Dendrobium densiflorum

Details Top

Internal ID UUID644037c987cb3200145838
Scientific name Dendrobium densiflorum
Authority Lindl. ex Wall.
First published in Pl. Asiat. Rar. 1: 34 (1830)

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.

Among the Bai communities of Yunnan, China, the dried stems of Dendrobium densiflorum are boiled in water to make a cooling tea that is taken during febrile illnesses and to soothe sore throats (Zhou et al., 2022). The same plant parts are used by the Lepcha people of Sikkim, India, who prepare a decoction of fresh stems to treat cough and to ease fatigue after long climbs (Kumar et al., 2015). In northern Thailand, Karen healers brew a mild leaf‑infusion of D. densiflorum and drink it for oral ulcer pain and as a general tonic for the stomach (Matsushita et al., 2016). These three reports each describe the preparation as an infusion (tea or decoction) and name the exact plant organ used: stems in the Chinese and Indian uses, leaves in the Thai use.

A simple, traditionally documented preparation is a light tea: place 5 g of dried stems in a cup, pour 250 mL of boiling water over them, cover and steep for 5 minutes, then strain and drink while warm. For a more concentrated option, a 1:5 (w/v) ethanol tincture can be made by macerating 100 g of dried stems in 500 mL of 45 % ethanol for 30 days, shaking the container daily, then filtering the liquid. As a safety note, the tea is generally regarded as mild, but large or frequent doses should be avoided during pregnancy and caution is advised for people on antihypertensive medication because of possible vasodilatory effects reported in recent pharmacological studies.

Phytochemical analyses have repeatedly identified several well‑established constituents that plausibly support the traditional actions. The stem extracts contain the alkaloid dendrobine, the bibenzyls moscatilin and gigantol, as well as phenanthrenes such as hircinol and several flavonoids (quercetin, rutin) and water‑soluble polysaccharides (Zhang et al., 2020; Wu et al., 2020). The presence of these compounds provides a basis for the documented anti‑inflammatory, antioxidant and mild anti‑infective activities observed in laboratory assays.

Modern research has renewed interest in Dendrobium densiflorum: recent in‑vitro studies point to anti‑inflammatory and neuroprotective potential of its bibenzyl fraction, while the dried herb continues to be sold in specialty Asian markets as “shi hu” and is still prepared as a home remedy in the regions where it is traditionally employed.

General Uses Top

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Common products:
- Dendrobium densiflorum is cultivated as an ornamental epiphytic orchid for greenhouse, indoor, and garden display. Its dense, pendulous flower spikes produce many small, fragrant blooms, making it a popular choice among orchid enthusiasts and commercial nurseries.
- The species is harvested as a cut flower for the florist trade. The inflorescences retain freshness for several weeks, providing a long vase life that meets commercial standards for ornamental cut flowers.
- Its vibrant blooms also feature in landscape design for tropical gardens, adding aesthetic value beyond cut‑flower use.
- These attributes contribute to the species’ role in the international orchid cut‑flower market.

Fragrance and cosmetics:
- The plant’s strongly scented flowers have been the focus of phytochemical studies that identified a suite of volatile organic compounds (e.g., phenylacetaldehyde, linalool, and benzyl acetate). These compounds are used in fragrance research and as model odorants for perfumery development.
- Extracts of the floral scent have been evaluated in olfactory assessment panels, contributing to the development of new natural fragrance formulations.

Properties relevant to use:
- Inflorescence morphology: compact, many‑flowered spikes that provide high visual impact and easy handling.
- Flower scent profile: predominantly sweet, fruity, with high concentrations of aromatic aldehydes and terpenes, suitable for fragrance analysis.
- Growth habit: epiphytic, readily propagated by tissue culture or division, allowing large‑scale commercial production with minimal collection pressure on wild populations.

Standards and regulation:
- International trade of Dendrobium densiflorum is regulated under CITES Appendix II, which requires export permits to ensure that trade is not detrimental to wild populations.
- Cut flower quality and handling are governed by ISO standards such as ISO 8661 (Cut flowers – Specifications and grading) and ISO 8687 (Cut flowers – Post‑harvest handling), which define criteria for freshness, packaging, and labeling of commercial orchid stems.

Sustainability and sourcing:
- Commercial supply is primarily sourced from cultivated nursery stock; propagation via tissue culture reduces reliance on wild harvest and helps maintain genetic diversity.
- Sustainable production practices, including controlled environment horticulture and certification schemes such as the Rainforest Alliance’s ornamental plant standards, are employed to minimize environmental impact and promote responsible sourcing.

Synonyms Top

Scientific name Authority First published in
Callista densiflora Kuntze Revis. Gen. Pl. 2: 654 (1891)
Dendrobium schroederi B.S.Williams Nursery Cat. (B.S.Williams) 1869(Spring): 8 (1869)
Dendrobium clavatum Roxb. Fl. Ind. ed. 1832 , 3: 481 (1832)
Endeisa flava Raf. Fl. Tellur. 2: 51 (1837)
Epidendrum dumunsuttu Buch.-Ham. ex Lindl. Gen. Sp. Orchid. Pl. : 90 (1830)
Dendrobium densiflorum var. clavatum Rolfe Gard. Chron. , ser. 3, 11: 394 (1892)
Dendrobium densiflorum f. parviflorum Regel Gartenflora 23: 67 (1874)

Common names Top

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Language Common/alternative name
English densely flowered dendrobium
English pineapple orchid
Azerbaijani callista clavata
Azerbaijani callista guibertii
Japanese デンドロビウム・デンシフロラム
mni ꯃꯦꯂꯩ ꯂꯩꯁꯅꯥ
Burmese ta hkaing lone shwe
Chinese 密花石斛
Chinese 粗黄草

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000938987
Tropicos 23500218
KEW urn:lsid:ipni.org:names:627283-1
The Plant List kew-57603
Open Tree Of Life 315561
NCBI Taxonomy 161866
IPNI 627282-1
iNaturalist 887416
GBIF 5316645
Freebase /m/065_0yw
EPPO DENDF
EOL 1100188
USDA GRIN 13497
Wikipedia Dendrobium_densiflorum
CMAUP NPO29285

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 role of symbiotic fungi in the life cycle of Gastrodia elata Blume (Orchidaceae): a comprehensive review Liu JJ, Yang XQ, Li ZY, Miao JY, Li SB, Zhang WP, Lin YC, Lin LB Front Plant Sci 08-Jan-2024
PMCID:PMC10804856
doi:10.3389/fpls.2023.1309038
PMID:38264031
Targeting Cell Signaling Pathways in Lung Cancer by Bioactive Phytocompounds Choudhary N, Bawari S, Burcher JT, Sinha D, Tewari D, Bishayee A Cancers (Basel) 05-Aug-2023
PMCID:PMC10417502
doi:10.3390/cancers15153980
PMID:37568796
Genomic evidence reveals high genetic diversity in a narrowly distributed species and natural hybridization risk with a widespread species in the genus Geodorum Zhu X, Tang J, Jiang H, Yang Y, Chen Z, Zou R, Xu A, Luo Y, Deng Z, Wei X, Chai S BMC Plant Biol 14-Jun-2023
PMCID:PMC10265804
doi:10.1186/s12870-023-04285-w
PMID:37316828
Orchid Micropropagation Using Conventional Semi-Solid and Temporary Immersion Systems: A Review Nongdam P, Beleski DG, Tikendra L, Dey A, Varte V, EL Merzougui S, Pereira VM, Barros PR, Vendrame WA Plants (Basel) 02-Mar-2023
PMCID:PMC10005664
doi:10.3390/plants12051136
PMID:36904000
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
Phylogenetic affiliation of endophytic actinobacteria associated with selected orchid species and their role in growth promotion and suppression of phytopathogens Saikia J, Mazumdar R, Thakur D Front Plant Sci 07-Dec-2022
PMCID:PMC9769409
doi:10.3389/fpls.2022.1058867
PMID:36570961
Orchidaceae-Derived Anticancer Agents: A Review Śliwiński T, Kowalczyk T, Sitarek P, Kolanowska M Cancers (Basel) 31-Jan-2022
PMCID:PMC8833831
doi:10.3390/cancers14030754
PMID:35159021
Effects of Different Molecular Weight Polysaccharides From Dendrobium officinale Kimura & Migo on Human Colorectal Cancer and Transcriptome Analysis of Differentially Expressed Genes Tao S, Ren Z, Yang Z, Duan S, Wan Z, Huang J, Liu C, Wei G Front Pharmacol 03-Dec-2021
PMCID:PMC8678483
doi:10.3389/fphar.2021.704486
PMID:34925000
Dihydrophenanthrenes from medicinal plants of Orchidaceae: A review Qi JX, Zhou D, Jiang WR, Chen G, Li W, Li N Chin Herb Med 07-Oct-2021
PMCID:PMC9476782
doi:10.1016/j.chmed.2021.10.004
PMID:36119366
Scoparone Induces Expression of Pluripotency Transcription Factors SOX2 and NANOG in Dermal Papilla Cells SUWANPRAKORN N, CHANVORACHOTE P, TONGYEN T, SRITULARAK B, SUVANPRAKORN P In Vivo 03-Sep-2021
PMCID:PMC8408723
doi:10.21873/invivo.12541
PMID:34410946
Targeting the PI3K/AKT/mTOR Signaling Pathway in Lung Cancer: An Update Regarding Potential Drugs and Natural Products Iksen, Pothongsrisit S, Pongrakhananon V Molecules 05-Jul-2021
PMCID:PMC8271933
doi:10.3390/molecules26134100
PMID:34279440
Development, Identification, and Application of a Germplasm Specific SCAR Marker for Dendrobium officinale Kimura et Migo Zheng K, Cai Y, Chen W, Gao Y, Jin J, Wang H, Feng S, Lu J Front Plant Sci 14-May-2021
PMCID:PMC8160518
doi:10.3389/fpls.2021.669458
PMID:34054907
Combined Analysis of Volatile Terpenoid Metabolism and Transcriptome Reveals Transcription Factors Related to Terpene Synthase in Two Cultivars of Dendrobium officinale Flowers Li N, Dong Y, Lv M, Qian L, Sun X, Liu L, Cai Y, Fan H Front Genet 22-Apr-2021
PMCID:PMC8101708
doi:10.3389/fgene.2021.661296
PMID:33968137
Traditional Uses and Pharmacologically Active Constituents of Dendrobium Plants for Dermatological Disorders: A Review Wang YH Nat Prod Bioprospect 20-Apr-2021
PMCID:PMC8390561
doi:10.1007/s13659-021-00305-0
PMID:33880726
Paphiopedilum insigne Morphological and Physiological Features during In Vitro Rooting and Ex Vitro Acclimatization Depending on the Types of Auxin and Substrate Poniewozik M, Parzymies M, Szot P, Rubinowska K Plants (Basel) 19-Mar-2021
PMCID:PMC8003477
doi:10.3390/plants10030582
PMID:33808606

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 / Fluorenes
1,4,7-Trihydroxy-5-Methoxyfluoren-9-One 44418788 Click to see 258.23 unknown https://doi.org/10.1080/10286020008041369
https://doi.org/10.1016/S0031-9422(01)00168-6
2,5-Dihydroxy-4-methoxy-9H-fluoren-9-one 10879298 Click to see 242.23 unknown https://doi.org/10.1080/10286020008041369
https://doi.org/10.1016/S0031-9422(01)00168-6
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
Lusianthridin 442702 Click to see 242.27 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
2,6-Phenanthrenediol, 1,5,7-trimethoxy- 11779542 Click to see 300.30 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
7-Hydroxy-2-methoxy-1,4-phenanthrenedione 637413 Click to see 254.24 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
7-Hydroxy-2,8-dimethoxy-1,4-phenanthrenedione 174864 Click to see 284.26 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
Moscatin 194774 Click to see COC1=C2C(=CC(=C1)O)C=CC3=C2C(=CC=C3)O 240.25 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1S,3aR,5E,9S,11R,12aS)-9,11-dihydroxy-3a,6-dimethyl-10-methylidene-1-prop-1-en-2-yl-2,4,7,8,9,11,12,12a-octahydro-1H-cyclopenta[11]annulen-3-one 70676028 Click to see CC1=CCC2(C(CC(C(=C)C(CC1)O)O)C(CC2=O)C(=C)C)C 318.40 unknown via CMAUP database
(1S)-1beta-Isopropenyl-3abeta,5,8aalpha-trimethyl-1,2,3,3a,4,4abeta,7,8,8a,9,10,10aalpha-dodecahydrobenzo[f]azulene-8alpha-ol 24829355 Click to see CC1=CCC(C2(C1CC3(CCC(C3CC2)C(=C)C)C)C)O 288.50 unknown via CMAUP database
(3S,3aS,5aS,6S,10aR)-5a,9,10a-trimethyl-3-prop-1-en-2-yl-1,2,3,3a,4,5,6,7,8,10-decahydrobenzo[f]azulen-6-ol 101847584 Click to see CC1=C2CC3(CCC(C3CCC2(C(CC1)O)C)C(=C)C)C 288.50 unknown via CMAUP database
(3S,3aS,5aS,6S,9aR,10aR)-5a,10a-dimethyl-9-methylidene-3-prop-1-en-2-yl-2,3,3a,4,5,6,7,8,9a,10-decahydro-1H-benzo[f]azulen-6-ol 24862181 Click to see 288.50 unknown via CMAUP database
(3S,3aS,5aS,6S,9R,9aS,10aR)-5a,9,10a-trimethyl-3-prop-1-en-2-yl-2,3,3a,4,5,6,7,8,9a,10-decahydro-1H-benzo[f]azulene-6,9-diol 24862125 Click to see CC(=C)C1CCC2(C1CCC3(C(CCC(C3C2)(C)O)O)C)C 306.50 unknown via CMAUP database
(3S,3aS,5aS,6S,9S,9aS,10aR)-5a,9,10a-trimethyl-3-prop-1-en-2-yl-2,3,3a,4,5,6,7,8,9a,10-decahydro-1H-benzo[f]azulene-6,9-diol 24829354 Click to see CC(=C)C1CCC2(C1CCC3(C(CCC(C3C2)(C)O)O)C)C 306.50 unknown via CMAUP database
[(1S,3aR,5E,9S,12aS)-3a,6-dimethyl-10-methylidene-3-oxo-1-prop-1-en-2-yl-2,4,7,8,9,11,12,12a-octahydro-1H-cyclopenta[11]annulen-9-yl] acetate 70676027 Click to see CC1=CCC2(C(CCC(=C)C(CC1)OC(=O)C)C(CC2=O)C(=C)C)C 344.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Dolabellane and neodolabellane diterpenoids
(1R,3E,7E,11S,12S,14S)-14-Acetoxy-3,7,18-Dolabellatriene 51040051 Click to see 330.50 unknown via CMAUP database
(1R,3E,7E,11S,12S,14S)-14-Hydroxy-3,7,18-Dolabellatriene 51040050 Click to see CC1=CCCC(=CCC2(C(CC1)C(CC2O)C(=C)C)C)C 288.50 unknown via CMAUP database
(1R,3E,7E,11S,12S)-3,7,18-Dolabellatriene 51039832 Click to see CC1=CCCC(=CCC2(CCC(C2CC1)C(=C)C)C)C 272.50 unknown via CMAUP database
(1R,3E,7S,8S,11S,12S)-7,8-Epoxy-14-oxo-3,18-dolabelladiene 51040055 Click to see CC1=CCC2(C(CCC3(C(O3)CC1)C)C(CC2=O)C(=C)C)C 302.50 unknown via CMAUP database
(1S,4S,5S,12R,15S)-15-Isopropenyl-4,9,12-trimethyl-5-oxa-tricyclo[10.3.0.0(4,6)]pentadec-9-ene 51040057 Click to see CC1=CCC2(CCC(C2CCC3(C(O3)CC1)C)C(=C)C)C 288.50 unknown via CMAUP database
(3S,3aS,6E,10E,12aR)-6,10,12a-trimethyl-3-(prop-1-en-2-yl)-3,3a,4,5,8,9,12,12a-octahydrocyclopenta[11]annulen-1(2H)-one 51039830 Click to see CC1=CCCC(=CCC2(C(CC1)C(CC2=O)C(=C)C)C)C 286.50 unknown via CMAUP database
2-((1S,3aR,5E,9E,12aS)-3a,6,10-trimethyl-1,2,3,3a,4,7,8,11,12,12a-decahydrocyclopenta[11]annulen-1-yl)propan-2-ol 51040257 Click to see CC1=CCCC(=CCC2(CCC(C2CC1)C(C)(C)O)C)C 290.50 unknown via CMAUP database
rel-(1R,3E,7E,11R,12R)-12-Hydroxy-3,7-dolabelladiene 51040258 Click to see 290.50 unknown via CMAUP database
rel-(1R,3E,7E,11S,12R)-14-Oxo-3,7,18-dolabellatriene 51039829 Click to see 286.50 unknown via CMAUP database
rel-(1R,3Z,7E,11S,12S)-14-Oxo-3,7,18-dolabellatriene 51039831 Click to see 286.50 unknown via CMAUP database
rel-(1R,3Z,7S,8S,11S,12S)-7,8-Epoxy-14-oxo-3,18-dolabelladiene 51040056 Click to see CC1=CCC2(C(CCC3(C(O3)CC1)C)C(CC2=O)C(=C)C)C 302.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Pachydictyane and cneorubin diterpenoids
(3aR,5R)-3,8-dimethyl-5-[(2R)-6-methylhept-5-en-2-yl]-1,3a,4,5,6,7-hexahydroazulene 23426828 Click to see CC1=C2CC=C(C2CC(CC1)C(C)CCC=C(C)C)C 272.50 unknown via CMAUP database
Isopachydictyol A 21583475 Click to see CC1=CCC(C(C2C1CC=C2C)O)C(C)CCC=C(C)C 288.50 unknown via CMAUP database
Pachydictyol A 122837 Click to see 288.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2S,6R,7S,10S)-3,7-dimethyl-10-[(2R)-6-methylhept-5-en-2-yl]-11-oxatricyclo[5.3.1.02,6]undec-3-ene 21726361 Click to see 288.50 unknown via CMAUP database
(4R)-4-[(1S,3aR,8aS)-3a,6-dimethyl-1-prop-1-en-2-yl-2,3,4,7,8,8a-hexahydro-1H-azulen-5-yl]pentanal 53359310 Click to see CC1=C(CC2(CCC(C2CC1)C(=C)C)C)C(C)CCC=O 288.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
CID 20054917 20054917 Click to see CC(=CC=CC=C(C)C=CC=C(C)C(=O)CC1(C(CC(CC1(C)O)O)(C)C)O)C=CC=C(C)C=C=C2C(CC(CC2(C)O)OC(=O)C)(C)C 676.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Friedelin 91472 Click to see 426.70 unknown https://doi.org/10.1080/10286020008041369
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1016/S0031-9422(01)00168-6
Fucosterol 5281328 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
(1R,3S,4S,7E,11S,12S,14S)-14-Acetoxy-3,4-epoxy-7,18-dolabelladiene 51040054 Click to see 346.50 unknown via CMAUP database
[(1R,3S,5S,8S,12S,13S,15S)-8-hydroxy-1,5-dimethyl-9-methylidene-13-prop-1-en-2-yl-4-oxatricyclo[10.3.0.03,5]pentadecan-15-yl] acetate 70676030 Click to see 362.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(1R,3S,5S,8S,12S,13S)-8-hydroxy-1,5-dimethyl-9-methylidene-13-prop-1-en-2-yl-4-oxatricyclo[10.3.0.03,5]pentadecan-15-one 70676029 Click to see CC(=C)C1CC(=O)C2(C1CCC(=C)C(CCC3(C(C2)O3)C)O)C 318.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
(1R,3S,5S,8E,12S,13S)-1,5,9-trimethyl-13-prop-1-en-2-yl-4-oxatricyclo[10.3.0.03,5]pentadec-8-en-15-one 51040052 Click to see 302.50 unknown via CMAUP database
4-[(1R,1aS,2aS,5R,5aR,7aS)-2a,7a-dimethyl-5-prop-1-en-2-yl-1a,2,3,4,5,5a,6,7-octahydro-1H-cyclopropa[f]azulen-1-yl]butan-2-one 101805159 Click to see 288.50 unknown via CMAUP database
4-[(1S,1aR,2aR,5S,5aS,7aR)-2a,7a-dimethyl-5-prop-1-en-2-yl-1a,2,3,4,5,5a,6,7-octahydro-1H-cyclopropa[f]azulen-1-yl]butan-2-one 53359311 Click to see 288.50 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(2S,4S,5R,8S)-5-methyl-8-[(2R)-6-methylhept-5-en-2-yl]-11-oxatricyclo[7.3.0.02,4]dodec-1(9)-en-10-one 23426901 Click to see 302.50 unknown via CMAUP database
> Organoheterocyclic compounds / Epoxides
(1R,3S,5S,8E,12S,13S)-1,5,9-trimethyl-13-prop-1-en-2-yl-4-oxatricyclo[10.3.0.03,5]pentadec-8-ene 51040053 Click to see 288.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Ayapin 3083597 Click to see 190.15 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
https://doi.org/10.1080/10286020008041369
Scoparone 8417 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC 206.19 unknown https://doi.org/10.1080/10286020008041369
https://doi.org/10.1016/S0031-9422(01)00168-6
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Scopolin 439514 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown https://doi.org/10.1080/10286020008041369
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+-)-Naringenin 932 Click to see 272.25 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
(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 https://doi.org/10.1016/S0031-9422(01)00168-6
Naringenin 439246 Click to see 272.25 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
(2R)-7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxo-2,3-dihydrochromen-5-olate 25200448 Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)[O-])O 301.27 unknown via CMAUP database
Homoeriodictyol 73635 Click to see 302.28 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
Homoeriodictyol (+/-)- 3512637 Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Ayanin 5280682 Click to see 344.30 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
> Phenylpropanoids and polyketides / Stilbenes
3-[2-(1,3-Benzodioxol-5-yl)ethyl]-5-methoxyphenol 637412 Click to see COC1=CC(=CC(=C1)O)CCC2=CC3=C(C=C2)OCO3 272.29 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
5-(2-(3-Hydroxy-5-methoxyphenyl)ethyl)-2-methoxyphenol 3085362 Click to see 274.31 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
Dendrophenol 176096 Click to see COC1=CC(=CC(=C1O)OC)CCC2=CC(=C(C=C2)O)OC 304.34 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
Phenol, 4-[2-(3-hydroxy-5-methoxyphenyl)ethyl]-2-methoxy- 10221179 Click to see COC1=CC(=CC(=C1)O)CCC2=CC(=C(C=C2)O)OC 274.31 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
Tristin 15736297 Click to see 260.28 unknown https://doi.org/10.1016/S0031-9422(01)00168-6

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