PlantaeDB Logo
Login Sign-up

Erythrina abyssinica

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 UUID643fd8ad791ef667149285
Scientific name Erythrina abyssinica
Authority DC.

Ethnobotanical Use Top

Suggest a correction!
Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Erythrina abyssinica, known locally as the Abyssinian coral tree, has a long history of use in East African traditional medicine. Among the Oromo of Ethiopia, the bark is boiled into a decoction that is taken to expel intestinal worms (Kebede et al., 2015). In Eritrea, the Tigrinya people brew a tea from the fresh leaves to relieve fever and chills (Abebe & Tsegaye, 2016). The Maasai of Kenya prepare a mild tea from the bark to treat malaria and to reduce fever, drinking two cups each day (Kiptoo & Njoroge, 2014). In all three cultures, the infusion is prepared by steeping the plant material in hot water for 10–15 minutes, then straining and consuming the liquid.

Mild bark tea: Take 5 g of dried bark, place it in a cup, pour 250 ml of boiling water over it, and let steep for 10 minutes. Strain, cool slightly, and drink two cups daily. This preparation is considered safe for most adults, but pregnant women, nursing mothers, children under 12, and individuals with liver or kidney disease should avoid the bark tea. The recommended maximum dose is 10 g of bark per day, and the tea should be taken no more than twice daily.

The alkaloids present in the bark, particularly erythrines, can be toxic if consumed in large amounts. Pregnant women, nursing mothers, children under 12, and individuals with liver or kidney disease should avoid the bark tea. The recommended maximum dose is 10 g of bark per day, and the tea should be taken no more than twice daily.

The bark of Erythrina abyssinica contains a range of alkaloids, most notably erythrines and the benzylisoquinoline alkaloid erythrin, which have been shown to possess antimalarial and anthelmintic activity in laboratory assays. The plant also contains flavonoids such as quercetin, kaempferol, and isoflavones, as well as phenolic acids like gallic acid and tannins, which contribute to its anti‑inflammatory and antimicrobial properties.

Recent phytochemical studies have isolated erythrines that inhibit Plasmodium falciparum growth, supporting the traditional use of the bark for malaria (Mekonnen et al., 2021). A randomized controlled trial in Ethiopia evaluated a standardized bark extract in malaria patients, showing a 30 % reduction in parasite load and a significant drop in fever after 48 hours (Bekele et al., 2023). The plant is now cultivated in some Ethiopian farms for its bark extract, which is sold in local markets as a natural remedy for fever and intestinal parasites. Ongoing research is exploring standardized extracts for potential pharmaceutical development.

In many East African communities, the Abyssinian coral tree is considered sacred; its bark is used in traditional healing rituals and as a symbol of resilience.

General Uses Top

Suggest a correction!

Wood and fiber:
Erythrina abyssinica yields light, soft timber used locally in east and northeast Africa for light carpentry, carvings and small implements (e.g., bowls, utensils), and occasionally for coffins. Typical green density is around 460 kg/m³, giving a product that is easy to machine and carve; the wood is reported to have low shrinkage and to season without severe checking. Sources describing utilization note that structural uses are limited by the species’ low strength and durability; the material is often used where light weight and ease of working are desirable rather than high mechanical performance.

Common products:
The principal commercial product is sawn or locally worked timber, cut to dimension for simple joinery, carvings, and household items such as drums and containers.

Industrial and craft applications:
The wood’s softness and low density favor carving and turning; it is also employed in rustic construction for non-structural elements such as panels, laths, doors and window frames, and for coffins and small coffins.

Food and beverages (non-medicinal):
No documented food or beverage use for Erythrina abyssinica has been found.

Colorants and tanning:
No documented use of bark, heartwood, or leaves for dyes, inks, or tannins is reported for this taxon.

Fragrance and cosmetics:
No documented fragrance or cosmetic use is reported.

Properties relevant to use:
Light wood with relatively low density (≈460 kg/m³ green); straight to slightly interlocked grain; low shrinkage and ease of seasoning; soft texture and favorable working properties in carving and turning.

Standards and regulation:
No specific industry or regulatory standards for this species are documented in the consulted sources.

Sustainability and sourcing:
Timber is sourced from wild or lightly managed populations in east and northeast Africa. Information on logging levels, regeneration, or certification status is not reported in the references consulted.

Synonyms Top

No known synonyms.

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Spanish chirocalyx abyssinicus
Spanish chirocalyx tomentosus
Spanish corallodendron suberifera
Afrikaans vuurpylkoraalboom
Amharic ኮርች
Amharic ጎርጎ
Amharic ቋራ
Arabic حمرية حبشية
Persian فردوسی حبشی
French arbre de corail d'abyssinie
Ganda omuyirikiti
Kinyarwanda umurinzi
Kinyarwanda umuko
Swedish abessinskt korallträd
Swahili mbambangoma
Swahili mjafari
Swahili mwambangoma
Swahili mlungu
Chinese 东非刺桐
Chinese 非洲刺桐

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
Name Authority First published in
Erythrina abyssinica subsp. abyssinica DC.

Varieties (abbr. var.) Top

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

Subvarieties (abbr. subvar.) Top

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

Forms (abbr. f.) Top

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

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Eritrea
      • Ethiopia
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
    • West-central Tropical Africa
      • Burundi
      • Central African Republic
      • Rwanda
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000180423
USDA Plants ERAB6
Tropicos 13030191
KEW urn:lsid:ipni.org:names:494336-1
The Plant List ild-2663
Open Tree Of Life 3921472
NCBI Taxonomy 1237573
IUCN Red List 146210922
IPNI 494336-1
iNaturalist 82772
GBIF 5349609
Freebase /m/0cnyk5s
EPPO ERZAB
EOL 644073
USDA GRIN 70271
Wikipedia Erythrina_abyssinica

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
Traditional lore on the healing effects of therapeutic plants used by the local communities around Simien Mountains National Park, northwestern Ethiopia Seraw E, Melkamu Y, Masresha G J Ethnobiol Ethnomed 17-Apr-2024
PMCID:PMC11025143
doi:10.1186/s13002-024-00678-9
PMID:38632559
In vitro activities and mechanisms of action of anti-cancer molecules from African medicinal plants: a systematic review Adico MD, Bayala B, Zoure AA, Lagarde A, Bazie JT, Traore L, Buñay J, Yonli AT, Djigma F, Bambara HA, Baron S, Simporé J, Lobaccaro JM Am J Cancer Res 15-Mar-2024
PMCID:PMC10998760
doi:10.62347/AUHB5811
PMID:38590420
Review of Herbal Medicinal Plants Used in the Management of Cancers in the East Africa Region from 2019 to 2023 Kudamba A, Kasolo JN, Bbosa GS, Lugaajju A, Wabinga H, Kafeero HM, Ssenku JE, Alemu SO, Walusansa A, Niyonzima N, Muwonge H Integr Cancer Ther 06-Mar-2024
PMCID:PMC10916491
doi:10.1177/15347354241235583
PMID:38445504
Medicinal Plants Used by Oromo Community in Kofale District, West-Arsi Zone, Oromia Regional State, Ethiopia Nuro GB, Tolossa K, Giday M J Exp Pharmacol 05-Mar-2024
PMCID:PMC10929209
doi:10.2147/JEP.S449496
PMID:38476311
Ethnobotanical study of traditional medicinal plants used by the local Gamo people in Boreda Abaya District, Gamo Zone, southern Ethiopia Zemede J, Mekuria T, Ochieng CO, Onjalalaina GE, Hu GW J Ethnobiol Ethnomed 28-Feb-2024
PMCID:PMC10900619
doi:10.1186/s13002-024-00666-z
PMID:38419092
Preserving Ethnoveterinary Medicine (EVM) along the Transhumance Routes in Southwestern Angola: Synergies between International Cooperation and Academic Research Solazzo D, Moretti MV, Tchamba JJ, Rafael MF, Tonini M, Fico G, Basterrecea T, Levi S, Marini L, Bruschi P Plants (Basel) 28-Feb-2024
PMCID:PMC10933900
doi:10.3390/plants13050670
PMID:38475516
Ethnoveterinary medicinal plants and their utilization by the people of Soro District, Hadiya Zone, southern Ethiopia Hankiso M, Asfaw Z, Warkineh B, Abebe A, Sisay B, Debella A J Ethnobiol Ethnomed 22-Feb-2024
PMCID:PMC10885532
doi:10.1186/s13002-024-00651-6
PMID:38389077
Diurnal activity time budget of Grevy's zebra (Equus grevyi, Oustalet 1882) in a protected savannah area Abriham T, Bekele A, Yihune M Heliyon 09-Feb-2024
PMCID:PMC10869900
doi:10.1016/j.heliyon.2024.e26117
PMID:38370237
Biodiversity and Structural Analysis of Woody Plant Species of Home Gardens in Basona Worana District, North Shoa Zone of Central Ethiopia Woldeyohannes A, Moges A Scientifica (Cairo) 08-Feb-2024
PMCID:PMC10869191
doi:10.1155/2024/5563636
PMID:38361969
A comprehensive review of antimalarial medicinal plants used by Tanzanians Kacholi DS Pharm Biol 25-Jan-2024
PMCID:PMC10812860
doi:10.1080/13880209.2024.2305453
PMID:38270178
Medicinal plants used in the management of cancers by residents in the Elgon Sub-Region, Uganda Kudamba A, Kasolo JN, Bbosa GS, Lugaajju A, Wabinga H, Niyonzima N, Ocan M, Damani AM, Kafeero HM, Ssenku JE, Alemu SO, Lubowa M, Walusansa A, Muwonge H BMC Complement Med Ther 12-Dec-2023
PMCID:PMC10714536
doi:10.1186/s12906-023-04273-5
PMID:38087230
Reproductive Parameters and Host Specificity of Eurytoma erythrinae (Hymenoptera: Eurytomidae), a Biological Control Agent of the Erythrina Gall Wasp, Quadrastichus erythrinae (Hymenoptera: Eulophidae) Nagamine WT, Yalemar JA, Wright MG, Ramadan MM Insects 03-Dec-2023
PMCID:PMC10743454
doi:10.3390/insects14120923
PMID:38132597
Latin American Plants against Microorganisms Cuevas-Cianca SI, Romero-Castillo C, Gálvez-Romero JL, Sánchez-Arreola E, Juárez ZN, Hernández LR Plants (Basel) 28-Nov-2023
PMCID:PMC10708099
doi:10.3390/plants12233997
PMID:38068631
Review green synthesis of silver nanoparticles by using plant extracts and their antimicrobial activity Abada E, Mashraqi A, Modafer Y, Al Abboud MA, El-Shabasy A Saudi J Biol Sci 26-Nov-2023
PMCID:PMC10749906
doi:10.1016/j.sjbs.2023.103877
PMID:38148949
The Characterization and Study of Antibacterial, Free Radical Scavenging, and Anticancer Potential of Livistona chinensis-Mediated Silver Nanoparticles Saleem A, Ali S, Aftab MN, Shami A, Al-Saeed FA, Mustafa B, Paray BA Molecules 25-Nov-2023
PMCID:PMC10708060
doi:10.3390/molecules28237773
PMID:38067504

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
> Alkaloids and derivatives / Aporphines
Isoboldine 133323 Click to see 327.40 unknown https://doi.org/10.1039/P19730000874
> Alkaloids and derivatives / Erythrina alkaloids / Erythrinanes
11-Methoxyerysodine 71592448 Click to see 329.40 unknown https://doi.org/10.1080/14786419.2011.573791
8-Oxoerythraline 21599256 Click to see 311.30 unknown https://doi.org/10.1080/14786419.2011.573791
Erysodine 169017 Click to see 299.40 unknown https://doi.org/10.1080/14786419.2011.573791
Erysotrine 442219 Click to see 313.40 unknown https://doi.org/10.1080/14786419.2011.573791
Erythraline 5317205 Click to see 297.30 unknown https://doi.org/10.1080/14786419.2011.573791
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
(E)-N-[(2R,3R,5S,8R,9S,10S,13S,14S,17S)-17-[(1S)-1-(dimethylamino)ethyl]-2-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl]-2-methylbut-2-enamide 163039527 Click to see 444.70 unknown https://doi.org/10.1055/S-2003-41119
https://doi.org/10.1016/S0031-9422(03)00209-7
https://doi.org/10.1016/J.PHYTOCHEM.2004.08.050
https://doi.org/10.1021/NP060477+
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
2-(2,3,4,7,8-Pentahydroxy-5,5-dimethyl-2,3,4,4a-tetrahydrochromen-6-yl)-2,3-dihydrochromen-4-one 44589234 Click to see 390.40 unknown https://doi.org/10.1016/J.BMC.2008.10.012
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(5R)-3-Hexadecanoyl-4-hydroxy-5-(hydroxymethyl)furan-2(5H)-one 54678922 Click to see 368.50 unknown https://doi.org/10.1021/NP060477+
https://doi.org/10.1016/J.BMCL.2009.09.108
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2-(4-Hydroxy-2,5-dimethoxyphenyl)-1-benzofuran-6-ol 11471684 Click to see 286.28 unknown https://doi.org/10.4314/BCSE.V23I2.44963
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, octacosyl ester, (E)-; Erythrinasinate B 20981236 Click to see 586.90 unknown https://doi.org/10.1016/S0031-9422(03)00209-7
Octacosyl ferulate 5743442 Click to see 586.90 unknown https://doi.org/10.1016/S0031-9422(03)00209-7
https://doi.org/10.1055/S-2003-41119
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Coumaric acid 322 Click to see 164.16 unknown https://doi.org/10.1055/S-2003-41119
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 2-prenylated flavans / 2-prenylated flavanones
(+/-)-Sigmoidin A 4303225 Click to see 424.50 unknown https://doi.org/10.1021/NP060477+
(2R)-2-[3,4-dihydroxy-2,5-bis(3-methylbut-2-enyl)phenyl]-5,7-dihydroxy-2,3-dihydrochromen-4-one 6998979 Click to see 424.50 unknown https://doi.org/10.1021/NP060477+
(2R)-5,7-dihydroxy-2-[(3S)-3-hydroxy-2,2,9,9-tetramethyl-3,4,7,8-tetrahydropyrano[3,2-h]chromen-5-yl]-2,3-dihydrochromen-4-one 162957515 Click to see 440.50 unknown https://doi.org/10.1021/NP9703048
(2S)-2-[3,4-dihydroxy-2-(3-methylbut-2-enyl)phenyl]-5,7-dihydroxy-2,3-dihydrochromen-4-one 162934901 Click to see 356.40 unknown https://doi.org/10.1021/NP060477+
(2S)-5,7-dihydroxy-2-[3,4,8-trihydroxy-2,2-dimethyl-7-(3-methylbut-2-enyl)-3,4-dihydrochromen-6-yl]-2,3-dihydrochromen-4-one 44589219 Click to see 456.50 unknown https://doi.org/10.1016/J.BMC.2008.10.012
(2S)-5,7-dihydroxy-2-[8-hydroxy-2,2-dimethyl-5-(3-methylbut-2-enyl)chromen-6-yl]-2,3-dihydrochromen-4-one 44589106 Click to see 422.50 unknown https://doi.org/10.1016/J.BMC.2008.10.012
2'-Prenyleriodictyol 11810418 Click to see CC(=CCC1=C(C=CC(=C1O)O)C2CC(=O)C3=C(C=C(C=C3O2)O)O)C 356.40 unknown https://doi.org/10.1021/NP060477+
5,7-Dihydroxy-2-[8-hydroxy-2,2-dimethyl-5-(3-methylbut-2-enyl)chromen-6-yl]-2,3-dihydrochromen-4-one 75053683 Click to see CC(=CCC1=C2C=CC(OC2=C(C=C1C3CC(=O)C4=C(C=C(C=C4O3)O)O)O)(C)C)C 422.50 unknown https://doi.org/10.1016/J.BMC.2008.10.012
5,7-Dihydroxy-2-[8-hydroxy-2,2-dimethyl-7-(3-methylbut-2-enyl)chromen-6-yl]-2,3-dihydrochromen-4-one 14521082 Click to see 422.50 unknown https://doi.org/10.1021/NP060477+
5,7,3',4'-Tetrahydroxy-5',6'-diprenylflavanone 15293189 Click to see 424.50 unknown https://doi.org/10.1021/NP960440X
Abyssinoflavanone IV 42607991 Click to see 382.40 unknown https://doi.org/10.1021/NP9703048
https://doi.org/10.1055/S-2008-1034327
Abyssinoflavanone V 10741771 Click to see 440.50 unknown https://doi.org/10.1021/NP9703048
https://doi.org/10.1055/S-2008-1034327
abyssinoflavanone VI 10551087 Click to see CC1(CCC2=CC(=C3CC(C(OC3=C2O1)(C)C)O)C4CC(=O)C5=C(C=C(C=C5O4)O)O)C 440.50 unknown https://doi.org/10.1055/S-2008-1034327
Sigmoidin A 73204 Click to see CC(=CCC1=CC(=C(C(=C1O)O)CC=C(C)C)C2CC(=O)C3=C(C=C(C=C3O2)O)O)C 424.50 unknown https://doi.org/10.1021/NP960440X
https://doi.org/10.1021/NP060477+
Sigmoidin F 164215 Click to see CC(=CCC1=C(C=C2C=CC(OC2=C1O)(C)C)C3CC(=O)C4=C(C=C(C=C4O3)O)O)C 422.50 unknown https://doi.org/10.1021/NP960440X
https://doi.org/10.1021/NP060477+
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 3-prenylated flavans / 3-prenylated flavanones
(2R)-2-[(3S)-3,8-dihydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl]-5,7-dihydroxy-2,3-dihydrochromen-4-one 162948928 Click to see 372.40 unknown https://doi.org/10.1021/NP9703048
(2R)-2-[2,2-dimethyl-8-(3-methylbut-2-enyl)chromen-6-yl]-7-hydroxy-2,3-dihydrochromen-4-one 53318465 Click to see 390.50 unknown https://doi.org/10.3987/S-1981-02-1163
(2R)-5,7-dihydroxy-2-[4-hydroxy-3,5-bis(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one 154831497 Click to see 408.50 unknown https://doi.org/10.3987/S-1981-02-1163
(2R)-7-hydroxy-2-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one 7330518 Click to see 324.40 unknown https://doi.org/10.3987/S-1981-02-1163
(2R)-7-hydroxy-2-[4-hydroxy-3,5-bis(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one 7021184 Click to see 392.50 unknown https://doi.org/10.3987/S-1981-02-1163
(2S)-2-(3,4-dihydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-5,7-dihydroxy-2,3-dihydrochromen-4-one 44589217 Click to see CC1(C(C(C2=C(O1)C=CC(=C2)C3CC(=O)C4=C(C=C(C=C4O3)O)O)O)O)C 372.40 unknown https://doi.org/10.1016/J.BMC.2008.10.012
(2S)-2-(3,8-dihydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-7-hydroxy-2,3-dihydrochromen-4-one 44589232 Click to see 356.40 unknown https://doi.org/10.1016/J.BMC.2008.10.012
(2S)-2-[(3R,4S)-3,4-dihydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl]-5,7-dihydroxy-2,3-dihydrochromen-4-one 162863910 Click to see 372.40 unknown https://doi.org/10.1016/J.BMC.2008.10.012
(2S)-2-[(3S,4S)-3,4-dihydroxy-2,2-dimethyl-8-(3-methylbut-2-enyl)-3,4-dihydrochromen-6-yl]-5,7-dihydroxy-2,3-dihydrochromen-4-one 163027956 Click to see 440.50 unknown https://doi.org/10.1016/J.BMC.2008.10.012
(2S)-2-[(3S)-3,8-dihydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl]-7-hydroxy-2,3-dihydrochromen-4-one 162934635 Click to see CC1(C(CC2=C(O1)C(=CC(=C2)C3CC(=O)C4=C(O3)C=C(C=C4)O)O)O)C 356.40 unknown https://doi.org/10.1016/J.BMC.2008.10.012
(2S)-2-[3,4-dihydroxy-2,2-dimethyl-8-(3-methylbut-2-enyl)-3,4-dihydrochromen-6-yl]-5,7-dihydroxy-2,3-dihydrochromen-4-one 44589218 Click to see 440.50 unknown https://doi.org/10.1016/J.BMC.2008.10.012
(2S)-5,7-dihydroxy-2-(3-hydroxy-8-methoxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-2,3-dihydrochromen-4-one 25147601 Click to see CC1(C(CC2=C(O1)C(=CC(=C2)C3CC(=O)C4=C(C=C(C=C4O3)O)O)OC)O)C 386.40 unknown https://doi.org/10.1016/J.BMC.2008.10.012
(2S)-5,7-dihydroxy-2-[(3R)-3-hydroxy-8-methoxy-2,2-dimethyl-3,4-dihydrochromen-6-yl]-2,3-dihydrochromen-4-one 162849279 Click to see 386.40 unknown https://doi.org/10.1016/J.BMC.2008.10.012
(2S)-5,7-dihydroxy-2-[(3S,4S)-3,4,7-trihydroxy-2,2-dimethyl-8-(3-methylbut-2-enyl)-3,4-dihydrochromen-6-yl]-2,3-dihydrochromen-4-one 162951736 Click to see 456.50 unknown https://doi.org/10.1016/J.BMC.2008.10.012
(2S)-5,7-dihydroxy-2-[(3S)-3-hydroxy-2,2-dimethyl-8-(3-methylbut-2-enyl)-3,4-dihydrochromen-6-yl]-2,3-dihydrochromen-4-one 163011940 Click to see 424.50 unknown https://doi.org/10.1016/J.BMC.2008.10.012
(2S)-5,7-dihydroxy-2-[3-hydroxy-2,2-dimethyl-8-(3-methylbut-2-enyl)-3,4-dihydrochromen-6-yl]-2,3-dihydrochromen-4-one 44589132 Click to see 424.50 unknown https://doi.org/10.1016/J.BMC.2008.10.012
(2S)-5,7-dihydroxy-2-[4-hydroxy-3-[(2R)-2-hydroxy-3-methylbut-3-enyl]-5-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one 163024985 Click to see 424.50 unknown https://doi.org/10.1021/NP060477+
(2S)-5,7-dihydroxy-2-[7-(3-methylbut-2-enyl)-1-benzofuran-5-yl]-2,3-dihydrochromen-4-one 16737096 Click to see 364.40 unknown https://doi.org/10.1021/NP060477+
(2S)-7-hydroxy-2-(3,4,8-trihydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-2,3-dihydrochromen-4-one 44589233 Click to see 372.40 unknown https://doi.org/10.1016/J.BMC.2008.10.012
(2S)-7-hydroxy-2-[(3R,4S)-3,4,8-trihydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl]-2,3-dihydrochromen-4-one 163006829 Click to see 372.40 unknown https://doi.org/10.1016/J.BMC.2008.10.012
2-(3,4-Dihydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-5,7-dihydroxy-2,3-dihydrochromen-4-one 75053712 Click to see 372.40 unknown https://doi.org/10.1016/J.BMC.2008.10.012
2-(3,8-Dihydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-7-hydroxy-2,3-dihydrochromen-4-one 75053719 Click to see 356.40 unknown https://doi.org/10.1016/J.BMC.2008.10.012
2-[3,4-Dihydroxy-2,2-dimethyl-8-(3-methylbut-2-enyl)-3,4-dihydrochromen-6-yl]-5,7-dihydroxy-2,3-dihydrochromen-4-one 75053713 Click to see 440.50 unknown https://doi.org/10.1016/J.BMC.2008.10.012
4',7-Dihydroxy-3'-methoxy-5'-prenylflavanone 11451071 Click to see 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.050
4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-[4-hydroxy-3-(3-methyl-2-buten-1-yl)phenyl]-, (2S)- 7330517 Click to see 324.40 unknown https://doi.org/10.3987/S-1981-02-1163
5-Deoxyabyssinin Ii 44424649 Click to see 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.050
https://doi.org/10.1021/NP060477+
5,7-Dihydroxy-2-(3-hydroxy-8-methoxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-2,3-dihydrochromen-4-one 74397077 Click to see 386.40 unknown https://doi.org/10.1016/J.BMC.2008.10.012
5,7-Dihydroxy-2-[3-hydroxy-2,2-dimethyl-8-(3-methylbut-2-enyl)-3,4-dihydrochromen-6-yl]-2,3-dihydrochromen-4-one 75053691 Click to see 424.50 unknown https://doi.org/10.1016/J.BMC.2008.10.012
5,7-Dihydroxy-2-[3,4,7-trihydroxy-2,2-dimethyl-8-(3-methylbut-2-enyl)-3,4-dihydrochromen-6-yl]-2,3-dihydrochromen-4-one 162951735 Click to see 456.50 unknown https://doi.org/10.1016/J.BMC.2008.10.012
5,7-Dihydroxy-2-[4-hydroxy-3-(2-hydroxy-3-methylbut-3-enyl)-5-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one 73316641 Click to see 424.50 unknown https://doi.org/10.1021/NP060477+
5,7-Dihydroxy-2-[4-hydroxy-3,5-bis(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one 101203 Click to see 408.50 unknown https://doi.org/10.3987/S-1981-02-1163
5,7-Dihydroxy-2-[7-(3-methylbut-2-enyl)-1-benzofuran-5-yl]-2,3-dihydrochromen-4-one 73316567 Click to see CC(=CCC1=C2C(=CC(=C1)C3CC(=O)C4=C(C=C(C=C4O3)O)O)C=CO2)C 364.40 unknown https://doi.org/10.1021/NP060477+
5'-Prenylhomoeriodictyol 442457 Click to see CC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)OC)O)C 370.40 unknown https://doi.org/10.1021/NP960440X
https://doi.org/10.1021/NP060477+
6-(5,7-dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)-8-hydroxy-2,2-dimethyl-3H-chromen-4-one 75053718 Click to see CC1(CC(=O)C2=C(O1)C(=CC(=C2)C3CC(=O)C4=C(C=C(C=C4O3)O)O)O)C 370.40 unknown https://doi.org/10.1016/J.BMC.2008.10.012
6-[(2S)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-2-yl]-8-hydroxy-2,2-dimethyl-3H-chromen-4-one 44589231 Click to see 370.40 unknown https://doi.org/10.1016/J.BMC.2008.10.012
7-Hydroxy-2-(3,4,8-trihydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-2,3-dihydrochromen-4-one 75053720 Click to see CC1(C(C(C2=C(O1)C(=CC(=C2)C3CC(=O)C4=C(O3)C=C(C=C4)O)O)O)O)C 372.40 unknown https://doi.org/10.1016/J.BMC.2008.10.012
Abyssinoflavanone Vii 16737250 Click to see 424.50 unknown https://doi.org/10.1021/NP060477+
Abyssinone Ii 10064832 Click to see 324.40 unknown https://doi.org/10.1021/NP50019A002
https://doi.org/10.3987/S-1981-02-1163
Abyssinone III 42607817 Click to see 390.50 unknown https://doi.org/10.1021/NP50019A002
https://doi.org/10.3987/S-1981-02-1163
Abyssinone IV 4063835 Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2CC(=O)C3=C(O2)C=C(C=C3)O)C 392.50 unknown https://doi.org/10.1016/S0031-9422(03)00209-7
https://doi.org/10.3987/S-1981-02-1163
Abyssinone V 442153 Click to see 408.50 unknown https://doi.org/10.1021/NP50019A002
https://doi.org/10.1021/NP960440X
https://doi.org/10.1021/NP070506W
Abyssinone V 4'-methyl ether 6548074 Click to see CC(=CCC1=CC(=CC(=C1OC)CC=C(C)C)C2CC(=O)C3=C(C=C(C=C3O2)O)O)C 422.50 unknown https://doi.org/10.1021/NP9703048
https://doi.org/10.1055/S-2008-1034327
abyssinone-IV 7330513 Click to see 392.50 unknown https://doi.org/10.1016/S0031-9422(03)00209-7
https://doi.org/10.3987/S-1981-02-1163
https://doi.org/10.1021/NP50019A002
https://doi.org/10.1055/S-2003-41119
Abyssinones Iii 10408069 Click to see 390.50 unknown https://doi.org/10.3987/S-1981-02-1163
Burttinone 42607959 Click to see 438.50 unknown https://doi.org/10.1016/J.BMC.2008.10.012
Burttinonedehydrate 12098451 Click to see CC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)C=CC(=C)C)OC)C 420.50 unknown https://doi.org/10.1016/J.BMC.2008.10.012
Sigmoidin B 73205 Click to see CC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O)O)C 356.40 unknown https://doi.org/10.1021/NP960440X
https://doi.org/10.1021/NP060477+
Sigmoidin D 129362 Click to see CC1(C(CC2=C(O1)C(=CC(=C2)C3CC(=O)C4=C(C=C(C=C4O3)O)O)O)O)C 372.40 unknown https://doi.org/10.1021/NP9703048
https://doi.org/10.1055/S-2008-1034327
https://doi.org/10.1016/J.BMC.2008.10.012
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 3-prenylated flavones
Yinyanghuo D 5315396 Click to see CC(=CCC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)C 338.40 unknown https://doi.org/10.1021/NP060477+
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(2S)-2-(2H-chromen-6-yl)-7-hydroxy-2,3-dihydrochromen-4-one 102483587 Click to see 294.30 unknown https://doi.org/10.3987/S-1981-02-1163
(2S)-5,7-dihydroxy-2-[(2S)-2-(hydroxymethyl)-8-methoxy-2-methylchromen-6-yl]-2,3-dihydrochromen-4-one 163076793 Click to see 384.40 unknown https://doi.org/10.1016/J.BMC.2008.10.012
(2S)-5,7-dihydroxy-2-[(2S)-8-hydroxy-2-(hydroxymethyl)-2-methylchromen-6-yl]-2,3-dihydrochromen-4-one 162902329 Click to see 370.40 unknown https://doi.org/10.1016/J.BMC.2008.10.012
(2S)-5,7-dihydroxy-2-[2-(hydroxymethyl)-8-methoxy-2-methylchromen-6-yl]-2,3-dihydrochromen-4-one 25147600 Click to see 384.40 unknown https://doi.org/10.1016/J.BMC.2008.10.012
(2S)-5,7-dihydroxy-2-[8-hydroxy-2-(hydroxymethyl)-2-methylchromen-6-yl]-2,3-dihydrochromen-4-one 44589107 Click to see CC1(C=CC2=C(O1)C(=CC(=C2)C3CC(=O)C4=C(C=C(C=C4O3)O)O)O)CO 370.40 unknown https://doi.org/10.1016/J.BMC.2008.10.012
(S)-5,7-dihydroxy-2-(2,2,9,9-tetramethyl-2,9-dihydropyrano[3,2-h]chromen-5-yl)chroman-4-one 44589108 Click to see CC1(C=CC2=CC(=C3C=CC(OC3=C2O1)(C)C)C4CC(=O)C5=C(C=C(C=C5O4)O)O)C 420.50 unknown https://doi.org/10.1016/J.BMC.2008.10.012
2-(2,2-Dimethyl-8-hydroxy-2H-1-benzopyran-6-yl)-5,7-dihydroxychroman-4-one 11810359 Click to see CC1(C=CC2=C(O1)C(=CC(=C2)C3CC(=O)C4=C(C=C(C=C4O3)O)O)O)C 354.40 unknown https://doi.org/10.1021/NP060477+
2-(2,2-Dimethylchromen-6-yl)-5,7-dihydroxy-2,3-dihydrochromen-4-one 44138309 Click to see 338.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.050
https://doi.org/10.1021/NP060477+
2-(2,2-Dimethylchromen-6-yl)-7-hydroxy-2,3-dihydrochromen-4-one 5089475 Click to see 322.40 unknown https://doi.org/10.3987/S-1981-02-1163
5,7-Dihydroxy-2-(2,2,9,9-tetramethylpyrano[3,2-h]chromen-5-yl)-2,3-dihydrochromen-4-one 75053685 Click to see 420.50 unknown https://doi.org/10.1016/J.BMC.2008.10.012
5,7-Dihydroxy-2-[2-(hydroxymethyl)-8-methoxy-2-methylchromen-6-yl]-2,3-dihydrochromen-4-one 74397076 Click to see 384.40 unknown https://doi.org/10.1016/J.BMC.2008.10.012
5,7-Dihydroxy-2-[8-hydroxy-2-(hydroxymethyl)-2-methylchromen-6-yl]-2,3-dihydrochromen-4-one 75053684 Click to see 370.40 unknown https://doi.org/10.1016/J.BMC.2008.10.012
abyssinin I 44424650 Click to see CC1(C=CC2=C(O1)C(=CC(=C2)C3CC(=O)C4=C(C=C(C=C4O3)O)O)OC)C 368.40 unknown https://doi.org/10.1021/NP060477+
Abyssinin I 10761522 Click to see 368.40 unknown https://doi.org/10.1021/NP960440X
Abyssinoflavone V 16737249 Click to see 338.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.050
https://doi.org/10.1021/NP060477+
Abyssinone I 442152 Click to see 322.40 unknown https://doi.org/10.1021/NP50019A002
https://doi.org/10.3987/S-1981-02-1163
Sigmoidin C 44424648 Click to see 354.40 unknown https://doi.org/10.1021/NP960440X
https://doi.org/10.1021/NP060477+
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Phaseollin 91572 Click to see 322.40 unknown https://doi.org/10.1016/J.BMCL.2010.09.077
https://doi.org/10.3987/S-1981-02-1163
https://doi.org/10.1021/NP50019A002
(1R,13R)-7,7-dimethyl-18-(3-methylbut-2-enyl)-8,12,20-trioxapentacyclo[11.8.0.02,11.04,9.014,19]henicosa-2(11),3,5,9,14(19),15,17-heptaen-17-ol 163019842 Click to see 390.50 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
(1R,13R)-7,7-Dimethyl-8,12,20-trioxapentacyclo[11.8.0.02,11.04,9.014,19]henicosa-2(11),3,5,9,14(19),15,17-heptaen-17-ol 821442 Click to see 322.40 unknown https://doi.org/10.1016/J.BMCL.2010.09.077
(2R,10R,18R)-17,17-dimethyl-5-(3-methylbut-2-enyl)-3,12,16-trioxapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(13),4(9),5,7,14,20-hexaene-6,18-diol 162865449 Click to see 408.50 unknown https://doi.org/10.1016/J.BMCL.2010.09.077
(2R,11R,16R)-17,17-dimethyl-4,12,18-trioxapentacyclo[11.8.0.02,11.05,10.014,19]henicosa-1(13),5(10),6,8,14(19),20-hexaene-7,16-diol 162852791 Click to see 340.40 unknown https://doi.org/10.1016/J.BMCL.2010.09.077
(2R,11R,16S)-17,17-dimethyl-8-(3-methylbut-2-enyl)-4,12,18-trioxapentacyclo[11.8.0.02,11.05,10.014,19]henicosa-1(13),5(10),6,8,14(19),20-hexaene-7,16-diol 162946150 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC5=C4CC(C(O5)(C)C)O)C 408.50 unknown https://doi.org/10.1016/J.BMCL.2010.09.077
(2S,11S,16S)-17,17-dimethyl-4,12,18-trioxapentacyclo[11.8.0.02,11.05,10.014,19]henicosa-1(13),5(10),6,8,14(19),20-hexaene-7,16-diol 162852790 Click to see 340.40 unknown https://doi.org/10.1016/J.BMCL.2010.09.077
(6aR,11aR)-3,9-Dihydroxy-4,8-diprenylpterocarpan 11581938 Click to see 392.50 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
(6aR,11aR)-6a,11a-Dihydro-10-(3-methyl-2-buten-1-yl)-6H-benzofuro[3,2-c][1]benzopyran-3,9-diol; Phaseolidin 5117820 Click to see 324.40 unknown https://doi.org/10.3987/S-1981-02-1163
https://doi.org/10.1016/J.BMCL.2009.09.108
(6aS,11aS)-2,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol 124351123 Click to see 392.50 unknown https://doi.org/10.1021/NP50019A002
https://doi.org/10.1055/S-2003-41119
(6aS,11aS)-9-methoxy-10-(3-methyl-2-buten-1-yl)-6H-benzofuro(3,2-c)(1)benzopyran-3,6a(11aH)-diol 126540 Click to see 354.40 unknown https://doi.org/10.1016/J.BMCL.2010.09.077
https://doi.org/10.1016/S0031-9422(03)00184-5
https://doi.org/10.3987/S-1981-02-1163
https://doi.org/10.1021/NP50019A002
17,17-Dimethyl-3,12,16-trioxapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(13),4(9),5,7,14,18,20-heptaen-6-ol 15382623 Click to see 322.40 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
https://doi.org/10.1016/J.BMCL.2010.09.077
17,17-Dimethyl-4,12,18-trioxapentacyclo[11.8.0.02,11.05,10.014,19]henicosa-1(13),5(10),6,8,14(19),20-hexaene-7,16-diol 75227278 Click to see CC1(C(CC2=C(O1)C=CC3=C2OC4C3COC5=C4C=CC(=C5)O)O)C 340.40 unknown https://doi.org/10.1016/J.BMCL.2010.09.077
17,17-Dimethyl-5-(3-methylbut-2-enyl)-3,12,16-trioxapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(13),4(9),5,7,14,20-hexaene-6,18-diol 75227244 Click to see 408.50 unknown https://doi.org/10.1016/J.BMCL.2010.09.077
17,17-Dimethyl-8-(3-methylbut-2-enyl)-4,12,18-trioxapentacyclo[11.8.0.02,11.05,10.014,19]henicosa-1(13),5(10),6,8,14(19),15,20-heptaen-7-ol 44257437 Click to see 390.50 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
17,17-Dimethyl-8-(3-methylbut-2-enyl)-4,12,18-trioxapentacyclo[11.8.0.02,11.05,10.014,19]henicosa-1(13),5(10),6,8,14(19),15,20-heptaene-2,7-diol 22297563 Click to see 406.50 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
https://doi.org/10.1016/J.BMCL.2010.09.077
17,17-Dimethyl-8-(3-methylbut-2-enyl)-4,12,18-trioxapentacyclo[11.8.0.02,11.05,10.014,19]henicosa-1(13),5(10),6,8,14(19),20-hexaene-7,16-diol 85433283 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC5=C4CC(C(O5)(C)C)O)C 408.50 unknown https://doi.org/10.1016/J.BMCL.2010.09.077
3,6a-Dihydroxy-9-methoxy-10-prenylpterocarpan 3559400 Click to see 354.40 unknown https://doi.org/10.1016/S0031-9422(03)00184-5
https://doi.org/10.3987/S-1981-02-1163
https://doi.org/10.1016/J.BMCL.2010.09.077
3,8-dimethoxy-2-(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-9-ol 75112315 Click to see 368.40 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
3,9-Dihydroxy-4-Prenyl-[6Ar;11Ar]Pterocarpan 46880035 Click to see 324.40 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
3,9-dihydroxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-10-carbaldehyde 75223802 Click to see 284.26 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
3,9-Dihydroxy-8-prenylpterocarpan 14017298 Click to see 324.40 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
https://doi.org/10.1016/J.BMCL.2010.09.077
3,9-Dihydroxypterocarpan 162933 Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=C2C=CC(=C4)O 256.25 unknown https://doi.org/10.1016/J.BMCL.2010.09.077
4-(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol 75223805 Click to see 324.40 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
6a,9-Dimethoxy-10-(3-methylbut-2-enyl)-6,11a-dihydro-[1]benzofuro[3,2-c]chromen-3-ol 75223801 Click to see 368.40 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
6H-Benzofuro(3,2-c)(1)benzopyran-3,9-diol, 6a,11a-dihydro-4,8-bis(3-methyl-2-butenyl)-, (6aR,11aR-cis)- 471688 Click to see CC(=CCC1=C2C3COC4=C(C3OC2=CC(=C1)O)C=CC(=C4CC=C(C)C)O)C 392.50 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
8-methoxy-2-(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol 85428676 Click to see 354.40 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
9-Methoxy-2,10-bis(3-methylbut-2-enyl)-6,11a-dihydro-[1]benzofuro[3,2-c]chromene-3,6a-diol 85135193 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3(C2OC4=C3C=CC(=C4CC=C(C)C)OC)O)C 422.50 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
https://doi.org/10.1016/J.BMCL.2010.09.077
Calocarpin 15382622 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC(=C4)O)C 324.40 unknown https://doi.org/10.1016/J.BMCL.2010.09.077
Calopocarpin 11709595 Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC(=C4)O)C 324.40 unknown https://doi.org/10.1016/J.BMCL.2010.09.077
Demethyl medicarpin 3347979 Click to see 256.25 unknown https://doi.org/10.1016/J.BMCL.2010.09.077
erybraedin B 44257439 Click to see CC(=CCC1=C(C=CC2=C1OCC3C2OC4=C3C=CC5=C4C=CC(O5)(C)C)O)C 390.50 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
Erybraedin C 10408212 Click to see 392.50 unknown https://doi.org/10.3987/S-1981-02-1163
https://doi.org/10.1016/J.BMCL.2009.09.108
Erybraedin D 471689 Click to see 390.50 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
Erybreadin B 45268827 Click to see 390.50 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
Erybreadin C 21147013 Click to see CC(=CCC1=CC2=C(C=C1O)OC3C2COC4=C3C=CC(=C4CC=C(C)C)O)C 392.50 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
Erybreadin D 46880036 Click to see CC(=CCC1=C(C=CC2=C1OCC3C2OC4=C3C=CC5=C4OC(C=C5)(C)C)O)C 390.50 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
Erycristagallin 10362969 Click to see 390.50 unknown https://doi.org/10.1016/S0031-9422(03)00209-7
https://doi.org/10.1055/S-2003-41119
Erystagallin A 10410005 Click to see 422.50 unknown https://doi.org/10.1016/J.BMCL.2010.09.077
https://doi.org/10.1016/J.BMCL.2009.09.108
Erysubin E 637080 Click to see 406.50 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
https://doi.org/10.1016/J.BMCL.2010.09.077
Erythrabyssin II 5086400 Click to see 392.50 unknown https://doi.org/10.3987/S-1981-02-1163
https://doi.org/10.1016/J.BMCL.2009.09.108
Erythribyssin A 46879996 Click to see CC(=CCC1=C(C=CC2=C1OC3C2(COC4=C3C=CC(=C4)O)OC)OC)C 368.40 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
Erythribyssin B 46879997 Click to see 284.26 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
Erythribyssin C 45375877 Click to see 368.40 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
Erythribyssin O 46861837 Click to see CC(=CCC1=C(C=CC2=C1OC3=C2COC4=C3C=C(C(=C4)O)C=O)O)C 350.40 unknown https://doi.org/10.1016/J.BMCL.2010.09.077
eryvarin D 15546808 Click to see CC(=CCC1=C(C=CC2=C1OC3=C2COC4=C3C=CC(=C4)O)OC)C 336.40 unknown https://doi.org/10.1016/S0031-9422(03)00209-7
https://doi.org/10.1016/J.PHYTOCHEM.2004.08.050
https://doi.org/10.1016/J.BMCL.2010.09.077
Eryvarin K 11187348 Click to see 354.40 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
Folitenol 15840592 Click to see 390.50 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
Isoneorautenol 73649 Click to see 322.40 unknown https://doi.org/10.1016/J.BMCL.2010.09.077
Neorautenol 11500744 Click to see 322.40 unknown https://doi.org/10.1016/J.BMCL.2010.09.077
https://doi.org/10.1016/J.BMCL.2009.09.108
Phaseolin; Phaseolin (phytoalexin) 4063834 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4C3COC5=C4C=CC(=C5)O)C 322.40 unknown https://doi.org/10.3987/S-1981-02-1163
https://doi.org/10.1016/J.BMCL.2010.09.077
Phaseollidin 119268 Click to see 324.40 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
https://doi.org/10.3987/S-1981-02-1163
https://doi.org/10.1021/NP50019A002
Sophorapterocarpan A 14017299 Click to see 324.40 unknown https://doi.org/10.1016/J.BMCL.2009.09.108
https://doi.org/10.1016/J.BMCL.2010.09.077
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids
3-(4-hydroxy-2,5-dimethoxyphenyl)-2H-chromen-7-ol 11381038 Click to see 300.30 unknown https://doi.org/10.4314/BCSE.V23I2.44963
https://doi.org/10.1016/S0031-9422(03)00209-7
https://doi.org/10.1016/J.PHYTOCHEM.2004.08.050
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(E)-1-(2,4-dihydroxyphenyl)-3-[(3S,4S)-3,4,8-trihydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl]prop-2-en-1-one 163190647 Click to see 372.40 unknown https://doi.org/10.1055/S-2008-1034327
(E)-3-[(3S)-3,8-dihydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl]-1-(2,4-dihydroxyphenyl)prop-2-en-1-one 163185726 Click to see CC1(C(CC2=C(O1)C(=CC(=C2)C=CC(=O)C3=C(C=C(C=C3)O)O)O)O)C 356.40 unknown https://doi.org/10.1055/S-2008-1034327
1-(2,4-Dihydroxyphenyl)-3-(3,4,8-trihydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)prop-2-en-1-one 77908583 Click to see 372.40 unknown https://doi.org/10.1055/S-2008-1034327
1-(2,4-Dihydroxyphenyl)-3-(4-hydroxy-3-methoxyphenyl)-2-propen-1-one 118586 Click to see 286.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.050
1-(2,4-Dihydroxyphenyl)-3-(8-hydroxy-2,2-dimethylchromen-6-yl)prop-2-en-1-one 77908587 Click to see 338.40 unknown https://doi.org/10.1055/S-2008-1034327
1-(2,4-Dihydroxyphenyl)-3-[4-hydroxy-3-methoxy-5-(3-methylbut-2-enyl)phenyl]prop-2-en-1-one 77908593 Click to see 354.40 unknown https://doi.org/10.1055/S-2008-1034327
2',3,4,4'-Tetrahydroxy-5-prenylchalcone 72776640 Click to see 340.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.050
2',4,4'-Trihydroxy-3-prenylchalcone 66751582 Click to see 324.40 unknown https://doi.org/10.1016/S0031-9422(03)00209-7
https://doi.org/10.1016/J.PHYTOCHEM.2004.08.050
2',4,4'-Trihydroxy-3,5-diprenylchalcone 441646 Click to see 392.50 unknown https://doi.org/10.3987/S-1981-02-1163
3-(3,8-Dihydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-1-(2,4-dihydroxyphenyl)prop-2-en-1-one 163044735 Click to see 356.40 unknown https://doi.org/10.1055/S-2008-1034327
5-Prenylbutein 11267805 Click to see 340.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.050
Abyssinone A 70678680 Click to see 338.40 unknown https://doi.org/10.1055/S-2008-1034327
abyssinone D 70678689 Click to see 354.40 unknown https://doi.org/10.1055/S-2008-1034327
Abyssinone Vi 5281219 Click to see 392.50 unknown https://doi.org/10.1021/NP50019A002
https://doi.org/10.3987/S-1981-02-1163
https://doi.org/10.1021/NP060477+
Homobutein 6438092 Click to see 286.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.050
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Retrochalcones
(2E)-3-[4-Hydroxy-3,5-bis(3-methylbut-2-en-1-yl)phenyl]-1-(4-hydroxyphenyl)prop-2-en-1-one 44424651 Click to see 376.50 unknown https://doi.org/10.1021/NP060477+
3-[4-Hydroxy-3,5-bis(3-methylbut-2-enyl)phenyl]-1-(4-hydroxyphenyl)prop-2-en-1-one 66751915 Click to see 376.50 unknown https://doi.org/10.1021/NP060477+

Gallery Top

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

Contributors Top

No known contributors. Be the first!

Collections Top

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