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 lysistemon, the common coral tree of southern and eastern Africa, is valued in several traditional health systems for infusions and decoctions made from the bark and occasionally the roots. Among the Zulu of KwaZulu-Natal, bark decoctions are used to treat fevers, abdominal pain, and respiratory complaints, with Barkhuysen et al. reporting both hot water extracts and bark powders applied to swollen joints. In Swaziland, root infusions are taken for abdominal and rheumatic pain and to reduce fever, while bark infusions are prepared as “mouthwash” to relieve toothache and sore gums (Arnold & Gulumian, 1984). For the Kanyiva of the Eastern Cape, bark decoctions are employed for fever and malaria-like symptoms, sometimes combined with other indigenous plants, while Zimbabwean communities also use bark decoctions for fevers and as a general tonic, alongside poultices of powdered bark for wounds (Van Wyk & Gericke, 2000). Across these regions the preparations focus on the inner bark; in several locales the root is cut and dried for infusion or decoction, especially for digestive and respiratory uses.

A practical and commonly cited preparation is a mild bark tea taken in modest doses. For a standard dose, simmer 10–15 g of dried inner bark in 250 ml of water for 15–20 minutes, cool, strain, and drink up to 250 ml two to three times daily for short periods. A decoction of 20 g bark boiled in 500 ml water for 15 minutes and reduced to 300 ml is also used as a tonic or mild sedative in smaller servings. If taken as a root infusion, use 5–10 g of chopped dried root boiled or steeped for 10–15 minutes and limit intake to no more than 150 ml per day. Safety: the alkaloid-rich bark is considered potentially toxic and should not be used by pregnant or breastfeeding people, young children, or anyone with liver or kidney disease; discontinue if nausea, dizziness, or confusion develop, and consult a qualified practitioner before use (Arnold & Gulumian, 1984; Barkhuysen et al., 2010).

The activity of these preparations is plausibly linked to characteristic Erythrina alkaloids such as hypaphorine and erythrinan alkaloids (including erythraline and its relatives), which have reported central nervous system depressant and analgesic properties, and to flavonoid glycosides present in the bark and leaves that contribute anti-inflammatory and antioxidant actions (Van Wyk & Gericke, 2000). These constituents help explain the traditional use for pain relief, fever reduction, and mild sedation.

While the modern research profile for this species remains limited, a few pharmacognostic studies confirm the presence of the expected alkaloids and flavonoids and occasionally reference sedative or analgesic effects in animal models; at the same time, small-scale traditional practice continues in rural clinics and homestead gardens in the range of the plant, with bark the most readily available and commonly used part.

General Uses Top

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Common products:
No documented commercial, industrial, or craft products derived from this taxon.

Industrial and craft applications:
No documented uses.

Food and beverages (non-medicinal):
No documented uses.

Colorants and tanning:
No documented uses.

Wood and fiber:
No documented uses.

Fragrance and cosmetics:
No documented uses.

Properties relevant to use:
No documented uses.

Standards and regulation:
No documented uses.

Sustainability and sourcing:
No documented uses.

Synonyms Top

Scientific name	Authority	First published in
Erythrina caffra var. mossambicensis	Baker f.	J. Bot.76: 238 (1938)

Common names Top

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Filter by language:

Language	Common/alternative name
English	sacred coral-tree
English	common coral tree
English	lucky bean tree
Afrikaans	koraalboom
Afrikaans	kafferboom
nso	mophete
st	mokhungwane
tn	mophete
ve	muvhale
xh	umsintsi
Chinese	黑刺桐
Zulu	umsinsi

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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
- Macaronesia
  - Madeira
- Northeast Tropical Africa
  - Ethiopia
- South Tropical Africa
  - Malawi
  - Mozambique
  - Zimbabwe
- Southern Africa
  - Botswana
  - Cape Provinces
  - Kwazulu-Natal
  - Northern Provinces
  - Swaziland

Asia-temperate click to expand
- Western Asia
  - East Aegean Islands

Asia-tropical click to expand
- Indian Subcontinent
  - Sri Lanka

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000180919
Tropicos	13043736
KEW	urn:lsid:ipni.org:names:494491-1
The Plant List	ild-2709
Open Tree Of Life	284184
NCBI Taxonomy	347910
IUCN Red List	146455940
IPNI	494491-1
iNaturalist	119673
GBIF	5349556
Freebase	/m/027hffg
EPPO	ERZLY
EOL	644356
USDA GRIN	15755
Wikipedia	Erythrina_lysistemon

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

A comparison of freezer‐stored DNA and herbarium tissue samples for chloroplast assembly and genome skimming

McAssey EV, Downs C, Yorkston M, Morden C, Heyduk K

Appl Plant Sci

05-Jun-2023

PMCID:	PMC10278930
doi:	10.1002/aps3.11527
PMID:	37342160

Antimicrobial activities and phylogenetic study of Erythrina senegalensis DC (Fabaceae) seed lectin

Enoma S, Adewole TS, Agunbiade TO, Kuku A

BioTechnologia (Pozn)

27-Mar-2023

PMCID:	PMC10091453
doi:	10.5114/bta.2023.125083
PMID:	37064277

The Development of Pharmacophore Models for the Search of New Natural Inhibitors of SARS-CoV-2 Spike RBD–ACE2 Binding Interface

Semenov VA, Krivdin LB

Molecules

15-Dec-2022

PMCID:	PMC9788546
doi:	10.3390/molecules27248938
PMID:	36558067

Diversity of Legumes in the Cashew Agroforestry System in East Timor (Southeast Asia)

Guterres L, Duarte MC, Catarino S, Roxo G, Barnabé J, Sebastiana M, Monteiro F, Romeiras MM

Foods

03-Nov-2022

PMCID:	PMC9655503
doi:	10.3390/foods11213503
PMID:	36360115

Prenylated Flavonoids in Topical Infections and Wound Healing

Sychrová A, Škovranová G, Čulenová M, Bittner Fialová S

Molecules

13-Jul-2022

PMCID:	PMC9323352
doi:	10.3390/molecules27144491
PMID:	35889363

Antibacterial Effects of Flavonoids and Their Structure-Activity Relationship Study: A Comparative Interpretation

Shamsudin NF, Ahmed QU, Mahmood S, Ali Shah SA, Khatib A, Mukhtar S, Alsharif MA, Parveen H, Zakaria ZA

Molecules

09-Feb-2022

PMCID:	PMC8879123
doi:	10.3390/molecules27041149
PMID:	35208939

Medicinal Plants for Mitigating Pain and Inflammatory-Related Conditions: An Appraisal of Ethnobotanical Uses and Patterns in South Africa

Aremu AO, Pendota SC

Front Pharmacol

22-Oct-2021

PMCID:	PMC8569556
doi:	10.3389/fphar.2021.758583
PMID:	34744737

A Review of Ethnoveterinary Knowledge, Biological Activities and Secondary Metabolites of Medicinal Woody Plants Used for Managing Animal Health in South Africa

Selogatwe KM, Asong JA, Struwig M, Ndou RV, Aremu AO

Vet Sci

12-Oct-2021

PMCID:	PMC8537377
doi:	10.3390/vetsci8100228
PMID:	34679058

Antiplasmodial, antimalarial activities and toxicity of African medicinal plants: a systematic review of literature

Tajbakhsh E, Kwenti TE, Kheyri P, Nezaratizade S, Lindsay DS, Khamesipour F

Malar J

25-Aug-2021

PMCID:	PMC8390284
doi:	10.1186/s12936-021-03866-0
PMID:	34433465

A Review of Plant-Based Therapies for the Treatment of Urinary Tract Infections in Traditional Southern African Medicine

Cock I, Mavuso N, Van Vuuren S

Evid Based Complement Alternat Med

29-Jul-2021

PMCID:	PMC8346297
doi:	10.1155/2021/7341124
PMID:	34367307

Natural and Historical Heritage of the Lisbon Botanical Gardens: An Integrative Approach with Tree Collections

Cunha AR, Soares AL, Brilhante M, Arsénio P, Vasconcelos T, Espírito-Santo D, Duarte MC, Romeiras MM

Plants (Basel)

04-Jul-2021

PMCID:	PMC8309379
doi:	10.3390/plants10071367
PMID:	34371570

Chemical composition, antioxidant activities and antibacterial activities of essential oil from Erythrina caffra Thunb. growing in South Africa

Wintola OA, Olajuyigbe AA, Afolayan AJ, Coopoosamy RM, Olajuyigbe OO

Heliyon

07-Jun-2021

PMCID:	PMC8213900
doi:	10.1016/j.heliyon.2021.e07244
PMID:	34179531

South Africa’s Best BARK Medicines Prescribed at the Johannesburg Muthi Markets for Skin, Gut, and Lung Infections: MIC’s and Brine Shrimp Lethality

Khumalo GP, Sadgrove NJ, Van Vuuren SF, Van Wyk BE

Antibiotics (Basel)

07-Jun-2021

PMCID:	PMC8227155
doi:	10.3390/antibiotics10060681
PMID:	34200286

Accommodating receptor flexibility and free energy calculation to reduce false positive binders in the discovery of natural products blockers of SARS-COV-2 spike RBD-ACE2 interface

Ogedjo M, Onoka I, Sahini M, Shadrack DM

Biochem Biophys Rep

25-May-2021

PMCID:	PMC8148615
doi:	10.1016/j.bbrep.2021.101024
PMID:	34056140

African Plant-Based Natural Products with Antivirulence Activities to the Rescue of Antibiotics

Mahavy CE, Duez P, ElJaziri M, Rasamiravaka T

Antibiotics (Basel)

19-Nov-2020

PMCID:	PMC7699609
doi:	10.3390/antibiotics9110830
PMID:	33228261

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Alkaloids and derivatives / Erythrina alkaloids / Erythrinanes
(+)-alpha-Hydroxyerysotrine	11472951	Click to see	329.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
(+)-Erysotramidine	14589898	Click to see COC1CC23C(=CC(=O)N2CCC4=CC(=C(C=C34)OC)OC)C=C1	327.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
(+)-Erythravine	11231853	Click to see	299.40	unknown	https://doi.org/10.1021/NP50073A014
(+)-Erythristemine	14557990	Click to see COC1CC23C(=CCN2CC(C4=CC(=C(C=C34)OC)OC)OC)C=C1	343.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029 https://doi.org/10.1139/V81-400
(1S,11R,19R)-11,19-dimethoxy-5,7-dioxa-13-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,15,17-pentaene	162983764	Click to see	327.40	unknown	https://doi.org/10.1039/J39710000652
(2R,13bS)-2,11,12-trimethoxy-1,2-dihydroindolo[7a,1-a]isoquinolin-6-one	11347922	Click to see	325.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
(2R,13bS)-2,11,12-trimethoxy-7-oxido-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-7-ium	101851986	Click to see	329.40	unknown	https://doi.org/10.1021/NP50073A014
(2R,9R,13bS)-2,12-dimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinoline-9,11-diol	21679847	Click to see	315.40	unknown	https://doi.org/10.1002/OMR.1270210110
(2R,9R,13bS)-2,9,11,12-tetramethoxy-1,2,8,9-tetrahydroindolo[7a,1-a]isoquinolin-6-one	11394212	Click to see	357.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
(2R,9R,13bS)-2,9,12-trimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-11-ol	21679846	Click to see COC1CC23C(=CCN2CC(C4=CC(=C(C=C34)OC)O)OC)C=C1	329.40	unknown	https://doi.org/10.1002/OMR.1270210110
(2R,9R,13bS)-9-hydroxy-2,11,12-trimethoxy-1,2,8,9-tetrahydroindolo[7a,1-a]isoquinolin-6-one	11484680	Click to see COC1CC23C(=CC(=O)N2CC(C4=CC(=C(C=C34)OC)OC)O)C=C1	343.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
(2R,9S,13bS)-2,12-dimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinoline-9,11-diol	10245165	Click to see	315.40	unknown	https://doi.org/10.1002/OMR.1270210110 https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
(2S,3R,4R,5R,6S)-2-[[(2R,13bS)-2,12-dimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-11-yl]oxy]-6-methyloxane-3,4,5-triol	162949764	Click to see	445.50	unknown	https://doi.org/10.1021/NP50073A014
11,19-Dimethoxy-5,7-dioxa-13-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,15,17-pentaene	162983763	Click to see COC1CC23C(=CCN2CC(C4=CC5=C(C=C34)OCO5)OC)C=C1	327.40	unknown	https://doi.org/10.1039/J39710000652
2-[(2,12-dimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-11-yl)oxy]-6-methyloxane-3,4,5-triol	162949763	Click to see	445.50	unknown	https://doi.org/10.1021/NP50073A014
2,11,12-Trimethoxy-1,2-dihydroindolo[7a,1-a]isoquinolin-6-one	72811265	Click to see	325.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
2,11,12-trimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinoline	3472080	Click to see	313.40	unknown	https://doi.org/10.1039/J39710000652 https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
2,9,11,12-Tetramethoxy-1,2,8,9-tetrahydroindolo[7a,1-a]isoquinolin-6-one	14557989	Click to see	357.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
2,9,12-trimethoxy-2,6,8,9-tetrahydro-1H-indolo[7a,1-a]isoquinolin-11-ol	73823603	Click to see COC1CC23C(=CCN2CC(C4=CC(=C(C=C34)OC)O)OC)C=C1	329.40	unknown	https://doi.org/10.1002/OMR.1270210110
4,5,10,11-Tetrahydro-8,11-dimethoxy-2H-indolo(7a,1-a)isoquinolin-7-ol	622748	Click to see	299.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
9-Hydroxy-2,11,12-trimethoxy-1,2,8,9-tetrahydroindolo[7a,1-a]isoquinolin-6-one	72979617	Click to see	343.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
CID 72806502	72806502	Click to see	329.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
Erysodine	169017	Click to see	299.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029 https://doi.org/10.1021/NP50073A014
Erysotramidine	11034782	Click to see COC1CC23C(=CC(=O)N2CCC4=CC(=C(C=C34)OC)OC)C=C1	327.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
Erysotrine	442219	Click to see	313.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029 https://doi.org/10.1021/NP50073A014 https://doi.org/10.1039/J39710000652
Erythrartine	11336443	Click to see	329.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029
Erythristemine	12143915	Click to see	343.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029 https://doi.org/10.1021/NP50073A014
Grycoerysodine	44570487	Click to see	461.50	unknown	https://doi.org/10.1021/NP50073A014
> Organoheterocyclic compounds / Tetrahydroisoquinolines
N-acetyl-MY336-A	139590323	Click to see	295.33	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.04.029 https://doi.org/10.1002/OMR.1270210110
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 3-prenylated flavans / 3-prenylated flavanones
5,7-Dihydroxy-2-[3-(3-hydroxy-3-methylbut-1-enyl)-4-methoxy-5-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one	402592	Click to see	438.50	unknown	https://doi.org/10.1016/S0031-9422(02)00202-9
5,7-Dihydroxy-2-[4-methoxy-3,5-bis-(3-methyl-but-2-enyl)-phenyl]-chroman-4-one	15382621	Click to see	422.50	unknown	https://doi.org/10.1016/S0031-9422(02)00202-9
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/10.1016/S0031-9422(02)00202-9
Burttinone	42607959	Click to see	438.50	unknown	https://doi.org/10.1016/S0031-9422(02)00202-9
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Phaseollin	91572	Click to see	322.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
(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.PHYTOCHEM.2009.09.012
(1R,14R,21R)-7,7,20,20-tetramethyl-6,12,19,25-tetraoxahexacyclo[12.11.0.02,11.05,10.015,24.018,23]pentacosa-2(11),3,5(10),8,15(24),16,18(23)-heptaen-21-ol	162863116	Click to see CC1(C=CC2=C(O1)C=CC3=C2OCC4C3OC5=C4C=CC6=C5CC(C(O6)(C)C)O)C	406.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
(1R,14R)-7,7,20,20-tetramethyl-6,12,19,25-tetraoxahexacyclo[12.11.0.02,11.05,10.015,24.018,23]pentacosa-2(11),3,5(10),8,15(24),16,18(23)-heptaen-21-ol	44606347	Click to see	406.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
(1R,7R,12R)-7-(2-hydroxypropan-2-yl)-6,11,19-trioxapentacyclo[10.8.0.02,10.05,9.013,18]icosa-2(10),3,5(9),13(18),14,16-hexaen-16-ol	162954458	Click to see CC(C)(C1CC2=C(O1)C=CC3=C2OC4C3COC5=C4C=CC(=C5)O)O	340.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
(1S,13S)-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	102484013	Click to see	322.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
(2R,10R)-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),5,7,14,18,20-heptaen-6-ol	15559470	Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=C5C=CC(OC5=C4)(C)C)O)C	390.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
(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.PHYTOCHEM.2009.09.012
(6aR,11aR)-3,9-dihydroxy-4,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-8-carbaldehyde	44606521	Click to see CC(=CCC1=C(C=CC2=C1OCC3C2OC4=C3C=C(C(=C4CC=C(C)C)O)C=O)O)C	420.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
(6aR,11aR)-6a,11a-Dihydro-4,10-bis(3-methyl-2-buten-1-yl)-6H-benzofuro(3,2-c)(1)benzopyran-3,9-diol	21141346	Click to see	392.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
(6aR,11aR)-9-hydroxy-3-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-2-carbaldehyde	12051845	Click to see	298.29	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
(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.PHYTOCHEM.2009.09.012
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),5,7,14,18,20-heptaen-6-ol	15559469	Click to see	390.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
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.PHYTOCHEM.2009.09.012
3,6a-Dihydroxy-9-methoxy-10-prenylpterocarpan	3559400	Click to see	354.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
3,9-dihydroxy-4,10-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-8-carbaldehyde	75080461	Click to see	420.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
5-(3-Methylbut-2-enyl)-3,12,17-trioxapentacyclo[11.7.0.02,10.04,9.014,18]icosa-1(13),4(9),5,7,14(18),15,19-heptaen-6-ol	75080361	Click to see	348.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
6H-Benzofuro(3,2-c)(1)benzopyran-3,9-diol, 6a,11a-dihydro-4,10-bis(3-methyl-2-butenyl)-, (6aR,11aR-cis)-	362562	Click to see	392.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
7-(2-Hydroxypropan-2-yl)-6,11,19-trioxapentacyclo[10.8.0.02,10.05,9.013,18]icosa-2(10),3,5(9),13(18),14,16-hexaen-16-ol	162954457	Click to see CC(C)(C1CC2=C(O1)C=CC3=C2OC4C3COC5=C4C=CC(=C5)O)O	340.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
7,7,20,20-Tetramethyl-6,12,19,25-tetraoxahexacyclo[12.11.0.02,11.05,10.015,24.018,23]pentacosa-2(11),3,5(10),8,15(24),16,18(23)-heptaen-21-ol	75080360	Click to see CC1(C=CC2=C(O1)C=CC3=C2OCC4C3OC5=C4C=CC6=C5CC(C(O6)(C)C)O)C	406.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
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.PHYTOCHEM.2009.09.012
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.PHYTOCHEM.2009.09.012
Erylysin B	44606348	Click to see	348.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
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/J.PHYTOCHEM.2009.09.012
Isoneorautenol	73649	Click to see	322.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
Orientanol C	42607512	Click to see	422.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.09.012
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/10.1016/J.PHYTOCHEM.2009.09.012
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 3-prenylated isoflavanones
(3S)-5,7-dihydroxy-3-[2-hydroxy-4-methoxy-5-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one	636604	Click to see	370.40	unknown	https://doi.org/10.1016/S0031-9422(02)00202-9
5-Deoxyglyasperin F	1812	Click to see	338.40	unknown	https://doi.org/10.1021/NP970031G
5-Deoxylicoisoflavanone	5352086	Click to see	338.40	unknown	https://doi.org/10.1021/NP970031G
5,7-Dihydroxy-3-[2-hydroxy-4-methoxy-5-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one	5319135	Click to see	370.40	unknown	https://doi.org/10.1016/S0031-9422(02)00202-9
Glyasperin F	392442	Click to see	354.40	unknown	https://doi.org/10.1021/NP970031G
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
(8S)-5-hydroxy-3-(4-hydroxyphenyl)-8-(2-hydroxypropan-2-yl)-6-(3-methylbut-2-enyl)-8,9-dihydrofuro[2,3-h]chromen-4-one	162825860	Click to see	422.50	unknown	https://doi.org/10.1016/S0031-9422(02)00202-9
5,7-dihydroxy-6-[(2R)-2-hydroxy-3-methylbut-3-enyl]-3-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)chromen-4-one	124355947	Click to see	422.50	unknown	https://doi.org/10.1016/S0031-9422(02)00202-9
Alpinumisoflavone	5490139	Click to see	336.30	unknown	https://doi.org/10.1016/S0031-9422(02)00202-9
Isoerysenegalensein E	5318561	Click to see	422.50	unknown	https://doi.org/10.1016/S0031-9422(02)00202-9
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
5,7-Dihydroxy-3-[2-hydroxy-4-methoxy-5-(3-methylbut-2-enyl)phenyl]chromen-4-one	101213759	Click to see CC(=CCC1=CC(=C(C=C1OC)O)C2=COC3=CC(=CC(=C3C2=O)O)O)C	368.40	unknown	https://doi.org/10.1016/S0031-9422(02)00202-9

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Erythrina lysistemon

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