MiMeDB: Showing metabocard for Fumisoquin A (MMDBc0012675)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 04:09:31 UTC

Update Date

2025-10-07 16:06:01 UTC

Metabolite ID

MMDBc0012675

Metabolite Identification

Common Name

Fumisoquin A

Description

Fumisoquin A is a secondary metabolite belonging to the class of quinones. There is limited literature available on this compound, indicating a need for further research to fully understand its properties and potential biological activities.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152106092D          

 20 22  0  0  0  0            999 V2000
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  5  1  1  0  0  0  0
  6  4  1  0  0  0  0
  6  5  2  0  0  0  0
  7  3  1  0  0  0  0
  8  2  1  0  0  0  0
  9  3  1  0  0  0  0
 10  9  1  0  0  0  0
 11  6  1  0  0  0  0
 11  8  2  0  0  0  0
 12  5  1  0  0  0  0
 12 10  1  0  0  0  0
 13  7  1  0  0  0  0
 14  7  1  0  0  0  0
 15  4  1  0  0  0  0
 15 10  1  0  0  0  0
 15 13  1  0  0  0  0
 16  8  1  0  0  0  0
 17  9  1  0  0  0  0
 18 11  1  0  0  0  0
 19 12  1  0  0  0  0
 20 13  2  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0012675

> <DATABASE_NAME>
MIME

> <SMILES>
NC1CC(O)C2C(O)C3=C(CN2C1=O)C(O)=C(O)C=C3

> <INCHI_IDENTIFIER>
InChI=1S/C13H16N2O5/c14-7-3-9(17)10-12(19)5-1-2-8(16)11(18)6(5)4-15(10)13(7)20/h1-2,7,9-10,12,16-19H,3-4,14H2

> <INCHI_KEY>
DGLVASJKYCTLGR-UHFFFAOYSA-N

> <FORMULA>
C13H16N2O5

> <MOLECULAR_WEIGHT>
280.28

> <EXACT_MASS>
280.105921623

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
27.20250137902395

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-amino-1,7,8,11-tetrahydroxy-1H,2H,3H,4H,6H,11H,11aH-pyrido[1,2-b]isoquinolin-4-one

> <ALOGPS_LOGP>
-1.92

> <JCHEM_LOGP>
-2.082907922238311

> <ALOGPS_LOGS>
-0.98

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
12.45516646789185

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.036609381151012

> <JCHEM_PKA_STRONGEST_BASIC>
8.00629125346627

> <JCHEM_POLAR_SURFACE_AREA>
127.25000000000001

> <JCHEM_REFRACTIVITY>
68.98490000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.96e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-amino-1,7,8,11-tetrahydroxy-1H,2H,3H,6H,11H,11aH-pyrido[1,2-b]isoquinolin-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-MAY-21         0                                  
HETATM    1  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.000   1.540   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0      -2.667   1.540   0.000  0.00  0.00           N+0
HETATM   15  N   UNK     0       1.334   2.310   0.000  0.00  0.00           N+0
HETATM   16  O   UNK     0       8.002   1.540   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       0.000   6.160   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       5.335   0.000   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       2.667   6.160   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       0.000  -0.000   0.000  0.00  0.00           O+0
CONECT    1    2    5                                                       
CONECT    2    1    8                                                       
CONECT    3    7    9                                                       
CONECT    4    6   15                                                       
CONECT    5    1    6   12                                                  
CONECT    6    4    5   11                                                  
CONECT    7    3   13   14                                                  
CONECT    8    2   11   16                                                  
CONECT    9    3   10   17                                                  
CONECT   10    9   12   15                                                  
CONECT   11    6    8   18                                                  
CONECT   12    5   10   19                                                  
CONECT   13    7   15   20                                                  
CONECT   14    7                                                            
CONECT   15    4   10   13                                                  
CONECT   16    8                                                            
CONECT   17    9                                                            
CONECT   18   11                                                            
CONECT   19   12                                                            
CONECT   20   13                                                            
MASTER        0    0    0    0    0    0    0    0   20    0   44    0
END

Synonyms

Not Available

Molecular Formula

C₁₃H₁₆N₂O₅

Average Mass

280.28

Monoisotopic Mass

280.105921623

IUPAC Name

3-amino-1,7,8,11-tetrahydroxy-1H,2H,3H,4H,6H,11H,11aH-pyrido[1,2-b]isoquinolin-4-one

Traditional Name

3-amino-1,7,8,11-tetrahydroxy-1H,2H,3H,6H,11H,11aH-pyrido[1,2-b]isoquinolin-4-one

CAS Registry Number

Not Available

SMILES

NC1CC(O)C2C(O)C3=C(CN2C1=O)C(O)=C(O)C=C3

InChI Identifier

InChI=1S/C13H16N2O5/c14-7-3-9(17)10-12(19)5-1-2-8(16)11(18)6(5)4-15(10)13(7)20/h1-2,7,9-10,12,16-19H,3-4,14H2

InChI Key

DGLVASJKYCTLGR-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetrahydroisoquinolines. These are tetrahydrogenated isoquinoline derivatives.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Tetrahydroisoquinolines

Sub Class

Not Available

Direct Parent

Tetrahydroisoquinolines

Alternative Parents

Substituents

Tetrahydroisoquinoline
Alpha-amino acid or derivatives
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Aralkylamine
Piperidinone
Delta-lactam
3-aminopiperidine
Benzenoid
Piperidine
Tertiary carboxylic acid amide
Secondary alcohol
Lactam
Carboxamide group
Amino acid or derivatives
Azacycle
Polyol
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Primary amine
Organooxygen compound
Organonitrogen compound
Primary aliphatic amine
Carbonyl group
Amine
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	29.6 g/L	ALOGPS
logP	-1.9	ALOGPS
logP	-2.1	ChemAxon
logS	-0.98	ALOGPS
pKa (Strongest Acidic)	9.04	ChemAxon
pKa (Strongest Basic)	8.01	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	127.25 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	68.98 m³·mol⁻¹	ChemAxon
Polarizability	27.2 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_3_2) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-09	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-09	View Spectrum
MS	Mass Spectrum (Electron Ionization)	Not Available	2022-08-06	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum

Chromatographic Retention Times and Retention Indices

Retention Times

Chromatography Type	Technique	Column	Deposition Date	Retention Time (s)
Liquid Chromatography	HILIC	Waters Acquity UPLC-BEH Amide column (eluted)	2025-10-23	459.8
Liquid Chromatography	HILIC	Accucore 150 Amide HILIC (eluted)	2025-10-23	346.5
Liquid Chromatography	Reversed-phase	Hypersil Gold 1.9 µm C18 (eluted)	2025-10-23	47.0
Liquid Chromatography	Reversed-phase	Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) (eluted)	2025-10-23	250.9
Liquid Chromatography	Reversed-phase	XBridge C18 3.5u 2.1x50 mm (eluted)	2025-10-23	280.7
Liquid Chromatography	Reversed-phase	Ascentis Express C18 (eluted)	2025-10-23	232.1
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-23	387.6
Liquid Chromatography	HILIC	Merck SeQuant ZIC-HILIC (eluted)	2025-10-23	873.5
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC (eluted)	2025-10-23	412.8
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-23	139.6
Liquid Chromatography	HILIC	Merck SeQuant ZIC-HILIC (eluted)	2025-10-23	658.2
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-23	155.5
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-23	66.6
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC column (eluted)	2025-10-23	411.6
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC column (eluted)	2025-10-23	607.3
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-23	41.6
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-23	201.8
Liquid Chromatography	Reversed-phase	Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex (eluted)	2025-10-23	676.1
Liquid Chromatography	Reversed-phase	Waters Atlantis T3 (2.1 x 150 mm, 5 um) (eluted)	2025-10-23	549.7

Retention Indices

Chromatography Type	Peak Label	SMILES	Stationary Phase	Deposition Date	Retention Index
Gas Chromatography	Fumisoquin A_TMS_1	C[Si](C)(C)OC1CC(N)C(=O)N2CC3=C(C=CC(O)=C3O)C(O)C12	standard non polar	2025-10-23	2568.0
Gas Chromatography	Fumisoquin A_TMS_2	C[Si](C)(C)OC1C2=CC=C(O)C(O)=C2CN2C(=O)C(N)CC(O)C12	standard non polar	2025-10-23	2437.9
Gas Chromatography	Fumisoquin A_TMS_3	C[Si](C)(C)OC1=C(O)C=CC2=C1CN1C(=O)C(N)CC(O)C1C2O	standard non polar	2025-10-23	1876.09
Gas Chromatography	Fumisoquin A_TMS_4	C[Si](C)(C)OC1=CC=C2C(=C1O)CN1C(=O)C(N)CC(O)C1C2O	standard non polar	2025-10-23	2131.06
Gas Chromatography	Fumisoquin A_TMS_5	C[Si](C)(C)NC1CC(O)C2C(O)C3=CC=C(O)C(O)=C3CN2C1=O	standard non polar	2025-10-23	2389.07
Gas Chromatography	Fumisoquin A_TMS_6	C[Si](C)(C)OC1=CC=C2C(=C1O)CN1C(=O)C(N)CC(O[Si](C)(C)C)C1C2O	standard non polar	2025-10-23	2066.66
Gas Chromatography	Fumisoquin A_TMS_7	C[Si](C)(C)OC1=C(O)C=CC2=C1CN1C(=O)C(N)CC(O[Si](C)(C)C)C1C2O	standard non polar	2025-10-23	961.407
Gas Chromatography	Fumisoquin A_TMS_8	C[Si](C)(C)OC1CC(N)C(=O)N2CC3=C(C=CC(O)=C3O)C(O[Si](C)(C)C)C12	standard non polar	2025-10-23	1395.09
Gas Chromatography	Fumisoquin A_TMS_9	C[Si](C)(C)NC1CC(O[Si](C)(C)C)C2C(O)C3=CC=C(O)C(O)=C3CN2C1=O	standard non polar	2025-10-23	2005.88
Gas Chromatography	Fumisoquin A_TMS_10	C[Si](C)(C)OC1=CC=C2C(=C1O)CN1C(=O)C(N)CC(O)C1C2O[Si](C)(C)C	standard non polar	2025-10-23	1783.03
Gas Chromatography	Fumisoquin A_TMS_11	C[Si](C)(C)OC1=C(O)C=CC2=C1CN1C(=O)C(N)CC(O)C1C2O[Si](C)(C)C	standard non polar	2025-10-23	2029.43
Gas Chromatography	Fumisoquin A_TMS_12	C[Si](C)(C)NC1CC(O)C2C(O[Si](C)(C)C)C3=CC=C(O)C(O)=C3CN2C1=O	standard non polar	2025-10-23	853.473
Gas Chromatography	Fumisoquin A_TMS_13	C[Si](C)(C)OC1=CC=C2C(=C1O[Si](C)(C)C)CN1C(=O)C(N)CC(O)C1C2O	standard non polar	2025-10-23	1990.29
Gas Chromatography	Fumisoquin A_TMS_14	C[Si](C)(C)NC1CC(O)C2C(O)C3=CC=C(O)C(O[Si](C)(C)C)=C3CN2C1=O	standard non polar	2025-10-23	1731.38
Gas Chromatography	Fumisoquin A_TMS_15	C[Si](C)(C)NC1CC(O)C2C(O)C3=CC=C(O[Si](C)(C)C)C(O)=C3CN2C1=O	standard non polar	2025-10-23	2057.84
Gas Chromatography	Fumisoquin A_TMS_16	C[Si](C)(C)N(C1CC(O)C2C(O)C3=CC=C(O)C(O)=C3CN2C1=O)[Si](C)(C)C	standard non polar	2025-10-23	1154.81
Gas Chromatography	Fumisoquin A_TMS_17	C[Si](C)(C)OC1=CC=C2C(=C1O[Si](C)(C)C)CN1C(=O)C(N)CC(O[Si](C)(C)C)C1C2O	standard non polar	2025-10-23	2782.91
Gas Chromatography	Fumisoquin A_TMS_18	C[Si](C)(C)OC1=CC=C2C(=C1O)CN1C(=O)C(N)CC(O[Si](C)(C)C)C1C2O[Si](C)(C)C	standard non polar	2025-10-23	1765.83
Gas Chromatography	Fumisoquin A_TMS_19	C[Si](C)(C)NC1CC(O[Si](C)(C)C)C2C(O)C3=CC=C(O[Si](C)(C)C)C(O)=C3CN2C1=O	standard non polar	2025-10-23	2109.75
Gas Chromatography	Fumisoquin A_TMS_20	C[Si](C)(C)OC1=C(O)C=CC2=C1CN1C(=O)C(N)CC(O[Si](C)(C)C)C1C2O[Si](C)(C)C	standard non polar	2025-10-23	1265.74
Gas Chromatography	Fumisoquin A_TMS_21	C[Si](C)(C)NC1CC(O[Si](C)(C)C)C2C(O)C3=CC=C(O)C(O[Si](C)(C)C)=C3CN2C1=O	standard non polar	2025-10-23	2200.56
Gas Chromatography	Fumisoquin A_TMS_22	C[Si](C)(C)NC1CC(O[Si](C)(C)C)C2C(O[Si](C)(C)C)C3=CC=C(O)C(O)=C3CN2C1=O	standard non polar	2025-10-23	1875.92
Gas Chromatography	Fumisoquin A_TMS_23	C[Si](C)(C)OC1CC(N([Si](C)(C)C)[Si](C)(C)C)C(=O)N2CC3=C(C=CC(O)=C3O)C(O)C12	standard non polar	2025-10-23	1718.88
Gas Chromatography	Fumisoquin A_TMS_24	C[Si](C)(C)OC1=CC=C2C(=C1O[Si](C)(C)C)CN1C(=O)C(N)CC(O)C1C2O[Si](C)(C)C	standard non polar	2025-10-23	1704.82
Gas Chromatography	Fumisoquin A_TMS_25	C[Si](C)(C)NC1CC(O)C2C(O[Si](C)(C)C)C3=CC=C(O[Si](C)(C)C)C(O)=C3CN2C1=O	standard non polar	2025-10-23	1445.46
Gas Chromatography	Fumisoquin A_TMS_26	C[Si](C)(C)NC1CC(O)C2C(O[Si](C)(C)C)C3=CC=C(O)C(O[Si](C)(C)C)=C3CN2C1=O	standard non polar	2025-10-23	2226.03
Gas Chromatography	Fumisoquin A_TMS_27	C[Si](C)(C)OC1C2=CC=C(O)C(O)=C2CN2C(=O)C(N([Si](C)(C)C)[Si](C)(C)C)CC(O)C12	standard non polar	2025-10-23	1991.66
Gas Chromatography	Fumisoquin A_TMS_28	C[Si](C)(C)NC1CC(O)C2C(O)C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CN2C1=O	standard non polar	2025-10-23	2161.8
Gas Chromatography	Fumisoquin A_TMS_29	C[Si](C)(C)OC1=C(O)C=CC2=C1CN1C(=O)C(N([Si](C)(C)C)[Si](C)(C)C)CC(O)C1C2O	standard non polar	2025-10-23	1928.44
Gas Chromatography	Fumisoquin A_TMS_30	C[Si](C)(C)OC1=CC=C2C(=C1O)CN1C(=O)C(N([Si](C)(C)C)[Si](C)(C)C)CC(O)C1C2O	standard non polar	2025-10-23	1353.48
Gas Chromatography	Fumisoquin A_TMS_31	C[Si](C)(C)OC1=CC=C2C(=C1O[Si](C)(C)C)CN1C(=O)C(N)CC(O[Si](C)(C)C)C1C2O[Si](C)(C)C	standard non polar	2025-10-23	1854.8
Gas Chromatography	Fumisoquin A_TMS_32	C[Si](C)(C)NC1CC(O[Si](C)(C)C)C2C(O)C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CN2C1=O	standard non polar	2025-10-23	1119.62
Gas Chromatography	Fumisoquin A_TMS_33	C[Si](C)(C)NC1CC(O[Si](C)(C)C)C2C(O[Si](C)(C)C)C3=CC=C(O[Si](C)(C)C)C(O)=C3CN2C1=O	standard non polar	2025-10-23	1071.62
Gas Chromatography	Fumisoquin A_TMS_34	C[Si](C)(C)OC1=CC=C2C(=C1O)CN1C(=O)C(N([Si](C)(C)C)[Si](C)(C)C)CC(O[Si](C)(C)C)C1C2O	standard non polar	2025-10-23	1662.38
Gas Chromatography	Fumisoquin A_TMS_35	C[Si](C)(C)NC1CC(O[Si](C)(C)C)C2C(O[Si](C)(C)C)C3=CC=C(O)C(O[Si](C)(C)C)=C3CN2C1=O	standard non polar	2025-10-23	2072.79
Gas Chromatography	Fumisoquin A_TMS_36	C[Si](C)(C)OC1=C(O)C=CC2=C1CN1C(=O)C(N([Si](C)(C)C)[Si](C)(C)C)CC(O[Si](C)(C)C)C1C2O	standard non polar	2025-10-23	2196.85
Gas Chromatography	Fumisoquin A_TMS_37	C[Si](C)(C)OC1CC(N([Si](C)(C)C)[Si](C)(C)C)C(=O)N2CC3=C(C=CC(O)=C3O)C(O[Si](C)(C)C)C12	standard non polar	2025-10-23	1120.15
Gas Chromatography	Fumisoquin A_TMS_38	C[Si](C)(C)NC1CC(O)C2C(O[Si](C)(C)C)C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CN2C1=O	standard non polar	2025-10-23	1526.44
Gas Chromatography	Fumisoquin A_TMS_39	C[Si](C)(C)OC1=CC=C2C(=C1O)CN1C(=O)C(N([Si](C)(C)C)[Si](C)(C)C)CC(O)C1C2O[Si](C)(C)C	standard non polar	2025-10-23	928.11
Gas Chromatography	Fumisoquin A_TMS_40	C[Si](C)(C)OC1=C(O)C=CC2=C1CN1C(=O)C(N([Si](C)(C)C)[Si](C)(C)C)CC(O)C1C2O[Si](C)(C)C	standard non polar	2025-10-23	2265.63
Gas Chromatography	Fumisoquin A_TMS_41	C[Si](C)(C)OC1=CC=C2C(=C1O[Si](C)(C)C)CN1C(=O)C(N([Si](C)(C)C)[Si](C)(C)C)CC(O)C1C2O	standard non polar	2025-10-23	1567.23
Gas Chromatography	Fumisoquin A_TMS_42	C[Si](C)(C)NC1CC(O[Si](C)(C)C)C2C(O[Si](C)(C)C)C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CN2C1=O	standard non polar	2025-10-23	1215.72
Gas Chromatography	Fumisoquin A_TMS_43	C[Si](C)(C)OC1=CC=C2C(=C1O[Si](C)(C)C)CN1C(=O)C(N([Si](C)(C)C)[Si](C)(C)C)CC(O[Si](C)(C)C)C1C2O	standard non polar	2025-10-23	2288.45
Gas Chromatography	Fumisoquin A_TMS_44	C[Si](C)(C)OC1=CC=C2C(=C1O)CN1C(=O)C(N([Si](C)(C)C)[Si](C)(C)C)CC(O[Si](C)(C)C)C1C2O[Si](C)(C)C	standard non polar	2025-10-23	2600.64
Gas Chromatography	Fumisoquin A_TMS_45	C[Si](C)(C)OC1=C(O)C=CC2=C1CN1C(=O)C(N([Si](C)(C)C)[Si](C)(C)C)CC(O[Si](C)(C)C)C1C2O[Si](C)(C)C	standard non polar	2025-10-23	1410.79
Gas Chromatography	Fumisoquin A_TMS_46	C[Si](C)(C)OC1=CC=C2C(=C1O[Si](C)(C)C)CN1C(=O)C(N([Si](C)(C)C)[Si](C)(C)C)CC(O)C1C2O[Si](C)(C)C	standard non polar	2025-10-23	1400.19
Gas Chromatography	Fumisoquin A_TMS_47	C[Si](C)(C)OC1=CC=C2C(=C1O[Si](C)(C)C)CN1C(=O)C(N([Si](C)(C)C)[Si](C)(C)C)CC(O[Si](C)(C)C)C1C2O[Si](C)(C)C	standard non polar	2025-10-23	1224.34
Gas Chromatography	Fumisoquin A_TMS_1	C[Si](C)(C)OC1CC(N)C(=O)N2CC3=C(C=CC(O)=C3O)C(O)C12	standard polar	2025-10-23	1484.32
Gas Chromatography	Fumisoquin A_TMS_2	C[Si](C)(C)OC1C2=CC=C(O)C(O)=C2CN2C(=O)C(N)CC(O)C12	standard polar	2025-10-23	2586.18
Gas Chromatography	Fumisoquin A_TMS_3	C[Si](C)(C)OC1=C(O)C=CC2=C1CN1C(=O)C(N)CC(O)C1C2O	standard polar	2025-10-23	1907.96
Gas Chromatography	Fumisoquin A_TMS_4	C[Si](C)(C)OC1=CC=C2C(=C1O)CN1C(=O)C(N)CC(O)C1C2O	standard polar	2025-10-23	1780.51
Gas Chromatography	Fumisoquin A_TMS_5	C[Si](C)(C)NC1CC(O)C2C(O)C3=CC=C(O)C(O)=C3CN2C1=O	standard polar	2025-10-23	1879.99
Gas Chromatography	Fumisoquin A_TMS_6	C[Si](C)(C)OC1=CC=C2C(=C1O)CN1C(=O)C(N)CC(O[Si](C)(C)C)C1C2O	standard polar	2025-10-23	2352.21
Gas Chromatography	Fumisoquin A_TMS_7	C[Si](C)(C)OC1=C(O)C=CC2=C1CN1C(=O)C(N)CC(O[Si](C)(C)C)C1C2O	standard polar	2025-10-23	2266.64
Gas Chromatography	Fumisoquin A_TMS_8	C[Si](C)(C)OC1CC(N)C(=O)N2CC3=C(C=CC(O)=C3O)C(O[Si](C)(C)C)C12	standard polar	2025-10-23	2161.43
Gas Chromatography	Fumisoquin A_TMS_9	C[Si](C)(C)NC1CC(O[Si](C)(C)C)C2C(O)C3=CC=C(O)C(O)=C3CN2C1=O	standard polar	2025-10-23	2428.37
Gas Chromatography	Fumisoquin A_TMS_10	C[Si](C)(C)OC1=CC=C2C(=C1O)CN1C(=O)C(N)CC(O)C1C2O[Si](C)(C)C	standard polar	2025-10-23	1661.56
Gas Chromatography	Fumisoquin A_TMS_11	C[Si](C)(C)OC1=C(O)C=CC2=C1CN1C(=O)C(N)CC(O)C1C2O[Si](C)(C)C	standard polar	2025-10-23	1675.1
Gas Chromatography	Fumisoquin A_TMS_12	C[Si](C)(C)NC1CC(O)C2C(O[Si](C)(C)C)C3=CC=C(O)C(O)=C3CN2C1=O	standard polar	2025-10-23	2247.53
Gas Chromatography	Fumisoquin A_TMS_13	C[Si](C)(C)OC1=CC=C2C(=C1O[Si](C)(C)C)CN1C(=O)C(N)CC(O)C1C2O	standard polar	2025-10-23	2090.25
Gas Chromatography	Fumisoquin A_TMS_14	C[Si](C)(C)NC1CC(O)C2C(O)C3=CC=C(O)C(O[Si](C)(C)C)=C3CN2C1=O	standard polar	2025-10-23	2054.21
Gas Chromatography	Fumisoquin A_TMS_15	C[Si](C)(C)NC1CC(O)C2C(O)C3=CC=C(O[Si](C)(C)C)C(O)=C3CN2C1=O	standard polar	2025-10-23	1708.01
Gas Chromatography	Fumisoquin A_TMS_16	C[Si](C)(C)N(C1CC(O)C2C(O)C3=CC=C(O)C(O)=C3CN2C1=O)[Si](C)(C)C	standard polar	2025-10-23	1543.51
Gas Chromatography	Fumisoquin A_TMS_17	C[Si](C)(C)OC1=CC=C2C(=C1O[Si](C)(C)C)CN1C(=O)C(N)CC(O[Si](C)(C)C)C1C2O	standard polar	2025-10-23	1414.3
Gas Chromatography	Fumisoquin A_TMS_18	C[Si](C)(C)OC1=CC=C2C(=C1O)CN1C(=O)C(N)CC(O[Si](C)(C)C)C1C2O[Si](C)(C)C	standard polar	2025-10-23	4302.02
Gas Chromatography	Fumisoquin A_TMS_19	C[Si](C)(C)NC1CC(O[Si](C)(C)C)C2C(O)C3=CC=C(O[Si](C)(C)C)C(O)=C3CN2C1=O	standard polar	2025-10-23	1275.72
Gas Chromatography	Fumisoquin A_TMS_20	C[Si](C)(C)OC1=C(O)C=CC2=C1CN1C(=O)C(N)CC(O[Si](C)(C)C)C1C2O[Si](C)(C)C	standard polar	2025-10-23	1906.27
Gas Chromatography	Fumisoquin A_TMS_21	C[Si](C)(C)NC1CC(O[Si](C)(C)C)C2C(O)C3=CC=C(O)C(O[Si](C)(C)C)=C3CN2C1=O	standard polar	2025-10-23	2931.23
Gas Chromatography	Fumisoquin A_TMS_22	C[Si](C)(C)NC1CC(O[Si](C)(C)C)C2C(O[Si](C)(C)C)C3=CC=C(O)C(O)=C3CN2C1=O	standard polar	2025-10-23	2346.21
Gas Chromatography	Fumisoquin A_TMS_23	C[Si](C)(C)OC1CC(N([Si](C)(C)C)[Si](C)(C)C)C(=O)N2CC3=C(C=CC(O)=C3O)C(O)C12	standard polar	2025-10-23	1726.88
Gas Chromatography	Fumisoquin A_TMS_24	C[Si](C)(C)OC1=CC=C2C(=C1O[Si](C)(C)C)CN1C(=O)C(N)CC(O)C1C2O[Si](C)(C)C	standard polar	2025-10-23	854.754
Gas Chromatography	Fumisoquin A_TMS_25	C[Si](C)(C)NC1CC(O)C2C(O[Si](C)(C)C)C3=CC=C(O[Si](C)(C)C)C(O)=C3CN2C1=O	standard polar	2025-10-23	2652.38
Gas Chromatography	Fumisoquin A_TMS_26	C[Si](C)(C)NC1CC(O)C2C(O[Si](C)(C)C)C3=CC=C(O)C(O[Si](C)(C)C)=C3CN2C1=O	standard polar	2025-10-23	1808.47
Gas Chromatography	Fumisoquin A_TMS_27	C[Si](C)(C)OC1C2=CC=C(O)C(O)=C2CN2C(=O)C(N([Si](C)(C)C)[Si](C)(C)C)CC(O)C12	standard polar	2025-10-23	2429.79
Gas Chromatography	Fumisoquin A_TMS_28	C[Si](C)(C)NC1CC(O)C2C(O)C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CN2C1=O	standard polar	2025-10-23	1488.89
Gas Chromatography	Fumisoquin A_TMS_29	C[Si](C)(C)OC1=C(O)C=CC2=C1CN1C(=O)C(N([Si](C)(C)C)[Si](C)(C)C)CC(O)C1C2O	standard polar	2025-10-23	2043.45
Gas Chromatography	Fumisoquin A_TMS_30	C[Si](C)(C)OC1=CC=C2C(=C1O)CN1C(=O)C(N([Si](C)(C)C)[Si](C)(C)C)CC(O)C1C2O	standard polar	2025-10-23	2416.08
Gas Chromatography	Fumisoquin A_TMS_31	C[Si](C)(C)OC1=CC=C2C(=C1O[Si](C)(C)C)CN1C(=O)C(N)CC(O[Si](C)(C)C)C1C2O[Si](C)(C)C	standard polar	2025-10-23	2804.62
Gas Chromatography	Fumisoquin A_TMS_32	C[Si](C)(C)NC1CC(O[Si](C)(C)C)C2C(O)C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CN2C1=O	standard polar	2025-10-23	1025.3
Gas Chromatography	Fumisoquin A_TMS_33	C[Si](C)(C)NC1CC(O[Si](C)(C)C)C2C(O[Si](C)(C)C)C3=CC=C(O[Si](C)(C)C)C(O)=C3CN2C1=O	standard polar	2025-10-23	1743.65
Gas Chromatography	Fumisoquin A_TMS_34	C[Si](C)(C)OC1=CC=C2C(=C1O)CN1C(=O)C(N([Si](C)(C)C)[Si](C)(C)C)CC(O[Si](C)(C)C)C1C2O	standard polar	2025-10-23	1498.81
Gas Chromatography	Fumisoquin A_TMS_35	C[Si](C)(C)NC1CC(O[Si](C)(C)C)C2C(O[Si](C)(C)C)C3=CC=C(O)C(O[Si](C)(C)C)=C3CN2C1=O	standard polar	2025-10-23	2096.46
Gas Chromatography	Fumisoquin A_TMS_36	C[Si](C)(C)OC1=C(O)C=CC2=C1CN1C(=O)C(N([Si](C)(C)C)[Si](C)(C)C)CC(O[Si](C)(C)C)C1C2O	standard polar	2025-10-23	2074.3
Gas Chromatography	Fumisoquin A_TMS_37	C[Si](C)(C)OC1CC(N([Si](C)(C)C)[Si](C)(C)C)C(=O)N2CC3=C(C=CC(O)=C3O)C(O[Si](C)(C)C)C12	standard polar	2025-10-23	1782.06
Gas Chromatography	Fumisoquin A_TMS_38	C[Si](C)(C)NC1CC(O)C2C(O[Si](C)(C)C)C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CN2C1=O	standard polar	2025-10-23	2389.34
Gas Chromatography	Fumisoquin A_TMS_39	C[Si](C)(C)OC1=CC=C2C(=C1O)CN1C(=O)C(N([Si](C)(C)C)[Si](C)(C)C)CC(O)C1C2O[Si](C)(C)C	standard polar	2025-10-23	2546.31
Gas Chromatography	Fumisoquin A_TMS_40	C[Si](C)(C)OC1=C(O)C=CC2=C1CN1C(=O)C(N([Si](C)(C)C)[Si](C)(C)C)CC(O)C1C2O[Si](C)(C)C	standard polar	2025-10-23	1450.66
Gas Chromatography	Fumisoquin A_TMS_41	C[Si](C)(C)OC1=CC=C2C(=C1O[Si](C)(C)C)CN1C(=O)C(N([Si](C)(C)C)[Si](C)(C)C)CC(O)C1C2O	standard polar	2025-10-23	1893.22
Gas Chromatography	Fumisoquin A_TMS_42	C[Si](C)(C)NC1CC(O[Si](C)(C)C)C2C(O[Si](C)(C)C)C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CN2C1=O	standard polar	2025-10-23	1977.91
Gas Chromatography	Fumisoquin A_TMS_43	C[Si](C)(C)OC1=CC=C2C(=C1O[Si](C)(C)C)CN1C(=O)C(N([Si](C)(C)C)[Si](C)(C)C)CC(O[Si](C)(C)C)C1C2O	standard polar	2025-10-23	1966.55
Gas Chromatography	Fumisoquin A_TMS_44	C[Si](C)(C)OC1=CC=C2C(=C1O)CN1C(=O)C(N([Si](C)(C)C)[Si](C)(C)C)CC(O[Si](C)(C)C)C1C2O[Si](C)(C)C	standard polar	2025-10-23	3001.46
Gas Chromatography	Fumisoquin A_TMS_45	C[Si](C)(C)OC1=C(O)C=CC2=C1CN1C(=O)C(N([Si](C)(C)C)[Si](C)(C)C)CC(O[Si](C)(C)C)C1C2O[Si](C)(C)C	standard polar	2025-10-23	2646.55
Gas Chromatography	Fumisoquin A_TMS_46	C[Si](C)(C)OC1=CC=C2C(=C1O[Si](C)(C)C)CN1C(=O)C(N([Si](C)(C)C)[Si](C)(C)C)CC(O)C1C2O[Si](C)(C)C	standard polar	2025-10-23	1543.03
Gas Chromatography	Fumisoquin A_TMS_47	C[Si](C)(C)OC1=CC=C2C(=C1O[Si](C)(C)C)CN1C(=O)C(N([Si](C)(C)C)[Si](C)(C)C)CC(O[Si](C)(C)C)C1C2O[Si](C)(C)C	standard polar	2025-10-23	2242.91

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Microbial Pathways

Pathways

Not Available

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Eukaryota/Fungi	Ascomycota	1	Human feces	Metabolic reconstruction

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78443694

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139586523

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

Not Available

General References

van Santen JA, Poynton EF, Iskakova D, McMann E, Alsup TA, Clark TN, Fergusson CH, Fewer DP, Hughes AH, McCadden CA, Parra J, Soldatou S, Rudolf JD, Janssen EM, Duncan KR, Linington RG: The Natural Products Atlas 2.0: a database of microbially-derived natural products. Nucleic Acids Res. 2022 Jan 7;50(D1):D1317-D1323. doi: 10.1093/nar/gkab941. [PubMed:34718710 ]

Showing metabocard for Fumisoquin A (MMDBc0012675)

MOL for #<Metabolite:0x00007f8ad5bdce20>

3D MOL for #<Metabolite:0x00007f8ad5bdce20>

3D SDF for #<Metabolite:0x00007f8ad5bdce20>

3D-SDF for #<Metabolite:0x00007f8ad5bdce20>

PDB for #<Metabolite:0x00007f8ad5bdce20>

3D PDB for #<Metabolite:0x00007f8ad5bdce20>

SMILES for #<Metabolite:0x00007f8ad5bdce20>

INCHI for #<Metabolite:0x00007f8ad5bdce20>

Structure for #<Metabolite:0x00007f8ad5bdce20>

3D Structure for #<Metabolite:0x00007f8ad5bdce20>