Tephrosia vogelii - Unknown
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Details Top

Internal ID UUID643fdd27ed513358105029
Scientific name Tephrosia vogelii
Authority Hook.f.
First published in W.J.Hooker, Niger Fl.: 296 (1849)

Description Top

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Tephrosia vogelii, also known as the Vogel's tephrosia, is a flowering plant native to tropical Africa. It has been used for centuries by farmers to deter pests and diseases, particularly on livestock. However, it is not suitable for human or livestock consumption due to its low nutritional value and potential toxicity. As a nitrogen-fixing plant, it can also be used as a source of green manure and intercropped with other plants. Tephrosia vogelii has been successfully used as an organic pesticide and has been found to be just as effective as conventional acaricides. It is adaptable to various growing conditions and can thrive in poor soils. Besides its use as a pesticide, Tephrosia vogelii has also been found to improve soil fertility and increase crop yields when intercropped with other plants. It is a cost-effective option for farmers, with seeds being sold at a low price. However, its use is limited by its toxicity to fish and its ban in certain areas due to its use as a fish poison. Overall, Tephrosia vogelii has many practical uses for farmers and is a valuable plant in tropical regions.

Synonyms Top

Scientific name Authority First published in
Cracca vogelii (Hook.f.) Kuntze Revis. Gen. Pl.1: 175 (1891)
Tephrosia periculosa Baker Bull. Misc. Inform. Kew1897: 258 (1897)
Tephrosia inebrians Welw. Apont.: 573 (1859)
Tephrosia megalantha Micheli Bull. Soc. Roy. Bot. Belgique, Compt. Rend. 36: 57 (1897)

Common names Top

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Language Common/alternative name
English vogel's tephrosia
dag bim
Kinyarwanda umurukuruku
Kinyarwanda umuruku
Vietnamese cốt khí lông vàng
Chinese 白花鐵富豆
Chinese 威氏鐵富豆
Chinese 西非灰毛豆
Chinese 白花铁富豆
Chinese 威氏铁富豆

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
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Ethiopia
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Cape Provinces
    • West Tropical Africa
      • Benin
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Mali
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Burundi
      • Cameroon
      • Central African Republic
      • Equatorial Guinea
      • Gabon
      • Gulf Of Guinea Islands
      • Rwanda
      • Zaïre
    • Western Indian Ocean
      • Comoros
      • Madagascar
  • Asia-temperate
    • China
      • China Southeast
      • Hainan
    • Eastern Asia
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • India
      • Sri Lanka
    • Indo-China
      • Thailand
    • Malesia
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea
  • Southern America
    • Brazil
      • Brazil Southeast
    • Caribbean
      • Jamaica
    • Western South America
      • Bolivia
      • Colombia
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000204544
USDA Plants TEVO2
Tropicos 13033611
INPN 721763
KEW urn:lsid:ipni.org:names:521002-1
The Plant List ild-5085
Open Tree Of Life 92899
NCBI Taxonomy 1157238
IUCN Red List 146197294
IPNI 521002-1
iNaturalist 280795
GBIF 5342354
Freebase /m/0fq14w1
EPPO TEPVO
EOL 688978
USDA GRIN 80185
Wikipedia Tephrosia_vogelii
CMAUP NPO26213

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 Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Higher Plant-Derived Biostimulants: Mechanisms of Action and Their Role in Mitigating Plant Abiotic Stress Martínez-Lorente SE, Martí-Guillén JM, Pedreño MÁ, Almagro L, Sabater-Jara AB Antioxidants (Basel) 06-Mar-2024
PMCID:PMC10967762
doi:10.3390/antiox13030318
PMID:38539851
Targeting oxidative stress with natural products: A novel strategy for esophageal cancer therapy Cao F, Zhang HL, Guo C, Xu XL, Yuan Q World J Gastrointest Oncol 15-Feb-2024
PMCID:PMC10900143
doi:10.4251/wjgo.v16.i2.287
PMID:38425393
Pest categorisation of Pratylenchus loosi Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Migheli Q, Vloutoglou I, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 16-Jan-2024
PMCID:PMC10790189
doi:10.2903/j.efsa.2024.8548
PMID:38229874
NopAA and NopD Signaling Association-Related Gene GmNAC27 Promotes Nodulation in Soybean (Glycine max) Wang Y, Jia X, Li Y, Ma S, Ma C, Xin D, Wang J, Chen Q, Liu C Int J Mol Sci 15-Dec-2023
PMCID:PMC10744329
doi:10.3390/ijms242417498
PMID:38139327
Ethnomedicinal Knowledge of Plants Used in Nonconventional Medicine in the Management of Diabetes Mellitus in Kinshasa (Democratic Republic of the Congo) Chiribagula Valentin B, Ndjolo Philippe O, Mboni Henry M, Mushagalusa Kasali F Evid Based Complement Alternat Med 20-Sep-2023
PMCID:PMC10533323
doi:10.1155/2023/4621883
PMID:37771953
G-type receptor-like kinase AsNIP43 interacts with rhizobia effector nodulation outer protein P and is required for symbiosis Liu Y, Lin Y, Wei F, Lv Y, Xie F, Chen D, Lin H, Li Y Plant Physiol 11-Jul-2023
PMCID:PMC10517198
doi:10.1093/plphys/kiad318
PMID:37432453
A comparison of the attractiveness of flowering plant blossoms versus attractive targeted sugar baits (ATSBs) in western Kenya Yalla N, Polo B, McDermott DP, Kosgei J, Omondi S, Agumba S, Moshi V, Abong’o B, Gimnig JE, Harris AF, Entwistle J, Long PR, Ochomo E PLoS One 06-Jun-2023
PMCID:PMC10243617
doi:10.1371/journal.pone.0286679
PMID:37279239
Nanoemulsions of terpene by-products from cannabidiol production have promising insecticidal effect on Callosobruchusmaculatus Fei T, Gwinn K, Leyva-Gutierrez FM, Wang T Heliyon 01-Apr-2023
PMCID:PMC10121836
doi:10.1016/j.heliyon.2023.e15101
PMID:37095909
Exploring Knowledge about Fang Traditional Medicine: An Informal Health Seeking Behaviour for Medical or Cultural Afflictions in Equatorial Guinea Jimenez-Fernandez R, Rodriguez Vázquez R, Marín-Morales D, Herraiz-Soria E, Losa-Iglesias ME, Becerro-de-Bengoa-Vallejo R, Corral-Liria I Healthcare (Basel) 09-Mar-2023
PMCID:PMC10048063
doi:10.3390/healthcare11060808
PMID:36981465
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
Smallholders’ knowledge about healing goat gastrointestinal parasite infections with wild plants in southern DR Congo Mavungu GN, Mutombo CS, Numbi DM, Nsenga SN, Muyumba WN, Pongombo CS, Bakari SA, Nachtergael A, Vandenput S, Okombe VE, Duez P Front Pharmacol 01-Mar-2023
PMCID:PMC10016610
doi:10.3389/fphar.2023.1124267
PMID:36937835
Phytochemicals as alternative fungicides for controlling plant diseases: A comprehensive review of their efficacy, commercial representatives, advantages, challenges for adoption, and possible solutions Deresa EM, Diriba TF Heliyon 17-Feb-2023
PMCID:PMC9984788
doi:10.1016/j.heliyon.2023.e13810
PMID:36879959
Therapeutic Potential of Phenolic Compounds in Medicinal Plants—Natural Health Products for Human Health Sun W, Shahrajabian MH Molecules 15-Feb-2023
PMCID:PMC9960276
doi:10.3390/molecules28041845
PMID:36838831
Traditional knowledge of plants used in hunting and fishing practices among Baka hunter-gatherers of eastern Cameroon Fongnzossie EF, Ngansop MT, Oishi T, Biwole AB, Biye EH, Ichikawa M J Ethnobiol Ethnomed 03-Jan-2023
PMCID:PMC9808952
doi:10.1186/s13002-022-00571-3
PMID:36597154

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
> Benzenoids / Phenol ethers / Anisoles
1,2,3-Trimethoxybenzene 12462 Click to see COC1=C(C(=CC=C1)OC)OC 168.19 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
[(2S,3R,4R)-2-(4-hydroxy-3-methoxyphenyl)-4-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-3-yl]methyl octadecanoate 102280073 Click to see CCCCCCCCCCCCCCCCCC(=O)OCC1C(COC1C2=CC(=C(C=C2)O)OC)CC3=CC(=C(C=C3)O)OC 626.90 unknown https://doi.org/10.1002/HLCA.200800272
[2-(4-Hydroxy-3-methoxyphenyl)-4-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-3-yl]methyl octadecanoate 162900406 Click to see CCCCCCCCCCCCCCCCCC(=O)OCC1C(COC1C2=CC(=C(C=C2)O)OC)CC3=CC(=C(C=C3)O)OC 626.90 unknown https://doi.org/10.1002/HLCA.200800272
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(3aS,4S,5S,8S,8aR)-8-methyl-3-methylidene-5-propan-2-yl-2,3a,4,6,7,8a-hexahydro-1H-azulene-4,5,8-triol 163070621 Click to see CC(C)C1(CCC(C2CCC(=C)C2C1O)(C)O)O 254.36 unknown https://doi.org/10.1002/HLCA.200800272
8-methyl-3-methylidene-5-propan-2-yl-2,3a,4,6,7,8a-hexahydro-1H-azulene-4,5,8-triol 163070620 Click to see CC(C)C1(CCC(C2CCC(=C)C2C1O)(C)O)O 254.36 unknown https://doi.org/10.1002/HLCA.200800272
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
3beta-(2-O-beta-D-Galactopyranosyl-beta-D-glucurono pyranosyloxy)olean-12-en-28-oic acid 101923141 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1)C)C(=O)O)C 795.00 unknown via CMAUP database
Araloside A 10079497 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)OC7C(C(C(O7)CO)O)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C 927.10 unknown via CMAUP database
Calenduloside E 176079 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C)C2C1)C)C(=O)O)C 632.80 unknown via CMAUP database
Calenduloside F 13909684 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C 795.00 unknown via CMAUP database
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylate 21669007 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)OC)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C 971.10 unknown via CMAUP database
Narcissiflorine 162878 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)OC7C(C(C(O7)CO)O)O)O)O)C)C)C2C1)C)C(=O)O)C 764.90 unknown via CMAUP database
Papyrioside LE 11803947 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC6(C(=CCC7C6(CCC8C7(CCC(C8(C)C)O)C)C)C4CC(C(=O)C5)(C)C)C)O)O)O)CO)O)O)O 941.10 unknown via CMAUP database
Papyrioside LF 10819773 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC6(C(=CCC7C6(CCC8C7(CCC(C8(C)C)O)C)C)C4CC(C(=O)C5)(C)C)C)O)O)O)COC(=O)C)O)O)O 983.10 unknown via CMAUP database
Scheffleraside II 101720880 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(C(O9)C(=O)O)O)O)O)C)(C)C)O)O)O)CO)O)O)O 1103.20 unknown via CMAUP database
Udosaponin B 21635582 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C 957.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-2,2,6a,6b,9,9,12a-heptamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 13878127 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)O)O)C)C)C2C1)C)C(=O)O)C 588.80 unknown via CMAUP database
3-Epipapyriogenin C 16112782 Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC2(CC1=O)C(=O)O)C)C)(C)C)O)C)C 468.70 unknown via CMAUP database
3-O-alpha-L-Arabinopyranosylechinocystic acid 15379012 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(CO6)O)O)O)C)C(=O)O)C 604.80 unknown via CMAUP database
3alpha,21beta,22alpha-Trihydroxyoleana-11,13(18)-diene-28-oic acid 16112781 Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1O)O)C(=O)O)C)C)(C)C)O)C)C 486.70 unknown via CMAUP database
Guaianin N 10395290 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1)C)C(=O)O)C 751.00 unknown via CMAUP database
Papyriogenin A 3081523 Click to see CC1(CC2=C3C=CC4C5(CCC(=O)C(C5CCC4(C3(CCC2(CC1=O)C(=O)O)C)C)(C)C)C)C 466.70 unknown via CMAUP database
Papyriogenin C 3081568 Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC2(CC1=O)C(=O)O)C)C)(C)C)O)C)C 468.70 unknown via CMAUP database
Papyriogenin D 101277260 Click to see CC1(CC2=C3C=CC4C5(CCC(=O)C(C5CCC4(C3(CCC2(CC1O)C(=O)O)C)C)(C)C)C)C 468.70 unknown via CMAUP database
Papyriogenin E 101277261 Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC2(CC1O)C(=O)O)C)C)(C)C)O)C)C 470.70 unknown via CMAUP database
Papyriogenin F 102239749 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC1=O)C(=O)O)C)C)(C)C)O)C)C 470.70 unknown via CMAUP database
Papyrioside LG 10605857 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC6(C(=CC=C7C6(CCC8C7(CCC(C8(C)C)O)C)C)C4CC(C(=O)C5)(C)C)C)O)O)O)CO)O)O)O 939.10 unknown via CMAUP database
Papyrioside LH 10748397 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC6(C(=CC=C7C6(CCC8C7(CCC(=O)C8(C)C)C)C)C4CC(C(=O)C5)(C)C)C)O)O)O)CO)O)O)O 937.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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 via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
28-Noroleana-11,13(18),17(22)-triene-3,21-dione 102588576 Click to see CC1(CC2=C3C=CC4C5(CCC(=O)C(C5CCC4(C3(CCC2=CC1=O)C)C)(C)C)C)C 420.60 unknown via CMAUP database
3alpha-Hydroxy-28-noroleana-11,13(18),17(22)-triene-21-one 102588575 Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC2=CC1=O)C)C)(C)C)O)C)C 422.60 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
1-Benzofuran-5-carbaldehyde 2773875 Click to see C1=CC2=C(C=CO2)C=C1C=O 146.14 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
praecansone B 10090306 Click to see CC1(C=CC2=C(C(=C(C=C2O1)OC)C(=O)C=C(C3=CC=CC=C3)O)OC)C 366.40 unknown https://doi.org/10.1016/S0031-9422(02)00078-X
> Organoheterocyclic compounds / Lactones / Beta propiolactones
Papyriogenin G 101967008 Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC26C(C1O)OC6=O)C)C)(C)C)O)C)C 468.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / 3,4-dihydrocoumarins
3,4-Dihydrocoumarin 660 Click to see C1CC(=O)OC2=CC=CC=C21 148.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
Phenylallyl alcohol 308 Click to see C1=CC=C(C=C1)C=CCO 134.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see C1=CC=C2C(=C1)C=CC(=O)O2 146.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Kaempferol 3,4',7-triacetate 44584293 Click to see CC(=O)OC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC(=O)C)O)OC(=O)C 412.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 5317847 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown https://doi.org/10.1016/S0031-9422(00)83511-6
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(00)83511-6
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(00)83511-6
Afzelin 5316673 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown via CMAUP database
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/S0031-9422(00)83511-6
Reynoutrin 5878729 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown https://doi.org/10.1016/S0031-9422(00)83511-6
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/S0031-9422(00)83511-6
Vitamin P 5293655 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/S0031-9422(00)83511-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
kaempferol 7-O-(2-E-p-coumaroyl-alpha-L-rhamnopyranoside) 11678667 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)OC(=O)C=CC5=CC=C(C=C5)O)O)O 578.50 unknown via CMAUP database
kaempferol 7-O-(2,3-di-E-p-coumaroyl-alpha-L-rhamnopyranoside) 11607311 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)OC(=O)C=CC5=CC=C(C=C5)O)OC(=O)C=CC6=CC=C(C=C6)O)O 724.70 unknown via CMAUP database
> 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 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(80)87050-6
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(80)87050-6
> 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/10.1016/S0031-9422(00)90838-0
https://doi.org/10.1002/ARDP.19322700609
https://doi.org/10.1016/S0031-9422(00)83511-6
(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/10.1016/S0031-9422(00)83511-6
https://doi.org/10.1016/S0031-9422(00)90838-0
https://doi.org/10.1002/ARDP.19322700609
3H-Bis(1)benzopyrano(3,4-b:6',5'-e)pyran-7(7aH)-one, 13,13a-dihydro-7a-hydroxy-9,10-dimethoxy-3,3-dimethyl-, (7aS-cis)- 184228 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/10.1002/ARDP.19322700609
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/S0031-9422(00)90838-0
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/S0031-9422(00)90838-0
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/10.1016/S0031-9422(00)83511-6
https://doi.org/10.1039/C39860000353
https://doi.org/10.1039/C39860000352
https://doi.org/10.1016/S0031-9422(00)90838-0
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/10.1002/ARDP.19352730102
rel-(7aR,13aR)-9,10-Dimethoxy-3,3-dimethyl-13,13a-dihydro-3H-pyrano[2,3-c:6,5-f']dichromen-7(7aH)-one 184223 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/10.1002/ARDP.19322700609
Rotenolon II 99189 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/S0031-9422(00)90838-0
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/S0031-9422(00)90838-0
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/S0031-9422(00)90838-0
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/10.1016/S0031-9422(00)83511-6
https://doi.org/10.1016/S0031-9422(00)90838-0

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