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Millettia usaramensis

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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 UUID643fdc5f5abe5823596950
Scientific name Millettia usaramensis
Authority Taub.
First published in H.G.A.Engler, Pflanzenw. Ost-Afrikas, C: 212 (1895)

Description Top

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Synonyms Top

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Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Millettia usaramensis subsp. australis J.B.Gillett Kew Bull.15: 30 (1961)
Millettia usaramensis subsp. usaramensis Taub. Unknown

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
    • Northeast Tropical Africa
      • Somalia
    • South Tropical Africa
      • Malawi
      • Mozambique
      • Zimbabwe

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000200818
Tropicos 13073060
KEW urn:lsid:ipni.org:names:507257-1
The Plant List ild-4726
Open Tree Of Life 3920671
NCBI Taxonomy 1258704
IUCN Red List 62519
IPNI 507257-1
iNaturalist 340144
GBIF 5355738
EOL 691008
USDA GRIN 436849
Wikipedia Millettia_usaramensis

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
Study on the absolute configuration and biological activity of rotenoids from the leaves and twigs of Millettia pyrrhocarpa Mattapha, Forest & Hawkins, sp. Nov Sananboonudom S, Kaewnoi A, Pompimon W, Narakaew S, Jiajaroen S, Chainok K, nuntasaen N, Suksen K, Chairoungdua A, Limthongkul J, Naparswad C, Pikulthong S, Meepowpan P, Wingwon B, Charoenphakinrattana N, Udomputtimekakul P BMC Complement Med Ther 04-May-2023
PMCID:PMC10161675
doi:10.1186/s12906-023-03963-4
PMID:37143007
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005
Accommodating receptor flexibility and free energy calculation to reduce false positive binders in the discovery of natural products blockers of SARS-COV-2 spike RBD-ACE2 interface Ogedjo M, Onoka I, Sahini M, Shadrack DM Biochem Biophys Rep 25-May-2021
PMCID:PMC8148615
doi:10.1016/j.bbrep.2021.101024
PMID:34056140
Diversification of African Tree Legumes in Miombo–Mopane Woodlands Maquia I, Catarino S, Pena AR, Brito DR, Ribeiro NS, Romeiras MM, Ribeiro-Barros AI Plants (Basel) 20-Jun-2019
PMCID:PMC6631767
doi:10.3390/plants8060182
PMID:31226765
Anti-plasmodial activities and X-ray crystal structures of rotenoids from Millettia usaramensis subspecies usaramensis. Yenesew A, Derese S, Midiwo JO, Oketch-Rabah HA, Lisgarten J, Palmer R, Heydenreich M, Peter MG, Akala H, Wangui J, Liyala P, Waters NC Phytochemistry 01-Oct-2003
doi:10.1016/S0031-9422(03)00373-X
PMID:13679101
Rotenoids, isoflavones and chalcones from the stem bark of Millettia usaramensis subspecies usaramensis Abiy Yenesew, Jacob O. Midiwo, Peter G. Waterman Elsevier BV 23-Apr-2003
doi:10.1016/S0031-9422(97)00424-X

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 / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
[(E)-3-[4-[(2E)-3,7-dimethylocta-2,6-dienoxy]phenyl]prop-2-enyl] acetate 101938913 Click to see CC(=CCCC(=CCOC1=CC=C(C=C1)C=CCOC(=O)C)C)C 328.40 unknown https://doi.org/10.1016/S0031-9422(97)00424-X
3-[4-(3,7-Dimethylocta-2,6-dienoxy)phenyl]prop-2-enyl acetate 162979479 Click to see CC(=CCCC(=CCOC1=CC=C(C=C1)C=CCOC(=O)C)C)C 328.40 unknown https://doi.org/10.1016/S0031-9422(97)00424-X
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8R,8aR,9R,10R,12aS,14aR,14bR)-8a-(acetyloxymethyl)-8,9-dihydroxy-4-(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-10-(2-methylpropanoyloxy)-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4-hydroxy-3,5-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]oxane-2-carboxylic acid 100917537 Click to see CC(C)C(=O)OC1C(C2(C(CC1(C)C)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)CO)OC6C(C(C(C(O6)C(=O)O)OC7C(C(C(C(O7)CO)O)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)COC(=O)C)O 1119.20 unknown https://doi.org/10.1016/S0031-9422(97)00424-X
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
3-[1-(3,4-Dihydroxyphenyl)ethyl]-7-hydroxy-6,8-dimethoxychromen-2-one 162851266 Click to see CC(C1=CC(=C(C=C1)O)O)C2=CC3=CC(=C(C(=C3OC2=O)OC)O)OC 358.30 unknown https://doi.org/10.1016/S0031-9422(97)00424-X
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Maxima isoflavone G 5385091 Click to see COC1=CC2=C(C=C1C3=COC4=C(C3=O)C=CC(=C4)O)OCO2 312.27 unknown https://doi.org/10.1016/S0031-9422(97)00424-X
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
3-(7-Hydroxy-1,3-benzodioxol-5-yl)-8,8-dimethylpyrano[2,3-f]chromen-4-one 101938912 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC=C(C3=O)C4=CC(=C5C(=C4)OCO5)O)C 364.30 unknown https://doi.org/10.1016/S0031-9422(97)00424-X
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/10.1016/S0031-9422(03)00373-X
https://doi.org/10.1016/S0031-9422(97)00424-X
Jamaicin 12304682 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC=C(C3=O)C4=CC5=C(C=C4OC)OCO5)C 378.40 unknown https://doi.org/10.1016/S0031-9422(97)00424-X
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(1R,13R,24R)-5,7,11,14,17,19-hexaoxahexacyclo[11.11.0.02,10.04,8.015,23.016,20]tetracosa-2,4(8),9,15(23),16(20),21-hexaene-1,24-diol 73897316 Click to see C1C2C(C(C3=C(O2)C4=C(C=C3)OCO4)O)(C5=CC6=C(C=C5O1)OCO6)O 358.30 unknown https://doi.org/10.1016/S0031-9422(97)00424-X
https://doi.org/10.1016/S0031-9422(03)00373-X
(1R,14R)-14-hydroxy-7,7-dimethyl-2,8,18,20,24-pentaoxahexacyclo[12.11.0.03,12.04,9.015,23.017,21]pentacosa-3(12),4(9),5,10,15,17(21),22-heptaen-13-one 15560543 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC6=C(C=C5C4(C3=O)O)OCO6)C 394.40 unknown https://doi.org/10.1016/S0031-9422(97)00424-X
(1R,14S)-14-hydroxy-7,7-dimethyl-2,8,18,20,24-pentaoxahexacyclo[12.11.0.03,12.04,9.015,23.017,21]pentacosa-3(12),4(9),5,10,15,17(21),22-heptaen-13-one 7330544 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC6=C(C=C5C4(C3=O)O)OCO6)C 394.40 unknown https://doi.org/10.1016/S0031-9422(97)00424-X
(1S,13R)-1-hydroxy-16,17-dimethoxy-5,7,11,14-tetraoxapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-2,4(8),9,15(20),16,18-hexaen-21-one 101938910 Click to see COC1=C(C2=C(C=C1)C(=O)C3(C(O2)COC4=CC5=C(C=C43)OCO5)O)OC 372.30 unknown https://doi.org/10.1016/S0031-9422(97)00424-X
(1S,13R)-1-hydroxy-5,7,11,14,17,19-hexaoxahexacyclo[11.11.0.02,10.04,8.015,23.016,20]tetracosa-2,4(8),9,15(23),16(20),21-hexaen-24-one 73897315 Click to see C1C2C(C3=CC4=C(C=C3O1)OCO4)(C(=O)C5=C(O2)C6=C(C=C5)OCO6)O 356.30 unknown https://doi.org/10.1016/S0031-9422(97)00424-X
https://doi.org/10.1016/S0031-9422(03)00373-X
1-Hydroxy-16,17-dimethoxy-5,7,11,14-tetraoxapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-2,4(8),9,15(20),16,18-hexaen-21-one 162930624 Click to see COC1=C(C2=C(C=C1)C(=O)C3(C(O2)COC4=CC5=C(C=C43)OCO5)O)OC 372.30 unknown https://doi.org/10.1016/S0031-9422(97)00424-X
1-Hydroxy-17-methoxy-16-(3-methylbut-2-enyl)-5,7,11,14-tetraoxapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-2,4(8),9,15(20),16,18-hexaen-21-one 78201089 Click to see CC(=CCC1=C(C=CC2=C1OC3COC4=CC5=C(C=C4C3(C2=O)O)OCO5)OC)C 410.40 unknown https://doi.org/10.1016/S0031-9422(03)00373-X
1-Hydroxy-5,7,11,14,17,19-hexaoxahexacyclo[11.11.0.02,10.04,8.015,23.016,20]tetracosa-2,4(8),9,15(23),16(20),21-hexaen-24-one 162911933 Click to see C1C2C(C3=CC4=C(C=C3O1)OCO4)(C(=O)C5=C(O2)C6=C(C=C5)OCO6)O 356.30 unknown https://doi.org/10.1016/S0031-9422(97)00424-X
5,7,11,14,17,19-Hexaoxahexacyclo[11.11.0.02,10.04,8.015,23.016,20]tetracosa-2,4(8),9,15(23),16(20),21-hexaene-1,24-diol 163028784 Click to see C1C2C(C(C3=C(O2)C4=C(C=C3)OCO4)O)(C5=CC6=C(C=C5O1)OCO6)O 358.30 unknown https://doi.org/10.1016/S0031-9422(97)00424-X
Dehydromillettone 7040274 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC6=C(C=C5OC4)OCO6)C 376.40 unknown https://doi.org/10.1016/S0031-9422(03)00373-X
Millettosin 15560542 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC6=C(C=C5C4(C3=O)O)OCO6)C 394.40 unknown https://doi.org/10.1016/S0031-9422(97)00424-X
Usararotenoid C 641748 Click to see CC(=CCC1=C(C=CC2=C1OC3COC4=CC5=C(C=C4C3(C2=O)O)OCO5)OC)C 410.40 unknown https://doi.org/10.1016/S0031-9422(03)00373-X
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
(2R)-1-[4-[(2E)-3,7-dimethylocta-2,6-dienoxy]-2-hydroxyphenyl]-2-hydroxy-3-(4-hydroxyphenyl)propan-1-one 163193581 Click to see CC(=CCCC(=CCOC1=CC(=C(C=C1)C(=O)C(CC2=CC=C(C=C2)O)O)O)C)C 410.50 unknown https://doi.org/10.1016/S0031-9422(97)00424-X
1-[4-(3,7-Dimethylocta-2,6-dienoxy)-2-hydroxyphenyl]-2-hydroxy-3-(4-hydroxyphenyl)propan-1-one 162892359 Click to see CC(=CCCC(=CCOC1=CC(=C(C=C1)C(=O)C(CC2=CC=C(C=C2)O)O)O)C)C 410.50 unknown https://doi.org/10.1016/S0031-9422(97)00424-X
alpha,4,2'-Trihydroxy-4-O-geranyldihydrochalcone 42607723 Click to see CC(=CCC(=CCOC1=CC(=C(C=C1)C(=O)C(CC2=CC=C(C=C2)O)O)O)C)C 396.50 unknown https://doi.org/10.1016/S0031-9422(97)00424-X
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
4'-Geranyloxy-4,2'-dihydroxychalcone 10318361 Click to see CC(=CCCC(=CCOC1=CC(=C(C=C1)C(=O)C=CC2=CC=C(C=C2)O)O)C)C 392.50 unknown https://doi.org/10.1016/S0031-9422(97)00424-X
GU17;ISL;Isoliquiritigen 425 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1016/S0031-9422(97)00424-X
Trihydroxychalcone 638278 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1016/S0031-9422(97)00424-X

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