MiMeDB: Showing metabocard for Fumonisin C3 (MMDBc0015663)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 06:27:35 UTC

Update Date

2025-10-07 16:06:26 UTC

Metabolite ID

MMDBc0015663

Metabolite Identification

Common Name

Fumonisin C3

Description

Fumonisin C3 is a member of the fumonisin chemical class, which consists of mycotoxins produced by certain species of the Fusarium fungus, notably Fusarium oxysporum. This metabolite has been identified in various agricultural products, including corn and wheat, where it can co-occur with other fumonisins such as fumonisin C1 and C4. The prevalence of fumonisin C3 in moldy corn was reported to be 11%, indicating its relatively lower occurrence compared to fumonisin C1 and C4, which were found at 71% and 43%, respectively (PMID:10049903 ). Fumonisin C3, along with hydroxylated fumonisin C1, was isolated from wheat cultures of Fusarium oxysporum, highlighting its production in specific fungal environments (PMID:8946739 ). The biological significance of fumonisin C3, like other fumonisins, may relate to its potential toxicity and role in plant-pathogen interactions, although detailed biological effects require further investigation. Understanding the chemistry and occurrence of fumonisin C3 is crucial for assessing its impact on food safety and public health.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152108272D          

 48 47  0  0  0  0            999 V2000
   13.9658   -5.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6802   -3.0493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.5381   -5.5243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6802   -5.5243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3947   -5.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1079   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3934   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8224   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6789   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1092   -5.5243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5368   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9645   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9658   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3947   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.9671   -3.0493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.3960   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.5381   -3.0493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.9671   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5355   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6802   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8237   -5.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.2526   -2.6368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.6815   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2513   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2500   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1092   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.6815   -2.6368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.1105   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8237   -2.6368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.2526   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8237   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.2526   -1.8118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.6815   -5.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8211   -4.2868    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   13.2513   -3.0493    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2500   -5.1118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.6815   -1.8118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.3960   -3.0493    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.8249   -3.8743    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.1105   -5.1118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.8237   -1.8118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.2526   -5.1118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.5381   -1.3993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.9671   -1.3993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.3960   -5.5243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.9671   -5.5243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.1092   -3.0493    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.5381   -3.8743    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  4  1  1  0  0  0  0
  5  4  1  0  0  0  0
  7  6  1  0  0  0  0
  8  6  1  0  0  0  0
  9  7  1  0  0  0  0
 10  5  1  0  0  0  0
 11  8  1  0  0  0  0
 12  9  1  0  0  0  0
 20  2  1  0  0  0  0
 20 13  1  0  0  0  0
 20 14  1  0  0  0  0
 21  3  1  0  0  0  0
 21 10  1  0  0  0  0
 22 15  1  0  0  0  0
 22 17  1  0  0  0  0
 23 16  1  0  0  0  0
 23 18  1  0  0  0  0
 24 11  1  0  0  0  0
 24 13  1  0  0  0  0
 25 12  1  0  0  0  0
 25 19  1  0  0  0  0
 26 14  1  0  0  0  0
 27 15  1  0  0  0  0
 28 16  1  0  0  0  0
 29 17  1  0  0  0  0
 30 18  1  0  0  0  0
 31 21  1  0  0  0  0
 31 26  1  0  0  0  0
 32 22  1  0  0  0  0
 33 23  1  0  0  0  0
 34 19  1  0  0  0  0
 35 24  1  0  0  0  0
 36 25  1  0  0  0  0
 37 27  2  0  0  0  0
 38 27  1  0  0  0  0
 39 28  2  0  0  0  0
 40 28  1  0  0  0  0
 41 29  2  0  0  0  0
 42 30  2  0  0  0  0
 43 32  2  0  0  0  0
 44 32  1  0  0  0  0
 45 33  2  0  0  0  0
 46 33  1  0  0  0  0
 47 26  1  0  0  0  0
 47 29  1  0  0  0  0
 48 30  1  0  0  0  0
 48 31  1  0  0  0  0
M  END


  Mrv1652305152108272D          

 48 47  0  0  0  0            999 V2000
   13.9658   -5.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6802   -3.0493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.5381   -5.5243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6802   -5.5243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3947   -5.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1079   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3934   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8224   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6789   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1092   -5.5243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5368   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9645   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9658   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3947   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.9671   -3.0493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.3960   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.5381   -3.0493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.9671   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5355   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6802   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8237   -5.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.2526   -2.6368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.6815   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2513   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2500   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1092   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.6815   -2.6368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.1105   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8237   -2.6368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.2526   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8237   -4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.2526   -1.8118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.6815   -5.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8211   -4.2868    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   13.2513   -3.0493    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2500   -5.1118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.6815   -1.8118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.3960   -3.0493    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.8249   -3.8743    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.1105   -5.1118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.8237   -1.8118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.2526   -5.1118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.5381   -1.3993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.9671   -1.3993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.3960   -5.5243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.9671   -5.5243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.1092   -3.0493    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.5381   -3.8743    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  4  1  1  0  0  0  0
  5  4  1  0  0  0  0
  7  6  1  0  0  0  0
  8  6  1  0  0  0  0
  9  7  1  0  0  0  0
 10  5  1  0  0  0  0
 11  8  1  0  0  0  0
 12  9  1  0  0  0  0
 20  2  1  0  0  0  0
 20 13  1  0  0  0  0
 20 14  1  0  0  0  0
 21  3  1  0  0  0  0
 21 10  1  0  0  0  0
 22 15  1  0  0  0  0
 22 17  1  0  0  0  0
 23 16  1  0  0  0  0
 23 18  1  0  0  0  0
 24 11  1  0  0  0  0
 24 13  1  0  0  0  0
 25 12  1  0  0  0  0
 25 19  1  0  0  0  0
 26 14  1  0  0  0  0
 27 15  1  0  0  0  0
 28 16  1  0  0  0  0
 29 17  1  0  0  0  0
 30 18  1  0  0  0  0
 31 21  1  0  0  0  0
 31 26  1  0  0  0  0
 32 22  1  0  0  0  0
 33 23  1  0  0  0  0
 34 19  1  0  0  0  0
 35 24  1  0  0  0  0
 36 25  1  0  0  0  0
 37 27  2  0  0  0  0
 38 27  1  0  0  0  0
 39 28  2  0  0  0  0
 40 28  1  0  0  0  0
 41 29  2  0  0  0  0
 42 30  2  0  0  0  0
 43 32  2  0  0  0  0
 44 32  1  0  0  0  0
 45 33  2  0  0  0  0
 46 33  1  0  0  0  0
 47 26  1  0  0  0  0
 47 29  1  0  0  0  0
 48 30  1  0  0  0  0
 48 31  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0015663

> <DATABASE_NAME>
MIME

> <SMILES>
CCCCC(C)C(OC(=O)CC(CC(O)=O)C(O)=O)C(CC(C)CC(O)CCCCCCC(O)CN)OC(=O)CC(CC(O)=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C33H57NO14/c1-4-5-10-21(3)31(48-30(42)18-23(33(45)46)16-28(39)40)26(47-29(41)17-22(32(43)44)15-27(37)38)14-20(2)13-24(35)11-8-6-7-9-12-25(36)19-34/h20-26,31,35-36H,4-19,34H2,1-3H3,(H,37,38)(H,39,40)(H,43,44)(H,45,46)

> <INCHI_KEY>
LTKGSCNZLUASHU-UHFFFAOYSA-N

> <FORMULA>
C33H57NO14

> <MOLECULAR_WEIGHT>
691.812

> <EXACT_MASS>
691.377905519

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
105

> <JCHEM_AVERAGE_POLARIZABILITY>
75.25028491957245

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[2-({19-amino-6-[(3,4-dicarboxybutanoyl)oxy]-11,18-dihydroxy-5,9-dimethylnonadecan-7-yl}oxy)-2-oxoethyl]butanedioic acid

> <ALOGPS_LOGP>
-0.48

> <JCHEM_LOGP>
0.37578359142811135

> <ALOGPS_LOGS>
-4.54

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-3

> <JCHEM_PKA>
3.745923310701054

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.1587785129559003

> <JCHEM_PKA_STRONGEST_BASIC>
9.591270431067855

> <JCHEM_POLAR_SURFACE_AREA>
268.2799999999999

> <JCHEM_REFRACTIVITY>
169.66100000000012

> <JCHEM_ROTATABLE_BOND_COUNT>
31

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.98e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[2-({19-amino-6-[(3,4-dicarboxybutanoyl)oxy]-11,18-dihydroxy-5,9-dimethylnonadecan-7-yl}oxy)-2-oxoethyl]butanedioic acid

> <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      26.069  -9.542   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      27.403  -5.692   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      32.738 -10.312   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      27.403 -10.312   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      28.737  -9.542   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      20.735  -8.002   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      19.401  -7.232   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      22.068  -7.232   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      18.067  -8.002   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      30.070 -10.312   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      23.402  -8.002   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      16.734  -7.232   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      26.069  -8.002   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      28.737  -8.002   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      35.405  -5.692   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      38.073  -7.232   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      32.738  -5.692   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      35.405  -7.232   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      14.066  -7.232   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      27.403  -7.232   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      31.404  -9.542   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      34.072  -4.922   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      36.739  -8.002   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      24.736  -7.232   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      15.400  -8.002   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      30.070  -7.232   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      36.739  -4.922   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      39.406  -8.002   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      31.404  -4.922   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      34.072  -8.002   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      31.404  -8.002   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      34.072  -3.382   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      36.739  -9.542   0.000  0.00  0.00           C+0
HETATM   34  N   UNK     0      12.733  -8.002   0.000  0.00  0.00           N+0
HETATM   35  O   UNK     0      24.736  -5.692   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      15.400  -9.542   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0      36.739  -3.382   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      38.073  -5.692   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      40.740  -7.232   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      39.406  -9.542   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0      31.404  -3.382   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0      34.072  -9.542   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0      32.738  -2.612   0.000  0.00  0.00           O+0
HETATM   44  O   UNK     0      35.405  -2.612   0.000  0.00  0.00           O+0
HETATM   45  O   UNK     0      38.073 -10.312   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0      35.405 -10.312   0.000  0.00  0.00           O+0
HETATM   47  O   UNK     0      30.070  -5.692   0.000  0.00  0.00           O+0
HETATM   48  O   UNK     0      32.738  -7.232   0.000  0.00  0.00           O+0
CONECT    1    4                                                            
CONECT    2   20                                                            
CONECT    3   21                                                            
CONECT    4    1    5                                                       
CONECT    5    4   10                                                       
CONECT    6    7    8                                                       
CONECT    7    6    9                                                       
CONECT    8    6   11                                                       
CONECT    9    7   12                                                       
CONECT   10    5   21                                                       
CONECT   11    8   24                                                       
CONECT   12    9   25                                                       
CONECT   13   20   24                                                       
CONECT   14   20   26                                                       
CONECT   15   22   27                                                       
CONECT   16   23   28                                                       
CONECT   17   22   29                                                       
CONECT   18   23   30                                                       
CONECT   19   25   34                                                       
CONECT   20    2   13   14                                                  
CONECT   21    3   10   31                                                  
CONECT   22   15   17   32                                                  
CONECT   23   16   18   33                                                  
CONECT   24   11   13   35                                                  
CONECT   25   12   19   36                                                  
CONECT   26   14   31   47                                                  
CONECT   27   15   37   38                                                  
CONECT   28   16   39   40                                                  
CONECT   29   17   41   47                                                  
CONECT   30   18   42   48                                                  
CONECT   31   21   26   48                                                  
CONECT   32   22   43   44                                                  
CONECT   33   23   45   46                                                  
CONECT   34   19                                                            
CONECT   35   24                                                            
CONECT   36   25                                                            
CONECT   37   27                                                            
CONECT   38   27                                                            
CONECT   39   28                                                            
CONECT   40   28                                                            
CONECT   41   29                                                            
CONECT   42   30                                                            
CONECT   43   32                                                            
CONECT   44   32                                                            
CONECT   45   33                                                            
CONECT   46   33                                                            
CONECT   47   26   29                                                       
CONECT   48   30   31                                                       
MASTER        0    0    0    0    0    0    0    0   48    0   94    0
END

Synonyms

Value	Source
2-[2-({19-amino-6-[(3,4-dicarboxybutanoyl)oxy]-11,18-dihydroxy-5,9-dimethylnonadecan-7-yl}oxy)-2-oxoethyl]butanedioate	Generator

Molecular Formula

C₃₃H₅₇NO₁₄

Average Mass

691.812

Monoisotopic Mass

691.377905519

IUPAC Name

2-[2-({19-amino-6-[(3,4-dicarboxybutanoyl)oxy]-11,18-dihydroxy-5,9-dimethylnonadecan-7-yl}oxy)-2-oxoethyl]butanedioic acid

Traditional Name

2-[2-({19-amino-6-[(3,4-dicarboxybutanoyl)oxy]-11,18-dihydroxy-5,9-dimethylnonadecan-7-yl}oxy)-2-oxoethyl]butanedioic acid

CAS Registry Number

Not Available

SMILES

CCCCC(C)C(OC(=O)CC(CC(O)=O)C(O)=O)C(CC(C)CC(O)CCCCCCC(O)CN)OC(=O)CC(CC(O)=O)C(O)=O

InChI Identifier

InChI=1S/C33H57NO14/c1-4-5-10-21(3)31(48-30(42)18-23(33(45)46)16-28(39)40)26(47-29(41)17-22(32(43)44)15-27(37)38)14-20(2)13-24(35)11-8-6-7-9-12-25(36)19-34/h20-26,31,35-36H,4-19,34H2,1-3H3,(H,37,38)(H,39,40)(H,43,44)(H,45,46)

InChI Key

LTKGSCNZLUASHU-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hexacarboxylic acids and derivatives. These are carboxylic acids containing exactly six carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Hexacarboxylic acids and derivatives

Direct Parent

Hexacarboxylic acids and derivatives

Alternative Parents

Substituents

Hexacarboxylic acid or derivatives
Fatty acid ester
Fatty acyl
1,2-aminoalcohol
Amino acid or derivatives
Carboxylic acid ester
Amino acid
Secondary alcohol
Carboxylic acid
Organic nitrogen compound
Organonitrogen compound
Primary aliphatic amine
Organooxygen compound
Primary amine
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
Amine
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.02 g/L	ALOGPS
logP	-0.48	ALOGPS
logP	0.38	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	3.16	ChemAxon
pKa (Strongest Basic)	9.59	ChemAxon
Physiological Charge	-3	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	268.28 Å²	ChemAxon
Rotatable Bond Count	31	ChemAxon
Refractivity	169.66 m³·mol⁻¹	ChemAxon
Polarizability	75.25 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	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_1_5) - 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)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-17	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	484.2
Liquid Chromatography	HILIC	Accucore 150 Amide HILIC (eluted)	2025-10-23	257.7
Liquid Chromatography	Reversed-phase	Hypersil Gold 1.9 µm C18 (eluted)	2025-10-23	628.8
Liquid Chromatography	Reversed-phase	Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) (eluted)	2025-10-23	565.8
Liquid Chromatography	Reversed-phase	XBridge C18 3.5u 2.1x50 mm (eluted)	2025-10-23	592.0
Liquid Chromatography	Reversed-phase	Ascentis Express C18 (eluted)	2025-10-23	141.9
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-23	2507.0
Liquid Chromatography	HILIC	Merck SeQuant ZIC-HILIC (eluted)	2025-10-23	555.6
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC (eluted)	2025-10-23	333.2
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-23	309.0
Liquid Chromatography	HILIC	Merck SeQuant ZIC-HILIC (eluted)	2025-10-23	114.4
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-23	158.5
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-23	196.9
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC column (eluted)	2025-10-23	271.3
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC column (eluted)	2025-10-23	287.1
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-23	207.9
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-23	453.1
Liquid Chromatography	Reversed-phase	Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex (eluted)	2025-10-23	1665.8
Liquid Chromatography	Reversed-phase	Waters Atlantis T3 (2.1 x 150 mm, 5 um) (eluted)	2025-10-23	1060.8

Retention Indices

Chromatography Type	Peak Label	SMILES	Stationary Phase	Deposition Date	Retention Index
Gas Chromatography	Fumonisin C3_TMS_1	CCCCC(C)C(OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O)C(CC(C)CC(O)CCCCCCC(O)CN)OC(=O)CC(CC(=O)O)C(=O)O	standard non polar	2025-10-23	2661.58
Gas Chromatography	Fumonisin C3_TMS_2	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O[Si](C)(C)C)C(CC(C)CC(O)CCCCCCC(O)CN)OC(=O)CC(CC(=O)O)C(=O)O	standard non polar	2025-10-23	2008.71
Gas Chromatography	Fumonisin C3_TMS_3	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(CCCCCCC(O)CN)O[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O	standard non polar	2025-10-23	1315.73
Gas Chromatography	Fumonisin C3_TMS_4	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(O)CCCCCCC(CN)O[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O	standard non polar	2025-10-23	1764.57
Gas Chromatography	Fumonisin C3_TMS_5	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(O)CCCCCCC(O)CN)OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O	standard non polar	2025-10-23	1764.88
Gas Chromatography	Fumonisin C3_TMS_6	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(O)CCCCCCC(O)CN)OC(=O)CC(CC(=O)O)C(=O)O[Si](C)(C)C	standard non polar	2025-10-23	2973.92
Gas Chromatography	Fumonisin C3_TMS_7	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(O)CCCCCCC(O)CN[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O	standard non polar	2025-10-23	2073.82
Gas Chromatography	Fumonisin C3_TMS_8	CCCCC(C)C(OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(CC(C)CC(O)CCCCCCC(O)CN)OC(=O)CC(CC(=O)O)C(=O)O	standard non polar	2025-10-23	3433.08
Gas Chromatography	Fumonisin C3_TMS_9	CCCCC(C)C(OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O)C(CC(C)CC(CCCCCCC(O)CN)O[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O	standard non polar	2025-10-23	1787.2
Gas Chromatography	Fumonisin C3_TMS_10	CCCCC(C)C(OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O)C(CC(C)CC(O)CCCCCCC(CN)O[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O	standard non polar	2025-10-23	2070.86
Gas Chromatography	Fumonisin C3_TMS_11	CCCCC(C)C(OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O)C(CC(C)CC(O)CCCCCCC(O)CN)OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O	standard non polar	2025-10-23	2684.61
Gas Chromatography	Fumonisin C3_TMS_12	CCCCC(C)C(OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O)C(CC(C)CC(O)CCCCCCC(O)CN)OC(=O)CC(CC(=O)O)C(=O)O[Si](C)(C)C	standard non polar	2025-10-23	2098.89
Gas Chromatography	Fumonisin C3_TMS_13	CCCCC(C)C(OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O)C(CC(C)CC(O)CCCCCCC(O)CN[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O	standard non polar	2025-10-23	1728.34
Gas Chromatography	Fumonisin C3_TMS_14	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O[Si](C)(C)C)C(CC(C)CC(CCCCCCC(O)CN)O[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O	standard non polar	2025-10-23	2500.87
Gas Chromatography	Fumonisin C3_TMS_15	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O[Si](C)(C)C)C(CC(C)CC(O)CCCCCCC(CN)O[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O	standard non polar	2025-10-23	2288.03
Gas Chromatography	Fumonisin C3_TMS_16	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O[Si](C)(C)C)C(CC(C)CC(O)CCCCCCC(O)CN)OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O	standard non polar	2025-10-23	2716.7
Gas Chromatography	Fumonisin C3_TMS_17	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O[Si](C)(C)C)C(CC(C)CC(O)CCCCCCC(O)CN)OC(=O)CC(CC(=O)O)C(=O)O[Si](C)(C)C	standard non polar	2025-10-23	2609.3
Gas Chromatography	Fumonisin C3_TMS_18	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O[Si](C)(C)C)C(CC(C)CC(O)CCCCCCC(O)CN[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O	standard non polar	2025-10-23	1639.18
Gas Chromatography	Fumonisin C3_TMS_19	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(CCCCCCC(CN)O[Si](C)(C)C)O[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O	standard non polar	2025-10-23	1504.43
Gas Chromatography	Fumonisin C3_TMS_20	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(CCCCCCC(O)CN)O[Si](C)(C)C)OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O	standard non polar	2025-10-23	680.487
Gas Chromatography	Fumonisin C3_TMS_21	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(CCCCCCC(O)CN)O[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O[Si](C)(C)C	standard non polar	2025-10-23	1997.52
Gas Chromatography	Fumonisin C3_TMS_22	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(CCCCCCC(O)CN[Si](C)(C)C)O[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O	standard non polar	2025-10-23	2833.63
Gas Chromatography	Fumonisin C3_TMS_23	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(O)CCCCCCC(CN)O[Si](C)(C)C)OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O	standard non polar	2025-10-23	124.659
Gas Chromatography	Fumonisin C3_TMS_24	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(O)CCCCCCC(CN)O[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O[Si](C)(C)C	standard non polar	2025-10-23	1588.45
Gas Chromatography	Fumonisin C3_TMS_25	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(O)CCCCCCC(CN[Si](C)(C)C)O[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O	standard non polar	2025-10-23	1108.33
Gas Chromatography	Fumonisin C3_TMS_26	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(O)CCCCCCC(O)CN)OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	standard non polar	2025-10-23	3174.12
Gas Chromatography	Fumonisin C3_TMS_27	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(O)CCCCCCC(O)CN[Si](C)(C)C)OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O	standard non polar	2025-10-23	928.845
Gas Chromatography	Fumonisin C3_TMS_28	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(O)CCCCCCC(O)CN[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O[Si](C)(C)C	standard non polar	2025-10-23	2479.37
Gas Chromatography	Fumonisin C3_TMS_29	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(O)CCCCCCC(O)CN([Si](C)(C)C)[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O	standard non polar	2025-10-23	3004.81
Gas Chromatography	Fumonisin C3_TMS_1	CCCCC(C)C(OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O)C(CC(C)CC(O)CCCCCCC(O)CN)OC(=O)CC(CC(=O)O)C(=O)O	standard polar	2025-10-23	1110.22
Gas Chromatography	Fumonisin C3_TMS_2	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O[Si](C)(C)C)C(CC(C)CC(O)CCCCCCC(O)CN)OC(=O)CC(CC(=O)O)C(=O)O	standard polar	2025-10-23	1513.82
Gas Chromatography	Fumonisin C3_TMS_3	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(CCCCCCC(O)CN)O[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O	standard polar	2025-10-23	1825.49
Gas Chromatography	Fumonisin C3_TMS_4	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(O)CCCCCCC(CN)O[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O	standard polar	2025-10-23	2290.64
Gas Chromatography	Fumonisin C3_TMS_5	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(O)CCCCCCC(O)CN)OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O	standard polar	2025-10-23	1803.7
Gas Chromatography	Fumonisin C3_TMS_6	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(O)CCCCCCC(O)CN)OC(=O)CC(CC(=O)O)C(=O)O[Si](C)(C)C	standard polar	2025-10-23	1773.66
Gas Chromatography	Fumonisin C3_TMS_7	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(O)CCCCCCC(O)CN[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O	standard polar	2025-10-23	1023.91
Gas Chromatography	Fumonisin C3_TMS_8	CCCCC(C)C(OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(CC(C)CC(O)CCCCCCC(O)CN)OC(=O)CC(CC(=O)O)C(=O)O	standard polar	2025-10-23	2160.18
Gas Chromatography	Fumonisin C3_TMS_9	CCCCC(C)C(OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O)C(CC(C)CC(CCCCCCC(O)CN)O[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O	standard polar	2025-10-23	434.441
Gas Chromatography	Fumonisin C3_TMS_10	CCCCC(C)C(OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O)C(CC(C)CC(O)CCCCCCC(CN)O[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O	standard polar	2025-10-23	1654.53
Gas Chromatography	Fumonisin C3_TMS_11	CCCCC(C)C(OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O)C(CC(C)CC(O)CCCCCCC(O)CN)OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O	standard polar	2025-10-23	651.012
Gas Chromatography	Fumonisin C3_TMS_12	CCCCC(C)C(OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O)C(CC(C)CC(O)CCCCCCC(O)CN)OC(=O)CC(CC(=O)O)C(=O)O[Si](C)(C)C	standard polar	2025-10-23	3162.37
Gas Chromatography	Fumonisin C3_TMS_13	CCCCC(C)C(OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O)C(CC(C)CC(O)CCCCCCC(O)CN[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O	standard polar	2025-10-23	1927.4
Gas Chromatography	Fumonisin C3_TMS_14	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O[Si](C)(C)C)C(CC(C)CC(CCCCCCC(O)CN)O[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O	standard polar	2025-10-23	1139.99
Gas Chromatography	Fumonisin C3_TMS_15	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O[Si](C)(C)C)C(CC(C)CC(O)CCCCCCC(CN)O[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O	standard polar	2025-10-23	3159.17
Gas Chromatography	Fumonisin C3_TMS_16	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O[Si](C)(C)C)C(CC(C)CC(O)CCCCCCC(O)CN)OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O	standard polar	2025-10-23	892.38
Gas Chromatography	Fumonisin C3_TMS_17	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O[Si](C)(C)C)C(CC(C)CC(O)CCCCCCC(O)CN)OC(=O)CC(CC(=O)O)C(=O)O[Si](C)(C)C	standard polar	2025-10-23	-130.812
Gas Chromatography	Fumonisin C3_TMS_18	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O[Si](C)(C)C)C(CC(C)CC(O)CCCCCCC(O)CN[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O	standard polar	2025-10-23	1558.88
Gas Chromatography	Fumonisin C3_TMS_19	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(CCCCCCC(CN)O[Si](C)(C)C)O[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O	standard polar	2025-10-23	2588.86
Gas Chromatography	Fumonisin C3_TMS_20	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(CCCCCCC(O)CN)O[Si](C)(C)C)OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O	standard polar	2025-10-23	1429.65
Gas Chromatography	Fumonisin C3_TMS_21	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(CCCCCCC(O)CN)O[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O[Si](C)(C)C	standard polar	2025-10-23	1461.88
Gas Chromatography	Fumonisin C3_TMS_22	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(CCCCCCC(O)CN[Si](C)(C)C)O[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O	standard polar	2025-10-23	2235.74
Gas Chromatography	Fumonisin C3_TMS_23	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(O)CCCCCCC(CN)O[Si](C)(C)C)OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O	standard polar	2025-10-23	1532.42
Gas Chromatography	Fumonisin C3_TMS_24	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(O)CCCCCCC(CN)O[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O[Si](C)(C)C	standard polar	2025-10-23	2600.89
Gas Chromatography	Fumonisin C3_TMS_25	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(O)CCCCCCC(CN[Si](C)(C)C)O[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O	standard polar	2025-10-23	-1277.21
Gas Chromatography	Fumonisin C3_TMS_26	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(O)CCCCCCC(O)CN)OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	standard polar	2025-10-23	2346.88
Gas Chromatography	Fumonisin C3_TMS_27	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(O)CCCCCCC(O)CN[Si](C)(C)C)OC(=O)CC(CC(=O)O[Si](C)(C)C)C(=O)O	standard polar	2025-10-23	846.632
Gas Chromatography	Fumonisin C3_TMS_28	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(O)CCCCCCC(O)CN[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O[Si](C)(C)C	standard polar	2025-10-23	878.403
Gas Chromatography	Fumonisin C3_TMS_29	CCCCC(C)C(OC(=O)CC(CC(=O)O)C(=O)O)C(CC(C)CC(O)CCCCCCC(O)CN([Si](C)(C)C)[Si](C)(C)C)OC(=O)CC(CC(=O)O)C(=O)O	standard polar	2025-10-23	2146.47

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

8970060

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10794752

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 Fumonisin C3 (MMDBc0015663)

MOL for #<Metabolite:0x00007f9acc3a9b20>

3D MOL for #<Metabolite:0x00007f9acc3a9b20>

3D SDF for #<Metabolite:0x00007f9acc3a9b20>

3D-SDF for #<Metabolite:0x00007f9acc3a9b20>

PDB for #<Metabolite:0x00007f9acc3a9b20>

3D PDB for #<Metabolite:0x00007f9acc3a9b20>

SMILES for #<Metabolite:0x00007f9acc3a9b20>

INCHI for #<Metabolite:0x00007f9acc3a9b20>

Structure for #<Metabolite:0x00007f9acc3a9b20>

3D Structure for #<Metabolite:0x00007f9acc3a9b20>