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Millettia pachycarpa

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643fd98114a90929005319
Scientific name Millettia pachycarpa
Authority Benth.
First published in F.A.W.Miquel, Pl. Jungh.: 250 (1852)

Description Top

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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)
Whitfordiodendron taiwaniana (Hayata) Ohwi
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)

Common names Top

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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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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

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
World Flora Online wfo-0000185902
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

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
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
Vegetation Classification and Distribution Patterns in the South Slope of Yarlung Zangbo Grand Canyon National Nature Reserve, Eastern Himalayas Wu PP, Wang Z, Jia NX, Dong SQ, Qu XY, Qiao XG, Liu CC, Guo K Plants (Basel) 28-Apr-2022
PMCID:PMC9105001
doi:10.3390/plants11091194
PMID:35567195
Nanotechnology-Based Bioactive Antifeedant for Plant Protection Melanie M, Miranti M, Kasmara H, Malini DM, Husodo T, Panatarani C, Joni IM, Hermawan W Nanomaterials (Basel) 14-Feb-2022
PMCID:PMC8879102
doi:10.3390/nano12040630
PMID:35214959

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 / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(2S,9S,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecane 46937024 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Boscialin 6442487 Click to see CC1CC(CC(C1(C=CC(=O)C)O)(C)C)O 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 CC1(C2CC(=O)C3(C(C2(C(O1)CC(=O)OC)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)C 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 CC1(C=CC2=C(O1)C=C(C3=C2OC=C(C3=O)C4=CCC(CC4)OC)O)C 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 CC1(C=CC2=C(O1)C=C(C3=C2OC=C(C3=O)C4=CCC(CC4)OC)O)C 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 C1=CC=C2C(=C1)C(=C(N2)C3=NC(=O)C4=CC=CC=C4N3)C=O 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
1,2-Dihydroxyrutaecarpine 23250595 Click to see C1CN2C(=NC3=C(C2=O)C=CC(=C3O)O)C4=C1C5=CC=CC=C5N4 319.30 unknown via CMAUP database
Rutaecarpine 65752 Click to see C1CN2C(=NC3=CC=CC=C3C2=O)C4=C1C5=CC=CC=C5N4 287.30 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine 68085 Click to see COC1=C2C=COC2=NC3=CC=CC=C31 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 CC(=CCC1=C2C(=CC3=C1OC(C(C3=O)O)C4=CC=C(C=C4)O)C=CC(O2)(C)C)C 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 CC(=CCC1=C2C(=C(C3=C1OC(C(C3=O)O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)C 422.50 unknown https://doi.org/10.1016/0031-9422(80)85140-5
Lupinifolinol 21721869 Click to see CC(=CCC1=C2C(=C(C3=C1OC(C(C3=O)O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)C 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 COC1=C(C(=CC=C1)OC)C2=C(C(=O)C3=C(O2)C4=C(C=C3)OC=C4)OC 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 COC1=CC=CC(=C1)C2=C(C(=O)C3=C(O2)C4=C(C=C3)OC=C4)OC 322.30 unknown via CMAUP database
3-Methoxy-2-(3,4,5-trimethoxyphenyl)furo[2,3-h]chromen-4-one 5320357 Click to see COC1=CC(=CC(=C1OC)OC)C2=C(C(=O)C3=C(O2)C4=C(C=C3)OC=C4)OC 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 CC(=CCCC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2=COC3=CC(=CC(=C3C2=O)O)O)C)C 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 CC(=CCCC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2=COC3=CC(=CC(=C3C2=O)O)O)C)C 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 CC(=CCCC(=CCC1=CC(=C(C(=C1O)O)CC=C(C)C)C2=COC3=CC(=CC(=C3C2=O)O)O)C)C 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 CC(=CCCC(=CCC1=CC(=C(C(=C1O)OC)CC=C(C)C)C2=COC3=CC(=CC(=C3C2=O)O)O)C)C 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 CC(=CCCC(=CCC1=CC(=C(C(=C1O)O)CC=C(C)C)C2=COC3=CC(=CC(=C3C2=O)O)O)C)C 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 CC(=CCCC(=CCC1=CC(=C(C(=C1O)OC)CC=C(C)C)C2=COC3=CC(=CC(=C3C2=O)O)O)C)C 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 CC(=CCC1=CC(=C(C(=C1O)OC)CC=C(C)C)C2=COC3=CC(=CC(=C3C2=O)O)O)C 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 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
(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 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
(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 CC(=CCC1=C2C(=C3C(=C1O)C(=O)C(=CO3)C4=CC(=C(C=C4)O)O)CC(O2)C(C)(C)O)C 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 CC1(CCC2=C(C3=C(C(=C2O1)CCC(C)(C)O)OC=C(C3=O)C4=C(C=C(C=C4)OC)OC)O)C 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 CC(=C)C(CC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)OO 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 CC(=C)C(CC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC=C(C=C4)O)O)CCC(O2)(C)C)OO 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 CC(=C)C(CC1=C2C(=C(C3=C1OC=C(C3=O)C4=CC=C(C=C4)O)O)C=CC(O2)(C)C)OO 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 CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=CC(=C(C=C3)O)O)CC(C(=C)C)O)O)C 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 CC(=CCC1=C(C2=C(C(=C1OC)CC=C(C)C)OC=C(C2=O)C3=CC=C(C=C3)O)O)C 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 CC(=CCC1=C(C(=C(C2=C1OC=C(C2=O)C3=CC=C(C=C3)O)O)CC(C(=C)C)O)O)C 422.50 unknown https://doi.org/10.1055/S-2005-916259
5,7,3'-Trihydroxy-4'-methoxy-6,8-diprenylisoflavone 13916925 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=CC(=C(C=C3)OC)O)CC=C(C)C)O)C 436.50 unknown https://doi.org/10.1016/0031-9422(83)85042-0
6,8-Diprenylgenistein 480783 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)CC=C(C)C)O)C 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 CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=CC(=C(C=C3)O)O)CC=C(C)C)O)C 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 CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O)C 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 CC(=CCC1=C2C(=C3C(=C1O)C(=O)C(=CO3)C4=CC(=C(C=C4)O)O)CC(O2)C(C)(C)O)C 438.50 unknown https://doi.org/10.1021/NP050341W
Isoerysenegalensein E 5318561 Click to see CC(=CCC1=C(C(=C(C2=C1OC=C(C2=O)C3=CC=C(C=C3)O)O)CC(C(=C)C)O)O)C 422.50 unknown https://doi.org/10.1021/NP050341W
https://doi.org/10.1055/S-2005-916259
Lupalbigenin 10001388 Click to see CC(=CCC1=C(C=CC(=C1)C2=COC3=C(C2=O)C(=C(C(=C3)O)CC=C(C)C)O)O)C 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 CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=CC(=C(C=C3)O)O)CC(C(=C)C)O)O)C 438.50 unknown https://doi.org/10.1021/NP050341W
Pomiferin 4871 Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C(=CO3)C4=CC(=C(C=C4)O)O)C=CC(O2)(C)C)C 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
Barbigerone 156793 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC=C(C3=O)C4=CC(=C(C=C4OC)OC)OC)C 394.40 unknown https://doi.org/10.1021/NP030554Q
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(-)-Deguelin;(-)-cis-Deguelin 606171 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)C 394.40 unknown https://doi.org/10.1021/NP030554Q
(Rac)-Tephrosin 4485131 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)C 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
12a-Hydroxyrotenonic acid 51136534 Click to see CC(=CCC1=C(C=CC2=C1OC3COC4=CC(=C(C=C4C3(C2=O)O)OC)OC)O)C 412.40 unknown https://doi.org/10.1016/0031-9422(82)80103-9
5'beta-Rotenone 5102 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
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 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
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 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
cis-12a-Hydroxyrot-2'-enonic acid 44257415 Click to see CC(=CCC1=C(C=CC2=C1OC3COC4=CC(=C(C=C4C3(C2=O)O)OC)OC)O)C 412.40 unknown https://doi.org/10.1016/0031-9422(82)80103-9
Deguelin 107935 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)C 394.40 unknown https://doi.org/10.1021/NP030554Q
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 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
Tephrosin 114909 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)C 410.40 unknown https://doi.org/10.1021/NP030554Q
US9328123, Rotenone 10023540 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC 394.40 unknown via CMAUP database
> 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 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
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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