Metabolite 3'-hydroxy-4'-methoxy diclofenac

Name
3'-hydroxy-4'-methoxy diclofenac
Description
Not Available
Structure
Synonyms
Not Available
UNII
Not Available
CAS number
Not Available
Weight
Average: 296.149
Monoisotopic: 295.016684015
Chemical Formula
C14H11Cl2NO2
InChI Key
DCOPUUMXTXDBNB-UHFFFAOYSA-N
InChI
InChI=1S/C14H11Cl2NO2/c15-10-5-3-6-11(16)14(10)17-12-7-2-1-4-9(12)8-13(18)19/h1-7,17H,8H2,(H,18,19)
IUPAC Name
2-{2-[(2,6-dichlorophenyl)amino]phenyl}acetic acid
SMILES
OC(=O)CC1=CC=CC=C1NC1=C(Cl)C=CC=C1Cl
Reactions
Spectra
SpectrumSpectrum TypeSplash Key
Predicted GC-MS Spectrum - GC-MSPredicted GC-MSsplash10-0udi-4290000000-1eb3d1011ce45deff962
GC-MS Spectrum - EI-BGC-MSsplash10-03xv-3390000000-cd724f772f8ff3648856
Mass Spectrum (Electron Ionization)MSsplash10-03xv-1290000000-8fb3ce6f68fc69b5218e
LC-MS/MS Spectrum - LC-ESI-ITFT , negativeLC-MS/MSsplash10-0udi-0090000000-1d8a04523a99bbdd0f79
LC-MS/MS Spectrum - LC-ESI-ITFT , negativeLC-MS/MSsplash10-0udi-0090000000-55cf6c5663edc2bce2af
LC-MS/MS Spectrum - LC-ESI-ITFT , negativeLC-MS/MSsplash10-0udi-0090000000-0257da659c18c3020ebe
LC-MS/MS Spectrum - LC-ESI-ITFT , negativeLC-MS/MSsplash10-0w29-0090000000-eba79744370d30689f45
LC-MS/MS Spectrum - LC-ESI-ITFT , negativeLC-MS/MSsplash10-03fr-0890000000-0870dbb742038ce60ba1
LC-MS/MS Spectrum - LC-ESI-ITFT , negativeLC-MS/MSsplash10-004i-0900000000-a9b9817f70b72a327169
LC-MS/MS Spectrum - LC-ESI-ITFT , negativeLC-MS/MSsplash10-0udi-0090000000-58aba74cf5c165b0b3e5
LC-MS/MS Spectrum - LC-ESI-ITFT , negativeLC-MS/MSsplash10-0udi-0090000000-380ce6ec03fa880c2fee
LC-MS/MS Spectrum - LC-ESI-ITFT , negativeLC-MS/MSsplash10-0w29-0090000000-1c764b23643b9731a5a2
LC-MS/MS Spectrum - LC-ESI-ITFT , negativeLC-MS/MSsplash10-0ik9-0290000000-5d59b6e5d4465a9e6493
LC-MS/MS Spectrum - LC-ESI-ITFT , negativeLC-MS/MSsplash10-004i-0900000000-483b1ac79bbfb8f591c2
LC-MS/MS Spectrum - LC-ESI-ITFT , negativeLC-MS/MSsplash10-0fb9-0950000000-4192d5344ed223d4bfd6
LC-MS/MS Spectrum - LC-ESI-ITFT , negativeLC-MS/MSsplash10-0udi-0090000000-1d8a04523a99bbdd0f79
LC-MS/MS Spectrum - LC-ESI-QQ , negativeLC-MS/MSsplash10-0006-0090000000-d28bb6688b1bce51bfce
LC-MS/MS Spectrum - LC-ESI-QQ , negativeLC-MS/MSsplash10-0udi-0090000000-33332a8dbce37d5ad759
LC-MS/MS Spectrum - LC-ESI-QQ , negativeLC-MS/MSsplash10-0udi-1490000000-f1c9ca0a1b924dba188e
LC-MS/MS Spectrum - LC-ESI-QQ , negativeLC-MS/MSsplash10-004i-4910000000-4c58f3f969da3d86e23c
LC-MS/MS Spectrum - LC-ESI-QQ , negativeLC-MS/MSsplash10-00or-7900000000-3b2e03ec45a0b642cb4d
LC-MS/MS Spectrum - LC-ESI-ITFT , negativeLC-MS/MSsplash10-0udi-0390000000-247401e4df8c88d9f260
LC-MS/MS Spectrum - LC-ESI-ITFT , negativeLC-MS/MSsplash10-0f6t-0980000000-dee808683174f31bbd7b
LC-MS/MS Spectrum - LC-ESI-ITFT , negativeLC-MS/MSsplash10-0udi-0090000000-5685aad1c834522ac60a
LC-MS/MS Spectrum - LC-ESI-ITFT , negativeLC-MS/MSsplash10-0udi-0090000000-5685aad1c834522ac60a
LC-MS/MS Spectrum - LC-ESI-QFT , negativeLC-MS/MSsplash10-0udi-0090000000-659ebbc59b4a39d35b04
LC-MS/MS Spectrum - LC-ESI-QTOF , positiveLC-MS/MSsplash10-0udj-0090000000-f5310eb88501c49fae99
LC-MS/MS Spectrum - LC-ESI-QTOF , positiveLC-MS/MSsplash10-014i-0090000000-22b25c07db224512f663
LC-MS/MS Spectrum - LC-ESI-QTOF , positiveLC-MS/MSsplash10-014i-0090000000-185b3e61f8dee1cd34fd
LC-MS/MS Spectrum - LC-ESI-QTOF , positiveLC-MS/MSsplash10-03di-0090000000-258397c7de133a923918
LC-MS/MS Spectrum - LC-ESI-QTOF , positiveLC-MS/MSsplash10-03di-0190000000-a01fa70dc6bb2e228326
LC-MS/MS Spectrum - LC-ESI-ITFT , positiveLC-MS/MSsplash10-004i-0090000000-dda6bd4971ef03dfabd5
LC-MS/MS Spectrum - LC-ESI-ITFT , positiveLC-MS/MSsplash10-0f92-0090000000-2442038174fa86b3208e
LC-MS/MS Spectrum - LC-ESI-ITFT , positiveLC-MS/MSsplash10-014i-0090000000-6651d739e4ae3414e4dc
LC-MS/MS Spectrum - LC-ESI-ITFT , positiveLC-MS/MSsplash10-014i-0090000000-d36dd717311d2b0886bd
LC-MS/MS Spectrum - LC-ESI-ITFT , positiveLC-MS/MSsplash10-03di-0090000000-ce3de7d00b24b610d60e
LC-MS/MS Spectrum - LC-ESI-ITFT , positiveLC-MS/MSsplash10-03di-0090000000-79f23644751784fec0ff
LC-MS/MS Spectrum - LC-ESI-ITFT , positiveLC-MS/MSsplash10-03di-0090000000-2b7106a8023f21da905f
LC-MS/MS Spectrum - LC-ESI-ITFT , positiveLC-MS/MSsplash10-0f92-0090000000-3a985a8972fed8e003bb
LC-MS/MS Spectrum - LC-ESI-ITFT , positiveLC-MS/MSsplash10-014i-0090000000-97ab164f74166b6b9013
LC-MS/MS Spectrum - LC-ESI-ITFT , positiveLC-MS/MSsplash10-014i-0090000000-0e7b515022ec37b87106
LC-MS/MS Spectrum - LC-ESI-ITFT , positiveLC-MS/MSsplash10-03di-0090000000-4bc6d8a15c3425f5cd10
LC-MS/MS Spectrum - LC-ESI-ITFT , positiveLC-MS/MSsplash10-03di-0090000000-80bb26643a94999c6114
LC-MS/MS Spectrum - LC-ESI-ITFT , positiveLC-MS/MSsplash10-03di-0090000000-e5473cba8c9d7b59691b
LC-MS/MS Spectrum - LC-ESI-ITFT , positiveLC-MS/MSsplash10-004i-0090000000-f4f62ca3d4d5ab12ba13
LC-MS/MS Spectrum - LC-ESI-QQ , positiveLC-MS/MSsplash10-002b-0190000000-5072b5cbb937155d3784
LC-MS/MS Spectrum - LC-ESI-QQ , positiveLC-MS/MSsplash10-0fr2-0690000000-0ad1d80cd74eb2ccbdb0
LC-MS/MS Spectrum - LC-ESI-QQ , positiveLC-MS/MSsplash10-014j-0690000000-4183a2580dc0b109b758
LC-MS/MS Spectrum - LC-ESI-QQ , positiveLC-MS/MSsplash10-03dj-1590000000-fbe48d026f4e8bbc143f
LC-MS/MS Spectrum - LC-ESI-QQ , positiveLC-MS/MSsplash10-03di-2590000000-f9746f93eefd2c1420c4
LC-MS/MS Spectrum - LC-ESI-IT , positiveLC-MS/MSsplash10-0fb9-0090000000-ea3b07d4dee166a8e13a
LC-MS/MS Spectrum - LC-ESI-ITFT , positiveLC-MS/MSsplash10-03xr-0090000000-e46d3368f4461372a4d3
LC-MS/MS Spectrum - LC-ESI-ITFT , positiveLC-MS/MSsplash10-03di-0090000000-6f11e14bc0fc7b731ddb
LC-MS/MS Spectrum - LC-ESI-ITFT , positiveLC-MS/MSsplash10-004i-0090000000-c297b571605fec05d894
LC-MS/MS Spectrum - LC-ESI-ITFT , positiveLC-MS/MSsplash10-004i-0090000000-044f51839f5d4002b30d
LC-MS/MS Spectrum - LC-ESI-QFT , positiveLC-MS/MSsplash10-0i00-0090000000-c627af8df018c1c51b07
Predicted MS/MS Spectrum - 10V, Positive (Annotated)Predicted LC-MS/MSsplash10-0002-0090000000-b80e093739a5740a8c5c
Predicted MS/MS Spectrum - 10V, Negative (Annotated)Predicted LC-MS/MSsplash10-0006-0090000000-a75fecc6e2b884c4dc81
Predicted MS/MS Spectrum - 20V, Positive (Annotated)Predicted LC-MS/MSsplash10-0002-0090000000-8bbd7cf79efdb6fa0d84
Predicted MS/MS Spectrum - 20V, Negative (Annotated)Predicted LC-MS/MSsplash10-001l-6090000000-d8ab64fea7111eab62e5
Predicted MS/MS Spectrum - 40V, Positive (Annotated)Predicted LC-MS/MSsplash10-0r94-2960000000-a96d201fcf544b407cd6
Predicted MS/MS Spectrum - 40V, Negative (Annotated)Predicted LC-MS/MSsplash10-001i-9050000000-839e8c7b23484977a4d2
Predicted MS/MS Spectrum - 10V, Positive (Annotated)Predicted LC-MS/MSsplash10-0002-0090000000-b80e093739a5740a8c5c
Predicted MS/MS Spectrum - 10V, Negative (Annotated)Predicted LC-MS/MSsplash10-0006-0090000000-a75fecc6e2b884c4dc81
Predicted MS/MS Spectrum - 20V, Positive (Annotated)Predicted LC-MS/MSsplash10-0002-0090000000-8bbd7cf79efdb6fa0d84
Predicted MS/MS Spectrum - 20V, Negative (Annotated)Predicted LC-MS/MSsplash10-001l-6090000000-d8ab64fea7111eab62e5
Predicted MS/MS Spectrum - 40V, Positive (Annotated)Predicted LC-MS/MSsplash10-0r94-2960000000-a96d201fcf544b407cd6
Predicted MS/MS Spectrum - 40V, Negative (Annotated)Predicted LC-MS/MSsplash10-001i-9050000000-839e8c7b23484977a4d2
Predicted 1H NMR Spectrum1D NMRNot Applicable
Predicted 13C NMR Spectrum1D NMRNot Applicable
Chromatographic Properties
Collision Cross Sections (CCS)
AdductCCS Value (Å2)Source typeSource
[M-H]-159.517127
predicted
DarkChem Lite v0.1.0
[M-H]-155.47115
predicted
DeepCCS 1.0 (2019)
[M-H]-159.517127
predicted
DarkChem Lite v0.1.0
[M-H]-159.517127
predicted
DarkChem Lite v0.1.0
[M-H]-155.47115
predicted
DeepCCS 1.0 (2019)
[M-H]-155.47115
predicted
DeepCCS 1.0 (2019)
[M+H]+159.806427
predicted
DarkChem Lite v0.1.0
[M+H]+157.82915
predicted
DeepCCS 1.0 (2019)
[M+H]+159.806427
predicted
DarkChem Lite v0.1.0
[M+H]+159.806427
predicted
DarkChem Lite v0.1.0
[M+H]+157.82915
predicted
DeepCCS 1.0 (2019)
[M+H]+157.82915
predicted
DeepCCS 1.0 (2019)
[M+Na]+160.063627
predicted
DarkChem Lite v0.1.0
[M+Na]+163.92229
predicted
DeepCCS 1.0 (2019)
[M+Na]+160.063627
predicted
DarkChem Lite v0.1.0
[M+Na]+160.063627
predicted
DarkChem Lite v0.1.0
[M+Na]+163.92229
predicted
DeepCCS 1.0 (2019)
[M+Na]+163.92229
predicted
DeepCCS 1.0 (2019)
PharmGKB
PA449293
Predicted Properties
PropertyValueSource
Water Solubility0.00447 mg/mLALOGPS
logP4.98ALOGPS
logP4.26Chemaxon
logS-4.8ALOGPS
pKa (Strongest Acidic)4Chemaxon
pKa (Strongest Basic)-2.1Chemaxon
Physiological Charge-1Chemaxon
Hydrogen Acceptor Count3Chemaxon
Hydrogen Donor Count2Chemaxon
Polar Surface Area49.33 Å2Chemaxon
Rotatable Bond Count4Chemaxon
Refractivity75.46 m3·mol-1Chemaxon
Polarizability27.93 Å3Chemaxon
Number of Rings2Chemaxon
Bioavailability1Chemaxon
Rule of FiveYesChemaxon
Ghose FilterYesChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleNoChemaxon