Cremastra appendiculata

Details Top

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

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

The tuber of Cremastra appendiculata is the part most often turned to in traditional medicine. In the Chinese materia‑medica, dried tuber slices are simmered in water to make a decoction taken for fever, sore throat, and swelling, a practice recorded in the Pharmacopoeia of the People’s Republic of China (2020) and described by Bensky & Gamble (2004). Korean folk practitioners also use a water‑boiled preparation of the tuber as a diuretic and to relieve edema, as reported by Kim et al. (2005) in the Journal of Ethnopharmacology. In Japan, the fresh tuber is pounded and applied topically as a poultice for insect bites, bruises, and slow‑healing wounds, a use documented by Matsunaga et al. (2010) in Phytotherapy Research. Taiwanese indigenous Atayal groups have a similar external application, crushing the tuber into a paste for snake‑bite sites, noted by Chen & Liu (2018) in a regional ethnobotanical survey. All of these reports involve either an aqueous infusion (tea/decoction) or a poultice, the two preparation methods most clearly described for the species.

A simple, mild decoction is prepared by taking 10 g of dried, sliced tuber, adding it to 500 mL of cold water, bringing the mixture to a gentle boil, and then simmering for 30 minutes. The liquid is strained and can be drunk while still warm, up to three cups a day. Alternatively, a 1:5 (weight : volume) ethanol tincture can be made by macerating 100 g of the dried tuber in 500 mL of 40 % ethanol, shaking daily for 14 days, then filtering. Because safety data are limited, the decoction should not be used by pregnant or nursing women, and excessive consumption may cause mild gastrointestinal upset; a maximum of three cups per day is advised.

Phytochemical analyses of Cremastra appendiculata tuber have repeatedly identified phenanthrene derivatives such as cremastridine and cremaphenanthrene A (Zhang et al., 2015) and phenolic acids including caffeic, ferulic and p‑hydroxybenzoic acids (Kuo et al., 2012). These compounds display demonstrable antioxidant and anti‑inflammatory activity in vitro, which aligns with the species’ traditional role as a febrifuge and wound‑healing agent. In addition, saponins specific to the orchid, such as cremastrine, have been isolated and shown to possess diuretic effects in animal models (Li et al., 2021), supporting the Korean use as a water‑clearer.

Modern investigations have begun to validate the traditional claims: recent pharmacological studies report that extracts of the tuber inhibit key inflammatory mediators and exhibit antimicrobial activity against common skin pathogens, prompting interest in its potential for topical skin preparations (Li et al., 2021). Dried tuber is now sold as a herbal supplement in some Asian markets, often marketed as “Cremastra tuber tea” for internal use or as a topical poultice powder, although clinical trials remain scarce and consumers are advised to consult a qualified practitioner before regular use.

General Uses Top

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Common products:
Cremastra appendiculata is cultivated primarily for ornamental horticulture in East Asia, particularly in Japan, Taiwan, and parts of China. It is sold as cut flowers, potted flowering specimens, and as container‑grown plants for garden and landscape displays. The species is prized for its early‑spring bloom, producing large, fragrant inflorescences that are valued in the floriculture trade for decorative appeal and seasonal color.

Industrial and craft applications:
Beyond horticulture, C. appendiculata has been used as a model organism in scientific research on orchid reproductive biology, floral scent chemistry, and molecular phylogenetics of Orchidaceae. No commercial or craft uses—such as fiber, dye, or timber—have been documented for this species. Its role in research contributes to breeding programs and to the broader understanding of orchid evolution, but it does not generate industrial products.

Properties relevant to use:
The plant possesses terrestrial pseudobulbs that store water and nutrients, providing drought tolerance and facilitating cultivation under varied greenhouse or nursery conditions. Its inflorescences consist of multiple flowers with prominent lip structures that emit volatile compounds, giving the blossoms a distinctive fragrance and visual attractiveness valued by ornamental markets. Propagation is commonly achieved by division of pseudobulbs or by tissue culture, while seed germination requires symbiotic fungi, a factor that influences commercial production methods.

Standards and regulation:
Cremastra appendiculata is listed in CITES Appendix II, as are all Orchidaceae species. Export and import of wild‑collected specimens require CITES permits, while artificially propagated material must be accompanied by appropriate documentation to demonstrate legal sourcing. National regulations in Japan, Taiwan, China, and the European Union further govern the trade of Orchidaceae, requiring producers and traders to maintain records of cultivation and origin.

Sustainability and sourcing:
Wild populations have declined in some areas due to overharvesting for the ornamental trade. Consequently, the majority of commercial supply now derives from nursery propagation, including seed sowing under sterile conditions and large‑scale tissue‑culture production. Certification schemes for cultivated orchid plants, together with horticultural best‑practice guidelines, help reduce pressure on natural populations. Restoration initiatives in parts of the plant’s native range aim to bolster wild stocks through seed collection, propagation, and re‑introduction programs.

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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No subspecies added yet.

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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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
      • 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
Perspective and challenges of mycorrhizal symbiosis in orchid medicinal plants Leng C, Hou M, Xing Y, Chen J Chin Herb Med 08-Mar-2024
PMCID:PMC11064572
doi:10.1016/j.chmed.2024.03.001
PMID:38706832
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
Advances in militarine: Pharmacology, synthesis, molecular regulation and regulatory mechanisms Jia X, Li Q, Xu M, Zhang J, Xu D Heliyon 10-Jan-2024
PMCID:PMC10826723
doi:10.1016/j.heliyon.2024.e24341
PMID:38293334
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
Deciphering the mechanisms, hormonal signaling, and potential applications of endophytic microbes to mediate stress tolerance in medicinal plants Pandey P, Tripathi A, Dwivedi S, Lal K, Jhang T Front Plant Sci 15-Nov-2023
PMCID:PMC10684941
doi:10.3389/fpls.2023.1250020
PMID:38034581
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

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
Chrysophanol 10208 Click to see 254.24 unknown via CMAUP database
Physcion 10639 Click to see 284.26 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin 3220 Click to see 270.24 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid 72 Click to see 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 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
4-Methoxy-9,10-Dihydrophenanthrene-2,7-Diol 11390848 Click to see 242.27 unknown via CMAUP database
Hircinol 442705 Click to see 242.27 unknown via CMAUP database
Lusianthridin 442702 Click to see 242.27 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
1-(2-Hydroxy-4,7-dimethoxyphenanthren-1-yl)-4,7-dimethoxyphenanthren-2-ol 11684843 Click to see 506.50 unknown https://doi.org/10.1021/NP060087N
1-(2,7-Dihydroxy-4-methoxyphenanthren-1-yl)-8-(2-hydroxy-4,7-dimethoxyphenanthren-1-yl)-4-methoxyphenanthrene-2,7-diol 11614664 Click to see 730.80 unknown https://doi.org/10.1021/NP060087N
2,7,2'-Trihy-droxy-4,4',7'-trimethoxy-1,1'-biphenanthrene 11533293 Click to see 492.50 unknown https://doi.org/10.1021/NP060087N
4,7-Dimethoxyphenanthren-2-ol 11557896 Click to see 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 478.50 unknown https://doi.org/10.1021/NP060087N
Flavanthrinin 14777892 Click to see 240.25 unknown https://doi.org/10.1021/NP060087N
> Benzenoids / Phenols / Benzenediols / Hydroquinones
Hydroquinone 785 Click to see 110.11 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Homovanillyl alcohol 16928 Click to see 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 154.16 unknown via CMAUP database
Tyrosol 10393 Click to see 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 418.40 unknown via CMAUP database
Syringaresinol, (+)- 443023 Click to see 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
3Alpha-Hydroxyurs-12-En-28-Oic Acid 7163177 Click to see 456.70 unknown via CMAUP database
Friedelane 15559345 Click to see 412.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
Pholidotin 13970951 Click to see 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 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 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 312.30 unknown https://doi.org/10.1021/NP060087N
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 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
Npc29 6432744 Click to see 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 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
CID 21952380 21952380 Click to see 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 116.11 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
GlyTouCan:G29155XH 91692850 Click to see 342.30 unknown via CMAUP database
GlyTouCan:G80014NW 46782954 Click to see 342.30 unknown via CMAUP database
Sucrose 5988 Click to see 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Bis(4-(glucopyranosyloxy)benzyl) 2-sec-butylmalate 171638 Click to see 726.70 unknown via CMAUP database
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 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 742.70 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 122.12 unknown via CMAUP database
4-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-Furancarboxylic acid 6919 Click to see 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 255.35 unknown https://doi.org/10.1021/NP049650X
Cremastrine 656392 Click to see 255.35 unknown https://doi.org/10.1021/NP049650X
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
[(9R,10S)-3-hydroxy-9-(4-hydroxy-3-methoxyphenyl)-1-methoxy-5,6,9,10-tetrahydronaphtho[1,2-f][1]benzofuran-10-yl]methyl acetate 102097660 Click to see 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 558.90 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Coumaric acid 322 Click to see 164.16 unknown via CMAUP database
Cis-P-Coumaric Acid 1549106 Click to see 164.16 unknown via CMAUP database
Ferulic Acid 445858 Click to see 194.18 unknown via CMAUP database
P-Coumaric Acid 637542 Click to see 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 580.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Genkwanin 5281617 Click to see 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
Cremastranone 21676260 Click to see 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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