view test-data/remove_spectra/require_compound_name.msp @ 17:7627b40601f6 draft default tip

planemo upload for repository https://github.com/RECETOX/galaxytools/tree/master/tools/matchms commit 8db07edd3b0d2ff778036dec410027ad58365488

FORMULA: C13H14O
CASNO: 2000130-22-2
ID: 7198
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|
COMPOUND_NAME: ((1R*,2R*)-1-Methyl-2-phenylethynylcyclopropyl)methanol
PARENT_MASS: 186.1044655
RETENTION_INDEX: 1588.0
PUBCHEMID: 130762197
NOMINAL_MASS: 186
INCHI: nan
NUM PEAKS: 20
51.0        89.92
63.0        89.92
77.0        179.84
88.0        39.96
89.0        59.95
91.0        49.95
102.0       149.86
113.0       49.95
115.0       229.79
127.0       139.87
128.0       999.0
129.0       199.82
144.0       99.91
155.0       119.89
156.0       14.89
157.0       1.1
158.0       0.1
186.0       39.96
187.0       5.89
188.0       0.5

FORMULA: C34H54O4
CASNO: 2000774-54-3
ID: 36905
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|
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
PARENT_MASS: 526.40221
RETENTION_INDEX: 3353.0
PUBCHEMID: 236415
NOMINAL_MASS: 526
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
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
NUM PEAKS: 14
189.0       419.62
203.0       249.77
216.0       149.86
262.0       79.93
276.0       49.95
393.0       149.86
423.0       219.8
453.0       179.84
466.0       999.0
526.0       179.84
527.0       68.94
528.0       14.29
529.0       2.1
530.0       0.2

IONMODE: negative
SPECTRUMTYPE: Centroid
COMPOUND_NAME: C001
RETENTION_TIME: 38.74
RETENTION_INDEX: None
NUM PEAKS: 16
138.9121    10186226.0
175.0641    26780143.0
196.8658    21390430.0
198.8647    21688594.0
206.9034    26130980.0
254.8252    23747536.0
258.8237    15532799.0
266.8652    9805546.0
312.7841    10051801.0
316.7777    10734168.0
372.7383    19374863.0
382.8218    12815572.0
392.7685    10913351.0
434.7287    9943329.0
440.7322    10603010.0
488.6825    12267966.0

SCANNUMBER: -1
IONMODE: positive
SPECTRUMTYPE: Centroid
FORMULA: C20H12
INCHIKEY: CSHWQDPOILHKBI-UHFFFAOYSA-N
SMILES: C1=CC2=C3C(=C1)C1=CC=CC4=C1C(=CC=C4)C3=CC=C2
AUTHORS: Price et al., RECETOX, Masaryk University (CZ)
INSTRUMENT: Q Exactive GC Orbitrap GC-MS/MS
IONIZATION: EI+
LICENSE: CC BY-NC
COMPOUND_NAME: Perylene
RETENTION_TIME: None
RETENTION_INDEX: 2886.9
ADDUCT: [M]+
COLLISION_ENERGY: 70eV
INSTRUMENT_TYPE: GC-EI-Orbitrap
CHARGE: 1
PARENT_MASS: 251.08595400000002
PRECURSOR_MZ: 251.08540542009078
NUM PEAKS: 3
250.07765   0.3282529462971431
252.09323   1.0
253.09656   0.20573802940517583