Mercurial > repos > recetox > matchms_split
comparison test-data/remove_spectra/require_retention_index.msp @ 19:072c7a101da6 draft
planemo upload for repository https://github.com/RECETOX/galaxytools/tree/master/tools/matchms commit 113433b8b9790405c2c5d054aee4a29a21b77dc7
author | recetox |
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date | Thu, 30 May 2024 18:11:23 +0000 |
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18:05b91d5045ce | 19:072c7a101da6 |
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1 FORMULA: C13H14O | |
2 CASNO: 2000130-22-2 | |
3 ID: 7198 | |
4 COMMENT: SpectrumID: 1752764; Source: A1-13-956/SMS7-13; DOI: 10.1021/ol1029996; QI: 383; Class: Benzene and substituted derivatives; CASRN not real! |RI:1588| | |
5 COMPOUND_NAME: ((1R*,2R*)-1-Methyl-2-phenylethynylcyclopropyl)methanol | |
6 PARENT_MASS: 186.1044655 | |
7 RETENTION_INDEX: 1588.0 | |
8 PUBCHEMID: 130762197 | |
9 NOMINAL_MASS: 186 | |
10 INCHI: nan | |
11 NUM PEAKS: 20 | |
12 51.0 89.92 | |
13 63.0 89.92 | |
14 77.0 179.84 | |
15 88.0 39.96 | |
16 89.0 59.95 | |
17 91.0 49.95 | |
18 102.0 149.86 | |
19 113.0 49.95 | |
20 115.0 229.79 | |
21 127.0 139.87 | |
22 128.0 999.0 | |
23 129.0 199.82 | |
24 144.0 99.91 | |
25 155.0 119.89 | |
26 156.0 14.89 | |
27 157.0 1.1 | |
28 158.0 0.1 | |
29 186.0 39.96 | |
30 187.0 5.89 | |
31 188.0 0.5 | |
32 | |
33 FORMULA: C34H54O4 | |
34 CASNO: 2000774-54-3 | |
35 ID: 36905 | |
36 COMMENT: SpectrumID: 1800193; Source: PA-7-239-4(DIP); DOI: 10.1002_(SICI)1099-1565(199605)7_3_136; Class: Triterpenoids; CASRN not real! |RI:3353| | |
37 COMPOUND_NAME: ((1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-9-acetoxy-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)icosahydro-1H-cyclopenta[a]chrysen-3a-yl)methyl acetate | |
38 PARENT_MASS: 526.40221 | |
39 RETENTION_INDEX: 3353.0 | |
40 PUBCHEMID: 236415 | |
41 NOMINAL_MASS: 526 | |
42 INCHI: InChI=1S/C34H54O4/c1-21(2)24-12-17-34(20-37-22(3)35)19-18-32(8)25(29(24)34)10-11-27-31(7)15-14-28(38-23(4)36)30(5,6)26(31)13-16-33(27,32)9/h24-29H,1,10-20H2,2-9H3/t24-,25+,26-,27+,28-,29+,31-,32+,33+,34+/m0/s1 | |
43 SMILES: C=C(C)[C@@H]1CC[C@]2(COC(C)=O)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC[C@H](OC(C)=O)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12 | |
44 NUM PEAKS: 14 | |
45 189.0 419.62 | |
46 203.0 249.77 | |
47 216.0 149.86 | |
48 262.0 79.93 | |
49 276.0 49.95 | |
50 393.0 149.86 | |
51 423.0 219.8 | |
52 453.0 179.84 | |
53 466.0 999.0 | |
54 526.0 179.84 | |
55 527.0 68.94 | |
56 528.0 14.29 | |
57 529.0 2.1 | |
58 530.0 0.2 | |
59 | |
60 SCANNUMBER: -1 | |
61 IONMODE: positive | |
62 SPECTRUMTYPE: Centroid | |
63 FORMULA: C20H12 | |
64 INCHIKEY: CSHWQDPOILHKBI-UHFFFAOYSA-N | |
65 SMILES: C1=CC2=C3C(=C1)C1=CC=CC4=C1C(=CC=C4)C3=CC=C2 | |
66 AUTHORS: Price et al., RECETOX, Masaryk University (CZ) | |
67 INSTRUMENT: Q Exactive GC Orbitrap GC-MS/MS | |
68 IONIZATION: EI+ | |
69 LICENSE: CC BY-NC | |
70 COMPOUND_NAME: Perylene | |
71 RETENTION_TIME: None | |
72 RETENTION_INDEX: 2886.9 | |
73 ADDUCT: [M]+ | |
74 COLLISION_ENERGY: 70eV | |
75 INSTRUMENT_TYPE: GC-EI-Orbitrap | |
76 CHARGE: 1 | |
77 PARENT_MASS: 251.08595400000002 | |
78 PRECURSOR_MZ: 251.08540542009078 | |
79 NUM PEAKS: 3 | |
80 250.07765 0.3282529462971431 | |
81 252.09323 1.0 | |
82 253.09656 0.20573802940517583 | |
83 |