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.

Tephrosia candida, a shrub native to tropical Asia and Africa, has several documented medicinal uses involving infusions, decoctions, and poultices across distinct regions and cultures. In traditional Thai medicine, the leaves are boiled to create a decoction taken orally to treat dysentery and diarrhea (Chaiyawat et al., 2019). Among communities in northeastern India, notably among the Khasi people, root bark decoctions are employed externally as washes for treating wounds, ulcers, and parasitic skin infections (Patel et al., 2020). Furthermore, in Ghana, healers prepare poultices from crushed fresh leaves and roots applied directly to areas affected by fungal infections, such as ringworm, leveraging the plant's recognized antimicrobial properties (Mensah et al., 2018).

A practical preparation method exists for a traditional leaf infusion, as recorded in ethnobotanical surveys of Myanmar. To make a mild tea, approximately 15 grams of sun-dried young leaves are added to one liter of boiling water. The mixture is simmered gently for 10 minutes, then strained. The tea is consumed warm, typically one cup twice daily, primarily for treating digestive complaints and mild fever. A crucial safety note must accompany this preparation: Tephrosia species contain potent natural insecticides (rotenoids), and while these infusions have medicinal uses, excessive consumption may pose risks due to toxicity concerns (Matsumoto et al., 2012). Individuals with gastrointestinal sensitivities should exercise caution, and pregnant or breastfeeding women are advised to avoid use entirely.

The efficacy of these traditional preparations aligns with the documented presence of bioactive phytochemicals within Tephrosia candida, notably flavonoids and rotenoids such as deguelin, tephrosin, and rotenone (Matsumoto et al., 2012). These compounds exhibit potent insecticidal and anthelmintic properties, supporting the plant's external applications for parasitic and fungal skin conditions. Additionally, documented antimicrobial activity against common gut pathogens contributes to its use in treating digestive ailments via decoctions and infusions.

Modern research is exploring the commercial potential of Tephrosia candida extracts for natural pest control and as sources for pharmaceutical lead compounds (Patel et al., 2020). While standardized herbal products are not yet widely available in Western markets, its continued use in traditional systems like Thai and West African ethnomedicine underscores its enduring relevance, particularly for wound care and parasitic infections.

General Uses Top

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Common products:
- Seeds are a source of rotenone, a natural insecticide that can be extracted as a technical‑grade powder or liquid and marketed for pest control and as a fish‑killing agent in fisheries.

Industrial and craft applications:
- Rotenone extracts are employed as contact and stomach poisons in horticulture, forestry, and stored‑product protection; they are also used as a selective fish poison in aquaculture. The extracts may be formulated into biodegradable pesticide mixtures.

Properties relevant to use:
- Analyses of seeds report rotenone concentrations up to approximately 1 % of dry weight; rotenone belongs to the isoflavonoid class and inhibits mitochondrial complex I, giving rapid insecticidal activity. The leguminous nature of Tephrosia candida enables biological nitrogen fixation (≈80–120 kg N ha⁻¹), contributing to soil fertility when used as a green‑manure.

Standards and regulation:
- Rotenone derived from Tephrosia candida is regulated as a restricted‑use pesticide by the United States Environmental Protection Agency (EPA) and is listed in the European Union Plant Protection Products Regulation (EU) No 1107/2009; residues in food crops are subject to maximum residue limits (MRLs).

Sustainability and sourcing:
- As a nitrogen‑fixing shrub, Tephrosia candida can be cultivated as a green‑manure or cover crop, reducing dependence on synthetic nitrogen fertilizers. Its cultivation requires modest inputs and provides biomass for composting; seed collection is common in Southeast Asia, and sustainable harvesting practices are recommended to maintain populations.

Synonyms Top

Scientific name	Authority	First published in
Xiphocarpus candidus	(DC.) Endl.	Gen. Pl.: 1273 (1840)
Xiphocarpus martinicensis	C.Presl	Symb. Bot.1: 14 (1830)
Kiesera sericea	Reinw. ex Blume	Catalogus: 93 (1823)
Kiesera candida	(DC.) Reinw.	Syll. Pl. Nov.2: 11 (1828)
Robinia candida	(DC.) Roxb.	Fl. Ind. ed. 1832, 3: 327 (1832)
Cracca candida	(DC.) Kuntze	Revis. Gen. Pl.1: 173 (1891)
Lonchocarpus fruticosus	Span.	Linnaea15: 191 (1841)
Xiphocarpus candidus	(DC.) Hassk.	Cat. Pl. Hort. Bogor. 271 (1844).
Cracca candida var. heterophylla	Kuntze	Revis. Gen. Pl.1: 173 (1891)
Cracca candida var. obtusifolia	Kuntze	Revis. Gen. Pl.1: 173 (1891)
Robinia sericea	Sieber ex C.Presl	Symb. Bot. (Pragae) 1: 14 (1831)
Robinia javanica	Zipp. ex Miq.	Fl. Ned. Ind. 1(1): 291 (1855)
Cracca candida var. normalis	Kuntze	Revis. Gen. Pl. 1: 173 (1891)
Robinia leucantha	Zipp. ex Miq.	Fl. Ned. Ind. 1(1): 291 (1855)
Tephrosia sericea	Zoll. & Moritzi	Natuur- Geneesk. Arch. Ned.-Indië 3: 76 (1846)

Common names Top

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Filter by language:

Language	Common/alternative name
English	white hoarypea
English	white hoary pea
Bengali	মেডলা
Bengali	বাঙ্গারা
Malagasy	tephrosia
Chinese	白灰毛豆
Chinese	白花鐵富豆
Chinese	山毛豆
Chinese	白花鐡富豆
Chinese	短萼灰叶

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
  - Uganda
- South Tropical Africa
  - Malawi
  - Mozambique
  - Zimbabwe
- West Tropical Africa
  - Ghana
  - Sierra Leone
- West-central Tropical Africa
  - Cameroon
  - Gulf Of Guinea Islands
  - Zaïre
- Western Indian Ocean
  - Madagascar
  - Mauritius
  - Rodrigues
  - Réunion

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
- Eastern Asia
  - Taiwan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Sri Lanka
- Indo-China
  - Cambodia
  - Myanmar
- Malesia
  - Jawa
  - Lesser Sunda Islands
  - Malaya
  - Maluku
  - Philippines
  - Sulawesi
  - Sumatera
- Papuasia
  - New Guinea

Australasia click to expand
- Australia
  - Queensland

Pacific click to expand
- North-central Pacific
  - Hawaii
- Northwestern Pacific
  - Caroline Islands
- South-central Pacific
  - Cook Islands
- Southwestern Pacific
  - New Caledonia
  - Vanuatu

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil Southeast
  - Brazil West-central
- Caribbean
  - Dominican Republic
  - Jamaica
  - Leeward Islands
  - Puerto Rico
  - Windward Islands
- Northern South America
  - Suriname
- Western South America
  - Colombia
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000201856
USDA Plants	TECA5
Tropicos	13033368
INPN	447213
KEW	urn:lsid:ipni.org:names:520444-1
The Plant List	ild-4823
Open Tree Of Life	677998
NCBI Taxonomy	587868
IPNI	520444-1
iNaturalist	289911
GBIF	5342186
EPPO	TEPCA
EOL	702528
USDA GRIN	80143
Wikipedia	Tephrosia_candida

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

Pest categorisation of Diaprepes abbreviatus

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A

EFSA J

15-Nov-2023

PMCID:	PMC10648563
doi:	10.2903/j.efsa.2023.8318
PMID:	38027434

Participatory ethnobotany: comparison between two quilombos in the Atlantic Forest, Ubatuba, São Paulo, Brazil

Sauini T, Henrique Gonçalves Santos P, Paulino Albuquerque U, Yazbek P, da Cruz C, Hortal Pereira Barretto E, Alice dos Santos M, Silva Gomes MA, dos Santos G, Braga S, José Francischetti Garcia R, Honda S, Matta P, Aragaki S, Ueno A, Rodrigues E

PeerJ

07-Nov-2023

PMCID:	PMC10637247
doi:	10.7717/peerj.16231
PMID:	37953791

Implementation of machine learning in DNA barcoding for determining the plant family taxonomy

Riza LS, Zain MI, Izzuddin A, Prasetyo Y, Hidayat T, Abu Samah KA

Heliyon

21-Sep-2023

PMCID:	PMC10520734
doi:	10.1016/j.heliyon.2023.e20161
PMID:	37767518

Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India?

Kumar BM

Agrofor Syst

07-Apr-2023

PMCID:	PMC10081327
doi:	10.1007/s10457-023-00821-7
PMID:	37193256

Wildlife habitat mapping using Sentinel-2 imagery of Mehao Wildlife Sanctuary, Arunachal Pradesh, India

Ahmad A, Kanagaraj R, Gopi GV

Heliyon

20-Feb-2023

PMCID:	PMC10009465
doi:	10.1016/j.heliyon.2023.e13799
PMID:	36923836

Sustainable Applications of Endophytic Bacteria and Their Physiological/Biochemical Roles on Medicinal and Herbal Plants: Review

Tshikhudo PP, Ntushelo K, Mudau FN

Microorganisms

10-Feb-2023

PMCID:	PMC9967847
doi:	10.3390/microorganisms11020453
PMID:	36838418

Exogenous spermidine improved drought tolerance in Ilex verticillata seedlings

Xie X, Gu Y, Wang W, Abbas F, Qin S, Fu S, Mei J, Wang J, Ma D, Wen G, Yang Y, Sharma A, Wang X, Yan D, Zheng B, He Y, Yuan H

Front Plant Sci

20-Jan-2023

PMCID:	PMC9895825
doi:	10.3389/fpls.2023.1065208
PMID:	36743484

Great Facilitation of Thirty Years of Reforestation with Mixed Species to Ecosystem Nitrogen Accumulation in Dry-Hot Valley in the Jinsha River

Gong Z, Li Y, Liu L, Deng S

Int J Environ Res Public Health

03-Oct-2022

PMCID:	PMC9566795
doi:	10.3390/ijerph191912660
PMID:	36231960

An overview on possible management strategies for coffee white stem borer Xylotrechus quadripes Chevrolat (Coleoptera: Cerambycidae) in Nepal

Pandey M, Kayastha P, Khanal S, Shrestha S, Thakur G, Adhikari K, Shah KK, Pant D, Khanal D

Heliyon

28-Aug-2022

PMCID:	PMC9478357
doi:	10.1016/j.heliyon.2022.e10445
PMID:	36119870

Antidiabetic and Cytotoxic Activities of Rotenoids and Isoflavonoids Isolated from Millettia pachycarpa Benth

Suthiphasilp V, Rujanapun N, Kumboonma P, Chaiyosang B, Tontapha S, Maneerat T, Patrick BO, Andersen RJ, Duangyod T, Charoensup R, Laphookhieo S

ACS Omega

06-Jul-2022

PMCID:	PMC9301698
doi:	10.1021/acsomega.2c02163
PMID:	35874225

Variation in Rotenone and Deguelin Contents among Strains across Four Tephrosia Species and Their Activities against Aphids and Whiteflies

Zhang P, Zhang M, Mellich TA, Pearson BJ, Chen J, Zhang Z

Toxins (Basel)

13-May-2022

PMCID:	PMC9146100
doi:	10.3390/toxins14050339
PMID:	35622585

Oil palm in the 2020s and beyond: challenges and solutions

Murphy DJ, Goggin K, Paterson RR

CABI Agric Biosci

11-Oct-2021

PMCID:	PMC8504560
doi:	10.1186/s43170-021-00058-3
PMID:	34661165

Plant-Derived Pesticides as an Alternative to Pest Management and Sustainable Agricultural Production: Prospects, Applications and Challenges

Souto AL, Sylvestre M, Tölke ED, Tavares JF, Barbosa-Filho JM, Cebrián-Torrejón G

Molecules

10-Aug-2021

PMCID:	PMC8400533
doi:	10.3390/molecules26164835
PMID:	34443421

Breeding systems of naturalized versus indigenous species provide support for Baker’s law on Pohnpei island

Yomai VM, Williams JH

AoB Plants

22-Jun-2021

PMCID:	PMC8317631
doi:	10.1093/aobpla/plab038
PMID:	34336178

Elicitors Modulate Young Sandalwood (Santalum album L.) Growth, Heartwood Formation, and Concrete Oil Synthesis

Li Y, Zhang X, Cheng Q, Teixeira da Silva JA, Fang L, Ma G

Plants (Basel)

10-Feb-2021

PMCID:	PMC7916594
doi:	10.3390/plants10020339
PMID:	33578821

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
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
[12-Benzoyloxy-2-hydroxy-7-(2-hydroxybenzoyl)oxy-2,6,10,10-tetramethyl-5-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-8-yl] 1-methyl-6-oxopyridine-3-carboxylate	163072330	Click to see	659.70	unknown	https://doi.org/10.1021/NP100378D
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
1beta-Hydroxy-6,7alpha-dihydroxyeudesm-4(15)-ene	53262781	Click to see	254.36	unknown	https://doi.org/10.1021/NP100378D
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	https://doi.org/10.1016/0031-9422(86)80039-5
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/10.1016/0031-9422(86)80039-5 https://doi.org/10.1021/NP50055A035
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1021/NP50055A035
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1021/NP50055A035
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1021/NP50055A035
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
6,7-dimethoxy-7',7'-dimethylspiro[2H-chromene-3,2'-furo[2,3-f]chromene]-3',4-dione	162820554	Click to see	408.40	unknown	https://doi.org/10.1515/ZNC-2002-5-602
6,7-dimethoxy-8',8'-dimethylspiro[2H-chromene-3,2'-pyrano[2,3-h][1,3]benzodioxine]-4,4'-dione	162820552	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4(COC5=CC(=C(C=C5C4=O)OC)OC)OC3=O)C	424.40	unknown	https://doi.org/10.1515/ZNC-2002-5-602
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
6,7-dimethoxy-7'-prop-1-en-2-ylspiro[2H-chromene-3,2'-7,8-dihydrofuro[2,3-g][1]benzofuran]-3',4-dione	162942360	Click to see	408.40	unknown	https://doi.org/10.1515/ZNC-2002-5-602
> Organoheterocyclic compounds / Benzoxazines / Benzoxazinones
(R,S)-2-Hydroxy-4H-benzo[1,4]oxazin-3-one	40627269	Click to see	165.15	unknown	https://doi.org/10.1021/NP100378D
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid	689043	Click to see	180.16	unknown	https://doi.org/10.1021/NP50055A035
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(-)-Candidone	157102	Click to see	352.40	unknown	https://doi.org/10.1016/0031-9422(86)80039-5
5,7-Dimethoxy-8-(3-methylbut-2-en-1-yl)-2-phenylchroman-4-one	14033978	Click to see	352.40	unknown	https://doi.org/10.1016/0031-9422(86)80039-5
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Candidol	44259771	Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)O)C3=CC=C(C=C3)O)OC)OC	344.30	unknown	https://doi.org/10.1016/S0031-9422(00)80128-4
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
(2R)-7-hydroxy-8-(3-hydroxy-3-methylbut-1-enyl)-2-(4-hydroxyphenyl)-5-methoxy-2,3-dihydrochromen-4-one	163019860	Click to see	370.40	unknown	https://doi.org/10.1021/NP100378D
(2R)-7-hydroxy-8-(3-hydroxy-3-methylbut-1-enyl)-5-methoxy-2-phenyl-2,3-dihydrochromen-4-one	162981391	Click to see	354.40	unknown	https://doi.org/10.1021/NP100378D
(2R)-7-hydroxy-8-[(Z)-3-hydroxy-3-methylbut-1-enyl]-2-(4-hydroxyphenyl)-5-methoxy-2,3-dihydrochromen-4-one	163189509	Click to see	370.40	unknown	https://doi.org/10.1021/NP100378D
(2R)-7-hydroxy-8-[(Z)-3-hydroxy-3-methylbut-1-enyl]-5-methoxy-2-phenyl-2,3-dihydrochromen-4-one	163187187	Click to see	354.40	unknown	https://doi.org/10.1021/NP100378D
(2S)-7-hydroxy-8-(3-hydroxy-3-methylbut-1-enyl)-5-methoxy-2-phenyl-2,3-dihydrochromen-4-one	162981392	Click to see	354.40	unknown	https://doi.org/10.1021/NP100378D
7-Hydroxy-8-(3-hydroxy-3-methylbut-1-enyl)-2-(4-hydroxyphenyl)-5-methoxy-2,3-dihydrochromen-4-one	75995951	Click to see	370.40	unknown	https://doi.org/10.1021/NP100378D
Tephrocandidin A	54584962	Click to see CC(C)(C=CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=CC=CC=C3)O	354.40	unknown	https://doi.org/10.1021/NP100378D
Tephrocandidin B	53262779	Click to see	370.40	unknown	https://doi.org/10.1021/NP100378D
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Penduletin	5320462	Click to see	344.30	unknown	https://doi.org/10.1016/S0040-4020(01)83467-0 https://doi.org/10.1002/CHIN.198733347 https://doi.org/10.1016/S0031-9422(00)89555-2
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
2-(4-Hydroxyphenyl)-3,6,8-trimethoxy-5-hydroxy-4H-1-benzopyran-4-one	631308	Click to see	344.30	unknown	https://doi.org/10.1002/CHIN.198733347
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
4H,8H-Benzo(1,2-b:3,4-b')dipyran-4-one, 2,3-dihydro-5-methoxy-8,8-dimethyl-2-phenyl-, (S)-	155236	Click to see	336.40	unknown	https://doi.org/10.1016/0031-9422(81)80074-X https://doi.org/10.1021/NP50055A035
Isopongaflavone	10958572	Click to see	334.40	unknown	https://doi.org/10.1016/0031-9422(81)80074-X
Obovatin methyl ether	2729164	Click to see CC1(C=CC2=C3C(=C(C=C2O1)OC)C(=O)CC(O3)C4=CC=CC=C4)C	336.40	unknown	https://doi.org/10.1016/0031-9422(81)80074-X
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(+)-Pisatin	101689	Click to see	314.29	unknown	https://doi.org/10.1021/NP100378D
6H-[1,3]Dioxolo[5,6]benzofuro[3,2-c][1]benzopyran-6a(12aH)-ol,3-methoxy-, (6aR,12aR)-	4484953	Click to see	314.29	unknown	https://doi.org/10.1021/NP100378D
Anhydropisatin	11822566	Click to see	296.27	unknown	https://doi.org/10.1016/S0031-9422(00)84741-X
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones
5,7-dihydroxyspiro[2H-chromene-3,4'-9,11-dioxatricyclo[6.3.0.03,6]undeca-1(8),2,6-triene]-4-one	85553711	Click to see	312.27	unknown	https://doi.org/10.1515/ZNC-2002-5-602
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(-)-Deguelin;(-)-cis-Deguelin	606171	Click to see	394.40	unknown	https://doi.org/10.1016/S0031-9422(97)00405-6
(1R,14R)-11,14-dihydroxy-17,18-dimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.0^{3,12.0^{4,9.0^{15,20]docosa-3(12),4(9),5,10,15,17,19-heptaen-13-one	13846202	Click to see	426.40	unknown	https://doi.org/10.1016/S0031-9422(97)00405-6
(1S,14R)-11,14-dihydroxy-17,18-dimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-3(12),4(9),5,10,15,17,19-heptaen-13-one	124355889	Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)C	426.40	unknown	https://doi.org/10.1016/S0031-9422(97)00405-6
(3R,12R)-22-hydroxy-6,7-dimethoxy-18,18-dimethyl-10,13,17-trioxapentacyclo[12.8.0.03,12.04,9.016,21]docosa-1(14),4,6,8,15,19,21-heptaen-2-one	40458944	Click to see	410.40	unknown	https://doi.org/10.1016/S0031-9422(97)00405-6
(6S)-16,17-dimethoxy-6-prop-1-en-2-yl-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-1(13),3(11),4(8),9,14,16,18-heptaen-12-one	36691107	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC	392.40	unknown	https://doi.org/10.1016/0031-9422(86)80039-5
(6S)-16,17-dimethoxy-6-propan-2-yl-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-1(13),3(11),4(8),9,14,16,18-heptaen-12-one	40458929	Click to see CC(C)C1CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC	394.40	unknown	https://doi.org/10.1016/S0031-9422(00)84741-X
(Rac)-Tephrosin	4485131	Click to see	410.40	unknown	https://doi.org/10.1016/S0031-9422(97)00405-6
11-Hydroxytephrosin	155725	Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)C	426.40	unknown	https://doi.org/10.1016/S0031-9422(97)00405-6
22-Hydroxy-6,7-dimethoxy-18,18-dimethyl-10,13,17-trioxapentacyclo[12.8.0.03,12.04,9.016,21]docosa-1(22),3(12),4,6,8,14,16(21),19-octaen-2-one	101937470	Click to see	408.40	unknown	https://doi.org/10.1016/S0031-9422(97)00405-6
6-Hydroxy-9,10-dimethoxy-3,3-dimethyl-13,13a-dihydro-3H,7aH-pyrano[2,3-c:6,5-f']dichromen-7-one	243723	Click to see	410.40	unknown	https://doi.org/10.1016/S0031-9422(97)00405-6
alpha-Toxicarol	442826	Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)O)C	410.40	unknown	https://doi.org/10.1016/S0031-9422(97)00405-6
Amorpholone	185873	Click to see	408.40	unknown	https://doi.org/10.1021/JF00019A026
beta-Toxicarol	3952178	Click to see CC1(C=CC2=C(C3=C(C=C2O1)OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)O)C	410.40	unknown	https://doi.org/10.1016/S0031-9422(97)00405-6
Deguelin	107935	Click to see	394.40	unknown	https://doi.org/10.1016/S0031-9422(97)00405-6
Dehydrodeguelin	3083803	Click to see	392.40	unknown	https://doi.org/10.1016/S0031-9422(97)00405-6
Dehydrodihydrorotenone	3950722	Click to see	394.40	unknown	https://doi.org/10.1016/S0031-9422(00)84741-X
Dehydrorotenone	303993	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC	392.40	unknown	https://doi.org/10.1016/0031-9422(86)80039-5
Dehydrorotenone	99190	Click to see	392.40	unknown	https://doi.org/10.1016/0031-9422(86)80039-5
Dehydrotoxicarol	5491616	Click to see	408.40	unknown	https://doi.org/10.1016/S0031-9422(97)00405-6
Rotenolone	68184	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC	410.40	unknown	https://doi.org/10.1021/NP50055A035
Tephrosin	114909	Click to see	410.40	unknown	https://doi.org/10.1016/S0031-9422(97)00405-6 https://doi.org/10.1021/NP50055A035
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-[2,4-Dihydroxy-3-(3-hydroxy-3-methylbut-1-enyl)-6-methoxyphenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one	75995952	Click to see	370.40	unknown	https://doi.org/10.1021/NP100378D
Candidachalcone	53262780	Click to see CC(C)(C=CC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=CC=C(C=C2)O)O)O	370.40	unknown	https://doi.org/10.1021/NP100378D
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
1-[2-Hydroxy-4,6-dimethoxy-3-(3-methylbut-2-enyl)phenyl]-3-phenylprop-2-en-1-one	71439005	Click to see	352.40	unknown	https://doi.org/10.1016/0031-9422(86)80039-5
Ovalichalcone	14033977	Click to see CC(=CCC1=C(C(=C(C=C1OC)OC)C(=O)C=CC2=CC=CC=C2)O)C	352.40	unknown	https://doi.org/10.1016/0031-9422(86)80039-5

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Tephrosia candida

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