Erythrina abyssinica, also known as lucky bean or flame tree, is a tree species belonging to the Fabaceae family. It is native to East Africa, Eastern DRC, and southern Africa, with its range overlapping with a similar species, Erythrina latissima, in Zimbabwe. The history of its description has been complicated due to confusion with other species, resulting in numerous synonyms. The tree produces attractive flowers that attract sunbirds, followed by long, cylindrical seed capsules containing bright red and black seeds. The seeds have various uses, including as a fish poison and decorative element in necklaces. The soft wood of the trunk is used for carving and making beehives and African drums.

Synonyms Top

No known synonyms.

Common names Top

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Filter by language:

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

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Name	Authority	First published in
Erythrina abyssinica subsp. abyssinica	DC.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- 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

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

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

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

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

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

Medicinal plants of the upper Aswa River catchment of northern Uganda - a cultural crossroads

Masters ET

J Ethnobiol Ethnomed

27-Oct-2023

PMCID:	PMC10605377
doi:	10.1186/s13002-023-00620-5
PMID:	37884931

Automated silylation of flavonoids using 3D printed microfluidics prior to chromatographic analysis: system development

Ncongwane TB, Ndinteh DT, Smit E

Anal Bioanal Chem

07-Oct-2023

PMCID:	PMC10684624
doi:	10.1007/s00216-023-04981-4
PMID:	37804326

Ethnomedicinal Knowledge of Plants Used in Nonconventional Medicine in the Management of Diabetes Mellitus in Kinshasa (Democratic Republic of the Congo)

Chiribagula Valentin B, Ndjolo Philippe O, Mboni Henry M, Mushagalusa Kasali F

Evid Based Complement Alternat Med

20-Sep-2023

PMCID:	PMC10533323
doi:	10.1155/2023/4621883
PMID:	37771953

Ethnobotanical study of nutraceutical plants used to manage opportunistic infections associated with HIV/AIDS in Acholi sub-region, Northern Uganda

Ikinyom N, Lamwaka AV, Malagala AT, Ndyomugyenyi EK

Trop Med Health

01-Sep-2023

PMCID:	PMC10472741
doi:	10.1186/s41182-023-00540-w
PMID:	37658427

Floristic composition and plant community distribution along environmental gradients in Guard dry Afromontane forest of Northwestern Ethiopia

Dagne Y, Birhanu L

BMC Ecol Evol

28-Aug-2023

PMCID:	PMC10463663
doi:	10.1186/s12862-023-02154-6
PMID:	37635212

Nutritional quality of indigenous legume browse in southern Ethiopia: farmers’ preference and correlation of local valuation of feed value with scientific indicators

Abraham G, Kechero Y, Andualem D

Front Vet Sci

21-Aug-2023

PMCID:	PMC10475582
doi:	10.3389/fvets.2023.1198212
PMID:	37671277

Medicinal Plants Used in the Management of Sexual Dysfunction, Infertility and Improving Virility in the East African Community: A Systematic Review

Kyarimpa C, Nagawa CB, Omara T, Odongo S, Ssebugere P, Lugasi SO, Gumula I

Evid Based Complement Alternat Med

12-Aug-2023

PMCID:	PMC10439835
doi:	10.1155/2023/6878852
PMID:	37600549

Biogenic Fabrication of Silver Nanoparticles Using Calotropis procera Flower Extract with Enhanced Biomimetics Attributes

Nagime PV, Singh S, Shaikh NM, Gomare KS, Chitme H, Abdel-Wahab BA, Alqahtany YS, Khateeb MM, Habeeb MS, Bakir MB

Materials (Basel)

30-May-2023

PMCID:	PMC10254777
doi:	10.3390/ma16114058
PMID:	37297192

Woody species diversity and regeneration status of Sub-Alpine forest of Mount Adama exclosure site, Northwestern highlands of Ethiopia

Mengistu DA, Bekele DA, Gela AG, Meshesha DT, Getahun MM

Heliyon

20-May-2023

PMCID:	PMC10220367
doi:	10.1016/j.heliyon.2023.e16473
PMID:	37251442

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 CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC	327.40	unknown	https://doi.org/10.1039/P19730000874
> Alkaloids and derivatives / Erythrina alkaloids / Erythrinanes
11-Methoxyerysodine	71592448	Click to see COC1CC23C(=CCN2CC(C4=CC(=C(C=C34)OC)O)OC)C=C1	329.40	unknown	https://doi.org/10.1080/14786419.2011.573791
8-Oxoerythraline	21599256	Click to see COC1CC23C(=CC(=O)N2CCC4=CC5=C(C=C34)OCO5)C=C1	311.30	unknown	https://doi.org/10.1080/14786419.2011.573791
Erysodine	169017	Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)OC)O)C=C1	299.40	unknown	https://doi.org/10.1080/14786419.2011.573791
Erysotrine	442219	Click to see COC1CC23C(=CCN2CCC4=CC(=C(C=C34)OC)OC)C=C1	313.40	unknown	https://doi.org/10.1080/14786419.2011.573791
Erythraline	5317205	Click to see COC1CC23C(=CCN2CCC4=CC5=C(C=C34)OCO5)C=C1	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 CC=C(C)C(=O)NC1CC2CCC3C4CCC(C4(CCC3C2(CC1O)C)C)C(C)N(C)C	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 CC1(C2C(C(C(OC2=C(C(=C1C3CC(=O)C4=CC=CC=C4O3)O)O)O)O)O)C	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 CCCCCCCCCCCCCCCC(=O)C1=C(C(OC1=O)CO)O	368.50	unknown	https://doi.org/10.1016/J.BMCL.2009.09.108 https://doi.org/10.1021/NP060477+
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2-(4-Hydroxy-2,5-dimethoxyphenyl)-1-benzofuran-6-ol	11471684	Click to see COC1=CC(=C(C=C1C2=CC3=C(O2)C=C(C=C3)O)OC)O	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 CCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC	586.90	unknown	https://doi.org/10.1016/S0031-9422(03)00209-7
Octacosyl (E)-ferulate	5743442	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC	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-Hydroxycinnamic acid	322	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	https://doi.org/10.1055/S-2003-41119
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 2-prenylated flavans / 2-prenylated flavanones
(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 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/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 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/10.1021/NP9703048
(2S)-2-[3,4-dihydroxy-2-(3-methylbut-2-enyl)phenyl]-5,7-dihydroxy-2,3-dihydrochromen-4-one	162934901	Click to see 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+
(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 CC(=CCC1=C(C2=C(C=C1C3CC(=O)C4=C(C=C(C=C4O3)O)O)C(C(C(O2)(C)C)O)O)O)C	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 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
2-[3,4-Dihydroxy-2,5-bis(3-methylbut-2-enyl)phenyl]-5,7-dihydroxy-2,3-dihydrochromen-4-one	4303225	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/NP060477+
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 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/NP060477+
5,7,3',4'-Tetrahydroxy-5',6'-diprenylflavanone	15293189	Click to see CC(=CCC1=C(C(=C(C=C1C2CC(=O)C3=C(C=C(C=C3O2)O)O)O)O)CC=C(C)C)C	424.50	unknown	https://doi.org/10.1021/NP960440X
Abyssinoflavanone IV	42607991	Click to see CC(=CCC1=C(C=C2CCOC2=C1O)C3CC(=O)C4=C(C=C(C=C4O3)O)O)C	382.40	unknown	https://doi.org/10.1021/NP9703048 https://doi.org/10.1055/S-2008-1034327
Abyssinoflavanone V	10741771	Click to see CC(=CCC1=C(C=C2CC(C(OC2=C1O)(C)C)O)C3CC(=O)C4=C(C=C(C=C4O3)O)O)C	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 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
(2R)-5,7-dihydroxy-2-[4-hydroxy-3,5-bis(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one	154831497	Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2CC(=O)C3=C(C=C(C=C3O2)O)O)C	408.50	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 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/10.3987/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 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-[(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 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-[(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 CC(=CCC1=C2C(=CC(=C1)C3CC(=O)C4=C(C=C(C=C4O3)O)O)C(C(C(O2)(C)C)O)O)C	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 CC(=CCC1=C2C(=CC(=C1)C3CC(=O)C4=C(C=C(C=C4O3)O)O)C(C(C(O2)(C)C)O)O)C	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 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-[(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 CC(=CCC1=C(C(=CC2=C1OC(C(C2O)O)(C)C)C3CC(=O)C4=C(C=C(C=C4O3)O)O)O)C	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 CC(=CCC1=CC(=CC2=C1OC(C(C2)O)(C)C)C3CC(=O)C4=C(C=C(C=C4O3)O)O)C	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 CC(=CCC1=CC(=CC2=C1OC(C(C2)O)(C)C)C3CC(=O)C4=C(C=C(C=C4O3)O)O)C	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 CC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)CC(C(=C)C)O)O)C	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 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+
(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 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
(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 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
2-(3,4-Dihydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-5,7-dihydroxy-2,3-dihydrochromen-4-one	75053712	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
2-(3,8-Dihydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-7-hydroxy-2,3-dihydrochromen-4-one	75053719	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
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 CC(=CCC1=C2C(=CC(=C1)C3CC(=O)C4=C(C=C(C=C4O3)O)O)C(C(C(O2)(C)C)O)O)C	440.50	unknown	https://doi.org/10.1016/J.BMC.2008.10.012
4',7-Dihydroxy-3'-methoxy-5'-prenylflavanone	11451071	Click to see CC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(O2)C=C(C=C3)O)OC)O)C	354.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.08.050
5-deoxyabyssinin II	44424649	Click to see CC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(O2)C=C(C=C3)O)OC)O)C	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 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
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 CC(=CCC1=CC(=CC2=C1OC(C(C2)O)(C)C)C3CC(=O)C4=C(C=C(C=C4O3)O)O)C	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 CC(=CCC1=C(C(=CC2=C1OC(C(C2O)O)(C)C)C3CC(=O)C4=C(C=C(C=C4O3)O)O)O)C	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 CC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)CC(C(=C)C)O)O)C	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 CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2CC(=O)C3=C(C=C(C=C3O2)O)O)C	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 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
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
Abssinone II	7330517	Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C=C(C=C3)O)O)C	324.40	unknown	https://doi.org/10.3987/S-1981-02-1163
abyssinoflavanone VII	16737250	Click to see CC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)CC(C(=C)C)O)O)C	424.50	unknown	https://doi.org/10.1021/NP060477+
abyssinone II	10064832	Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C=C(C=C3)O)O)C	324.40	unknown	https://doi.org/10.1021/NP50019A002 https://doi.org/10.3987/S-1981-02-1163
Abyssinone III	42607817	Click to see CC(=CCC1=CC(=CC2=C1OC(C=C2)(C)C)C3CC(=O)C4=C(O3)C=C(C=C4)O)C	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 CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2CC(=O)C3=C(C=C(C=C3O2)O)O)C	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 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 https://doi.org/10.1021/NP50019A002 https://doi.org/10.1055/S-2003-41119
Abyssinones Iii	10408069	Click to see CC(=CCC1=CC(=CC2=C1OC(C=C2)(C)C)C3CC(=O)C4=C(O3)C=C(C=C4)O)C	390.50	unknown	https://doi.org/10.3987/S-1981-02-1163
Burttinone	42607959	Click to see CC(=CCC1=C(C(=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)C=CC(C)(C)O)OC)C	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
ent-abyssinone II	7330518	Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C=C(C=C3)O)O)C	324.40	unknown	https://doi.org/10.3987/S-1981-02-1163
ent-abyssinone III	53318465	Click to see CC(=CCC1=CC(=CC2=C1OC(C=C2)(C)C)C3CC(=O)C4=C(O3)C=C(C=C4)O)C	390.50	unknown	https://doi.org/10.3987/S-1981-02-1163
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 C1C=CC2=C(O1)C=CC(=C2)C3CC(=O)C4=C(O3)C=C(C=C4)O	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 CC1(C=CC2=C(O1)C(=CC(=C2)C3CC(=O)C4=C(C=C(C=C4O3)O)O)OC)CO	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 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
(2S)-5,7-dihydroxy-2-[2-(hydroxymethyl)-8-methoxy-2-methylchromen-6-yl]-2,3-dihydrochromen-4-one	25147600	Click to see CC1(C=CC2=C(O1)C(=CC(=C2)C3CC(=O)C4=C(C=C(C=C4O3)O)O)OC)CO	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
(2S)-5,7-Dihydroxy-3'-methoxy-6'',6''-dimethylpyrano[2'',3'':4',5']flavanone	10761522	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/NP960440X
(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 CC1(C=CC2=C(O1)C=CC(=C2)C3CC(=O)C4=C(C=C(C=C4O3)O)O)C	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 CC1(C=CC2=C(O1)C=CC(=C2)C3CC(=O)C4=C(O3)C=C(C=C4)O)C	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 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
5,7-Dihydroxy-2-[2-(hydroxymethyl)-8-methoxy-2-methylchromen-6-yl]-2,3-dihydrochromen-4-one	74397076	Click to see CC1(C=CC2=C(O1)C(=CC(=C2)C3CC(=O)C4=C(C=C(C=C4O3)O)O)OC)CO	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 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
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+
Abyssinoflavone V	16737249	Click to see CC1(C=CC2=C(O1)C=CC(=C2)C3CC(=O)C4=C(C=C(C=C4O3)O)O)C	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 CC1(C=CC2=C(O1)C=CC(=C2)C3CC(=O)C4=C(O3)C=C(C=C4)O)C	322.40	unknown	https://doi.org/10.1021/NP50019A002 https://doi.org/10.3987/S-1981-02-1163
sigmoidin C	44424648	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/NP960440X https://doi.org/10.1021/NP060477+
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(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 CC(=CCC1=C(C=CC2=C1OCC3C2OC4=C3C=C5C=CC(OC5=C4)(C)C)O)C	390.50	unknown	https://doi.org/10.1016/J.BMCL.2009.09.108
(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 CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=C5CC(C(OC5=C4)(C)C)O)O)C	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 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
(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 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
(6aR,11aR)-10-(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol	5117820	Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=CC(=C4)O)O)C	324.40	unknown	https://doi.org/10.3987/S-1981-02-1163 https://doi.org/10.1016/J.BMCL.2009.09.108
(6aR,11aR)-3,9-Dihydroxy-4,8-diprenylpterocarpan	11581938	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
(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 CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC(=C4CC=C(C)C)O)C	392.50	unknown	https://doi.org/10.1021/NP50019A002 https://doi.org/10.1055/S-2003-41119
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 CC1(C=CC2=CC3=C(C=C2O1)OCC4C3OC5=C4C=CC(=C5)O)C	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 CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=C5CC(C(OC5=C4)(C)C)O)O)C	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 CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC5=C4C=CC(O5)(C)C)C	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 CC(=CCC1=CC2=C(C=C1O)OCC3(C2OC4=C3C=CC5=C4C=CC(O5)(C)C)O)C	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 CC(=CCC1=C(C=CC2=C1OC3C2(COC4=C3C=CC(=C4)O)O)OC)C	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 CC(=CCC1=CC2=C(C=C1OC)OCC3C2OC4=CC(=C(C=C34)OC)O)C	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 CC(=CCC1=C(C=CC2=C1OCC3C2OC4=C3C=CC(=C4)O)O)C	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 C1C2C(C3=C(O1)C=C(C=C3)O)OC4=C2C=CC(=C4C=O)O	284.26	unknown	https://doi.org/10.1016/J.BMCL.2009.09.108
3,9-Dihydroxy-8-prenylpterocarpan	14017298	Click to see CC(=CCC1=CC2=C(C=C1O)OC3C2COC4=C3C=CC(=C4)O)C	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 CC(=CCC1=C(C=CC2=C1OCC3C2OC4=C3C=CC(=C4)O)O)C	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 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
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 CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=CC(=C(C=C34)OC)O)C	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
CID 10408212	10408212	Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC(=C4CC=C(C)C)O)C	392.50	unknown	https://doi.org/10.3987/S-1981-02-1163 https://doi.org/10.1016/J.BMCL.2009.09.108
CID 821442	821442	Click to see CC1(C=CC2=CC3=C(C=C2O1)OC4C3COC5=C4C=CC(=C5)O)C	322.40	unknown	https://doi.org/10.1016/J.BMCL.2010.09.077
Cristacarpin	126540	Click to see CC(=CCC1=C(C=CC2=C1OC3C2(COC4=C3C=CC(=C4)O)O)OC)C	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
Demethyl medicarpin	3347979	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
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 D	471689	Click to see CC(=CCC1=C(C=CC2=C1OCC3C2OC4=C3C=C5C=CC(OC5=C4)(C)C)O)C	390.50	unknown	https://doi.org/10.1016/J.BMCL.2009.09.108
Erybreadin B	45268827	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
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 CC(=CCC1=CC2=C(C=C1O)OCC3=C2OC4=C3C=CC(=C4CC=C(C)C)O)C	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 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.2010.09.077 https://doi.org/10.1016/J.BMCL.2009.09.108
Erysubin E	637080	Click to see CC(=CCC1=CC2=C(C=C1O)OCC3(C2OC4=C3C=CC5=C4C=CC(O5)(C)C)O)C	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 CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC(=C4CC=C(C)C)O)C	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 C1C2C(C3=C(O1)C=C(C=C3)O)OC4=C2C=CC(=C4C=O)O	284.26	unknown	https://doi.org/10.1016/J.BMCL.2009.09.108
Erythribyssin C	45375877	Click to see CC(=CCC1=CC2=C(C=C1OC)OCC3C2OC4=CC(=C(C=C34)OC)O)C	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 CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=CC(=C(C=C34)OC)O)C	354.40	unknown	https://doi.org/10.1016/J.BMCL.2009.09.108
Folitenol	15840592	Click to see CC(=CCC1=CC2=C(C=C1O)OCC3C2OC4=C3C=CC5=C4C=CC(O5)(C)C)C	390.50	unknown	https://doi.org/10.1016/J.BMCL.2009.09.108
Homoedudiol	14017299	Click to see CC(=CCC1=CC2=C(C=C1O)OC3C2COC4=C3C=CC(=C4)O)C	324.40	unknown	https://doi.org/10.1016/J.BMCL.2009.09.108 https://doi.org/10.1016/J.BMCL.2010.09.077
Isoneorautenol	73649	Click to see CC1(C=CC2=CC3=C(C=C2O1)OC4C3COC5=C4C=CC(=C5)O)C	322.40	unknown	https://doi.org/10.1016/J.BMCL.2010.09.077
Neorautenol	11500744	Click to see CC1(C=CC2=CC3=C(C=C2O1)OCC4C3OC5=C4C=CC(=C5)O)C	322.40	unknown	https://doi.org/10.1016/J.BMCL.2009.09.108 https://doi.org/10.1016/J.BMCL.2010.09.077
Phaseolin	91572	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4C3COC5=C4C=CC(=C5)O)C	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
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 CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=CC(=C4)O)O)C	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
> 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 COC1=CC(=C(C=C1C2=CC3=C(C=C(C=C3)O)OC2)OC)O	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 CC1(C(C(C2=C(O1)C(=CC(=C2)C=CC(=O)C3=C(C=C(C=C3)O)O)O)O)O)C	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 CC1(C(C(C2=C(O1)C(=CC(=C2)C=CC(=O)C3=C(C=C(C=C3)O)O)O)O)O)C	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 COC1=C(C=CC(=C1)C=CC(=O)C2=C(C=C(C=C2)O)O)O	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 CC1(C=CC2=C(O1)C(=CC(=C2)C=CC(=O)C3=C(C=C(C=C3)O)O)O)C	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 CC(=CCC1=C(C(=CC(=C1)C=CC(=O)C2=C(C=C(C=C2)O)O)OC)O)C	354.40	unknown	https://doi.org/10.1055/S-2008-1034327
2',3,4,4'-Tetrahydroxy-5-prenylchalcone	72776640	Click to see CC(=CCC1=C(C(=CC(=C1)C=CC(=O)C2=C(C=C(C=C2)O)O)O)O)C	340.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.08.050
2',4,4'-Trihydroxy-3-prenylchalcone	66751582	Click to see CC(=CCC1=C(C=CC(=C1)C=CC(=O)C2=C(C=C(C=C2)O)O)O)C	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 CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C=CC(=O)C2=C(C=C(C=C2)O)O)C	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 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
5-Prenylbutein	11267805	Click to see CC(=CCC1=C(C(=CC(=C1)C=CC(=O)C2=C(C=C(C=C2)O)O)O)O)C	340.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.08.050
Abyssinone A	70678680	Click to see CC1(C=CC2=C(O1)C(=CC(=C2)C=CC(=O)C3=C(C=C(C=C3)O)O)O)C	338.40	unknown	https://doi.org/10.1055/S-2008-1034327
abyssinone D	70678689	Click to see CC(=CCC1=C(C(=CC(=C1)C=CC(=O)C2=C(C=C(C=C2)O)O)OC)O)C	354.40	unknown	https://doi.org/10.1055/S-2008-1034327
Abyssinone VI	5281219	Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C=CC(=O)C2=C(C=C(C=C2)O)O)C	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 COC1=C(C=CC(=C1)C=CC(=O)C2=C(C=C(C=C2)O)O)O	286.28	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.08.050
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Retrochalcones
(E)-3-[4-hydroxy-3,5-bis(3-methylbut-2-enyl)phenyl]-1-(4-hydroxyphenyl)prop-2-en-1-one	44424651	Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C=CC(=O)C2=CC=C(C=C2)O)C	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 CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C=CC(=O)C2=CC=C(C=C2)O)C	376.50	unknown	https://doi.org/10.1021/NP060477+

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Erythrina abyssinica

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