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Markhamia lutea

Markhamia lutea - 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 UUID6440274677d80017630493
Scientific name Markhamia lutea
Authority K.Schum.
First published in Nat. Pflanzenfam. 4(3b): 242 (1895)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Muenteria lutea Seem. J. Bot. 8: 211 (1870)
Markhamia platycalyx Sprague Hooker's Icon. Pl. 28: t. 2800 (1905)
Markhamia hildebrandtii Sprague Hooker's Icon. Pl. 28: t. 2800 (1905)
Spathodea lutea Benth. Niger Fl. : 461 (1849)
Dolichandrone hildebrandtii Baker Bull. Misc. Inform. Kew 1894: 31 (1894)
Dolichandrone lutea (Benth.) Benth. & Hook.f. ex B.D.Jacks. Index Kew. 1: 785 (1893)
Dolichandrone platycalyx Baker Bull. Misc. Inform. Kew 1894: 30 (1894)

Common names Top

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Language Common/alternative name
English siala
Finnish kameruninputkitrumpetti
Hebrew מרקמיה צהובה
Italian albero siala
Italian tromba del nilo
Italian tulipano del nilo
Japanese マーカミア・ルテア

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
      • Sudan
    • West Tropical Africa
      • Ghana
      • Ivory Coast
      • Nigeria
      • Togo
    • West-central Tropical Africa
      • Burundi
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Gulf Of Guinea Islands
      • Rwanda
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000779039
USDA Plants MALU4
Tropicos 3701602
KEW urn:lsid:ipni.org:names:110020-1
The Plant List kew-317580
Open Tree Of Life 5145156
NCBI Taxonomy 1548301
IUCN Red List 144259403
IPNI 110020-1
iNaturalist 431279
GBIF 5668625
Freebase /m/0kmhjvj
EPPO MKMLU
USDA GRIN 105224
Wikipedia Markhamia_lutea

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
Diversity and Distribution of Avifauna in the Northeast of Addis Ababa, Central Ethiopia Desalegn T, Abebe B ScientificWorldJournal 18-Apr-2024
PMCID:PMC11045286
doi:10.1155/2024/5592074
PMID:38665230
A comprehensive review of antimalarial medicinal plants used by Tanzanians Kacholi DS Pharm Biol 25-Jan-2024
PMCID:PMC10812860
doi:10.1080/13880209.2024.2305453
PMID:38270178
Ethnobotanical study of medicinal plants used by the people of Mosop, Nandi County in Kenya Maiyo ZC, Njeru SN, Toroitich FJ, Indieka SA, Obonyo MA Front Pharmacol 19-Jan-2024
PMCID:PMC10834697
doi:10.3389/fphar.2023.1328903
PMID:38313073
Critical Review on the Use of Extractives of Naturally Durable Woods as Natural Wood Protectants Kirker GT, Hassan B, Mankowski ME, Eller FJ Insects 18-Jan-2024
PMCID:PMC10816604
doi:10.3390/insects15010069
PMID:38249075
Pest categorisation of Diaprepes abbreviatus Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 15-Nov-2023
PMCID:PMC10648563
doi:10.2903/j.efsa.2023.8318
PMID:38027434
Chimpanzees select comfortable nesting tree species Lacroux C, Krief S, Douady S, Cornette R, Durand S, Aleeje A, Asalu E, Pouydebat E Sci Rep 07-Oct-2023
PMCID:PMC10560204
doi:10.1038/s41598-023-44192-6
PMID:37805595
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
Assessing plant diversity change in logged and unlogged dense semi-deciduous production forest of eastern Cameroon Hubert Kpoumie Mounmemi, Mensah Ekué MR, Funwi Preasious Forbi, Roger Kabelong Banoho LP, Tiokeng B, Maffo Maffo NL, Lagarde Jean Betti, Carole Mireil Votio Tchoupou, Amandine Flore Yonkeu Ntonmen, Taedoumg HE, Zapfack L Heliyon 12-May-2023
PMCID:PMC10199262
doi:10.1016/j.heliyon.2023.e16199
PMID:37215910
Contrasting warming responses of photosynthesis in early- and late-successional tropical trees Mujawamariya M, Wittemann M, Dusenge ME, Manishimwe A, Ntirugulirwa B, Zibera E, Nsabimana D, Wallin G, Uddling J Tree Physiol 27-Mar-2023
PMCID:PMC10335848
doi:10.1093/treephys/tpad035
PMID:36971469
A review of efficacy and safety of Ugandan anti-malarial plants with application of RITAM score Angupale JR, Tusiimire J, Ngwuluka NC Malar J 17-Mar-2023
PMCID:PMC10021060
doi:10.1186/s12936-023-04486-6
PMID:36932389
Tree species composition along environmental and disturbance gradients in tropical sub-montane forests, Tanzania Lolila NJ, Shirima DD, Mauya EW PLoS One 08-Mar-2023
PMCID:PMC9994703
doi:10.1371/journal.pone.0282528
PMID:36888683
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
Adoption of novel climate-smart farming systems for enhanced carbon stock and carbon dioxide equivalent emission reduction in cattle corridor areas of Uganda Fatumah N, Mohammed S, Ashraf N, Abasi K, Shadia N Heliyon 26-Feb-2023
PMCID:PMC10008977
doi:10.1016/j.heliyon.2023.e14114
PMID:36923883
Multi-Step In Silico Discovery of Natural Drugs against COVID-19 Targeting Main Protease Elkaeed EB, Youssef FS, Eissa IH, Elkady H, Alsfouk AA, Ashour ML, El Hassab MA, Abou-Seri SM, Metwaly AM Int J Mol Sci 21-Jun-2022
PMCID:PMC9266348
doi:10.3390/ijms23136912
PMID:35805916
Ethnomedicinal, Phytochemical and Pharmacological Investigations of Tetradenia riparia (Hochst.) Codd (Lamiaceae) Panda SK, Gazim ZC, Swain SS, Bento MC, Sena JD, Mukazayire MJ, Van Puyvelde L, Luyten W Front Pharmacol 02-Jun-2022
PMCID:PMC9201335
doi:10.3389/fphar.2022.896078
PMID:35721148

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
> Benzenoids / Naphthalenes / Naphthoquinones
Lapachol 3884 Click to see CC(=CCC1=C(C2=CC=CC=C2C(=O)C1=O)O)C 242.27 unknown https://doi.org/10.1021/NP50037A031
> Lignans, neolignans and related compounds / Furanoid lignans
(+)-Paulownin 3321512 Click to see C1C2C(OCC2(C(O1)C3=CC4=C(C=C3)OCO4)O)C5=CC6=C(C=C5)OCO6 370.40 unknown https://doi.org/10.1021/NP50037A031
Paulownin 3084131 Click to see C1C2C(OCC2(C(O1)C3=CC4=C(C=C3)OCO4)O)C5=CC6=C(C=C5)OCO6 370.40 unknown https://doi.org/10.1021/NP50037A031
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1021/NP50037A031
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
2-Epitormentic acid 490364 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.020
Arjunic Acid 15385516 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1O)C)C(=O)O)C 488.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.020
CID 21325844 21325844 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1O)C)C(=O)O)C 488.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.020
Jacarandic acid 13653335 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.020
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3S,4S,6S,7S,8R,11S,12S,15R,16R)-15-[(2R,5R)-5-hydroperoxy-6-methylhept-6-en-2-yl]-4-hydroxy-7,12,16-trimethyl-6-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxypentacyclo[9.7.0.01,3.03,8.012,16]octadecane-7-carboxylic acid 163030558 Click to see CC(CCC(C(=C)C)OO)C1CCC2(C1(CCC34C2CCC5C3(C4)C(CC(C5(C)C(=O)O)OC6C(C(C(CO6)O)O)O)O)C)C 636.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.020
(1S,3S,4S,6S,7S,8R,11S,12S,15R,16R)-15-[(2R,5R)-5-hydroperoxy-6-methylhept-6-en-2-yl]-4,6-dihydroxy-7,12,16-trimethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecane-7-carboxylic acid 162927598 Click to see CC(CCC(C(=C)C)OO)C1CCC2(C1(CCC34C2CCC5C3(C4)C(CC(C5(C)C(=O)O)O)O)C)C 504.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.020
(1S,3S,4S,6S,7S,8R,11S,12S,15R,16R)-15-[(2R)-5-hydroperoxy-6-methylhept-6-en-2-yl]-4,6-dihydroxy-7,12,16-trimethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecane-7-carboxylic acid 44472194 Click to see CC(CCC(C(=C)C)OO)C1CCC2(C1(CCC34C2CCC5C3(C4)C(CC(C5(C)C(=O)O)O)O)C)C 504.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.020
(1S,3S,4S,6S,7S,8R,11S,12S,15R,16R)-15-[(E,2R)-6-hydroperoxy-6-methylhept-4-en-2-yl]-4,6-dihydroxy-7,12,16-trimethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecane-7-carboxylic acid 44472304 Click to see CC(CC=CC(C)(C)OO)C1CCC2(C1(CCC34C2CCC5C3(C4)C(CC(C5(C)C(=O)O)O)O)C)C 504.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.020
(1S,3S,4S,6S,7S,8R,11S,12S,15R,16R)-4-hydroxy-7,12,16-trimethyl-15-[(2R)-6-methyl-5-oxohept-6-en-2-yl]-6-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxypentacyclo[9.7.0.01,3.03,8.012,16]octadecane-7-carboxylic acid 162971036 Click to see CC(CCC(=O)C(=C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)C(CC(C5(C)C(=O)O)OC6C(C(C(CO6)O)O)O)O)C)C 618.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.020
(1S,3S,4S,6S,7S,8R,11S,12S,15R,16R)-4,6-dihydroxy-7,12,16-trimethyl-15-[(2R)-6-methyl-5-oxohept-6-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecane-7-carboxylic acid 44472305 Click to see CC(CCC(=O)C(=C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)C(CC(C5(C)C(=O)O)O)O)C)C 486.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.020
15-(5-Hydroperoxy-6-methylhept-6-en-2-yl)-4-hydroxy-7,12,16-trimethyl-6-(3,4,5-trihydroxyoxan-2-yl)oxypentacyclo[9.7.0.01,3.03,8.012,16]octadecane-7-carboxylic acid 163030557 Click to see CC(CCC(C(=C)C)OO)C1CCC2(C1(CCC34C2CCC5C3(C4)C(CC(C5(C)C(=O)O)OC6C(C(C(CO6)O)O)O)O)C)C 636.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.020
15-(5-Hydroperoxy-6-methylhept-6-en-2-yl)-4,6-dihydroxy-7,12,16-trimethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecane-7-carboxylic acid 162927597 Click to see CC(CCC(C(=C)C)OO)C1CCC2(C1(CCC34C2CCC5C3(C4)C(CC(C5(C)C(=O)O)O)O)C)C 504.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.020
15-(6-Hydroperoxy-6-methylhept-4-en-2-yl)-4,6-dihydroxy-7,12,16-trimethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecane-7-carboxylic acid 162870269 Click to see CC(CC=CC(C)(C)OO)C1CCC2(C1(CCC34C2CCC5C3(C4)C(CC(C5(C)C(=O)O)O)O)C)C 504.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.020
4-Hydroxy-7,12,16-trimethyl-15-(6-methyl-5-oxohept-6-en-2-yl)-6-(3,4,5-trihydroxyoxan-2-yl)oxypentacyclo[9.7.0.01,3.03,8.012,16]octadecane-7-carboxylic acid 162971035 Click to see CC(CCC(=O)C(=C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)C(CC(C5(C)C(=O)O)OC6C(C(C(CO6)O)O)O)O)C)C 618.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.020
4,6-Dihydroxy-7,12,16-trimethyl-15-(6-methyl-5-oxohept-6-en-2-yl)pentacyclo[9.7.0.01,3.03,8.012,16]octadecane-7-carboxylic acid 162900151 Click to see CC(CCC(=O)C(=C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)C(CC(C5(C)C(=O)O)O)O)C)C 486.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.020
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
(1S,3S,4S,6S,7S,8R,11S,12S,15R,16R)-15-[(E,2R)-6-hydroperoxy-6-methylhept-4-en-2-yl]-4-hydroxy-7,12,16-trimethyl-6-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxypentacyclo[9.7.0.01,3.03,8.012,16]octadecane-7-carboxylic acid 163089346 Click to see CC(CC=CC(C)(C)OO)C1CCC2(C1(CCC34C2CCC5C3(C4)C(CC(C5(C)C(=O)O)OC6C(C(C(CO6)O)O)O)O)C)C 636.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.020
15-(6-Hydroperoxy-6-methylhept-4-en-2-yl)-4-hydroxy-7,12,16-trimethyl-6-(3,4,5-trihydroxyoxan-2-yl)oxypentacyclo[9.7.0.01,3.03,8.012,16]octadecane-7-carboxylic acid 163089345 Click to see CC(CC=CC(C)(C)OO)C1CCC2(C1(CCC34C2CCC5C3(C4)C(CC(C5(C)C(=O)O)OC6C(C(C(CO6)O)O)O)O)C)C 636.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.020
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.020
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.020
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1021/NP50037A031
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
[(2R,3R,4S,5R,6R)-3,5-diacetyloxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-4-[(2S,3R,4R,5S,6S)-3,4,5-triacetyloxy-6-methyloxan-2-yl]oxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 10700689 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 834.80 unknown https://doi.org/10.1021/NP9703914
[(2R,3R,4S,5R,6R)-5-acetyloxy-2-(acetyloxymethyl)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-4-[(2S,3R,4R,5S,6S)-3,4,5-triacetyloxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 10605522 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C)OCCC3=CC(=C(C=C3)O)O)COC(=O)C)OC(=O)C=CC4=CC(=C(C=C4)O)O)OC(=O)C)OC(=O)C)OC(=O)C 834.80 unknown https://doi.org/10.1021/NP9703914
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[(2R,3R,4S,5R,6R)-2-(acetyloxymethyl)-5-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 155545808 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(CO3)(CO)O)O)OCCC4=CC(=C(C=C4)O)O)COC(=O)C)OC(=O)C=CC5=CC(=C(C=C5)O)O)O)O)O 798.70 unknown https://doi.org/10.1021/NP9703914
[(2R,3R,4S,5R,6R)-5-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3-hydroxy-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 154496940 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(CO3)(CO)O)O)OCCC4=CC(=C(C=C4)O)O)COC(=O)C=CC5=CC(=C(C=C5)O)O)O)O)O)O 756.70 unknown https://doi.org/10.1021/NP9703914
[(2R,3R,4S,5R,6R)-5-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3-hydroxy-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 10605213 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(CO3)(CO)O)O)OCCC4=CC(=C(C=C4)O)O)COC(=O)C=CC5=CC(=C(C=C5)O)OC)O)O)O)O 770.70 unknown https://doi.org/10.1021/NP9703914
Luteoside A 10629144 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(CO3)(CO)O)O)OCCC4=CC(=C(C=C4)O)O)COC(=O)C)OC(=O)C=CC5=CC(=C(C=C5)O)O)O)O)O 798.70 unknown https://doi.org/10.1021/NP9703914
Luteoside B 10818886 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(CO3)(CO)O)O)OCCC4=CC(=C(C=C4)O)O)COC(=O)C=CC5=CC(=C(C=C5)O)O)O)O)O)O 756.70 unknown https://doi.org/10.1021/NP9703914
Luteoside C 10723884 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(CO3)(CO)O)O)OCCC4=CC(=C(C=C4)O)O)COC(=O)C=CC5=CC(=C(C=C5)O)OC)O)O)O)O 770.70 unknown https://doi.org/10.1021/NP9703914
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
beta-Lapachone 3885 Click to see CC1(CCC2=C(O1)C3=CC=CC=C3C(=O)C2=O)C 242.27 unknown https://doi.org/10.1021/NP50037A031
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 154496101 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1021/NP9703914
{6-[2-(3,4-Dihydroxyphenyl)ethoxy]-3,5-dihydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 73323377 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1021/NP9703914
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]-beta-D-glucopyranoside 132274946 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1021/NP9703914
Acteoside;Kusaginin;TJC160 354009 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1021/NP9703914
Isoacteoside 6476333 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1021/NP9703914
Isoverbascoside Noaacetate 10796065 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C)OCCC3=CC(=C(C=C3)OC(=O)C)OC(=O)C)COC(=O)C=CC4=CC(=C(C=C4)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 1002.90 unknown https://doi.org/10.1021/NP9703914
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1021/NP9703914
Verbascoside Nonaacetate 9897969 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C)OCCC3=CC(=C(C=C3)OC(=O)C)OC(=O)C)COC(=O)C)OC(=O)C=CC4=CC(=C(C=C4)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 1002.90 unknown https://doi.org/10.1021/NP9703914

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