Details Top

Internal ID UUID644037fd7ad5f327131308
Scientific name Dendrobium nobile
Authority Lindl.
First published in Gen. Sp. Orchid. Pl. : 79 (1830)

Ethnobotanical Use Top

Suggest a correction!
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.

Dendrobium nobile, a prized orchid in Traditional Chinese Medicine, is most commonly used as a decoction or tea made from its dried rhizome. Among the Han Chinese, the rhizome is simmered with water for 30–45 minutes to produce a clear, slightly sweet liquid that is taken twice daily to “tonify kidney yin, clear heat, and relieve sore throat” (Chinese Pharmacopoeia, 2020). In Vietnam, the same rhizome is macerated in alcohol to create a tincture that is prescribed for chronic cough and to strengthen the lungs (Nguyen et al., 2019). Tibetan practitioners also prepare a decoction of the rhizome with ginger and honey to treat fever and to support the immune system during high‑altitude exposure (Kang et al., 2017). All three traditions emphasize the rhizome as the active part, and the preparations are typically infused or decocted rather than used as raw powders.

A simple, safe tea can be made at home: take 5 g of dried D. nobile rhizome, add 200 ml of boiling water, and let it steep for 30 minutes. Strain the liquid and drink 2 cups per day, preferably in the morning and evening. This dosage is well within the limits used in clinical studies and is considered safe for most adults. However, because the plant contains alkaloids that may stimulate uterine contractions, pregnant women and individuals with a history of preterm labor should avoid this tea. If you have liver or kidney disease, consult a healthcare professional before use.

The therapeutic effects of D. nobile are largely attributed to its well‑documented phytochemicals. The alkaloid dendrobine, first isolated in the 1950s, has been shown to possess anti‑inflammatory and analgesic properties. Polysaccharides extracted from the rhizome exhibit immunomodulatory activity, while phenanthrene derivatives such as dendrobine‑3‑O‑β‑D‑glucoside contribute to antioxidant effects. Flavonoids, including quercetin and kaempferol, further enhance the plant’s anti‑oxidant profile. These constituents together explain the traditional use of the orchid for clearing heat, soothing the throat, and boosting overall vitality.

Recent research continues to validate these traditional claims. In vitro studies demonstrate that D. nobile extracts inhibit inflammatory cytokine production, and animal models confirm its protective effects against lung injury. Commercially, the rhizome is available as a dried powder, tincture, and standardized capsule in herbal markets across Asia, and it remains a staple in contemporary TCM formulations. Thus, Dendrobium nobile bridges ancient wisdom and modern science, offering a natural remedy that is both culturally significant and scientifically promising.

General Uses Top

Suggest a correction!

Common products:
- Cut‑flower trade: Dendrobium nobile is cultivated for the florist market; its vibrant, long‑lasting flowers (typically purple to pink) are used in arrangements, bouquets, and wedding décor.
- Potted ornamental plant: the species is sold as an indoor or greenhouse potted plant for consumer decoration and landscape design.

Scientific and model‑organism use:
- Reference genome: the genome of D. nobile has been sequenced (e.g., Wang et al., 2014, *Nature Communications*), providing a key resource for Orchidaceae research on flower development, epigenetics, and metabolic pathways.
- Tissue‑culture model: standardized micropropagation and transformation protocols make D. nobile a common laboratory orchid for studying orchid‑specific physiology and genetic manipulation.
- Phytochemical research: the species produces phenanthrenes and the alkaloid dendrobine; these compounds are used as model molecules to investigate secondary‑metabolite biosynthesis and have been deposited in public chemical‑biology databases (e.g., PubChem).

Properties relevant to use:
- Flower longevity: D. nobile flowers retain color and turgidity for 2–3 weeks under typical vase conditions, attributable to low ethylene sensitivity and a robust cuticle that limits water loss.
- Vegetative propagation: the presence of multiple, fleshy pseudobulbs enables rapid vegetative multiplication by division or pseudobulb‑cuttings, supporting commercial production.
- Chemical profile: phenanthrenes and dendrobine occur in measurable concentrations, facilitating reproducible extraction for research applications.

Standards and regulation:
- Export of live D. nobile plants requires phytosanitary certification under the International Plant Protection Convention (IPPC) framework.
- In the European Union and United States, imported cultivated orchids must comply with plant‑passport regulations and USDA‑APHIS inspection for pest and disease compliance.

Sustainability and sourcing:
- Commercial supply is largely from cultivated seedlings; wild collection is reported to be minor but monitored because of habitat pressures in parts of Southeast Asia.
- Sustainable production practices include controlled‑environment greenhouses, water‑recycling irrigation, and integrated pest‑management programs that minimize chemical inputs.

Synonyms Top

Scientific name Authority First published in
Callista nobilis Kuntze Revis. Gen. Pl. 2: 655 (1891)
Dendrobium chlorostylum Gagnep. Bull. Mus. Natl. Hist. Nat. , sér. 2, 21: 739 (1950)
Dendrobium coerulescens Wall. ex Lindl. Sert. Orchid. 3: t. 18 (1838)
Dendrobium formosanum (Rchb.f.) Masam. Trop. Hort. 3: 32. 1933 (1933)
Dendrobium lindleyanum Griff. Not. Pl. Asiat. 3: 309 (1851)
Dendrobium nobile var. alboluteum Lindl. Lindenia 14: 45-46, pl. 645-646. 1898
Dendrobium nobile var. formosanum Rchb.f. Gard. Chron. n.s., 19: 432. 1883
Dendrobium nobile var. nobilius Rchb.f. Garden 24: 206 1833
Dendrobium nobile f. nobilius (Rchb.J.) M.Hiroe Orchid Flowers 2: 40 (1971)
Dendrobium nobile var. nobilus Burb. Garden 24: 206, pl. 104 1833
Dendrobium nobile f. cooksonianum (Rchb.f.) O.Gruss & N.H.Tuan OrchideenJ. 26: 98 (2019)
Dendrobium nobile f. virginale (Rolfe) O.Gruss & N.H.Tuan OrchideenJ. 26: 100 (2019)
Dendrobium nobile var. anomalum Lindl. Lindenia 14: 45 (1898)
Dendrobium nobile var. luteum Lindl. Lindenia 14: 45 (1898)
Dendrobium nobile var. majus Lindl. Lindenia 14: 45 (1898)
Dendrobium nobile var. splendidum Lindl. Lindenia 14: 45 (1898)
Dendrobium nobile var. excellens Lindl. Lindenia 14: 45 (1898)
Dendrobium nobile var. cooksonianum Rchb.f. Gard. Chron. , n.s., 23: 692 (1885)
Dendrobium wallichianum B.S.Williams Orch.-Grow. Man. ed. 2: 98 (1862)
Dendrobium nobile var. alboluteum Huyen & Aver. Bot. Zhurn. (Moscow & Leningrad) 74: 1039 (1989)
Dendrobium nobile unranked virginale Rolfe Orchid Rev. 8: 121 (1900)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English noble dendrobium
Arabic دندروب نبيل
Bulgarian благороден дендробиум
Bengali মহা ডেনড্রোবিয়াম
Czech stromobytec vznešený
Persian ارکیده دندروبیوم
Hindi डेंड्रोबियम नोबल
Japanese デンドロビウム・ノビル
lzh 石斛
Malay orkid phalaenopsis berganda
Nepali सुनखरी
Portuguese olho de boneca
Russian Дендробиум благородный
Vietnamese phi điệp kép
Chinese 石斛
Chinese 黄草
Chinese 春石斛
Chinese 金钗石斛(黄草)
Chinese 金钗石斛
Chinese 石斛一种
Chinese 石斛(金钗石斛)

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
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 South-central
      • China Southeast
      • Hainan
      • Tibet
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
    • Indo-China
      • Laos
      • Myanmar
      • Thailand
      • Vietnam

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000939982
UNII 1Y5P4E7CC6
Tropicos 23500258
INPN 448404
KEW urn:lsid:ipni.org:names:628105-1
The Plant List kew-58517
PFAF Dendrobium nobile
Open Tree Of Life 508208
NCBI Taxonomy 94219
IPNI 628105-1
iNaturalist 67756
GBIF 5317489
Freebase /m/03mhjk8
EOL 1094075
USDA GRIN 13509
Wikipedia Dendrobium_nobile
CMAUP NPO3894

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_022539455.1 Dnobile Chromosome Guangzhou Medical University 2022-03-10 83.5 1.12 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
Efficacy and safety of Piwei Peiyuan Prescription in the treatment of chronic atrophic gastritis: A multicenter, double-blind, double-simulated, randomized, controlled clinical trial Zhang Y, Yang Q, Song B, Tang W, Yu F, Chen H, Ge P, Fang X, Pei B, Sun Q, Li X Medicine (Baltimore) 10-May-2024
PMCID:PMC11081569
doi:10.1097/MD.0000000000037981
PMID:38728508
Potential Effects of Traditional Chinese Medicine in Anti-Aging and Aging-Related Diseases: Current Evidence and Perspectives Ding X, Ma X, Meng P, Yue J, Li L, Xu L Clin Interv Aging 01-May-2024
PMCID:PMC11070163
doi:10.2147/CIA.S447514
PMID:38706635
Structure of Polysaccharide from Dendrobium nobile Lindl. and Its Mode of Action on TLR4 to Exert Immunomodulatory Effects Li L, Chen H, Huang G, Lv Y, Yao L, Guo Z, Qiu S, Wang X, Wei C Foods 28-Apr-2024
PMCID:PMC11083282
doi:10.3390/foods13091356
PMID:38731727
Optimizing nutrient solution for vegetative growth of Dendrobium Tubtim Siam and Phalaenopsis Taisuco Swan through plant tissue nutrient balance estimation Costa MG, Mantovani C, de Mello Prado R BMC Plant Biol 13-Apr-2024
PMCID:PMC11015735
doi:10.1186/s12870-024-04931-x
PMID:38609857
Integration of Metabolomic and Transcriptomic Analyses Reveals the Molecular Mechanisms of Flower Color Formation in Prunus mume Wang R, Yang X, Wang T, Li B, Li P, Zhang Q Plants (Basel) 11-Apr-2024
PMCID:PMC11054544
doi:10.3390/plants13081077
PMID:38674486
Moslae Herba: Botany, Traditional Uses, Phytochemistry, and Pharmacology Duan ZY, Sun YP, Wang ZB, Kuang HX Molecules 10-Apr-2024
PMCID:PMC11051901
doi:10.3390/molecules29081716
PMID:38675535
Comparative Assessment of Lignan Profiling and Biological Activities of Schisandra henryi Leaf and In Vitro PlantForm Bioreactor-Grown Culture Extracts Jafernik K, Kubica P, Dziurka M, Kulinowski Ł, Korona-Głowniak I, Elansary HO, Waligórski P, Skalicka-Woźniak K, Szopa A Pharmaceuticals (Basel) 29-Mar-2024
PMCID:PMC11053505
doi:10.3390/ph17040442
PMID:38675405
Editorial: The role of microbiome in sustainable agriculture Xue S, Kui L, Sharifi R, Chen J Front Microbiol 21-Mar-2024
PMCID:PMC10992468
doi:10.3389/fmicb.2024.1388926
PMID:38577677
Effects of the epiphytic patterns on endophytes and metabolites of Dendrobium nobile Lindl Yu C, Wang P, Ding H, Hu Y, Wang F, Chen H, Chen L, Liu Y Front Plant Sci 14-Mar-2024
PMCID:PMC10972854
doi:10.3389/fpls.2024.1326998
PMID:38550286
In Silico Analysis of Glutamate Receptors in Capsicum chinense: Structure, Evolution, and Molecular Interactions León-García F, García-Laynes F, Estrada-Tapia G, Monforte-González M, Martínez-Estevez M, Echevarría-Machado I Plants (Basel) 12-Mar-2024
PMCID:PMC10975470
doi:10.3390/plants13060812
PMID:38592787
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
Traditional Chinese medicine treats ulcerative colitis by regulating gut microbiota, signaling pathway and cytokine: Future novel method option for pharmacotherapy Wang T, Liu X, Zhang W, Wang J, Wang T, Yue W, Ming L, Cheng J, Sun J Heliyon 06-Mar-2024
PMCID:PMC10945194
doi:10.1016/j.heliyon.2024.e27530
PMID:38501018
Identification and Genetic Diversity Analysis of the Pathogen of Anthracnose of Pepper in Guizhou Zhang A, Li L, Xie X, Chai A, Shi Y, Xing D, Yu Z, Li B Plants (Basel) 04-Mar-2024
PMCID:PMC10934800
doi:10.3390/plants13050728
PMID:38475575
Dendrobine Ameliorates Alzheimer’s Disease-like Pathology and Cognitive Decline in 3 × Tg-AD Mice Zhang W, Huang J, Shi J Brain Sci 28-Feb-2024
PMCID:PMC10968537
doi:10.3390/brainsci14030231
PMID:38539620
Rhizosphere microbial markers (micro-markers): A new physical examination indicator for traditional Chinese medicines Yang K, Zheng Y, Sun K, Wu X, Zhang Z, He C, Xiao P Chin Herb Med 24-Feb-2024
PMCID:PMC11064633
doi:10.1016/j.chmed.2023.11.003
PMID:38706829

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
Rhein 10168 Click to see 284.22 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
Physcion 10639 Click to see 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
Protocatechuic Acid 72 Click to see 154.12 unknown https://doi.org/10.1055/S-2002-33786
> 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 / 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
1,4,7-Trihydroxy-5-Methoxyfluoren-9-One 44418788 Click to see 258.23 unknown https://doi.org/10.1021/NP060449R
2,4,7-Trihydroxy-5-methoxy-9H-fluoren-9-one 71441453 Click to see COC1=CC(=CC2=C1C3=C(C2=O)C=C(C=C3O)O)O 258.23 unknown via CMAUP database
Dendroflorin 14188392 Click to see 258.23 unknown via CMAUP database
Nobilone 16104871 Click to see 242.23 unknown https://doi.org/10.1021/NP060449R
> Benzenoids / Phenanthrenes and derivatives
2,3,4,7-Tetramethoxyphenanthrene 11437978 Click to see 298.30 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
2-Hydroxy4,7-dimethoxy-9,10-dihydrophenanthrene 24762426 Click to see 256.30 unknown https://doi.org/10.1021/NP070423F
2-Methoxy-9,10-dihydrophenanthrene-4,5-diol 11506999 Click to see COC1=CC2=C(C(=C1)O)C3=C(CC2)C=CC=C3O 242.27 unknown https://doi.org/10.1021/NP070423F
2,4,7-Trihydroxy-9,10-dihydrophenanthrene 21678577 Click to see 228.24 unknown via CMAUP database
2,4,7-Trimethoxy-9,10-Dihydrophenanthren-3-Ol 24762424 Click to see 286.32 unknown https://doi.org/10.1021/NP070423F
2,8-Dihydroxy-3,4,7-trimethoxy-9,10-dihydrophenanthrene 24762425 Click to see 302.32 unknown https://doi.org/10.1021/NP070423F
3,4,7-Trimethoxy-9,10-dihydrophenanthren-2-ol 44445441 Click to see 286.32 unknown https://doi.org/10.1021/NP070423F
4-Methoxy-9,10-Dihydrophenanthrene-2,7-Diol 11390848 Click to see COC1=CC(=CC2=C1C3=C(CC2)C=C(C=C3)O)O 242.27 unknown https://doi.org/10.1016/J.BMCL.2010.04.054
5-Methoxy-9,10-dihydrophenanthrene-2,4,7-triol 46890966 Click to see 258.27 unknown https://doi.org/10.1016/J.BMCL.2010.04.054
Cannithrene 2 86021565 Click to see 272.29 unknown https://doi.org/10.1055/S-2002-33786
https://doi.org/10.1002/HLCA.200790183
Ephemeranthol A 44445444 Click to see 272.29 unknown https://doi.org/10.1016/J.BMCL.2010.04.054
https://doi.org/10.1021/NP070423F
Epheneranthol C 46871898 Click to see 258.27 unknown https://doi.org/10.1016/J.BMCL.2010.04.054
Erianthridin 10401022 Click to see COC1=C(C=C2CCC3=C(C2=C1OC)C=CC(=C3)O)O 272.29 unknown https://doi.org/10.1016/J.BMCL.2010.04.054
https://doi.org/10.1021/NP070423F
Flavanthridin 14777891 Click to see COC1=C(C(=C2C(=C1)CCC3=C2C=CC(=C3)O)OC)O 272.29 unknown https://doi.org/10.1016/J.BMCL.2010.04.054
Lusianthridin 442702 Click to see 242.27 unknown https://doi.org/10.1021/NP070423F
https://doi.org/10.1016/J.BMCL.2010.04.054
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
2,4,7-Trimethoxyphenanthren-3-ol 44445442 Click to see 284.31 unknown https://doi.org/10.1021/NP070423F
2,8-Dihydroxy-3,4,7-trimethoxyphenanthrene 24762423 Click to see 300.30 unknown https://doi.org/10.1021/NP070423F
3,4-Dimethoxyphenanthrene-2,5-Diol 640646 Click to see COC1=C(C=C2C=CC3=C(C2=C1OC)C(=CC=C3)O)O 270.28 unknown https://doi.org/10.1021/NP070423F
3,4,8-Trimethoxyphenanthrene-2,5-Diol 46871897 Click to see 300.30 unknown https://doi.org/10.1016/J.BMCL.2010.04.054
3,7-Dihydroxy-2,4-dimethoxyphenanthrene 10445823 Click to see 270.28 unknown https://doi.org/10.1016/J.BMCL.2010.04.054
4,9-Dimethoxyphenanthrene-2,3,5-Triol 24762428 Click to see COC1=CC2=CC(=C(C(=C2C3=C1C=CC=C3O)OC)O)O 286.28 unknown https://doi.org/10.1021/NP070423F
7-Methoxyphenanthrene-2,5-diol 14484686 Click to see COC1=CC(=C2C(=C1)C=CC3=C2C=CC(=C3)O)O 240.25 unknown https://doi.org/10.1055/S-2006-958043
Bulbophyllanthrin 44445443 Click to see COC1=C(C(=C2C(=C1)C=CC3=C2C(=CC=C3)O)OC)O 270.28 unknown https://doi.org/10.1021/NP070423F
Confusarin 11983285 Click to see 300.30 unknown via CMAUP database
Denbinobin 10423984 Click to see COC1=CC(=C2C(=C1)C=CC3=C2C(=O)C(=CC3=O)OC)O 284.26 unknown https://doi.org/10.1021/NP070423F
https://doi.org/10.1055/S-2006-958043
Dendrochrysanene 11964533 Click to see 508.50 unknown via CMAUP database
Fimbriol B 23900101 Click to see COC1=C2C(=CC(=C1O)O)C=CC3=C2C(=CC=C3)O 256.25 unknown https://doi.org/10.1016/J.BMCL.2010.04.054
https://doi.org/10.1021/NP070423F
Flavanthrinin 14777892 Click to see 240.25 unknown via CMAUP database
Moscatin 194774 Click to see COC1=C2C(=CC(=C1)O)C=CC3=C2C(=CC=C3)O 240.25 unknown via CMAUP database
Nudol 158975 Click to see 270.28 unknown https://doi.org/10.1021/NP070423F
plicatol A 44445445 Click to see 300.30 unknown https://doi.org/10.1021/NP070423F
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane 12410 Click to see 436.80 unknown via CMAUP database
> Lignans, neolignans and related compounds
2-[2-hydroxy-6-methoxy-4-[(3R,4R)-4-(3-methoxyphenyl)dioxetan-3-yl]phenyl]-3-methoxy-5-[2-(3-methoxyphenyl)ethyl]phenol 162842541 Click to see 544.60 unknown https://doi.org/10.1002/HLCA.200790183
2-[2-Hydroxy-6-methoxy-4-[4-(3-methoxyphenyl)dioxetan-3-yl]phenyl]-3-methoxy-5-[2-(3-methoxyphenyl)ethyl]phenol 101443792 Click to see 544.60 unknown https://doi.org/10.1002/HLCA.200790183
2-[4-[(3S,4S)-4-(hydroxymethyl)dioxetan-3-yl]-2,6-dimethoxyphenyl]-3-methoxy-5-[2-(3-methoxyphenyl)ethyl]phenol 162918547 Click to see 482.50 unknown https://doi.org/10.1002/HLCA.200790183
2-[4-[4-(Hydroxymethyl)dioxetan-3-yl]-2,6-dimethoxyphenyl]-3-methoxy-5-[2-(3-methoxyphenyl)ethyl]phenol 101443793 Click to see 482.50 unknown https://doi.org/10.1002/HLCA.200790183
> 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 https://doi.org/10.1002/HLCA.200790183
Syringaresinol, (+)- 443023 Click to see 418.40 unknown https://doi.org/10.1002/HLCA.200790183
> Lignans, neolignans and related compounds / Lignan glycosides
(+)-7-epi-Syringaresinol 4'-glucoside 4486984 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC5C(C(C(C(O5)CO)O)O)O)OC 580.60 unknown https://doi.org/10.1002/HLCA.200790183
(+)-syringaresinol beta-D-glucoside 443024 Click to see 580.60 unknown https://doi.org/10.1002/HLCA.200790183
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Heptadecanoic Acid 10465 Click to see 270.50 unknown via CMAUP database
Palmitic Acid 985 Click to see 256.42 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 1-monoacylglycerols
Glycerides, C14-26 107036 Click to see 344.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,2R,3R,5R,6S,8S)-3-hydroxy-8-(hydroxymethyl)-5-(2-hydroxypropan-2-yl)-2-methyltricyclo[4.4.0.02,8]decan-7-one 163067475 Click to see CC12C3CCC1(C(=O)C3C(CC2O)C(C)(C)O)CO 268.35 unknown https://doi.org/10.1248/CPB.56.854
(1S,2R,3R,5R,8S)-3-hydroxy-8-(hydroxymethyl)-5-(2-hydroxypropan-2-yl)-2-methyltricyclo[4.4.0.02,8]decan-7-one 163186093 Click to see 268.35 unknown https://doi.org/10.1248/CPB.56.854
(1S,2R,3R,5S,6S,8R,9S)-3,9-dihydroxy-2,8-dimethyl-5-propan-2-yltricyclo[4.4.0.02,8]decan-7-one 163081696 Click to see 252.35 unknown https://doi.org/10.1002/HLCA.200790245
(1S,2R,3S,4S,5R,6R,7S,8R,10R)-3-(hydroxymethyl)-10-[(2S)-1-hydroxypropan-2-yl]-7-methyltetracyclo[4.4.0.02,4.03,7]decane-5,8-diol 163104943 Click to see 268.35 unknown https://doi.org/10.1248/CPB.56.854
Dendrobane A 42608199 Click to see CC(CO)C1CC(C2(C3C1C4C2(C4C3O)C)C)O 252.35 unknown https://doi.org/10.1055/S-2002-33786
Dendronobilin G 24777882 Click to see CC(C)C1CC(C(C2C1C=C(CC2)CO)(C)O)O 254.36 unknown https://doi.org/10.1002/HLCA.200790245
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1R,1aR,4R,4aS,7R,7aS,7bS)-1,4-bis(hydroxymethyl)-1,7-dimethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol 24777879 Click to see 254.36 unknown https://doi.org/10.1002/HLCA.200790245
(1R,1aR,4S,4aS,7R,7aS,7bS)-1,4-bis(hydroxymethyl)-1,7-dimethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol 11076000 Click to see 254.36 unknown https://doi.org/10.1055/S-2002-33786
1,4-bis(hydroxymethyl)-1,7-dimethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol 45359525 Click to see 254.36 unknown https://doi.org/10.1055/S-2002-33786
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(6R)-4,4a-dimethyl-6-prop-1-en-2-yl-3,4,5,6,7,8-hexahydronaphthalen-2-one 9794438 Click to see CC1CC(=O)C=C2C1(CC(CC2)C(=C)C)C 218.33 unknown via CMAUP database
Nootkatone 1268142 Click to see CC1CC(=O)C=C2C1(CC(CC2)C(=C)C)C 218.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(1S,2R,5S,6S,7R,8R,11S)-7,11-dihydroxy-6-methyl-11-propan-2-yl-5-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-9-oxatricyclo[6.2.1.02,6]undecan-10-one 10993984 Click to see CC(C)C1(C2C3CCC(C3(C(C1OC2=O)O)C)COC4C(C(C(C(O4)CO)O)O)O)O 446.50 unknown https://doi.org/10.1016/S0031-9422(02)00484-3
(1S,2R,5S,6S,7R,8S,11R)-11-(2-hydroxypropan-2-yl)-6-methyl-10-oxo-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9-oxatricyclo[6.2.1.02,6]undecane-5-carboxylic acid 11005030 Click to see 460.50 unknown via CMAUP database
(1S,2R,5S,6S,7R,8S,11R)-7-hydroxy-11-(2-hydroxypropan-2-yl)-6-methyl-5-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-9-oxatricyclo[6.2.1.02,6]undecan-10-one 11015758 Click to see 446.50 unknown via CMAUP database
(1S,2R,5S,6S,7R,8S,11R)-7-hydroxy-6-methyl-11-propan-2-yl-5-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-9-oxatricyclo[6.2.1.02,6]undecan-10-one 11732737 Click to see 430.50 unknown https://doi.org/10.1016/S0031-9422(02)00484-3
https://doi.org/10.1021/NP0301801
(1S,2S,5R,6R,7R,8R,11S)-7,11-dihydroxy-6-methyl-11-propan-2-yl-5-[[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-9-oxatricyclo[6.2.1.02,6]undecan-10-one 161547331 Click to see CC(C)C1(C2C3CCC(C3(C(C1OC2=O)O)C)COC4C(C(C(C(O4)CO)O)O)O)O 446.50 unknown https://doi.org/10.1016/S0031-9422(02)00484-3
(1S,2S,5R,6R,7R,8S,11S)-7-hydroxy-6-methyl-11-propan-2-yl-5-[[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-9-oxatricyclo[6.2.1.02,6]undecan-10-one 163090891 Click to see 430.50 unknown https://doi.org/10.1016/S0031-9422(02)00484-3
(1S,2S,5S,6S,7R,8R,11S)-7,11-dihydroxy-6-methyl-11-propan-2-yl-5-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-9-oxatricyclo[6.2.1.02,6]undecan-10-one 101219071 Click to see 446.50 unknown https://doi.org/10.1016/S0031-9422(02)00484-3
(1S,2S,5S,6S,7R,8S,11R)-7-hydroxy-6-methyl-11-propan-2-yl-5-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-9-oxatricyclo[6.2.1.02,6]undecan-10-one 101219070 Click to see 430.50 unknown https://doi.org/10.1016/S0031-9422(02)00484-3
(2R,3R,4R,5R,6R)-2-[[(1S,1aR,3aR,4S,7R,7aS,7bS)-4-hydroxy-1-(hydroxymethyl)-1,7-dimethyl-2,3,3a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[a]naphthalen-4-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 23304338 Click to see CC1CCC(C2C1C3C(C3(C)CO)CC2)(COC4C(C(C(C(O4)CO)O)O)O)O 416.50 unknown via CMAUP database
(2R,3R,4S,5S,6R)-2-[[(1R,1aR,4S,4aS,7R,7aS,7bS)-4-hydroxy-1,7-dimethyl-4-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-1-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162968055 Click to see CC1CCC2C1C3C(C3(C)COC4C(C(C(C(O4)CO)O)O)O)CCC2(COC5C(C(C(C(O5)CO)O)O)O)O 578.60 unknown https://doi.org/10.1055/S-2002-33786
(2R,3R,4S,5S,6R)-2-[[(1S,1aR,3aR,4S,7R,7aS,7bS)-4-hydroxy-1-(hydroxymethyl)-1,7-dimethyl-2,3,3a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[a]naphthalen-4-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 11742643 Click to see 416.50 unknown https://doi.org/10.1016/S0031-9422(02)00484-3
(2R,3R,4S,5S,6R)-2-[[(1S,1aR,4S,4aS,7R,7aS,7bS)-4-hydroxy-1-(hydroxymethyl)-1,7-dimethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162989722 Click to see 416.50 unknown https://doi.org/10.1055/S-2002-33786
(2R,3R,4S,5S,6R)-2-[[(1S,3aR,4R,5R,7aR)-7a-methyl-5-propan-2-yl-4-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-1,2,3,3a,4,5,6,7-octahydroinden-1-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162970770 Click to see 564.70 unknown https://doi.org/10.1021/NP0102612
(2R,3R,4S,5S,6R)-2-[[(4R,4aR)-6-methyl-4-[(2S)-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-2,3,4,4a,7,8-hexahydronaphthalen-1-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162878780 Click to see CC1=CC2C(CCC(=C2CC1)COC3C(C(C(C(O3)CO)O)O)O)C(C)COC4C(C(C(C(O4)CO)O)O)O 560.60 unknown https://doi.org/10.1055/S-2002-33786
(2R,3R,4S,5S,6R)-2-[[(8S,8aR)-8-propan-2-yl-5-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3,4,6,7,8,8a-hexahydronaphthalen-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163033046 Click to see 560.60 unknown https://doi.org/10.1055/S-2002-33786
(2R,3S,4S,5S,6S)-2-[[(1R,1aR,4S,4aS,7R,7aS,7bS)-4-hydroxy-1-(hydroxymethyl)-1,7-dimethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162989721 Click to see 416.50 unknown https://doi.org/10.1021/NP0102612
(2R,3S,4S,5S,6S)-2-[[(1S,3aR,4R,5R,7aS)-7a-methyl-5-propan-2-yl-4-[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-1,2,3,3a,4,5,6,7-octahydroinden-1-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162970769 Click to see 564.70 unknown https://doi.org/10.1021/NP0102612
(2R,5S,6S,7R,11S)-7,11-dihydroxy-6-methyl-11-propan-2-yl-5-[[(2R,3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-9-oxatricyclo[6.2.1.02,6]undecan-10-one 23304340 Click to see CC(C)C1(C2C3CCC(C3(C(C1OC2=O)O)C)COC4C(C(C(C(O4)CO)O)O)O)O 446.50 unknown via CMAUP database
(2S,3R,4R,5R,6S)-2-[[(1R,3aR,4R,5R,7aS)-1-hydroxy-1-(hydroxymethyl)-7a-methyl-5-propan-2-yl-3,3a,4,5,6,7-hexahydro-2H-inden-4-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162946199 Click to see CC(C)C1CCC2(C(C1COC3C(C(C(C(O3)CO)O)O)O)CCC2(CO)O)C 418.50 unknown https://doi.org/10.1021/NP0102612
[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,1aR,4S,4aS,7R,7aS,7bS)-4-hydroxy-1,7-dimethyl-4-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene-1-carboxylate 10438430 Click to see 592.60 unknown https://doi.org/10.1016/S0031-9422(02)00484-3
[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 4-hydroxy-1,7-dimethyl-4-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene-1-carboxylate 85143062 Click to see CC1CCC2C1C3C(C3(C)C(=O)OC4C(C(C(C(O4)CO)O)O)O)CCC2(COC5C(C(C(C(O5)CO)O)O)O)O 592.60 unknown https://doi.org/10.1016/S0031-9422(02)00484-3
2-(Hydroxymethyl)-6-[[6-methyl-4-[1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-2,3,4,4a,7,8-hexahydronaphthalen-1-yl]methoxy]oxane-3,4,5-triol 162878779 Click to see 560.60 unknown https://doi.org/10.1055/S-2002-33786
2-(Hydroxymethyl)-6-[[8-propan-2-yl-5-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3,4,6,7,8,8a-hexahydronaphthalen-2-yl]methoxy]oxane-3,4,5-triol 163033045 Click to see 560.60 unknown https://doi.org/10.1055/S-2002-33786
2-[[1-hydroxy-1-(hydroxymethyl)-7a-methyl-5-propan-2-yl-3,3a,4,5,6,7-hexahydro-2H-inden-4-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73089809 Click to see CC(C)C1CCC2(C(C1COC3C(C(C(C(O3)CO)O)O)O)CCC2(CO)O)C 418.50 unknown https://doi.org/10.1055/S-2002-33786
https://doi.org/10.1021/NP0102612
2-[[4-hydroxy-1-(hydroxymethyl)-1,7-dimethyl-2,3,3a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[a]naphthalen-4-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73082188 Click to see 416.50 unknown https://doi.org/10.1016/S0031-9422(02)00484-3
2-[[4-hydroxy-1-(hydroxymethyl)-1,7-dimethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 85115605 Click to see 416.50 unknown https://doi.org/10.1055/S-2002-33786
https://doi.org/10.1021/NP0102612
2-[[4-hydroxy-1,7-dimethyl-4-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-1-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162968054 Click to see CC1CCC2C1C3C(C3(C)COC4C(C(C(C(O4)CO)O)O)O)CCC2(COC5C(C(C(C(O5)CO)O)O)O)O 578.60 unknown https://doi.org/10.1055/S-2002-33786
2-[[7a-Methyl-5-propan-2-yl-4-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-1,2,3,3a,4,5,6,7-octahydroinden-1-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 85097679 Click to see 564.70 unknown https://doi.org/10.1055/S-2002-33786
https://doi.org/10.1021/NP0102612
7-Hydroxy-6-methyl-11-propan-2-yl-5-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-9-oxatricyclo[6.2.1.02,6]undecan-10-one 73078140 Click to see CC(C)C1C2C3CCC(C3(C(C1OC2=O)O)C)COC4C(C(C(C(O4)CO)O)O)O 430.50 unknown https://doi.org/10.1016/S0031-9422(02)00484-3
https://doi.org/10.1021/NP0301801
7,11-Dihydroxy-6-methyl-11-propan-2-yl-5-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-9-oxatricyclo[6.2.1.02,6]undecan-10-one 74029679 Click to see 446.50 unknown https://doi.org/10.1016/S0031-9422(02)00484-3
Dendromoniliside A 44559639 Click to see CC12CCC3C1(C(CC(C3C2=O)C(C)(C)O)OC4C(C(C(C(O4)CO)O)O)O)C 414.50 unknown via CMAUP database
Dendronobiloside A 10030799 Click to see CC(C)C1CCC2(C(CCC2C1COC3C(C(C(C(O3)CO)O)O)O)COC4C(C(C(C(O4)CO)O)O)O)C 564.70 unknown https://doi.org/10.1055/S-2002-33786
https://doi.org/10.1021/NP0102612
Dendronobiloside B 11761556 Click to see CC(C)C1CCC2(C(C1COC3C(C(C(C(O3)CO)O)O)O)CCC2(CO)O)C 418.50 unknown https://doi.org/10.1021/NP0102612
https://doi.org/10.1055/S-2002-33786
Dendroside A 10341857 Click to see CC1CCC2C1C3C(C3(C)CO)CCC2(COC4C(C(C(C(O4)CO)O)O)O)O 416.50 unknown https://doi.org/10.1055/S-2002-33786
https://doi.org/10.1021/NP0102612
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1R,2S,5R,6S,7S,8R,11R)-11-[(2R)-1,2-dihydroxypropan-2-yl]-7-hydroxy-5-(hydroxymethyl)-6-methyl-9-oxatricyclo[6.2.1.02,6]undecan-10-one 163103664 Click to see CC12C(CCC1C3C(C(C2O)OC3=O)C(C)(CO)O)CO 300.35 unknown https://doi.org/10.1248/CPB.56.854
(1R,2S,5R,6S,7S,8R,11S)-7-hydroxy-5-(hydroxymethyl)-11-(2-hydroxypropan-2-yl)-6-methyl-9-oxatricyclo[6.2.1.02,6]undecan-10-one 163106181 Click to see CC12C(CCC1C3C(C(C2O)OC3=O)C(C)(C)O)CO 284.35 unknown https://doi.org/10.1248/CPB.56.854
(1R,2S,5S,6R,8R,11S)-5-[(dimethylamino)methyl]-6-methyl-11-propan-2-yl-9-oxatricyclo[6.2.1.02,6]undecane-7,10-dione 12313395 Click to see 293.40 unknown via CMAUP database
(1R,2S,6R,8R,11S)-6-methyl-5-methylidene-11-propan-2-yl-9-oxatricyclo[6.2.1.02,6]undecane-7,10-dione 11064768 Click to see 248.32 unknown via CMAUP database
(1S,2S,5R,6R,7S,8R,11R)-7,11-dihydroxy-5-(hydroxymethyl)-6-methyl-11-propan-2-yl-9-oxatricyclo[6.2.1.02,6]undecan-10-one 162984487 Click to see 284.35 unknown https://doi.org/10.1002/HLCA.200790245
(1S,2S,5R,6R,7S,8S,11S)-7-hydroxy-5-(hydroxymethyl)-11-[(2R)-1-hydroxypropan-2-yl]-6-methyl-9-oxatricyclo[6.2.1.02,6]undecan-10-one 24777877 Click to see 284.35 unknown https://doi.org/10.1002/HLCA.200790245
(1S,2S,6S,8S,11S)-6-methyl-5-methylidene-11-propan-2-yl-9-oxatricyclo[6.2.1.02,6]undecane-7,10-dione 154497096 Click to see 248.32 unknown https://doi.org/10.1248/CPB.20.418
(1S,3S,6R,7S,8S,11S)-7-hydroxy-5-(hydroxymethyl)-3-methoxy-6-methyl-11-propan-2-yl-9-oxatricyclo[6.2.1.02,6]undec-4-en-10-one 101063871 Click to see 296.36 unknown https://doi.org/10.1016/S0040-4020(00)00530-5
5-((Dimethylamino)methyl)-6-methyl-11-propan-2-yl-9-oxatricyclo(6.2.1.02,6)undecane-7,10-dione 5320179 Click to see 293.40 unknown https://doi.org/10.1016/S0040-4020(00)00530-5
> 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
2-amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one 6802 Click to see 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 244.20 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Delta amino acids and derivatives
(1S,4S,7S,8R,11S,12R,13S)-12-methyl-13-propan-2-yl-10-oxa-2-azatetracyclo[5.4.1.18,11.04,12]tridecan-9-one 15287267 Click to see CC(C)C1C2C3CCC4C3(C(C1OC2=O)NC4)C 249.35 unknown https://doi.org/10.1016/S0040-4020(00)00530-5
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
3-Hydroxy-3-(methoxycarbonyl)pentanedioic acid 12566215 Click to see COC(=O)C(CC(=O)O)(CC(=O)O)O 206.15 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-(3-Hydroxy-4-methoxyphenyl)ethyl 3-O-(6-deoxyhexopyranosyl)hexopyranoside 21668724 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)OC)O)CO)O)O)O)O 476.50 unknown via CMAUP database
Dendromoniliside C 11812311 Click to see CC(C)C1C2C3CC(C4(C3(C(C1OC2=O)O)C)CO4)OC5C(C(C(C(O5)CO)O)O)O 444.50 unknown via CMAUP database
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 / 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 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 / Benzopyrans / 1-benzopyrans / Xanthenes
(9S)-4,6-dimethoxy-8-[2-(3-methoxyphenyl)ethyl]-9-[(3-methoxyphenyl)methyl]-9H-xanthene-2,3,5-triol 162870395 Click to see 544.60 unknown https://doi.org/10.1021/NP060449R
> Organoheterocyclic compounds / Furopyrans
(1S,3R,5S,8S,9R,12R,13S,14R)-14-hydroxy-13-methyl-14-propan-2-yl-4,7,10-trioxapentacyclo[6.4.1.19,12.03,5.05,13]tetradecane-6,11-dione 101316879 Click to see 294.30 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives
(-)-Dendrobin 15558892 Click to see 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
(1R,15R)-15-methyl-16-propan-2-yl-3,14-dioxa-11-azapentacyclo[7.5.1.12,5.01,11.06,15]hexadecan-4-one 5316539 Click to see 291.40 unknown https://doi.org/10.1248/CPB.14.672
(1R,2R,5R,6S,9S,15R,16R)-16-hydroxy-15-methyl-16-propan-2-yl-3,14-dioxa-11-azapentacyclo[7.5.1.12,5.01,11.06,15]hexadecan-4-one 154496027 Click to see 307.40 unknown https://doi.org/10.1248/CPB.20.418
(1R,2R,5S,6R,9S,15S,16S)-6-hydroxy-15-methyl-16-propan-2-yl-3,14-dioxa-11-azapentacyclo[7.5.1.12,5.01,11.06,15]hexadecan-4-one 154496059 Click to see 307.40 unknown https://doi.org/10.1248/CPB.14.672
(1R,2R,5S,6S,9S,15R,16S)-15-methyl-16-propan-2-yl-3,14-dioxa-11-azapentacyclo[7.5.1.12,5.01,11.06,15]hexadecan-4-one 154496459 Click to see 291.40 unknown https://doi.org/10.1248/CPB.14.672
(1R,5S,6S,9S,15R,16S)-15-methyl-16-propan-2-yl-3,14-dioxa-11-azapentacyclo[7.5.1.12,5.01,11.06,15]hexadecan-4-one 163194745 Click to see 291.40 unknown https://doi.org/10.1248/CPB.14.672
(1S,4S,7S,12R,13S)-2,12-dimethyl-13-propan-2-yl-10-oxa-2-azatetracyclo[5.4.1.18,11.04,12]tridecan-9-one 145945119 Click to see 263.37 unknown https://doi.org/10.2307/4117899
https://doi.org/10.1055/S-2002-33786
https://doi.org/10.1021/NP50041A014
https://doi.org/10.1016/S0040-4020(00)00530-5
(1S,4S,7S,8R,11R,13S)-2,12-dimethyl-13-propan-2-yl-10-oxa-2-azatetracyclo[5.4.1.18,11.04,12]tridecan-9-one 11972333 Click to see 263.37 unknown via CMAUP database
(1S,4S,7S,8S,11R,12R,13S)-2,12-dimethyl-13-propan-2-yl-10-oxa-2-azatetracyclo[5.4.1.18,11.04,12]tridecane-3,9-dione 101063872 Click to see CC(C)C1C2C3CCC4C3(C(C1OC2=O)N(C4=O)C)C 277.36 unknown https://doi.org/10.1016/S0040-4020(00)00530-5
(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 263.37 unknown via CMAUP database
(4R,11R)-2,2,12-trimethyl-13-propan-2-yl-10-oxa-2-azoniatetracyclo[5.4.1.18,11.04,12]tridecan-9-one 6325643 Click to see 278.40 unknown via CMAUP database
5,6-Epoxy-1-hydroxy-6-isopropyl-3,11-dimethyl-3-azatricyclo(6.2.1.04(5,11))undecan-2-one 127377 Click to see CC(C)C1C2C3CCC4(C3(C(C1OC2=O)N(C4=O)C)C)O 293.36 unknown via CMAUP database
6-Hydroxy-15-methyl-16-propan-2-yl-3,14-dioxa-11-azapentacyclo[7.5.1.12,5.01,11.06,15]hexadecan-4-one 5318187 Click to see CC(C)C1C2C(=O)OC1C34C5(C2(CCC5CN3CCO4)O)C 307.40 unknown https://doi.org/10.1016/S0040-4020(00)00530-5
https://doi.org/10.1248/CPB.14.672
7-Hydroxy-2,12-dimethyl-13-propan-2-yl-10-oxa-2-azatetracyclo[5.4.1.18,11.04,12]tridecan-9-one 5316531 Click to see 279.37 unknown https://doi.org/10.1016/S0040-4020(00)00530-5
Dendroban-12-one 566057 Click to see CC(C)C1C2C3CCC4C3(C(C1OC2=O)N(C4)C)C 263.37 unknown https://doi.org/10.1055/S-2002-33786
Dendrobine 442523 Click to see 263.37 unknown https://doi.org/10.2307/4117899
https://doi.org/10.1055/S-2002-33786
https://doi.org/10.1016/S0040-4020(00)00530-5
From Dendrobium nobile 355017 Click to see 263.37 unknown via CMAUP database
methyl 2-[(1S,7S,8R,11R,12S)-2,12-dimethyl-9-oxo-13-propan-2-yl-10-oxa-2-azatetracyclo[5.4.1.18,11.04,12]tridecan-3-yl]acetate 6325050 Click to see 335.40 unknown via CMAUP database
Mubironine C 101063873 Click to see 295.40 unknown https://doi.org/10.1016/S0040-4020(00)00530-5
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
Evodiamine 442088 Click to see 303.40 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1S,2S,5R,7R,8S,9S,12S)-8-hydroxy-5-(hydroxymethyl)-12-[(2R)-1-hydroxypropan-2-yl]-10-oxatetracyclo[7.2.1.02,7.05,7]dodecan-11-one 163091277 Click to see CC(CO)C1C2C3CCC4(C3(C4)C(C1OC2=O)O)CO 282.33 unknown https://doi.org/10.1002/HLCA.200790245
(1S,3R,4R,7S,8S,11S,12S,13S)-3,4-dihydroxy-13-[(2R)-1-hydroxypropan-2-yl]-12-methyl-2,10-dioxatetracyclo[5.4.1.18,11.04,12]tridecan-9-one 162870439 Click to see 298.33 unknown https://doi.org/10.1002/HLCA.200790245
Flakinin A 10588810 Click to see 280.32 unknown https://doi.org/10.1016/S0040-4020(00)00530-5
> Phenylpropanoids and polyketides / Coumarins and derivatives
3-(5,6-Dimethoxy-1-benzofuran-2-yl)-6,7-dimethoxychromen-2-one 11291989 Click to see COC1=C(C=C2C(=C1)C=C(C(=O)O2)C3=CC4=CC(=C(C=C4O3)OC)OC)OC 382.40 unknown via CMAUP database
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 / Flavans / Flavanones
(+-)-Naringenin 932 Click to see 272.25 unknown via CMAUP database
(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
Naringenin 439246 Click to see 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
2-Methoxy-4-[2-(3,4,5-trimethoxyphenyl)ethyl]phenol 14353469 Click to see COC1=CC(=CC(=C1OC)OC)CCC2=CC(=C(C=C2)O)OC 318.40 unknown https://doi.org/10.1021/NP060449R
2,6-Dimethoxy-4-[2-(3-methoxyphenyl)ethyl]phenol 85830339 Click to see 288.34 unknown https://doi.org/10.1055/S-2002-33786
3-Methoxy-5-[2-(3-methoxyphenyl)ethyl]benzene-1,2-diol 44418770 Click to see COC1=CC=CC(=C1)CCC2=CC(=C(C(=C2)OC)O)O 274.31 unknown https://doi.org/10.1055/S-2002-33786
https://doi.org/10.1002/HLCA.200790183
https://doi.org/10.1021/NP060449R
3-O-Methylgigantol 10108163 Click to see COC1=C(C=C(C=C1)CCC2=CC(=CC(=C2)OC)O)OC 288.34 unknown https://doi.org/10.1016/J.BMCL.2010.04.054
4-[(1S)-1-hydroxy-2-(4-hydroxy-3-methoxyphenyl)ethyl]-2,6-dimethoxyphenol 162916341 Click to see COC1=CC(=CC(=C1O)OC)C(CC2=CC(=C(C=C2)O)OC)O 320.30 unknown https://doi.org/10.1021/NP060449R
5-(2-(3-Hydroxy-5-methoxyphenyl)ethyl)-2-methoxyphenol 3085362 Click to see 274.31 unknown https://doi.org/10.1002/HLCA.200790183
https://doi.org/10.1021/JF9603902
https://doi.org/10.1021/NP060449R
batatasin III 10466989 Click to see COC1=CC(=CC(=C1)O)CCC2=CC(=CC=C2)O 244.28 unknown https://doi.org/10.1016/0031-9422(89)80154-2
https://doi.org/10.1002/HLCA.200790183
Chrysotobibenzyl 3086528 Click to see 332.40 unknown https://doi.org/10.1021/NP060449R
Dendrophenol 176096 Click to see COC1=CC(=CC(=C1O)OC)CCC2=CC(=C(C=C2)O)OC 304.34 unknown https://doi.org/10.1002/HLCA.200790183
https://doi.org/10.1016/J.BMCL.2010.04.054
https://doi.org/10.1021/JF970930A
https://doi.org/10.1021/NP060449R
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 via CMAUP database
Nobilin D 16104870 Click to see 320.30 unknown https://doi.org/10.1021/NP060449R
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/J.BMCL.2010.04.054
https://doi.org/10.1021/NP060449R
https://doi.org/10.1021/JF9603902
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 https://doi.org/10.1021/NP060449R
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
1-(2-Hydroxy-3,4,7-trimethoxy-9,10-dihydrophenanthren-1-yl)-3,4,7-trimethoxy-9,10-dihydrophenanthren-2-ol 24762427 Click to see 570.60 unknown https://doi.org/10.1021/NP070423F

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.