Da Costa Fernando B FB

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Unknown (18)
Metabolomics (3)

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MetaboLights (3)

Technology Type

Mass spectrometry (3)

Instrument Platform

Liquid Chromatography MS - Alternating (LC-MS (Alternating)) (1)
Liquid Chromatography MS - Negative (LC-MS (Negative)) (1)
Liquid Chromatography MS - Positive (LC-MS (Positive)) (1)
Exactive (Thermo Scientific) (1)

Publication Date

2020 (1)
2019 (1)
2018 (1)

CHEBI ID

CHEBI:65751 (3)
CHEBI:28527 (3)
CHEBI:17521 (3)
CHEBI:141126 (2)
CHEBI:141118 (2)
CHEBI:141136 (2)
CHEBI:5995 (2)
CHEBI:520 (2)
CHEBI:16860 (2)
CHEBI:28499 (2)
CHEBI:16243 (2)
CHEBI:17558 (2)
CHEBI:67486 (2)
CHEBI:28230 (2)
CHEBI:145104 (1)
CHEBI:145103 (1)
CHEBI:145102 (1)
CHEBI:145101 (1)
CHEBI:145100 (1)
CHEBI:145098 (1)
CHEBI:145099 (1)
CHEBI:145097 (1)
CHEBI:145095 (1)
CHEBI:145093 (1)
CHEBI:145092 (1)
CHEBI:141117 (1)
CHEBI:141151 (1)
CHEBI:141150 (1)
CHEBI:141149 (1)
CHEBI:141148 (1)

Metabolite Name

Polymatin B (2)
Longipilin acetate (2)
15-hydroxy-eremantholide B (1)
Viguilenin (1)
1b,2a-epoxy tagitinin C (1)
Flavonol 3-o-glycosylated (1)
Pinocembrin (1)
2-oxo-8b-methacryloyloxy-guaia-3,10(14),11(13)-trien-6a,12-olide (1)
Galangin (1)
Genkwanin (1)
3,4',5-trihydroxy-7-methoxyflavone (1)
15-hydroxy-eremantholide b (1)
Hispidulin (1)
3,4,5-tri-O-E-caffeoylquinic acid (1)
Hirsutinolide (1)
3-O-caffeoyl-2-(2-butyl)-2-hydroxybutanedioic acid (1)
Budlein B (1)
4,5-di-O-E-caffeoylquinic acid (1)
3,4-di-O-E-caffeoylquinic acid (1)
Apigenin-7-O-glucoside (1)
Spiraeoside (1)
3,5-di-O-E-caffeoylquinic acid (1)
3-O-caffeoyl-2-(2-propyl)-2-hydroxybutanedioic acid (1)
1,5-di-O-E-caffeoylquinic acid (1)
Kaempferol-3-O-rutinoside (1)
Kaempferol-3-O-glucoside (1)
Quercetin-3-O-glucoronoside (1)
Quercetin-3-O-arabino-rhamnoside (1)
Luteolin-7-O-glucoside (1)
Methyl 5-O-E-caffeoylquinate (1)

Release Date

2021 (7)
2025 (3)
2024 (3)
2022 (2)
2023 (1)
2020 (1)
2015 (1)

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Untargeted LC-MS metabolomic studies of Asteraceae species to discover inhibitors of Leishmania major dihydroorotate dehydrogenase

INTRODUCTION: Interesting data about the family Asteraceae as a new source of Leishmania major dihydroorotate dehydrogenase (LmDHODH) inhibitors are presented. This key macromolecular target for parasites causing neglected diseases catalyzes the fourth reaction of the de novo pyr...

2019-10-14 | MTBLS722 | MetaboLights

Biogeography shaped the metabolome of the genus Espeletia: a phytochemical perspective on an Andean adaptive radiation

The páramo ecosystem has the highest rate of diversification across plant lineages on earth, of which the genus Espeletia (Asteraceae) is a prime example. The current distribution and molecular phylogeny of Espeletia suggest the influence of Andean geography and past climatic fluctuations on the div...

2018-11-20 | MTBLS445 | MetaboLights

Metabolomic and gene expression approaches reveal the developmental and environmental regulation of the secondary metabolism of yacón (Smallanthus sonchifolius, Asteraceae)

Acting as chemical defense or signaling compounds, secondary metabolites (SMs) play an essential role in the evolutionary success of many angiosperm plant families. However, the adaptive advantages that SMs confer, and the influence of environmental and developmental factors on SMs expression, remai...

2020-03-24 | MTBLS840 | MetaboLights

Coumarin/β-Cyclodextrin Inclusion Complexes Promote Acceleration and Improvement of Wound Healing.

Not available

S-EPMC11194811 | biostudies-literature

A cluster randomized trial of a multifaceted quality improvement intervention in Brazilian intensive care units: study protocol.

Not available

S-EPMC4342101 | biostudies-literature

Anastomotic leak after manual circular stapled left-sided bowel surgery: analysis of technology-, disease-, and patient-related factors.

Not available

S-EPMC11498054 | biostudies-literature

Global Burden of Cardiovascular Diseases and Risks, 1990-2022.

Not available