydroxyfriedelan-16-one 101679786 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CC(=O)C5(C4CC(CC5)(C)C)C)C)C)C)C)O 442.70 unknown via CMAUP database
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Maytensifolin B 21636453 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CC(=O)C5(C4CC(CC5)(C)C)C)C)C)C)C 440.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Cerveratrum-type alkaloids
(6S,23R)-20-hydroxy-6,23-dimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosan-17-one 5315861 Click to see CC1CCC2CC3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C 399.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 6432744 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
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/10.1007/S10600-009-9329-7
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
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 via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
2-amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one 6802 Click to see C1=NC2=C(N1C3C(C(C(O3)CO)O)O)NC(=NC2=O)N 283.24 unknown via CMAUP database
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
Uridine 6029 Click to see C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O 244.20 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
alpha-D-Glucopyranoside, beta-D-fructofuranosyl 91692850 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
Sucrose 5988 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
Sucrose NF 46782954 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5-Hydroxymethylfurfural 237332 Click to see C1=C(OC(=C1)C=O)CO 126.11 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
(7aR)-6-hydroxy-4,4,7a-trimethyl-6,7-dihydro-5H-1-benzofuran-2-one 12311356 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 unknown via CMAUP database
Loliolide 100332 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 unknown via CMAUP database
> Organoheterocyclic compounds / Furopyrans
Aduncin 101316879 Click to see CC(C)C1(C2C3CC4C5(C3(C(C1OC2=O)OC5=O)C)O4)O 294.30 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives
(-)-Dendrobin 15558892 Click to see CC(C)C1C2C3CCC4C3(C(C1OC2=O)N(C4)C)C 263.37 unknown via CMAUP database
(11R,12R,13S)-2,12-dimethyl-13-propan-2-yl-10-oxa-2-azatetracyclo[5.4.1.18,11.04,12]tridecan-9-one 118701398 Click to see CC(C)C1C2C3CCC4C3(C(C1OC2=O)N(C4)C)C 263.37 unknown via CMAUP database
(1S,4S,7S,8S,11S,12R,13S)-2,12-Dimethyl-13-propan-2-yl-10-oxa-2-azatetracyclo[5.4.1.18,11.04,12]tridecan-9-one 3037126 Click to see CC(C)C1C2C3CCC4C3(C(C1OC2=O)N(C4)C)C 263.37 unknown via CMAUP database
Dendroban-12-one 566057 Click to see CC(C)C1C2C3CCC4C3(C(C1OC2=O)N(C4)C)C 263.37 unknown via CMAUP database
Dendrobine 442523 Click to see CC(C)C1C2C3CCC4C3(C(C1OC2=O)N(C4)C)C 263.37 unknown via CMAUP database
From Dendrobium nobile 355017 Click to see CC(C)C1C2C3CCC4C3(C(C1OC2=O)N(C4)C)C 263.37 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Ayapin 3083597 Click to see C1OC2=C(O1)C=C3C(=C2)C=CC(=O)O3 190.15 unknown via CMAUP database
Scoparone 8417 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC 206.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Amentoflavone 5281600 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O 538.50 unknown via CMAUP database
Podocarpusflavone A 5320644 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O 552.50 unknown via CMAUP database
Putraflavone 5320646 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)OC)O)O 566.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown via CMAUP database
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one 932 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown via CMAUP database
Naringenin 439246 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Chrysotobibenzyl 3086528 Click to see COC1=C(C=C(C=C1)CCC2=CC(=C(C(=C2)OC)OC)OC)OC 332.40 unknown https://doi.org/10.1007/S10600-009-9329-7
Crepidatin 14353469 Click to see COC1=CC(=CC(=C1OC)OC)CCC2=CC(=C(C=C2)O)OC 318.40 unknown via CMAUP database
Dendrophenol 176096 Click to see COC1=CC(=CC(=C1O)OC)CCC2=CC(=C(C=C2)O)OC 304.34 unknown via CMAUP database
Dihydroresveratrol 185914 Click to see C1=CC(=CC=C1CCC2=CC(=CC(=C2)O)O)O 230.26 unknown via CMAUP database
Erianin 356759 Click to see COC1=C(C=C(C=C1)CCC2=CC(=C(C(=C2)OC)OC)OC)O 318.40 unknown https://doi.org/10.1007/S10600-009-9329-7
Phenol, 4-[2-(3,4-dimethoxyphenyl)ethyl]-2,6-dimethoxy- 5315860 Click to see COC1=C(C=C(C=C1)CCC2=CC(=C(C(=C2)OC)O)OC)OC 318.40 unknown via CMAUP database

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