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Paepalanthus latipes

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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 UUID644002ae3f413996761238
Scientific name Paepalanthus latipes
Authority Silveira
First published in Floral. Mont. 1: 230 (1928)

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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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000485786
Tropicos 100237297
KEW urn:lsid:ipni.org:names:180400-2
The Plant List kew-256854
Open Tree Of Life 3965656
NCBI Taxonomy 1858759
IPNI 180400-2
GBIF 5287130
EOL 231703

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
Review on Compounds Isolated from Eriocaulaceae Family and Evaluation of Biological Activities by Machine Learning Moreira LL, de Menezes RP, Scotti L, Scotti MT, Lacerda Júnior V, Borges WD Molecules 24-Oct-2022
PMCID:PMC9654208
doi:10.3390/molecules27217186
PMID:36364014
Efficacy and Mechanisms of Flavonoids against the Emerging Opportunistic Nontuberculous Mycobacteria Mickymaray S, Alfaiz FA, Paramasivam A Antibiotics (Basel) 27-Jul-2020
PMCID:PMC7460331
doi:10.3390/antibiotics9080450
PMID:32726972
Phenolic Compounds as Promising Drug Candidates in Tuberculosis Therapy Mazlun MH, Sabran SF, Mohamed M, Abu Bakar MF, Abdullah Z Molecules 04-Jul-2019
PMCID:PMC6651284
doi:10.3390/molecules24132449
PMID:31277371
A new cytotoxic naphthoquinone from Paepalanthus latipes. Kitagawa RR, Raddi MS, Santos LC, Vilegas W Chem Pharm Bull (Tokyo) 01-Dec-2004
doi:10.1248/CPB.52.1487
PMID:15577252
Quercetagetin 7-methyl ether glycosides from Paepalanthus vellozioides and Paepalanthus latipes W. Vilegas, C.J. Nehme, A.L. Dokkeddal, S. Piacente, L. Rastrelli, C. Pizza Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(99)00009-6
New naphthopyranone glycosides from Paepalanthus vellozioides and Paepalanthus latipes. Vilegas W, Dokkeddal AL, Piacente S, Rastrelli L, Pizza C J Nat Prod 01-May-1999
doi:10.1021/NP980082T
PMID:10346959

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 / Naphthopyrans / Naphthopyranones / Naphthopyranone glycosides
(3R)-10-hydroxy-7-methoxy-3-methyl-9-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydrobenzo[g]isochromen-1-one 10812811 Click to see CC1CC2=CC3=CC(=CC(=C3C(=C2C(=O)O1)O)OC4C(C(C(C(O4)CO)O)O)O)OC 436.40 unknown https://doi.org/10.1021/NP980082T
(3R)-10-hydroxy-7-methoxy-3-methyl-9-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-3,4-dihydrobenzo[g]isochromen-1-one 10769846 Click to see CC1CC2=CC3=CC(=CC(=C3C(=C2C(=O)O1)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)OC 598.50 unknown https://doi.org/10.1021/NP980082T
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5,6-dihydroxy-7-methoxy-4-oxochromen-3-yl]oxy-5-[(2S,3R,4S,5S,6R)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid 163067812 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(C(O3)C(=O)O)O)O)OC4C(C(C(C(O4)CO)O)O)OC(=O)C=CC5=CC(=C(C=C5)O)O)C6=CC(=C(C=C6)O)O)O)O 832.70 unknown https://doi.org/10.1016/S0031-9422(99)00009-6
(2R,3S,4S,5S,6R)-6-[2-(3,4-dihydroxyphenyl)-5,6-dihydroxy-7-methoxy-4-oxochromen-3-yl]oxy-3-[(2S,3R,4S,5R,6S)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,5-dihydroxyoxane-2-carboxylic acid 163195524 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(C(O3)C(=O)O)OC4C(C(C(C(O4)CO)O)O)OC(=O)C=CC5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O)O 832.70 unknown https://doi.org/10.1016/S0031-9422(99)00009-6
(2S,3S,4R,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5,6-dihydroxy-7-methoxy-4-oxochromen-3-yl]oxy-3-[(2S,3R,4S,5S,6R)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,5-dihydroxyoxane-2-carboxylic acid 100978775 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(C(O3)C(=O)O)OC4C(C(C(C(O4)CO)O)O)OC(=O)C=CC5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O)O 832.70 unknown https://doi.org/10.1016/S0031-9422(99)00009-6
6-[2-(3,4-Dihydroxyphenyl)-5,6-dihydroxy-7-methoxy-4-oxochromen-3-yl]oxy-3-[3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,5-dihydroxyoxane-2-carboxylic acid 162850270 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(C(O3)C(=O)O)OC4C(C(C(C(O4)CO)O)O)OC(=O)C=CC5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O)O 832.70 unknown https://doi.org/10.1016/S0031-9422(99)00009-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
3,5,6-Trihydroxy-2-[3-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-7-methoxychromen-4-one 74978504 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)O)C3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 494.40 unknown https://doi.org/10.1016/S0031-9422(99)00009-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,6-dihydroxy-7-methoxy-3-[(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 163057401 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O)O 494.40 unknown https://doi.org/10.1016/S0031-9422(99)00009-6
2-(3,4-Dihydroxyphenyl)-5,6-dihydroxy-7-methoxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 74978464 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O)O 494.40 unknown https://doi.org/10.1016/S0031-9422(99)00009-6
3-[(2R,3S,4R,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,6-dihydroxy-7-methoxychromen-4-one 163021540 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=C(C(=C4C3=O)O)O)OC)C5=CC(=C(C=C5)O)O)CO)O)O)O)O)O 640.50 unknown https://doi.org/10.1016/S0031-9422(99)00009-6
3-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,6-dihydroxy-7-methoxychromen-4-one 162963135 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(C(O3)CO)OC4C(C(C(C(O4)CO)O)O)O)O)O)C5=CC(=C(C=C5)O)O)O)O 656.50 unknown https://doi.org/10.1016/S0031-9422(99)00009-6
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,6-dihydroxy-7-methoxychromen-4-one 74978505 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=C(C(=C4C3=O)O)O)OC)C5=CC(=C(C=C5)O)O)CO)O)O)O)O)O 640.50 unknown https://doi.org/10.1016/S0031-9422(99)00009-6
> Phenylpropanoids and polyketides / Isochromanequinones
10-Hydroxy-5,7-dimethoxy-3-methylbenzo[g]isochromene-1,6,9-trione 11347623 Click to see CC1=CC2=C(C(=C3C(=O)C=C(C(=O)C3=C2OC)OC)O)C(=O)O1 316.26 unknown https://doi.org/10.1248/CPB.52.1487
3,4,3',4'-Bisdehydroxanthomegnin 101305718 Click to see CC1=CC2=CC3=C(C(=C2C(=O)O1)O)C(=O)C(=C(C3=O)OC)C4=C(C(=O)C5=C(C4=O)C(=C6C(=C5)C=C(OC6=O)C)O)OC 570.50 unknown https://doi.org/10.1248/CPB.52.1487

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