MiMeDB: Showing metabocard for Marcfortine C (MMDBc0005947)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-14 23:21:47 UTC

Update Date

2022-08-31 06:24:41 UTC

Metabolite ID

MMDBc0005947

Metabolite Identification

Common Name

Marcfortine C

Description

Marcfortine C belongs to the class of organic compounds known as alpha amino acid amides. These are amide derivatives of alpha amino acids. Based on a literature review a small amount of articles have been published on Marcfortine C.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152101212D          

 34 40  0  0  1  0            999 V2000
    7.8380    1.1308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6703    2.1780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2963    3.9720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4681    3.3926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3384    0.5867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7822    1.2184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3437    2.5754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2750    2.7047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0211    0.6534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1552    0.8230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8357    0.7838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0994    1.9983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4841    1.8479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0087    3.2143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3312    2.9614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4997    1.1770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1660    1.8036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7952    2.0644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9332    2.6027    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6862    1.1633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2569    1.2606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4114    2.2840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1301    1.5545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6591    3.2310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1784    3.0034    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5518    1.5956    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6141    2.4962    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4559    1.4602    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0043    2.1740    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9235    2.2060    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7875    0.6289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0517    2.8043    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6098    2.1948    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1388    2.3803    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0  0  0  0
  8  7  2  0  0  0  0
 10  5  1  0  0  0  0
 11  9  2  0  0  0  0
 12  6  1  0  0  0  0
 16  9  1  0  0  0  0
 17  7  1  0  0  0  0
 18  8  1  0  0  0  0
 18 16  2  0  0  0  0
 19 13  1  0  0  0  0
 20 16  1  0  0  0  0
 20 17  2  0  0  0  0
 23  1  1  0  0  0  0
 23  2  1  0  0  0  0
 23 11  1  0  0  0  0
 24  3  1  0  0  0  0
 24  4  1  0  0  0  0
 24 19  1  0  0  0  0
 25 14  1  1  0  0  0
 25 15  1  0  0  0  0
 25 19  1  0  0  0  0
 26 10  1  0  0  0  0
 26 13  1  0  0  0  0
 26 21  1  0  0  0  0
 27 14  1  6  0  0  0
 27 17  1  0  0  0  0
 27 22  1  0  0  0  0
 27 24  1  0  0  0  0
 28 20  1  0  0  0  0
 28 22  2  0  0  0  0
 29 21  2  0  0  0  0
 29 25  1  0  0  0  0
 30 12  1  0  0  0  0
 30 15  1  0  0  0  0
 26 30  1  1  0  0  0
 31 21  1  0  0  0  0
 32 22  1  0  0  0  0
 33 18  1  0  0  0  0
 33 23  1  0  0  0  0
 19 34  1  6  0  0  0
M  END


  Mrv1652305152101212D          

 34 40  0  0  1  0            999 V2000
    7.8380    1.1308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6703    2.1780    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2963    3.9720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4681    3.3926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3384    0.5867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7822    1.2184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3437    2.5754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2750    2.7047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0211    0.6534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1552    0.8230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8357    0.7838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0994    1.9983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4841    1.8479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0087    3.2143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3312    2.9614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4997    1.1770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1660    1.8036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7952    2.0644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9332    2.6027    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6862    1.1633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2569    1.2606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4114    2.2840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1301    1.5545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6591    3.2310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1784    3.0034    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5518    1.5956    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6141    2.4962    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4559    1.4602    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.0043    2.1740    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.9235    2.2060    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7875    0.6289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0517    2.8043    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6098    2.1948    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1388    2.3803    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0  0  0  0
  8  7  2  0  0  0  0
 10  5  1  0  0  0  0
 11  9  2  0  0  0  0
 12  6  1  0  0  0  0
 16  9  1  0  0  0  0
 17  7  1  0  0  0  0
 18  8  1  0  0  0  0
 18 16  2  0  0  0  0
 19 13  1  0  0  0  0
 20 16  1  0  0  0  0
 20 17  2  0  0  0  0
 23  1  1  0  0  0  0
 23  2  1  0  0  0  0
 23 11  1  0  0  0  0
 24  3  1  0  0  0  0
 24  4  1  0  0  0  0
 24 19  1  0  0  0  0
 25 14  1  1  0  0  0
 25 15  1  0  0  0  0
 25 19  1  0  0  0  0
 26 10  1  0  0  0  0
 26 13  1  0  0  0  0
 26 21  1  0  0  0  0
 27 14  1  6  0  0  0
 27 17  1  0  0  0  0
 27 22  1  0  0  0  0
 27 24  1  0  0  0  0
 28 20  1  0  0  0  0
 28 22  2  0  0  0  0
 29 21  2  0  0  0  0
 29 25  1  0  0  0  0
 30 12  1  0  0  0  0
 30 15  1  0  0  0  0
 26 30  1  1  0  0  0
 31 21  1  0  0  0  0
 32 22  1  0  0  0  0
 33 18  1  0  0  0  0
 33 23  1  0  0  0  0
 19 34  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0005947

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@]12C[C@]34CCCCN3C[C@@]1(C[C@@]1(C(O)=NC3=C1C=CC1=C3C=CC(C)(C)O1)C2(C)C)N=C4O

> <INCHI_IDENTIFIER>
InChI=1S/C27H33N3O3/c1-23(2)11-9-16-18(33-23)8-7-17-20(16)28-22(32)27(17)14-25-15-30-12-6-5-10-26(30,21(31)29-25)13-19(25)24(27,3)4/h7-9,11,19H,5-6,10,12-15H2,1-4H3,(H,28,32)(H,29,31)/t19-,25-,26+,27-/m1/s1

> <INCHI_KEY>
MEDWEEBWLKOHES-ABMOCFRJSA-N

> <FORMULA>
C27H33N3O3

> <MOLECULAR_WEIGHT>
447.579

> <EXACT_MASS>
447.252191935

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
50.70509653868678

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1'S,3R,8'S,10'R)-7,7,11',11'-tetramethyl-7H-3',14'-diazaspiro[chromeno[5,6-b]pyrrole-3,12'-tetracyclo[6.5.2.0^{1,10}.0^{3,8}]pentadecan]-14'-ene-2,15'-diol

> <ALOGPS_LOGP>
3.49

> <JCHEM_LOGP>
2.202798021375147

> <ALOGPS_LOGS>
-4.79

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
4.420160592473669

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.265331967341579

> <JCHEM_PKA_STRONGEST_BASIC>
7.02332945411076

> <JCHEM_POLAR_SURFACE_AREA>
77.65

> <JCHEM_REFRACTIVITY>
129.46649999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.25e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1'S,3R,8'S,10'R)-7,7,11',11'-tetramethyl-3',14'-diazaspiro[chromeno[5,6-b]pyrrole-3,12'-tetracyclo[6.5.2.0^{1,10}.0^{3,8}]pentadecan]-14'-ene-2,15'-diol

> <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      17.449   3.106   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      17.058   1.166   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.022  -0.325   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.353   1.145   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.316   2.484   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.710   4.002   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.042   0.666   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.551   0.362   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.096   4.133   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.368   1.306   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      15.606   3.828   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.255   4.185   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.592   1.186   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.649   3.203   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.588   3.213   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.078   2.977   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.550   2.126   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      13.570   1.518   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.304   0.722   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      11.568   3.281   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.622  -0.238   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.281   4.270   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      16.097   2.369   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.814   1.200   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.598   1.985   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.978   1.225   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.137   2.737   0.000  0.00  0.00           C+0
HETATM   28  N   UNK     0      10.784   4.607   0.000  0.00  0.00           N+0
HETATM   29  N   UNK     0       6.151   0.224   0.000  0.00  0.00           N+0
HETATM   30  N   UNK     0       4.068   2.836   0.000  0.00  0.00           N+0
HETATM   31  O   UNK     0       3.978  -1.637   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       8.126   5.289   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0      15.079   1.214   0.000  0.00  0.00           O+0
HETATM   34  H   UNK     0       7.842  -0.720   0.000  0.00  0.00           H+0
CONECT    1   23                                                            
CONECT    2   23                                                            
CONECT    3   24                                                            
CONECT    4   24                                                            
CONECT    5    6   10                                                       
CONECT    6    5   12                                                       
CONECT    7    8   17                                                       
CONECT    8    7   18                                                       
CONECT    9   11   16                                                       
CONECT   10    5   26                                                       
CONECT   11    9   23                                                       
CONECT   12    6   30                                                       
CONECT   13   19   26                                                       
CONECT   14   25   27                                                       
CONECT   15   25   30                                                       
CONECT   16    9   18   20                                                  
CONECT   17    7   20   27                                                  
CONECT   18    8   16   33                                                  
CONECT   19   13   24   25   34                                             
CONECT   20   16   17   28                                                  
CONECT   21   26   29   31                                                  
CONECT   22   27   28   32                                                  
CONECT   23    1    2   11   33                                             
CONECT   24    3    4   19   27                                             
CONECT   25   14   15   19   29                                             
CONECT   26   10   13   21   30                                             
CONECT   27   14   17   22   24                                             
CONECT   28   20   22                                                       
CONECT   29   21   25                                                       
CONECT   30   12   15   26                                                  
CONECT   31   21                                                            
CONECT   32   22                                                            
CONECT   33   18   23                                                       
CONECT   34   19                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   80    0
END

Synonyms

Not Available

Molecular Formula

C₂₇H₃₃N₃O₃

Average Mass

447.579

Monoisotopic Mass

447.252191935

IUPAC Name

(1'S,3R,8'S,10'R)-7,7,11',11'-tetramethyl-7H-3',14'-diazaspiro[chromeno[5,6-b]pyrrole-3,12'-tetracyclo[6.5.2.0^{1,10}.0^{3,8}]pentadecan]-14'-ene-2,15'-diol

Traditional Name

(1'S,3R,8'S,10'R)-7,7,11',11'-tetramethyl-3',14'-diazaspiro[chromeno[5,6-b]pyrrole-3,12'-tetracyclo[6.5.2.0^{1,10}.0^{3,8}]pentadecan]-14'-ene-2,15'-diol

CAS Registry Number

Not Available

SMILES

[H][C@]12C[C@]34CCCCN3C[C@@]1(C[C@@]1(C(O)=NC3=C1C=CC1=C3C=CC(C)(C)O1)C2(C)C)N=C4O

InChI Identifier

InChI=1S/C27H33N3O3/c1-23(2)11-9-16-18(33-23)8-7-17-20(16)28-22(32)27(17)14-25-15-30-12-6-5-10-26(30,21(31)29-25)13-19(25)24(27,3)4/h7-9,11,19H,5-6,10,12-15H2,1-4H3,(H,28,32)(H,29,31)/t19-,25-,26+,27-/m1/s1

InChI Key

MEDWEEBWLKOHES-ABMOCFRJSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alpha amino acid amides. These are amide derivatives of alpha amino acids.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Alpha amino acid amides

Alternative Parents

Substituents

Alpha-amino acid amide
2,2-dimethyl-1-benzopyran
Azaspirodecane
Benzopyran
Piperazino-1,2-a-piperidine
1-benzopyran
Quinolizidine
Indole or derivatives
Dihydroindole
Alkyl aryl ether
Delta-lactam
Aralkylamine
N-alkylpiperazine
Piperidinone
1,4-diazinane
Piperazine
Benzenoid
Piperidine
Secondary carboxylic acid amide
Tertiary amine
Tertiary aliphatic amine
Carboxamide group
Lactam
Organoheterocyclic compound
Azacycle
Ether
Oxacycle
Amine
Organic nitrogen compound
Organonitrogen compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organooxygen compound
Organic oxygen compound
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	0.0072 g/L	ALOGPS
logP	3.49	ALOGPS
logP	2.2	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	2.27	ChemAxon
pKa (Strongest Basic)	7.02	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	77.65 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	129.47 m³·mol⁻¹	ChemAxon
Polarizability	50.71 Å³	ChemAxon
Number of Rings	7	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_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
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-23	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

Metabolic Reactions

Not Available

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

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

C00023602

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

102514133

PDB ID

Not Available

ChEBI ID

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 Marcfortine C (MMDBc0005947)

MOL for #<Metabolite:0x0000556b6a3fa1d0>

3D MOL for #<Metabolite:0x0000556b6a3fa1d0>

3D SDF for #<Metabolite:0x0000556b6a3fa1d0>

3D-SDF for #<Metabolite:0x0000556b6a3fa1d0>

PDB for #<Metabolite:0x0000556b6a3fa1d0>

3D PDB for #<Metabolite:0x0000556b6a3fa1d0>

SMILES for #<Metabolite:0x0000556b6a3fa1d0>

INCHI for #<Metabolite:0x0000556b6a3fa1d0>

Structure for #<Metabolite:0x0000556b6a3fa1d0>

3D Structure for #<Metabolite:0x0000556b6a3fa1d0>