MassBank Record: MSBNK-Nihon_Univ-NU000068
ACCESSION: MSBNK-Nihon_Univ-NU000068
RECORD_TITLE: 3alpha,4beta-Dihydroxy-5beta-cholan-24-oic acid Methyl ester; EI-B; MS
DATE: 2016.01.19 (Created 2008.12.03, modified 2011.05.06)
AUTHORS: Takashi Iida, Department of Chemistry, College of Humanities and Sciences, Nihon University. Koichi Metori, Chemical Analytical Center, College of Pharmacy, Nihon Univercity.
LICENSE: CC BY-NC-SA
PUBLICATION: Iida, T., Momose, T., Chang, F. C., Goto, J., and Nambara, T. 1989. Potential bile acid metabolites. XV. Synthesis of 4 beta-hydroxylated bile acids; unique bile acids in human fetal bile [PMID: 2632079]. Chem Pharm Bull. 37: 3323-3329. doi:10.1248/cpb.37.3323
COMMENT: Mass spectral data were collected from the publications cited in LipidBank
COMMENT: Because the base peak (m/z=388.0) observed was scaled out, its relative intensity was adjusted so that other peaks could be shown in an appropriate range.
CH$NAME: 3alpha,4beta-Dihydroxy-5beta-cholan-24-oic acid Methyl ester
CH$COMPOUND_CLASS: Natural Product; BILE ACID
CH$FORMULA: C25H42O4
CH$EXACT_MASS: 406.30831
CH$SMILES: C(C1(C)4)([H])(C(C)CCC(=O)OC)CCC1(C(C3([H])CC4)([H])CCC(C3(C)2)([H])C(O)C(O)CC2)[H]
CH$IUPAC: InChI=1S/C25H42O4/c1-15(5-10-22(27)29-4)17-8-9-18-16-6-7-20-23(28)21(26)12-14-25(20,3)19(16)11-13-24(17,18)2/h15-21,23,26,28H,5-14H2,1-4H3/t15-,16+,17-,18+,19+,20-,21-,23-,24-,25-/m1/s1
CH$LINK: LIPIDBANK
BBA0022
CH$LINK: INCHIKEY
BJTZAKSSYSISDQ-NTMHHKLKSA-N
AC$INSTRUMENT: JEOL JMS-01SG-2
AC$INSTRUMENT_TYPE: EI-B
AC$MASS_SPECTROMETRY: MS_TYPE MS
AC$MASS_SPECTROMETRY: ION_MODE POSITIVE
AC$MASS_SPECTROMETRY: IONIZATION_POTENTIAL 60 eV
AC$MASS_SPECTROMETRY: SOURCE_TEMPERATURE 140-160 C
MS$FOCUSED_ION: BASE_PEAK 388.0
MS$FOCUSED_ION: ION_TYPE [M]+*
PK$SPLASH: splash10-052r-7955000000-1c0c8c460ef2b57f2c87
PK$NUM_PEAK: 191
PK$PEAK: m/z int. rel.int.
53 33 33
54 12 12
55 335 335
56 18 18
57 138 138
59 68 68
67 210 210
68 59 59
69 230 230
70 19 19
71 62 62
73 50 50
74 43 43
77 39 39
78 15 15
79 133 133
80 53 53
81 262 262
82 100 100
83 87 87
84 32 32
85 42 42
86 11 11
87 32 32
88 10 10
91 112 112
92 39 39
93 156 156
94 76 76
95 183 183
96 47 47
97 37 37
103 8 8
104 6 6
105 214 214
106 37 37
107 208 208
108 62 62
109 125 125
110 47 47
111 28 28
112 18 18
113 10 10
114 47 47
115 32 32
116 8 8
117 26 26
118 10 10
119 180 180
120 48 48
121 201 201
122 68 68
123 86 86
124 32 32
125 10 10
126 15 15
127 28 28
128 14 14
129 10 10
131 115 115
132 18 18
133 101 101
134 18 18
135 55 55
136 100 100
137 39 39
138 15 15
141 50 50
142 12 12
143 35 35
144 10 10
145 58 58
146 33 33
147 61 61
148 19 19
149 120 120
150 19 19
151 22 22
154 39 39
155 8 8
156 6 6
157 58 58
158 21 21
159 77 77
160 17 17
161 64 64
162 48 48
163 35 35
164 14 14
165 89 89
168 3 3
171 36 36
172 11 11
173 48 48
174 12 12
175 36 36
176 47 47
177 19 19
178 10 10
179 18 18
181 37 37
182 69 69
183 19 19
185 28 28
186 3 3
187 18 18
188 28 28
189 21 21
190 14 14
191 46 46
199 14 14
200 7 7
201 12 12
203 55 55
204 10 10
206 4 4
207 6 6
208 3 3
209 15 15
213 304 304
214 66 66
215 64 64
216 36 36
217 33 33
218 10 10
219 19 19
220 4 4
222 6 6
227 11 11
228 46 46
229 46 46
230 17 17
231 237 237
232 173 173
233 39 39
234 11 11
235 32 32
245 7 7
246 55 55
247 26 26
248 10 10
249 208 208
250 65 65
251 10 10
255 47 47
256 18 18
263 7 7
264 178 178
265 39 39
266 10 10
272 8 8
273 35 35
274 10 10
285 11 11
289 10 10
301 24 24
302 8 8
303 60 60
304 10 10
314 14 14
315 59 59
316 33 33
317 22 22
318 35 35
319 15 15
328 9 9
330 86 86
331 22 22
332 7 7
333 11 11
334 14 14
338 10 10
339 35 35
355 33 33
356 42 42
357 42 42
358 32 32
359 11 11
370 227 227
371 131 131
372 18 18
373 21 21
374 15 15
375 18 18
388 999 999
389 184 184
390 10 10
404 14 14
406 167 167
407 20 20
408 8 8
//
system version 2.2.8-SNAPSHOT