Common Name
LM ID
Instrument
Adduct / Ion
Submitter
Resolvin D1
SCIEX QTRAP 6500 LC-MS/MS System
[M-H]-
Ed Dennis, Oswald Quehenberger, Aaron Armando
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Structure
Common name
Resolvin D1
LMID
Systematic name
7S,8R,17S-trihydroxy-4Z,9E,11E,13Z,15E,19Z-docosahexaenoic acid
m/z
375
Adduct / Ion
[M-H]-
Charge
-1
Ion source
ESI
Instrument
SCIEX QTRAP 6500 LC-MS/MS System
Resolution
N/A
For high resolution data only
Ion mode
Negative
Collision Energy (CE)
-24
Column
Not Available
Mobile phase A
60/40 Water/Acetonitrile, 0.02% Acetic Acid
Mobile phase B
50/50 Isopropanol/Acetonitrile
Retention time (min)
2
Amount injected
10ng
DOI for method
Date acquired
Submitters
Ed Dennis, Oswald Quehenberger, Aaron Armando
Source of standard
Cayman Chemical
Resolvin D1
Thermo Fisher Orbitrap ID-X Tribrid
[M-H]-
Jean-Marie Galano.Ángel Sánchez Illana.Thierry Durand
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Structure
Common name
Resolvin D1
LMID
Systematic name
7S,8R,17S-trihydroxy-4Z,9E,11E,13Z,15E,19Z-docosahexaenoic acid
m/z
375.2177
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)
5.93
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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ensity":66300},{"mz":315.6,"intensity":961},{"mz":319.43,"intensity":4729},{"mz":321.52,"intensity":8765},{"mz":327.45,"intensity":4800},{"mz":331.17,"intensity":32510},{"mz":334.34,"intensity":889},{"mz":336.58,"intensity":1617},{"mz":339.17,"intensity":18780},{"mz":342.98,"intensity":2131},{"mz":347.38,"intensity":4507},{"mz":356.56,"intensity":8209},{"mz":357.15,"intensity":73300},{"mz":363.89,"intensity":5009},{"mz":375.11,"intensity":384300}]
Structure
Common name
Resolvin D1
LMID
Systematic name
7S,8R,17S-trihydroxy-4Z,9E,11E,13Z,15E,19Z-docosahexaenoic acid
m/z
375.2
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)
3.52
Amount injected
0.25 ng
DOI for method
Date acquired
March 2025
Submitters
Wheelock/Hagn
Source of standard
Cayman Chemical