MassBank Record: MSBNK-Osaka_Univ-OUF00011
ACCESSION: MSBNK-Osaka_Univ-OUF00011
RECORD_TITLE: 1-Methyladenosine; GC-EI-TOF; MS; n TMS; RT:1017.608 sec
DATE: 2016.01.19 (Created 2010.05.20, modified 2013.04.24)
AUTHORS: Tsujimoto Y, Tsugawa H, Bamba T, Fukusaki E, engineering department, Osaka Univ.
LICENSE: CC BY-SA
COMMENT: The chemical compound was chemically modified with N-methyl-N-trimethylsilyl-trifluoroacetamide (MSTFA) before GC-MS analysis. When it has two or more functional groups, this modification gave a mixture of the TMS derivatives having different number of TMS groups at different functional groups.
CH$NAME: 1-Methyladenosine
CH$COMPOUND_CLASS: Natural Product
CH$FORMULA: C11H15N5O4
CH$EXACT_MASS: 281.11240
CH$SMILES: OCC([H])(O1)C([H])(O)C([H])(O)C([H])1n(c3)c(N=2)c(n3)C(=N)N(C)C2
CH$IUPAC: InChI=1S/C11H15N5O4/c1-15-3-14-10-6(9(15)12)13-4-16(10)11-8(19)7(18)5(2-17)20-11/h3-5,7-8,11-12,17-19H,2H2,1H3/t5-,7-,8-,11-/m1/s1
CH$LINK: CAS
15763-06-1
CH$LINK: CHEMSPIDER
17216227
CH$LINK: INCHIKEY
GFYLSDSUCHVORB-IOSLPCCCSA-N
CH$LINK: COMPTOX
DTXSID30864632
AC$INSTRUMENT: Pegasus III TOF-MS system, Leco; GC 6890, Agilent Technologies
AC$INSTRUMENT_TYPE: GC-EI-TOF
AC$MASS_SPECTROMETRY: MS_TYPE MS
AC$MASS_SPECTROMETRY: ION_MODE POSITIVE
AC$MASS_SPECTROMETRY: HELIUM_FLOW 1 ml/min
AC$MASS_SPECTROMETRY: ION_SOURCE_TEMPERATURE 200 C
AC$MASS_SPECTROMETRY: SCAN_RANGE_M/Z 85-500
AC$CHROMATOGRAPHY: COLUMN_NAME CP-SIL 8 CB LOW BLEED/MS
AC$CHROMATOGRAPHY: INJECTION_TEMPERATURE 230 C
AC$CHROMATOGRAPHY: OVEN_TEMPERATURE 80 C (Duration 2 min)-330 C (rate: 15 C/min; Duration 6 min)
AC$CHROMATOGRAPHY: RETENTION_INDEX 2742.504
AC$CHROMATOGRAPHY: RETENTION_TIME 1017.608 sec
AC$CHROMATOGRAPHY: TRANSFARLINE_TEMPERATURE 250 C
MS$DATA_PROCESSING: WHOLE ChromaTOF ver. 2.32 (LECO)
PK$SPLASH: splash10-0a4i-0790000000-1516313b8da901f28bba
PK$NUM_PEAK: 199
PK$PEAK: m/z int. rel.int.
85 18 18
86 12 12
87 9 9
88 8 8
89 22 22
90 3 3
91 2 2
92 4 4
93 4 4
94 7 7
95 7 7
96 6 6
97 19 19
98 8 8
99 27 27
100 10 10
101 33 33
102 7 7
103 275 275
104 28 28
105 14 14
106 3 3
107 3 3
108 4 4
109 4 4
110 5 5
111 24 24
112 5 5
113 32 32
114 6 6
115 75 75
116 18 18
117 60 60
118 8 8
119 12 12
120 3 3
121 5 5
122 5 5
123 7 7
124 6 6
125 8 8
126 5 5
127 8 8
128 3 3
129 63 63
130 10 10
131 30 30
132 8 8
133 51 51
134 10 10
135 11 11
136 6 6
137 6 6
138 10 10
139 3 3
140 3 3
141 10 10
142 5 5
143 35 35
144 6 6
145 23 23
146 4 4
147 157 157
148 32 32
149 25 25
150 9 9
151 12 12
152 8 8
153 12 12
154 3 3
155 4 4
156 2 2
157 20 20
158 6 6
159 4 4
160 3 3
161 3 3
162 5 5
163 10 10
164 11 11
165 31 31
166 7 7
167 3 3
168 1 1
169 59 59
170 9 9
171 9 9
172 2 2
173 3 3
174 4 4
175 4 4
176 10 10
177 10 10
178 6 6
179 10 10
180 6 6
181 4 4
182 2 2
183 1 1
185 1 1
186 1 1
187 2 2
188 2 2
189 20 20
190 41 41
191 22 22
192 9 9
193 6 6
194 2 2
195 1 1
196 1 1
201 1 1
202 1 1
203 4 4
204 8 8
205 42 42
206 999 999
207 168 168
208 50 50
209 7 7
210 1 1
211 1 1
215 3 3
216 1 1
217 44 44
218 17 17
219 12 12
220 85 85
221 21 21
222 23 23
223 5 5
224 1 1
229 6 6
230 6 6
231 10 10
232 6 6
233 3 3
234 5 5
235 2 2
236 1 1
237 2 2
238 1 1
239 1 1
243 30 30
244 11 11
245 15 15
246 7 7
247 3 3
248 3 3
249 2 2
250 6 6
251 4 4
252 1 1
257 3 3
258 1 1
259 64 64
260 17 17
261 8 8
262 3 3
263 2 2
264 2 2
265 1 1
276 7 7
277 4 4
278 59 59
279 17 17
280 9 9
281 3 3
291 1 1
292 6 6
293 3 3
294 4 4
295 1 1
304 1 1
305 1 1
306 1 1
307 1 1
308 1 1
319 2 2
320 21 21
321 8 8
322 3 3
323 1 1
333 1 1
334 1 1
335 1 1
336 7 7
337 3 3
338 1 1
349 1 1
351 1 1
352 1 1
392 3 3
393 1 1
408 1 1
465 1 1
466 4 4
467 2 2
468 1 1
//
system version 2.2.8-SNAPSHOT