Salix babylonica - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Salix babylonica - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID644036b610456952198296
Scientific name Salix babylonica
Authority L.
First published in Sp. Pl. : 1017 (1753)

Description Top

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Salix babylonica, also known as Babylon willow or weeping willow, is a species of willow tree native to northern China. It has been cultivated for thousands of years in Asia and was traded along the Silk Road to other regions such as southwest Asia and Europe. This medium to large-sized deciduous tree can grow up to 20-25 meters tall and has a short lifespan of 40-75 years. Its leaves are narrow, light green, and turn a golden yellow in the autumn. The tree is dioecious, with male and female catkins on separate trees. It is commonly grown for its ornamental value and for wood production in China. In other regions, it has been less successful due to susceptibility to disease and frost. There are many cultivars of Salix babylonica, including the popular weeping form, as well as hybrids with other willow species. The name "Babylon" in its scientific name and common names comes from a misunderstanding by Linnaeus that this was the tree mentioned in the Bible in Psalm 137. However, the trees mentioned in the Bible were actually poplars, not willows.

Synonyms Top

Scientific name Authority First published in
Ficus salix H.Lév. & Vaniot Repert. Spec. Nov. Regni Veg. 4: 66 (1907)
Salix lasiogyne Seemen Salic. Jap. : 32 (1903)
Salix lenta Fries Novit. Fl. Suec. Mant. 1: 78 (1835)
Salix jeholensis Nakai Rep. Exped. Manchoukuo Sect. IV 4: 74 (1936)
Salix annularis J.Forbes Salict. Woburn. : 41 (1829)
Salix dependens Nakai Bull. Soc. Dendrol. France 1928: 49 (1928)
Salix capitata Y.L.Chou & Skvortsov Ill. Fl. Ligneous Pl. N. E. China : 551 (1958)
Salix yuhkii Kimura Sci. Rep. Tohoku Imp. Univ., Ser. 4, Biol. 18: 544 (1950)
Salix subfragilis Andersson Mem. Amer. Acad. Arts , n.s., 6: 450 (1859)
Salix neolasiogyne Nakai & Nakai Bull. Soc. Dendrol. France 1928: 47 (1928)
Salix napoleonis F.W.Schultz Arch. Fl. : 239 (1856)
Salix ohsidare Kimura Bot. Mag. (Tokyo) 59: 79 (1946)
Salix matsudana Koidz. Bot. Mag. (Tokyo) 29: 312 (1915)
Salix pseudolasiogyne H.Lév. Repert. Spec. Nov. Regni Veg. 10: 436 (1912)
Salix pseudogilgiana H.Lév. Repert. Spec. Nov. Regni Veg. 10: 436 (1912)
Salix pseudomatsudana Y.L.Chou & Skvortsov Ill. Fl. Ligneous Pl. N. E. China : 552 (1955)
Salix pendula Moench Methodus (Moench) 336. 1794
Salix pendula Gaterau Descr. Pl. Montauban 168. 1789
Salix pseudomatsudana Y.L.Chou & Skvortsov Ill. Fl. Ligneous Pl. N. E. China : 552 (1955)
Salix babylonica var. lavallei Dode Bull. Soc. Dendrol. France 73: 93 1930
Salix babylonica f. seiko Kimura Sci. Rep. Tohoku Imp. Univ., Ser. 4, Biol. 24: 115 1958
Salix matsudana var. tortuosa A.Vilm. J. Soc. Natl. Hort. France sér. 4, 25: 350. 1924
Salix matsudana f. tortuosa (Vilm.) Rehder J. Arnold Arbor. 6: 206 1925
Salix pingliensis Y.L.Chou Bull. Bot. Res., Harbin 1(1-2): 163 (1981)
Salix matsudana var. pseudomatsudana (Y.L.Chou & Skv.) Y.L.Chou Fl. Reipubl. Popularis Sin. 20(2): 134 (1984)
Salix chinensis Burm.f. Fl. Indica : 211 (1768)
Salix cantoniensis Hance J. Bot. 6: 48 (1868)
Salix babylonica var. szechuanica Goerz Bull. Fan Mem. Inst. Biol., Bot. 6(1): 2–3 1935
Salix jishiensis C.F.Fang & J.Q.Wang Bull. Bot. Res., Harbin 1(4): 124 (1981)
Salix babylonica f. villosa C.F.Fang Bull. Bot. Res., Harbin 1(1–2): 159. 1981
Salix matsudana var. anshanensis Z.Wang & J.Z.Yan Bull. Bot. Res., Harbin 1(1-2): 176 (1981)
Salix babylonica var. glandulipilosa P.I Mao & W.Z.Li Bull. Bot. Res., Harbin 6(2): 79 (1986)

Common names Top

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Language Common/alternative name
English weeping willow
English peking willow
English babylon willow
Spanish sauce llorón
Spanish sauce lloron
Spanish sauce crespo
Spanish sáuce lloron
Spanish sáuce llorón
Afrikaans treurwilger
Arabic صفصاف بابلي
Arabic خلاف
Arabic ام شعور صفصاف
Arabic صفصاف مستحي
Azerbaijani sallaq söyüd
Azerbaijani vavilon söyüdü
Azerbaijani ağlar söyüd
Azerbaijani babil söyüdü
azb آغلار سؤیود
Belarusian Вярба вавілонская
Belarusian Вярба плакучая
Bulgarian плачеща върба
Bengali বেবিলন উইলো
Catalan desmai
Czech vrba babylónská
Welsh helygen frau wylofus
German (echte) trauerweide
German babylonische weide
German chinesische trauerweide
German chinesische weide
German trauer-weide
German echte trauerweide
Basque zume negarti
Basque sahats negarti
Persian بید بابل
Persian بید گریان
Persian بید مجنون
Finnish itkupaju
French saule pleureur
Irish saileach shilte
Irish saileach shilte shíneach
Galician salgueiro chorón
Hebrew ערבת בבל
Croatian Žalosna vrba
Croatian tužna vrba
Upper Sorbian wisata wjerba
Hungarian babiloni szomorúfűz
Armenian ուռենի բաբելոնական
Indonesian dedalu tangis
Icelandic grátvíðir
Italian salice piangente
Japanese ロッカク
Japanese イトヤナギ
Japanese オオシダレ
Japanese オオシダレヤナギ
Japanese シダリヤナギ
Japanese セイコヤナギ
Japanese ロッカクヤナギ
Japanese シダレヤナギ
Georgian მტირალა ტირიფი
Georgian ძეწნა
Korean 살릭스 바빌로니카
Korean 수양버들
Lithuanian svyruoklinis gluosnis
Macedonian жална врба
Malay dedalu cina
Burmese မိုးမခ
Burmese မိုးမခပင်
Nepali बैंश
Dutch treurwilg
Dutch wierzba płacząca
Dutch kronkelwilg
Polish wierzba żałobna
Polish wierzba płacząca
Portuguese salgueiro-chorão
Portuguese chourão
Portuguese salgueiro chorão
Portuguese salso-chorão
Romanian salcia pletoasă
Romanian salcie pletoasă
Russian Ива вавилонская
Russian Ива плакучая
sc salighe
Albanian shelgu pikëllues
Swedish tårpil
Thai หลิว
Tonga hakoloaʻani
Tonga uilou
Turkish salkım söğüt
Ukrainian Вавілонська верба
Ukrainian Верба плакуча
Uzbek majnuntol
Chinese
Chinese 柳枝
Chinese 柳絮
Chinese 柳花
Chinese 水柳
Chinese 垂柳
Chinese 垂柳(柳)
Chinese 杨柳枝
Chinese 柳屑
Chinese 柳根
Chinese 柳白皮
Chinese 垂丝柳
Chinese 清明柳

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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No subvariety added yet.

Forms (abbr. f.) Top

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Name Authority First published in
Salix babylonica f. pendula (C.K.Schneid.) Geerinck Taxonomania 6: 8 (2002)
Salix babylonica f. rokkaku Kimura J. Jap. Bot. 53: 193 (1978)
Salix babylonica f. tortuosa Y.L.Chou Bull. Bot. Res., Harbin 1(1-2): 159 (1981)
Salix babylonica f. umbraculifera (Rehder) Geerinck Taxonomania 6: 8 (2002)

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
  • Africa
    • Northern Africa
      • Algeria
      • Morocco
    • South Tropical Africa
      • Zimbabwe
    • Southern Africa
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Lesotho
      • Northern Provinces
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • China
      • China North-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
      • Qinghai
    • Eastern Asia
      • Japan
      • Korea
    • Middle Asia
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Western Asia
      • Afghanistan
      • Iran
      • Iraq
      • Lebanon-Syria
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
      • Pakistan
      • West Himalaya
    • Indo-China
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
  • Australasia
    • Australia
      • New South Wales
      • Queensland
      • South Australia
      • Tasmania
      • Victoria
  • Europe
    • Eastern Europe
      • Krym
      • South European Russia
    • Middle Europe
      • Austria
      • Belgium
      • Hungary
    • Southeastern Europe
      • Romania
  • Northern America
    • Mexico
      • Mexico Central
    • North-central U.S.A.
      • Illinois
    • Northeastern U.S.A.
      • New York
    • Northwestern U.S.A.
      • Colorado
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Delaware
      • District Of Columbia
      • Florida
      • Georgia
      • Kentucky
      • Louisiana
      • Maryland
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia
    • Southwestern U.S.A.
      • California
  • Pacific
    • South-central Pacific
      • Tubuai Islands
    • Southwestern Pacific
      • Fiji
  • Southern America
    • Caribbean
      • Bermuda
      • Cuba
      • Dominican Republic
      • Haiti
      • Puerto Rico
    • Southern South America
      • Argentina Northwest
      • Chile Central
      • Chile North

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000930856
UNII 629X19YOW6
Florida Plant Atlas 2003
Flora of Alabama 3317
Canadensys 9075
USDA Plants SABA
Tropicos 28300082
INPN 119954
Flora of Italy 187
KEW urn:lsid:ipni.org:names:777133-1
The Plant List kew-5004552
Missouri Botanical Garden 286787
Open Tree Of Life 164204
Observations.org 121654
NCBI Taxonomy 75706
NBN Atlas NBNSYS0000004910
Nature Serve 2.160018
IUCN Red List 61960227
IPNI 777133-1
iNaturalist 58316
GBIF 5372639
Freebase /m/0669pl
EPPO SAXBA
Elurikkus 7003
Calflora (Californian flora) 7262
USDA GRIN 32683
Wikipedia Salix_babylonica
CMAUP NPO14692
CMAUP NPO22503

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_040801835.1 Saba01F-Hap-a Chromosome Chinese Academy of Sciences (CAS) 2024-07-22 64.0x 624.01 Mb

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
Comprehensive evaluation and application of woody plants in the green spaces of parks in saline–Alkaline areas from a low-carbon perspective: A case study of Tianjin Qiaoyuan Park Bai J, Wang H PLoS One 10-May-2024
PMCID:PMC11086879
doi:10.1371/journal.pone.0303341
PMID:38728347
Commodity risk assessment of Tilia cordata and Tilia platyphyllos plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 03-May-2024
PMCID:PMC11066761
doi:10.2903/j.efsa.2024.8803
PMID:38707495
Measurement of mass force field driving water refilling of cuttage Xu M, Li K, Xue Y, Wang F, Liu Z, Xiao T Sci Rep 18-Apr-2024
PMCID:PMC11026483
doi:10.1038/s41598-024-59716-x
PMID:38637680
High Trunk Truncation as a Potential Sustainable Management Option for Asian Longhorned Beetle on Salix babylonica Huang C, Wang H, Hai X, Wang Z, Lyu F Insects 16-Apr-2024
PMCID:PMC11050171
doi:10.3390/insects15040278
PMID:38667408
Body Size of Female Strepsipteran Parasites (Strepsiptera, Xenidae, Xenos) Depends on Several Key Factors in a Vespine Wasp (Hymenoptera, Vespidae, Vespa) Kudô K, Oyaizu W, Kusama R, Yamaguchi Y, Koji S Insects 12-Apr-2024
PMCID:PMC11050309
doi:10.3390/insects15040266
PMID:38667396
Pest categorisation of Eulecanium giganteum Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Akrivou A, Kertesz V, Papachristos D, Sfyra O, MacLeod A EFSA J 03-Apr-2024
PMCID:PMC10988561
doi:10.2903/j.efsa.2024.8666
PMID:38576539
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
Apple crown and collar canker and necrosis caused by Cytospora balanejica sp. nov. in Iran Azizi R, Ghosta Y, Ahmadpour A Sci Rep 19-Mar-2024
PMCID:PMC10951349
doi:10.1038/s41598-024-57235-3
PMID:38504125
Local knowledge of homegarden plants in Miao ethnic communities in Laershan region, Xiangxi area, China Luo J, Li Q, He J, Yan J, Zhang S, Chang X, Wu T J Ethnobiol Ethnomed 18-Mar-2024
PMCID:PMC10946099
doi:10.1186/s13002-024-00676-x
PMID:38500123
Assessing Alien Plant Invasions in Urban Environments: A Case Study of Tshwane University of Technology and Implications for Biodiversity Conservation Nelufule T, Shivambu TC, Shivambu N, Moshobane MC, Seoraj-Pillai N, Nangammbi T Plants (Basel) 18-Mar-2024
PMCID:PMC10975853
doi:10.3390/plants13060872
PMID:38592858
Higher Plant-Derived Biostimulants: Mechanisms of Action and Their Role in Mitigating Plant Abiotic Stress Martínez-Lorente SE, Martí-Guillén JM, Pedreño MÁ, Almagro L, Sabater-Jara AB Antioxidants (Basel) 06-Mar-2024
PMCID:PMC10967762
doi:10.3390/antiox13030318
PMID:38539851
Shrouded in history: Unveiling the ways of life of an early Muslim population in Santarém, Portugal (8th– 10th century AD) MacRoberts RA, Liberato M, Roca-Rada X, Valente MJ, Relvado C, Matos Fernandes T, Barrocas Dias C, Llamas B, Vasconcelos Vilar H, Schöne BR, Ribeiro S, Santos JF, Teixeira JC, Maurer AF PLoS One 06-Mar-2024
PMCID:PMC10917335
doi:10.1371/journal.pone.0299958
PMID:38446809
A Comprehensive Analysis of Immunoglobulin E Levels, Allergen-Specific Sensitivities, and Clinical Manifestations in Allergic Dermatological Conditions: A Multicenter Retrospective Study in China Zhao J, Liang S, Zhou B, Li M, Li L Clin Cosmet Investig Dermatol 01-Mar-2024
PMCID:PMC10913895
doi:10.2147/CCID.S451117
PMID:38444403
Characterization of the complete chloroplast genome of ‘Quanhong poplar’ (Populus deltoides W. Bartram ex Humphry Marshall, 2011) Zhuang W, Li Y, Shu X, Wang Z, Wang Y, Wang T Mitochondrial DNA B Resour 23-Feb-2024
PMCID:PMC10896124
doi:10.1080/23802359.2024.2318391
PMID:38410200
Impacts of willow (Salix babylonica L.) leaf extract on growth, cecal microbial population, and blood biochemical parameters of broilers Farag SA, El-Keredy A, Abd El Gawad SA, Swelum AA, Tellez-Isaias G, Abouzeid AE Poult Sci 16-Dec-2023
PMCID:PMC10805942
doi:10.1016/j.psj.2023.103386
PMID:38176372

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
> Benzenoids / Benzene and substituted derivatives / Phenylmethylamines
2-(Aminomethyl)phenol 70267 Click to see C1=CC=C(C(=C1)CN)O 123.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
2alpha-Hydroxy-3beta-acetyloxy-betulic acid 67993145 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)OC(=O)C)O)C)C)C(=O)O 514.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown via CMAUP database
Canophyllol 7330581 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)CO)C)C)C)C 442.70 unknown via CMAUP database
Epifriedelanol 119242 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown via CMAUP database
Friedelane 15559345 Click to see CC1CCCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 412.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3S,4R,5R,6S)-2-(hydroxymethyl)-6-[2-(hydroxymethyl)phenoxy]oxane-3,4,5-triol 6931410 Click to see C1=CC=C(C(=C1)CO)OC2C(C(C(C(O2)CO)O)O)O 286.28 unknown via CMAUP database
1-[4-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethanone 10447381 Click to see CC(=O)C1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O 298.29 unknown via CMAUP database
benzyl 2-[(2S,3R,4S,5S,6R)-3-acetyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxybenzoate 162895560 Click to see CC(=O)OC1C(C(C(OC1OC2=C(C=C(C=C2)O)C(=O)OCC3=CC=CC=C3)CO)O)O 448.40 unknown https://doi.org/10.1016/0031-9422(88)80716-7
Benzyl 2-[3-acetyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxybenzoate 162895559 Click to see CC(=O)OC1C(C(C(OC1OC2=C(C=C(C=C2)O)C(=O)OCC3=CC=CC=C3)CO)O)O 448.40 unknown https://doi.org/10.1016/0031-9422(88)80716-7
Benzyl 5-hydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoate 4486614 Click to see C1=CC=C(C=C1)COC(=O)C2=C(C=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O 406.40 unknown https://doi.org/10.1016/0031-9422(88)80716-7
o-Hydroxyphenyl beta-D-glucoside 14334960 Click to see C1=CC=C(C(=C1)O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown https://doi.org/10.1016/0031-9422(88)80716-7
Pyrocatechol monoglucoside 9900144 Click to see C1=CC=C(C(=C1)O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown https://doi.org/10.1016/0031-9422(88)80716-7
Salicin 439503 Click to see C1=CC=C(C(=C1)CO)OC2C(C(C(C(O2)CO)O)O)O 286.28 unknown https://doi.org/10.1016/0031-9422(88)80716-7
Tremuloidin 3083619 Click to see C1=CC=C(C=C1)C(=O)OC2C(C(C(OC2OC3=CC=CC=C3CO)CO)O)O 390.40 unknown https://doi.org/10.1016/S0031-9422(00)85563-6
Trichocarpin 442989 Click to see C1=CC=C(C=C1)COC(=O)C2=C(C=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O 406.40 unknown https://doi.org/10.1016/0031-9422(88)80716-7
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(1S,2S,13S,15R)-15-[(Z)-4,4-dimethoxy-3-methylbut-2-enyl]-7-[(2E)-3,7-dimethylocta-2,6-dienyl]-6,8-dihydroxy-17,17-dimethyl-5-(3-methylbut-2-enyl)-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraene-10,14-dione 10532388 Click to see CC(=CCCC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=CC4CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C(OC)OC)CC=C(C)C)O)C)C 660.80 unknown via CMAUP database
(1S,2S,13S,15R)-6-[(2E)-3,7-dimethylocta-2,6-dienoxy]-8-hydroxy-17,17-dimethyl-5,15-bis(3-methylbut-2-enyl)-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4(9),5,7,11-tetraene-10,14-dione 25208760 Click to see CC(=CCCC(=CCOC1=C(C2=C(C(=C1)O)C(=O)C3=CC4CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C)CC=C(C)C)C)C 600.80 unknown via CMAUP database
(1S,2S,13S,15R)-6,8-dihydroxy-17,17-dimethyl-5,13,15-tris(3-methylbut-2-enyl)-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraene-10,14-dione 10554272 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=CC4(CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C)CC=C(C)C)C 532.70 unknown via CMAUP database
(1S,2S,13S,15R)-6,8-dihydroxy-17,17-dimethyl-5,15-bis(3-methylbut-2-enyl)-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraene-10,14-dione 57393978 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=CC4CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C)C 464.50 unknown via CMAUP database
(1S,2S,13S,15R)-6,8-dihydroxy-17,17-dimethyl-5,7,15-tris(3-methylbut-2-enyl)-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraene-10,14-dione 101389904 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=CC4CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C)CC=C(C)C)O)C 532.70 unknown via CMAUP database
(E)-4-[(1S,2S,13S,15R)-6,8-dihydroxy-17,17-dimethyl-5,7-bis(3-methylbut-2-enyl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enoic acid 46867195 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=CC4CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C(=O)O)CC=C(C)C)O)C 562.60 unknown via CMAUP database
(E)-4-[(1S,2S,13S,15R)-7-[(2E)-3,7-dimethylocta-2,6-dienyl]-6,8-dihydroxy-17,17-dimethyl-5-(3-methylbut-2-enyl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enal 10603834 Click to see CC(=CCCC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=CC4CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C=O)CC=C(C)C)O)C)C 614.80 unknown via CMAUP database
(Z)-4-[(1S,2S,13S,15R)-6,8-dihydroxy-17,17-dimethyl-5,7-bis(3-methylbut-2-enyl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enoic acid 101389902 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=CC4CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C(=O)O)CC=C(C)C)O)C 562.60 unknown via CMAUP database
(Z)-4-[(1S,2S,13S,15R)-7-[(2E)-3,7-dimethylocta-2,6-dienyl]-6,8-dihydroxy-17,17-dimethyl-5-(3-methylbut-2-enyl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enal 10841474 Click to see CC(=CCCC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=CC4CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C=O)CC=C(C)C)O)C)C 614.80 unknown via CMAUP database
1,5-Dihydroxyxanthone 5480299 Click to see C1=CC2=C(C(=C1)O)OC3=CC=CC(=C3C2=O)O 228.20 unknown via CMAUP database
Buchanaxanthone 5481840 Click to see COC1=C(C=CC2=C1OC3=CC=CC(=C3C2=O)O)O 258.23 unknown via CMAUP database
Deoxygambogenin 10817397 Click to see CC(=CCCC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=CC4CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C)CC=C(C)C)O)C)C 600.80 unknown via CMAUP database
Euxanthone 5281631 Click to see C1=CC(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O 228.20 unknown via CMAUP database
Gambogenic Acid 10794070 Click to see CC(=CCCC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=CC4CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C(=O)O)CC=C(C)C)O)C)C 630.80 unknown via CMAUP database
Isogambogenic acid 101389903 Click to see CC(=CCCC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=CC4CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C(=O)O)CC=C(C)C)O)C)C 630.80 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 2-prenylated xanthones
1,3,5-Trihydroxy-2-prenyl-9H-xanthene-9-one 9995643 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C=CC=C3O)O)C 312.30 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 8-prenylated xanthones
Calabaxanthone 341188 Click to see CC(=CCC1=C(C=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C=C4)(C)C)O)OC)C 392.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
(1S,2S,17R,19R)-12-hydroxy-19-[(E)-4-hydroxy-3-methylbut-2-enyl]-17-methoxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaene-14,18-dione 25208912 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)(C(=O)C5(OC6(C)C)CC=C(C)CO)OC)O)C=CC(O2)(C)C)C 576.70 unknown via CMAUP database
(1S,2S,17S,19R)-12-hydroxy-19-[(E)-4-hydroxy-3-methylbut-2-enyl]-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaene-14,18-dione 101389908 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)CO)O)C=CC(O2)(C)C)C 546.60 unknown via CMAUP database
(1S,2S,17S,19R)-12-hydroxy-8,8,21,21-tetramethyl-5,19-bis(3-methylbut-2-enyl)-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaene-14,18-dione 11432549 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C)O)C=CC(O2)(C)C)C 530.60 unknown via CMAUP database
(1S,2S,17S,19R)-19-[(Z)-4,4-dimethoxy-3-methylbut-2-enyl]-12-hydroxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaene-14,18-dione 10769730 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(OC)OC)O)C=CC(O2)(C)C)C 590.70 unknown via CMAUP database
(1S,2S,8R,17S,19R)-12-hydroxy-8,21,21-trimethyl-5,19-bis(3-methylbut-2-enyl)-8-(4-methylpent-3-enyl)-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaene-14,18-dione 101690778 Click to see CC(=CCCC1(C=CC2=C(C3=C(C(=C2O1)CC=C(C)C)OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C)O)C)C 598.80 unknown via CMAUP database
(E)-4-[(1S,2S,15R,16S,17S,19R)-12-hydroxy-16-methoxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11-tetraen-19-yl]-2-methylbut-2-enal 11801290 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C(C4C3=O)OC)C(=O)C5(OC6(C)C)CC=C(C)C=O)O)C=CC(O2)(C)C)C 576.70 unknown via CMAUP database
(E)-4-[(1S,2S,17S,19R)-12-hydroxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]-2-methylbut-2-enoic acid 101389907 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C=CC(O2)(C)C)C 560.60 unknown via CMAUP database
(E)-4-[(1S,2S,8R,17S,19R)-12-hydroxy-8,21,21-trimethyl-5-(3-methylbut-2-enyl)-8-(4-methylpent-3-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]-2-methylbut-2-enoic acid 70697925 Click to see CC(=CCCC1(C=CC2=C(C3=C(C(=C2O1)CC=C(C)C)OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C)C 628.70 unknown via CMAUP database
(Z)-2-(hydroxymethyl)-4-[(1S,2S,8R,17S,19R)-12-hydroxy-8,21,21-trimethyl-5-(3-methylbut-2-enyl)-8-(4-methylpent-3-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]but-2-enoic acid 102402040 Click to see CC(=CCCC1(C=CC2=C(C3=C(C(=C2O1)CC=C(C)C)OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(CO)C(=O)O)O)C)C 644.70 unknown via CMAUP database
(Z)-2-(hydroxymethyl)-4-[(1S,2S,8S,17S,19R)-12-hydroxy-8,21,21-trimethyl-5-(3-methylbut-2-enyl)-8-(4-methylpent-3-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]but-2-enoic acid 102402042 Click to see CC(=CCCC1(C=CC2=C(C3=C(C(=C2O1)CC=C(C)C)OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(CO)C(=O)O)O)C)C 644.70 unknown via CMAUP database
(Z)-4-[(1R,2R,17R,19S)-12-hydroxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]-2-methylbut-2-enoic acid 102533562 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C=CC(O2)(C)C)C 560.60 unknown via CMAUP database
(Z)-4-[(1S,2S,15R,16S,17S,19R)-12-hydroxy-16-methoxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11-tetraen-19-yl]-2-methylbut-2-enoic acid 10507667 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C(C4C3=O)OC)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C=CC(O2)(C)C)C 592.70 unknown via CMAUP database
(Z)-4-[(1S,2S,17S,19R)-12-hydroxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]-2-methylbut-2-enoic acid 54580250 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C=CC(O2)(C)C)C 560.60 unknown via CMAUP database
(Z)-4-[(1S,2S,8R,17R,19R)-12-hydroxy-17-methoxy-8,21,21-trimethyl-5-(3-methylbut-2-enyl)-8-(4-methylpent-3-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]-2-methylbut-2-enoic acid 25208439 Click to see CC(=CCCC1(C=CC2=C(C3=C(C(=C2O1)CC=C(C)C)OC45C6CC(C=C4C3=O)(C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)OC)O)C)C 658.80 unknown via CMAUP database
(Z)-4-[(1S,2S,8S,17R,19R)-12-hydroxy-17-methoxy-8,21,21-trimethyl-5-(3-methylbut-2-enyl)-8-(4-methylpent-3-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]-2-methylbut-2-enoic acid 25208762 Click to see CC(=CCCC1(C=CC2=C(C3=C(C(=C2O1)CC=C(C)C)OC45C6CC(C=C4C3=O)(C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)OC)O)C)C 658.80 unknown via CMAUP database
6-Deoxyjacareubin 5281629 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=CC=C4)O)C 310.30 unknown via CMAUP database
7-Methoxydeoxymorellin 70697915 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)(C(=O)C5(OC6(C)C)CC=C(C)C)OC)O)C=CC(O2)(C)C)C 560.70 unknown via CMAUP database
CID 12313004 12313004 Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C=O)O)C=CC(O2)(C)C)C 544.60 unknown via CMAUP database
Epigambogic acid 101406629 Click to see CC(=CCCC1(C=CC2=C(C3=C(C(=C2O1)CC=C(C)C)OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C)C 628.70 unknown via CMAUP database
Gambogic Acid 9852185 Click to see CC(=CCCC1(C=CC2=C(C3=C(C(=C2O1)CC=C(C)C)OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C)C 628.70 unknown via CMAUP database
Gambogic acid B 101377135 Click to see CCOC1C2CC3C(OC(C2=O)(C34C1C(=O)C5=C(O4)C(=C6C(=C5O)C=CC(O6)(C)CCC=C(C)C)CC=C(C)C)CC=C(C)C(=O)O)(C)C 674.80 unknown via CMAUP database
Gambogoic acid A 101377134 Click to see CC(=CCCC1(C=CC2=C(C3=C(C(=C2O1)CC=C(C)C)OC45C6CC(C(C4C3=O)OC)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C)C 660.80 unknown via CMAUP database
Jacareubin 5281644 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=C(C=C4)O)O)C 326.30 unknown via CMAUP database
S-Isogambogic acid 102402041 Click to see CC(=CCCC1(C=CC2=C(C3=C(C(=C2O1)CC=C(C)C)OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C)C 628.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
(10S,11S)-10,11,16,16-tetramethyl-6-propyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1,5,7,13,17-pentaene-4,12-dione 12444385 Click to see CCCC1=CC(=O)OC2=C3C=CC(OC3=C4C(=O)C(C(OC4=C12)C)C)(C)C 368.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Luteolin 4'-glucoside 12304737 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 448.40 unknown https://doi.org/10.1016/0031-9422(88)80716-7
Luteolin-4'-o-glucoside 5319116 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 448.40 unknown https://doi.org/10.1016/0031-9422(88)80716-7
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin 7-O-glucoside 5385553 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/0031-9422(88)80716-7
kaempferol 7-O-glucoside 10095180 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/0031-9422(88)80716-7
Kaempferol-7-o-glucoside 5480982 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/0031-9422(88)80716-7
Thalictiin 5464455 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/0031-9422(88)80716-7
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
Cyanidin 128861 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2O)O)O)O)O 287.24 unknown https://doi.org/10.1016/S0031-9422(00)88609-4
> Phenylpropanoids and polyketides / Neoflavonoids / Prenylated neoflavonoids
(10R,11R)-10,11,16,16-tetramethyl-6-phenyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1,5,7,13,17-pentaene-4,12-dione 11014914 Click to see CC1C(OC2=C3C(=CC(=O)OC3=C4C=CC(OC4=C2C1=O)(C)C)C5=CC=CC=C5)C 402.40 unknown via CMAUP database

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