Common Name
LM ID
Instrument
Adduct / Ion
Submitter
2,3-Dinor-8-iso-PGF2alpha
SCIEX QTRAP 6500 LC-MS/MS System
[M-H]-
Ed Dennis, Oswald Quehenberger, Aaron Armando
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Structure
Common name
2,3-Dinor-8-iso-PGF2alpha
LMID
Systematic name
9S,11R,15S-trihydroxy-2,3-dinor-5Z,13E-prostadienoic acid-cyclo[8S,12R]
m/z
325
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)
-19
Column
Not Available
Mobile phase A
60/40 Water/Acetonitrile, 0.02% Acetic Acid
Mobile phase B
50/50 Isopropanol/Acetonitrile
Retention time (min)
0.77
Amount injected
10ng
DOI for method
Date acquired
Submitters
Ed Dennis, Oswald Quehenberger, Aaron Armando
Source of standard
Cayman Chemical
2,3-Dinor-8-iso-PGF2alpha
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
2,3-Dinor-8-iso-PGF2alpha
LMID
Systematic name
9S,11R,15S-trihydroxy-2,3-dinor-5Z,13E-prostadienoic acid-cyclo[8S,12R]
m/z
325.2021
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)
7.55
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
2,3-Dinor-8-iso-PGF2alpha
Thermo Fisher Orbitrap ID-X Tribrid
[M-H]-
Jean-Marie Galano.Ángel Sánchez Illana.Thierry Durand
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Structure
Common name
2,3-Dinor-8-iso-PGF2alpha
LMID
Systematic name
9S,11R,15S-trihydroxy-2,3-dinor-5Z,13E-prostadienoic acid-cyclo[8S,12R]
m/z
325.2021
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
N/A
Mobile phase A
N/A
Mobile phase B
N/A
Retention time (min)
N/A
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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Structure
Common name
2,3-Dinor-8-iso-PGF2alpha
LMID
Systematic name
9S,11R,15S-trihydroxy-2,3-dinor-5Z,13E-prostadienoic acid-cyclo[8S,12R]
m/z
325.2
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)
15
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)
1.29
Amount injected
0.25 ng
DOI for method
Date acquired
March 2025
Submitters
Wheelock/Hagn
Source of standard
Cayman Chemical