Common Name
LM ID
Instrument
Adduct / Ion
Submitter
4-F3t-NeuroP
Thermo Scientific Q Exactive Focus Orbitrap LC-MS/MS System
[M-H]-
Jean-Marie Galano.Ángel Sánchez Illana.Thierry Durand
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Structure
Common name
4-F3t-NeuroP
LMID
Systematic name
(4S,E)-6-((1S,2R,3R,5S)-3,5-dihydroxy-2-((2Z,5Z)-undeca-2,5,8-dien-1-yl)cyclopentyl)-4-hydroxyhex-5-enoic acid
m/z
379.2488
Adduct / Ion
[M-H]-
Charge
-1
Ion source
ESI
Instrument
Thermo Scientific Q Exactive Focus Orbitrap LC-MS/MS System
Resolution
17000
For high resolution data only
Ion mode
Negative
Collision Energy (CE)
30eV
Column
Kinetex EVO C18 (100 × 2.1 mm column 1.7 µm)
Mobile phase A
0.3 mL/min binary gradient using H2O (0.1% HCOOH)
Mobile phase B
CH3CN:CH3OH 8:2, (0.1% HCOOH)
Retention time (min)
13.81
Amount injected
5μl
DOI for method
Date acquired
October 2023
Submitters
Jean-Marie Galano.Ángel Sánchez Illana.Thierry Durand
Source of standard
Synthesized in-house
4-F3t-NeuroP
Thermo Fisher Orbitrap ID-X Tribrid
[M-H]-
Jean-Marie Galano.Ángel Sánchez Illana.Thierry Durand
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Structure
Common name
4-F3t-NeuroP
LMID
Systematic name
(4S,E)-6-((1S,2R,3R,5S)-3,5-dihydroxy-2-((2Z,5Z)-undeca-2,5,8-dien-1-yl)cyclopentyl)-4-hydroxyhex-5-enoic acid
m/z
379.2491
Adduct / Ion
[M-H]-
Charge
-1
Ion source
ESI
Instrument
Thermo Fisher Orbitrap ID-X Tribrid
Resolution
60000
For high resolution data only
Ion mode
Negative
Collision Energy (CE)
stepped HCD collision energy 20–40–60%
Column
Kinetex C18 (100 × 2.1 mm, 1.7 µm)
Mobile phase A
H2O (0.1% HCOOH)
Mobile phase B
CH3CN (0.1% HCOOH) binary gradient at 0.5 m L/min
Retention time (min)
6.25
Amount injected
10 µL
DOI for method
Date acquired
October 2023
Submitters
Jean-Marie Galano.Ángel Sánchez Illana.Thierry Durand
Source of standard
Synthesized in-house
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nsity":4655},{"mz":351.28,"intensity":3684},{"mz":361.1,"intensity":759600},{"mz":376.79,"intensity":4151},{"mz":379.09,"intensity":8363000}]
Structure
Common name
4-F3t-NeuroP
LMID
Systematic name
(4S,E)-6-((1S,2R,3R,5S)-3,5-dihydroxy-2-((2Z,5Z)-undeca-2,5,8-dien-1-yl)cyclopentyl)-4-hydroxyhex-5-enoic acid
m/z
379.2
Adduct / Ion
[M-H]-
Charge
-1
Ion source
ESI
Instrument
Waters Xevo TQ-XS Triple Quadrupole
Resolution
N/A
For high resolution data only
Ion mode
Negative
Collision Energy (CE)
18
Column
Waters Acquity Premier BEH C18 with VanGuard FIT, 130 Å, 1.7 µm, 2.1 x 100 mm
Mobile phase A
Milli-Q H2O + 0.1 % (v/v) acetic acid
Mobile phase B
ACN:IPA (90:10)
Retention time (min)
4.43
Amount injected
0.25 ng
DOI for method
Date acquired
March 2025
Submitters
Wheelock/Hagn
Source of standard
Université de Montpellier (Durand/Galano/Oger)