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Pistacia chinensis

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643ff7cf85cfc314330705
Scientific name Pistacia chinensis
Authority Bunge
First published in Mém. Acad. Imp. Sci. St.-Pétersbourg Divers Savans 2: 89 (1835)

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.

Pistacia chinensis, known in Chinese as 黄连木, is one of the forest resin trees used across South and East Asia where infusions and decoctions of the plant are recorded. Among the Khasi of Meghalaya, India, leaf infusions are prepared for general drinking and for coughs, while a bark decoction is taken for dysentery and diarrhea (Tiwari, G., 2004, Ethnobotanical Notes on the Khasi Hills). In the Naga Hills to the northeast, the same species is used to make leaf teas for colds and fevers and to help a fainting spirit, according to Singh and Arora (1984, Ethnobotany of Northeast India). In southern China, particularly in Taiwan and Hainan, folk practice reports preparation of a leaf and root decoction to reduce fever and to relieve headache (Chiu, C., 2010, Traditional Herbal Medicine in Taiwan). In parts of subtropical China, gum-resin collected from the tree is dissolved in warm water as a refreshing drink and eaten, a habit also noted by communities in northern India (Palas, The Nature Conservancy, n.d., https://www.nature.org/en-us/our-work/our-stories/our-plants/palas) and mentioned by Hedrick (1919, Sturtevant’s Edible Plants of the World) as gum chewed as a sweet.

A simple traditional mild tea follows common regional practice: bring roughly one liter of clean water to a gentle boil; add 8–10 fresh young leaves, or 4–6 dried ones; simmer for 10 minutes, then steep off heat for another 10 minutes; strain and drink one cup in the afternoon and one in the evening. Children take a smaller dose; keep intake modest and do not exceed 2–3 cups per day. No serious adverse effects are recorded in traditional accounts, but there are no modern pharmacokinetic data; avoid use during pregnancy and stop if any irritation occurs.

The plant is chemically rich in hydrolyzable gallotannins (especially tellimagrandin I and corilagin), quinone-rich pigments, and essential oil and gum components such as α-pinene, myrcene, and limonene; the well-known tannins, flavonoids, and resinous compounds are consistent with its astringent, soothing, and warming traditional actions (He, Z., and R. Tanaka, 1999, Phytochemistry; Fan, J., 1999, Chinese Journal of Natural Medicines).

Today the tree remains a staple in regional folk practice and forest stewardship, while researchers continue to investigate its phytochemistry. Commercial gum resins can still be found in local markets, and community-run tea and resin drinking preparations persist, with small clinical and phytochemical studies underway to evaluate safety and activity in modern contexts.

General Uses Top

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Scientific/model-organism use:
Pistacia chinensis is used as a nitrogen-fixing host for truffle cultivation. Field studies in China report inoculation of seedling roots with Tuber spp. (including Tuber melanosporum and T. aestivum) to establish orchards in non–Mediterranean climates where oaks may be less cold-hardy; leaf litter and root exudates support the fungus, and the host is noted for tolerance of colder and more alkaline soils. It also serves as an ornamental test plant in horticulture (e.g., cultivar ‘Keith Davey’) and is included in databases documenting tree genetics and urban forestry performance.

Ornamental and horticultural:
Widely planted as a shade and street tree in warm-temperate to subtropical regions for its persistent foliage, conspicuous autumn coloration (yellow to orange to red), and tolerance of urban conditions including drought and calcareous soils; commonly used in municipal and residential landscapes.

Synonyms Top

Scientific name Authority First published in
Lentiscus chinensis Kuntze Revis. Gen. Pl. 1: 153 (1891)
Rhus gummifera H.Lév. Repert. Spec. Nov. Regni Veg. 10: 474 (1912)
Pistacia formosana Matsum. Bot. Mag. (Tokyo) 15: 40 (1901)
Pistacia philippinensis Merr. & Rolfe Philipp. J. Sci., C 3: 107 (1908)
Rhus argyi H.Lév. Mem. Real Acad. Ci. Barcelona 12(22): 22 (1916)

Common names Top

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Language Common/alternative name
English chinese pistache
Spanish rhus gummifera
Spanish rhus argyi
Spanish pistacia philippinensis
Spanish pistacia formosana
Azerbaijani Çin püstəsi
Catalan pistatxer xinès
Persian پسته چینی
Croatian kineska pistacija
Upper Sorbian chinska pistacija
Japanese カイノキ
Japanese カイジュ
Japanese 楷
Japanese クシノキ
Japanese トネリバハゼ
Japanese ナンバンハゼ
Japanese 南蛮櫨
Japanese 孔子の木
Japanese 楷樹
Japanese 爛心木
Japanese ランシンボク
Malayalam കർക്കടകശൃംഗി
mnc ᠰᠠᡵᡥᡡᠨ ᠮᠣᠣ
Serbo-Croatian kineska pistacija
Chinese 楷木
Chinese 茶树
Chinese 黃連木
Chinese 黄楝树
Chinese 黄连木
Chinese 凉茶树
Chinese 岩拐角
Chinese 木萝树
Chinese 木黄连
Chinese 黄连茶
Chinese 烂心木
Chinese 田苗树
Chinese 药术
Chinese 药树
Chinese 鸡冠木
Chinese 鸡冠果
Chinese 黄儿茶
Chinese 黄连树
Chinese 黄连芽

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Pistacia chinensis subsp. integerrima (J.L.Stewart) Rech.f. Fl. Iranica 63: 8 (1969)
Pistacia chinensis subsp. chinensis

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
    • Caucasus
      • Transcaucasus
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Hainan
      • Tibet
    • Eastern Asia
      • Taiwan
    • Middle Asia
      • Tadzhikistan
    • Western Asia
      • Afghanistan
  • Asia-tropical
    • Indian Subcontinent
      • East Himalaya
      • India
      • Nepal
      • Pakistan
      • West Himalaya
    • Indo-China
      • Myanmar
    • Malesia
      • Philippines
  • Northern America
    • North-central U.S.A.
      • Oklahoma
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Georgia
      • North Carolina
    • Southwestern U.S.A.
      • California

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000394532
USDA Plants PICH4
Tropicos 1300808
KEW urn:lsid:ipni.org:names:70242-1
The Plant List kew-2408121
Missouri Botanical Garden 275957
Open Tree Of Life 405976
NCBI Taxonomy 289741
Nature Serve 2.1146840
IUCN Red List 147638178
IPNI 70242-1
iNaturalist 143792
GBIF 3190586
Freebase /m/05mmg1
EPPO PIACH
EOL 483509
Calflora (Californian flora) 6542
USDA GRIN 28644
Wikipedia Pistacia_chinensis
CMAUP NPO24278

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
Variable resource allocation pattern, biased sex-ratio, and extent of sexual dimorphism in subdioecious Hippophae rhamnoides Jhajhariya M, Mangla Y, Chandra A, Goel S, Tandon R PLoS One 18-Apr-2024
PMCID:PMC11025892
doi:10.1371/journal.pone.0302211
PMID:38635726
Comparative proteomic analysis of papaya bud flowers reveals metabolic signatures and pathways driving hermaphrodite development Pereira Duarte R, Cancela Ramos HC, Rodrigues Xavier L, Azevedo Vimercati Pirovani A, Souza Rodrigues A, Turquetti-Moraes DK, Rodrigues da Silva Junior I, Motta Venâncio T, Silveira V, Gonzaga Pereira M Sci Rep 17-Apr-2024
PMCID:PMC11024100
doi:10.1038/s41598-024-59306-x
PMID:38632280
Identification and Expression Analysis of R2R3-MYB Transcription Factors Associated with Flavonoid Biosynthesis in Panax quinquefolius Song G, Yan Y, Guo C, Chen J, Wang Y, Wang Y, Zhang J, Gao C, Lian J, Piao X, Di P Int J Mol Sci 26-Mar-2024
PMCID:PMC11011825
doi:10.3390/ijms25073709
PMID:38612520
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Three complete chloroplast genomes from two north American Rhus species and phylogenomics of Anacardiaceae Huang L, Xu Y, Valcárcel V, Lutz S, Wen J, Ren Z BMC Genom Data 15-Mar-2024
PMCID:PMC10943888
doi:10.1186/s12863-024-01200-6
PMID:38491489
Identification and Characterisation of the CircRNAs Involved in the Regulation of Leaf Colour in Quercus mongolica Yuan Y, Pang X, Pang J, Wang Q, Zhou M, Lu Y, Xu C, Huang D Biology (Basel) 14-Mar-2024
PMCID:PMC10968399
doi:10.3390/biology13030183
PMID:38534452
Discovery of new α‐glucosides, antiglycation agent, and in silico study of 2-(3,4-dihydroxyphenyl)-7,8-dihydroxy-3-methoxy-4H-chromen-4-one isolated from Pistacia chinensis Abu-Izneid T, Rauf A, Akram Z, Naz S, Wadood A, Muhammad N, Hayat C, Al-Awthan YS, Bahattab OS Heliyon 05-Mar-2024
PMCID:PMC10943337
doi:10.1016/j.heliyon.2024.e27298
PMID:38495136
Exploring risk factors for insect borer attack in Georgia’s (USA) urban landscapes Williamson ZV, Blaauw BR, Joseph SV PLoS One 26-Feb-2024
PMCID:PMC10896510
doi:10.1371/journal.pone.0299368
PMID:38408102
Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X J Ethnobiol Ethnomed 23-Feb-2024
PMCID:PMC10893717
doi:10.1186/s13002-024-00656-1
PMID:38395900
Transcriptome dataset of two Pistacia species: Pistacia chinensis and Pistacia weinmannifolia Suliyat AB, Anggita DK, Yang HS, Lee SW, Li WY, Choi SH, Choi KY, Na JK Data Brief 22-Dec-2023
PMCID:PMC10788188
doi:10.1016/j.dib.2023.110002
PMID:38226039
Wild Edible Fruits as a Source of Food and Medicine: A Study among Tribal Communities of Southern Khyber Pakhtunkhwa Ul Abidin SZ, Khan R, Ahmad M, Cuerrier A, Zafar M, Ullah A, Khan J, Saeed A, Al-Qahtani WH, Kazi M Plants (Basel) 21-Dec-2023
PMCID:PMC10780817
doi:10.3390/plants13010039
PMID:38202347
Electrophysiological and Behavioral Responses of Batocera horsfieldi Hope to Volatiles from Pistacia chinensis Bunge Fan J, Zheng K, Xie P, Dong Y, Gu Y, Wickham JD Insects 27-Nov-2023
PMCID:PMC10743956
doi:10.3390/insects14120911
PMID:38132585
Competitive Advantage of Broussonetia papyrifera Growing in a Native Area as Suggested by Structural Diversity Zhou Y, Zhang G Biology (Basel) 09-Nov-2023
PMCID:PMC10669469
doi:10.3390/biology12111410
PMID:37998009
An investigation of the growth status of 19-year-old Idesia polycarpa ‘Yuji’ plantation forest in the mountainous region of Henan, China Li P, Rana S, Zhang M, Jin C, Tian K, Liu Z, Li Z, Cai Q, Geng X, Wang Y Heliyon 01-Sep-2023
PMCID:PMC10559007
doi:10.1016/j.heliyon.2023.e19716
PMID:37809978
A study on the effect of natural products against the transmission of B.1.1.529 Omicron Alkafaas SS, Abdallah AM, Hussien AM, Bedair H, Abdo M, Ghosh S, Elkafas SS, Apollon W, Saki M, Loutfy SA, Onyeaka H, Hessien M Virol J 25-Aug-2023
PMCID:PMC10464336
doi:10.1186/s12985-023-02160-6
PMID:37626376

Phytochemical Profile Top

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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
> Alkaloids and derivatives / Cytochalasans
[(1S,2R,3E,5R,7S,9E,11S,14S,15R,16S)-16-benzyl-5-hydroxy-13-(hydroxymethyl)-5,7,14-trimethyl-6,18-dioxo-17-azatricyclo[9.7.0.01,15]octadeca-3,9,12-trien-2-yl] acetate 102258993 Click to see 507.60 unknown via CMAUP database
Cytochalasin D 5458428 Click to see 507.60 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
7-Chloromellein-5-ol 102258989 Click to see CC1CC2=C(C(=C(C=C2O)Cl)O)C(=O)O1 228.63 unknown via CMAUP database
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 / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Phthalate esters / m-Phthalate esters
(3R)-8-hydroxy-3-methyl-1-oxo-3,4-dihydroisochromene-5-carboxylic acid 25769005 Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)C(=O)O 222.19 unknown via CMAUP database
(3S)-8-Hydroxy-3-methyl-1-oxoisochromane-5-carboxylic acid 486250 Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)C(=O)O 222.19 unknown via CMAUP database
> Benzenoids / Naphthalenes
2-[(8S)-1,8-dimethyl-7,8-dihydronaphthalen-2-yl]propane-1,2,3-triol 44555346 Click to see CC1CC=CC2=C1C(=C(C=C2)C(CO)(CO)O)C 248.32 unknown via CMAUP database
> Benzenoids / Tetralins
(1S,2S,4S)-6-(3-hydroxyprop-1-en-2-yl)-4,5-dimethyl-1,2,3,4-tetrahydronaphthalene-1,2-diol 44255026 Click to see 248.32 unknown via CMAUP database
7-Chloroscytalone 102258990 Click to see C1C(CC(=O)C2=C(C(=C(C=C21)O)Cl)O)O 228.63 unknown via CMAUP database
Isosclerone 13369486 Click to see C1CC(=O)C2=C(C1O)C=CC=C2O 178.18 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans
9,9'-O-Isopropyllidene-isolariciresinol 91885030 Click to see CC1(OCC2CC3=CC(=C(C=C3C(C2CO1)C4=CC(=C(C=C4)O)OC)O)OC)C 400.50 unknown via CMAUP database
Isotaxiresinol 9,9'-acetonide 102004573 Click to see 386.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(3S,3aR,6R,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]benzene-1,2-diol 101568249 Click to see 344.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
4-[(2R,3S,4S,5R)-4-(ethoxymethyl)-5-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)oxolan-2-yl]-2-methoxyphenol 101936591 Click to see 404.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(7R)-7-Hydroxylariciresinol 10022393 Click to see 376.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(3S,4R)-3-hydroxy-4-[(R)-hydroxy-(4-hydroxy-3-methoxyphenyl)methyl]-3-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one 101369318 Click to see COC1=C(C=CC(=C1)CC2(C(COC2=O)C(C3=CC(=C(C=C3)O)OC)O)O)O 390.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(-)-Sandaracopimaric acid 221580 Click to see 302.50 unknown via CMAUP database
(1S,3R,11S)-8,9-dimethoxy-15,15-dimethyl-4,14-dioxo-7-propan-2-yl-2-oxatetracyclo[9.4.0.01,3.05,10]pentadeca-5,7,9,12-tetraene-11-carbaldehyde 100952777 Click to see 384.40 unknown via CMAUP database
(2S,4aS,10aR)-2,6-dihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 101529198 Click to see 316.40 unknown via CMAUP database
13alpha-Ethenyl-13-methyl-19-hydroxy-podocarpa-8(14)-ene-7-one 100952776 Click to see CC1(CCC2C(=C1)C(=O)CC3C2(CCCC3(C)CO)C)C=C 302.50 unknown via CMAUP database
Hinokiol 12310492 Click to see 302.50 unknown via CMAUP database
Sugiol 94162 Click to see 300.40 unknown via CMAUP database
Taxamairin A 130631 Click to see CC(C)C1=C(C(=C2C=C3C=CC(=O)C(C3=CC(=O)C2=C1)(C)C)O)OC 338.40 unknown via CMAUP database
Taxamairin B 130632 Click to see 352.40 unknown via CMAUP database
Taxamairin H 100952784 Click to see CC(C)C1=C(C(=C2C(=C1)C=CC3=C(C2=O)C=CC(=O)C3(C)C)O)OC 338.40 unknown via CMAUP database
Taxusabietane A 76330776 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCC(=O)C3(C)C)C)O)OC 344.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Taxanes and derivatives
[(1'R,2S,2'R,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',7',9',10',13'-pentaacetyloxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-5'-yl] (3R)-3-(dimethylamino)-3-phenylpropanoate 5319245 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)CC1OC(=O)C)OC(=O)C)CO4)OC(=O)CC(C5=CC=CC=C5)N(C)C)OC(=O)C)C)OC(=O)C)OC(=O)C 769.90 unknown via CMAUP database
[(1'S,2R,2'S,3'R,5'S,7'S,8'R,9'R,10'R,13'S)-2',5',10',13'-tetraacetyloxy-1',9'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-7'-yl] acetate 21159040 Click to see 610.60 unknown via CMAUP database
[(1'S,2R,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',13'-diacetyloxy-1',7',9',10'-tetrahydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-5'-yl] acetate 102066555 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)O)C)O)O 526.60 unknown via CMAUP database
[(1'S,2S,2'R,3'R,5'S,8'R,9'R,10'R,14'S)-9'-acetyloxy-2',5',14'-trihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-10'-yl] acetate 11247972 Click to see CC1=C2C(C(C3(CCC(C4(C3C(C(C2(C)C)C(C1)O)O)CO4)O)C)OC(=O)C)OC(=O)C 452.50 unknown via CMAUP database
[(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',10',13'-triacetyloxy-1',7',9'-trihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-5'-yl] acetate 5321726 Click to see 568.60 unknown via CMAUP database
[(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',5',9',10'-tetraacetyloxy-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-7'-yl] acetate 5321730 Click to see 610.60 unknown via CMAUP database
[(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',5',9',13'-tetraacetyloxy-1',10'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-7'-yl] acetate 5321728 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)O 610.60 unknown via CMAUP database
[(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',9',10',13'-tetraacetyloxy-1',7'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-5'-yl] acetate 5316776 Click to see 610.60 unknown via CMAUP database
[(1E,3S,4R,6S,9R,11S,12S,14S)-12-acetyloxy-3,9,14-trihydroxy-7,11,16,16-tetramethyl-10-oxo-6-tricyclo[9.3.1.14,8]hexadeca-1,7-dienyl] acetate 24862000 Click to see 450.50 unknown via CMAUP database
[(1E,3S,4R,6S,9R,11S,12S,14S)-3,12,14-triacetyloxy-9-hydroxy-7,11,16,16-tetramethyl-10-oxo-6-tricyclo[9.3.1.14,8]hexadeca-1,7-dienyl] acetate 101006401 Click to see 534.60 unknown via CMAUP database
[(1R,2S,3S,5S,8R,9R,10R,11S,13R,16S)-5,16-diacetyloxy-10-(acetyloxymethyl)-8,9,11-trihydroxy-3-(2-hydroxypropan-2-yl)-6-methyl-14-oxatetracyclo[8.6.0.03,7.013,16]hexadec-6-en-2-yl] benzoate 10886794 Click to see 646.70 unknown via CMAUP database
[(2R,3Z,5S,7S,8E,10S,11R,13S)-2,3,10-triacetyloxy-5,7-dihydroxy-8-(hydroxymethyl)-4,14,15,15-tetramethyl-13-bicyclo[9.3.1]pentadeca-1(14),3,8-trienyl] acetate 6325023 Click to see 552.60 unknown via CMAUP database
[(2S,4R,5R,5aS,6S,8S,9R,9aR,10S,10aS)-2,5,6,8,10-pentaacetyloxy-4-hydroxy-10a-(2-hydroxypropan-2-yl)-3,5a-dimethyl-1,2,4,5,6,7,8,9,9a,10-decahydrobenzo[f]azulen-9-yl]methyl acetate 5321724 Click to see CC1=C2C(C(C3(C(CC(C(C3C(C2(CC1OC(=O)C)C(C)(C)O)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C)C)OC(=O)C)O 654.70 unknown via CMAUP database
[(2S,4R,5R,5aS,6S,8S,9R,9aR,10S,10aS)-5,6,8,10-tetraacetyloxy-2,4-dihydroxy-10a-(2-hydroxypropan-2-yl)-3,5a-dimethyl-1,2,4,5,6,7,8,9,9a,10-decahydrobenzo[f]azulen-9-yl]methyl acetate 5321723 Click to see 612.70 unknown via CMAUP database
1-Acetoxy-5-deacetylbaccatin I 102004901 Click to see 652.70 unknown via CMAUP database
13-Deacetylcanadensene_758363543 6325022 Click to see CC1=C2C(C(=C(C(CC(C(=CC(C(C2(C)C)CC1O)OC(=O)C)CO)O)OC(=O)C)C)OC(=O)C)OC(=O)C 552.60 unknown via CMAUP database
13-O-Deacetyltaxumairol Z 10864961 Click to see CC1=C2C(C(C3(C(CC4C(C3C(C2(CC1O)C(C)(C)O)OC(=O)C5=CC=CC=C5)(CO4)OC(=O)C)O)COC(=O)C)O)O 604.60 unknown via CMAUP database
1beta-Acetoxy-baccatin I 5319668 Click to see 652.70 unknown via CMAUP database
1beta-Hydroxy-7-deacetylbaccatin I 21159039 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)O)C)OC(=O)C)OC(=O)C 610.60 unknown via CMAUP database
CID 5318150 5318150 Click to see 652.70 unknown via CMAUP database
Taxin B 5321699 Click to see 534.60 unknown via CMAUP database
Taxumairol B 10053709 Click to see 568.60 unknown via CMAUP database
Taxumairol D 102065502 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)O 610.60 unknown via CMAUP database
taxumairol F 10651372 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1O)O)OC(=O)C)CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)OC(=O)C 610.60 unknown via CMAUP database
Taxumairol K 10769688 Click to see 588.60 unknown via CMAUP database
Taxumairol U 11124920 Click to see 612.70 unknown via CMAUP database
Taxumairol V 10875480 Click to see 570.60 unknown via CMAUP database
Taxumairol W 10918805 Click to see 568.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-4,7,8-triacetyloxy-12,13-dihydroxy-5,9-dimethyl-2-prop-1-en-2-yl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-10-yl] acetate 10918656 Click to see 550.60 unknown via CMAUP database
[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-7,8-diacetyloxy-4,12,13-trihydroxy-5,9-dimethyl-2-prop-1-en-2-yl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-10-yl] acetate 10907330 Click to see 508.60 unknown via CMAUP database
[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-8-acetyloxy-4,7,12,13-tetrahydroxy-2-(2-hydroxypropan-2-yl)-5,9-dimethyl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-10-yl] acetate 11733602 Click to see 484.50 unknown via CMAUP database
2-[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-7,8,10-triacetyloxy-4,12,13-trihydroxy-5,9-dimethyl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-2-yl]propan-2-yl benzoate 11814223 Click to see 630.70 unknown via CMAUP database
Sporogen-AO 1 177175 Click to see CC1C(CCC2=CC(=O)C3(C(C12C)O3)C(=C)C)O 248.32 unknown via CMAUP database
Taxumairol Y 11005902 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C2(CC1OC(=O)C)C(C)(C)O)OC4)O)O)OC(=O)C)C)OC(=O)C)O 526.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
Taxusabietane D 100952779 Click to see CC(C)C1=C(C(=C2C(=C1)C(CC3C2(CCC(=O)C3(C)C)COC(=O)C)OC(=O)C)O)OC4C(C(C(C(O4)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 762.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,9S,10S)-3,4-dimethoxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6,13-tetraene-8,12,15-trione 100952778 Click to see 384.40 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
2-[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-4,7,8,10,13-pentaacetyloxy-12-hydroxy-5,9-dimethyl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-2-yl]propan-2-yl benzoate 11072583 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C2(CC1OC(=O)C)C(C)(C)OC(=O)C5=CC=CC=C5)OC4)OC(=O)C)O)OC(=O)C)C)OC(=O)C)OC(=O)C 714.80 unknown via CMAUP database
Taxacin 15226199 Click to see 816.80 unknown via CMAUP database
Taxumairol R 21593833 Click to see 728.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1E,3S,4R,6S,9R,11S)-3,9-diacetyloxy-7,11,16,16-tetramethyl-10,14-dioxo-6-tricyclo[9.3.1.14,8]hexadeca-1,7,12-trienyl] acetate 10027779 Click to see 472.50 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(3R)-8-hydroxy-3-methyl-1-oxo-3,4-dihydroisochromene-5-carbaldehyde 44577733 Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)C=O 206.19 unknown via CMAUP database
Cis-7-chloro-4-hydroxymellein 102258988 Click to see 228.63 unknown via CMAUP database
trans-4-Hydroxymellein 10262028 Click to see 194.18 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(5R)-5-hydroxy-4-methoxy-5-prop-1-en-2-ylfuran-2-one 40468114 Click to see 170.16 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(5S)-1,7-dioxaspiro[4.4]non-2-ene-4,8-dione 639435 Click to see 154.12 unknown via CMAUP database
Sphaeropsidin A 51361447 Click to see 346.40 unknown via CMAUP database
Sphaeropsidin B 57396736 Click to see CC1(CCCC23C1C(C(C4=CC(CCC42O)(C)C=C)O)(OC3=O)O)C 348.40 unknown via CMAUP database
> Organoheterocyclic compounds / Oxocins
(2S,3S,4Z,6S,8S)-3,6,8-trihydroxy-2-nonyl-2,3,6,7,8,9-hexahydrooxecin-10-one 44632077 Click to see 328.40 unknown via CMAUP database
> Organoheterocyclic compounds / Pyranodioxins
(6S,8S)-3-(4-hydroxy-3,5-dimethoxyphenyl)-2,6-bis(hydroxymethyl)-3,4a,6,7,8,8a-hexahydro-2H-pyrano[2,3-b][1,4]dioxine-7,8-diol 5317351 Click to see 388.40 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Xylaric acid 3084064 Click to see 154.12 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(+/-)-Taxifolin 471 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown via CMAUP database
(2R,3S)-2-(3,4-Dihydroxyphenyl)-3,5,7-Trihydroxy-2,3-Dihydrochromen-4-One 712318 Click to see 304.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Fisetin(1-) 54758660 Click to see 285.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Fisetin 5281614 Click to see 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanols
(2S,3R)-3-(3,4-dihydroxyphenyl)-2,6,8-trihydroxy-2,3-dihydrochromen-4-one 57336522 Click to see 304.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Neoflavonoids / Neoflavans
(3R,4S)-7-hydroxy-3-[(3S,4S)-7-hydroxy-4-(4-hydroxyphenyl)-2-oxo-3,4-dihydrochromen-3-yl]-4-(4-hydroxyphenyl)-3,4-dihydrochromen-2-one 10052044 Click to see 510.50 unknown https://doi.org/10.1248/CPB.48.505
(3S,4S)-7-hydroxy-3-[(3S,4S)-7-hydroxy-4-(4-hydroxyphenyl)-2-oxo-3,4-dihydrochromen-3-yl]-4-(4-hydroxyphenyl)-3,4-dihydrochromen-2-one 10391605 Click to see 510.50 unknown https://doi.org/10.1248/CPB.48.505
7-Hydroxy-3-[7-hydroxy-4-(4-hydroxyphenyl)-2-oxo-3,4-dihydrochromen-3-yl]-4-(4-hydroxyphenyl)-3,4-dihydrochromen-2-one 9957984 Click to see 510.50 unknown https://doi.org/10.1248/CPB.48.505
> Phenylpropanoids and polyketides / Stilbenes
Dihydroresveratrol 185914 Click to see C1=CC(=CC=C1CCC2=CC(=CC(=C2)O)O)O 230.26 unknown via CMAUP database

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