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Afrocarpus gracilior

Afrocarpus gracilior - 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 UUID644007bee98b7094290680
Scientific name Afrocarpus gracilior
Authority (Pilg.) C.N.Page
First published in Notes Roy. Bot. Gard. Edinburgh 45: 383 (1988 publ. 1989)

Description Top

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Afrocarpus gracilior is a species of coniferous tree in the family Podocarpaceae, native to eastern Africa. It is a medium-sized tree, growing 20-40 m tall, with a trunk diameter of 50-80 cm. The leaves are spirally arranged, lanceolate, 2-6 cm long and 3-5 mm broad on mature trees. The seed cones are highly modified, with a single 2 cm diameter seed with a thin fleshy coating. It is an important timber tree in its native range, where it is harvested for local use and export, and is also grown in plantations elsewhere in the world. It is also cultivated as an ornamental tree, and planted as a shade tree. It is a common species found in many types of tropical mountain forest habitat, and is a dominant species in some areas. Nevertheless, it may be in slow decline due to deforestation and logging.

Synonyms Top

Scientific name Authority First published in
Nageia falcata var. gracilior (Pilg.) Silba J. Int. Conifer Preserv. Soc. 7: 27 (2000)
Podocarpus gracilior Pilg. Pflanzenr. , IV, 5: 71 (1903)
Decussocarpus gracilior (Pilg.) de Laub. J. Arnold Arbor. 50: 359 (1969)
Afrocarpus falcatus subsp. gracilior (Pilg.) Silba J. Int. Conifer Preserv. Soc. 17: 21 (2010)

Common names Top

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Language Common/alternative name
English east african yellowwood
Afrikaans oos-afrikaanse geelhout
German schlankes afrogelbholz
Persian چوبزرد شرق آفریقا
Japanese アフリカマキ
Chinese 细叶非洲杉

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
      • Eritrea
      • Ethiopia
      • Sudan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000522642
Tropicos 25600066
KEW urn:lsid:ipni.org:names:946474-1
The Plant List kew-2624886
Missouri Botanical Garden 252993
Open Tree Of Life 875161
NCBI Taxonomy 165205
IUCN Red List 42439
IPNI 946474-1
iNaturalist 135424
GBIF 2687628
Freebase /m/026v3q5
EPPO PODGR
EOL 1033605
USDA GRIN 417624
Wikipedia Afrocarpus_gracilior
CMAUP NPO28741

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
Proteomics and metabolomics analyses of camptothecin-producing Aspergillus terreus reveal the integration of PH domain-containing proteins and peptidylprolyl cis/trans isomerase in restoring the camptothecin biosynthesis Rady AM, El-Sayed AS, El-Baz AF, Abdel-Fattah GG, Magdeldin S, Ahmed E, Osama A, Hassanein SE, Saed H, Yassin M Microbiol Spectr 19-Oct-2023
PMCID:PMC10714794
doi:10.1128/spectrum.02281-23
PMID:37855596
Way to efficient microbial paclitaxel mass production Li C, Qi Y, Sun Z, Jiang M, Li C Synth Syst Biotechnol 19-Oct-2023
PMCID:PMC10632112
doi:10.1016/j.synbio.2023.10.002
PMID:37954482
Phytochemical and metabolic profiling of the different Podocarpus species in Egypt: Potential antimicrobial and antiproliferative activities Mohamed NZ, Shaaban L, Safan S, El-Sayed AS Heliyon 09-Sep-2023
PMCID:PMC10559778
doi:10.1016/j.heliyon.2023.e20034
PMID:37810029
Perplexing Polyphenolics: The Isolations, Syntheses, Reappraisals, and Bioactivities of Flavonoids, Isoflavonoids, and Neoflavonoids from 2016 to 2022 Umer SM, Shamim S, Khan KM, Saleem RS Life (Basel) 09-Mar-2023
PMCID:PMC10058313
doi:10.3390/life13030736
PMID:36983891
Diversity, Distribution, Systematics and Conservation Status of Podocarpaceae Khan R, Hill RS, Liu J, Biffin E Plants (Basel) 03-Mar-2023
PMCID:PMC10005643
doi:10.3390/plants12051171
PMID:36904033
Arthropod Ectoparasites of Two Rodent Species Occurring in Varied Elevations on Tanzania’s Second Highest Mountain Gebrezgiher GB, Makundi RH, Katakweba AA, Belmain SR, Lyimo CM, Meheretu Y Biology (Basel) 02-Mar-2023
PMCID:PMC10045264
doi:10.3390/biology12030394
PMID:36979086
No cell is an island: characterising the leaf epidermis using epidermalmorph, a new R package Brown MJ, Jordan GJ New Phytol 15-Nov-2022
PMCID:PMC10098627
doi:10.1111/nph.18519
PMID:36205061
A Review on Medicinal Plants Used in the Management of Respiratory Problems in Ethiopia over a Twenty-Year Period (2000–2021) Haile AA, Tsegay BA, Seid A, Adnew W, Moges A Evid Based Complement Alternat Med 27-Jun-2022
PMCID:PMC9252637
doi:10.1155/2022/2935015
PMID:35795271
Endophytic Fungi: Key Insights, Emerging Prospects, and Challenges in Natural Product Drug Discovery Tiwari P, Bae H Microorganisms 04-Feb-2022
PMCID:PMC8876476
doi:10.3390/microorganisms10020360
PMID:35208814
Current Practices for Reference Gene Selection in RT-qPCR of Aspergillus: Outlook and Recommendations for the Future Archer M, Xu J Genes (Basel) 24-Jun-2021
PMCID:PMC8307107
doi:10.3390/genes12070960
PMID:34202507
Candidate Anti-COVID-19 Medicinal Plants from Ethiopia: A Review of Plants Traditionally Used to Treat Viral Diseases Tegen D, Dessie K, Damtie D Evid Based Complement Alternat Med 04-Jun-2021
PMCID:PMC8219417
doi:10.1155/2021/6622410
PMID:34221083
Production, bioprocess optimization and γ-irradiation of Penicillium polonicum, as a new Taxol producing endophyte from Ginko biloba Abdel-Fatah SS, El-Batal AI, El-Sherbiny GM, Khalaf MA, El-Sayed AS Biotechnol Rep (Amst) 24-Apr-2021
PMCID:PMC8120861
doi:10.1016/j.btre.2021.e00623
PMID:34026575
Deep learning approaches for natural product discovery from plant endophytic microbiomes Aghdam SA, Brown AM Environ Microbiome 18-Mar-2021
PMCID:PMC7972023
doi:10.1186/s40793-021-00375-0
PMID:33758794
Plant associated fungal endophytes as a source of natural bioactive compounds Rai N, Kumari Keshri P, Verma A, Kamble SC, Mishra P, Barik S, Kumar Singh S, Gautam V Mycology 27-Jan-2021
PMCID:PMC8451683
doi:10.1080/21501203.2020.1870579
PMID:34552808
A Compressive Review about Taxol®: History and Future Challenges Gallego-Jara J, Lozano-Terol G, Sola-Martínez RA, Cánovas-Díaz M, de Diego Puente T Molecules 17-Dec-2020
PMCID:PMC7767101
doi:10.3390/molecules25245986
PMID:33348838

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Triacontane 12535 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 422.80 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan lactones
9-Hydroxy-5-(3,4,5-trimethoxyphenyl)-3,5,5a,8,8a,9-hexahydro-[2]benzofuro[6,5-f][1,2]benzodioxol-6-one 45358776 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=C2C=C5COOC5=C4)O 414.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Byzantionoside B 14135395 Click to see CC1=CC(=O)CC(C1CCC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C 372.50 unknown https://doi.org/10.1016/J.PHYTOL.2012.02.005
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexacosanol 68171 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCO 382.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(+)-Totarol 326995 Click to see CC(C)C1=C(C=CC2=C1CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://doi.org/10.1016/S0031-9422(00)80328-3
(4b,8,8-trimethyl-10-oxo-2-propan-2-yl-6,7,8a,9-tetrahydro-5H-phenanthren-3-yl) acetate 14287360 Click to see CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)OC(=O)C 342.50 unknown https://doi.org/10.1016/S0031-9422(00)80328-3
[(4bS,8aS)-4b,8,8-trimethyl-10-oxo-2-propan-2-yl-6,7,8a,9-tetrahydro-5H-phenanthren-3-yl] acetate 14287361 Click to see CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)OC(=O)C 342.50 unknown https://doi.org/10.1016/S0031-9422(00)80328-3
Totarol 92783 Click to see CC(C)C1=C(C=CC2=C1CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://doi.org/10.1016/S0031-9422(00)80328-3
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Taxanes and derivatives
Paclitaxel 36314 Click to see CC1=C2C(C(=O)C3(C(CC4C(C3C(C(C2(C)C)(CC1OC(=O)C(C(C5=CC=CC=C5)NC(=O)C6=CC=CC=C6)O)O)OC(=O)C7=CC=CC=C7)(CO4)OC(=O)C)O)C)OC(=O)C 853.90 unknown https://doi.org/10.1016/S0305-1978(98)00118-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,4S,5R,9S)-4,5-Epoxy-4,11,11-trimethyl-8-methylenebicyclo[7.2.0]undecane 9991037 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
(2E,4E)-5-[(1R,3S,5R,8S)-3,8-dihydroxy-1,5-dimethyl-6-oxabicyclo[3.2.1]octan-8-yl]-3-(hydroxymethyl)penta-2,4-dienoic acid 102524768 Click to see CC12CC(CC(C1(C=CC(=CC(=O)O)CO)O)(OC2)C)O 298.33 unknown https://doi.org/10.1016/J.PHYTOL.2012.02.005
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(4aS,5S)-3-(2-hydroxypropan-2-yl)-4a,5-dimethyl-5,6,7,8-tetrahydronaphthalen-2-one 14830797 Click to see CC1CCCC2=CC(=O)C(=CC12C)C(C)(C)O 234.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1S,3R,4aS)-3,7-dihydroxy-8-(1-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylate 163081939 Click to see CC(CO)C1=C(C=CC2=C1CCC3C2(CC(CC3(C)C(=O)OC4C(C(C(C(O4)CO)O)O)O)O)C)O 510.60 unknown https://doi.org/10.1016/J.PHYTOL.2012.02.005
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
20-Hydroxyecdysone 5459840 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown https://doi.org/10.1016/J.PHYTOL.2012.02.005
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
Ponasterone A 115127 Click to see CC(C)CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O 464.60 unknown https://doi.org/10.1016/J.PHYTOL.2012.02.005
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / C-glycosyl compounds
(2S,3S,4S,5R)-2,5-bis(hydroxymethyl)-2-methoxyoxolane-3,4-diol 6325664 Click to see COC1(C(C(C(O1)CO)O)O)CO 194.18 unknown via CMAUP database
methyl beta-D-fructofuranoside 128889 Click to see COC1(C(C(C(O1)CO)O)O)CO 194.18 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Volkenin 181811 Click to see C1C(C=CC1(C#N)OC2C(C(C(C(O2)CO)O)O)O)O 287.27 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Dianthoside 5316639 Click to see CC1=C(C(=O)C=CO1)OC2C(C(C(C(O2)CO)O)O)O 288.25 unknown via CMAUP database
Sucrose 5988 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoic acid 54036359 Click to see C1=CC(=CC=C1C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 326.30 unknown via CMAUP database
Arbutin 440936 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
D-(-)-Fructose 5984 Click to see C(C(C(C(C(=O)CO)O)O)O)O 180.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal 107526 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown via CMAUP database
D-Rhamnose 5460029 Click to see CC(C(C(C(C=O)O)O)O)O 164.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Teuhetenone A 15153216 Click to see CC12CCCC(C1=CC(=O)CC2)(C)O 194.27 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
(10S)-10,14-dimethyl-5-propan-2-yl-3,6,16-trioxapentacyclo[8.6.1.02,4.04,9.014,17]heptadeca-8,12-diene-7,15-dione 5320647 Click to see CC(C)C1C23C(O2)C4C5C(C3=CC(=O)O1)(CC=CC5(C(=O)O4)C)C 330.40 unknown via CMAUP database
(1S,2R,4R,5R,10S,14R,17R)-10,14-dimethyl-5-propan-2-yl-3,6,16-trioxapentacyclo[8.6.1.02,4.04,9.014,17]heptadeca-8,12-diene-7,15-dione 162942513 Click to see CC(C)C1C23C(O2)C4C5C(C3=CC(=O)O1)(CC=CC5(C(=O)O4)C)C 330.40 unknown https://doi.org/10.1007/BF01990665
(1S,2R,5R,14R,17R)-10,14-dimethyl-5-propan-2-yl-3,6,16-trioxapentacyclo[8.6.1.02,4.04,9.014,17]heptadeca-8,12-diene-7,15-dione 163188369 Click to see CC(C)C1C23C(O2)C4C5C(C3=CC(=O)O1)(CC=CC5(C(=O)O4)C)C 330.40 unknown https://doi.org/10.1007/BF01990665
Nagilactone 319648 Click to see CC(C)C1=C2C(C3C4C(C(C5C(C4(C2=CC(=O)O1)C)O5)O)(C(=O)O3)C)O 362.40 unknown https://doi.org/10.1016/J.PHYTOL.2012.02.005
Nagilactone B 3084329 Click to see CC(C)C1=C2C(C3C4C(CC(C(C4(C2=CC(=O)O1)C)O)O)(C(=O)O3)C)O 364.40 unknown https://doi.org/10.1016/J.PHYTOL.2012.02.005
Nagilactone D 3084330 Click to see CCC1=C2CC3C4C(C(C5C(C4(C2=CC(=O)O1)C)O5)O)(C(=O)O3)C 332.30 unknown https://doi.org/10.1016/J.PHYTOL.2012.02.005
Nagilactone F 181498 Click to see CC(C)C1C2=CC3C4C(C2=CC(=O)O1)(CCCC4(C(=O)O3)C)C 316.40 unknown https://doi.org/10.1016/J.PHYTOL.2012.02.005
Podolactone B 442078 Click to see CC12C3C(C4C5(O4)C(OC(=O)C=C5C3(C6C(C1O)O6)C)C(C)(CO)O)OC2=O 394.40 unknown https://doi.org/10.1016/J.PHYTOL.2012.02.005
Podolide 99535 Click to see CC(C)C1C23C(O2)C4C5C(C3=CC(=O)O1)(CC=CC5(C(=O)O4)C)C 330.40 unknown https://doi.org/10.1016/J.PHYTOL.2012.02.005
https://doi.org/10.1007/BF01990665
> Organoheterocyclic compounds / Oxepanes
(1S,2S,4R,5R,6R,9R)-12-ethyl-5-hydroxy-1,6-dimethyl-3,8,13-trioxapentacyclo[7.6.1.02,4.06,16.011,15]hexadec-11(15)-ene-7,14-dione 162856674 Click to see CCC1C2=C(C(=O)O1)C3(C4C(C2)OC(=O)C4(C(C5C3O5)O)C)C 320.30 unknown https://doi.org/10.1016/J.PHYTOL.2012.02.005
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Glochidioboside 24982202 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCOC4C(C(C(C(O4)CO)O)O)O 522.50 unknown https://doi.org/10.1016/J.PHYTOL.2012.02.005
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Ginkgetin 5271805 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O 566.50 unknown https://doi.org/10.1016/J.PHYTOL.2012.02.005
Kayaflavone 9894522 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)OC 580.50 unknown https://doi.org/10.1016/S0031-9422(00)81743-4
Podocarpusflavone A 5320644 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O 552.50 unknown https://doi.org/10.1007/BF01990665
https://doi.org/10.1016/S0031-9422(00)81743-4
https://doi.org/10.1016/J.PHYTOL.2012.02.005
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
8-C-(2-Rhamnosyl-6-deoxyhexopyranosulyl)luteolin 102040777 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2=O)O)C)C3=C(C=C(C4=C3OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O)O 576.50 unknown via CMAUP database
Luteolin 8-C-E-propenoic acid 16109839 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C(=C3O2)C=CC(=O)O)O)O)O)O 356.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
(1S)-1,5-anhydro-2-O-(6-deoxy-beta-L-mannopyranosyl)-1-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-8-yl]-D-glucitol 86289611 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2C3=C(C=C(C4=C3OC(=CC4=O)C5=CC=C(C=C5)O)O)O)CO)O)O)O)O)O 578.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Laricitin 3-O-(6-beta-D-glucopyranosyl-beta-D-glucopyranoside) 102401707 Click to see COC1=CC(=CC(=C1O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O 656.50 unknown via CMAUP database
Quercetin 3-gentiobioside 5320834 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O 626.50 unknown via CMAUP database
Syringetin 3-O-(6-beta-D-glucopyranosyl-beta-D-glucopyranoside) 16109838 Click to see COC1=CC(=CC(=C1O)OC)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O 670.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
4''-O-(4-Hydroxy-Z-cinnamoyl)cosmosiin 16109840 Click to see C1=CC(=CC=C1C=CC(=O)OC2C(OC(C(C2O)O)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O 578.50 unknown via CMAUP database
Apigenin 7-O-(6''-O-p-Z-coumaroyl-beta-D-glucopyranoside) 16109837 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O 578.50 unknown via CMAUP database
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
Echinacin 6439941 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O 578.50 unknown via CMAUP database
Echinaticin 101321313 Click to see C1=CC(=CC=C1C=CC(=O)OC2C(OC(C(C2O)O)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O 578.50 unknown via CMAUP database
Thermopsoside 11294177 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown via CMAUP database
Tricin 7-glucoside 5322022 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O 492.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Apigenin 7,4'-dimethyl ether 5281601 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O 298.29 unknown via CMAUP database
Velutin 5464381 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)OC)O 314.29 unknown via CMAUP database

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