MiMeDB: Showing metabocard for Territrem B (MMDBc0012635)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 04:07:51 UTC

Update Date

2025-10-07 16:06:01 UTC

Metabolite ID

MMDBc0012635

Metabolite Identification

Common Name

Territrem B

Description

Territrem B is a meroterpenoid, a chemical class that combines elements of terpenes and other organic compounds, and is characterized as a significant metabolite derived from the fermentation extract of fungi such as Alternaria sp. This compound has been identified as an acetylcholinesterase (AChE) inhibitor, demonstrating notable activity against various biological targets, including the prevention of Phytophthora blight caused by Phytophthora capsici (PMID:40638848 ). The compound's structure allows it to bind to AChE, affecting both the active and peripheral sites, which contributes to its inhibitory potency (PMIDs:24900610, 24573600). Additionally, in vitro studies have shown that territrem B can reduce apoptotic cell death under normal culture conditions when used alongside other AChE inhibitors (PMID:32761307 ). Its unique conformational characteristics, particularly in the E-ring, are believed to influence its binding affinity and mechanism of action against AChE (PMID:40863500 ). Overall, territrem B represents a promising natural product with potential applications in both agricultural and medicinal fields due to its bioactive properties.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152106072D          

 40 45  0  0  1  0            999 V2000
   -0.6448    1.5408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0276    2.3096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9695    3.0411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4430    2.4350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5235   -0.4217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8755    1.7325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0680    2.8569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2451    2.6853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4014    1.6627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4417    0.2343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7521    1.6162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2671   -0.0854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7105    0.8439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6143    0.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0092    0.9369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5352    0.8672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1846    0.9137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9274    1.5930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2261    1.6860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2664    0.2576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0262    0.2631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0613    0.6841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6586    0.9834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9677    0.1646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1792    1.4986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6703    2.2723    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4703    1.1255    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9792    1.8566    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2781    1.5465    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5963   -0.3333    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5755   -0.5612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3646    2.4070    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0586    0.7512    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6183    2.4118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6989   -0.4450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4833    1.0067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7825    0.7835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7924    0.1878    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4949    2.2955    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8849    0.6361    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0  0  0  0
 15  9  2  0  0  0  0
 15 10  1  0  0  0  0
 16 13  1  0  0  0  0
 17 11  2  0  0  0  0
 17 15  1  0  0  0  0
 18 11  1  0  0  0  0
 18 16  2  0  0  0  0
 19  9  1  0  0  0  0
 20 10  2  0  0  0  0
 21 12  1  0  0  0  0
 22 12  1  0  0  0  0
 23 19  2  0  0  0  0
 23 20  1  0  0  0  0
 24 16  1  0  0  0  0
 25  1  1  0  0  0  0
 25  2  1  0  0  0  0
 25 22  1  0  0  0  0
 26  3  1  6  0  0  0
 26  7  1  0  0  0  0
 27 14  1  6  0  0  0
 27 21  1  0  0  0  0
 28  8  1  0  0  0  0
 28 25  1  0  0  0  0
 28 27  1  0  0  0  0
 29 13  1  0  0  0  0
 29 26  1  0  0  0  0
 29 27  1  0  0  0  0
 30 21  2  0  0  0  0
 31 24  2  0  0  0  0
 28 32  1  1  0  0  0
 29 33  1  1  0  0  0
 34  4  1  0  0  0  0
 34 19  1  0  0  0  0
 35  5  1  0  0  0  0
 35 20  1  0  0  0  0
 36  6  1  0  0  0  0
 36 23  1  0  0  0  0
 37 14  1  0  0  0  0
 37 22  1  0  0  0  0
 38 17  1  0  0  0  0
 38 24  1  0  0  0  0
 39 18  1  0  0  0  0
 39 26  1  0  0  0  0
 40 22  1  0  0  0  0
M  END


  Mrv1652305152106072D          

 40 45  0  0  1  0            999 V2000
   -0.6448    1.5408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0276    2.3096    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9695    3.0411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4430    2.4350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5235   -0.4217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8755    1.7325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0680    2.8569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2451    2.6853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4014    1.6627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4417    0.2343    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7521    1.6162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2671   -0.0854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7105    0.8439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6143    0.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0092    0.9369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5352    0.8672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1846    0.9137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9274    1.5930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2261    1.6860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2664    0.2576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0262    0.2631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0613    0.6841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6586    0.9834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9677    0.1646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1792    1.4986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6703    2.2723    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4703    1.1255    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9792    1.8566    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2781    1.5465    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5963   -0.3333    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5755   -0.5612    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3646    2.4070    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0586    0.7512    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6183    2.4118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6989   -0.4450    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4833    1.0067    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7825    0.7835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7924    0.1878    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4949    2.2955    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8849    0.6361    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0  0  0  0
 15  9  2  0  0  0  0
 15 10  1  0  0  0  0
 16 13  1  0  0  0  0
 17 11  2  0  0  0  0
 17 15  1  0  0  0  0
 18 11  1  0  0  0  0
 18 16  2  0  0  0  0
 19  9  1  0  0  0  0
 20 10  2  0  0  0  0
 21 12  1  0  0  0  0
 22 12  1  0  0  0  0
 23 19  2  0  0  0  0
 23 20  1  0  0  0  0
 24 16  1  0  0  0  0
 25  1  1  0  0  0  0
 25  2  1  0  0  0  0
 25 22  1  0  0  0  0
 26  3  1  6  0  0  0
 26  7  1  0  0  0  0
 27 14  1  6  0  0  0
 27 21  1  0  0  0  0
 28  8  1  0  0  0  0
 28 25  1  0  0  0  0
 28 27  1  0  0  0  0
 29 13  1  0  0  0  0
 29 26  1  0  0  0  0
 29 27  1  0  0  0  0
 30 21  2  0  0  0  0
 31 24  2  0  0  0  0
 28 32  1  1  0  0  0
 29 33  1  1  0  0  0
 34  4  1  0  0  0  0
 34 19  1  0  0  0  0
 35  5  1  0  0  0  0
 35 20  1  0  0  0  0
 36  6  1  0  0  0  0
 36 23  1  0  0  0  0
 37 14  1  0  0  0  0
 37 22  1  0  0  0  0
 38 17  1  0  0  0  0
 38 24  1  0  0  0  0
 39 18  1  0  0  0  0
 39 26  1  0  0  0  0
 40 22  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0012635

> <DATABASE_NAME>
MIME

> <SMILES>
[H]C12CC(=O)[C@@]3(CO1)[C@@](O)(CC[C@@]1(C)OC4=C(C[C@]31O)C(=O)OC(=C4)C1=CC(OC)=C(OC)C(OC)=C1)C2(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C29H34O10/c1-25(2)22-12-21(30)27(14-37-22)28(25,32)8-7-26(3)29(27,33)13-16-18(39-26)11-17(38-24(16)31)15-9-19(34-4)23(36-6)20(10-15)35-5/h9-11,22,32-33H,7-8,12-14H2,1-6H3/t22?,26-,27+,28-,29-/m1/s1

> <INCHI_KEY>
ATLGSZPVKAPATP-QNEAMCJZSA-N

> <FORMULA>
C29H34O10

> <MOLECULAR_WEIGHT>
542.581

> <EXACT_MASS>
542.215197295

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
73

> <JCHEM_AVERAGE_POLARIZABILITY>
56.46181243147564

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,11R,14R)-2,14-dihydroxy-11,15,15-trimethyl-7-(3,4,5-trimethoxyphenyl)-6,10,17-trioxapentacyclo[14.2.2.0^{1,14}.0^{2,11}.0^{4,9}]icosa-4(9),7-diene-5,19-dione

> <ALOGPS_LOGP>
1.82

> <JCHEM_LOGP>
1.3132805429999987

> <ALOGPS_LOGS>
-4.01

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.789528487968852

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.81947615247098

> <JCHEM_PKA_STRONGEST_BASIC>
-3.401757332893901

> <JCHEM_POLAR_SURFACE_AREA>
129.98000000000002

> <JCHEM_REFRACTIVITY>
138.87589999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.33e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,11R,14R)-2,14-dihydroxy-11,15,15-trimethyl-7-(3,4,5-trimethoxyphenyl)-6,10,17-trioxapentacyclo[14.2.2.0^{1,14}.0^{2,11}.0^{4,9}]icosa-4(9),7-diene-5,19-dione

> <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      -1.204   2.876   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.051   4.311   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.543   5.677   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      15.760   4.545   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      15.911  -0.787   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      16.568   3.234   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.860   5.333   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.324   5.013   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      11.949   3.104   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.025   0.437   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.871   3.017   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.499  -0.159   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.060   1.575   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.013   0.700   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.217   1.749   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.599   1.619   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.678   1.705   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.331   2.974   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      13.489   3.147   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      13.564   0.481   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.916   0.491   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.114   1.277   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      14.296   1.836   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.406   0.307   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.334   2.797   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.985   4.242   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.745   2.101   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.828   3.466   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.252   2.887   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       2.980  -0.622   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       6.674  -1.048   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       0.681   4.493   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       3.843   1.402   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      14.221   4.502   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      14.371  -0.831   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      15.835   1.879   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       1.461   1.463   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0       8.946   0.351   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0       6.524   4.285   0.000  0.00  0.00           O+0
HETATM   40  H   UNK     0      -1.652   1.187   0.000  0.00  0.00           H+0
CONECT    1   25                                                            
CONECT    2   25                                                            
CONECT    3   26                                                            
CONECT    4   34                                                            
CONECT    5   35                                                            
CONECT    6   36                                                            
CONECT    7    8   26                                                       
CONECT    8    7   28                                                       
CONECT    9   15   19                                                       
CONECT   10   15   20                                                       
CONECT   11   17   18                                                       
CONECT   12   21   22                                                       
CONECT   13   16   29                                                       
CONECT   14   27   37                                                       
CONECT   15    9   10   17                                                  
CONECT   16   13   18   24                                                  
CONECT   17   11   15   38                                                  
CONECT   18   11   16   39                                                  
CONECT   19    9   23   34                                                  
CONECT   20   10   23   35                                                  
CONECT   21   12   27   30                                                  
CONECT   22   12   25   37   40                                             
CONECT   23   19   20   36                                                  
CONECT   24   16   31   38                                                  
CONECT   25    1    2   22   28                                             
CONECT   26    3    7   29   39                                             
CONECT   27   14   21   28   29                                             
CONECT   28    8   25   27   32                                             
CONECT   29   13   26   27   33                                             
CONECT   30   21                                                            
CONECT   31   24                                                            
CONECT   32   28                                                            
CONECT   33   29                                                            
CONECT   34    4   19                                                       
CONECT   35    5   20                                                       
CONECT   36    6   23                                                       
CONECT   37   14   22                                                       
CONECT   38   17   24                                                       
CONECT   39   18   26                                                       
CONECT   40   22                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   90    0
END

Synonyms

Not Available

Molecular Formula

C₂₉H₃₄O₁₀

Average Mass

542.581

Monoisotopic Mass

542.215197295

IUPAC Name

(1S,2S,11R,14R)-2,14-dihydroxy-11,15,15-trimethyl-7-(3,4,5-trimethoxyphenyl)-6,10,17-trioxapentacyclo[14.2.2.0^{1,14}.0^{2,11}.0^{4,9}]icosa-4(9),7-diene-5,19-dione

Traditional Name

(1S,2S,11R,14R)-2,14-dihydroxy-11,15,15-trimethyl-7-(3,4,5-trimethoxyphenyl)-6,10,17-trioxapentacyclo[14.2.2.0^{1,14}.0^{2,11}.0^{4,9}]icosa-4(9),7-diene-5,19-dione

CAS Registry Number

Not Available

SMILES

[H]C12CC(=O)[C@@]3(CO1)[C@@](O)(CC[C@@]1(C)OC4=C(C[C@]31O)C(=O)OC(=C4)C1=CC(OC)=C(OC)C(OC)=C1)C2(C)C

InChI Identifier

InChI=1S/C29H34O10/c1-25(2)22-12-21(30)27(14-37-22)28(25,32)8-7-26(3)29(27,33)13-16-18(39-26)11-17(38-24(16)31)15-9-19(34-4)23(36-6)20(10-15)35-5/h9-11,22,32-33H,7-8,12-14H2,1-6H3/t22?,26-,27+,28-,29-/m1/s1

InChI Key

ATLGSZPVKAPATP-QNEAMCJZSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthopyrans

Sub Class

Not Available

Direct Parent

Naphthopyrans

Alternative Parents

Substituents

Naphthopyran
Naphthalene
Phenoxy compound
Anisole
Phenol ether
Methoxybenzene
Alkyl aryl ether
Pyranone
Monocyclic benzene moiety
Oxane
Pyran
Benzenoid
Heteroaromatic compound
Cyclic alcohol
Vinylogous ester
Tertiary alcohol
Lactone
Ketone
Oxacycle
Ether
Dialkyl ether
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Carbonyl group
Alcohol
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.053 g/L	ALOGPS
logP	1.82	ALOGPS
logP	1.31	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	12.82	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	129.98 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	138.88 m³·mol⁻¹	ChemAxon
Polarizability	56.46 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_1_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

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

This table shows at most 5 pathways. For the full list of associated pathways:

See All Associated Bacterial Pathways

Name	SMPDB/PathBank	Species

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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139586514

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

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 Territrem B (MMDBc0012635)

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