SeMPI 2.0

Cluster scaffolds:

O *

1

Putative metabolites:


Name Rank Metabolite Score Similarity MCS Score Post-Mod Score Post-Mod Info Source Link Smiles Molview Full Name Figure
Phosphinothricintripeptide 0 0.38 0.36 0.48 0.0 Glyco:0/2 MIBiG Source CP(=O)([O-])CCC([NH3+])C(=O)[O-] view Phosphinothricintripeptide P O O- NH3+ O O-
FR900098 1 0.36 0.33 0.47 0.0 Glyco:0/2 MIBiG Source CC(=O)N(O)CCCP(=O)(O)O view FR900098 O N OH P O OH OH
ectoine 2 0.35 0.3 0.48 0.0 Glyco:0/2 MIBiG Source CC1=NCC[C@@H](C(=O)O)N1 view ectoine N O OH NH
2-Hydroxymethylclavam 3 0.35 0.29 0.48 0.0 Glyco:0/2 MIBiG Source O=C1C[C@@H]2O[C@@H](CO)CN12 view 2-Hydroxymethylclavam O O OH N H
d-cycloserine 9 0.34 0.34 0.43 0.0 Glyco:0/2 MIBiG Source N[C@@H]1CONC1=O view d-cycloserine H2N O NH O
Fosfomycin 4 0.35 0.4 0.4 0.0 Glyco:0/2 MIBiG Source C[C@@H]1O[C@@H]1P(=O)([O-])[O-].[Na+].[Na+] view Fosfomycin O P O O- O- Na+ Na+
itaconic acid 5 0.34 0.25 0.5 0.0 Glyco:0/2 MIBiG Source C=C(CC(=O)O)C(=O)O view itaconic acid O HO O HO
terrein 6 0.34 0.29 0.47 0.0 Glyco:0/2 MIBiG Source C/C=C/C1=CC(=O)[C@@H](O)[C@@H]1O view terrein O OH OH
Clavam-2-carboxylate 7 0.34 0.27 0.47 0.0 Glyco:0/2 MIBiG Source O=C(O)[C@H]1CN2C(=O)C[C@@H]2O1 view Clavam-2-carboxylate O OH N O O H
citrulline 8 0.34 0.27 0.47 0.0 Glyco:0/2 MIBiG Source NC(=O)NCCC[C@H](N)C(=O)O view citrulline H2N O NH NH2 O OH
SCB1 38 0.25 0.22 0.34 0.0 Glyco:0/2 MIBiG Source CC(C)CCCC[C@H](O)[C@H]1C(=O)OC[C@H]1CO view SCB1 OH O O HO
2-hydroxyethylclavam 10 0.33 0.26 0.47 0.0 Glyco:0/2 MIBiG Source O=C1C[C@@H]2O[C@@H](CCO)CN12 view 2-hydroxyethylclavam O O HO N H
Anatoxin-a 11 0.33 0.27 0.46 0.0 Glyco:0/2 MIBiG Source CC(=O)C1=CCC[C@@H]2CC[C@H]1N2 view Anatoxin-a O NH H H
3-methylarginine 12 0.33 0.26 0.46 0.0 Glyco:0/2 MIBiG Source CC(CC[NH+]=C(N)N)C([NH3+])C(=O)[O-] view 3-methylarginine NH+ H2N NH2 NH3+ O O-
methylenomycin 13 0.33 0.27 0.45 0.0 Glyco:0/2 MIBiG Source C=C1C(=O)C2(C)OC2(C)C1C(=O)O view methylenomycin O O O OH
Homoanatoxin-a 14 0.32 0.25 0.45 0.0 Glyco:0/2 MIBiG Source CCC(=O)C1=CCC[C@@H]2CC[C@H]1N2 view Homoanatoxin-a O NH H H
thiolactomycin 15 0.32 0.24 0.45 0.0 Glyco:0/2 MIBiG Source C=C/C(C)=C/[C@@]1(C)SC(=O)C(C)=C1O view thiolactomycin S O OH
fusaric acid 16 0.32 0.24 0.45 0.0 Glyco:0/2 MIBiG Source CCCCc1ccc(C(=O)O)nc1 view fusaric acid O OH N
coronafacic acid 17 0.31 0.24 0.44 0.0 Glyco:0/2 MIBiG Source CC[C@H]1C=C(C(=O)O)[C@H]2CCC(=O)[C@H]2C1 view coronafacic acid O OH O H H
2,4-Diacetylphloroglucinol 18 0.31 0.23 0.44 0.0 Glyco:0/2 MIBiG Source CC(=O)c1c(O)cc(O)c(C(C)=O)c1O view 2,4-Diacetylphloroglucinol O HO OH O OH
clavulanic acid 19 0.3 0.22 0.44 0.0 Glyco:0/2 MIBiG Source O=C(O)[C@H]1/C(=C/CO)O[C@@H]2CC(=O)N21 view clavulanic acid O OH HO O O N H
thiolutin 20 0.3 0.21 0.44 0.0 Glyco:0/2 MIBiG Source CC(=O)Nc1c2sscc-2n(C)c1=O view thiolutin O NH S S N O
cetoniacytone A 21 0.3 0.21 0.44 0.0 Glyco:0/2 MIBiG Source CC(=O)NC1=CC(=O)[C@]2(CO)O[C@@H]2[C@H]1O view cetoniacytone A O NH O OH O OH H
Tu 3010 22 0.3 0.22 0.43 0.0 Glyco:0/2 MIBiG Source C=C/C(C)=C/[C@@]1(CC(N)=O)SC(=O)C(CC)=C1O view Tu 3010 H2N O S O OH
albaflavenone 23 0.3 0.22 0.43 0.0 Glyco:0/2 MIBiG Source CC1=C2C(=O)C[C@H](C)[C@]23CC[C@@H](C3)C1(C)C view albaflavenone O H
U-68204 24 0.3 0.22 0.43 0.0 Glyco:0/2 MIBiG Source C=C/C(C)=C/[C@@]1(CC)SC(=O)C(CC(N)=O)=C1O view U-68204 S O NH2 O OH
A-factor 25 0.3 0.22 0.43 0.0 Glyco:0/2 MIBiG Source CC(C)CCCCC(=O)C1C(=O)OC[C@H]1CO view A-factor O O O HO
botryenalol 26 0.29 0.22 0.42 0.0 Glyco:0/2 MIBiG Source CC(=O)O[C@H]1C[C@@H](C)C(C=O)=C2[C@@H]1C(C)(C)C[C@]2(C)CO view botryenalol O O O HO H
botryendial 27 0.29 0.22 0.42 0.0 Glyco:0/2 MIBiG Source CC(=O)O[C@H]1C[C@@H](C)C(C=O)=C2[C@@H]1C(C)(C)C[C@]2(C)C=O view botryendial O O O O H
Xenocyloin B 28 0.28 0.19 0.42 0.0 Glyco:0/2 MIBiG Source CCC(C)C(=O)[C@@H](O)Cc1c[nH]c2ccccc12 view Xenocyloin B O OH NH
bacilysin 29 0.28 0.19 0.42 0.0 Glyco:0/2 MIBiG Source C[C@H](N)C(=O)OC(=O)[C@@H](N)CC1CCC(=O)[C@@H]2O[C@H]12 view bacilysin NH2 O O O NH2 O O H H
botrydial 30 0.28 0.21 0.41 0.0 Glyco:0/2 MIBiG Source CC(=O)O[C@H]1C[C@@H](C)[C@H](C=O)[C@@]2(O)[C@@H]1C(C)(C)C[C@]2(C)C=O view botrydial O O O HO O H
desosamine 31 0.28 0.26 0.37 0.0 Glyco:0/2 MIBiG Source CC1CC(N(C)C)C(O)C(O)O1 view desosamine N OH OH O
desosamine 32 0.28 0.26 0.37 0.0 Glyco:0/2 MIBiG Source C[C@@H]1C[C@H](N(C)C)[C@@H](O)[C@H](O)O1 view desosamine N OH OH O
2-Formyloxymethylclavam 33 0.28 0.24 0.37 0.0 Glyco:0/2 MIBiG Source O=COC[C@H]1CN2C(=O)C[C@@H]2O1 view 2-Formyloxymethylclavam O O N O O H
2-methylisoborneol 34 0.28 0.24 0.37 0.0 Glyco:0/2 MIBiG Source CC1(O)CC2CCC1(C)C2(C)C view 2-methylisoborneol OH
asperlactone 35 0.27 0.25 0.36 0.0 Glyco:0/2 MIBiG Source C[C@@H]1O[C@H]1C1=C[C@H]([C@H](C)O)OC1=O view asperlactone O OH O O
(-)-Mellein 36 0.26 0.22 0.36 0.0 Glyco:0/2 MIBiG Source C[C@@H]1Cc2cccc(O)c2C(=O)O1 view (-)-Mellein OH O O
Alanylclavam 37 0.26 0.22 0.35 0.0 Glyco:0/2 MIBiG Source N[C@@H](C[C@H]1CN2C(=O)C[C@@H]2O1)C(=O)O view Alanylclavam NH2 N O O O HO H
isoflavipucine 39 0.25 0.21 0.34 0.0 Glyco:0/2 MIBiG Source Cc1cc2c(c(=O)[nH]1)OC(C(=O)CC(C)C)O2 view isoflavipucine O NH O O O
thienamycin 40 0.25 0.21 0.34 0.0 Glyco:0/2 MIBiG Source C[C@@H](O)[C@@H]1C(=O)N2C(C(=O)O)=C(SCCN)C[C@H]12 view thienamycin OH O N O HO S NH2 H
SCB2 41 0.25 0.21 0.34 0.0 Glyco:0/2 MIBiG Source CCCCCCC[C@H](O)[C@H]1C(=O)OC[C@H]1CO view SCB2 OH O O HO
tabtoxin 42 0.25 0.21 0.34 0.0 Glyco:0/2 MIBiG Source C[C@@H](O)[C@H](NC(=O)[C@@H](N)CC[C@]1(O)CNC1=O)C(=O)O view tabtoxin OH NH O NH2 OH NH O O OH
SCB3 43 0.25 0.2 0.34 0.0 Glyco:0/2 MIBiG Source CCC(C)CCCC[C@H](O)[C@H]1C(=O)OC[C@H]1CO view SCB3 OH O O HO
2-amino-4-methoxy-trans-3-butenoic acid 44 0.24 0.23 0.3 0.0 Glyco:0/2 MIBiG Source CO/C=C/[C@H](N)C(=O)O view 2-amino-4-methoxy-trans-3-butenoic acid O NH2 O OH
terreic acid 45 0.24 0.27 0.28 0.0 Glyco:0/2 MIBiG Source CC1=C(O)C(=O)[C@@H]2O[C@@H]2C1=O view terreic acid OH O O O H H
shanorellin 46 0.23 0.25 0.27 0.0 Glyco:0/2 MIBiG Source CC1=C(O)C(C)=C(CO)C(=O)C1=O view shanorellin HO OH O O
4-deoxygadusol 47 0.23 0.25 0.27 0.0 Glyco:0/2 MIBiG Source COC1=C(O)C[C@@](O)(CO)CC1=O view 4-deoxygadusol O OH HO HO O
Argimycin PIII 48 0.21 0.21 0.27 0.0 Glyco:0/2 MIBiG Source C/C=C/C=C/C=C/C1=NCCCC1 view Argimycin PIII N
mycosporine glycine 49 0.2 0.19 0.26 0.0 Glyco:0/2 MIBiG Source COC1=C(NCC(=O)O)C[C@@](O)(CO)CC1=O view mycosporine glycine O NH O OH OH OH O

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