MassBank Record: MSBNK-Keio_Univ-KO009138
ACCESSION: MSBNK-Keio_Univ-KO009138
RECORD_TITLE: Octopine; LC-ESI-IT; MS2; m/z: 247; [M+H]+
DATE: 2011.05.10 (Created 2008.05.12)
AUTHORS: Ojima Y, Kakazu Y, Horai H, Soga T, Institute for Advanced Biosciences, Keio Univ.
LICENSE: CC BY-NC-SA
COMMENT: KEIO_ID O009
CH$NAME: Octopine
CH$NAME: L-Arginine, N2-[(1R)-1-carboxyethyl]-
CH$NAME: D-(+)-Octopine
CH$NAME: Arginine, N2-(1-carboxyethyl)-, L-
CH$NAME: D-Octopine
CH$NAME: N2-(D-1-Carboxyethyl)-L-arginine
CH$NAME: L-Arginine, N2-(1-carboxyethyl)-, (R)-
CH$NAME: N2-(1-Carboxyethyl)-L-arginine
CH$COMPOUND_CLASS: N/A
CH$FORMULA: C9H18N4O4
CH$EXACT_MASS: 246.13281
CH$SMILES: NC(=N)NCCC[C@@H](C(O)=O)N[C@@H](C)C(O)=O
CH$IUPAC: InChI=1S/C9H18N4O4/c1-5(7(14)15)13-6(8(16)17)3-2-4-12-9(10)11/h5-6,13H,2-4H2,1H3,(H,14,15)(H,16,17)(H4,10,11,12)/t5-,6-/m0/s1
CH$LINK: CAS
34522-32-2
CH$LINK: CHEBI
15805
CH$LINK: KEGG
C04137
CH$LINK: NIKKAJI
J18.376H
CH$LINK: PUBCHEM
SID:6823
CH$LINK: INCHIKEY
IMXSCCDUAFEIOE-WDSKDSINSA-N
CH$LINK: COMPTOX
DTXSID50487423
AC$INSTRUMENT: LC/MSD Trap XCT, Agilent Technologies
AC$INSTRUMENT_TYPE: LC-ESI-IT
AC$MASS_SPECTROMETRY: MS_TYPE MS2
AC$MASS_SPECTROMETRY: ION_MODE POSITIVE
AC$MASS_SPECTROMETRY: COLLISION_ENERGY 0.70
MS$FOCUSED_ION: PRECURSOR_M/Z 247
MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+
MS$DATA_PROCESSING: WHOLE LC/MSD Trap Control and Data Analysis
PK$SPLASH: splash10-0059-0930000000-df62b2a822d2271224a0
PK$ANNOTATION: m/z struct. num formula mass
70.2 1 1 C4H8N 70.06567
142.1 0 1 C7H12NO2 142.0868
158.1 1 1 C6H12N3O2 158.09295
175.1 1 1 C6H15N4O2 175.1195
188.1 1 1 C8H14NO4 188.09228
201.1 0 1 C8H17N4O2 201.13515
229.1 0 1 C9H17N4O3 229.13007
230.1 1 1 C9H16N3O4 230.11408
PK$NUM_PEAK: 160
PK$PEAK: m/z int. rel.int.
68.2 15.17 1
69.4 29.09 2
70.2 1600.34 137
71.1 42.74 4
72.2 214.44 18
73.2 10.43 1
75.1 12.04 1
77.1 4.91 1
79.1 10.48 1
80.4 5.04 1
81.1 36.09 3
83.1 42.52 4
84.2 4.48 1
85.2 30.17 3
86.2 41.35 4
87.1 227.65 20
88.2 1.35 1
89.1 14.04 1
90.0 15.04 1
91.1 42.17 4
93.0 23.43 2
94.2 2.83 1
95.1 125.00 11
96.1 86.13 7
97.1 274.48 24
98.1 1419.12 122
99.1 37.91 3
100.1 75.39 6
101.1 68.17 6
102.2 7.22 1
103.1 20.09 2
105.1 199.96 17
106.1 5.96 1
107.1 224.78 19
108.1 27.78 2
109.1 145.26 12
111.2 78.48 7
112.1 6408.00 549
113.1 1768.46 152
114.1 1858.81 159
115.0 102.78 9
116.1 1396.64 120
117.0 43.52 4
118.1 27.48 2
119.1 88.96 8
120.0 8.35 1
121.1 116.78 10
122.1 14.17 1
123.1 131.26 11
124.2 14.52 1
125.1 98.69 8
126.1 5.52 1
127.1 18.48 2
128.2 3.09 1
129.0 74.78 6
130.1 4860.75 417
131.1 298.74 26
133.1 146.26 13
134.1 75.74 6
135.1 200.13 17
136.0 152.96 13
137.0 59.00 5
138.0 14.70 1
139.1 58.22 5
140.1 246.00 21
141.1 1749.91 150
142.1 9677.96 830
143.1 46.30 4
144.1 1250.03 107
145.1 165.30 14
146.0 15.35 1
147.1 124.31 11
148.1 16.35 1
149.1 133.65 11
150.1 86.48 7
151.1 44.52 4
153.0 12.61 1
154.1 3.83 1
155.1 31.22 3
156.1 114.52 10
157.1 781.47 67
158.1 5636.82 483
159.1 256.87 22
160.1 258.04 22
161.1 58.91 5
162.1 42.74 4
163.1 144.00 12
164.1 23.35 2
165.1 32.17 3
166.1 7.65 1
167.1 494.65 42
168.1 93.13 8
169.2 62.83 5
171.1 55.17 5
172.1 89.30 8
173.1 230.13 20
174.1 1856.33 159
175.1 8894.27 763
176.1 38.39 3
177.1 178.13 15
178.1 20.70 2
179.2 38.65 3
181.1 3.43 1
183.1 44.56 4
184.1 115.52 10
185.1 1278.38 110
186.1 321.52 28
187.1 916.64 79
188.1 7883.92 676
189.0 423.47 36
190.2 8.26 1
191.1 246.82 21
192.1 8.09 1
193.2 11.48 1
194.0 6.13 1
195.1 2.22 1
196.0 4.57 1
199.0 10.35 1
200.1 34.00 3
201.1 1924.94 165
202.1 391.08 34
203.2 273.52 23
204.1 34.83 3
205.1 311.35 27
205.9 8.52 1
206.9 4.09 1
207.9 4.39 1
209.0 20.87 2
210.1 8.87 1
211.1 83.83 7
212.1 331.91 28
213.1 8.52 1
214.2 23.61 2
215.1 78.78 7
217.0 6.17 1
218.1 44.39 4
219.1 138.61 12
223.2 4.52 1
224.1 8.74 1
225.0 2.13 1
226.1 3.91 1
227.2 13.00 1
228.2 106.13 9
229.1 11652.47 999
230.1 5534.35 474
231.1 30.39 3
232.0 2.00 1
233.2 12.52 1
235.0 7.83 1
243.3 15.26 1
245.1 94.65 8
246.2 248.87 21
247.1 616.38 53
247.9 23.43 2
249.0 16.83 1
264.9 6.96 1
266.4 4.61 1
267.7 1.65 1
282.9 3.39 1
297.0 4.17 1
//