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Millettia duchesnei

Millettia duchesnei - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fdc3419f59644968619
Scientific name Millettia duchesnei
Authority De Wild.
First published in Ann. Mus. Congo Belge, Bot., sér. 5, 1: 138 (1904)

Description Top

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Synonyms Top

No known synonyms.

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
    • West-central Tropical Africa
      • Cabinda
      • Cameroon
      • Gabon
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000199865
Tropicos 13060061
KEW urn:lsid:ipni.org:names:507348-1
The Plant List ild-4634
Open Tree Of Life 3920667
NCBI Taxonomy 2708899
IPNI 507348-1
GBIF 5355755
Freebase /m/0fq1x93
EOL 686568
USDA GRIN 436846
Wikipedia Millettia_duchesnei

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
Pharmacological Activity of Eriodictyol: The Major Natural Polyphenolic Flavanone Deng Z, Hassan S, Rafiq M, Li H, He Y, Cai Y, Kang X, Liu Z, Yan T Evid Based Complement Alternat Med 12-Dec-2020
PMCID:PMC7752289
doi:10.1155/2020/6681352
PMID:33414838
Flavonoids and Their Anti-Diabetic Effects: Cellular Mechanisms and Effects to Improve Blood Sugar Levels AL-Ishaq RK, Abotaleb M, Kubatka P, Kajo K, Büsselberg D Biomolecules 01-Sep-2019
PMCID:PMC6769509
doi:10.3390/biom9090430
PMID:31480505
Antidiabetic properties of dietary flavonoids: a cellular mechanism review Vinayagam R, Xu B Nutr Metab (Lond) 23-Dec-2015
PMCID:PMC4690284
doi:10.1186/s12986-015-0057-7
PMID:26705405
Rotenoid derivatives and other constituents of the twigs of Millettia duchesnei. Ngandeu F, Bezabih M, Ngamga D, Tchinda AT, Ngadjui BT, Abegaz BM, Dufat H, Tillequin F Phytochemistry 01-Jan-2008
doi:10.1016/J.PHYTOCHEM.2007.05.038
PMID:17640692

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
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans
(6,7-dimethoxy-3,4-dihydro-2H-chromen-4-yl)-(4-hydroxy-1-benzofuran-5-yl)methanone 101837049 Click to see COC1=C(C=C2C(=C1)C(CCO2)C(=O)C3=C(C4=C(C=C3)OC=C4)O)OC 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.038
[(4R)-6,7-dimethoxy-3,4-dihydro-2H-chromen-4-yl]-(4-hydroxy-1-benzofuran-5-yl)methanone 162877368 Click to see COC1=C(C=C2C(=C1)C(CCO2)C(=O)C3=C(C4=C(C=C3)OC=C4)O)OC 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.038
[(4S)-6,7-dimethoxy-3,4-dihydro-2H-chromen-4-yl]-(4-hydroxy-1-benzofuran-5-yl)methanone 162877367 Click to see COC1=C(C=C2C(=C1)C(CCO2)C(=O)C3=C(C4=C(C=C3)OC=C4)O)OC 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.038
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+/-)-Eriodictyol 11095 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.038
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.038
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids
17,18-Dimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-1(14),3(12),4(9),5,10,15,17,19-octaene-13,22-dione 135019234 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4=O)OC)OC)C 406.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.038
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(1)Benzopyrano(3,4-b)furo(2,3-h)(1)benzopyran-6(6aH)-one,12,12a-dihydro-6a-hydroxy-8,9-dimethoxy-, (6aS-cis)- 183157 Click to see COC1=C(C=C2C(=C1)C3(C(CO2)OC4=C(C3=O)C=CC5=C4C=CO5)O)OC 368.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.038
(1R,13S)-13-hydroxy-16,17-dimethoxy-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),5,9,14,16,18-heptaen-12-one 162999570 Click to see COC1=C(C=C2C(=C1)C3(C(CO2)OC4=C(C3=O)C=CC5=C4C=CO5)O)OC 368.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.038
(1S,12S,13S)-12,16,17-trimethoxy-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),5,9,14,16,18-heptaene 163044383 Click to see COC1C2C(COC3=CC(=C(C=C23)OC)OC)OC4=C1C=CC5=C4C=CO5 368.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.038
(1S,13R)-16,17-dimethoxy-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),5,9,14,16,18-heptaen-12-one 162920961 Click to see COC1=C(C=C2C(=C1)C3C(CO2)OC4=C(C3=O)C=CC5=C4C=CO5)OC 352.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.038
(22S)-17,18,22-trimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-1(14),3(12),4(9),5,10,15,17,19-octaen-13-one 163004444 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4OC)OC)OC)C 422.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.038
(22S)-22-hydroxy-17,18-dimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-1(14),3(12),4(9),5,10,15,17,19-octaen-13-one 163043659 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4O)OC)OC)C 408.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.038
12,16,17-Trimethoxy-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),5,9,14,16,18-heptaene 163044382 Click to see COC1C2C(COC3=CC(=C(C=C23)OC)OC)OC4=C1C=CC5=C4C=CO5 368.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.038
13-Hydroxy-16,17-dimethoxy-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),5,9,14,16,18-heptaen-12-one 13846201 Click to see COC1=C(C=C2C(=C1)C3(C(CO2)OC4=C(C3=O)C=CC5=C4C=CO5)O)OC 368.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.038
17,18,22-Trimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-1(14),3(12),4(9),5,10,15,17,19-octaen-13-one 163004443 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4OC)OC)OC)C 422.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.038
22-Hydroxy-17,18-dimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-1(14),3(12),4(9),5,10,15,17,19-octaen-13-one 163043658 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4O)OC)OC)C 408.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.038
Dehydrodeguelin 3083803 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC)C 392.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.038
Derride 13846199 Click to see COC1=C(C=C2C(=C1)C3C(CO2)OC4=C(C3=O)C=CC5=C4C=CO5)OC 352.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.038
Elliptone 160477 Click to see COC1=C(C=C2C(=C1)C3C(CO2)OC4=C(C3=O)C=CC5=C4C=CO5)OC 352.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.038

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