MiMeDB: Showing metabocard for Neosartoricin (MMDBc0012421)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 03:57:42 UTC

Update Date

2025-10-07 16:06:00 UTC

Metabolite ID

MMDBc0012421

Metabolite Identification

Common Name

Neosartoricin

Description

Neosartoricin is a polyketide belonging to the class of secondary metabolites. It has been implicated in various biological processes, particularly in the regulation of secondary metabolism. Transcriptomic analyses have linked the enzyme FphB to the biosynthesis of neosartoricin B, suggesting its role in modulating the associated gene cluster and the production of related compounds such as hexadehydroastechrome (PMID:40985688 ). The exploration of biosynthetic gene clusters (BGCs) and secondary metabolites (SMs) has revealed that co-culture with bacteria and specific growth conditions can enhance the production of neosartoricin (PMID:38667937 ). Furthermore, neosartoricin B has been successfully produced in artificial consortia involving cyanobacteria and filamentous fungi, with nitrogen levels playing a critical role in its biosynthesis (PMID:36859469 ). The compound also serves as a precursor in the formation of other metabolites, such as hancockinone A, through enzymatic processes involving cytochrome P450 (PMID:34747627 ). Additionally, neosartoricin's structural relationship with other compounds highlights its potential relevance in the pathogenesis of certain fungal strains (PMID:23758576 ). The activation of silent clusters has further facilitated the isolation of neosartoricin, underscoring its significance in fungal secondary metabolism (PMID:23368997 ).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152105572D          

 36 38  0  0  1  0            999 V2000
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1178   -0.5152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8697    0.8920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5269    1.3808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4000    0.2600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0572    0.7488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2125    0.4033    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7751   -0.0265    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9966    0.4623    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.8875    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0  0  0  0
 12  1  1  0  0  0  0
 12  2  1  0  0  0  0
 12  5  2  0  0  0  0
 13  3  1  0  0  0  0
  7 13  1  4  0  0  0
 14  4  1  0  0  0  0
 15  8  2  0  0  0  0
 15  9  1  0  0  0  0
 16  7  2  0  0  0  0
 16 10  1  0  0  0  0
 17  6  1  0  0  0  0
 18  8  1  0  0  0  0
 18 17  2  0  0  0  0
 19 11  1  0  0  0  0
 19 17  1  0  0  0  0
 20  9  2  0  0  0  0
 21 18  1  0  0  0  0
 21 20  1  0  0  0  0
 22 19  2  0  0  0  0
 23 21  2  0  0  0  0
 23 22  1  0  0  0  0
 24 22  1  0  0  0  0
 25 24  1  0  0  0  0
 26 10  1  1  0  0  0
 26 11  1  0  0  0  0
 26 25  1  0  0  0  0
 27 13  2  0  0  0  0
 28 14  2  0  0  0  0
 29 15  1  0  0  0  0
 30 16  1  0  0  0  0
 31 20  1  0  0  0  0
 32 23  1  0  0  0  0
 33 24  2  0  0  0  0
 26 34  1  6  0  0  0
 35 14  1  0  0  0  0
 25 35  1  6  0  0  0
 25 36  1  1  0  0  0
M  END


  Mrv1652305152105572D          

 36 38  0  0  1  0            999 V2000
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1178   -0.5152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8697    0.8920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5269    1.3808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4000    0.2600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0572    0.7488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2125    0.4033    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7751   -0.0265    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9966    0.4623    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.8875    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0  0  0  0
 12  1  1  0  0  0  0
 12  2  1  0  0  0  0
 12  5  2  0  0  0  0
 13  3  1  0  0  0  0
  7 13  1  4  0  0  0
 14  4  1  0  0  0  0
 15  8  2  0  0  0  0
 15  9  1  0  0  0  0
 16  7  2  0  0  0  0
 16 10  1  0  0  0  0
 17  6  1  0  0  0  0
 18  8  1  0  0  0  0
 18 17  2  0  0  0  0
 19 11  1  0  0  0  0
 19 17  1  0  0  0  0
 20  9  2  0  0  0  0
 21 18  1  0  0  0  0
 21 20  1  0  0  0  0
 22 19  2  0  0  0  0
 23 21  2  0  0  0  0
 23 22  1  0  0  0  0
 24 22  1  0  0  0  0
 25 24  1  0  0  0  0
 26 10  1  1  0  0  0
 26 11  1  0  0  0  0
 26 25  1  0  0  0  0
 27 13  2  0  0  0  0
 28 14  2  0  0  0  0
 29 15  1  0  0  0  0
 30 16  1  0  0  0  0
 31 20  1  0  0  0  0
 32 23  1  0  0  0  0
 33 24  2  0  0  0  0
 26 34  1  6  0  0  0
 35 14  1  0  0  0  0
 25 35  1  6  0  0  0
 25 36  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0012421

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]1(OC(C)=O)C(=O)C2=C(C[C@@]1(O)CC(O)=CC(C)=O)C(CC=C(C)C)=C1C=C(O)C=C(O)C1=C2O

> <INCHI_IDENTIFIER>
InChI=1S/C26H28O9/c1-12(2)5-6-17-18-8-15(29)9-20(31)21(18)23(32)22-19(17)11-26(34,10-16(30)7-13(3)27)25(24(22)33)35-14(4)28/h5,7-9,25,29-32,34H,6,10-11H2,1-4H3/t25-,26+/m1/s1

> <INCHI_KEY>
KVVYTLCXDTXZPI-FTJBHMTQSA-N

> <FORMULA>
C26H28O9

> <MOLECULAR_WEIGHT>
484.501

> <EXACT_MASS>
484.173332482

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
50.216276713784545

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3R)-3,6,8,9-tetrahydroxy-3-(2-hydroxy-4-oxopent-2-en-1-yl)-10-(3-methylbut-2-en-1-yl)-1-oxo-1,2,3,4-tetrahydroanthracen-2-yl acetate

> <ALOGPS_LOGP>
2.68

> <JCHEM_LOGP>
3.033523617666665

> <ALOGPS_LOGS>
-4.35

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.479993757505376

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.658580562080143

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5537079282443003

> <JCHEM_POLAR_SURFACE_AREA>
161.58999999999997

> <JCHEM_REFRACTIVITY>
129.6443

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.17e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R)-3,6,8,9-tetrahydroxy-3-(2-hydroxy-4-oxopent-2-en-1-yl)-10-(3-methylbut-2-en-1-yl)-1-oxo-2,4-dihydroanthracen-2-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-MAY-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-MAY-21         0                                  
HETATM    1  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.820  -0.962   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.335   4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -5.357   1.665   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.850   2.577   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.000   1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -6.347   0.485   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.001   3.850   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -3.840   1.398   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -7.863   0.753   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      -4.001   2.310   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       8.002   1.540   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      -3.313  -0.049   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       5.335   6.160   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       2.667   6.160   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       0.000   6.160   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      -1.860   0.863   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      -2.667   4.620   0.000  0.00  0.00           O+0
HETATM   36  H   UNK     0      -1.334   5.390   0.000  0.00  0.00           H+0
CONECT    1   12                                                            
CONECT    2   12                                                            
CONECT    3   13                                                            
CONECT    4   14                                                            
CONECT    5    6   12                                                       
CONECT    6    5   17                                                       
CONECT    7   13   16                                                       
CONECT    8   15   18                                                       
CONECT    9   15   20                                                       
CONECT   10   16   26                                                       
CONECT   11   19   26                                                       
CONECT   12    1    2    5                                                  
CONECT   13    3    7   27                                                  
CONECT   14    4   28   35                                                  
CONECT   15    8    9   29                                                  
CONECT   16    7   10   30                                                  
CONECT   17    6   18   19                                                  
CONECT   18    8   17   21                                                  
CONECT   19   11   17   22                                                  
CONECT   20    9   21   31                                                  
CONECT   21   18   20   23                                                  
CONECT   22   19   23   24                                                  
CONECT   23   21   22   32                                                  
CONECT   24   22   25   33                                                  
CONECT   25   24   26   35   36                                             
CONECT   26   10   11   25   34                                             
CONECT   27   13                                                            
CONECT   28   14                                                            
CONECT   29   15                                                            
CONECT   30   16                                                            
CONECT   31   20                                                            
CONECT   32   23                                                            
CONECT   33   24                                                            
CONECT   34   26                                                            
CONECT   35   14   25                                                       
CONECT   36   25                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   76    0
END

Synonyms

Not Available

Molecular Formula

C₂₆H₂₈O₉

Average Mass

484.501

Monoisotopic Mass

484.173332482

IUPAC Name

(2S,3R)-3,6,8,9-tetrahydroxy-3-(2-hydroxy-4-oxopent-2-en-1-yl)-10-(3-methylbut-2-en-1-yl)-1-oxo-1,2,3,4-tetrahydroanthracen-2-yl acetate

Traditional Name

(2S,3R)-3,6,8,9-tetrahydroxy-3-(2-hydroxy-4-oxopent-2-en-1-yl)-10-(3-methylbut-2-en-1-yl)-1-oxo-2,4-dihydroanthracen-2-yl acetate

CAS Registry Number

Not Available

SMILES

[H][C@@]1(OC(C)=O)C(=O)C2=C(C[C@@]1(O)CC(O)=CC(C)=O)C(CC=C(C)C)=C1C=C(O)C=C(O)C1=C2O

InChI Identifier

InChI=1S/C26H28O9/c1-12(2)5-6-17-18-8-15(29)9-20(31)21(18)23(32)22-19(17)11-26(34,10-16(30)7-13(3)27)25(24(22)33)35-14(4)28/h5,7-9,25,29-32,34H,6,10-11H2,1-4H3/t25-,26+/m1/s1

InChI Key

KVVYTLCXDTXZPI-FTJBHMTQSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anthracenes. These are organic compounds containing a system of three linearly fused benzene rings.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Anthracenes

Sub Class

Not Available

Direct Parent

Anthracenes

Alternative Parents

Substituents

Anthracene
1-naphthol
2-naphthol
Tetralin
Aryl alkyl ketone
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alpha-acyloxy ketone
Vinylogous acid
Alpha,beta-unsaturated ketone
Tertiary alcohol
Enone
Acryloyl-group
Ketone
Carboxylic acid ester
Polyol
Monocarboxylic acid or derivatives
Enol
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.022 g/L	ALOGPS
logP	2.68	ALOGPS
logP	3.03	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	7.66	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	161.59 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	129.64 m³·mol⁻¹	ChemAxon
Polarizability	50.22 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_4_12) - 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

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 (void)	2025-10-23	22.6
Liquid Chromatography	HILIC	Accucore 150 Amide HILIC (void)	2025-10-23	27.9
Liquid Chromatography	Reversed-phase	Hypersil Gold 1.9 µm C18 (eluted)	2025-10-23	539.0
Liquid Chromatography	Reversed-phase	Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) (eluted)	2025-10-23	572.4
Liquid Chromatography	Reversed-phase	XBridge C18 3.5u 2.1x50 mm (eluted)	2025-10-23	687.8
Liquid Chromatography	Reversed-phase	Ascentis Express C18 (eluted)	2025-10-23	189.5
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-23	2902.4
Liquid Chromatography	HILIC	Merck SeQuant ZIC-HILIC (void)	2025-10-23	102.9
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC (eluted)	2025-10-23	421.8
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-23	289.9
Liquid Chromatography	HILIC	Merck SeQuant ZIC-HILIC (eluted)	2025-10-23	138.5
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-23	128.9
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-23	137.4
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC column (eluted)	2025-10-23	42.2
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC column (eluted)	2025-10-23	341.9
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-23	84.9
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-23	476.0
Liquid Chromatography	Reversed-phase	Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex (eluted)	2025-10-23	1926.9
Liquid Chromatography	Reversed-phase	Waters Atlantis T3 (2.1 x 150 mm, 5 um) (eluted)	2025-10-23	1084.8

Retention Indices

Chromatography Type	Peak Label	SMILES	Stationary Phase	Deposition Date	Retention Index
Gas Chromatography	Neosartoricin_TMS_1	CC(=O)C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O)=CC1=C2CC=C(C)C	standard non polar	2025-10-23	1715.83
Gas Chromatography	Neosartoricin_TMS_2	CC(=O)C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	2359.64
Gas Chromatography	Neosartoricin_TMS_3	CC(=O)C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C	standard non polar	2025-10-23	2067.05
Gas Chromatography	Neosartoricin_TMS_4	CC(=O)C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C	standard non polar	2025-10-23	756.643
Gas Chromatography	Neosartoricin_TMS_5	CC(=O)C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O)=CC1=C2CC=C(C)C	standard non polar	2025-10-23	2410.93
Gas Chromatography	Neosartoricin_TMS_6	C=C(C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	2466.59
Gas Chromatography	Neosartoricin_TMS_7	CC(=O)C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	1509.73
Gas Chromatography	Neosartoricin_TMS_8	CC(=O)C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O)=CC1=C2CC=C(C)C	standard non polar	2025-10-23	1902.74
Gas Chromatography	Neosartoricin_TMS_9	CC(=O)C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C	standard non polar	2025-10-23	2548.92
Gas Chromatography	Neosartoricin_TMS_10	CC(=O)C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C	standard non polar	2025-10-23	1673.74
Gas Chromatography	Neosartoricin_TMS_11	C=C(C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	1399.38
Gas Chromatography	Neosartoricin_TMS_12	CC(=O)C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	504.762
Gas Chromatography	Neosartoricin_TMS_13	CC(=O)C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	2514.79
Gas Chromatography	Neosartoricin_TMS_14	CC(=O)C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	2119.25
Gas Chromatography	Neosartoricin_TMS_15	C=C(C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	1146.91
Gas Chromatography	Neosartoricin_TMS_16	CC(=O)C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C	standard non polar	2025-10-23	2548.87
Gas Chromatography	Neosartoricin_TMS_17	CC(=O)C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C	standard non polar	2025-10-23	2213.02
Gas Chromatography	Neosartoricin_TMS_18	C=C(C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	2779.07
Gas Chromatography	Neosartoricin_TMS_19	CC(=O)C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C	standard non polar	2025-10-23	2711.65
Gas Chromatography	Neosartoricin_TMS_20	C=C(C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	1097.72
Gas Chromatography	Neosartoricin_TMS_21	C=C(C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	1247.01
Gas Chromatography	Neosartoricin_TMS_22	CC(=O)C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	2613.71
Gas Chromatography	Neosartoricin_TMS_23	CC(=O)C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	1305.96
Gas Chromatography	Neosartoricin_TMS_24	CC(=O)C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	2592.81
Gas Chromatography	Neosartoricin_TMS_25	C=C(C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	2039.12
Gas Chromatography	Neosartoricin_TMS_26	CC(=O)C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C	standard non polar	2025-10-23	1813.3
Gas Chromatography	Neosartoricin_TMS_27	CC(=O)C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C	standard non polar	2025-10-23	2698.79
Gas Chromatography	Neosartoricin_TMS_28	C=C(C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	1661.92
Gas Chromatography	Neosartoricin_TMS_29	CC(=O)C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C	standard non polar	2025-10-23	1761.39
Gas Chromatography	Neosartoricin_TMS_30	C=C(C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	2362.9
Gas Chromatography	Neosartoricin_TMS_31	C=C(C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	1261.28
Gas Chromatography	Neosartoricin_TMS_32	CC(=O)C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	2413.38
Gas Chromatography	Neosartoricin_TMS_33	CC(=O)C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	1869.69
Gas Chromatography	Neosartoricin_TMS_34	C=C(C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	826.381
Gas Chromatography	Neosartoricin_TMS_35	CC(=O)C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	2603.49
Gas Chromatography	Neosartoricin_TMS_36	C=C(C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	2388.15
Gas Chromatography	Neosartoricin_TMS_37	C=C(C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	2307.52
Gas Chromatography	Neosartoricin_TMS_38	CC(=O)C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C	standard non polar	2025-10-23	3364.38
Gas Chromatography	Neosartoricin_TMS_39	C=C(C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	1642.34
Gas Chromatography	Neosartoricin_TMS_40	C=C(C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	2127.79
Gas Chromatography	Neosartoricin_TMS_41	C=C(C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	1929.93
Gas Chromatography	Neosartoricin_TMS_42	CC(=O)C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	1846.65
Gas Chromatography	Neosartoricin_TMS_43	CC(=O)C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	2668.93
Gas Chromatography	Neosartoricin_TMS_44	C=C(C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	3112.41
Gas Chromatography	Neosartoricin_TMS_45	CC(=O)C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	1637.99
Gas Chromatography	Neosartoricin_TMS_46	C=C(C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	2473.72
Gas Chromatography	Neosartoricin_TMS_47	C=C(C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	870.448
Gas Chromatography	Neosartoricin_TMS_48	CC(=O)C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C	standard non polar	2025-10-23	2656.73
Gas Chromatography	Neosartoricin_TMS_49	C=C(C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	3232.72
Gas Chromatography	Neosartoricin_TMS_50	C=C(C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	1170.61
Gas Chromatography	Neosartoricin_TMS_51	C=C(C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	1674.99
Gas Chromatography	Neosartoricin_TMS_52	CC(=O)C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	1658.51
Gas Chromatography	Neosartoricin_TMS_53	C=C(C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	1698.41
Gas Chromatography	Neosartoricin_TMS_54	C=C(C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	2659.81
Gas Chromatography	Neosartoricin_TMS_55	C=C(C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	1411.83
Gas Chromatography	Neosartoricin_TMS_56	C=C(C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	2308.14
Gas Chromatography	Neosartoricin_TMS_57	CC(=O)C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	2572.9
Gas Chromatography	Neosartoricin_TMS_58	C=C(C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	3242.22
Gas Chromatography	Neosartoricin_TMS_59	C=C(C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	1868.35
Gas Chromatography	Neosartoricin_TMS_60	C=C(C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	1873.68
Gas Chromatography	Neosartoricin_TMS_61	C=C(C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	2957.84
Gas Chromatography	Neosartoricin_TMS_62	C=C(C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-23	1892.59
Gas Chromatography	Neosartoricin_TMS_1	CC(=O)C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O)=CC1=C2CC=C(C)C	standard polar	2025-10-23	2280.68
Gas Chromatography	Neosartoricin_TMS_2	CC(=O)C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	606.503
Gas Chromatography	Neosartoricin_TMS_3	CC(=O)C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C	standard polar	2025-10-23	1892.26
Gas Chromatography	Neosartoricin_TMS_4	CC(=O)C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C	standard polar	2025-10-23	2445.81
Gas Chromatography	Neosartoricin_TMS_5	CC(=O)C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O)=CC1=C2CC=C(C)C	standard polar	2025-10-23	1805.25
Gas Chromatography	Neosartoricin_TMS_6	C=C(C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	1528.29
Gas Chromatography	Neosartoricin_TMS_7	CC(=O)C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	3645.53
Gas Chromatography	Neosartoricin_TMS_8	CC(=O)C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O)=CC1=C2CC=C(C)C	standard polar	2025-10-23	3149.49
Gas Chromatography	Neosartoricin_TMS_9	CC(=O)C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C	standard polar	2025-10-23	2592.4
Gas Chromatography	Neosartoricin_TMS_10	CC(=O)C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C	standard polar	2025-10-23	1351.39
Gas Chromatography	Neosartoricin_TMS_11	C=C(C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	1422.59
Gas Chromatography	Neosartoricin_TMS_12	CC(=O)C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	1899.09
Gas Chromatography	Neosartoricin_TMS_13	CC(=O)C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	2485.57
Gas Chromatography	Neosartoricin_TMS_14	CC(=O)C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	2161.95
Gas Chromatography	Neosartoricin_TMS_15	C=C(C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-23	3497.98
Gas Chromatography	Neosartoricin_TMS_16	CC(=O)C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C	standard polar	2025-10-23	2066.18
Gas Chromatography	Neosartoricin_TMS_17	CC(=O)C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C	standard polar	2025-10-23	2974.0
Gas Chromatography	Neosartoricin_TMS_18	C=C(C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	1672.41
Gas Chromatography	Neosartoricin_TMS_19	CC(=O)C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C	standard polar	2025-10-23	3050.82
Gas Chromatography	Neosartoricin_TMS_20	C=C(C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	3310.66
Gas Chromatography	Neosartoricin_TMS_21	C=C(C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	1297.74
Gas Chromatography	Neosartoricin_TMS_22	CC(=O)C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	1312.25
Gas Chromatography	Neosartoricin_TMS_23	CC(=O)C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	1422.3
Gas Chromatography	Neosartoricin_TMS_24	CC(=O)C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	1479.7
Gas Chromatography	Neosartoricin_TMS_25	C=C(C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-23	2745.01
Gas Chromatography	Neosartoricin_TMS_26	CC(=O)C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C	standard polar	2025-10-23	1059.84
Gas Chromatography	Neosartoricin_TMS_27	CC(=O)C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C	standard polar	2025-10-23	388.32
Gas Chromatography	Neosartoricin_TMS_28	C=C(C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	2889.29
Gas Chromatography	Neosartoricin_TMS_29	CC(=O)C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C	standard polar	2025-10-23	1631.54
Gas Chromatography	Neosartoricin_TMS_30	C=C(C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	1708.3
Gas Chromatography	Neosartoricin_TMS_31	C=C(C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	2461.1
Gas Chromatography	Neosartoricin_TMS_32	CC(=O)C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	2118.44
Gas Chromatography	Neosartoricin_TMS_33	CC(=O)C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	2938.74
Gas Chromatography	Neosartoricin_TMS_34	C=C(C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-23	3523.98
Gas Chromatography	Neosartoricin_TMS_35	CC(=O)C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	2111.26
Gas Chromatography	Neosartoricin_TMS_36	C=C(C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-23	2010.76
Gas Chromatography	Neosartoricin_TMS_37	C=C(C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-23	2282.96
Gas Chromatography	Neosartoricin_TMS_38	CC(=O)C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C	standard polar	2025-10-23	3064.19
Gas Chromatography	Neosartoricin_TMS_39	C=C(C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	3042.12
Gas Chromatography	Neosartoricin_TMS_40	C=C(C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	1511.66
Gas Chromatography	Neosartoricin_TMS_41	C=C(C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	151.901
Gas Chromatography	Neosartoricin_TMS_42	CC(=O)C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	2793.55
Gas Chromatography	Neosartoricin_TMS_43	CC(=O)C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	1874.39
Gas Chromatography	Neosartoricin_TMS_44	C=C(C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-23	2076.83
Gas Chromatography	Neosartoricin_TMS_45	CC(=O)C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	3104.96
Gas Chromatography	Neosartoricin_TMS_46	C=C(C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-23	2844.6
Gas Chromatography	Neosartoricin_TMS_47	C=C(C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-23	1392.5
Gas Chromatography	Neosartoricin_TMS_48	CC(=O)C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C	standard polar	2025-10-23	-668.388
Gas Chromatography	Neosartoricin_TMS_49	C=C(C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	2474.54
Gas Chromatography	Neosartoricin_TMS_50	C=C(C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	2654.38
Gas Chromatography	Neosartoricin_TMS_51	C=C(C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	1991.15
Gas Chromatography	Neosartoricin_TMS_52	CC(=O)C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	1984.53
Gas Chromatography	Neosartoricin_TMS_53	C=C(C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-23	1586.39
Gas Chromatography	Neosartoricin_TMS_54	C=C(C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-23	1321.2
Gas Chromatography	Neosartoricin_TMS_55	C=C(C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-23	2121.53
Gas Chromatography	Neosartoricin_TMS_56	C=C(C=C(O)C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	1636.97
Gas Chromatography	Neosartoricin_TMS_57	CC(=O)C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	1385.48
Gas Chromatography	Neosartoricin_TMS_58	C=C(C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-23	1385.5
Gas Chromatography	Neosartoricin_TMS_59	C=C(C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-23	2366.6
Gas Chromatography	Neosartoricin_TMS_60	C=C(C=C(C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-23	2043.41
Gas Chromatography	Neosartoricin_TMS_61	C=C(C=C(O)C[C@]1(O[Si](C)(C)C)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C	standard polar	2025-10-23	2103.68
Gas Chromatography	Neosartoricin_TMS_62	C=C(C=C(C[C@]1(O)CC2=C(C(=O)[C@H]1OC(C)=O)C(O[Si](C)(C)C)=C1C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=CC1=C2CC=C(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-23	476.853

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

78437704

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139031680

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 Neosartoricin (MMDBc0012421)

MOL for #<Metabolite:0x00007f2e3a67a768>

3D MOL for #<Metabolite:0x00007f2e3a67a768>

3D SDF for #<Metabolite:0x00007f2e3a67a768>

3D-SDF for #<Metabolite:0x00007f2e3a67a768>

PDB for #<Metabolite:0x00007f2e3a67a768>

3D PDB for #<Metabolite:0x00007f2e3a67a768>

SMILES for #<Metabolite:0x00007f2e3a67a768>

INCHI for #<Metabolite:0x00007f2e3a67a768>

Structure for #<Metabolite:0x00007f2e3a67a768>

3D Structure for #<Metabolite:0x00007f2e3a67a768>