Common products:
- Rotenone, a lipophilic, non‑volatile secondary metabolite extracted from the roots, stems, and leaves of Derris taiwaniana, is the primary commercial product derived from the species.

Industrial and craft applications:
- Rotenone from D. taiwaniana is formulated into natural insecticide and acaricide preparations used for horticultural and agricultural pest control. Historically, it has also been employed as a piscicide in fish‑eradication programs within aquaculture.

Properties relevant to use:
- Rotenone (C₂₃H₂₂O₆) inhibits mitochondrial complex I, causing rapid paralysis in insects. Its low water solubility and good solubility in organic solvents allow incorporation into emulsifiable concentrates, dusts, or granule formulations. The compound is stable under typical storage conditions, retaining potency for several months.

Standards and regulation:
- Rotenone appears in the United Nations Food and Agriculture Organization (FAO) International Code of Conduct on Pesticide Management and is listed in national pesticide registries (e.g., US EPA’s list of registered pesticide active ingredients; EU Biocidal Products Regulation (BPR) Annex I for restricted substances). Commercial products must comply with labeling, residue limits, and environmental safety requirements set by these regulatory frameworks.

Sustainability and sourcing:
- Roots and aerial tissues of D. taiwaniana are harvested from wild populations and cultivated plots. Sustainable harvesting practices—such as replanting, crop rotation, and monitoring of population density—are advocated to prevent overexploitation. Domestication programs aim to improve extraction yields and ensure a consistent supply while minimizing impact on natural habitats.

Synonyms Top

Scientific name	Authority	First published in
Millettia dunnii	Merr.	Philipp. J. Sci., C13: 139 (1918)
Millettia taiwaniana	(Hayata) Hayata	Icon. Pl. Formosan.9: 22 (1920)
Millettia fooningensis	Hu	Acta Phytotax. Sin.3: 360 (1955)
Pongamia taiwaniana	Hayata	Icon. Pl. Formosan.3: 79 (1913)
Phaseoloides pachycarpa	(Benth.) Kuntze	Revis. Gen. Pl.1: 201 (1891)
Whitfordiodendron taiwanianum	(Hayata) Ohwi	J. Jap. Bot.12: 660 (1936)
Millettia pachycarpa	Benth.	Pl. Jungh. : 250 (1852)

Common names Top

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Filter by language:

Language	Common/alternative name
Persian	میلتیا پچیکارپا
nan	lô͘-tîn
nan	hî-tîn
pwn	qayu
szy	nipaluma-luten, loten
trv	cudu
Chinese	苦檀子
Chinese	台湾鱼藤
Chinese	苦檀根
Chinese	苦檀叶
Chinese	臺灣魚藤
Chinese	台灣魚藤
Chinese	厚果鸡血藤
Chinese	厚果崖豆藤（厚果鸡血藤）
Chinese	厚果崖豆藤
Chinese	厚果崖豆树
Chinese	厚果崖豆
Chinese	冲天子

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
Tropicos	13035938
KEW	urn:lsid:ipni.org:names:507475-1
The Plant List	ild-32233
Open Tree Of Life	404083
NCBI Taxonomy	690557
IUCN Red List	147636173
IPNI	507475-1
iNaturalist	559362
GBIF	5355731
Freebase	/m/0bh7bby
EOL	643630
USDA GRIN	24314
Wikipedia	Millettia_pachycarpa
CMAUP	NPO22654
World Flora Online	wfo-1200008664

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

Acute rotenone poisoning: A scoping review

Tat J, Heskett K, Boss GR

Heliyon

21-Mar-2024

PMCID:	PMC11021885
doi:	10.1016/j.heliyon.2024.e28334
PMID:	38633629

Ethnobotanical contributions to global fishing communities: a review

Mendoza JN, Hanazaki N, Prūse B, Martini A, Bittner MV, Kochalski S, Macusi E, Ciriaco A, Mattalia G, Sõukand R

J Ethnobiol Ethnomed

02-Dec-2023

PMCID:	PMC10693712
doi:	10.1186/s13002-023-00630-3
PMID:	38042774

Anthelmintic evaluation of three ayurvedic formulations: a transmission electron microscopy study in Raillietina sp. (Cestoda)

Chen RP, Soren AD, Yadav AK

J Parasit Dis

24-Oct-2023

PMCID:	PMC10667176
doi:	10.1007/s12639-023-01630-6
PMID:	38009143

Application of Zebrafish as a Model for Anti-Cancer Activity Evaluation and Toxicity Testing of Natural Products

Shen Y, Sheng R, Guo R

Pharmaceuticals (Basel)

01-Jun-2023

PMCID:	PMC10305033
doi:	10.3390/ph16060827
PMID:	37375774

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

Phenolic Phytochemicals for Prevention and Treatment of Colorectal Cancer: A Critical Evaluation of In Vivo Studies

De S, Paul S, Manna A, Majumder C, Pal K, Casarcia N, Mondal A, Banerjee S, Nelson VK, Ghosh S, Hazra J, Bhattacharjee A, Mandal SC, Pal M, Bishayee A

Cancers (Basel)

03-Feb-2023

PMCID:	PMC9913554
doi:	10.3390/cancers15030993
PMID:	36765950

Novel Indole-Containing Hybrids Derived from Millepachine: Synthesis, Biological Evaluation and Antitumor Mechanism Study

Liang B, Zou Q, Yu L, Wang Y, Yan J, Huang B

Molecules

03-Feb-2023

PMCID:	PMC9921564
doi:	10.3390/molecules28031481
PMID:	36771147

Efforts in Bioprospecting Research: A Survey of Novel Anticancer Phytochemicals Reported in the Last Decade

Anifowose SO, Alqahtani WS, Al-Dahmash BA, Sasse F, Jalouli M, Aboul-Soud MA, Badjah-Hadj-Ahmed AY, Elnakady YA

Molecules

28-Nov-2022

PMCID:	PMC9738008
doi:	10.3390/molecules27238307
PMID:	36500400

Integrated genomics and proteomics analysis of Paenibacillus peoriae IBSD35 and insights into its antimicrobial characteristics

Ngashangva N, Mukherjee PK, Sharma C, Kalita MC, Sarangthem I

Sci Rep

07-Nov-2022

PMCID:	PMC9640621
doi:	10.1038/s41598-022-23613-y
PMID:	36344671

The toxicological effects of Eryngium foetidum extracts on zebrafish embryos and larvae depend on the type of extract, dose, and exposure time.

Castro TF, Carneiro WF, Reichel T, Fabem SL, Machado MR, de Souza KK, Resende LV, Murgas LD

Toxicol Res (Camb)

03-Oct-2022

PMCID:	PMC9618102
doi:	10.1093/toxres/tfac067
PMID:	36337237

Stem cambial variants of Taiwan lianas

Yang SZ, Chen PH, Chen JJ

Bot Stud

24-Sep-2022

PMCID:	PMC9509506
doi:	10.1186/s40529-022-00358-5
PMID:	36153445

A Mini-Review Regarding the Modalities to Study Neurodevelopmental Disorders-Like Impairments in Zebrafish—Focussing on Neurobehavioural and Psychological Responses

Curpăn AS, Balmus IM, Dobrin RP, Ciobica A, Chele GE, Gorgan DL, Boloș A

Brain Sci

28-Aug-2022

PMCID:	PMC9496774
doi:	10.3390/brainsci12091147
PMID:	36138883

Identification of phenolics from miracle berry (Synsepalum dulcificum) leaf extract and its antiangiogenesis and anticancer activities

Ma FY, Zhang XM, Li Y, Zhang M, Tu XH, Du LQ

Front Nutr

15-Aug-2022

PMCID:	PMC9420939
doi:	10.3389/fnut.2022.970019
PMID:	36046137

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

Plant Antimicrobial Peptides (PAMPs): Features, Applications, Production, Expression, and Challenges

Bakare OO, Gokul A, Fadaka AO, Wu R, Niekerk LA, Barker AM, Keyster M, Klein A

Molecules

09-Jun-2022

PMCID:	PMC9229691
doi:	10.3390/molecules27123703
PMID:	35744828

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 / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(1S,2S,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecane	46937024	Click to see	234.38	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Boscialin	6442487	Click to see	226.31	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
methyl 2-[(1R,2R,4S,7S,8S,11R,12R,13R,16R)-7-(furan-3-yl)-1,8,12,15,15-pentamethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.02,4.02,8.012,16]octadecan-13-yl]acetate	21576498	Click to see	486.60	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
5-Hydroxy-3-(4-methoxycyclohexen-1-yl)-8,8-dimethylpyrano[2,3-h]chromen-4-one	162963490	Click to see	354.40	unknown	https://doi.org/10.1016/0031-9422(83)85042-0
5-hydroxy-3-[(4R)-4-methoxycyclohexen-1-yl]-8,8-dimethylpyrano[2,3-h]chromen-4-one	162963491	Click to see	354.40	unknown	https://doi.org/10.1016/0031-9422(83)85042-0
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Quinazolines
2-(4-oxo-1H-quinazolin-2-yl)-1H-indole-3-carbaldehyde	21576497	Click to see	289.29	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
1-Hydroxyrutaecarpine	10447696	Click to see C1CN2C(=NC3=C(C2=O)C=CC=C3O)C4=C1C5=CC=CC=C5N4	303.30	unknown	via CMAUP database
18,19-Dihydroxy-3,13,21-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(21),2(10),4,6,8,15(20),16,18-octaen-14-one	23250595	Click to see	319.30	unknown	via CMAUP database
Rutaecarpine	65752	Click to see	287.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine	68085	Click to see	199.20	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
Tocris-1610	6603986	Click to see CC1=C(C(=C(C(=C1O)C(=O)C)O)CC2=C(C(=C3C(=C2O)C=CC(O3)(C)C)C(=O)C=CC4=CC=CC=C4)O)O	516.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(7R,8R)-7-hydroxy-8-(4-hydroxyphenyl)-2,2-dimethyl-10-(3-methylbut-2-enyl)-7,8-dihydropyrano[3,2-g]chromen-6-one	162821291	Click to see	406.50	unknown	https://doi.org/10.1016/0031-9422(80)85140-5
5,7-Dihydroxy-8-(4-hydroxyphenyl)-2,2-dimethyl-10-(3-methylbut-2-enyl)-7,8-dihydropyrano[3,2-g]chromen-6-one	56664587	Click to see	422.50	unknown	https://doi.org/10.1016/0031-9422(80)85140-5
Lupinifolinol	21721869	Click to see	422.50	unknown	https://doi.org/10.1016/0031-9422(80)85140-5
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Furanoflavones
18,19-Dimethoxy-2,7,14-trioxapentacyclo[11.8.0.03,11.04,8.016,21]henicosa-1(13),3(11),4(8),5,9,16,18,20-octaen-12-one	5320359	Click to see COC1=C(C=C2C(=C1)COC3=C2OC4=C(C3=O)C=CC5=C4C=CO5)OC	350.30	unknown	via CMAUP database
2-(2,6-Dimethoxyphenyl)-3-methoxyfuro[2,3-h]chromen-4-one	5320356	Click to see	352.30	unknown	via CMAUP database
2-(3,4-Dimethoxyphenyl)-3-methoxyfuro[2,3-h]chromen-4-one	5320355	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C4=C(C=C3)OC=C4)OC)OC	352.30	unknown	via CMAUP database
3-Methoxy-2-(3-methoxyphenyl)furo[2,3-h]chromen-4-one	5320358	Click to see	322.30	unknown	via CMAUP database
3-Methoxy-2-(3,4,5-trimethoxyphenyl)furo[2,3-h]chromen-4-one	5320357	Click to see	382.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
3-[3-(3,7-Dimethylocta-2,6-dienyl)-4-hydroxy-5-(3-methylbut-2-enyl)phenyl]-5,7-dihydroxychromen-4-one	162910396	Click to see	474.60	unknown	https://doi.org/10.1021/NP030554Q
3-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-4-hydroxy-5-(3-methylbut-2-enyl)phenyl]-5,7-dihydroxychromen-4-one	21580241	Click to see	474.60	unknown	https://doi.org/10.1021/NP030554Q
3',5'-Diprenylgenistein	44257287	Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2=COC3=CC(=CC(=C3C2=O)O)O)C	406.50	unknown	https://doi.org/10.1021/NP030554Q
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones / 2-prenylated isoflavones
3-[5-(3,7-Dimethylocta-2,6-dienyl)-3,4-dihydroxy-2-(3-methylbut-2-enyl)phenyl]-5,7-dihydroxychromen-4-one	162843994	Click to see	490.60	unknown	https://doi.org/10.1021/NP030554Q
3-[5-(3,7-Dimethylocta-2,6-dienyl)-4-hydroxy-3-methoxy-2-(3-methylbut-2-enyl)phenyl]-5,7-dihydroxychromen-4-one	162886247	Click to see	504.60	unknown	https://doi.org/10.1021/NP030554Q
3-[5-[(2E)-3,7-dimethylocta-2,6-dienyl]-3,4-dihydroxy-2-(3-methylbut-2-enyl)phenyl]-5,7-dihydroxychromen-4-one	11317821	Click to see	490.60	unknown	https://doi.org/10.1021/NP030554Q
3-[5-[(2E)-3,7-dimethylocta-2,6-dienyl]-4-hydroxy-3-methoxy-2-(3-methylbut-2-enyl)phenyl]-5,7-dihydroxychromen-4-one	21580240	Click to see	504.60	unknown	https://doi.org/10.1021/NP030554Q
5,7-Dihydroxy-3-[4-hydroxy-3-methoxy-2,5-bis(3-methylbut-2-enyl)phenyl]chromen-4-one	11154818	Click to see	436.50	unknown	https://doi.org/10.1021/NP030554Q
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
(2S)-4-hydroxy-6-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-g]chromen-5-one	162842930	Click to see	422.50	unknown	https://doi.org/10.1055/S-2005-916259
(2S)-6-(3,4-dihydroxyphenyl)-4-hydroxy-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-g]chromen-5-one	124356353	Click to see	438.50	unknown	https://doi.org/10.1055/S-2005-916259
(8R)-3-(3,4-dihydroxyphenyl)-5-hydroxy-8-(2-hydroxypropan-2-yl)-6-(3-methylbut-2-enyl)-8,9-dihydrofuro[2,3-h]chromen-4-one	162921041	Click to see	438.50	unknown	https://doi.org/10.1021/NP050341W
1'',2''-Dihydro-2'-hydroxycycloosajin	44257321	Click to see CC1(CCC2=C3C(=C4C(=C2O1)CCC(O4)(C)C)C(=O)C(=CO3)C5=C(C=C(C=C5)OC)O)C	436.50	unknown	https://doi.org/10.1016/0031-9422(81)85179-5
1'',2''-Dihydro-8-hydroxyisopentanyl-2'-methoxy-4'-O-methylalpinumisoflavone	44257322	Click to see	468.50	unknown	https://doi.org/10.1016/0031-9422(81)85179-5
1'',2''-Dihydro-8-hydroxyisopentanyl-3'-methoxy-4'-O-methylalpinumisoflavone	44257311	Click to see CC1(CCC2=C(C3=C(C(=C2O1)CCC(C)(C)O)OC=C(C3=O)C4=CC(=C(C=C4)OC)OC)O)C	468.50	unknown	https://doi.org/10.1016/0031-9422(81)85179-5
10-(2-Hydroperoxy-3-methylbut-3-enyl)-5-hydroxy-7-(4-hydroxyphenyl)-2,2-dimethylpyrano[3,2-g]chromen-6-one	11407932	Click to see	436.50	unknown	https://doi.org/10.1021/NP030554Q
10-[(2R)-2-hydroperoxy-3-methylbut-3-enyl]-5-hydroxy-7-(4-hydroxyphenyl)-2,2-dimethyl-3,4-dihydropyrano[3,2-g]chromen-6-one	163106743	Click to see	438.50	unknown	https://doi.org/10.1021/NP030554Q
10-[(2S)-2-hydroperoxy-3-methylbut-3-enyl]-5-hydroxy-7-(4-hydroxyphenyl)-2,2-dimethylpyrano[3,2-g]chromen-6-one	162886390	Click to see	436.50	unknown	https://doi.org/10.1021/NP030554Q
3-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2R)-2-hydroxy-3-methylbut-3-enyl]-8-(3-methylbut-2-enyl)chromen-4-one	124355911	Click to see CC(=CCC1=C(C(=C(C2=C1OC=C(C2=O)C3=CC(=C(C=C3)O)O)O)CC(C(=C)C)O)O)C	438.50	unknown	https://doi.org/10.1021/NP050341W
3-(3,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2R)-2-hydroxy-3-methylbut-3-enyl]-6-(3-methylbut-2-enyl)chromen-4-one	124355913	Click to see	438.50	unknown	https://doi.org/10.1021/NP050341W
4-Hydroxy-6-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-g]chromen-5-one	195652	Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC=C(C=C4)O)O)CC(O2)C(C)(C)O)C	422.50	unknown	https://doi.org/10.1055/S-2005-916259
5-(3-Hydroxy-4-methoxyphenyl)-10,10,16,16-tetramethyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1,4,7,13-tetraen-6-one	162980576	Click to see CC1(CCC2=C3C(=C4C(=C2O1)CCC(O4)(C)C)C(=O)C(=CO3)C5=CC(=C(C=C5)OC)O)C	436.50	unknown	https://doi.org/10.1016/0031-9422(81)85179-5
5-Hydroxy-3-(4-hydroxyphenyl)-7-methoxy-6,8-bis(3-methylbut-2-enyl)chromen-4-one	101274082	Click to see	420.50	unknown	https://doi.org/10.1055/S-2005-916259
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/10.1055/S-2005-916259
5,7,3'-Trihydroxy-4'-methoxy-6,8-diprenylisoflavone	13916925	Click to see	436.50	unknown	https://doi.org/10.1016/0031-9422(83)85042-0
6,8-Diprenylgenistein	480783	Click to see	406.50	unknown	https://doi.org/10.1021/NP030554Q https://doi.org/10.1016/0031-9422(83)85042-0 https://doi.org/10.1016/0031-9422(80)85140-5 https://doi.org/10.1055/S-2005-916259
6,8-Diprenylorobol	21148065	Click to see	422.50	unknown	https://doi.org/10.1016/0031-9422(83)85042-0 https://doi.org/10.1055/S-2005-916259 https://doi.org/10.1016/0031-9422(80)85140-5
Alpinumisoflavone	5490139	Click to see	336.30	unknown	https://doi.org/10.1021/NP030554Q
Auriculasin	5358846	Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC(=C(C=C4)O)O)O)C=CC(O2)(C)C)C	420.50	unknown	https://doi.org/10.1021/NP030554Q
Furowanin A	11582970	Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC(=C(C=C4)O)O)O)CC(O2)C(C)(C)O)C	438.50	unknown	https://doi.org/10.1055/S-2005-916259
Furowanin B	11655056	Click to see	438.50	unknown	https://doi.org/10.1021/NP050341W
Isoerysenegalensein E	5318561	Click to see	422.50	unknown	https://doi.org/10.1021/NP050341W https://doi.org/10.1055/S-2005-916259
Lupalbigenin	10001388	Click to see	406.50	unknown	https://doi.org/10.1016/0031-9422(80)85140-5
Millewanin G	11662094	Click to see CC(=CCC1=C(C(=C(C2=C1OC=C(C2=O)C3=CC(=C(C=C3)O)O)O)CC(C(=C)C)O)O)C	438.50	unknown	https://doi.org/10.1021/NP050341W
Millewanin H	11597321	Click to see	438.50	unknown	https://doi.org/10.1021/NP050341W
Pomiferin	4871	Click to see	420.50	unknown	https://doi.org/10.1016/0031-9422(83)85042-0
Warangalone	5379679	Click to see CC(=CCC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)C	404.50	unknown	https://doi.org/10.1055/S-2005-916259 https://doi.org/10.1021/NP030554Q https://doi.org/10.1021/NP050341W
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
8,8-Dimethyl-3-(2,4,5-trimethoxyphenyl)-4H,8H-benzo(1,2-b:3,4-b')dipyran-4-one	156793	Click to see	394.40	unknown	https://doi.org/10.1021/NP030554Q
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(-)-Deguelin;(-)-cis-Deguelin	606171	Click to see	394.40	unknown	https://doi.org/10.1021/NP030554Q
(6Ar,12aR)-9,12a-dihydroxy-2,3-dimethoxy-8-(3-methylbut-2-enyl)-6,6a-dihydrochromeno[3,4-b]chromen-12-one	51136534	Click to see	412.40	unknown	https://doi.org/10.1016/0031-9422(82)80103-9
(Rac)-Tephrosin	4485131	Click to see	410.40	unknown	https://doi.org/10.1021/NP030554Q
12-Hydroxyrotenone	161176	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC	410.40	unknown	via CMAUP database
5'beta-Rotenone	5102	Click to see	394.40	unknown	https://doi.org/10.1016/0031-9422(82)80103-9
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/10.1021/NP030554Q
9-hydroxy-2,3-dimethoxy-8-(3-methylbut-2-enyl)-6a,12a-dihydro-6H-chromeno[3,4-b]chromen-12-one	4303568	Click to see CC(=CCC1=C(C=CC2=C1OC3COC4=CC(=C(C=C4C3C2=O)OC)OC)O)C	396.40	unknown	https://doi.org/10.1016/0031-9422(82)80103-9
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/10.1021/NP030554Q
CID 303992	303992	Click to see	410.40	unknown	https://doi.org/10.1016/0031-9422(82)80103-9
cis-12a-Hydroxyrot-2'-enonic acid	44257415	Click to see	412.40	unknown	https://doi.org/10.1016/0031-9422(82)80103-9
Deguelin	107935	Click to see	394.40	unknown	https://doi.org/10.1021/NP030554Q
Npc311014	10023540	Click to see	394.40	unknown	via CMAUP database
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/10.1016/0031-9422(82)80103-9
Rotenone	6758	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC	394.40	unknown	https://doi.org/10.1016/0031-9422(82)80103-9
Rotenonic acid	6708539	Click to see	396.40	unknown	https://doi.org/10.1016/0031-9422(82)80103-9
Tephrosin	114909	Click to see	410.40	unknown	https://doi.org/10.1021/NP030554Q
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(5-Hydroxy-2,2-dimethylchromen-6-yl)-3-(4-methoxyphenyl)prop-2-en-1-one	85152577	Click to see	336.40	unknown	https://doi.org/10.1016/0031-9422(83)85042-0
4-Methoxylonchocarpin	10472189	Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)OC)C	336.40	unknown	https://doi.org/10.1016/0031-9422(83)85042-0

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Derris taiwaniana

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