Cremastra appendiculata - Unknown
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Details Top

Internal ID UUID6440363b7e794760356252
Scientific name Cremastra appendiculata
Authority (D.Don) Makino
First published in Bot. Mag. (Tokyo) 18: 24 (1904)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cremastra wallichiana Lindl. Gen. Sp. Orchid. Pl. : 173 (1833)
Cymbidium appendiculatum D.Don Prodr. Fl. Nepal. : 36 (1825)
Aplectrum appendiculatum (Blume) F.Maek. Wild Orchids Japan Colour 60, without basionym ref. 1971
Cremastra appendiculata Schltr. Repert. Spec. Nov. Regni Veg. Beih. 4: 225 in obs. 1919
Cremastra appendiculata var. triloba (Hayata) S.S.Ying Chin. Fl. 26: 4. 1976

Common names Top

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Language Common/alternative name
Japanese サイハイラン
Chinese 山慈姑
Chinese 条叶垂头菊
Chinese 山慈菇
Chinese 杜鹃兰
Chinese 翅柱杜鹃兰
Chinese 山慈菇叶
Chinese 杜鹃兰(毛慈姑)
Chinese 馬鞭蘭
Chinese 多变杜鹃兰
Chinese 土贝母
Chinese 毛慈姑

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Cremastra appendiculata var. appendiculata Unknown
Cremastra appendiculata var. variabilis (Blume) I.D.Lund Nordic J. Bot. 8: 201 (1988)

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-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Tibet
    • Eastern Asia
      • Japan
      • Korea
      • Taiwan
    • Russian Far East
      • Kuril Islands
      • Sakhalin
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
      • Nepal
    • Indo-China
      • Laos
      • Myanmar
      • Thailand
      • Vietnam

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000926764
UNII S311HE10NG
KEW urn:lsid:ipni.org:names:624633-1
The Plant List kew-48775
Open Tree Of Life 214424
NCBI Taxonomy 459596
IPNI 624633-1
iNaturalist 452023
GBIF 2789676
Freebase /m/011qdhxf
EPPO KREAP
EOL 1092314
USDA GRIN 413947
Wikipedia Cremastra_appendiculata
CMAUP NPO1756

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
The protective effect of traditional Chinese medicine Jinteng Qingbi granules on rats with rheumatoid arthritis Wan Y, Sun W, Yang J, Wang H, Wang W, Ye W, Cheng G, Li B, Ren J, Kou Q Front Pharmacol 13-Mar-2024
PMCID:PMC10965689
doi:10.3389/fphar.2024.1327647
PMID:38545550
Hyperuricemia research progress in model construction and traditional Chinese medicine interventions Zhou H, Yang J, Yuan X, Song X, Zhang X, Cao T, Zhang J Front Pharmacol 07-Mar-2024
PMCID:PMC10955118
doi:10.3389/fphar.2024.1294755
PMID:38515855
Antitumour mechanisms of traditional Chinese medicine elicited by regulating tumour-associated macrophages in solid tumour microenvironments Gao J, Tan W, Yuan L, Wang H, Wen J, Sun K, Chen X, Wang S, Deng W Heliyon 02-Mar-2024
PMCID:PMC10923716
doi:10.1016/j.heliyon.2024.e27220
PMID:38463777
Traditional and contemporary herbal medicines in management of cancer: A scoping review Imtiaz I, Schloss J, Bugarcic A J Ayurveda Integr Med 23-Feb-2024
PMCID:PMC10901831
doi:10.1016/j.jaim.2024.100904
PMID:38395014
Traditional Chinese Medicine is Associated with the Reduction in Endpoint Events in Patients with Gouty Arthritis: Cohort Study and Association Rule Analysis Chen Y, Liu J, Cong C, Li Y, Hu Y Int J Gen Med 13-Feb-2024
PMCID:PMC10874188
doi:10.2147/IJGM.S451097
PMID:38371521
Diversity of Mycorrhizal Fungi in Temperate Orchid Species: Comparison of Culture-Dependent and Culture-Independent Methods Mennicken S, de Paula CC, Vogt-Schilb H, Jersáková J J Fungi (Basel) 23-Jan-2024
PMCID:PMC10890429
doi:10.3390/jof10020092
PMID:38392764
Bioprospecting of endophytic fungi from medicinal plant Anisomeles indica L. for their diverse role in agricultural and industrial sectors Toppo P, Jangir P, Mehra N, Kapoor R, Mathur P Sci Rep 05-Jan-2024
PMCID:PMC10770348
doi:10.1038/s41598-023-51057-5
PMID:38182714
The complete chloroplast genome of Chrysoglossum ornatum (Epidendroideae, Orchidaceae) and its phylogenetic analysis Tan CJ, Yan RR, Yu P, Lu GQ, Wu W, Hu GX Mitochondrial DNA B Resour 03-Jan-2024
PMCID:PMC10769113
doi:10.1080/23802359.2023.2296920
PMID:38187007
Symbiotic seed germination and seedling growth of mycorrhizal fungi in Paphiopedilum hirsutissimun (Lindl.Ex Hook.) Stein from China Tian F, Wang JC, Bai XX, Yang YB, Huang L, Liao XF Plant Signal Behav 17-Dec-2023
PMCID:PMC10730140
doi:10.1080/15592324.2023.2293405
PMID:38104263
1,5,6-Trimethoxy-2,7-dihydroxyphenanthrene from Dendrobium officinale Exhibited Antitumor Activities for HeLa Cells Liang C, Zhang C, Zhuo Y, Gong B, Xu W, Zhang G Int J Mol Sci 19-Oct-2023
PMCID:PMC10607032
doi:10.3390/ijms242015375
PMID:37895055
Autoactivation of mycorrhizal symbiosis signaling through gibberellin deactivation in orchid seed germination Miura C, Furui Y, Yamamoto T, Kanno Y, Honjo M, Yamaguchi K, Suetsugu K, Yagame T, Seo M, Shigenobu S, Yamato M, Kaminaka H Plant Physiol 30-Sep-2023
PMCID:PMC10756758
doi:10.1093/plphys/kiad517
PMID:37776523
The orchid seed coat: a developmental and functional perspective Lee YI, Yeung EC Bot Stud 27-Sep-2023
PMCID:PMC10533777
doi:10.1186/s40529-023-00400-0
PMID:37755558
Medicinal plant genomics Siadjeu C, Pucker B BMC Genomics 01-Aug-2023
PMCID:PMC10391748
doi:10.1186/s12864-023-09542-8
PMID:37528364
Identification, Biological Function Profiling and Biosynthesis of Secondary Metabolites in Medicinal Orchids Li K, Wu F, Chen M, Xiao Z, Xu Y, Xu M, Liu J, Xu D Metabolites 07-Jul-2023
PMCID:PMC10385179
doi:10.3390/metabo13070829
PMID:37512536
Integrated gut microbiota and metabolome analysis reveals the mechanism of Xiaoai Jiedu recipe in ameliorating colorectal cancer Qiu W, Xie H, Chen H, Zhou H, Wang Z, Zhou H Front Oncol 22-Jun-2023
PMCID:PMC10325652
doi:10.3389/fonc.2023.1184786
PMID:37427121

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 / Anthraquinones
Chrysophanic acid 10208 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3O 254.24 unknown via CMAUP database
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 / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin 3220 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)O 270.24 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown via CMAUP database
> 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 / Phenanthrenes and derivatives / Hydrophenanthrenes
7-Methoxy-9,10-dihydrophenanthrene-2,5-diol 442702 Click to see COC1=CC2=C(C3=C(CC2)C=C(C=C3)O)C(=C1)O 242.27 unknown via CMAUP database
Coelonin 11390848 Click to see COC1=CC(=CC2=C1C3=C(CC2)C=C(C=C3)O)O 242.27 unknown via CMAUP database
Hircinol 442705 Click to see COC1=CC(=CC2=C1C3=C(CC2)C=CC=C3O)O 242.27 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
4,4',4'',7''-Tetramethoxy-1,1':8',1''-terphenanthrene-2,2',2'',7,7'-pentaol 11614664 Click to see COC1=CC2=C(C=C1)C3=C(C=C(C(=C3C=C2)C4=C(C=CC5=C4C=CC6=C(C(=CC(=C56)OC)O)C7=C8C=CC9=C(C8=C(C=C7O)OC)C=CC(=C9)O)O)O)OC 730.80 unknown https://doi.org/10.1021/NP060087N
4,4',7,7'-Tetramethoxy-1,1'-biphenanthrene-2,2'-diol 11684843 Click to see COC1=CC2=C(C=C1)C3=C(C=C(C(=C3C=C2)C4=C5C=CC6=C(C5=C(C=C4O)OC)C=CC(=C6)OC)O)OC 506.50 unknown https://doi.org/10.1021/NP060087N
4,4',7'-Trimethoxy-1,1'-biphenanthrene-2,2',7-triol 11533293 Click to see COC1=CC2=C(C=C1)C3=C(C=C(C(=C3C=C2)C4=C5C=CC6=C(C5=C(C=C4O)OC)C=CC(=C6)O)O)OC 492.50 unknown https://doi.org/10.1021/NP060087N
4,7-Dimethoxyphenanthrene-2-ol 11557896 Click to see COC1=CC2=C(C=C1)C3=C(C=C(C=C3C=C2)O)OC 254.28 unknown https://doi.org/10.1021/NP060087N
Blestriarene B 442695 Click to see COC1=C2C(=C(C(=C1)O)C3=C4C=CC5=C(C4=C(C=C3O)OC)C=CC(=C5)O)CCC6=C2C=CC(=C6)O 480.50 unknown via CMAUP database
Cirrhopetalanthin 9982511 Click to see COC1=C2C3=C(C=CC2=C(C(=C1)O)C4=C5C=CC6=C(C5=C(C=C4O)OC)C=CC(=C6)O)C=C(C=C3)O 478.50 unknown https://doi.org/10.1021/NP060087N
Flavanthrinin 14777892 Click to see COC1=C2C(=CC(=C1)O)C=CC3=C2C=CC(=C3)O 240.25 unknown https://doi.org/10.1021/NP060087N
> Benzenoids / Phenols / Benzenediols / Hydroquinones
Hydroquinone 785 Click to see C1=CC(=CC=C1O)O 110.11 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Homovanillyl alcohol 16928 Click to see COC1=C(C=CC(=C1)CCO)O 168.19 unknown via CMAUP database
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Hydroxytyrosol 82755 Click to see C1=CC(=C(C=C1CCO)O)O 154.16 unknown via CMAUP database
Tyrosol 10393 Click to see C1=CC(=CC=C1CCO)O 138.16 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
2-Dodecyl-3-methylbutanedioic acid 99891 Click to see CCCCCCCCCCCCC(C(C)C(=O)O)C(=O)O 300.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Epiursolic acid 7163177 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
Friedelane 15559345 Click to see CC1CCCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 412.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
Pholidotin 13970951 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)C)C 586.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
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 via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
(1R)-1-hydroxy-4,7-dimethoxy-1-(2-oxopropyl)phenanthren-2-one 163002432 Click to see CC(=O)CC1(C2=C(C3=C(C=C2)C=C(C=C3)OC)C(=CC1=O)OC)O 326.30 unknown https://doi.org/10.1021/NP060087N
(1S)-1,7-dihydroxy-4-methoxy-1-(2-oxopropyl)phenanthren-2-one 162955161 Click to see CC(=O)CC1(C2=C(C3=C(C=C2)C=C(C=C3)O)C(=CC1=O)OC)O 312.30 unknown https://doi.org/10.1021/NP060087N
1-Hydroxy-4,7-dimethoxy-1-(2-oxopropyl)phenanthren-2-one 11645552 Click to see CC(=O)CC1(C2=C(C3=C(C=C2)C=C(C=C3)OC)C(=CC1=O)OC)O 326.30 unknown https://doi.org/10.1021/NP060087N
1,7-Dihydroxy-4-methoxy-1-(2-oxopropyl)phenanthren-2-one 11716581 Click to see CC(=O)CC1(C2=C(C3=C(C=C2)C=C(C=C3)O)C(=CC1=O)OC)O 312.30 unknown https://doi.org/10.1021/NP060087N
> 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 via CMAUP database
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
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
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
L-Pyroglutamic acid 7405 Click to see C1CC(=O)NC1C(=O)O 129.11 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(E)-but-2-enedioate;hydron 21883788 Click to see [H+].[H+].C(=CC(=O)[O-])C(=O)[O-] 116.07 unknown via CMAUP database
Butanedioate;hydron 21952380 Click to see [H+].[H+].C(CC(=O)[O-])C(=O)[O-] 118.09 unknown via CMAUP database
> Organic acids and derivatives / Keto acids and derivatives / Gamma-keto acids and derivatives
Levulinic acid 11579 Click to see CC(=O)CCC(=O)O 116.11 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 / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Dactylorhin A 10819499 Click to see CC(C)CC(CC(=O)OCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)(C(=O)OCC3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 888.90 unknown via CMAUP database
Gastrodin 115067 Click to see C1=CC(=CC=C1CO)OC2C(C(C(C(O2)CO)O)O)O 286.28 unknown via CMAUP database
Ibotanolide B 6442827 Click to see C1=CC(=C(C=C1CCO)O)OC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O 478.40 unknown via CMAUP database
Loroglossin 185907 Click to see CC(C)CC(C(C(=O)OCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)O)(C(=O)OCC3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O 742.70 unknown via CMAUP database
Militarine 171638 Click to see CC(C)CC(CC(=O)OCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)(C(=O)OCC3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O 726.70 unknown via CMAUP database
Vanilloloside 44577222 Click to see COC1=C(C=CC(=C1)CO)OC2C(C(C(C(O2)CO)O)O)O 316.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see C1=CC(=CC=C1C=O)O 122.12 unknown via CMAUP database
p-Hydroxybenzaldehyde-d5 10701848 Click to see C1=CC(=CC=C1C=O)O 127.15 unknown via CMAUP database
> 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 via CMAUP database
> Organoheterocyclic compounds / Pyrrolizidines
2,3,5,6,7,8-hexahydro-1H-pyrrolizin-1-ylmethyl 2-hydroxy-3-methylpentanoate 78202315 Click to see CCC(C)C(C(=O)OCC1CCN2C1CCC2)O 255.35 unknown https://doi.org/10.1021/NP049650X
Cremastrine 656392 Click to see CCC(C)C(C(=O)OCC1CCN2C1CCC2)O 255.35 unknown https://doi.org/10.1021/NP049650X
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Shanciol H 102097660 Click to see CC(=O)OCC1C(OC2=C1C=C3C(=C2)CCC4=C3C(=CC(=C4)O)OC)C5=CC(=C(C=C5)O)OC 462.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Hexacosyl (E)-ferulate 5318033 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 558.90 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
cis-p-Coumaric acid 1549106 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown via CMAUP database
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 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
Kayaflavone 9894522 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)OC 580.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Genkwanin 5281617 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
3-(3-Hydroxy-4-methoxybenzyl)-5,7-dihydroxy-6-methoxychroman-4-one 21676260 Click to see COC1=C(C=C(C=C1)CC2COC3=C(C2=O)C(=C(C(=C3)O)OC)O)O 346.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
batatasin III 10466989 Click to see COC1=CC(=CC(=C1)O)CCC2=CC(=CC=C2)O 244.28 unknown via CMAUP database

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