MiMeDB: Showing metabocard for Eremofortin C (MMDBc0004650)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-14 22:33:46 UTC

Update Date

2025-10-07 16:04:54 UTC

Metabolite ID

MMDBc0004650

Metabolite Identification

Common Name

Eremofortin C

Description

Eremofortin C is a secondary metabolite belonging to the chemical class of eremophilanes, produced by the fungus Penicillium roqueforti. This compound has garnered attention in the field of biochemistry due to its role in the biosynthetic pathways of eremophilanes, which are elucidated through bioinformatics-guided studies (PMID:38568215 ). Eremofortin C (EC) and its related compound, PR toxin, are both significant secondary metabolites of P. roqueforti, with various factors influencing their production, including the presence of corn extract which enhances the biosynthesis of EC and PR toxin (PMID:1768131 ; PMID:1819047 ). The transformation of eremofortin C into PR toxin has been documented, highlighting its biochemical relevance (PMID:4073900 ). Furthermore, studies have characterized the enzyme responsible for this transformation, providing insights into the enzymatic processes involved in secondary metabolite biosynthesis (PMID:16346812 ). The concentration required for inhibition of binding of PR toxin to its antibody has also been quantified, demonstrating the potency of eremofortin C in biochemical assays (PMID:30978841 ). Overall, eremofortin C exemplifies the intricate chemistry and biological significance of fungal secondary metabolites.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152100332D          

 27 30  0  0  1  0            999 V2000
    0.7339    0.2836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6647   -0.2251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2720    0.9672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9992    1.1190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5321    3.1344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1899    1.6507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1357    1.6721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0949    1.0254    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2028    0.4584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9940    2.4508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2908    3.0761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9179    1.0837    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8170    2.5091    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2789    1.8255    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6330    1.7090    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3354    1.8724    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6518    2.3343    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3624    0.8788    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5638    1.2002    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7528    3.7597    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3798    0.4002    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6399    2.5674    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3937    2.6953    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5569    0.3419    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7408    1.1420    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7587    3.3320    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1018    1.8838    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  1  1  6  0  0  0
  9  2  1  0  0  0  0
 10  5  2  0  0  0  0
 11  5  1  0  0  0  0
 12  8  1  0  0  0  0
 13 10  1  0  0  0  0
 14 12  1  0  0  0  0
 14 13  1  0  0  0  0
 15  3  1  6  0  0  0
 15  6  1  0  0  0  0
 15  8  1  0  0  0  0
 15 10  1  0  0  0  0
 16  4  1  6  0  0  0
 16  7  1  1  0  0  0
 17  6  1  0  0  0  0
 17 11  1  0  0  0  0
 17 16  1  0  0  0  0
 18  7  1  0  0  0  0
 19  9  2  0  0  0  0
 20 11  2  0  0  0  0
 21  9  1  0  0  0  0
 12 21  1  6  0  0  0
 22 13  1  0  0  0  0
 22 14  1  0  0  0  0
 23 16  1  0  0  0  0
 17 23  1  6  0  0  0
  8 24  1  1  0  0  0
 12 25  1  1  0  0  0
 13 26  1  1  0  0  0
 14 27  1  1  0  0  0
M  END


  Mrv1652305152100332D          

 27 30  0  0  1  0            999 V2000
    0.7339    0.2836    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6647   -0.2251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2720    0.9672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9992    1.1190    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5321    3.1344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1899    1.6507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1357    1.6721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0949    1.0254    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2028    0.4584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9940    2.4508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2908    3.0761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9179    1.0837    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8170    2.5091    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2789    1.8255    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6330    1.7090    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3354    1.8724    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6518    2.3343    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3624    0.8788    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5638    1.2002    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7528    3.7597    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3798    0.4002    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6399    2.5674    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3937    2.6953    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5569    0.3419    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7408    1.1420    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7587    3.3320    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1018    1.8838    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  1  1  6  0  0  0
  9  2  1  0  0  0  0
 10  5  2  0  0  0  0
 11  5  1  0  0  0  0
 12  8  1  0  0  0  0
 13 10  1  0  0  0  0
 14 12  1  0  0  0  0
 14 13  1  0  0  0  0
 15  3  1  6  0  0  0
 15  6  1  0  0  0  0
 15  8  1  0  0  0  0
 15 10  1  0  0  0  0
 16  4  1  6  0  0  0
 16  7  1  1  0  0  0
 17  6  1  0  0  0  0
 17 11  1  0  0  0  0
 17 16  1  0  0  0  0
 18  7  1  0  0  0  0
 19  9  2  0  0  0  0
 20 11  2  0  0  0  0
 21  9  1  0  0  0  0
 12 21  1  6  0  0  0
 22 13  1  0  0  0  0
 22 14  1  0  0  0  0
 23 16  1  0  0  0  0
 17 23  1  6  0  0  0
  8 24  1  1  0  0  0
 12 25  1  1  0  0  0
 13 26  1  1  0  0  0
 14 27  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0004650

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]12O[C@]1([H])[C@]([H])(OC(C)=O)[C@]([H])(C)[C@@]1(C)C[C@]3(O[C@]3(C)CO)C(=O)C=C21

> <INCHI_IDENTIFIER>
InChI=1S/C17H22O6/c1-8-12(21-9(2)19)14-13(22-14)10-5-11(20)17(6-15(8,10)3)16(4,7-18)23-17/h5,8,12-14,18H,6-7H2,1-4H3/t8-,12+,13-,14+,15+,16+,17-/m0/s1

> <INCHI_KEY>
AVFUXCSVVLQAGL-VIEAGMIOSA-N

> <FORMULA>
C17H22O6

> <MOLECULAR_WEIGHT>
322.357

> <EXACT_MASS>
322.141638428

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
33.140637438962656

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1aR,2R,3R,3'R,3aR,5R,7bS)-3'-(hydroxymethyl)-3,3',3a-trimethyl-6-oxo-2,3,3a,4,6,7b-hexahydro-1aH-spiro[naphtho[1,2-b]oxirene-5,2'-oxirane]-2-yl acetate

> <ALOGPS_LOGP>
1.11

> <JCHEM_LOGP>
0.6557754949999995

> <ALOGPS_LOGS>
-2.47

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.92475178313218

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.255981181659315

> <JCHEM_PKA_STRONGEST_BASIC>
-3.120016479191409

> <JCHEM_POLAR_SURFACE_AREA>
88.66

> <JCHEM_REFRACTIVITY>
79.23749999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.08e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1aR,2R,3R,3'R,3aR,5R,7bS)-3'-(hydroxymethyl)-3,3',3a-trimethyl-6-oxo-2,3,4,7b-tetrahydro-1aH-spiro[naphtho[1,2-b]oxirene-5,2'-oxirane]-2-yl acetate

> <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       1.370   0.529   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.841  -0.420   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.508   1.805   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.865   2.089   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.993   5.851   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.355   3.081   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.987   3.121   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.044   1.914   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.978   0.856   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.856   4.575   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.543   5.742   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.580   2.023   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.392   4.684   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.254   3.408   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.182   3.190   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.493   3.495   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.217   4.357   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -4.410   1.641   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       6.652   2.240   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -1.405   7.018   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       4.442   0.747   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       4.928   4.792   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      -2.602   5.031   0.000  0.00  0.00           O+0
HETATM   24  H   UNK     0       2.906   0.638   0.000  0.00  0.00           H+0
HETATM   25  H   UNK     0       5.116   2.132   0.000  0.00  0.00           H+0
HETATM   26  H   UNK     0       3.283   6.220   0.000  0.00  0.00           H+0
HETATM   27  H   UNK     0       5.790   3.516   0.000  0.00  0.00           H+0
CONECT    1    8                                                            
CONECT    2    9                                                            
CONECT    3   15                                                            
CONECT    4   16                                                            
CONECT    5   10   11                                                       
CONECT    6   15   17                                                       
CONECT    7   16   18                                                       
CONECT    8    1   12   15   24                                             
CONECT    9    2   19   21                                                  
CONECT   10    5   13   15                                                  
CONECT   11    5   17   20                                                  
CONECT   12    8   14   21   25                                             
CONECT   13   10   14   22   26                                             
CONECT   14   12   13   22   27                                             
CONECT   15    3    6    8   10                                             
CONECT   16    4    7   17   23                                             
CONECT   17    6   11   16   23                                             
CONECT   18    7                                                            
CONECT   19    9                                                            
CONECT   20   11                                                            
CONECT   21    9   12                                                       
CONECT   22   13   14                                                       
CONECT   23   16   17                                                       
CONECT   24    8                                                            
CONECT   25   12                                                            
CONECT   26   13                                                            
CONECT   27   14                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   60    0
END

Synonyms

Not Available

Molecular Formula

C₁₇H₂₂O₆

Average Mass

322.357

Monoisotopic Mass

322.141638428

IUPAC Name

(1aR,2R,3R,3'R,3aR,5R,7bS)-3'-(hydroxymethyl)-3,3',3a-trimethyl-6-oxo-2,3,3a,4,6,7b-hexahydro-1aH-spiro[naphtho[1,2-b]oxirene-5,2'-oxirane]-2-yl acetate

Traditional Name

(1aR,2R,3R,3'R,3aR,5R,7bS)-3'-(hydroxymethyl)-3,3',3a-trimethyl-6-oxo-2,3,4,7b-tetrahydro-1aH-spiro[naphtho[1,2-b]oxirene-5,2'-oxirane]-2-yl acetate

CAS Registry Number

Not Available

SMILES

[H][C@@]12O[C@]1([H])[C@]([H])(OC(C)=O)[C@]([H])(C)[C@@]1(C)C[C@]3(O[C@]3(C)CO)C(=O)C=C21

InChI Identifier

InChI=1S/C17H22O6/c1-8-12(21-9(2)19)14-13(22-14)10-5-11(20)17(6-15(8,10)3)16(4,7-18)23-17/h5,8,12-14,18H,6-7H2,1-4H3/t8-,12+,13-,14+,15+,16+,17-/m0/s1

InChI Key

AVFUXCSVVLQAGL-VIEAGMIOSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxepanes. Oxepanes are compounds containing an oxepane ring, which is a seven-member saturated aliphatic heterocycle with one oxygen and six carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Oxepanes

Sub Class

Not Available

Direct Parent

Oxepanes

Alternative Parents

Substituents

Cyclohexenone
Oxepane
Carboxylic acid ester
Ketone
Carboxylic acid derivative
Dialkyl ether
Oxirane
Ether
Monocarboxylic acid or derivatives
Oxacycle
Alcohol
Carbonyl group
Organic oxide
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Primary alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	1.08 g/L	ALOGPS
logP	1.11	ALOGPS
logP	0.66	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	14.26	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	88.66 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	79.24 m³·mol⁻¹	ChemAxon
Polarizability	33.14 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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_1_1) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-10	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-22	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-22	View Spectrum

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

This table shows at most 5 pathways. For the full list of associated pathways:

See All Associated Bacterial Pathways

Name	SMPDB/PathBank

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

C00016971

Chemspider ID

19979710

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21119861

PDB ID

Not Available

ChEBI ID

Not Available

CMMC Knowledgebase

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

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 Eremofortin C (MMDBc0004650)

MOL for #<Metabolite:0x00007fd44b48ddd0>

3D MOL for #<Metabolite:0x00007fd44b48ddd0>

3D SDF for #<Metabolite:0x00007fd44b48ddd0>

3D-SDF for #<Metabolite:0x00007fd44b48ddd0>

PDB for #<Metabolite:0x00007fd44b48ddd0>

3D PDB for #<Metabolite:0x00007fd44b48ddd0>

SMILES for #<Metabolite:0x00007fd44b48ddd0>

INCHI for #<Metabolite:0x00007fd44b48ddd0>

Structure for #<Metabolite:0x00007fd44b48ddd0>

3D Structure for #<Metabolite:0x00007fd44b48ddd0>