MiMeDB: Showing metabocard for BZR-cotoxin IV (MMDBc0013989)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 05:09:06 UTC

Update Date

2025-10-07 16:06:13 UTC

Metabolite ID

MMDBc0013989

Metabolite Identification

Common Name

BZR-cotoxin IV

Description

BZR-cotoxin IV is a cyclic peptide, a class of compounds characterized by a peptide chain that forms a ring structure. This metabolite has been identified in the context of fungal endophytes, specifically isolated from Bipolaris sorokiniana LK12, alongside other bioactive compounds such as sorokiniol and BZR-cotoxin I (PMID:27277006 ). Cyclic peptides like BZR-cotoxin IV are known for their diverse biological activities, which can include antimicrobial, antifungal, and cytotoxic properties, making them of interest in pharmacological research. The unique structural features of cyclic peptides often contribute to their stability and bioactivity, enhancing their potential as therapeutic agents. Understanding the chemistry and biological implications of BZR-cotoxin IV may lead to novel applications in medicine and agriculture, particularly in developing new strategies for disease management in crops or novel drug formulations. Further studies are warranted to elucidate the full spectrum of biological activities and mechanisms of action associated with BZR-cotoxin IV.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652305152107092D          

 72 74  0  0  1  0            999 V2000
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 40 72  1  6  0  0  0
M  END


  Mrv1652305152107092D          

 72 74  0  0  1  0            999 V2000
    2.8856    1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 50 41  2  0  0  0  0
 51 35  1  0  0  0  0
 51 44  2  0  0  0  0
 52 38  1  0  0  0  0
 52 42  2  0  0  0  0
 53 39  1  0  0  0  0
 53 43  2  0  0  0  0
 54 10  1  0  0  0  0
 54 36  1  0  0  0  0
 54 46  1  0  0  0  0
 37 55  1  4  0  0  0
 41 56  1  4  0  0  0
 42 57  1  4  0  0  0
 43 58  1  4  0  0  0
 44 59  1  4  0  0  0
 60 45  1  0  0  0  0
 61 46  2  0  0  0  0
 62 47  2  0  0  0  0
 63 40  1  0  0  0  0
 63 47  1  0  0  0  0
 29 64  1  6  0  0  0
 30 65  1  1  0  0  0
 31 66  1  1  0  0  0
 34 67  1  6  0  0  0
 35 68  1  6  0  0  0
 36 69  1  6  0  0  0
 38 70  1  6  0  0  0
 39 71  1  6  0  0  0
 40 72  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0013989

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@](C)(CC)[C@]1([H])N=C(O)[C@]([H])(CC2=CC=CC=C2)N=C(O)[C@@]([H])(C)N=C(O)CN=C(O)[C@@]([H])(N=C(O)[C@]([H])(CC2=CC=CC=C2)N=C(O)[C@]([H])(CC(C)C)N(C)C(=O)[C@@]([H])(OC1=O)C(C)C)[C@@]([H])(C)CC

> <INCHI_IDENTIFIER>
InChI=1S/C47H69N7O9/c1-11-29(7)38-45(60)48-26-37(55)49-31(9)41(56)50-34(24-32-19-15-13-16-20-32)43(58)53-39(30(8)12-2)47(62)63-40(28(5)6)46(61)54(10)36(23-27(3)4)44(59)51-35(42(57)52-38)25-33-21-17-14-18-22-33/h13-22,27-31,34-36,38-40H,11-12,23-26H2,1-10H3,(H,48,60)(H,49,55)(H,50,56)(H,51,59)(H,52,57)(H,53,58)/t29-,30-,31+,34-,35-,36-,38-,39-,40-/m0/s1

> <INCHI_KEY>
HYRIAKASPMEAMO-VKJNQXOZSA-N

> <FORMULA>
C47H69N7O9

> <MOLECULAR_WEIGHT>
876.109

> <EXACT_MASS>
875.51567683

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
132

> <JCHEM_AVERAGE_POLARIZABILITY>
93.88646984436674

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S,6S,9R,15S,18S,21S,24S)-6,18-dibenzyl-3,15-bis[(2S)-butan-2-yl]-5,8,11,14,17,20-hexahydroxy-9,22-dimethyl-21-(2-methylpropyl)-24-(propan-2-yl)-1-oxa-4,7,10,13,16,19,22-heptaazacyclotetracosa-4,7,10,13,16,19-hexaene-2,23-dione

> <ALOGPS_LOGP>
4.38

> <JCHEM_LOGP>
9.127931096333334

> <ALOGPS_LOGS>
-5.14

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
3.620428176847179

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.1807032953844083

> <JCHEM_PKA_STRONGEST_BASIC>
1.7579502049771485

> <JCHEM_POLAR_SURFACE_AREA>
242.14999999999995

> <JCHEM_REFRACTIVITY>
239.06280000000018

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.39e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,6S,9R,15S,18S,21S,24S)-6,18-dibenzyl-3,15-bis[(2S)-butan-2-yl]-5,8,11,14,17,20-hexahydroxy-24-isopropyl-9,22-dimethyl-21-(2-methylpropyl)-1-oxa-4,7,10,13,16,19,22-heptaazacyclotetracosa-4,7,10,13,16,19-hexaene-2,23-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       5.386   3.644   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.366 -12.065   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -6.498  -2.757   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.612  -0.871   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.345  -9.473   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.655  -8.139   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.322   3.352   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.391 -11.268   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.211  -3.778   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.182  -3.937   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.899   4.042   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.967 -10.578   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.171 -12.993   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.881   5.767   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.505 -12.223   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.837 -12.223   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -3.215   4.997   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.548   4.997   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.505 -10.683   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.837 -10.683   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -3.215   3.457   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.548   3.457   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -3.921  -3.448   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.171  -8.373   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.881   1.147   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.635  -0.420   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -5.010  -2.359   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -2.115  -8.139   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.810   2.953   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.480 -10.179   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.724  -4.177   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       7.171  -9.913   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -1.881   2.687   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.837  -7.603   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -0.548   0.377   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -2.434  -3.049   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       7.405  -1.754   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       3.209   1.466   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       2.081  -8.692   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -1.345  -6.806   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       7.325  -5.664   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       0.786   1.147   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       4.504  -8.373   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -2.035  -1.562   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       4.696   1.067   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -2.115  -5.472   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       0.594  -8.293   0.000  0.00  0.00           C+0
HETATM   48  N   UNK     0       5.095  -0.420   0.000  0.00  0.00           N+0
HETATM   49  N   UNK     0       6.635  -3.088   0.000  0.00  0.00           N+0
HETATM   50  N   UNK     0       5.837  -6.063   0.000  0.00  0.00           N+0
HETATM   51  N   UNK     0      -0.548  -1.163   0.000  0.00  0.00           N+0
HETATM   52  N   UNK     0       2.120   0.377   0.000  0.00  0.00           N+0
HETATM   53  N   UNK     0       3.170  -7.603   0.000  0.00  0.00           N+0
HETATM   54  N   UNK     0      -1.345  -4.138   0.000  0.00  0.00           N+0
HETATM   55  O   UNK     0       8.945  -1.754   0.000  0.00  0.00           O+0
HETATM   56  O   UNK     0       8.414  -6.753   0.000  0.00  0.00           O+0
HETATM   57  O   UNK     0       0.786   2.687   0.000  0.00  0.00           O+0
HETATM   58  O   UNK     0       4.504  -9.913   0.000  0.00  0.00           O+0
HETATM   59  O   UNK     0      -3.124  -0.473   0.000  0.00  0.00           O+0
HETATM   60  O   UNK     0       5.785   2.156   0.000  0.00  0.00           O+0
HETATM   61  O   UNK     0      -3.655  -5.472   0.000  0.00  0.00           O+0
HETATM   62  O   UNK     0      -0.495  -9.382   0.000  0.00  0.00           O+0
HETATM   63  O   UNK     0       0.195  -6.806   0.000  0.00  0.00           O+0
HETATM   64  H   UNK     0       2.411   4.441   0.000  0.00  0.00           H+0
HETATM   65  H   UNK     0       2.878 -11.667   0.000  0.00  0.00           H+0
HETATM   66  H   UNK     0       8.122  -2.689   0.000  0.00  0.00           H+0
HETATM   67  H   UNK     0       7.171  -6.833   0.000  0.00  0.00           H+0
HETATM   68  H   UNK     0      -1.881  -0.393   0.000  0.00  0.00           H+0
HETATM   69  H   UNK     0      -2.832  -4.537   0.000  0.00  0.00           H+0
HETATM   70  H   UNK     0       1.721   1.864   0.000  0.00  0.00           H+0
HETATM   71  H   UNK     0       3.569  -9.090   0.000  0.00  0.00           H+0
HETATM   72  H   UNK     0      -0.575  -8.139   0.000  0.00  0.00           H+0
CONECT    1   11                                                            
CONECT    2   12                                                            
CONECT    3   27                                                            
CONECT    4   27                                                            
CONECT    5   28                                                            
CONECT    6   28                                                            
CONECT    7   29                                                            
CONECT    8   30                                                            
CONECT    9   31                                                            
CONECT   10   54                                                            
CONECT   11    1   29                                                       
CONECT   12    2   30                                                       
CONECT   13   15   16                                                       
CONECT   14   17   18                                                       
CONECT   15   13   19                                                       
CONECT   16   13   20                                                       
CONECT   17   14   21                                                       
CONECT   18   14   22                                                       
CONECT   19   15   32                                                       
CONECT   20   16   32                                                       
CONECT   21   17   33                                                       
CONECT   22   18   33                                                       
CONECT   23   27   36                                                       
CONECT   24   32   34                                                       
CONECT   25   33   35                                                       
CONECT   26   37   48                                                       
CONECT   27    3    4   23                                                  
CONECT   28    5    6   40                                                  
CONECT   29    7   11   38   64                                             
CONECT   30    8   12   39   65                                             
CONECT   31    9   41   49   66                                             
CONECT   32   19   20   24                                                  
CONECT   33   21   22   25                                                  
CONECT   34   24   43   50   67                                             
CONECT   35   25   42   51   68                                             
CONECT   36   23   44   54   69                                             
CONECT   37   26   49   55                                                  
CONECT   38   29   45   52   70                                             
CONECT   39   30   47   53   71                                             
CONECT   40   28   46   63   72                                             
CONECT   41   31   50   56                                                  
CONECT   42   35   52   57                                                  
CONECT   43   34   53   58                                                  
CONECT   44   36   51   59                                                  
CONECT   45   38   48   60                                                  
CONECT   46   40   54   61                                                  
CONECT   47   39   62   63                                                  
CONECT   48   26   45                                                       
CONECT   49   31   37                                                       
CONECT   50   34   41                                                       
CONECT   51   35   44                                                       
CONECT   52   38   42                                                       
CONECT   53   39   43                                                       
CONECT   54   10   36   46                                                  
CONECT   55   37                                                            
CONECT   56   41                                                            
CONECT   57   42                                                            
CONECT   58   43                                                            
CONECT   59   44                                                            
CONECT   60   45                                                            
CONECT   61   46                                                            
CONECT   62   47                                                            
CONECT   63   40   47                                                       
CONECT   64   29                                                            
CONECT   65   30                                                            
CONECT   66   31                                                            
CONECT   67   34                                                            
CONECT   68   35                                                            
CONECT   69   36                                                            
CONECT   70   38                                                            
CONECT   71   39                                                            
CONECT   72   40                                                            
MASTER        0    0    0    0    0    0    0    0   72    0  148    0
END

Synonyms

Not Available

Molecular Formula

C₄₇H₆₉N₇O₉

Average Mass

876.109

Monoisotopic Mass

875.51567683

IUPAC Name

(3S,6S,9R,15S,18S,21S,24S)-6,18-dibenzyl-3,15-bis[(2S)-butan-2-yl]-5,8,11,14,17,20-hexahydroxy-9,22-dimethyl-21-(2-methylpropyl)-24-(propan-2-yl)-1-oxa-4,7,10,13,16,19,22-heptaazacyclotetracosa-4,7,10,13,16,19-hexaene-2,23-dione

Traditional Name

(3S,6S,9R,15S,18S,21S,24S)-6,18-dibenzyl-3,15-bis[(2S)-butan-2-yl]-5,8,11,14,17,20-hexahydroxy-24-isopropyl-9,22-dimethyl-21-(2-methylpropyl)-1-oxa-4,7,10,13,16,19,22-heptaazacyclotetracosa-4,7,10,13,16,19-hexaene-2,23-dione

CAS Registry Number

Not Available

SMILES

[H][C@](C)(CC)[C@]1([H])N=C(O)[C@]([H])(CC2=CC=CC=C2)N=C(O)[C@@]([H])(C)N=C(O)CN=C(O)[C@@]([H])(N=C(O)[C@]([H])(CC2=CC=CC=C2)N=C(O)[C@]([H])(CC(C)C)N(C)C(=O)[C@@]([H])(OC1=O)C(C)C)[C@@]([H])(C)CC

InChI Identifier

InChI=1S/C47H69N7O9/c1-11-29(7)38-45(60)48-26-37(55)49-31(9)41(56)50-34(24-32-19-15-13-16-20-32)43(58)53-39(30(8)12-2)47(62)63-40(28(5)6)46(61)54(10)36(23-27(3)4)44(59)51-35(42(57)52-38)25-33-21-17-14-18-22-33/h13-22,27-31,34-36,38-40H,11-12,23-26H2,1-10H3,(H,48,60)(H,49,55)(H,50,56)(H,51,59)(H,52,57)(H,53,58)/t29-,30-,31+,34-,35-,36-,38-,39-,40-/m0/s1

InChI Key

HYRIAKASPMEAMO-VKJNQXOZSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclic depsipeptides. These are natural or synthetic compounds having sequences of amino and hydroxy carboxylic acid residues (usually α-amino and α-hydroxy acids) connected in a ring. The residues are commonly but not necessarily regularly alternating.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Peptidomimetics

Sub Class

Depsipeptides

Direct Parent

Cyclic depsipeptides

Alternative Parents

Substituents

Cyclic depsipeptide
Macrolide lactam
Alpha-amino acid ester
Macrolactam
Macrolide
Alpha-amino acid or derivatives
Monocyclic benzene moiety
Benzenoid
Tertiary carboxylic acid amide
Cyclic carboximidic acid
Carboxamide group
Carboxylic acid ester
Lactam
Lactone
Propargyl-type 1,3-dipolar organic compound
Organic 1,3-dipolar compound
Monocarboxylic acid or derivatives
Azacycle
Oxacycle
Organoheterocyclic compound
Polyol
Carboxylic acid derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
Organic nitrogen compound
Carbonyl group
Organopnictogen compound
Hydrocarbon derivative
Organonitrogen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.0064 g/L	ALOGPS
logP	4.38	ALOGPS
logP	9.13	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	3.18	ChemAxon
pKa (Strongest Basic)	1.76	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	242.15 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	239.06 m³·mol⁻¹	ChemAxon
Polarizability	93.89 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	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 LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	Not Available	2022-08-10	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	Not Available	2022-08-10	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	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

78441285

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139586891

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 BZR-cotoxin IV (MMDBc0013989)

MOL for #<Metabolite:0x00007f6d708e5280>

3D MOL for #<Metabolite:0x00007f6d708e5280>

3D SDF for #<Metabolite:0x00007f6d708e5280>

3D-SDF for #<Metabolite:0x00007f6d708e5280>

PDB for #<Metabolite:0x00007f6d708e5280>

3D PDB for #<Metabolite:0x00007f6d708e5280>

SMILES for #<Metabolite:0x00007f6d708e5280>

INCHI for #<Metabolite:0x00007f6d708e5280>

Structure for #<Metabolite:0x00007f6d708e5280>

3D Structure for #<Metabolite:0x00007f6d708e5280>