MiMeDB: Showing metabocard for Fumonisin B2 (MMDBc0006640)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 00:07:15 UTC

Update Date

2022-12-15 22:51:43 UTC

Metabolite ID

MMDBc0006640

Metabolite Identification

Common Name

Fumonisin B2

Description

fumonisin b2, also known as FB2, belongs to the class of organic compounds known as fumonisins. These are diesters of propane-1,2,3-tricarboxylic acid (TCA) and similar long-chain aminopolyol backbones (for FB1: 2S-amino-12S,16R-dimethyl-3S,5R,10R,14S,15R-pentahydroxyeicosane). Structurally, fumonisins resemble the sphingoid bases sphinganine (SA) and sphingosine (SO) to which TCA groups have been added at the C-14 and C-15 positions. Thus, fumonisin B2 is considered to be a sphingoid base. fumonisin b2 is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. Based on a literature review a significant number of articles have been published on fumonisin b2.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152102072D          

 58 57  0  0  1  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
    6.8211   -4.2868    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
   12.5368   -4.2868    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
   13.2513   -3.8743    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
   13.9658   -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
   10.3934   -3.8743    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
    8.9645   -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  1  0  0  0  0  0  0  0  0  0
   16.8237   -5.1118    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5355   -3.8743    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.2526   -2.6368    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   19.6815   -4.2868    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.6789   -4.2868    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.2500   -4.2868    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   16.1092   -3.8743    0.0000 C   0  0  1  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  2  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
    7.5355   -3.0493    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.6789   -5.1118    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
   13.9658   -3.4618    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   16.8237   -5.9368    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5355   -4.6993    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   18.2526   -3.4618    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   19.6815   -3.4618    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6789   -3.4618    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2500   -3.4618    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   16.1092   -4.6993    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   17.5381   -4.6993    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  1  1  0  0  0  0
  6  5  1  0  0  0  0
  8  7  1  0  0  0  0
  9  7  1  0  0  0  0
 10  8  1  0  0  0  0
 11  9  1  0  0  0  0
 12  6  1  0  0  0  0
 13 10  1  0  0  0  0
 20  2  1  6  0  0  0
 20 11  1  0  0  0  0
 20 14  1  0  0  0  0
 21  3  1  6  0  0  0
 21 12  1  0  0  0  0
 22  4  1  0  0  0  0
 23 15  1  6  0  0  0
 23 17  1  0  0  0  0
 24 16  1  1  0  0  0
 24 18  1  0  0  0  0
 25 13  1  0  0  0  0
 25 19  1  0  0  0  0
 26 19  1  0  0  0  0
 26 22  1  0  0  0  0
 27 14  1  0  0  0  0
 28 15  1  0  0  0  0
 29 16  1  0  0  0  0
 30 17  1  0  0  0  0
 31 18  1  0  0  0  0
 32 21  1  0  0  0  0
 32 27  1  0  0  0  0
 33 23  1  0  0  0  0
 34 24  1  0  0  0  0
 22 35  1  1  0  0  0
 25 36  1  6  0  0  0
 26 37  1  1  0  0  0
 38 28  2  0  0  0  0
 39 28  1  0  0  0  0
 40 29  2  0  0  0  0
 41 29  1  0  0  0  0
 42 30  2  0  0  0  0
 43 31  2  0  0  0  0
 44 33  2  0  0  0  0
 45 33  1  0  0  0  0
 46 34  2  0  0  0  0
 47 34  1  0  0  0  0
 27 48  1  1  0  0  0
 48 30  1  0  0  0  0
 49 31  1  0  0  0  0
 32 49  1  6  0  0  0
 20 50  1  1  0  0  0
 21 51  1  1  0  0  0
 22 52  1  1  0  0  0
 23 53  1  1  0  0  0
 24 54  1  6  0  0  0
 25 55  1  6  0  0  0
 26 56  1  1  0  0  0
 27 57  1  1  0  0  0
 32 58  1  1  0  0  0
M  END


  Mrv1652305152102072D          

 58 57  0  0  1  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
    6.8211   -4.2868    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
   12.5368   -4.2868    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
   13.2513   -3.8743    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
   13.9658   -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
   10.3934   -3.8743    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
    8.9645   -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  1  0  0  0  0  0  0  0  0  0
   16.8237   -5.1118    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5355   -3.8743    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.2526   -2.6368    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   19.6815   -4.2868    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.6789   -4.2868    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.2500   -4.2868    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   16.1092   -3.8743    0.0000 C   0  0  1  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  2  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
    7.5355   -3.0493    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.6789   -5.1118    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
   13.9658   -3.4618    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   16.8237   -5.9368    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5355   -4.6993    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   18.2526   -3.4618    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   19.6815   -3.4618    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6789   -3.4618    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2500   -3.4618    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   16.1092   -4.6993    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   17.5381   -4.6993    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  1  1  0  0  0  0
  6  5  1  0  0  0  0
  8  7  1  0  0  0  0
  9  7  1  0  0  0  0
 10  8  1  0  0  0  0
 11  9  1  0  0  0  0
 12  6  1  0  0  0  0
 13 10  1  0  0  0  0
 20  2  1  6  0  0  0
 20 11  1  0  0  0  0
 20 14  1  0  0  0  0
 21  3  1  6  0  0  0
 21 12  1  0  0  0  0
 22  4  1  0  0  0  0
 23 15  1  6  0  0  0
 23 17  1  0  0  0  0
 24 16  1  1  0  0  0
 24 18  1  0  0  0  0
 25 13  1  0  0  0  0
 25 19  1  0  0  0  0
 26 19  1  0  0  0  0
 26 22  1  0  0  0  0
 27 14  1  0  0  0  0
 28 15  1  0  0  0  0
 29 16  1  0  0  0  0
 30 17  1  0  0  0  0
 31 18  1  0  0  0  0
 32 21  1  0  0  0  0
 32 27  1  0  0  0  0
 33 23  1  0  0  0  0
 34 24  1  0  0  0  0
 22 35  1  1  0  0  0
 25 36  1  6  0  0  0
 26 37  1  1  0  0  0
 38 28  2  0  0  0  0
 39 28  1  0  0  0  0
 40 29  2  0  0  0  0
 41 29  1  0  0  0  0
 42 30  2  0  0  0  0
 43 31  2  0  0  0  0
 44 33  2  0  0  0  0
 45 33  1  0  0  0  0
 46 34  2  0  0  0  0
 47 34  1  0  0  0  0
 27 48  1  1  0  0  0
 48 30  1  0  0  0  0
 49 31  1  0  0  0  0
 32 49  1  6  0  0  0
 20 50  1  1  0  0  0
 21 51  1  1  0  0  0
 22 52  1  1  0  0  0
 23 53  1  1  0  0  0
 24 54  1  6  0  0  0
 25 55  1  6  0  0  0
 26 56  1  1  0  0  0
 27 57  1  1  0  0  0
 32 58  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0006640

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@](C)(CCCCCC[C@@]([H])(O)C[C@]([H])(O)[C@]([H])(C)N)C[C@]([H])(OC(=O)C[C@@]([H])(CC(O)=O)C(O)=O)[C@]([H])(OC(=O)C[C@@]([H])(CC(O)=O)C(O)=O)[C@]([H])(C)CCCC

> <INCHI_IDENTIFIER>
InChI=1S/C34H59NO14/c1-5-6-12-21(3)32(49-31(43)18-24(34(46)47)16-29(40)41)27(48-30(42)17-23(33(44)45)15-28(38)39)14-20(2)11-9-7-8-10-13-25(36)19-26(37)22(4)35/h20-27,32,36-37H,5-19,35H2,1-4H3,(H,38,39)(H,40,41)(H,44,45)(H,46,47)/t20-,21+,22-,23+,24+,25+,26-,27-,32+/m0/s1

> <INCHI_KEY>
UXDPXZQHTDAXOZ-STOIETHLSA-N

> <FORMULA>
C34H59NO14

> <MOLECULAR_WEIGHT>
705.839

> <EXACT_MASS>
705.393555584

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
108

> <JCHEM_AVERAGE_POLARIZABILITY>
76.1002011656214

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R)-2-(2-{[(5R,6R,7S,9S,16R,18S,19S)-19-amino-6-{[(3R)-3,4-dicarboxybutanoyl]oxy}-16,18-dihydroxy-5,9-dimethylicosan-7-yl]oxy}-2-oxoethyl)butanedioic acid

> <ALOGPS_LOGP>
-0.28

> <JCHEM_LOGP>
0.7195988357625273

> <ALOGPS_LOGS>
-4.67

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-3

> <JCHEM_PKA>
3.74591811490538

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.158762261475544

> <JCHEM_PKA_STRONGEST_BASIC>
9.52972988204402

> <JCHEM_POLAR_SURFACE_AREA>
268.28

> <JCHEM_REFRACTIVITY>
174.03620000000015

> <JCHEM_ROTATABLE_BOND_COUNT>
31

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.50e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
fumonisin B2

> <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      12.733  -8.002   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      27.403 -10.312   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      28.737  -9.542   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      23.402  -8.002   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      24.736  -7.232   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      20.735  -8.002   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      26.069  -8.002   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      30.070 -10.312   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      19.401  -7.232   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      16.734  -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      14.066  -7.232   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      34.072  -4.922   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      36.739  -8.002   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      18.067  -8.002   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      15.400  -8.002   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      30.070  -7.232   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      36.739  -4.922   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      39.406  -8.002   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      31.404  -4.922   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      34.072  -8.002   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      31.404  -8.002   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      34.072  -3.382   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      36.739  -9.542   0.000  0.00  0.00           C+0
HETATM   35  N   UNK     0      14.066  -5.692   0.000  0.00  0.00           N+0
HETATM   36  O   UNK     0      18.067  -9.542   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0      15.400  -9.542   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      36.739  -3.382   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      38.073  -5.692   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      40.740  -7.232   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0      39.406  -9.542   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0      31.404  -3.382   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0      34.072  -9.542   0.000  0.00  0.00           O+0
HETATM   44  O   UNK     0      32.738  -2.612   0.000  0.00  0.00           O+0
HETATM   45  O   UNK     0      35.405  -2.612   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0      38.073 -10.312   0.000  0.00  0.00           O+0
HETATM   47  O   UNK     0      35.405 -10.312   0.000  0.00  0.00           O+0
HETATM   48  O   UNK     0      30.070  -5.692   0.000  0.00  0.00           O+0
HETATM   49  O   UNK     0      32.738  -7.232   0.000  0.00  0.00           O+0
HETATM   50  H   UNK     0      26.069  -6.462   0.000  0.00  0.00           H+0
HETATM   51  H   UNK     0      31.404 -11.082   0.000  0.00  0.00           H+0
HETATM   52  H   UNK     0      14.066  -8.772   0.000  0.00  0.00           H+0
HETATM   53  H   UNK     0      34.072  -6.462   0.000  0.00  0.00           H+0
HETATM   54  H   UNK     0      36.739  -6.462   0.000  0.00  0.00           H+0
HETATM   55  H   UNK     0      18.067  -6.462   0.000  0.00  0.00           H+0
HETATM   56  H   UNK     0      15.400  -6.462   0.000  0.00  0.00           H+0
HETATM   57  H   UNK     0      30.070  -8.772   0.000  0.00  0.00           H+0
HETATM   58  H   UNK     0      32.738  -8.772   0.000  0.00  0.00           H+0
CONECT    1    5                                                            
CONECT    2   20                                                            
CONECT    3   21                                                            
CONECT    4   22                                                            
CONECT    5    1    6                                                       
CONECT    6    5   12                                                       
CONECT    7    8    9                                                       
CONECT    8    7   10                                                       
CONECT    9    7   11                                                       
CONECT   10    8   13                                                       
CONECT   11    9   20                                                       
CONECT   12    6   21                                                       
CONECT   13   10   25                                                       
CONECT   14   20   27                                                       
CONECT   15   23   28                                                       
CONECT   16   24   29                                                       
CONECT   17   23   30                                                       
CONECT   18   24   31                                                       
CONECT   19   25   26                                                       
CONECT   20    2   11   14   50                                             
CONECT   21    3   12   32   51                                             
CONECT   22    4   26   35   52                                             
CONECT   23   15   17   33   53                                             
CONECT   24   16   18   34   54                                             
CONECT   25   13   19   36   55                                             
CONECT   26   19   22   37   56                                             
CONECT   27   14   32   48   57                                             
CONECT   28   15   38   39                                                  
CONECT   29   16   40   41                                                  
CONECT   30   17   42   48                                                  
CONECT   31   18   43   49                                                  
CONECT   32   21   27   49   58                                             
CONECT   33   23   44   45                                                  
CONECT   34   24   46   47                                                  
CONECT   35   22                                                            
CONECT   36   25                                                            
CONECT   37   26                                                            
CONECT   38   28                                                            
CONECT   39   28                                                            
CONECT   40   29                                                            
CONECT   41   29                                                            
CONECT   42   30                                                            
CONECT   43   31                                                            
CONECT   44   33                                                            
CONECT   45   33                                                            
CONECT   46   34                                                            
CONECT   47   34                                                            
CONECT   48   27   30                                                       
CONECT   49   31   32                                                       
CONECT   50   20                                                            
CONECT   51   21                                                            
CONECT   52   22                                                            
CONECT   53   23                                                            
CONECT   54   24                                                            
CONECT   55   25                                                            
CONECT   56   26                                                            
CONECT   57   27                                                            
CONECT   58   32                                                            
MASTER        0    0    0    0    0    0    0    0   58    0  114    0
END

Synonyms

Value	Source
FB2	ChEBI
Fumonisin-b2	MeSH

Molecular Formula

C₃₄H₅₉NO₁₄

Average Mass

705.839

Monoisotopic Mass

705.393555584

IUPAC Name

(2R)-2-(2-{[(5R,6R,7S,9S,16R,18S,19S)-19-amino-6-{[(3R)-3,4-dicarboxybutanoyl]oxy}-16,18-dihydroxy-5,9-dimethylicosan-7-yl]oxy}-2-oxoethyl)butanedioic acid

Traditional Name

fumonisin B2

CAS Registry Number

Not Available

SMILES

[H][C@](C)(CCCCCC[C@@]([H])(O)C[C@]([H])(O)[C@]([H])(C)N)C[C@]([H])(OC(=O)C[C@@]([H])(CC(O)=O)C(O)=O)[C@]([H])(OC(=O)C[C@@]([H])(CC(O)=O)C(O)=O)[C@]([H])(C)CCCC

InChI Identifier

InChI=1S/C34H59NO14/c1-5-6-12-21(3)32(49-31(43)18-24(34(46)47)16-29(40)41)27(48-30(42)17-23(33(44)45)15-28(38)39)14-20(2)11-9-7-8-10-13-25(36)19-26(37)22(4)35/h20-27,32,36-37H,5-19,35H2,1-4H3,(H,38,39)(H,40,41)(H,44,45)(H,46,47)/t20-,21+,22-,23+,24+,25+,26-,27-,32+/m0/s1

InChI Key

UXDPXZQHTDAXOZ-STOIETHLSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fumonisins. These are diesters of propane-1,2,3-tricarboxylic acid (TCA) and similar long-chain aminopolyol backbones (for FB1: 2S-amino-12S,16R-dimethyl-3S,5R,10R,14S,15R-pentahydroxyeicosane). Structurally, fumonisins resemble the sphingoid bases sphinganine (SA) and sphingosine (SO) to which TCA groups have been added at the C-14 and C-15 positions.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Fumonisins

Direct Parent

Fumonisins

Alternative Parents

Substituents

Fumonisin skeleton
Fumonisin-skeleton
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
Organopnictogen compound
Carbonyl group
Organic oxygen compound
Amine
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

fumonisin (CHEBI:38225 )
Mycotoxins (C19242 )
Sphingoid base analogs (LMSP01080023 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.015 g/L	ALOGPS
logP	-0.28	ALOGPS
logP	0.72	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	3.16	ChemAxon
pKa (Strongest Basic)	9.53	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	174.04 m³·mol⁻¹	ChemAxon
Polarizability	76.1 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_2_3) - 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)		2022-08-22	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

Cytoplasm
Extracellular
Membrane

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

Source Type	Source Sub-type	Species	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

C00056538

Chemspider ID

2015284

KEGG Compound ID

C19242

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

2733489

PDB ID

Not Available

ChEBI ID

38225

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 Fumonisin B2 (MMDBc0006640)

MOL for #<Metabolite:0x00007fecf043bf40>

3D MOL for #<Metabolite:0x00007fecf043bf40>

3D SDF for #<Metabolite:0x00007fecf043bf40>

3D-SDF for #<Metabolite:0x00007fecf043bf40>

PDB for #<Metabolite:0x00007fecf043bf40>

3D PDB for #<Metabolite:0x00007fecf043bf40>

SMILES for #<Metabolite:0x00007fecf043bf40>

INCHI for #<Metabolite:0x00007fecf043bf40>

Structure for #<Metabolite:0x00007fecf043bf40>

3D Structure for #<Metabolite:0x00007fecf043bf40>