Mass2Motif: motif_23

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Mass2Motif Annotation

The following are the full annotation and the short annotation (used for network visualisation) assigned to this Mass2Motif.

Annotation: Desosamine [deoxyaminosugar found in macrolides]

Short Annotation: Desosamine [deoxyaminosugar found in macrolides]

Mass2Motif Details

The following table shows the fragment and loss features that are explained by this Mass2Motifs and their corresponding probabilities. After thresholding to save the model, the total probability left in this motif is 1.0000000000000013. The column MAGMa Substructure Annotation shows substructures and the counts of MAGMa annotations for documents linked above threshold to this motif in this experiment. Hovering over each MAGMa substructure shows a plot of the substructure.

Feature Probability MAGMA Substructure Annotation
loss_158.0925 0.085
  • COC1(C)CCOC(C)C1O (6)
fragment_258.0675 0.048
  • CN1Cc2c(C=O)ncn2-c2ccc(F)cc2C1=O (4)
fragment_158.1175 0.043
  • CC1CC(C(O)CO1)N(C)C (12)
  • CC1CC(CC(O)O1)N(C)C (2)
  • [O-][N+]12CCCC1C(CO)CC2 (1)
  • CNC(C)C(=O)OCC(C)C (1)
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loss_46.0425 0.037
  • CCO (6)
  • CC.O (1)
fragment_304.1075 0.036
fragment_276.0775 0.036
  • CN1Cc2c(ncn2-c2ccc(F)cc2C1=O)C(=O)O (3)
loss_28.0275 0.035
  • CC (3)
loss_157.0925 0.034
  • CCC(=O)OC(CC)C(C)O (6)
fragment_591.4175 0.034
  • CCC1OC(=O)C(C)C(O)C(C)C(OC2OC(C)CC(C2O)N(C)C)C(C)(O)CC(C)CN(C)C(C)C(O)C1(C)O (2)
fragment_116.1075 0.034
  • CC(O)CCN(C)C (13)
  • CC(O)CNC(C)C (2)
  • CC1CNCC(C)O1 (1)
  • CCCNCC(C)O (1)
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fragment_749.5175 0.032
  • CCC1OC(=O)C(C)C(OC2CC(C)(OC)C(O)C(C)O2)C(C)C(OC2OC(C)CC(N(C)C)C2O)C(C)(O)CC(C)CN(C)C(C)C(O)C1(C)O (3)
fragment_748.4875 0.031
  • CCC1OC(=O)C(C)C(OC2CC(C)(OC)C(O)C(C)O2)C(C)C(OC2OC(C)CC(N(C)C)C2O)C(C)(OC)CC(C)C(=O)C(C)C(O)C1(C)O (2)
loss_87.0675 0.028
  • CC.CNC=O (4)
  • C1COCCN1 (2)
  • CCNCCO (1)
fragment_734.4675 0.024
  • CCC1OC(=O)C(C)C(OC2CC(C)(OC)C(O)C(C)O2)C(C)C(OC2OC(C)CC(N(C)C)C2O)C(C)(O)CC(C)C(=O)C(C)C(O)C1(C)O (1)
fragment_590.3875 0.022
  • CCC1OC(=O)C(C)C(O)C(C)C(OC2OC(C)CC(C2O)N(C)C)C(C)(CC(C)C(=O)C(C)C(O)C1(C)O)OC (1)
fragment_735.4725 0.022
fragment_576.3775 0.019
  • CCC1OC(=O)C(C)C(O)C(C)C(OC2OC(C)CC(C2O)N(C)C)C(C)(O)CC(C)C(=O)C(C)C(O)C1(C)O (1)
loss_176.1075 0.018
  • COC1(C)CC(O)OC(C)C1O (3)
fragment_159.1175 0.015
fragment_251.0375 0.014
  • O=S(=O)(c1ccc(O)cc1)c1ccc(O)cc1 (1)
fragment_750.5225 0.014
fragment_156.9975 0.013
  • O=[SH](=O)c1ccc(O)cc1 (1)
fragment_749.4875 0.013
fragment_189.0475 0.012
  • O=Cc1cc(F)ccc1-n1ccnc1 (4)
loss_115.0625 0.012
  • CCOC=O.CNC (4)
  • C1COCCN1.C=O (1)
fragment_592.4225 0.011
  • COC1(C)CC(OCC(C)C(OC2OC(C)CC(C2O)N(C)C)C(C)(O)CC(C)CN(C)C(C)CO)OC(C)C1O (3)
fragment_577.3775 0.011
  • COC1(C)CC(OCC(C)C(OC2OC(C)CC(C2O)N(C)C)C(C)(O)CC(C)C(=O)C(C)CO)OC(C)C1O (2)
loss_75.0675 0.010
  • CCO.CN (3)
fragment_229.0425 0.010
  • Cc1c(C=O)ncn1-c1ccc(F)cc1C=O (3)
fragment_558.3625 0.009
  • CCC1OC(=O)C(C)CC(C)C(OC2OC(C)CC(C2O)N(C)C)C(C)(O)CC(C)C(=O)C(C)C(O)C1(C)O (4)
fragment_591.3925 0.007
  • COC1(C)CC(OCC(C)C(OC2OC(C)CC(C2O)N(C)C)C(C)(CC(C)C(=O)C(C)CO)OC)OC(C)C1O (2)
fragment_677.4575 0.007
fragment_162.0375 0.007
loss_142.0725 0.007
  • CCO.Fc1ccccc1 (1)
fragment_217.0425 0.007
  • Cc1c(ncn1-c1ccc(F)cc1)C(=O)O (4)
fragment_573.4125 0.007
  • CCC1OC(=O)C(C)CC(C)C(OC2OC(C)CC(C2O)N(C)C)C(C)(O)CC(C)CN(C)C(C)C(O)C1(C)O (2)
fragment_305.1125 0.007
loss_129.9925 0.006
loss_27.0275 0.006
  • C.C (2)
  • CC (1)
loss_156.0875 0.006
  • CCC(=O)OC(CC)C(C)O (2)
loss_103.0625 0.006
  • CCOC=O.CN (2)
fragment_201.0475 0.006
  • Cc1cncn1-c1ccc(F)cc1C=O (2)
fragment_98.0975 0.005
  • CCCCN(C)C (5)
  • CCCNCCC (2)
fragment_277.0825 0.005
  • CCOC(=O)c1cn(cn1)-c1ccc(F)cc1C(N)=O (2)
fragment_173.0525 0.005
  • Cc1cncn1-c1ccc(F)cc1 (1)
loss_131.0575 0.005
  • CCOC=O.CNC=O (1)
fragment_259.0725 0.005
  • CN1Cc2c(C=O)ncn2-c2ccc(F)cc2C1=O (2)
loss_175.0975 0.005
fragment_115.0775 0.005
  • CC1CCC(O)CO1 (1)
fragment_127.0775 0.005
loss_101.0475 0.004
  • CCOC=O.CN (3)
fragment_113.0575 0.004
  • CC1CCC(O)CO1 (1)
fragment_203.0625 0.004
  • Cc1cncn1-c1ccc(F)cc1C=O (3)
loss_156.0525 0.004
  • CCOC(=O)c1cncn1.O (1)
fragment_148.0575 0.004
  • CN(C)Cc1cccc(F)c1 (1)
loss_142.0075 0.004
fragment_109.0275 0.004
fragment_230.0725 0.004
  • CN1Cc2cncn2-c2ccc(F)cc2C1=O (3)
fragment_750.4925 0.004
fragment_751.5175 0.004
fragment_678.4625 0.004
loss_74.0375 0.003
  • CCOC=O (4)
  • CC.O=CO (1)
fragment_559.3675 0.003
  • CCC1OC(=O)C(C)CC(C)C(OC2OC(C)CC(C2O)N(C)C)C(C)(O)CC(C)C(=O)C(C)C(O)C1(C)O (2)
loss_139.9925 0.003
loss_190.1225 0.003
  • C.COC1(C)CC(O)OC(C)C1O (1)
fragment_593.4225 0.003
  • COC1(C)CC(OCC(C)C(OC2OC(C)CCC2O)C(C)(O)CC(C)CN(C)C(C)C(O)C(C)O)OC(C)C1O (1)
fragment_522.3425 0.003
  • CCC1OC(=O)C(C)CC(C)C(OC2OC(C)CC(C2O)N(C)C)C(C)CC(C)C(=O)C(C)CC1(C)O (1)
fragment_716.4575 0.003
  • CCC1OC(=O)C(C)C(OC2CC(C)(OC)C(O)C(C)O2)C(C)C(OC2OC(C)CC(C2O)N(C)C)C(C)CC(C)C(=O)C(C)C(O)C1(C)O (1)
loss_170.0675 0.003
loss_86.0625 0.002
fragment_574.4125 0.002
  • CCC1OC(=O)C(C)CC(C)C(OC2OC(C)CC(C2O)N(C)C)C(C)(O)CC(C)CN(C)C(C)C(O)C1(C)O (1)
loss_45.0375 0.002
  • CCO (3)
fragment_398.2875 0.002
  • CCC1OC(=O)C(C)CC(C)CC(C)(O)CC(C)CN(C)C(C)C(O)C1(C)O (2)
fragment_434.3125 0.002
  • CCC1OC(=O)C(C)C(O)C(C)C(O)C(C)(O)CC(C)CN(C)C(C)C(O)C1(C)O (1)
loss_185.9975 0.002
  • O.cS(=O)(=O)c1ccc(O)cc1 (1)
fragment_659.4425 0.002
fragment_134.0375 0.002
  • CNCc1ncnc1C=O (1)
fragment_215.0275 0.002
loss_89.0825 0.002
fragment_540.3525 0.002
  • CCC1OC(=O)C(C)CC(C)C(OC2OC(C)CC(C2O)N(C)C)C(C)CC(C)C(=O)C(C)C(O)C1(C)O (1)
fragment_316.2125 0.002
  • COC(C)(COC1OC(C)CC(C1O)N(C)C)CC(C)C=O (1)
fragment_717.4575 0.002
  • CCC1OC(=O)C(C)C(OC2CC(C)(OC)C(O)C(C)O2)C(C)C(OC2OC(C)CC(C2O)N(C)C)C(C)CC(C)C(=O)C(C)C(O)C1(C)O (1)
loss_71.0725 0.002
  • CC.CNC (1)
loss_18.0125 0.002
  • O (4)
fragment_233.0375 0.002
loss_194.1175 0.002
fragment_186.1475 0.002
  • CC(C)CN(C)C(=O)C(O)C(C)C (1)
fragment_736.4725 0.002
fragment_679.4375 0.002
  • CCC1OC(=O)C(C)C(O)C(C)C(OC2OC(C)CC(C2O)N(C)C)C(C)(O)CC(C)C(=NOCOCCOC)C(C)C(O)C1(C)O (1)
loss_114.0625 0.002
fragment_592.3925 0.002
fragment_117.1125 0.001
  • CC(O)CNC(C)C (1)
  • CCCNCC(C)O (1)
loss_63.0675 0.001
fragment_241.0375 0.001

Counts of Classyfire Substituent terms

Term name Count in motif Percentage in motif Percentage in experiment Absolute difference
Hydrocarbon derivative 30 83.3 78.1 5.2
Organic nitrogen compound 27 75 60.8 14.2
Organonitrogen compound 27 75 60.8 14.2
Organic oxide 26 72.2 62.0 10.2
Organopnictogen compound 25 69.4 46.6 22.9
Carboxylic acid derivative 23 63.9 35.2 28.7
Amine 20 55.6 25.0 30.5
Carboxylic acid ester 18 50 13.9 36.1
Ether 18 50 30.9 19.1
Monocarboxylic acid or derivatives 16 44.4 19.7 24.8
Dialkyl ether 16 44.4 7.7 36.7
Tertiary amine 16 44.4 14.6 29.9
Tertiary aliphatic amine 16 44.4 13.7 30.7
Organic oxygen compound 16 44.4 69.8 25.3
Organooxygen compound 16 44.4 68.4 23.9
Alcohol 15 41.7 18.9 22.7
Oxacycle 15 41.7 27.5 14.2
Carbonyl group 15 41.7 41.3 0.3
Organoheterocyclic compound 15 41.7 38.0 3.6
Secondary alcohol 14 38.9 14.3 24.6
Amino acid or derivatives 14 38.9 10.7 28.2
Azacycle 13 36.1 46.4 10.3
Aliphatic heteromonocyclic compound 12 33.3 2.2 31.2
Tertiary alcohol 12 33.3 5.5 27.8
1,2-aminoalcohol 12 33.3 3.3 30.0
Acetal 11 30.6 4.4 26.1
Macrolide 11 30.6 1.6 28.9
Aminoglycoside core 11 30.6 0.5 30.1
Oxane 11 30.6 3.4 27.2
Lactone 11 30.6 12.7 17.9
Glycosyl compound 10 27.8 2.4 25.4
O-glycosyl compound 10 27.8 1.7 26.1
Monosaccharide 10 27.8 2.8 25.0
Ketone 9 25 11.9 13.1
Cyclic ketone 9 25 5.2 19.8
Benzenoid 8 22.2 45.0 22.8
Organohalogen compound 8 22.2 14.1 8.2
Heteroaromatic compound 8 22.2 36.8 14.6
Carboxamide group 8 22.2 24.1 1.9
Polyol 7 19.4 4.9 14.6
Tertiary carboxylic acid amide 7 19.4 12.0 7.5
Aromatic heteropolycyclic compound 7 19.4 40.3 20.9
Lactam 6 16.7 10.3 6.3
Aryl halide 6 16.7 10.8 5.9
Aromatic homomonocyclic compound 6 16.7 9.6 7.1
Vinylogous amide 5 13.9 4.9 9.0
Organofluoride 5 13.9 5.2 8.7
Azole 5 13.9 8.1 5.8
Imidazole 4 11.1 4.0 7.1
Imidazo[1,5-a][1,4]benzodiazepine 4 11.1 0.1 11.0
N-substituted imidazole 4 11.1 3.2 7.9
Aryl fluoride 4 11.1 3.2 7.9
Para-diazepine 4 11.1 0.2 10.9
Imidazole-4-carbonyl group 4 11.1 0.2 10.9
Aldehyde 4 11.1 1.1 10.0
Benzoyl 4 11.1 7.2 3.9
Aromatic heteromonocyclic compound 4 11.1 14.3 3.2
Monocyclic benzene moiety 4 11.1 26.6 15.5
Fatty acid ester 3 8.3 2.5 5.8
Pyrrolidine 3 8.3 5.8 2.5
Fatty acyl 3 8.3 5.9 2.4
N-alkylpyrrolidine 3 8.3 2.2 6.1
Secondary aliphatic amine 3 8.3 4.4 4.0
Phenoxy compound 3 8.3 11.4 3.0
Phenol ether 3 8.3 13.0 4.6
Alkyl aryl ether 3 8.3 24.7 16.4
Secondary amine 3 8.3 5.3 3.1
Morpholine 3 8.3 0.8 7.5
Aralkylamine 3 8.3 10.5 2.2
1-hydroxy-2-unsubstituted benzenoid 2 5.6 8.9 3.3
Phenol 2 5.6 6.8 1.3
Toluene 2 5.6 2.3 3.2
Benzylether 2 5.6 0.6 4.9
Tricarboxylic acid or derivatives 2 5.6 0.6 4.9
Halobenzene 2 5.6 6.1 0.6
Organochloride 2 5.6 8.7 3.1
Pyridine 2 5.6 8.5 2.9
Alkyl halide 2 5.6 3.3 2.2
Oxazinane 2 5.6 0.8 4.7
Pyrrolidone 2 5.6 1.1 4.5
Pyrrole 2 5.6 7.6 2.1
Diphenylmethane 2 5.6 2.1 3.5
2-pyrrolidone 2 5.6 1.0 4.5
3-phenylpyrrolidine 2 5.6 0.2 5.4
Oxime ether 1 2.8 0.1 2.7
Sulfone 1 2.8 0.5 2.3
Organosulfur compound 1 2.8 7.6 4.8
Sulfonyl 1 2.8 4.0 1.2
Benzenesulfonyl group 1 2.8 2.7 0.1
Vinylogous acid 1 2.8 5.4 2.6
1-hydroxy-4-unsubstituted benzenoid 1 2.8 5.3 2.5
Dihydroxybenzoic acid 1 2.8 0.2 2.6
Resorcinol 1 2.8 0.4 2.4
O-hydroxybenzoic acid ester 1 2.8 0.1 2.7
Salicylic acid or derivatives 1 2.8 0.5 2.2
P-hydroxybenzoic acid alkyl ester 1 2.8 0.1 2.7
M-cresol 1 2.8 0.3 2.5
Trialkyl amine oxide 1 2.8 0.1 2.7
Organic salt 1 2.8 0.7 2.0
N-oxide 1 2.8 0.1 2.7
Organic zwitterion 1 2.8 1.1 1.7
Hydroxy acid 1 2.8 0.7 2.0
Beta-hydroxy acid 1 2.8 0.8 2.0
1,2-diol 1 2.8 0.8 2.0
Aliphatic heteropolycyclic compound 1 2.8 3.5 0.8
Trisubstituted n-oxide 1 2.8 0.1 2.7
Pyrrolizidine 1 2.8 0.0 2.8
Imidolactam 1 2.8 3.8 1.0
Aryl chloride 1 2.8 7.2 4.4
Alkanolamine 1 2.8 1.1 1.7
1,3-thiazol-2-amine 1 2.8 0.4 2.4
N-arylpiperazine 1 2.8 1.6 1.2
Aromatic anilide 1 2.8 0.2 2.6
2-heteroaryl carboxamide 1 2.8 1.2 1.6
Thiazolecarboxylic acid or derivatives 1 2.8 0.2 2.6
2,5-disubstituted 1,3-thiazole 1 2.8 0.1 2.7
Chlorobenzene 1 2.8 4.2 1.4
Piperazine 1 2.8 2.9 0.1
Secondary carboxylic acid amide 1 2.8 15.3 12.5
Pyrimidine 1 2.8 4.5 1.7
1,4-diazinane 1 2.8 2.9 0.1
Aminopyrimidine 1 2.8 2.3 0.5
Primary alcohol 1 2.8 5.5 2.7
Thiazole 1 2.8 1.7 1.1
N-alkylpiperazine 1 2.8 3.1 0.3
Thiazolecarboxamide 1 2.8 0.1 2.7
Dialkylarylamine 1 2.8 3.4 0.7
Aminoquinoline 1 2.8 0.8 1.9
Acridine 1 2.8 0.1 2.7
Primary aromatic amine 1 2.8 3.3 0.5
Aminopyridine 1 2.8 0.7 2.1
4-aminoquinoline 1 2.8 0.1 2.6
Primary amine 1 2.8 6.3 3.5
Methylpyridine 1 2.8 0.7 2.1
Carboxylic acid 1 2.8 13.3 10.5
Pyridine carboxylic acid or derivatives 1 2.8 1.7 1.0
Pyridine carboxylic acid 1 2.8 1.1 1.7
Naphthyridine carboxylic acid 1 2.8 0.1 2.7
Alkyl chloride 1 2.8 1.2 1.5
Chloroacetamide 1 2.8 0.1 2.7
Benzoate ester 1 2.8 1.5 1.3
Dicarboxylic acid or derivatives 1 2.8 4.2 1.4
Trifluoromethylbenzene 1 2.8 0.8 1.9
Alkyl fluoride 1 2.8 2.1 0.6
Phenylpiperidine 1 2.8 0.8 2.0
3-aroylfuran 1 2.8 0.1 2.7
Organoiodide 1 2.8 0.2 2.5
Aryl iodide 1 2.8 0.2 2.5
Furan 1 2.8 2.2 0.6
Aryl-phenylketone 1 2.8 0.7 2.0
Iodobenzene 1 2.8 0.2 2.6
Benzofuran 1 2.8 1.8 0.9
Carboximidic acid 1 2.8 3.9 1.1
Organic 1,3-dipolar compound 1 2.8 9.9 7.2
Propargyl-type 1,3-dipolar organic compound 1 2.8 9.9 7.1
Acetophenone 1 2.8 0.4 2.4
Aryl alkyl ketone 1 2.8 3.2 0.4
Carboximidic acid derivative 1 2.8 4.9 2.1
Alkyl-phenylketone 1 2.8 1.0 1.8

Counts of Mass2Motif Features

Two bar plots will appear below this message. The first shows the proportion of the total intensity of these features explained by this Mass2Motif. Red bars show the total intensity (across the whole dataset), blue bars show the proportion explained by the selected Mass2Motif. The second shows the number of times each feature in this Mass2Motif appears in the documents associated with this Mass2Motif.

Fragmentation Spectra Explained by Mass2Motif

The following table lists all fragmentation spectra that are explained by this Mass2Motif at the threshold specified in the experiment option.

Fragmentation spectraPrecursor MassParent massAnnotationProbabilityOverlap Score
CCMSLIB00000077129.ms 749.5158 749.5158 Azithromycin [M+H] 0.927 0.284
CCMSLIB00000078309.ms 749.5158 749.5158 Azithromycin (Zithromax) [M+H] 0.874 0.213
CCMSLIB00000006289.ms 734.4685 734.4685 Erythromycin M+H 0.864 0.239
CCMSLIB00000078102.ms 304.1092 304.1092 Flumazenil [M+H] 0.853 0.278
CCMSLIB00000005237.ms 304.1092 304.1092 Flumazenil M+H 0.850 0.144
CCMSLIB00000078509.ms 748.4842 748.4842 "Clarithromycin (Biaxin, Klacid)" [M+H] 0.828 0.229
CCMSLIB00000085629.ms 837.5318 837.5318 MLS002154033-01!Roxithromycin80214-83-1 M+H 0.814 0.203
CCMSLIB00000085433.ms 342.2064 342.2064 MLS001148185-01! M+H 0.807 0.040
CCMSLIB00000078915.ms 304.1092 304.1092 "ethyl 8-fluoro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate" [M+H] 0.758 0.252
CCMSLIB00000085014.ms 304.1092 304.1092 MLS001076354-01! M+H 0.743 0.265
CCMSLIB00000078998.ms 748.4842 748.4842 CLARITHROMYCIN [M+H] 0.731 0.233
CCMSLIB00000223877.ms 582.3637 582.3637 Rosamicin M+H 0.718 0.087
CCMSLIB00000078217.ms 734.4685 734.4685 Erythromycin (E-Mycin) [M+H] 0.688 0.243
CCMSLIB00000004873.ms 748.4842 748.4842 Clarithromycin M+H 0.610 0.099
CCMSLIB00000084786.ms 749.5158 749.5158 MLS001201763-01!Azithromycin M+H 0.567 0.221
CCMSLIB00000579625.ms 251.0373 251.0373 Bisphenol S M+H 0.563 0.040
CCMSLIB00000080001.ms 197.0808 197.0808 MLS002695995-01! M+H 0.486 0.043
CCMSLIB00000478608.ms 591.4215 591.4215 DescladinoseAzithromycin M+H 0.421 0.088
CCMSLIB00000006292.ms 734.4685 734.4685 Erythromycin M+H 0.405 0.130
CCMSLIB00000078722.ms 302.1962 302.1962 NCGC00160190-01!HELIOCURASSAVICINE N-OXYDE M+H 0.332 0.059
CCMSLIB00000004930.ms 326.2326 326.2326 Bisoprolol M+H 0.315 0.035
CCMSLIB00000579651.ms 282.2791 282.2791 Dodemorph M+H 0.284 0.039
CCMSLIB00000086045.ms 862.5159 862.5159 MLS001074901-01!erythromycin ethylsuccinate M+H 0.176 0.082
CCMSLIB00000006077.ms 488.1630 488.1630 Dasatinib M+H 0.173 0.028
CCMSLIB00000085457.ms 199.1230 199.1230 "MLS001401372-01!9-AMINO-1,2,3,4-TETRAHYDROACRIDINE HYDROCHLORIDE" M+H 0.137 0.042
CCMSLIB00000078462.ms 233.0921 233.0921 Nalidixic acid (NegGram) [M+H] 0.116 0.045
CCMSLIB00000579877.ms 296.1412 296.1412 0144_Pethoxamid M+H 0.113 0.037
CCMSLIB00000579692.ms 223.0965 223.0965 Diethyl phthalate M+H 0.097 0.037
CCMSLIB00000077069.ms 862.5159 862.5159 Eryped [M+H] 0.071 0.082
CCMSLIB00000079081.ms 379.2380 379.2380 DOXAPRAM HYDROCHLORIDE [M+H] 0.069 0.040
CCMSLIB00000085144.ms 404.1444 404.1444 "MLS002153399-01!L-733,060 hydrochloride" M+H 0.065 0.028
CCMSLIB00000078631.ms 379.2380 379.2380 Doxapram HCl [M+H] 0.064 0.028
CCMSLIB00000085508.ms 646.0310 646.0310 MLS001076313-01!19774-82-4 M+H 0.061 0.042
CCMSLIB00000078999.ms 770.4661 770.4661 CLARITHROMYCIN [M+Na] 0.061 0.085
CCMSLIB00000577703.ms 612.3855 612.3855 Enniatin_J1_51868_dereplictor_pv_1.21096e-15 M+H 0.053 0.045
CCMSLIB00000078619.ms 337.2122 337.2122 Acebutolol HCl [M+H] 0.052 0.035

Fragmentation Spectra Plot

The fragmentation spectra of molecules explained by this Mass2Motif are plotted below. Features (fragments and losses) explained by this Mass2Motif will be coloured red, while parent ion is coloured in blue. Click Next and Previous to cycle through the fragmentation spectra.

Result goes here: