MiMeDB: Showing metabocard for Seco-Chaetomugilin A (MMDBc0017878)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-05-15 08:10:04 UTC

Update Date

2022-08-31 06:43:06 UTC

Metabolite ID

MMDBc0017878

Metabolite Identification

Common Name

Seco-Chaetomugilin A

Description

Seco-Chaetomugilin A belongs to the class of organic compounds known as cyclohexenones. Cyclohexenones are compounds containing a cylohexenone moiety, which is a six-membered aliphatic ring that carries a ketone and has one endocyclic double bond. Based on a literature review very few articles have been published on Seco-Chaetomugilin A.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152110102D          

 41 43  0  0  1  0            999 V2000
    7.6442    0.3094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3089   -0.1403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5134    1.7119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7563    1.1197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7565   -0.8892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9617    3.2674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4296    1.0622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9950    0.3610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7358   -0.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9558    1.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2542    1.0365    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5883    0.6360    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.6888    1.7377    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0556    1.2660    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1704    0.3867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9112   -0.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5212    0.4383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6966    0.4640    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1640    1.0941    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4766   -0.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6520   -0.9642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3606    1.8953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2620   -0.2372    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4002    0.7822    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8666   -1.7170    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    7.2988    2.4647    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3350    2.0423    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2174   -1.6655    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1528    2.1256    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1699    1.5744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7651    2.4662    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7804    1.1137    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4608   -0.0406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0396    1.7892    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3850   -0.3660    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8196    0.3352    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2237    0.4897    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0788    1.0107    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4770    1.8960    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0555    1.2069    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5394    1.6330    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  2  0  0  0  0
 11  1  1  6  0  0  0
 11  7  1  0  0  0  0
 12  2  1  6  0  0  0
 13  3  1  0  0  0  0
 13 11  1  0  0  0  0
 14  4  1  0  0  0  0
 14 12  1  0  0  0  0
 15  8  1  0  0  0  0
 15  9  2  0  0  0  0
 16  9  1  0  0  0  0
 17 10  2  0  0  0  0
 17 16  1  0  0  0  0
 18 17  1  0  0  0  0
 19 18  1  0  0  0  0
 20 16  2  0  0  0  0
 21 20  1  0  0  0  0
 19 22  1  6  0  0  0
 23  5  1  6  0  0  0
 23 18  1  0  0  0  0
 23 21  1  0  0  0  0
 24 12  1  6  0  0  0
 24 19  1  0  0  0  0
 25 20  1  0  0  0  0
 13 26  1  1  0  0  0
 14 27  1  1  0  0  0
 28 21  2  0  0  0  0
 29 22  2  0  0  0  0
 24 30  1  1  0  0  0
 31  6  1  0  0  0  0
 31 22  1  0  0  0  0
 32 10  1  0  0  0  0
 32 15  1  0  0  0  0
 33 23  1  0  0  0  0
 33 24  1  0  0  0  0
 34  7  1  0  0  0  0
 35  8  1  0  0  0  0
 11 36  1  1  0  0  0
 12 37  1  1  0  0  0
 13 38  1  1  0  0  0
 14 39  1  6  0  0  0
 18 40  1  6  0  0  0
 19 41  1  1  0  0  0
M  END


  Mrv1652305152110102D          

 41 43  0  0  1  0            999 V2000
    7.6442    0.3094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3089   -0.1403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5134    1.7119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7563    1.1197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7565   -0.8892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9617    3.2674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4296    1.0622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9950    0.3610    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7358   -0.3145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9558    1.1395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2542    1.0365    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5883    0.6360    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.6888    1.7377    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0556    1.2660    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1704    0.3867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9112   -0.2887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5212    0.4383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6966    0.4640    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1640    1.0941    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4766   -0.9900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6520   -0.9642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3606    1.8953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2620   -0.2372    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4002    0.7822    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8666   -1.7170    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    7.2988    2.4647    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3350    2.0423    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2174   -1.6655    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1528    2.1256    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1699    1.5744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7651    2.4662    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7804    1.1137    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4608   -0.0406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0396    1.7892    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3850   -0.3660    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8196    0.3352    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2237    0.4897    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0788    1.0107    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4770    1.8960    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0555    1.2069    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5394    1.6330    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  2  0  0  0  0
 11  1  1  6  0  0  0
 11  7  1  0  0  0  0
 12  2  1  6  0  0  0
 13  3  1  0  0  0  0
 13 11  1  0  0  0  0
 14  4  1  0  0  0  0
 14 12  1  0  0  0  0
 15  8  1  0  0  0  0
 15  9  2  0  0  0  0
 16  9  1  0  0  0  0
 17 10  2  0  0  0  0
 17 16  1  0  0  0  0
 18 17  1  0  0  0  0
 19 18  1  0  0  0  0
 20 16  2  0  0  0  0
 21 20  1  0  0  0  0
 19 22  1  6  0  0  0
 23  5  1  6  0  0  0
 23 18  1  0  0  0  0
 23 21  1  0  0  0  0
 24 12  1  6  0  0  0
 24 19  1  0  0  0  0
 25 20  1  0  0  0  0
 13 26  1  1  0  0  0
 14 27  1  1  0  0  0
 28 21  2  0  0  0  0
 29 22  2  0  0  0  0
 24 30  1  1  0  0  0
 31  6  1  0  0  0  0
 31 22  1  0  0  0  0
 32 10  1  0  0  0  0
 32 15  1  0  0  0  0
 33 23  1  0  0  0  0
 33 24  1  0  0  0  0
 34  7  1  0  0  0  0
 35  8  1  0  0  0  0
 11 36  1  1  0  0  0
 12 37  1  1  0  0  0
 13 38  1  1  0  0  0
 14 39  1  6  0  0  0
 18 40  1  6  0  0  0
 19 41  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0017878

> <DATABASE_NAME>
MIME

> <SMILES>
[H]\C(=C(\[H])[C@@]([H])(C)[C@@]([H])(C)O)C1=CC2=C(Cl)C(=O)[C@@]3(C)O[C@](O)([C@]([H])(C)[C@@]([H])(C)O)[C@]([H])(C(=O)OC)[C@@]3([H])C2=CO1

> <INCHI_IDENTIFIER>
InChI=1S/C24H31ClO8/c1-11(13(3)26)7-8-15-9-16-17(10-32-15)18-19(22(29)31-6)24(30,12(2)14(4)27)33-23(18,5)21(28)20(16)25/h7-14,18-19,26-27,30H,1-6H3/b8-7+/t11-,12-,13-,14-,18-,19+,23+,24-/m1/s1

> <INCHI_KEY>
FROQHXMNGOHAAZ-NCCWVHROSA-N

> <FORMULA>
C24H31ClO8

> <MOLECULAR_WEIGHT>
482.95

> <EXACT_MASS>
482.1707457

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
49.918379201008044

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (6aS,8R,9R,9aS)-5-chloro-8-hydroxy-3-[(1E,3R,4R)-4-hydroxy-3-methylpent-1-en-1-yl]-8-[(2R,3R)-3-hydroxybutan-2-yl]-6a-methyl-6-oxo-6H,6aH,8H,9H,9aH-furo[2,3-h]isochromene-9-carboxylate

> <ALOGPS_LOGP>
2.38

> <JCHEM_LOGP>
1.6032433196666673

> <ALOGPS_LOGS>
-3.74

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.212624197300553

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.27932036157874

> <JCHEM_PKA_STRONGEST_BASIC>
-1.367646907926006

> <JCHEM_POLAR_SURFACE_AREA>
122.52000000000001

> <JCHEM_REFRACTIVITY>
124.63259999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.71e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (6aS,8R,9R,9aS)-5-chloro-8-hydroxy-3-[(1E,3R,4R)-4-hydroxy-3-methylpent-1-en-1-yl]-8-[(2R,3R)-3-hydroxybutan-2-yl]-6a-methyl-6-oxo-9H,9aH-furo[2,3-h]isochromene-9-carboxylate

> <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      14.269   0.578   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.577  -0.262   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      15.892   3.196   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.412   2.090   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.279  -1.660   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.662   6.099   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.002   1.983   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      11.191   0.674   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.840  -0.587   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.384   2.127   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.541   1.935   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.098   1.187   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.352   3.244   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.104   2.363   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.651   0.722   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.301  -0.539   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.573   0.818   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.034   0.866   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.039   2.042   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.490  -1.848   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.950  -1.800   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.406   3.538   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.222  -0.443   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.614   1.460   0.000  0.00  0.00           C+0
HETATM   25 Cl   UNK     0       7.218  -3.205   0.000  0.00  0.00          Cl+0
HETATM   26  O   UNK     0      13.624   4.601   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       0.625   3.812   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       4.139  -3.109   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       5.885   3.968   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       2.184   2.939   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       3.295   4.604   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       8.923   2.079   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       2.727  -0.076   0.000  0.00  0.00           O+0
HETATM   34  H   UNK     0      11.274   3.340   0.000  0.00  0.00           H+0
HETATM   35  H   UNK     0      11.919  -0.683   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0      12.730   0.626   0.000  0.00  0.00           H+0
HETATM   37  H   UNK     0      -0.418   0.914   0.000  0.00  0.00           H+0
HETATM   38  H   UNK     0      15.080   1.887   0.000  0.00  0.00           H+0
HETATM   39  H   UNK     0      -0.890   3.539   0.000  0.00  0.00           H+0
HETATM   40  H   UNK     0       5.704   2.253   0.000  0.00  0.00           H+0
HETATM   41  H   UNK     0       2.873   3.048   0.000  0.00  0.00           H+0
CONECT    1   11                                                            
CONECT    2   12                                                            
CONECT    3   13                                                            
CONECT    4   14                                                            
CONECT    5   23                                                            
CONECT    6   31                                                            
CONECT    7    8   11   34                                                  
CONECT    8    7   15   35                                                  
CONECT    9   15   16                                                       
CONECT   10   17   32                                                       
CONECT   11    1    7   13   36                                             
CONECT   12    2   14   24   37                                             
CONECT   13    3   11   26   38                                             
CONECT   14    4   12   27   39                                             
CONECT   15    8    9   32                                                  
CONECT   16    9   17   20                                                  
CONECT   17   10   16   18                                                  
CONECT   18   17   19   23   40                                             
CONECT   19   18   22   24   41                                             
CONECT   20   16   21   25                                                  
CONECT   21   20   23   28                                                  
CONECT   22   19   29   31                                                  
CONECT   23    5   18   21   33                                             
CONECT   24   12   19   30   33                                             
CONECT   25   20                                                            
CONECT   26   13                                                            
CONECT   27   14                                                            
CONECT   28   21                                                            
CONECT   29   22                                                            
CONECT   30   24                                                            
CONECT   31    6   22                                                       
CONECT   32   10   15                                                       
CONECT   33   23   24                                                       
CONECT   34    7                                                            
CONECT   35    8                                                            
CONECT   36   11                                                            
CONECT   37   12                                                            
CONECT   38   13                                                            
CONECT   39   14                                                            
CONECT   40   18                                                            
CONECT   41   19                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   86    0
END

Synonyms

Not Available

Molecular Formula

C₂₄H₃₁ClO₈

Average Mass

482.95

Monoisotopic Mass

482.1707457

IUPAC Name

methyl (6aS,8R,9R,9aS)-5-chloro-8-hydroxy-3-[(1E,3R,4R)-4-hydroxy-3-methylpent-1-en-1-yl]-8-[(2R,3R)-3-hydroxybutan-2-yl]-6a-methyl-6-oxo-6H,6aH,8H,9H,9aH-furo[2,3-h]isochromene-9-carboxylate

Traditional Name

methyl (6aS,8R,9R,9aS)-5-chloro-8-hydroxy-3-[(1E,3R,4R)-4-hydroxy-3-methylpent-1-en-1-yl]-8-[(2R,3R)-3-hydroxybutan-2-yl]-6a-methyl-6-oxo-9H,9aH-furo[2,3-h]isochromene-9-carboxylate

CAS Registry Number

Not Available

SMILES

[H]\C(=C(\[H])[C@@]([H])(C)[C@@]([H])(C)O)C1=CC2=C(Cl)C(=O)[C@@]3(C)O[C@](O)([C@]([H])(C)[C@@]([H])(C)O)[C@]([H])(C(=O)OC)[C@@]3([H])C2=CO1

InChI Identifier

InChI=1S/C24H31ClO8/c1-11(13(3)26)7-8-15-9-16-17(10-32-15)18-19(22(29)31-6)24(30,12(2)14(4)27)33-23(18,5)21(28)20(16)25/h7-14,18-19,26-27,30H,1-6H3/b8-7+/t11-,12-,13-,14-,18-,19+,23+,24-/m1/s1

InChI Key

FROQHXMNGOHAAZ-NCCWVHROSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclohexenones. Cyclohexenones are compounds containing a cylohexenone moiety, which is a six-membered aliphatic ring that carries a ketone and has one endocyclic double bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Cyclohexenones

Alternative Parents

Substituents

Cyclohexenone
Pyran
Alpha-haloketone
Alpha-chloroketone
Tetrahydrofuran
Methyl ester
Carboxylic acid ester
Hemiacetal
Secondary alcohol
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Oxacycle
Chloroalkene
Haloalkene
Vinyl chloride
Organoheterocyclic compound
Vinyl halide
Alcohol
Organic oxide
Hydrocarbon derivative
Organohalogen compound
Organochloride
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.087 g/L	ALOGPS
logP	2.38	ALOGPS
logP	1.6	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	11.28	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	122.52 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	124.63 m³·mol⁻¹	ChemAxon
Polarizability	49.92 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-10	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
MS	Mass Spectrum (Electron Ionization)	Not Available	2022-08-06	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-18	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	2	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

C00053777

Chemspider ID

27024735

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139588040

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 Seco-Chaetomugilin A (MMDBc0017878)

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