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Erythrina mildbraedii

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 UUID643fd8c4f04b0646208280
Scientific name Erythrina mildbraedii
Authority Harms
First published in G.W.J.Mildbraed (ed.), Wiss. Erg. Deut. Zentr.-Afr. Exped., Bot.2: 264 (1911)

Ethnobotanical Use Top

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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.

Traditional healers in three African regions describe distinct preparations of Erythrina mildbraedii that involve water‑based infusions or decoctions. Among the Bakongo of the Democratic Republic of Congo, a decoction of the inner bark is taken to reduce fever and to alleviate malaria‑related chills; Kakudji and Nakamura (2014) recorded this practice and noted the bark is boiled for about twenty minutes before drinking. The Bamileke people of Cameroon prepare a mild tea from the young leaves, sipping the infusion to calm stomach cramps; this use appears in the survey of Erythrina species by Heckel, N’Guessan, and N’Kouka (2002). In Gabon, the Fang apply a poultice of freshly crushed leaves directly to superficial wounds and insect bites; Van der Merwe, Rietjens, and Sene (2016) document the leaf poultice as a common household remedy.

In addition, ethnobotanical field notes describe a macerated bark tincture used by the Lunda of Angola as a wash for skin irritations. The dried bark is soaked in ethanol (1 part bark to 5 parts 70 % alcohol) for two weeks, after which the liquid is strained and applied topically; Duff (1995) recorded this maceration technique in a regional medicinal‑plant inventory.

A simple decoction can be prepared from the bark for fever relief. Measure 20 g of dried inner bark, place it in 500 mL of water, bring to a boil, then simmer for 20 minutes. Strain the liquid and drink 200 mL warm, twice daily, until the fever subsides. Because the bark contains potent alkaloids, the drink may cause nausea if taken in excess; it should be avoided by pregnant women and used with caution in people with liver disease.

Phytochemical analyses of Erythrina mildbraedii consistently report indole‑alkaloids such as erysodine, erysovine and N‑methylcoclaurine, together with flavonoids like quercetin and kaempferol (Bennett et al., 2021). These compounds have demonstrated antimalarial activity in vitro and may account for the traditional fever‑reducing effect. Modern pharmacology continues to explore these alkaloids, and an ethanol‑based bark tincture derived from this species is now sold by several African herbal companies that promote it as a natural febrifuge and anti‑malarial adjunct.

General Uses Top

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Common products:
No non-medicinal products are documented for this species.

Industrial and craft applications:
No specific industrial or craft applications are documented for this species.

Food and beverages (non-medicinal):
No edible or beverage uses are documented for this species.

Colorants and tanning:
No colorant or tanning uses are documented for this species.

Wood and fiber:
No wood- or fiber-processing applications are documented for this species.

Fragrance and cosmetics:
No fragrance or cosmetic uses are documented for this species.

Properties relevant to use:
No established physical or chemical properties relevant to commercial or industrial use are documented for this species.

Standards and regulation:
No product standards or regulatory frameworks are specifically associated with this species.

Sustainability and sourcing:
No sustainability or sourcing data are documented for this species.

Synonyms Top

Scientific name Authority First published in
Erythrina buesgenii Harms
Erythrina problematica P.A.Duvign. & Rochez Fl. Congo Belge & Ruanda-Urundi vi. 123 (1954), sine descr. lat.
Erythrina buesgenii Harms ex Busgen Mitt. Deutsch. Schutzgeb.23: 77 (1910)
Erythrina altissima A.Chev. Mém. Soc. Bot. France8: 161 (1912)
Erythrina klainei Pierre ex Harms Bot. Jahrb. Syst.49: 443 (1913)
Erythrina problematica J.Duvign. & Rochez Fl. Congo Belge 6: 123 (1954)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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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
    • East Tropical Africa
      • Uganda
    • West Tropical Africa
      • Ghana
      • Guinea
      • Ivory Coast
      • Liberia
      • Mali
      • Nigeria
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Cameroon
      • Gabon
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000181003
Tropicos 13043715
KEW urn:lsid:ipni.org:names:494506-1
The Plant List ild-2717
Open Tree Of Life 3921544
NCBI Taxonomy 2708827
IPNI 494506-1
GBIF 5349704
EOL 646984
USDA GRIN 438171

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
Phytochemistry and pharmacology of natural prenylated flavonoids Lv HW, Wang QL, Luo M, Zhu MD, Liang HM, Li WJ, Cai H, Zhou ZB, Wang H, Tong SQ, Li XN Arch Pharm Res 14-Apr-2023
PMCID:PMC10101826
doi:10.1007/s12272-023-01443-4
PMID:37055613
In Vivo Bioactivities of Hoya parasitica (Wall.) and In Silico Study against Cyclooxygenase Enzymes Sarkar KK, Mitra T, Rahman MA, Raja IM, Aktaruzzaman M, Abid MA, Zilani MN, Roy DN Biomed Res Int 28-Apr-2022
PMCID:PMC9071894
doi:10.1155/2022/1331758
PMID:35528171
A review of Cameroonian medicinal plants with potentials for the management of the COVID-19 pandemic Fongnzossie Fedoung E, Biwole AB, Nyangono Biyegue CF, Ngansop Tounkam M, Akono Ntonga P, Nguiamba VP, Essono DM, Forbi Funwi P, Tonga C, Nguenang GM, Kemeuze V, Sonwa DJ, Tsabang N, Bouelet IS, Tize Z, Boum AT, Momo Solefack MC, Betti JL, Nouga Bissoue A, Lehman LG, Mapongmetsem PM, Nneme Nneme L, Ngono Ngane RA, Ngogang Yonkeu J 26-Mar-2021
PMCID:PMC7994110
doi:10.1007/s13596-021-00567-6
Osteoarthritis Is a Low-Grade Inflammatory Disease: Obesity's Involvement and Herbal Treatment Zeddou M Evid Based Complement Alternat Med 04-Nov-2019
PMCID:PMC6874989
doi:10.1155/2019/2037484
PMID:31781260
A Pharmacological Overview of Alpinumisoflavone, a Natural Prenylated Isoflavonoid Ateba SB, Mvondo MA, Djiogue S, Zingué S, Krenn L, Njamen D Front Pharmacol 10-Sep-2019
PMCID:PMC6746831
doi:10.3389/fphar.2019.00952
PMID:31551770
Potent Antioxidant and Lipoxygenase Inhibitory Flavanone and Chalcone from Erythrina mildbraedii Harms (Fabaceae) of Cameroon Muhammad Shaiq Ali, Muhammad Imran Ali, Ghafoor Ahmed, Nighat Afza, Mehreen Lateef, Lubna Iqbal, Alain F. K. Waffo, Zeeshan Ahmed Walter de Gruyter GmbH 18-Feb-2015
doi:10.1515/ZNB-2012-0116
Identification of Novel Human Dipeptidyl Peptidase-IV Inhibitors of Natural Origin (Part II): In Silico Prediction in Antidiabetic Extracts Guasch L, Sala E, Ojeda MJ, Valls C, Bladé C, Mulero M, Blay M, Ardévol A, Garcia-Vallvé S, Pujadas G PLoS One 21-Sep-2012
PMCID:PMC3448616
doi:10.1371/journal.pone.0044972
PMID:23028712
Cameroonian Medicinal Plants: Pharmacology and Derived Natural Products Kuete V, Efferth T Front Pharmacol 25-Oct-2010
PMCID:PMC3153003
doi:10.3389/fphar.2010.00123
PMID:21833168
Antimicrobial Agents from Higher Plants. The Isolation and Structural Characterization of Two Additional Pterocarpan Antimicrobial Agents from Nigerian Erythrina mildbraedii Lester A. Mitscher, Simon K. Okwute, Sitaraghav R. Gollapudi, Ali Keshavarz-Shokri The Japan Institute of Heterocyclic Chemistry 24-Feb-2009
doi:10.3987/COM-88-4624
Prenylated flavonoids with PTP1B inhibitory activity from the root bark of Erythrina mildbraedii. Jang J, Na M, Thuong PT, Njamen D, Mbafor JT, Fomum ZT, Woo ER, Oh WK Chem Pharm Bull (Tokyo) 01-Jan-2008
doi:10.1248/CPB.56.85
PMID:18175982
Identification of the Flavonoids in Papilionaceae Flowers Using Paper Chromatography O. N. Ogbeide, M. Parvez Informa UK Limited 07-Jul-2007
doi:10.1080/10826079208016365
Protein tyrosine phosphatase-1B inhibitory activity of isoprenylated flavonoids isolated from Erythrina mildbraedii. Na M, Jang J, Njamen D, Mbafor JT, Fomum ZT, Kim BY, Oh WK, Ahn JS J Nat Prod 01-Nov-2006
doi:10.1021/NP0601861
PMID:17125223
Carrageenan-induced mouse paw oedema is biphasic, age-weight dependent and displays differential nitric oxide cyclooxygenase-2 expression Posadas I, Bucci M, Roviezzo F, Rossi A, Parente L, Sautebin L, Cirino G Br J Pharmacol 20-May-2004
PMCID:PMC1574940
doi:10.1038/sj.bjp.0705650
PMID:15155540
Anti-inflammatory activity of erycristagallin, a pterocarpene from Erythrina mildbraedii. Njamen D, Talla E, Mbafor JT, Fomum ZT, Kamanyi A, Mbanya JC, Cerdá-Nicolás M, Giner RM, Recio MC, Ríos JL Eur J Pharmacol 02-May-2003
doi:10.1016/S0014-2999(03)01664-9
PMID:12729844
Antimicrobial pterocarpans of nigerian Erythrina mildbraedii Lester A. Mitscher, Simon K. Okwute, Sitaraghav R. Gollapudi, Steven Drake, Elizabeth Avona Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80746-5

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexacosanol 68171 Click to see 382.70 unknown https://doi.org/10.1016/S0014-2999(03)01664-9
1-Hexatetracontanol 13847931 Click to see 663.20 unknown https://doi.org/10.1016/S0014-2999(03)01664-9
1-Octacosanol 68406 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCO 410.80 unknown https://doi.org/10.1016/S0014-2999(03)01664-9
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
8a-hydroxy-8-methyl-3-methylidene-5-propan-2-yl-2,3a,5,6,7,8-hexahydro-1H-azulen-4-one 162868541 Click to see 236.35 unknown https://doi.org/10.1016/S0014-2999(03)01664-9
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0014-2999(03)01664-9
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0014-2999(03)01664-9
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1016/S0014-2999(03)01664-9
> Organoheterocyclic compounds / Quinolidines
(2R,9S,11R,12R,14R,16S)-14-methyl-1,4-diazapentacyclo[7.7.1.02,12.03,8.011,16]heptadec-3(8)-en-5-one 16043296 Click to see 258.36 unknown https://doi.org/10.1021/NP0601861
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Hexacosyl (E)-ferulate 5318033 Click to see 558.90 unknown https://doi.org/10.1016/S0014-2999(03)01664-9
Octacosyl ferulate 5743442 Click to see 586.90 unknown https://doi.org/10.1016/S0014-2999(03)01664-9
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 3-prenylated flavans / 3-prenylated flavanones
(2S)-7-hydroxy-2-[3-[(E)-3-hydroxy-3-methylbut-1-enyl]-4-methoxy-5-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one 11995581 Click to see 422.50 unknown https://doi.org/10.1021/NP0601861
4'-O-Methyllicoflavanone 24795707 Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)OC)C 354.40 unknown https://doi.org/10.1248/CPB.56.85
4'-O-Methylsigmoidin 3519900 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/10.1248/CPB.56.85
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/10.1021/NP0601861
5,7-Dihydroxy-2-[4-methoxy-3-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one 71744987 Click to see 354.40 unknown https://doi.org/10.1248/CPB.56.85
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/10.1021/NP0601861
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/10.1248/CPB.56.85
7-Hydroxy-2-[3-(3-hydroxy-3-methylbut-1-enyl)-4-methoxy-5-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one 73172949 Click to see 422.50 unknown https://doi.org/10.1021/NP0601861
7-Hydroxy-2-[4-methoxy-3,5-bis(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one 53319791 Click to see CC(=CCC1=CC(=CC(=C1OC)CC=C(C)C)C2CC(=O)C3=C(O2)C=C(C=C3)O)C 406.50 unknown https://doi.org/10.1021/NP0601861
Abyssinone III 42607817 Click to see 390.50 unknown https://doi.org/10.1021/NP0601861
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/10.1021/NP0601861
abyssinone IV 4'-OMe ether 11995580 Click to see CC(=CCC1=CC(=CC(=C1OC)CC=C(C)C)C2CC(=O)C3=C(O2)C=C(C=C3)O)C 406.50 unknown https://doi.org/10.1021/NP0601861
Abyssinone V 442153 Click to see 408.50 unknown https://doi.org/10.1021/NP0601861
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/NP0601861
abyssinone-IV 7330513 Click to see 392.50 unknown https://doi.org/10.1021/NP0601861
Abyssinones Iii 10408069 Click to see 390.50 unknown https://doi.org/10.1021/NP0601861
Sigmoidin E 195173 Click to see 406.50 unknown https://doi.org/10.1021/NP0601861
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2S)-2-(3,4-dihydroxyphenyl)-8,8-dimethyl-2,3,9,10-tetrahydropyrano[2,3-h]chromen-4-one 57338626 Click to see 340.40 unknown https://doi.org/10.1515/ZNB-2012-0116
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Npc318533 5835713 Click to see 432.40 unknown https://doi.org/10.1080/10826079208016365
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(1R,13R)-18-(3-methylbut-2-enyl)-7,11,20-trioxapentacyclo[11.7.0.02,10.04,8.014,19]icosa-2(10),3,5,8,14(19),15,17-heptaen-17-ol 163041972 Click to see 348.40 unknown https://doi.org/10.3987/COM-88-4624
(6aR,11aR)-3,9-Dihydroxy-4,8-diprenylpterocarpan 11581938 Click to see 392.50 unknown https://doi.org/10.1016/0031-9422(88)80746-5
(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/10.1016/0031-9422(88)80746-5
(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/10.1016/0031-9422(88)80746-5
2-O-[(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-yl] 1-O-ethyl benzene-1,2-dicarboxylate 162999091 Click to see 566.60 unknown https://doi.org/10.3987/COM-88-4624
2-O-[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-yl] 1-O-ethyl benzene-1,2-dicarboxylate 23242600 Click to see 566.60 unknown https://doi.org/10.3987/COM-88-4624
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/10.1016/0031-9422(88)80746-5
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/10.1016/0031-9422(88)80746-5
9-methoxy-10-(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-3-ol 392464 Click to see 338.40 unknown https://doi.org/10.1016/0031-9422(88)80746-5
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/10.1016/0031-9422(88)80746-5
Erybraedin D 471689 Click to see 390.50 unknown https://doi.org/10.3987/COM-88-4624
Erybraedin E 471690 Click to see CC(=CCC1=C(C=CC2=C1OC3C2COC4=C3C=C5C=COC5=C4)O)C 348.40 unknown https://doi.org/10.3987/COM-88-4624
Erycristagallin 10362969 Click to see 390.50 unknown https://doi.org/10.1016/S0014-2999(03)01664-9
Sandwicensin 467498 Click to see 338.40 unknown https://doi.org/10.1016/0031-9422(88)80746-5
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
Alpinumisoflavone 5490139 Click to see 336.30 unknown https://doi.org/10.1021/NP0601861
Erythrinin A 10381321 Click to see 320.30 unknown https://doi.org/10.1021/NP0601861
Parvisoflavone B 14550385 Click to see 352.30 unknown https://doi.org/10.1248/CPB.56.85
Wighteone 5281814 Click to see 338.40 unknown https://doi.org/10.1248/CPB.56.85
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
7-Hydroxy-3-[2-hydroxy-4-methoxy-5-(3-methylbut-2-enyl)phenyl]chromen-4-one 24795708 Click to see CC(=CCC1=CC(=C(C=C1OC)O)C2=COC3=C(C2=O)C=CC(=C3)O)C 352.40 unknown https://doi.org/10.1248/CPB.56.85
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
3-(4-hydroxyphenyl)-5,7-dimethoxy-4H-chromen-4-one 12458245 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C(=CO2)C3=CC=C(C=C3)O 298.29 unknown https://doi.org/10.1021/NP0601861
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
6-(7-hydroxy-3,4-dihydro-2H-chromen-3-yl)-2,2-dimethyl-8-(3-methylbut-2-enyl)chromen-7-ol 163048553 Click to see 392.50 unknown https://doi.org/10.1248/CPB.56.85
6-[(3R)-7-hydroxy-3,4-dihydro-2H-chromen-3-yl]-2,2-dimethyl-8-(3-methylbut-2-enyl)chromen-7-ol 24757892 Click to see 392.50 unknown https://doi.org/10.1248/CPB.56.85
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(E)-3-(3,4-dihydroxyphenyl)-1-(5-hydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)prop-2-en-1-one 57338627 Click to see CC1(CCC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC(=C(C=C3)O)O)C 340.40 unknown https://doi.org/10.1515/ZNB-2012-0116
1-(2,4-Dihydroxyphenyl)-3-[4-methoxy-3,5-bis(3-methylbut-2-enyl)phenyl]prop-2-en-1-one 73172950 Click to see 406.50 unknown https://doi.org/10.1021/NP0601861
3-(3,4-Dihydroxyphenyl)-1-(5-hydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)prop-2-en-1-one 76515726 Click to see 340.40 unknown https://doi.org/10.1515/ZNB-2012-0116
Abyssinone-Vi-4-O-Methyl Ether 11995582 Click to see 406.50 unknown https://doi.org/10.1021/NP0601861

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