MiMeDB: Showing metabocard for Altertoxin III (MMDBc0013190)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-05-15 04:32:14 UTC

Update Date

2025-10-07 16:06:05 UTC

Metabolite ID

MMDBc0013190

Metabolite Identification

Common Name

Altertoxin III

Description

Altertoxin III is a hydroxyperylenequinone compound, classified within the broader category of secondary metabolites. It has been identified as a notable metabolite through various biochemical assays and isolation techniques. The noncytotoxic concentration range of altertoxin III has been established to be between 0.2 and 0.04 micrograms/ml in metabolic communication assays (PMID:2913335 ). Additionally, its biological activity has been investigated in the context of Epstein-Barr virus early antigen induction and murine fibroblast cell transformation systems, where it was compared alongside altertoxin I (PMID:20702343 ). The structural characterization of altertoxin III, along with other altertoxins, was achieved using advanced analytical techniques such as mass spectrometry, infrared, ultraviolet, and proton magnetic resonance spectroscopy, confirming its classification as a hydroxyperylenequinone (PMID:3535674 ). This compound's unique chemical properties and biological activities suggest potential implications in further research, particularly in the fields of toxicology and pharmacology.

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004161508372D          

 26 32  0  0  0  0            999 V2000
    2.0328   -3.1569    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5411   -2.4944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7215   -2.5891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2298   -1.9266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5576   -1.1696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0659   -0.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7537   -0.6018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5732   -0.6964    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2454    0.0607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9176    0.8177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4093    1.4802    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0980    0.9124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2298    1.6694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2620    2.3319    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0493    1.7641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5411    1.1016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2132    0.3446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7050   -0.3179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5245   -0.2232    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3441   -0.1286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0163   -0.8857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6884   -1.6427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1802   -2.3052    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8689   -1.7374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3772   -1.0749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3937    0.2499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
  2 24  1  0  0  0  0
 24 25  2  0  0  0  0
  5 25  1  0  0  0  0
 18 25  1  0  0  0  0
 17 26  2  0  0  0  0
  6 26  1  0  0  0  0
 12 26  1  0  0  0  0
M  END


  Mrv1533004161508372D          

 26 32  0  0  0  0            999 V2000
    2.0328   -3.1569    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5411   -2.4944    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7215   -2.5891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2298   -1.9266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5576   -1.1696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0659   -0.5071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7537   -0.6018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5732   -0.6964    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2454    0.0607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9176    0.8177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4093    1.4802    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0980    0.9124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2298    1.6694    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2620    2.3319    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0493    1.7641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5411    1.1016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2132    0.3446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7050   -0.3179    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5245   -0.2232    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3441   -0.1286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0163   -0.8857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6884   -1.6427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1802   -2.3052    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8689   -1.7374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3772   -1.0749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3937    0.2499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
  2 24  1  0  0  0  0
 24 25  2  0  0  0  0
  5 25  1  0  0  0  0
 18 25  1  0  0  0  0
 17 26  2  0  0  0  0
  6 26  1  0  0  0  0
 12 26  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0013190

> <DATABASE_NAME>
MIME

> <SMILES>
OC1=CC=C2C3C4OC4C(=O)C4=C(O)C=CC(C5C6OC6C(=O)C1=C25)=C34

> <INCHI_IDENTIFIER>
InChI=1S/C20H12O6/c21-7-3-1-5-9-12(18-20(26-18)15(23)13(7)9)6-2-4-8(22)14-10(6)11(5)17-19(25-17)16(14)24/h1-4,11-12,17-22H

> <INCHI_KEY>
CJGDIPRCPKGNLW-UHFFFAOYSA-N

> <FORMULA>
C20H12O6

> <MOLECULAR_WEIGHT>
348.31

> <EXACT_MASS>
348.063388106

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
33.61847003371763

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
8,18-dihydroxy-4,14-dioxaheptacyclo[10.8.1.1²,⁷.0³,⁵.0¹³,¹⁵.0¹⁷,²¹.0¹¹,²²]docosa-1(21),7(22),8,10,17,19-hexaene-6,16-dione

> <ALOGPS_LOGP>
2.67

> <JCHEM_LOGP>
2.7376487486666665

> <ALOGPS_LOGS>
-2.86

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.784527712268808

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.182466159238341

> <JCHEM_PKA_STRONGEST_BASIC>
-3.967131448291798

> <JCHEM_POLAR_SURFACE_AREA>
99.66

> <JCHEM_REFRACTIVITY>
88.31959999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.84e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
8,18-dihydroxy-4,14-dioxaheptacyclo[10.8.1.1²,⁷.0³,⁵.0¹³,¹⁵.0¹⁷,²¹.0¹¹,²²]docosa-1(21),7(22),8,10,17,19-hexaene-6,16-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  O   UNK     0       3.795  -5.893   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       2.877  -4.656   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.347  -4.833   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.429  -3.596   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.041  -2.183   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.123  -0.947   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.407  -1.123   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -2.937  -1.300   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -2.325   0.113   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.713   1.526   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -2.631   2.763   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -0.183   1.703   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.429   3.116   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -0.489   4.353   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       1.959   3.293   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.877   2.056   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.265   0.643   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.183  -0.593   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.712  -0.417   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.242  -0.240   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.630  -1.653   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.018  -3.066   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       5.936  -4.303   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       3.489  -3.243   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.571  -2.007   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.735   0.467   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   24                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   25                                                  
CONECT    6    5    7   26                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7    9                                                       
CONECT    9    8    7   10                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   26                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   26                                                  
CONECT   18   17   19   25                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19   21                                                       
CONECT   21   20   19   22                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22    2   25                                                  
CONECT   25   24    5   18                                                  
CONECT   26   17    6   12                                                  
MASTER        0    0    0    0    0    0    0    0   26    0   64    0
END

Synonyms

Not Available

Molecular Formula

C₂₀H₁₂O₆

Average Mass

348.31

Monoisotopic Mass

348.063388106

IUPAC Name

8,18-dihydroxy-4,14-dioxaheptacyclo[10.8.1.1²,⁷.0³,⁵.0¹³,¹⁵.0¹⁷,²¹.0¹¹,²²]docosa-1(21),7(22),8,10,17,19-hexaene-6,16-dione

Traditional Name

8,18-dihydroxy-4,14-dioxaheptacyclo[10.8.1.1²,⁷.0³,⁵.0¹³,¹⁵.0¹⁷,²¹.0¹¹,²²]docosa-1(21),7(22),8,10,17,19-hexaene-6,16-dione

CAS Registry Number

Not Available

SMILES

OC1=CC=C2C3C4OC4C(=O)C4=C(O)C=CC(C5C6OC6C(=O)C1=C25)=C34

InChI Identifier

InChI=1S/C20H12O6/c21-7-3-1-5-9-12(18-20(26-18)15(23)13(7)9)6-2-4-8(22)14-10(6)11(5)17-19(25-17)16(14)24/h1-4,11-12,17-22H

InChI Key

CJGDIPRCPKGNLW-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenanthrenes and derivatives. These are polycyclic compounds containing a phenanthrene moiety, which is a tricyclic aromatic compound with three non-linearly fused benzene.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Phenanthrenes and derivatives

Sub Class

Not Available

Direct Parent

Phenanthrenes and derivatives

Alternative Parents

Substituents

Anthracene
Phenanthrene
Tetralin
Aryl alkyl ketone
Aryl ketone
1-hydroxy-2-unsubstituted benzenoid
Phenol
Vinylogous acid
Ketone
Dialkyl ether
Oxirane
Ether
Oxacycle
Organoheterocyclic compound
Organic oxide
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
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	0.48 g/L	ALOGPS
logP	2.67	ALOGPS
logP	2.74	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	8.18	ChemAxon
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	99.66 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	88.32 m³·mol⁻¹	ChemAxon
Polarizability	33.62 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_2_1) - 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
MS	Mass Spectrum (Electron Ionization)	Not Available	2022-08-06	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; Human supragingival plaque	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

78169696

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 Altertoxin III (MMDBc0013190)

MOL for #<Metabolite:0x00007f28890c97f8>

3D MOL for #<Metabolite:0x00007f28890c97f8>

3D SDF for #<Metabolite:0x00007f28890c97f8>

3D-SDF for #<Metabolite:0x00007f28890c97f8>

PDB for #<Metabolite:0x00007f28890c97f8>

3D PDB for #<Metabolite:0x00007f28890c97f8>

SMILES for #<Metabolite:0x00007f28890c97f8>

INCHI for #<Metabolite:0x00007f28890c97f8>

Structure for #<Metabolite:0x00007f28890c97f8>

3D Structure for #<Metabolite:0x00007f28890c97f8>