PlantaeDB Logo
Login Sign-up

Empetrum nigrum

Empetrum nigrum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Upload a new image!

Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID6440199865d9c398138417
Scientific name Empetrum nigrum
Authority L.
First published in Sp. Pl. : 1022 (1753)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Chamaetaxus nigra (L.) Bubani Fl. Pyren. 1: 118 (1897)
Empetrum erectum Loefl. Iter Hispan. 16 1758

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English black crowberry
English crowberry
Arabic حجرية سوداء الثمر
Belarusian Багноўка чорная
Bulgarian черен емпетрум
Czech šicha černá
Welsh creiglusen creiglus
Welsh creiglusen creiglus
Danish almindelig revling
German schwarze krähenbeere
Esperanto nigra empetro
Estonian harilik kukemari
Persian سنگروی سیاه
Finnish variksenmarja
French camarine noire
frr swinbei
Irish lus na feannóige
Hebrew אמפטרומיות
ik paunġaq
Icelandic krækilyng
Japanese ガンコウラン
Japanese セイヨウガンコウラン
Kazakh Субүлдірген
Korean 시로미
koi Пончӧд
kv Пончӧд
Lithuanian juodoji varnauogė
Malayalam എംപെട്രം നൈഗ്രം
Norwegian Bokmål krekling
Dutch kraaihei
Norwegian Nynorsk krekling
olo kuornahus
Polish bażyna czarna
Russian водяника
Russian Водяника чёрная
se čáhppesmuorji
Samogitian varnougė
sjd Чиммнушш
Slovak šucha čierna
smn čyemenjâs
smn čapismyerji
smn vuorâččâsmyerji
sms čuõʹmmjõš
stq heedebäie
Swedish kråkbär
Ukrainian Водянка чорна
Chinese 岩高兰

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
Name Authority First published in
Empetrum nigrum subsp. albidum (V.N.Vassil.) Kuvaev Bot. Zhurn. (Moscow & Leningrad) 81(10): 113 (1996)
Empetrum nigrum subsp. androgynum (V.N.Vassil.) Kuvaev Bot. Zhurn. (Moscow & Leningrad) 81(10): 113 (1996)
Empetrum nigrum subsp. asiaticum (Nakai ex H.Ito) Kuvaev Bot. Zhurn. (Moscow & Leningrad) 81(10): 113 (1996)
Empetrum nigrum subsp. caucasicum (Juz.) Kuvaev Bot. Zhurn. (Moscow & Leningrad) 81(10): 113 (1996)
Empetrum nigrum subsp. hermaphroditum (Hagerup) Böcher Meddel. Grønland 147(9): 81 (1952)
Empetrum nigrum subsp. kardakovii (V.N.Vassil.) Kuvaev Bot. Zhurn. (Moscow & Leningrad) 81(10): 113 (1996)
Empetrum nigrum subsp. nigrum
Empetrum nigrum subsp. stenopetalum (V.N.Vassil.) Nedol. Konsp. Dendrofl. Ross. Dal'nego Vostoka 40. (1995)

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!
Expose seeds to natural outdoor winter conditions for 3 months, then gradually increase light and temperature in the spring.
Germination Successful Only with GA3: for these seeds, the use of Gibberellic Acid is not just beneficial but essential for germination to occur.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • China
      • China North-central
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
    • Middle Asia
      • Kazakhstan
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Kamchatka
      • Khabarovsk
      • Kuril Islands
      • Magadan
      • Primorye
      • Sakhalin
    • Siberia
      • Altay
      • Buryatiya
      • Chita
      • Irkutsk
      • Krasnoyarsk
      • Tuva
      • West Siberia
      • Yakutskiya
    • Western Asia
      • Turkey
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • North European Russia
      • Northwest European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Finland
      • Føroyar
      • Great Britain
      • Iceland
      • Ireland
      • Norway
      • Svalbard
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Romania
      • Yugoslavia
    • Southwestern Europe
      • France
      • Spain
  • Northern America
    • Eastern Canada
      • Labrador
      • New Brunswick
      • Newfoundland
      • Nova Scotia
      • Ontario
      • Prince Edward Island
      • Québec
    • North-central U.S.A.
      • Minnesota
    • Northeastern U.S.A.
      • Maine
      • Michigan
      • New Hampshire
      • New York
      • Vermont
    • Northwestern U.S.A.
      • Oregon
      • Washington
    • Southwestern U.S.A.
      • California
    • Subarctic America
      • Alaska
      • Aleutian Islands
      • Greenland
      • Northwest Territorie
      • Nunavut
      • Yukon
    • Western Canada
      • Alberta
      • British Columbia
      • Manitoba
      • Saskatchewan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000667231
UNII FA1WUY08F1
Canadensys 5514
USDA Plants EMNI
Tropicos 11900005
INPN 96069
Flora of Italy 3741
KEW urn:lsid:ipni.org:names:30371508-2
The Plant List kew-2788473
PFAF Empetrum nigrum
Open Tree Of Life 760250
Observations.org 6730
NCBI Taxonomy 191066
NBN Atlas NBNSYS0000004598
Nature Serve 2.154886
IPNI 30371508-2
iNaturalist 76812
GBIF 2888370
Freebase /m/05254mh
FEIS plants/shrub/empnig
EPPO EMPHI
EOL 586630
Elurikkus 4532
Calflora (Californian flora) 2959
USDA GRIN 15127
Wikipedia Empetrum_nigrum
CMAUP NPO19152

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
Bacterial and fungal communities in sub-Arctic tundra heaths are shaped by contrasting snow accumulation and nutrient availability Männistö MK, Ahonen SH, Ganzert L, Tiirola M, Stark S, Häggblom MM FEMS Microbiol Ecol 28-Mar-2024
PMCID:PMC10996926
doi:10.1093/femsec/fiae036
PMID:38549428
The Arctic Plant Aboveground Biomass Synthesis Dataset Berner LT, Orndahl KM, Rose M, Tamstorf M, Arndal MF, Alexander HD, Humphreys ER, Loranty MM, Ludwig SM, Nyman J, Juutinen S, Aurela M, Happonen K, Mikola J, Mack MC, Vankoughnett MR, Iversen CM, Salmon VG, Yang D, Kumar J, Grogan P, Danby RK, Scott NA, Olofsson J, Siewert MB, Deschamps L, Lévesque E, Maire V, Morneault A, Gauthier G, Gignac C, Boudreau S, Gaspard A, Kholodov A, Bret-Harte MS, Greaves HE, Walker D, Gregory FM, Michelsen A, Kumpula T, Villoslada M, Ylänne H, Luoto M, Virtanen T, Forbes BC, Hölzel N, Epstein H, Heim RJ, Bunn A, Holmes RM, Hung JK, Natali SM, Virkkala AM, Goetz SJ Sci Data 20-Mar-2024
PMCID:PMC10954756
doi:10.1038/s41597-024-03139-w
PMID:38509110
Fecal DNA metabarcoding reveals seasonal and annual variation in willow ptarmigan diet Ingvaldsen EW, Østnes JE, Kleven O, Davey M, Fossøy F, Nilsen EB R Soc Open Sci 28-Feb-2024
PMCID:PMC10898975
doi:10.1098/rsos.231518
PMID:38420626
Arthropod diversity in the alpine tundra using metabarcoding: Spatial and temporal differences in alpha‐ and beta‐diversity Hein N, Astrin JJ, Beckers N, Giebner H, Langen K, Löffler J, Misof B, Fonseca VG Ecol Evol 09-Feb-2024
PMCID:PMC10857931
doi:10.1002/ece3.10969
PMID:38343576
Antioxidant and Antifungal Activities and Characterization of Phenolic Compounds Using High-Performance Liquid Chromatography and Mass Spectrometry (HPLC-MS) in Empetrum rubrum Vahl ex Willd. Schneider C, González-Reyes M, Vergara C, Fuica-Carrasco C, Zapata P Plants (Basel) 09-Feb-2024
PMCID:PMC10893491
doi:10.3390/plants13040497
PMID:38498437
Vaccinium uliginosum L. (bog bilberry) and the search for its alleged toxicity: a review Vaneková Z, Holloway P, Rollinger JM Front Toxicol 31-Jan-2024
PMCID:PMC10864615
doi:10.3389/ftox.2024.1358840
PMID:38357417
Vascular plants and mosses as bioindicators of variability of the coastal pine forest (Empetro nigri-Pinetum) Wolski GJ, Sobisz Z, Mitka J, Kruk A, Jukonienė I, Popiela A Sci Rep 02-Jan-2024
PMCID:PMC10761821
doi:10.1038/s41598-023-50189-y
PMID:38167576
Structural Studies of Mexican Husk Tomato (Physalis ixocarpa) Fruit Cutin Arrieta-Baez D, Quezada Huerta C, Rojas-Torres GS, Perea-Flores MD, Mendoza-León HF, Gómez-Patiño MB Molecules 28-Dec-2023
PMCID:PMC10780591
doi:10.3390/molecules29010184
PMID:38202766
Relating Paramagnetic Properties to Molecular Parameters of Humic Acids Isolated from Permafrost Peatlands in the European Arctic Lodygin E, Vasilevich R, Abakumov E Molecules 23-Dec-2023
PMCID:PMC10779841
doi:10.3390/molecules29010104
PMID:38202687
Rust Fungi on Medicinal Plants in Guizhou Province with Descriptions of Three New Species Wu Q, He M, Liu T, Hu H, Liu L, Zhao P, Li Q J Fungi (Basel) 21-Sep-2023
PMCID:PMC10532644
doi:10.3390/jof9090953
PMID:37755061
Mid-to-late Holocene climate variability in coastal East Asia and its impact on ancient Korean societies Park J, Bahk J, Park J, Kim H, Choi J Sci Rep 16-Sep-2023
PMCID:PMC10505234
doi:10.1038/s41598-023-42551-x
PMID:37717094
Use climatic space‐for‐time substitutions with care: Not only climate, but also local environment affect performance of the key forest species bilberry along elevation gradient Auestad I, Rydgren K, Halvorsen R, Avdem I, Berge R, Bollingberg I, Lima O Ecol Evol 16-Aug-2023
PMCID:PMC10432774
doi:10.1002/ece3.10401
PMID:37600486
Regional differences in water beetle communities networks settling in dystrophic lakes in northern Poland Pakulnicka J, Kruk M Sci Rep 05-Aug-2023
PMCID:PMC10404283
doi:10.1038/s41598-023-39689-z
PMID:37543705
The Liverwort and Hornwort Flora of Jeju Island, Republic of Korea: A Volcanic Island with a Unique Mixture of Subtropical, Temperate, Boreal, and Arctomontane Taxa Choi SS, Bakalin VA, Bum HM, Park SJ, Kim DS, Ahn US, Moon MO Plants (Basel) 20-Jun-2023
PMCID:PMC10301385
doi:10.3390/plants12122384
PMID:37376013
The relative importance of abiotic and biotic environmental conditions for taxonomic, phylogenetic, and functional diversity of spiders across spatial scales Måsviken J, Dalén L, Norén K, Dalerum F Oecologia 01-Jun-2023
PMCID:PMC10307692
doi:10.1007/s00442-023-05383-0
PMID:37261510

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
2-[(1S,2R,4R,4aR,6R,8R,8aS)-4-acetyloxy-8-benzoyloxy-1-(cyanomethyl)-6-ethenyl-4a-hydroxy-1,6-dimethyl-5-oxo-2,3,4,7,8,8a-hexahydronaphthalen-2-yl]-2-methylpropanoic acid 15548729 Click to see CC(=O)OC1CC(C(C2C1(C(=O)C(CC2OC(=O)C3=CC=CC=C3)(C)C=C)O)(C)CC#N)C(C)(C)C(=O)O 525.60 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
[(2S,3S,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-7,10-diacetyloxy-5-benzoyloxy-3-ethenyl-2,6,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 10032594 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)C=C)(C)O)O)C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C 692.70 unknown via CMAUP database
5,6,7-Trimethoxy-9,10-dihydrophenanthren-4-ol 85670360 Click to see COC1=C(C(=C2C(=C1)CCC3=C2C(=CC=C3)O)OC)OC 286.32 unknown https://doi.org/10.1111/J.1438-8677.1992.TB00302.X
Cannithrene 2 86021565 Click to see COC1=C(C2=C(CCC3=C2C(=CC(=C3)OC)O)C=C1)O 272.29 unknown https://doi.org/10.1111/J.1438-8677.1992.TB00302.X
Neoorthosiphol A 10055454 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)C=C)(C)O)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)O)(C)C 692.70 unknown via CMAUP database
Staminol B 11802781 Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(C(C(C3=O)(C)O)C=C)OC(=O)C5=CC=CC=C5)O)O)(C)C)OC(=O)C 692.70 unknown via CMAUP database
staminol C 11490943 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)C=C)(C)O)O)C)OC(=O)C)O)OC(=O)C5=CC=CC=C5)(C)C 692.70 unknown via CMAUP database
staminol D 11455867 Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)C=C)(C)O)O)C)OC(=O)C)(C)C 568.60 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
3-Cyclohexa-2,4-dien-1-yl-1-(4-hydroxy-2-methoxyphenyl)prop-2-en-1-one 129848354 Click to see COC1=C(C=CC(=C1)O)C(=O)C=CC2CC=CC=C2 256.30 unknown https://doi.org/10.1111/J.1438-8677.1992.TB00302.X
> Hydrocarbons / Saturated hydrocarbons / Cycloalkanes
Cyclodotriacontane 14041902 Click to see C1CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC1 448.80 unknown https://doi.org/10.1007/BF00598088
Cyclohexacosane 12268263 Click to see C1CCCCCCCCCCCCCCCCCCCCCCCCC1 364.70 unknown https://doi.org/10.1007/BF00598088
Cyclooctacosane 520451 Click to see C1CCCCCCCCCCCCCCCCCCCCCCCCCCC1 392.70 unknown https://doi.org/10.1007/BF00598088
Cyclotetracosane 520449 Click to see C1CCCCCCCCCCCCCCCCCCCCCCC1 336.60 unknown https://doi.org/10.1007/BF00598088
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
Chaetopenoid D 139583487 Click to see CCC(CO)C=CC=CC(=O)OC1C=CC2=CC(C(CC2(C1C)C)O)O 362.50 unknown https://doi.org/10.1007/BF00598088
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(13R)-1alpha-(Benzoyloxy)-2alpha-acetoxy-3alpha,7alpha,8-trihydroxypimara-15-ene-11,14-dione 101228589 Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(=O)CC(C3=O)(C)C=C)O)O)(C)C)O 528.60 unknown via CMAUP database
(13R)-1alpha-(Benzoyloxy)-2alpha,8-dihydroxy-3alpha,7alpha-diacetoxypimara-15-ene-11,14-dione 101228590 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)O)OC(=O)C)(C)C 570.60 unknown via CMAUP database
(13R)-1alpha,11alpha-Bis(benzoyloxy)-2alpha,6beta,8-trihydroxy-3alpha,7alpha-diacetoxypimara-15-ene-14-one 10930480 Click to see CC(=O)OC1C(C2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C)O 692.70 unknown via CMAUP database
(13R)-1alpha,11alpha-Bis(benzoyloxy)-2alpha,7alpha,8-trihydroxy-3alpha-acetoxypimara-15-ene-14-one 10919284 Click to see CC(=O)OC1C(C(C2(C(C1(C)C)CC(C3(C2C(CC(C3=O)(C)C=C)OC(=O)C4=CC=CC=C4)O)O)C)OC(=O)C5=CC=CC=C5)O 634.70 unknown via CMAUP database
(13S)-1alpha,11alpha-Bis(benzoyloxy)-3alpha,7alpha-diacetoxy-2alpha,8beta,12alpha-trihydroxypimara-15-ene-14-one 10032595 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)O)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C 692.70 unknown via CMAUP database
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-6,7-diacetyloxy-5-benzoyloxy-2-ethenyl-10,10a-dihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 10327179 Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(CC(C3=O)(C)C=C)OC(=O)C5=CC=CC=C5)O)O)(C)C)OC(=O)C 676.70 unknown via CMAUP database
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-6,7,10-triacetyloxy-5-benzoyloxy-2-ethenyl-10a-hydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 9987409 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C 718.80 unknown via CMAUP database
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,9S,10R,10aR)-6,10-diacetyloxy-5-benzoyloxy-2-ethenyl-7,9,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 10101175 Click to see CC(=O)OC1C(C(C2C(C(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(CC(C3=O)(C)C=C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)O)(C)C)O 692.70 unknown via CMAUP database
[(2S,3S,4R,4aS,4bR,7R,8aR,9R,10aS)-9-acetyloxy-4-benzoyloxy-7-ethenyl-3,8a-dihydroxy-1,1,4a,7-tetramethyl-5,8-dioxo-2,3,4,4b,6,9,10,10a-octahydrophenanthren-2-yl] benzoate 10258500 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)O)OC(=O)C5=CC=CC=C5)(C)C 632.70 unknown via CMAUP database
[(2S,3S,4R,4aS,4bS,5R,7R,8aR,9R,10aS)-2,3-diacetyloxy-7-ethenyl-5,8a,9-trihydroxy-1,1,4a,7-tetramethyl-8-oxo-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-4-yl] benzoate 10076785 Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(CC(C3=O)(C)C=C)O)O)O)(C)C)OC(=O)C 572.60 unknown via CMAUP database
[(2S,3S,4S,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-7,10-diacetyloxy-5-benzoyloxy-2-ethenyl-3,6,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 44583688 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)O)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C 692.70 unknown via CMAUP database
[(4aR,4bR,7R,8aR,9R,10aR)-3-acetyloxy-7-ethenyl-8a-hydroxy-1,1,4a,7-tetramethyl-2,5,8-trioxo-6,9,10,10a-tetrahydro-4bH-phenanthren-9-yl] acetate 10072248 Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C)(C)C 446.50 unknown via CMAUP database
orthosiphol A 15385858 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)O)(C)C 676.70 unknown via CMAUP database
orthosiphol B 15385859 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C 676.70 unknown via CMAUP database
orthosiphol D 44583689 Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C)(C)C 552.60 unknown via CMAUP database
orthosiphol I 10674582 Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(=O)CC(C3=O)(C)C=C)O)O)(C)C)OC(=O)C 570.60 unknown via CMAUP database
orthosiphol J 10438744 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)OC(=O)C)(C)C 612.70 unknown via CMAUP database
Orthosiphol K 10054824 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)O)(C)C 634.70 unknown via CMAUP database
Orthosiphol L 10101176 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)O)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)O)(C)C 692.70 unknown via CMAUP database
Orthosiphol M 10030927 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)O)(C)C 570.60 unknown via CMAUP database
Orthosiphol N 10258499 Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(=O)CC(C3=O)(C)C=C)O)O)(C)C)OC(=O)C5=CC=CC=C5 632.70 unknown via CMAUP database
orthosiphol O 10032464 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)OC(=O)C5=CC=CC=C5)(C)C 676.70 unknown via CMAUP database
Orthosiphol S 10099906 Click to see CC1(C2CC(C3(C(C2(C(C(=O)C1OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5)C)C(=O)CC(C3=O)(C)C=C)O)O)C 588.60 unknown via CMAUP database
orthosiphol T 11082749 Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(CC(C3=O)(C)C=C)OC(=O)C5=CC=CC=C5)O)O)(C)C)O 634.70 unknown via CMAUP database
Orthosiphol U 637182 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)OC(=O)C)(C)C 614.70 unknown via CMAUP database
Orthosiphol V 10951947 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)O)OC(=O)C)(C)C 572.60 unknown via CMAUP database
Orthosiphol W 11071897 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)O)(C)C 572.60 unknown via CMAUP database
Orthosiphol X 10054823 Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(CC(C3=O)(C)C=C)O)O)O)(C)C)OC(=O)C5=CC=CC=C5 634.70 unknown via CMAUP database
Orthosiphol Y 11144807 Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(=O)C(CC3O)(C)C=C)O)C)OC(=O)C)(C)C 448.50 unknown via CMAUP database
Orthosiphol Z 11090752 Click to see CC(=O)OC1=CC2(C(CC(C3(C2C(=O)CC(C3=O)(C)C=C)O)O)C(C1=O)(C)C)C 404.50 unknown via CMAUP database
orthosiphonone A 10439492 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)OC(=O)C5=CC=CC=C5)(C)C 674.70 unknown via CMAUP database
orthosiphonone C 11226314 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)O)OC(=O)C4=CC=CC=C4)O)(C)C 528.60 unknown via CMAUP database
Siphonol A 10952715 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)CO)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C 734.80 unknown via CMAUP database
Siphonol B 11017910 Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)CO)C(CC(C3=O)(C)C=C)OC(=O)C5=CC=CC=C5)O)O)(C)C)OC(=O)C 692.70 unknown via CMAUP database
Siphonol C 11115145 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)CO)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C 692.70 unknown via CMAUP database
SiphonolD 11828707 Click to see CC(=O)OCC12C(CC(C3(C1C(CC(C3=O)(C)C=C)OC(=O)C4=CC=CC=C4)O)O)C(C(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C 734.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Norstaminone A 10414921 Click to see CC(=O)C(=CC1C(=O)C(CC2C1(C(C(C(C2(C)C)O)OC(=O)C)OC(=O)C3=CC=CC=C3)C)OC(=O)C)C=C 540.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Vomifoliol 5280462 Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C 224.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
(4R,5S,8R,9S,10S,13R,14S,17R)-4,5,9,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-1,2,4,6,7,8,10,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 162962010 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC4C(C)CCC=C(C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/0040-4039(95)01286-Q
4,5,9,13,14-Pentamethyl-17-(6-methylhept-5-en-2-yl)-1,2,4,6,7,8,10,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 85181507 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC4C(C)CCC=C(C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/0040-4039(95)01286-Q
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,4S,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-4,9-dihydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 21604188 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C(=O)O 472.70 unknown via CMAUP database
(3R,4aR,6aR,6bS,8aS,11R,12S,12aS,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 293273 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO 442.70 unknown https://doi.org/10.1016/0040-4039(95)01286-Q
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
Erythrodiol 101761 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)CO)C 442.70 unknown https://doi.org/10.1016/0040-4039(95)01286-Q
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/0040-4039(95)01286-Q
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/0040-4039(95)01286-Q
Uvaol 92802 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO 442.70 unknown https://doi.org/10.1016/0040-4039(95)01286-Q
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
Siphonol E 10963687 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=O)O)CO)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C 736.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
14-deoxo-14-O-acetylorthosiphol Y 21578028 Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(C(CC3O)(C)C=C)OC(=O)C)O)C)OC(=O)C)(C)C 492.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
Asperglaucide 10026486 Click to see CC(=O)OCC(CC1=CC=CC=C1)NC(=O)C(CC2=CC=CC=C2)NC(=O)C3=CC=CC=C3 444.50 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
Norstaminolactone A 11146922 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C14OC(=O)C(O4)(C(C3OC(=O)C5=CC=CC=C5)CNC)C)C)OC(=O)C6=CC=CC=C6)OC(=O)C)O)(C)C 707.80 unknown via CMAUP database
Staminol A 10628761 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)C=C)(C)O)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C 734.80 unknown via CMAUP database
Staminolactone A 10770905 Click to see CC(=O)OC1C(C(C2CC(C34C(C2(C1OC(=O)C5=CC=CC=C5)C)C(C(C(O3)(C(=O)O4)C)C=C)OC(=O)C6=CC=CC=C6)O)(C)C)OC(=O)C 690.70 unknown via CMAUP database
Staminolactone B 10676125 Click to see CC(=O)OC1C(C(C2CC(C34C(C2(C1OC(=O)C5=CC=CC=C5)C)C(C(C(O3)(OC4=O)C)C=C)OC(=O)C6=CC=CC=C6)O)(C)C)OC(=O)C 690.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
2-[(1S,2R,4R,4aR,6R,8R,8aS)-4-acetyloxy-8-benzoyloxy-1-(carboxymethyl)-6-ethenyl-4a-hydroxy-1,6-dimethyl-5-oxo-2,3,4,7,8,8a-hexahydronaphthalen-2-yl]-2-methylpropanoic acid 15548710 Click to see CC(=O)OC1CC(C(C2C1(C(=O)C(CC2OC(=O)C3=CC=CC=C3)(C)C=C)O)(C)CC(=O)O)C(C)(C)C(=O)O 544.60 unknown via CMAUP database
secoorthosiphol B 15548728 Click to see CC(=O)OC1CC(C(C2C1(C(=O)C(CC2OC(=O)C3=CC=CC=C3)(C)C=C)O)(C)CC(=O)O)C(C)(C)C(=O)OC 558.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives
L-Tartaric acid 444305 Click to see C(C(C(=O)O)O)(C(=O)O)O 150.09 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
[(1S,2S,3R,4S,5S,7S,9R,10R,12R,15S,16S,17S)-4,9-diacetyloxy-3-benzoyloxy-5,10,15-trihydroxy-2,6,6,12-tetramethyl-11,13-dioxatetracyclo[8.7.0.02,7.012,16]heptadecan-17-yl] benzoate 10963538 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(OC4(C(C3OC(=O)C5=CC=CC=C5)C(CO4)O)C)O)C)OC(=O)C6=CC=CC=C6)OC(=O)C)O)(C)C 696.70 unknown via CMAUP database
Norstaminol A 11765116 Click to see CC(=O)OC1C(C(C2CC3C4(O3)C(C2(C1OC(=O)C5=CC=CC=C5)C)C(C6C(COC6(O4)C)O)OC(=O)C7=CC=CC=C7)(C)C)OC(=O)C 678.70 unknown via CMAUP database
Norstaminol C 10951829 Click to see CC(=O)C1=CC2C3(C(CC(C24OCC1O4)OC(=O)C)C(C(C(C3OC(=O)C5=CC=CC=C5)OC(=O)C)O)(C)C)C 556.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-rosmarinic acid 639655 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown via CMAUP database
2-Propenoic acid, 3-(3,4-dihydroxyphenyl)-, ethyl ester 66883 Click to see CCOC(=O)C=CC1=CC(=C(C=C1)O)O 208.21 unknown via CMAUP database
Methyl 3,4-dihydroxycinnamate 92202 Click to see COC(=O)C=CC1=CC(=C(C=C1)O)O 194.18 unknown via CMAUP database
Methyl rosmarinate 6479915 Click to see COC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O 374.30 unknown via CMAUP database
p-Hydroxyphenethyl trans-ferulate 637308 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCCC2=CC=C(C=C2)O)O 314.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid 2518 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown https://doi.org/10.1111/J.1438-8677.1992.TB00302.X
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1111/J.1438-8677.1992.TB00302.X
https://doi.org/10.1081/JLC-100100418
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown https://doi.org/10.1081/JLC-100100418
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1081/JLC-100100418
https://doi.org/10.1007/BF00598202
Rhamnocitrin 5320946 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1111/J.1438-8677.1992.TB00302.X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one 5353915 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1081/JLC-100100418
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/BF00598202
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/BF00598202
Avicularin 5490064 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O 434.30 unknown https://doi.org/10.1007/BF00598202
Guaijaverin 5481224 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown https://doi.org/10.1007/BF00598202
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/BF00598202
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/BF00598202
quercetin 3-O-alpha-L-fucopyranoside 5359430 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1081/JLC-100100418
Reynoutrin 5878729 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown https://doi.org/10.1007/BF00598202
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1081/JLC-100100418
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-3',4',6,7-tetramethoxyflavone 152430 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC 358.30 unknown via CMAUP database
5-Hydroxy-3',4',7-trimethoxyflavone 5272653 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O)OC 328.30 unknown via CMAUP database
6-Hydroxy-5,7-dimethoxy-2-(4-methoxyphenyl)-4H-chromen-4-one 243760 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)OC 328.30 unknown via CMAUP database
Eupatorin 97214 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown via CMAUP database
Ladanein 3084066 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)O 314.29 unknown via CMAUP database
Salvigenin 161271 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O 328.30 unknown via CMAUP database
Sinensetin 145659 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)OC)OC 372.40 unknown via CMAUP database
Tetramethylscutellarein 96118 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)OC 342.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
2-(3,4-Dimethoxyphenyl)-6,7,8-trimethoxy-4H-1-benzopyran-4-one 44584772 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=CC(=C(C(=C3O2)OC)OC)OC)OC 372.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
1-(2-Hydroxy-4-methoxyphenyl)-3-phenylpropan-1-one 1214726 Click to see COC1=CC(=C(C=C1)C(=O)CCC2=CC=CC=C2)O 256.30 unknown https://doi.org/10.1111/J.1438-8677.1992.TB00302.X
1-(2-Hydroxy-4,6-dimethoxyphenyl)-3-phenylpropan-1-one 270058 Click to see COC1=CC(=C(C(=C1)OC)C(=O)CCC2=CC=CC=C2)O 286.32 unknown https://doi.org/10.1111/J.1438-8677.1992.TB00302.X
Uvangoletin 6483649 Click to see COC1=CC(=CC(=C1C(=O)CCC2=CC=CC=C2)O)O 272.29 unknown https://doi.org/10.1111/J.1438-8677.1992.TB00302.X
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2-Hydroxy-4-methoxyphenyl)-3-phenylprop-2-en-1-one 265720 Click to see COC1=CC(=C(C=C1)C(=O)C=CC2=CC=CC=C2)O 254.28 unknown https://doi.org/10.1111/J.1438-8677.1992.TB00302.X
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
2'-Methoxy-4'-hydroxydihydrochalcone 42607666 Click to see COC1=C(C=CC(=C1)O)C(=O)CCC2=CC=CC=C2 256.30 unknown https://doi.org/10.1111/J.1438-8677.1992.TB00302.X
> Phenylpropanoids and polyketides / Stilbenes
3'-O-Methylbatatasin III 442711 Click to see COC1=CC=CC(=C1)CCC2=CC(=CC(=C2)OC)O 258.31 unknown https://doi.org/10.1055/S-2006-959382
5-[2-(2-Hydroxyphenyl)ethyl]-2,3-dimethoxy-phenol 10754781 Click to see COC1=CC(=CC(=C1OC)O)CCC2=CC=CC=C2O 274.31 unknown https://doi.org/10.1016/S0031-9422(97)00955-2
batatasin III 10466989 Click to see COC1=CC(=CC(=C1)O)CCC2=CC(=CC=C2)O 244.28 unknown https://doi.org/10.1055/S-2006-959382

Biological Material Top ebay Auctions

Please wait .. loading items ..

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.